#apoe4 — Public Fediverse posts
Live and recent posts from across the Fediverse tagged #apoe4, aggregated by home.social.
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https://www.europesays.com/it/589585/ Alzheimer, un esame del sangue può anticipare il rischio di declino cognitivo #Alzheimer #APOE4 #BetaAmiloide #biomarcatore #DeficitCognitivo #Health #IT #Italia #Italy #PTau217 #PETAmiloide #plasma #rischio #Salute #tau
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DATE: July 17, 2026 at 07:00AM
SOURCE: PSYPOST.ORG** Research quality varies widely from fantastic to small exploratory studies. Please check research methods when conclusions are very important to you. **
-------------------------------------------------TITLE: Study finds complex association between dietary fat intake and brain atrophy in older adults
An analysis of Vanderbilt Memory and Aging Project study data found that a high-fat diet was associated with a faster reduction in temporal lobe volume in cognitively unimpaired participants. However, in individuals with mild cognitive impairment, adherence to the same type of diet was associated with a slower enlargement of the inferior lateral ventricle area of the brain. The paper was published in Alzheimer’s Dementia.
As people age, their risk of developing dementia increases, although dementia is not an inevitable part of normal aging. Dementias are disorders involving progressive declines in memory, reasoning, language, judgment, or other cognitive abilities that interfere with daily life. The most common type of dementia is Alzheimer’s disease. This disease is associated with an abnormal accumulation of proteins called amyloid plaques and tau tangles in the brain.
Aside from Alzheimer’s disease, dementias also include vascular dementia (resulting from reduced blood flow or damage to brain tissues caused by strokes or small-vessel disease), Lewy body dementia, frontotemporal dementia, and others. The exact causes of dementias are not fully understood, but scientists believe that they are caused by a complex interaction between genetic predispositions and the environment. Up to 40% of the risk is attributable to modifiable lifestyle factors, including diet.
Lei Fan, a researcher at Vanderbilt University Medical Center, and colleagues examined whether dietary fat intake was associated with changes in gray matter atrophy rates detected using neuroimaging over time in older adults. They were also interested in interactions of these changes with cognitive status, their dependence on sex, and whether an individual is a carrier of the APOE ε4 gene variant. APOE ε4 is a gene variant that increases the risk of developing Alzheimer’s disease.
These researchers analyzed data from the Vanderbilt Memory and Aging Project. This is a longitudinal observational study that investigates vascular and neurological health and the aging of older individuals free of clinical dementia at enrollment. The data came from 758 participants of the Vanderbilt Memory and Aging Project Legacy Cohort and the Expansion Cohort. Their average age was 67 years. About 47% were men, and 35% were carriers of the APOE ε4 gene variant.
The Legacy Cohort recruitment began in September 2012, and all participants were required to be at least 60 years old, have adequate auditory and visual acuity, and have a reliable study partner. The Expansion Cohort recruited individuals aged 50 years or older and recruitment started in August 2021.
Depending on their assessed cognitive status, participants were categorized as either cognitively unimpaired or mildly cognitively impaired. Participants completed magnetic resonance imaging of their brains at enrollment in the study and on at least one more occasion. They also completed a questionnaire called the Quick Food Scan fat screener, allowing study authors to estimate their total dietary fat intake. Data were collected at the start of the study, 18 months later, and then 3, 5, 7, and 9 years after the start of the study.
Results showed that, cross-sectionally at baseline, neither total fat intake nor the percentage of energy derived from fats was associated with the total volume of the brain’s gray matter or with the volumes of specific lobes of the brain. However, longitudinally over an average of 4.6 years, individuals deriving a higher percentage of their energy from fats tended to show a slower rate of enlargement of the interior lateral ventricle volume. This association was weak, and it disappeared when study authors corrected their detection thresholds for multiple comparisons.
Further analysis showed that the percentage of energy derived from fat was associated with a faster reduction in temporal lobe volume in cognitively unimpaired participants. In contrast, in individuals with mild cognitive impairment, a higher percentage of energy derived from fat was associated with slower enlargement of the inferior lateral ventricle region of the brain.
The temporal lobe is a region of the brain that supports memory and language. The inferior lateral ventricles are spaces filled with fluids near the temporal lobe. Their enlargement reflects the loss of brain tissue in surrounding areas.
“A high-fat diet is associated with accelerated gray matter atrophy, particularly in [Alzheimer’s disease-relevant] regions such as the temporal lobe, in [cognitively unimpaired] adults, but is associated with slower atrophy in individuals with existing [mild cognitive impairment], which is mainly driven by APOE ε4 carriers and/or female individuals,” the study authors concluded.
“Different mechanisms may be involved in the fat–neurodegeneration relationship across cognitive statuses. Halted atrophy associated with a high-fat diet, observed exclusively in individuals with existing [mild cognitive impairment], may reflect the role of fat as part of a compensatory mechanism in response to progressive [Alzheimer’s disease] pathology and metabolic challenges.”
The study contributes to the scientific understanding of the links between diet and mental health. However, it should be noted that the design of this study does not allow any causal inferences to be derived from the results. It is also limited by the fact that the cohort was predominantly white, well-educated, and relatively healthy. Additionally, a single self-reported dietary fat assessment at baseline may not reflect long-term variations in dietary intake.
The paper, “High-fat diet is associated with accelerated gray matter atrophy in cognitively unimpaired older adults but slower atrophy in individuals with existing mild cognitive impairment,” was authored by Lei Fan, Yunyi Sun, Dandan Liu, W. Hudson Robb, Kimberly R. Pechman, Niranjana Shashikumar, Yukti Vyas, Bennett A. Landman, Timothy J. Hohman, and Angela L. Jefferson.
-------------------------------------------------
Private, vetted email list for mental health professionals: https://www.clinicians-exchange.org
Unofficial Psychology Today Xitter to toot feed at Psych Today Unofficial Bot @PTUnofficialBot
-------------------------------------------------
#psychology #counseling #socialwork #psychotherapy @psychotherapist @psychotherapists @psychology @socialpsych @socialwork @psychiatry #mentalhealth #psychiatry #healthcare #depression #psychotherapist #HighFatDiet #BrainAtrophy #TemporalLobe #MildCognitiveImpairment #Alzheimer'sDiseaseResearch #APOE4 #CognitiveHealth #DementiaPrevention #Neuroimaging #VanderbiltMemoryAgingProject
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DATE: July 17, 2026 at 07:00AM
SOURCE: PSYPOST.ORG** Research quality varies widely from fantastic to small exploratory studies. Please check research methods when conclusions are very important to you. **
-------------------------------------------------TITLE: Study finds complex association between dietary fat intake and brain atrophy in older adults
An analysis of Vanderbilt Memory and Aging Project study data found that a high-fat diet was associated with a faster reduction in temporal lobe volume in cognitively unimpaired participants. However, in individuals with mild cognitive impairment, adherence to the same type of diet was associated with a slower enlargement of the inferior lateral ventricle area of the brain. The paper was published in Alzheimer’s Dementia.
As people age, their risk of developing dementia increases, although dementia is not an inevitable part of normal aging. Dementias are disorders involving progressive declines in memory, reasoning, language, judgment, or other cognitive abilities that interfere with daily life. The most common type of dementia is Alzheimer’s disease. This disease is associated with an abnormal accumulation of proteins called amyloid plaques and tau tangles in the brain.
Aside from Alzheimer’s disease, dementias also include vascular dementia (resulting from reduced blood flow or damage to brain tissues caused by strokes or small-vessel disease), Lewy body dementia, frontotemporal dementia, and others. The exact causes of dementias are not fully understood, but scientists believe that they are caused by a complex interaction between genetic predispositions and the environment. Up to 40% of the risk is attributable to modifiable lifestyle factors, including diet.
Lei Fan, a researcher at Vanderbilt University Medical Center, and colleagues examined whether dietary fat intake was associated with changes in gray matter atrophy rates detected using neuroimaging over time in older adults. They were also interested in interactions of these changes with cognitive status, their dependence on sex, and whether an individual is a carrier of the APOE ε4 gene variant. APOE ε4 is a gene variant that increases the risk of developing Alzheimer’s disease.
These researchers analyzed data from the Vanderbilt Memory and Aging Project. This is a longitudinal observational study that investigates vascular and neurological health and the aging of older individuals free of clinical dementia at enrollment. The data came from 758 participants of the Vanderbilt Memory and Aging Project Legacy Cohort and the Expansion Cohort. Their average age was 67 years. About 47% were men, and 35% were carriers of the APOE ε4 gene variant.
The Legacy Cohort recruitment began in September 2012, and all participants were required to be at least 60 years old, have adequate auditory and visual acuity, and have a reliable study partner. The Expansion Cohort recruited individuals aged 50 years or older and recruitment started in August 2021.
Depending on their assessed cognitive status, participants were categorized as either cognitively unimpaired or mildly cognitively impaired. Participants completed magnetic resonance imaging of their brains at enrollment in the study and on at least one more occasion. They also completed a questionnaire called the Quick Food Scan fat screener, allowing study authors to estimate their total dietary fat intake. Data were collected at the start of the study, 18 months later, and then 3, 5, 7, and 9 years after the start of the study.
Results showed that, cross-sectionally at baseline, neither total fat intake nor the percentage of energy derived from fats was associated with the total volume of the brain’s gray matter or with the volumes of specific lobes of the brain. However, longitudinally over an average of 4.6 years, individuals deriving a higher percentage of their energy from fats tended to show a slower rate of enlargement of the interior lateral ventricle volume. This association was weak, and it disappeared when study authors corrected their detection thresholds for multiple comparisons.
Further analysis showed that the percentage of energy derived from fat was associated with a faster reduction in temporal lobe volume in cognitively unimpaired participants. In contrast, in individuals with mild cognitive impairment, a higher percentage of energy derived from fat was associated with slower enlargement of the inferior lateral ventricle region of the brain.
The temporal lobe is a region of the brain that supports memory and language. The inferior lateral ventricles are spaces filled with fluids near the temporal lobe. Their enlargement reflects the loss of brain tissue in surrounding areas.
“A high-fat diet is associated with accelerated gray matter atrophy, particularly in [Alzheimer’s disease-relevant] regions such as the temporal lobe, in [cognitively unimpaired] adults, but is associated with slower atrophy in individuals with existing [mild cognitive impairment], which is mainly driven by APOE ε4 carriers and/or female individuals,” the study authors concluded.
“Different mechanisms may be involved in the fat–neurodegeneration relationship across cognitive statuses. Halted atrophy associated with a high-fat diet, observed exclusively in individuals with existing [mild cognitive impairment], may reflect the role of fat as part of a compensatory mechanism in response to progressive [Alzheimer’s disease] pathology and metabolic challenges.”
The study contributes to the scientific understanding of the links between diet and mental health. However, it should be noted that the design of this study does not allow any causal inferences to be derived from the results. It is also limited by the fact that the cohort was predominantly white, well-educated, and relatively healthy. Additionally, a single self-reported dietary fat assessment at baseline may not reflect long-term variations in dietary intake.
The paper, “High-fat diet is associated with accelerated gray matter atrophy in cognitively unimpaired older adults but slower atrophy in individuals with existing mild cognitive impairment,” was authored by Lei Fan, Yunyi Sun, Dandan Liu, W. Hudson Robb, Kimberly R. Pechman, Niranjana Shashikumar, Yukti Vyas, Bennett A. Landman, Timothy J. Hohman, and Angela L. Jefferson.
-------------------------------------------------
Private, vetted email list for mental health professionals: https://www.clinicians-exchange.org
Unofficial Psychology Today Xitter to toot feed at Psych Today Unofficial Bot @PTUnofficialBot
-------------------------------------------------
#psychology #counseling #socialwork #psychotherapy @psychotherapist @psychotherapists @psychology @socialpsych @socialwork @psychiatry #mentalhealth #psychiatry #healthcare #depression #psychotherapist #HighFatDiet #BrainAtrophy #TemporalLobe #MildCognitiveImpairment #Alzheimer'sDiseaseResearch #APOE4 #CognitiveHealth #DementiaPrevention #Neuroimaging #VanderbiltMemoryAgingProject
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DATE: July 17, 2026 at 07:00AM
SOURCE: PSYPOST.ORG** Research quality varies widely from fantastic to small exploratory studies. Please check research methods when conclusions are very important to you. **
-------------------------------------------------TITLE: Study finds complex association between dietary fat intake and brain atrophy in older adults
An analysis of Vanderbilt Memory and Aging Project study data found that a high-fat diet was associated with a faster reduction in temporal lobe volume in cognitively unimpaired participants. However, in individuals with mild cognitive impairment, adherence to the same type of diet was associated with a slower enlargement of the inferior lateral ventricle area of the brain. The paper was published in Alzheimer’s Dementia.
As people age, their risk of developing dementia increases, although dementia is not an inevitable part of normal aging. Dementias are disorders involving progressive declines in memory, reasoning, language, judgment, or other cognitive abilities that interfere with daily life. The most common type of dementia is Alzheimer’s disease. This disease is associated with an abnormal accumulation of proteins called amyloid plaques and tau tangles in the brain.
Aside from Alzheimer’s disease, dementias also include vascular dementia (resulting from reduced blood flow or damage to brain tissues caused by strokes or small-vessel disease), Lewy body dementia, frontotemporal dementia, and others. The exact causes of dementias are not fully understood, but scientists believe that they are caused by a complex interaction between genetic predispositions and the environment. Up to 40% of the risk is attributable to modifiable lifestyle factors, including diet.
Lei Fan, a researcher at Vanderbilt University Medical Center, and colleagues examined whether dietary fat intake was associated with changes in gray matter atrophy rates detected using neuroimaging over time in older adults. They were also interested in interactions of these changes with cognitive status, their dependence on sex, and whether an individual is a carrier of the APOE ε4 gene variant. APOE ε4 is a gene variant that increases the risk of developing Alzheimer’s disease.
These researchers analyzed data from the Vanderbilt Memory and Aging Project. This is a longitudinal observational study that investigates vascular and neurological health and the aging of older individuals free of clinical dementia at enrollment. The data came from 758 participants of the Vanderbilt Memory and Aging Project Legacy Cohort and the Expansion Cohort. Their average age was 67 years. About 47% were men, and 35% were carriers of the APOE ε4 gene variant.
The Legacy Cohort recruitment began in September 2012, and all participants were required to be at least 60 years old, have adequate auditory and visual acuity, and have a reliable study partner. The Expansion Cohort recruited individuals aged 50 years or older and recruitment started in August 2021.
Depending on their assessed cognitive status, participants were categorized as either cognitively unimpaired or mildly cognitively impaired. Participants completed magnetic resonance imaging of their brains at enrollment in the study and on at least one more occasion. They also completed a questionnaire called the Quick Food Scan fat screener, allowing study authors to estimate their total dietary fat intake. Data were collected at the start of the study, 18 months later, and then 3, 5, 7, and 9 years after the start of the study.
Results showed that, cross-sectionally at baseline, neither total fat intake nor the percentage of energy derived from fats was associated with the total volume of the brain’s gray matter or with the volumes of specific lobes of the brain. However, longitudinally over an average of 4.6 years, individuals deriving a higher percentage of their energy from fats tended to show a slower rate of enlargement of the interior lateral ventricle volume. This association was weak, and it disappeared when study authors corrected their detection thresholds for multiple comparisons.
Further analysis showed that the percentage of energy derived from fat was associated with a faster reduction in temporal lobe volume in cognitively unimpaired participants. In contrast, in individuals with mild cognitive impairment, a higher percentage of energy derived from fat was associated with slower enlargement of the inferior lateral ventricle region of the brain.
The temporal lobe is a region of the brain that supports memory and language. The inferior lateral ventricles are spaces filled with fluids near the temporal lobe. Their enlargement reflects the loss of brain tissue in surrounding areas.
“A high-fat diet is associated with accelerated gray matter atrophy, particularly in [Alzheimer’s disease-relevant] regions such as the temporal lobe, in [cognitively unimpaired] adults, but is associated with slower atrophy in individuals with existing [mild cognitive impairment], which is mainly driven by APOE ε4 carriers and/or female individuals,” the study authors concluded.
“Different mechanisms may be involved in the fat–neurodegeneration relationship across cognitive statuses. Halted atrophy associated with a high-fat diet, observed exclusively in individuals with existing [mild cognitive impairment], may reflect the role of fat as part of a compensatory mechanism in response to progressive [Alzheimer’s disease] pathology and metabolic challenges.”
The study contributes to the scientific understanding of the links between diet and mental health. However, it should be noted that the design of this study does not allow any causal inferences to be derived from the results. It is also limited by the fact that the cohort was predominantly white, well-educated, and relatively healthy. Additionally, a single self-reported dietary fat assessment at baseline may not reflect long-term variations in dietary intake.
The paper, “High-fat diet is associated with accelerated gray matter atrophy in cognitively unimpaired older adults but slower atrophy in individuals with existing mild cognitive impairment,” was authored by Lei Fan, Yunyi Sun, Dandan Liu, W. Hudson Robb, Kimberly R. Pechman, Niranjana Shashikumar, Yukti Vyas, Bennett A. Landman, Timothy J. Hohman, and Angela L. Jefferson.
-------------------------------------------------
Private, vetted email list for mental health professionals: https://www.clinicians-exchange.org
Unofficial Psychology Today Xitter to toot feed at Psych Today Unofficial Bot @PTUnofficialBot
-------------------------------------------------
#psychology #counseling #socialwork #psychotherapy @psychotherapist @psychotherapists @psychology @socialpsych @socialwork @psychiatry #mentalhealth #psychiatry #healthcare #depression #psychotherapist #HighFatDiet #BrainAtrophy #TemporalLobe #MildCognitiveImpairment #Alzheimer'sDiseaseResearch #APOE4 #CognitiveHealth #DementiaPrevention #Neuroimaging #VanderbiltMemoryAgingProject
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https://www.europesays.com/at/256020/ Diabetes-Medikamente senken Alzheimer-Risiko: neue Studien, Antikörper & Diagnostik #AI #Alzheimer #Amyloid #Antikörper #ApoE4 #ARTIFICIALINTELLIGENCE #AT #Austria #Biomarker #Blutdruck #Bluttest #Cpla2 #Diabetes #Diagnostik #Ernährung #Gesundheit #GLP1 #Health #KI #KünstlicheIntelligenz #Lithium #Österreich #Prävention #Sglt2
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https://www.europesays.com/at/252320/ Alzheimer-Prävention: SGLT2-Hemmer senken Risiko um 43 Prozent #AlzheimerPrävention #ApoE4 #AT #Austria #Bluttests #Forschung #Gen #Gesundheit #Health #Hirnentzündungen #Österreich #Risiko #Sglt2Hemmer #Symptomen
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https://www.europesays.com/at/246229/ DHA bringt offenbar keine Gedächtnissteigerung: Was Fischölstudien für die Alzheimer-Prävention bedeuten #AI #Alzheimers #ApoE4 #ARTIFICIALINTELLIGENCE #AT #Austria #Bluttest #Dha #DigitaleTherapie #Fischöl #Früherkennung #Gesundheit #Gesundheitsdaten #Health #Hippocampus #KI #KünstlicheIntelligenz #Netzhaut #Omega3 #Österreich #Placebo #Prvention #Studie
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https://www.europesays.com/be-fr/154641/ Alzheimer : une bactérie courante détectée dans l’œil pourrait aggraver la maladie #Alzheimer #antibiotiques #APOE4 #BE #BEFr #Belgique #Belgium #BêtaAmyloïde #CedarsSinai #ChlamydiaPneumoniae #DéclinCognitif #dépistage #Health #ImagerieRétinienne #inflammation #MayaKoronyoHamaoui #NatureCommunications #Neurodégénérescence #rétine #Santé
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DATE: June 25, 2026 at 12:00PM
SOURCE: PSYPOST.ORG** Research quality varies widely from fantastic to small exploratory studies. Please check research methods when conclusions are very important to you. **
-------------------------------------------------TITLE: High-fat diets and pesticide exposure alter memory differently based on genes and sex
How diet, early chemical contact, genetic risk, and biological sex combine to shape memory function over a lifetime remains a major scientific puzzle. A new study published in Neurotoxicology reveals that consuming a high-fat diet and surviving early exposure to a common pesticide alters memory in wildly different ways depending on an animal’s genetic makeup and sex. The results suggest that nutritional advice for protecting the brain should be highly personalized rather than offered as a universal rule.
The brain constantly adapts to outside forces during its lifetime. During early childhood, the brain forms synaptic connections rapidly, making it highly sensitive to industrial chemicals in the environment. One of the most prevalent environmental risks comes from pesticides frequently used in agriculture and public health interventions.
Chlorpyrifos is a common organophosphate insecticide used heavily in commercial farming. It kills insects by attacking their nervous systems, but it can also affect humans and other mammals. The chemical blocks an enzyme responsible for clearing away a specific neurotransmitter called acetylcholine.
Acetylcholine acts as a chemical messenger heavily involved in learning, memory, and muscle movement. When the clearing enzyme is blocked, acetylcholine builds up, leading to severe overstimulation of the nervous system. While the European Union banned chlorpyrifos in recent years, it remains widely used in many other countries.
Along with chemical exposures, daily diet dictates how the animal brain functions. Researchers often use high-fat diets in laboratory settings to replicate metabolic diseases and study brain decline in rodents. Diets rich in fat have been frequently linked to immune system inflammation and memory loss, though experimental outcomes are not always the same across different studies.
Beyond diet and agricultural pesticides, genetics heavily dictate how the brain ages over time. The APOE gene (apolipoprotein E) is one of the most heavily studied genetic risk factors for memory decline in humans. This gene provides instructions for making a protein that helps transport cholesterol and other essential fats through the bloodstream and the central nervous system.
People naturally carry different versions of this gene, known as alleles. The most common version across human populations is APOE3, which functions adequately for most people. However, another version called APOE4 is widely recognized as a major risk factor for neurodegenerative conditions like Alzheimer’s disease. The APOE4 version alters how fats bind and travel through the blood, resulting in metabolic differences that researchers are still trying to understand.
Because these environmental and genetic factors are normally studied in isolation, researchers wanted to understand what happens when an animal experiences all of them sequentially. Laia Guardia-Escote, a behavioral researcher at the Universitat Rovira i Virgili in Spain, led a team to investigate whether specific genes, sex, a high-fat diet, and pesticide exposure interact to change adult memory capacity. Investigating these combined impacts offers a much more realistic model of everyday environmental risk.
The researchers used specialized laboratory mice for their experiment. These mice were genetically modified to carry the human versions of the APOE gene, producing mice with either the human APOE3 or APOE4 alleles. They were raised alongside a control group with normal, unaltered mouse genes.
Shortly after birth, the infant mice were divided into different experimental groups. Between their tenth and fifteenth days of life, some mice received liquid drops of chlorpyrifos by mouth. This specific timeframe was chosen because it mirrors the developmental milestones of the human brain immediately around birth.
The given dose of chlorpyrifos was relatively low. It was not high enough to cause systemic toxicity or immediate behavioral poisoning in the animals. The goal was to simulate the kind of low-level exposure a growing child might experience through everyday environmental residue on unwashed food.
The mice then grew up under standard laboratory conditions until they reached three months of age. At this point, the researchers changed their feeding routines. Half of the mice continued eating standard laboratory food, while the other half were fed a highly specialized diet composed of more than sixty percent fat.
After eight weeks on these diets, the researchers tracked how much weight the mice gained. As expected, the animals eating the high-fat diet gained more body weight than the ones casually munching on standard chow. Male mice also gained more weight than female mice in general.
The genetic makeup of the mice also influenced their physical response to the dietary intervention. The mice carrying the APOE3 gene gained the most body weight compared to the other genetic groups. Past studies suggest that the APOE3 version of the protein is simply more efficient at storing dietary energy as body fat, leading to accelerated weight gain.
To see how these variables influenced memory, the researchers placed the mice in a classic cognitive test called the Morris Water Maze. The maze consists of a large, circular pool of opaque water with a small platform hidden just below the water’s surface. Mice are natural swimmers, but they prefer to stand on solid ground, motivating them to find the hidden platform as quickly as possible.
Over five days of testing, researchers repeatedly placed the animals in the pool from varying starting locations. The mice had to rely on visual markers placed on the walls of the room to learn the actual location of the hidden platform. The team recorded how long it took the animals to navigate to safety during each swim maneuver.
All the different groups of mice successfully learned how to navigate the maze. However, the early-life exposure to the pesticide altered the learning speeds in unexpected ways. Postnatal chlorpyrifos exposure actually decreased the time it took APOE3 males and APOE4 females to find the platform, meaning they performed temporarily better than their unexposed counterparts.
Conversely, the pesticide exposure slowed down the learning process for the APOE3 females. This stark contrast highlights that an environmental toxin can have entirely different behavioral effects depending on the biological sex and genetic background of the subject. The researchers suspect the temporary memory boost in the APOE4 females might relate to how the pesticide interacts with their naturally lower baseline levels of acetylcholine.
After the initial learning phase, the researchers tested the animals’ spatial memory retention by completely removing the safety platform from the pool. They then tracked how much time the mice spent swimming in the specific quadrant of the pool where the platform used to be. A longer time spent searching the correct area indicates strong spatial memory.
Male mice generally demonstrated highly capable memories, easily recalling the former location of the platform. There was one notable exception. The APOE4 males that consumed the high-fat diet struggled to remember the location during the longest memory tests.
The APOE4 male mice could learn the initial task just fine. Yet they seemingly lost their long-term memory of the location after eating the high-fat diet for two months. This highlights a specific vulnerability to metabolic challenges for this genetic group.
Memory retention in the female mice was much more variable across the different groups. The APOE4 female mice who were fed standard chow entirely failed to remember where the hidden platform was located. Unexpectedly, exposing the APOE4 females to either the high-fat diet or the pesticide improved their memory retention relative to the control group.
However, when the female mice experienced both the pesticide exposure and the high-fat diet combined, their memory performance dropped. This combination acted synergistically to impair brain function. Males did not show this combined vulnerability, suggesting that female brains might be more susceptible to the combined stress of early toxins and late-in-life metabolic changes.
The researchers also tested the animals on cognitive flexibility by moving the platform to the opposite side of the pool and placing a visible marker directly on it. While all groups managed to complete the task, the APOE4 mice took the longest time to adapt to the new location. They also swam slower than the other genetic groups, suggesting a general difficulty in changing established behaviors.
There are some limitations to consider when interpreting these experimental results. The researchers note that they did not track specific anxiety behaviors in the pool, such as swimming exclusively around the edges to look for an exit. High anxiety can sometimes look like poor memory in a water maze, muddying the interpretation of the swimming patterns.
The study also did not directly measure hormonal differences, like the specific levels of estrogen circulating in the female mice. It is entirely possible that environmental chemicals like chlorpyrifos bind to hormone receptors in the brain, altering memory capacity. Future research will need to look directly at the molecular and cellular physiological changes occurring inside these specific brain regions.
Scientists have yet to determine why certain combinations, like high dietary fat and pesticides, hurt females more than males, while other singular factors seem strangely protective in the short term. The results illustrate that dietary guidelines intended to protect against memory loss should eventually account for a person’s biological and genetic profile. Generalized health advice may not be equally beneficial for everyone.
The study, “Impact of a high-fat diet on spatial learning and memory: The role of sex, APOE genotype, and postnatal chlorpyrifos exposure,” was authored by Laia Guardia-Escote, Judit Biosca-Brull, Jordi Blanco, Maria Cabré, Pia Basaure, Cristian Pérez-Fernández, Fernando Sánchez-Santed, José L. Domingo, and Maria Teresa Colomina.
-------------------------------------------------
Private, vetted email list for mental health professionals: https://www.clinicians-exchange.org
Unofficial Psychology Today Xitter to toot feed at Psych Today Unofficial Bot @PTUnofficialBot
-------------------------------------------------
#psychology #counseling #socialwork #psychotherapy @psychotherapist @psychotherapists @psychology @socialpsych @socialwork @psychiatry #mentalhealth #psychiatry #healthcare #depression #psychotherapist #HighFatDiet #PesticideExposure # APOEgenotype #APOE4 #MemoryAndLearning #SexDifferences #Chlorpyrifos #SpatialMemory #GeneDietInteraction #PersonalizedNutrition
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DATE: June 25, 2026 at 12:00PM
SOURCE: PSYPOST.ORG** Research quality varies widely from fantastic to small exploratory studies. Please check research methods when conclusions are very important to you. **
-------------------------------------------------TITLE: High-fat diets and pesticide exposure alter memory differently based on genes and sex
How diet, early chemical contact, genetic risk, and biological sex combine to shape memory function over a lifetime remains a major scientific puzzle. A new study published in Neurotoxicology reveals that consuming a high-fat diet and surviving early exposure to a common pesticide alters memory in wildly different ways depending on an animal’s genetic makeup and sex. The results suggest that nutritional advice for protecting the brain should be highly personalized rather than offered as a universal rule.
The brain constantly adapts to outside forces during its lifetime. During early childhood, the brain forms synaptic connections rapidly, making it highly sensitive to industrial chemicals in the environment. One of the most prevalent environmental risks comes from pesticides frequently used in agriculture and public health interventions.
Chlorpyrifos is a common organophosphate insecticide used heavily in commercial farming. It kills insects by attacking their nervous systems, but it can also affect humans and other mammals. The chemical blocks an enzyme responsible for clearing away a specific neurotransmitter called acetylcholine.
Acetylcholine acts as a chemical messenger heavily involved in learning, memory, and muscle movement. When the clearing enzyme is blocked, acetylcholine builds up, leading to severe overstimulation of the nervous system. While the European Union banned chlorpyrifos in recent years, it remains widely used in many other countries.
Along with chemical exposures, daily diet dictates how the animal brain functions. Researchers often use high-fat diets in laboratory settings to replicate metabolic diseases and study brain decline in rodents. Diets rich in fat have been frequently linked to immune system inflammation and memory loss, though experimental outcomes are not always the same across different studies.
Beyond diet and agricultural pesticides, genetics heavily dictate how the brain ages over time. The APOE gene (apolipoprotein E) is one of the most heavily studied genetic risk factors for memory decline in humans. This gene provides instructions for making a protein that helps transport cholesterol and other essential fats through the bloodstream and the central nervous system.
People naturally carry different versions of this gene, known as alleles. The most common version across human populations is APOE3, which functions adequately for most people. However, another version called APOE4 is widely recognized as a major risk factor for neurodegenerative conditions like Alzheimer’s disease. The APOE4 version alters how fats bind and travel through the blood, resulting in metabolic differences that researchers are still trying to understand.
Because these environmental and genetic factors are normally studied in isolation, researchers wanted to understand what happens when an animal experiences all of them sequentially. Laia Guardia-Escote, a behavioral researcher at the Universitat Rovira i Virgili in Spain, led a team to investigate whether specific genes, sex, a high-fat diet, and pesticide exposure interact to change adult memory capacity. Investigating these combined impacts offers a much more realistic model of everyday environmental risk.
The researchers used specialized laboratory mice for their experiment. These mice were genetically modified to carry the human versions of the APOE gene, producing mice with either the human APOE3 or APOE4 alleles. They were raised alongside a control group with normal, unaltered mouse genes.
Shortly after birth, the infant mice were divided into different experimental groups. Between their tenth and fifteenth days of life, some mice received liquid drops of chlorpyrifos by mouth. This specific timeframe was chosen because it mirrors the developmental milestones of the human brain immediately around birth.
The given dose of chlorpyrifos was relatively low. It was not high enough to cause systemic toxicity or immediate behavioral poisoning in the animals. The goal was to simulate the kind of low-level exposure a growing child might experience through everyday environmental residue on unwashed food.
The mice then grew up under standard laboratory conditions until they reached three months of age. At this point, the researchers changed their feeding routines. Half of the mice continued eating standard laboratory food, while the other half were fed a highly specialized diet composed of more than sixty percent fat.
After eight weeks on these diets, the researchers tracked how much weight the mice gained. As expected, the animals eating the high-fat diet gained more body weight than the ones casually munching on standard chow. Male mice also gained more weight than female mice in general.
The genetic makeup of the mice also influenced their physical response to the dietary intervention. The mice carrying the APOE3 gene gained the most body weight compared to the other genetic groups. Past studies suggest that the APOE3 version of the protein is simply more efficient at storing dietary energy as body fat, leading to accelerated weight gain.
To see how these variables influenced memory, the researchers placed the mice in a classic cognitive test called the Morris Water Maze. The maze consists of a large, circular pool of opaque water with a small platform hidden just below the water’s surface. Mice are natural swimmers, but they prefer to stand on solid ground, motivating them to find the hidden platform as quickly as possible.
Over five days of testing, researchers repeatedly placed the animals in the pool from varying starting locations. The mice had to rely on visual markers placed on the walls of the room to learn the actual location of the hidden platform. The team recorded how long it took the animals to navigate to safety during each swim maneuver.
All the different groups of mice successfully learned how to navigate the maze. However, the early-life exposure to the pesticide altered the learning speeds in unexpected ways. Postnatal chlorpyrifos exposure actually decreased the time it took APOE3 males and APOE4 females to find the platform, meaning they performed temporarily better than their unexposed counterparts.
Conversely, the pesticide exposure slowed down the learning process for the APOE3 females. This stark contrast highlights that an environmental toxin can have entirely different behavioral effects depending on the biological sex and genetic background of the subject. The researchers suspect the temporary memory boost in the APOE4 females might relate to how the pesticide interacts with their naturally lower baseline levels of acetylcholine.
After the initial learning phase, the researchers tested the animals’ spatial memory retention by completely removing the safety platform from the pool. They then tracked how much time the mice spent swimming in the specific quadrant of the pool where the platform used to be. A longer time spent searching the correct area indicates strong spatial memory.
Male mice generally demonstrated highly capable memories, easily recalling the former location of the platform. There was one notable exception. The APOE4 males that consumed the high-fat diet struggled to remember the location during the longest memory tests.
The APOE4 male mice could learn the initial task just fine. Yet they seemingly lost their long-term memory of the location after eating the high-fat diet for two months. This highlights a specific vulnerability to metabolic challenges for this genetic group.
Memory retention in the female mice was much more variable across the different groups. The APOE4 female mice who were fed standard chow entirely failed to remember where the hidden platform was located. Unexpectedly, exposing the APOE4 females to either the high-fat diet or the pesticide improved their memory retention relative to the control group.
However, when the female mice experienced both the pesticide exposure and the high-fat diet combined, their memory performance dropped. This combination acted synergistically to impair brain function. Males did not show this combined vulnerability, suggesting that female brains might be more susceptible to the combined stress of early toxins and late-in-life metabolic changes.
The researchers also tested the animals on cognitive flexibility by moving the platform to the opposite side of the pool and placing a visible marker directly on it. While all groups managed to complete the task, the APOE4 mice took the longest time to adapt to the new location. They also swam slower than the other genetic groups, suggesting a general difficulty in changing established behaviors.
There are some limitations to consider when interpreting these experimental results. The researchers note that they did not track specific anxiety behaviors in the pool, such as swimming exclusively around the edges to look for an exit. High anxiety can sometimes look like poor memory in a water maze, muddying the interpretation of the swimming patterns.
The study also did not directly measure hormonal differences, like the specific levels of estrogen circulating in the female mice. It is entirely possible that environmental chemicals like chlorpyrifos bind to hormone receptors in the brain, altering memory capacity. Future research will need to look directly at the molecular and cellular physiological changes occurring inside these specific brain regions.
Scientists have yet to determine why certain combinations, like high dietary fat and pesticides, hurt females more than males, while other singular factors seem strangely protective in the short term. The results illustrate that dietary guidelines intended to protect against memory loss should eventually account for a person’s biological and genetic profile. Generalized health advice may not be equally beneficial for everyone.
The study, “Impact of a high-fat diet on spatial learning and memory: The role of sex, APOE genotype, and postnatal chlorpyrifos exposure,” was authored by Laia Guardia-Escote, Judit Biosca-Brull, Jordi Blanco, Maria Cabré, Pia Basaure, Cristian Pérez-Fernández, Fernando Sánchez-Santed, José L. Domingo, and Maria Teresa Colomina.
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#psychology #counseling #socialwork #psychotherapy @psychotherapist @psychotherapists @psychology @socialpsych @socialwork @psychiatry #mentalhealth #psychiatry #healthcare #depression #psychotherapist #HighFatDiet #PesticideExposure # APOEgenotype #APOE4 #MemoryAndLearning #SexDifferences #Chlorpyrifos #SpatialMemory #GeneDietInteraction #PersonalizedNutrition
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DATE: June 25, 2026 at 12:00PM
SOURCE: PSYPOST.ORG** Research quality varies widely from fantastic to small exploratory studies. Please check research methods when conclusions are very important to you. **
-------------------------------------------------TITLE: High-fat diets and pesticide exposure alter memory differently based on genes and sex
How diet, early chemical contact, genetic risk, and biological sex combine to shape memory function over a lifetime remains a major scientific puzzle. A new study published in Neurotoxicology reveals that consuming a high-fat diet and surviving early exposure to a common pesticide alters memory in wildly different ways depending on an animal’s genetic makeup and sex. The results suggest that nutritional advice for protecting the brain should be highly personalized rather than offered as a universal rule.
The brain constantly adapts to outside forces during its lifetime. During early childhood, the brain forms synaptic connections rapidly, making it highly sensitive to industrial chemicals in the environment. One of the most prevalent environmental risks comes from pesticides frequently used in agriculture and public health interventions.
Chlorpyrifos is a common organophosphate insecticide used heavily in commercial farming. It kills insects by attacking their nervous systems, but it can also affect humans and other mammals. The chemical blocks an enzyme responsible for clearing away a specific neurotransmitter called acetylcholine.
Acetylcholine acts as a chemical messenger heavily involved in learning, memory, and muscle movement. When the clearing enzyme is blocked, acetylcholine builds up, leading to severe overstimulation of the nervous system. While the European Union banned chlorpyrifos in recent years, it remains widely used in many other countries.
Along with chemical exposures, daily diet dictates how the animal brain functions. Researchers often use high-fat diets in laboratory settings to replicate metabolic diseases and study brain decline in rodents. Diets rich in fat have been frequently linked to immune system inflammation and memory loss, though experimental outcomes are not always the same across different studies.
Beyond diet and agricultural pesticides, genetics heavily dictate how the brain ages over time. The APOE gene (apolipoprotein E) is one of the most heavily studied genetic risk factors for memory decline in humans. This gene provides instructions for making a protein that helps transport cholesterol and other essential fats through the bloodstream and the central nervous system.
People naturally carry different versions of this gene, known as alleles. The most common version across human populations is APOE3, which functions adequately for most people. However, another version called APOE4 is widely recognized as a major risk factor for neurodegenerative conditions like Alzheimer’s disease. The APOE4 version alters how fats bind and travel through the blood, resulting in metabolic differences that researchers are still trying to understand.
Because these environmental and genetic factors are normally studied in isolation, researchers wanted to understand what happens when an animal experiences all of them sequentially. Laia Guardia-Escote, a behavioral researcher at the Universitat Rovira i Virgili in Spain, led a team to investigate whether specific genes, sex, a high-fat diet, and pesticide exposure interact to change adult memory capacity. Investigating these combined impacts offers a much more realistic model of everyday environmental risk.
The researchers used specialized laboratory mice for their experiment. These mice were genetically modified to carry the human versions of the APOE gene, producing mice with either the human APOE3 or APOE4 alleles. They were raised alongside a control group with normal, unaltered mouse genes.
Shortly after birth, the infant mice were divided into different experimental groups. Between their tenth and fifteenth days of life, some mice received liquid drops of chlorpyrifos by mouth. This specific timeframe was chosen because it mirrors the developmental milestones of the human brain immediately around birth.
The given dose of chlorpyrifos was relatively low. It was not high enough to cause systemic toxicity or immediate behavioral poisoning in the animals. The goal was to simulate the kind of low-level exposure a growing child might experience through everyday environmental residue on unwashed food.
The mice then grew up under standard laboratory conditions until they reached three months of age. At this point, the researchers changed their feeding routines. Half of the mice continued eating standard laboratory food, while the other half were fed a highly specialized diet composed of more than sixty percent fat.
After eight weeks on these diets, the researchers tracked how much weight the mice gained. As expected, the animals eating the high-fat diet gained more body weight than the ones casually munching on standard chow. Male mice also gained more weight than female mice in general.
The genetic makeup of the mice also influenced their physical response to the dietary intervention. The mice carrying the APOE3 gene gained the most body weight compared to the other genetic groups. Past studies suggest that the APOE3 version of the protein is simply more efficient at storing dietary energy as body fat, leading to accelerated weight gain.
To see how these variables influenced memory, the researchers placed the mice in a classic cognitive test called the Morris Water Maze. The maze consists of a large, circular pool of opaque water with a small platform hidden just below the water’s surface. Mice are natural swimmers, but they prefer to stand on solid ground, motivating them to find the hidden platform as quickly as possible.
Over five days of testing, researchers repeatedly placed the animals in the pool from varying starting locations. The mice had to rely on visual markers placed on the walls of the room to learn the actual location of the hidden platform. The team recorded how long it took the animals to navigate to safety during each swim maneuver.
All the different groups of mice successfully learned how to navigate the maze. However, the early-life exposure to the pesticide altered the learning speeds in unexpected ways. Postnatal chlorpyrifos exposure actually decreased the time it took APOE3 males and APOE4 females to find the platform, meaning they performed temporarily better than their unexposed counterparts.
Conversely, the pesticide exposure slowed down the learning process for the APOE3 females. This stark contrast highlights that an environmental toxin can have entirely different behavioral effects depending on the biological sex and genetic background of the subject. The researchers suspect the temporary memory boost in the APOE4 females might relate to how the pesticide interacts with their naturally lower baseline levels of acetylcholine.
After the initial learning phase, the researchers tested the animals’ spatial memory retention by completely removing the safety platform from the pool. They then tracked how much time the mice spent swimming in the specific quadrant of the pool where the platform used to be. A longer time spent searching the correct area indicates strong spatial memory.
Male mice generally demonstrated highly capable memories, easily recalling the former location of the platform. There was one notable exception. The APOE4 males that consumed the high-fat diet struggled to remember the location during the longest memory tests.
The APOE4 male mice could learn the initial task just fine. Yet they seemingly lost their long-term memory of the location after eating the high-fat diet for two months. This highlights a specific vulnerability to metabolic challenges for this genetic group.
Memory retention in the female mice was much more variable across the different groups. The APOE4 female mice who were fed standard chow entirely failed to remember where the hidden platform was located. Unexpectedly, exposing the APOE4 females to either the high-fat diet or the pesticide improved their memory retention relative to the control group.
However, when the female mice experienced both the pesticide exposure and the high-fat diet combined, their memory performance dropped. This combination acted synergistically to impair brain function. Males did not show this combined vulnerability, suggesting that female brains might be more susceptible to the combined stress of early toxins and late-in-life metabolic changes.
The researchers also tested the animals on cognitive flexibility by moving the platform to the opposite side of the pool and placing a visible marker directly on it. While all groups managed to complete the task, the APOE4 mice took the longest time to adapt to the new location. They also swam slower than the other genetic groups, suggesting a general difficulty in changing established behaviors.
There are some limitations to consider when interpreting these experimental results. The researchers note that they did not track specific anxiety behaviors in the pool, such as swimming exclusively around the edges to look for an exit. High anxiety can sometimes look like poor memory in a water maze, muddying the interpretation of the swimming patterns.
The study also did not directly measure hormonal differences, like the specific levels of estrogen circulating in the female mice. It is entirely possible that environmental chemicals like chlorpyrifos bind to hormone receptors in the brain, altering memory capacity. Future research will need to look directly at the molecular and cellular physiological changes occurring inside these specific brain regions.
Scientists have yet to determine why certain combinations, like high dietary fat and pesticides, hurt females more than males, while other singular factors seem strangely protective in the short term. The results illustrate that dietary guidelines intended to protect against memory loss should eventually account for a person’s biological and genetic profile. Generalized health advice may not be equally beneficial for everyone.
The study, “Impact of a high-fat diet on spatial learning and memory: The role of sex, APOE genotype, and postnatal chlorpyrifos exposure,” was authored by Laia Guardia-Escote, Judit Biosca-Brull, Jordi Blanco, Maria Cabré, Pia Basaure, Cristian Pérez-Fernández, Fernando Sánchez-Santed, José L. Domingo, and Maria Teresa Colomina.
-------------------------------------------------
Private, vetted email list for mental health professionals: https://www.clinicians-exchange.org
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-------------------------------------------------
#psychology #counseling #socialwork #psychotherapy @psychotherapist @psychotherapists @psychology @socialpsych @socialwork @psychiatry #mentalhealth #psychiatry #healthcare #depression #psychotherapist #HighFatDiet #PesticideExposure # APOEgenotype #APOE4 #MemoryAndLearning #SexDifferences #Chlorpyrifos #SpatialMemory #GeneDietInteraction #PersonalizedNutrition
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Pesquisadores do Gladstone Institutes descobriram um mecanismo cerebral que pode explicar o maior risco de Alzheimer em portadores do gene APOE4. O estudo, publicado na revista Nature Aging, mostra que alterações na atividade neuronal podem ocorrer anos antes de problemas de memória.
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Learn how positive beliefs about aging, certain personality traits, and the MIND diet can lower dementia risk, even for those with genetic predispositions.
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https://newsletter.tf/positive-age-beliefs-cut-dementia-risk-gene-carriers/
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New research shows positive age beliefs can make individuals with a high genetic risk for dementia nearly 50% less likely to develop it.
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Dr. Juan Fortea discusses his groundbreaking research redefining APOE4 homozygosity as a genetic cause of Alzheimer’s and his upcoming webinar
WASHINGTON, Oct. 21, 2025 /PRNewswire/ — APOE4 Alzheimer’s Alliance Board Member Perry S. Chen discusses Dr. Fortea’s groundbreaking…
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https://www.newsbeep.com/us/241771/ -
Dr. Juan Fortea discusses his groundbreaking research redefining APOE4 homozygosity as a genetic cause of Alzheimer’s and his upcoming webinar
WASHINGTON, Oct. 21, 2025 /PRNewswire/ — APOE4 Alzheimer’s Alliance Board Member Perry S. Chen discusses Dr. Fortea’s groundbreaking…
#NewsBeep #News #US #USA #UnitedStates #UnitedStatesOfAmerica #Genetics #Alzheimer's #APOE4 #Fortea #Research #Science
https://www.newsbeep.com/us/241771/ -
Dr. Juan Fortea discusses his groundbreaking research redefining APOE4 homozygosity as a genetic cause of Alzheimer’s and his upcoming webinar
WASHINGTON, Oct. 21, 2025 /PRNewswire/ — APOE4 Alzheimer’s Alliance Board Member Perry S. Chen discusses Dr. Fortea’s groundbreaking…
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https://www.newsbeep.com/uk/216164/ -
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Thirty years on, our research linking viral infections with Alzheimer’s is finally getting the attention it deserves
#Health #Alzheimers #ColdSoreVirus #HerpesSimplex #Vaccines #DementiaResearch #Neuroscience #Brain #APOE4 #VirusLink #Dementia #Shingles
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Thirty years on, our research linking viral infections with Alzheimer’s is finally getting the attention it deserves
#Health #Alzheimers #ColdSoreVirus #HerpesSimplex #Vaccines #DementiaResearch #Neuroscience #Brain #APOE4 #VirusLink #Dementia #Shingles
https://the-14.com/thirty-years-on-our-research-linking-viral-infections-with-alzheimers-is-finally-getting-the-attention-it-deserves/ -
Thirty years on, our research linking viral infections with Alzheimer’s is finally getting the attention it deserves
#Health #Alzheimers #ColdSoreVirus #HerpesSimplex #Vaccines #DementiaResearch #Neuroscience #Brain #APOE4 #VirusLink #Dementia #Shingles
https://the-14.com/thirty-years-on-our-research-linking-viral-infections-with-alzheimers-is-finally-getting-the-attention-it-deserves/ -
Thirty years on, our research linking viral infections with Alzheimer’s is finally getting the attention it deserves
#Health #Alzheimers #ColdSoreVirus #HerpesSimplex #Vaccines #DementiaResearch #Neuroscience #Brain #APOE4 #VirusLink #Dementia #Shingles
https://the-14.com/thirty-years-on-our-research-linking-viral-infections-with-alzheimers-is-finally-getting-the-attention-it-deserves/ -
Thirty years on, our research linking viral infections with Alzheimer’s is finally getting the attention it deserves
#Health #Alzheimers #ColdSoreVirus #HerpesSimplex #Vaccines #DementiaResearch #Neuroscience #Brain #APOE4 #VirusLink #Dementia #Shingles
https://the-14.com/thirty-years-on-our-research-linking-viral-infections-with-alzheimers-is-finally-getting-the-attention-it-deserves/ -
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.
-
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.
-
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.
-
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.
-
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.
-
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.
-
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.
-
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.
-
A HS student emailed me out of the blue to do an interview as part of her capstone project on #Alzheimer's. I spoke w/her about #brain science & #caregiving. She's 18, her family has the #APOE4 gene - a risk factor for the disease - & she will study neuroscience to find a cure for Alzheimer's. She's smart, determined, & I had chills listening to her story and her passion. The senseless, fascistic #NIH cuts are imperiling the potential, the future of people like her, & our own.