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Maternal psychosocial risk factors and child gestational epigenetic age in a South African birth cohort study.
Koen, Nastassja; Jones, Meaghan J; Nhapi, Raymond T; Lake, Marilyn T; Donald, Kirsten A; Barnett, Whitney; Hoffman, Nadia; MacIsaac, Julia L; Morin, Alexander M; Lin, David T S; Kobor, Michael S; Koenen, Karestan C; Zar, Heather J; Stein, Dan J.
Afiliação
  • Koen N; Department of Psychiatry and Mental Health, University of Cape Town, Cape Town, South Africa. nastassja.koen@uct.ac.za.
  • Jones MJ; South African Medical Research Council (SAMRC) Unit on Risk and Resilience in Mental Disorders, Cape Town, South Africa. nastassja.koen@uct.ac.za.
  • Nhapi RT; Neuroscience Institute, University of Cape Town, Cape Town, South Africa. nastassja.koen@uct.ac.za.
  • Lake MT; Biochemistry and Medical Genetics, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Children's Hospital Research Institute of Manitoba, Winnipeg, Manitoba, Canada.
  • Donald KA; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, South Africa.
  • Barnett W; Division of Epidemiology and Biostatistics, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.
  • Hoffman N; Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, South Africa.
  • MacIsaac JL; Neuroscience Institute, University of Cape Town, Cape Town, South Africa.
  • Morin AM; Division of Developmental Paediatrics, Department of Paediatrics and Child Health, Red Cross War Memorial Children's Hospital, University of Cape Town, Cape Town, South Africa.
  • Lin DTS; Department of Paediatrics & Child Health and SAMRC Unit on Child and Adolescent Health, University of Cape Town, Cape Town, South Africa.
  • Kobor MS; Department of Psychiatry and Mental Health, University of Cape Town, Cape Town, South Africa.
  • Koenen KC; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada.
  • Zar HJ; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada.
  • Stein DJ; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, University of British Columbia, Vancouver, Canada.
Transl Psychiatry ; 11(1): 358, 2021 07 02.
Article em En | MEDLINE | ID: mdl-34215722
Accelerated epigenetic aging relative to chronological age has been found to be associated with higher risk of mortality in adults. However, little is known about whether and how in utero exposures might shape child gestational epigenetic age (EA) at birth. We aimed to explore associations between maternal psychosocial risk factors and deviation in child gestational EA at birth (i.e., greater or lower EA relative to chronological age) in a South African birth cohort study-the Drakenstein Child Health Study. Maternal psychosocial risk factors included trauma/stressor exposure; posttraumatic stress disorder (PTSD); depression; psychological distress; and alcohol/tobacco use. Child gestational EA at birth was calculated using an epigenetic clock previously devised for neonates; and gestational EA deviation was calculated as the residuals of the linear model between EA and chronological gestational age. Bivariate linear regression was then used to explore unadjusted associations between maternal/child risk factors and child gestational EA residuals at birth. Thereafter, a multivariable regression method was used to determine adjusted associations. Data from 271 maternal-child dyads were included in the current analysis. In the multivariable regression model, maternal PTSD was significantly and negatively associated with child gestational EA residuals at birth (ß = -1.95; p = 0.018), controlling for study site, sex of the child, head circumference at birth, birthweight, mode of delivery, maternal estimated household income, body mass index (BMI) at enrolment, HIV status, anaemia, psychological distress, and prenatal tobacco or alcohol use. Given the novelty of this preliminary finding, and its potential translational relevance, further studies to delineate underlying biological pathways and to explore clinical implications of EA deviation are warranted.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epigênese Genética Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Epigênese Genética Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Child / Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2021 Tipo de documento: Article