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Association between maternal depression symptoms and child telomere length.
Walker, Caroline G; Thayer, Zaneta M; Marks, Emma J; Ly, Kien N; Pillai, Avinesh; Waldie, Karen; Underwood, Lisa; Snell, Russell G; Knowles, Sarah D; Cha, Jane E; Morton, Susan M B.
  • Walker CG; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand. Electronic address: caroline.walker@auckland.ac.nz.
  • Thayer ZM; Department of Anthropology, Dartmouth College, Hanover, NH, USA.
  • Marks EJ; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand.
  • Ly KN; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand.
  • Pillai A; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand; Department of Statistics, University of Auckland, Auckland, New Zealand.
  • Waldie K; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand; School of Psychology, University of Auckland, Auckland, New Zealand.
  • Underwood L; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand.
  • Snell RG; School of Biological Sciences, Centre for Brain Research, University of Auckland, Auckland, New Zealand.
  • Knowles SD; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand; Auckland Museum, Auckland, New Zealand.
  • Cha JE; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand.
  • Morton SMB; Centre for Longitudinal Research - He Ara ki Mua and Growing Up in New Zealand, University of Auckland, New Zealand.
J Psychiatr Res ; 174: 319-325, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38685189
ABSTRACT
The biological mechanisms that explain how adverse early life events influence adult disease risk are poorly understood. One proposed mechanism is via the induction of accelerated biological aging, for which telomere length is considered a biomarker. We aimed to determine if maternal depression pre- and post-partum was associated with telomere length in children at 4 years of age (n = 4299). Mothers completed structured questionnaires assessing depression during pregnancy (Edinburgh Depression Scale), at 9 months (Edinburgh Depression Scale), and at 54 months postpartum (Patient Health Questionnaire 9). Regression methods were used to investigate the relationship between telomere length (DNA from saliva) and maternal depression score recorded at each stage. Significant covariates included in the final model were maternal age at pregnancy; child sex; child ethnicity; gestational age group, and rurality group. Child telomere length was found to be longer if their mother had a higher depression score at both postpartum time points tested (9 months of age; coefficient 0.003, SE = 0.001, P = 0.01, 54 months of age; coefficient 0.003, SE = 0.002, P = 0.02). Although these findings seem paradoxical, increased telomere length may be an adaptive response to early life stressors. We propose several testable hypotheses for these results and to determine if the positive association between depression and telomere length is a developmental adaptation or an indirect consequence of environmental factors.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Depresión Límite: Adult / Child, preschool / Female / Humans / Infant / Male / Pregnancy Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Depresión Límite: Adult / Child, preschool / Female / Humans / Infant / Male / Pregnancy Idioma: En Año: 2024 Tipo del documento: Article