Publications by authors named "Jonah Fisher"

Article Synopsis
  • This study investigates how educational attainment affects dementia and cognitive impairment through the lens of DNA methylation age acceleration, while considering the interactions between exposures and mediators.
  • Researchers examined data from 2016 participants and found associations indicating that both lower education levels and accelerated biological aging (GrimAge) are linked to a higher risk of cognitive impairment.
  • The study reveals that while the mediation effect of GrimAge on dementia related to education is modest, a significant portion of the effect stems from the interaction between low education and biological aging, highlighting the relationship between social disadvantage and cognitive health.
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Background: The effects of adverse life events on physical and psychological health, with DNA methylation (DNAm) as a critical underlying mechanism, have been extensively studied. However, the epigenetic resemblance between mother and child in the context of neglectful caregiving, and whether it may be shaped by the emotional impact of maternal stressful events and the duration of co-residence (indexed by child age), remains unknown. The present study examined mother-child similarity in methylation profiles, considering the potential effect of mother adversity, mother empathy, neglect-control group, child age (an index of years of mother-child co-residence), and mother age.

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Importance: Children who are socioeconomically disadvantaged are at increased risk for high body mass index (BMI) and multiple diseases in adulthood. The developmental origins of health and disease hypothesis proposes that early life conditions affect later-life health in a manner that is only partially modifiable by later-life experiences.

Objective: To examine whether epigenetic measures of BMI developed in adults are valid biomarkers of childhood BMI and if they are sensitive to early life social determinants of health.

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Article Synopsis
  • Childhood adversity affects DNA methylation patterns, potentially changing health outcomes throughout development, particularly during sensitive periods.
  • The study looked at data from the Avon Longitudinal Study of Parents and Children, focusing on various types of childhood adversity and its impact on DNA methylation at age 15.
  • Using structured life course modeling, researchers evaluated how timing, accumulation, and recency of adversity influence adolescent DNA methylation and aimed to replicate findings with other studies.
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Article Synopsis
  • * Researchers analyzed saliva samples from 796 children at ages 9 and 15 and found 8,430 sites on autosomal chromosomes where DNA methylation levels differed by sex, with a significant 76.2% showing higher levels in females.
  • * The consistent results between ages 9 and 15 suggest that these sex-differential DNA methylation patterns are stable over time, contributing to our understanding of why some diseases show differing prevalence based on sex.
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Children who are socioeconomically disadvantaged are at increased risk for high body mass index (BMI) and multiple diseases in adulthood. The developmental origins of health and disease hypothesis proposes that early life conditions affect later-life health in a manner that is only partially modifiable by later-life experiences. Epigenetic mechanisms may regulate the influence of early life conditions on later life health.

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Studies of DNA methylation have revealed the biological mechanisms by which life adversity confers risk for later physical and mental health problems. What remains unknown is the "biologically embedding" of maternal adverse experiences resulting in maladaptive parenting and whether these epigenetic effects are transmitted to the next generation. This study focuses on neglectful mothering indexed by a severe disregard for the basic and psychological needs of the child.

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Prenatal maternal smoking is associated with low birthweight, neurological disorders, and asthma in exposed children. DNA methylation signatures can function as biomarkers of prenatal smoke exposure. However, the robustness of DNA methylation signatures across child ages, genetic ancestry groups, or tissues is not clear.

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DNA methylation clocks are used as molecular estimators of epigenetic age, but with little evidence in mothers and none in neglectful mothering. We investigated differences in epigenetic age acceleration (EAA) and the role of empathy using the PhenoAge clock. We collected saliva samples from mothers with extreme disregard for their child's needs (50 in the neglect group, NG) and mothers with non-neglectful caregiving (87 in the control group, CG).

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Objectives: This study aims to examine the relationship between childhood socioeconomic position (SEP) and cognitive function in later life within nationally representative samples of older adults in the United States and England, investigate whether these effects are mediated by later-life SEP, and determine whether social mobility from childhood to adulthood affects cognitive function and decline.

Method: Using data from the Health and Retirement Study (HRS) and the English Longitudinal Survey of Ageing (ELSA), we examined the relationships between measures of SEP, cognitive performance and decline using individual growth curve models.

Results: High childhood SEP was associated with higher cognitive performance at baseline in both cohorts and did not affect the rate of decline.

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Saliva is a widely used biological sample, especially in pediatric research, containing a heterogenous mixture of immune and epithelial cells. Associations of exposure or disease with saliva DNA methylation can be influenced by cell-type proportions. Here, we developed a saliva cell-type DNA methylation reference panel to estimate interindividual cell-type heterogeneity in whole saliva studies.

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