Association between spontaneous activity of the default mode network hubs and leukocyte telomere length in late childhood and early adolescence

J Psychosom Res. 2019 Dec:127:109864. doi: 10.1016/j.jpsychores.2019.109864. Epub 2019 Oct 30.

Abstract

The impact of early life stress on mental health and telomere length shortening have been reported. Changes in brain default mode network (DMN) were found to be related to a myriad of psychiatric conditions in which stress may play a role. In this context, family environment and adverse childhood experiences (ACEs) are potential causes of stress. This is a hypothesis-driven study focused on testing two hypotheses: (i) there is an association between telomere length and the function of two main hubs of DMN: the posterior cingulate cortex (PCC) and the medial prefrontal cortex (mPFC); (ii) this association is modulated by family environment and/or ACEs. To the best of our knowledge, this is the first study investigating these hypotheses. Resting-state functional magnetic resonance imaging data and blood sample were collected from 389 subjects (6-15 age range). We assessed DMN fractional amplitude of low-frequency fluctuations (fALFF) and leukocyte telomere length (LTL). We fitted general linear models to test the main effects of LTL on DMN hubs and the interaction effects with Family Environment Scale (FES) and ACEs. The results did not survive a strict Bonferroni correction. However, uncorrected p-values suggest that LTL was positively correlated with fALFF in PCC and a FES interaction between FES and LTL at mPFC. Although marginal, our results encourage further research on the interaction between DMN hubs, telomere length and family environment, which may play a role on the biological embedding of stress.

Keywords: Adolescence; Brain development; Childhood; Default-mode; Leukocyte telomere length; Resting state; Stress; Telomere.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Brain Mapping / methods*
  • Child
  • Female
  • Humans
  • Leukocytes / metabolism*
  • Magnetic Resonance Imaging / methods*
  • Male
  • Telomere / metabolism*