Evidence map›Paper›PMID 31628984›Full record

ArticleJournal of the American Academy of Child and Adolescent Psychiatry2020

Depressive Symptoms Predict Change in Telomere Length and Mitochondrial DNA Copy Number Across Adolescence.

Kathryn L Humphreys, Lucinda M Sisk, Erika M Manczak, Jue Lin, Ian H Gotlib

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Academy of Child and Adolescent Psychiatry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
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  5. Review
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  10. Observational
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  15. Biomarkers of aging through the life course: A Recent Literature Update.Current opinion in epidemiology and public health · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Sex differences in myelin content of white matter tracts in adolescents with depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 5 institutions in 1 country.

Kathryn L HumphreysVanderbilt University, Nashville, TN. Electronic address: k.humphreys@vanderbilt.edu.
Lucinda M SiskYale University, New Haven, Connecticut.
Erika M ManczakUniversity of Denver, Colorado.
Jue LinUniversity of California, San Francisco.
Ian H GotlibStanford University, California.
Stanford University · USUniversity of California, San Francisco · USUniversity of Denver · USVanderbilt University · USYale University · US

Funding

A BIOBEHAVIORAL RESEARCH TRAINING PROGRAMT32MH019938 · NIMH · STANFORD UNIVERSITY · PI Corey J Keller, RACHEL MANBER · 1994 to 2026
$9.4M
Psychobiological Mechanisms Underlying the Association Between Early Life Stress and Depression Across AdolescenceR37MH101495 · NIMH · STANFORD UNIVERSITY · PI IAN H GOTLIB · 2018 to 2026
$6.6M
Telomere Length as a Mediator Between Early Life Stress and Child Health OutcomesF32MH107129 · NIMH · STANFORD UNIVERSITY · PI HUMPHREYS, KATHRYN LEIGH · 2015 to 2017
$169k
NIMH NIH HHS F32 MH107129NIMH NIH HHS R37 MH101495NIMH NIH HHS T32 MH019938
6 · The paper itself

Abstract

objectiveSeveral studies have found associations between a diagnosis or symptoms of major depressive disorder and markers of cellular aging and dysfunction. These investigations, however, are predominantly cross-sectional and focus on adults. In the present study, we used a prospective longitudinal design to test the cross-sectional association between depressive symptoms in adolescents and telomere length (TL) as well as mitochondrial DNA copy number (mtDNA-cn).

methodA total of 121 adolescents (mean age = 11.38 years, SD = 1.03; 39% male adolescents and 61% female adolescents) were followed for approximately 2 years. At baseline and follow-up, participants provided saliva for DNA extraction, from which measures of TL and mtDNA-cn were obtained. Depressive symptoms were obtained via the Children's Depression Inventory.

resultsThere was no association between depressive symptoms and markers of cellular aging at baseline; however, depressive symptoms at baseline predicted higher rates of telomere erosion (β = -0.201, p = .016) and greater increases in mtDNA-cn (β = 0.190, p = .012) over the follow-up period. Markers of cellular aging at baseline did not predict subsequent changes in depressive symptoms. Furthermore, including the number of stressful life events did not alter these patterns of findings.

conclusionThese results indicate that depressive symptoms precede changes in cellular aging and dysfunction, rather than the reverse.

Indexed as

DepressionMajor Depressive DisorderAdolescentAdultChildCross-Sectional StudiesDNA Copy Number VariationsDNA, MitochondrialFemaleHumansMaleProspective StudiesTelomereDNA, Mitochondrialadolescencecellular agingdepressionmitochondrial DNA copy numbertelomeres

Identifiers

PMID31628984
PMCPMC7160006
OpenAlexW2980653549

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.