Evidence map›Paper›PMID 36153290›Full record

ArticleThe American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry2023

Late-Life Depression is Associated With Increased Levels of GDF-15, a Pro-Aging Mitokine.

Emma Mastrobattista, Eric J Lenze, Charles F Reynolds, Benoit H Mulsant, Julie Wetherell, Gregory F Wu, Daniel M Blumberger, Jordan F Karp, Meryl A Butters, Ana Paula Mendes-Silva and 3 more

Open access · greenAbstract read
In one paragraph

Article in The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Review
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  4. Pharmacotherapy of major depressive disorder in older adults: from an evidence-informed stepwise algorithm to precision medicine.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  5. Mechanistic insights into the liver-brain axis during chronic liver disease.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  6. Premature aging in serious mental illness.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
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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

13 authors at 7 institutions in 2 countries.

Emma MastrobattistaUConn Center on Aging (EM, BSD), University of Connecticut, Farmington, CT.
Eric J LenzeDepartment of Psychiatry (EJL), Washington University School of Medicine, St Louis, MO.
Charles F ReynoldsDepartment of Psychiatry (CFR, MAB), University of Pittsburgh School of Medicine, Pittsburgh, PA.
Benoit H MulsantDepartment of Psychiatry (BHM, DMB, APMS, ELV), Temerty Faculty of Medicine, University of Toronto, Centre for Addiction and Mental Health, Toronto, ON Canada.
Julie WetherellVA San Diego Healthcare System (JW), Mental Health Impact Unit 3, University of California, San Diego Department of Psychiatry.
Gregory F WuDepartment of Neurology (GFW), Washington University, St Louis, MO.
Daniel M BlumbergerDepartment of Psychiatry (BHM, DMB, APMS, ELV), Temerty Faculty of Medicine, University of Toronto, Centre for Addiction and Mental Health, Toronto, ON Canada.
Jordan F KarpDepartment of Psychiatry (JFK), The University of Arizona College of Medicine, Tucson, AZ.
Meryl A ButtersDepartment of Psychiatry (CFR, MAB), University of Pittsburgh School of Medicine, Pittsburgh, PA.
Ana Paula Mendes-SilvaDepartment of Psychiatry (BHM, DMB, APMS, ELV), Temerty Faculty of Medicine, University of Toronto, Centre for Addiction and Mental Health, Toronto, ON Canada.
Erica L VieiraDepartment of Psychiatry (BHM, DMB, APMS, ELV), Temerty Faculty of Medicine, University of Toronto, Centre for Addiction and Mental Health, Toronto, ON Canada.
George TsengDepartment of Biostatistics (GT), University of Pittsburgh School of Public Health, PA.
Breno S DinizUConn Center on Aging (EM, BSD), University of Connecticut, Farmington, CT; Department of Psychiatry (BSD), UConn School of Medicine, Farmington, CT. Electronic address: diniz@uchc.edu.
University of Pittsburgh · USCentre for Addiction and Mental Health · CAUConn Health · USUniversity of Toronto · CAWashington University in St. Louis · USUniversity of Arizona · USUniversity of California, San Diego · US

Funding

Remediating Age Related-Cognitive Decline: Mindfulness-Based Stress Reduction and ExerciseR01AG049369 · NIA · WASHINGTON UNIVERSITY · PI LENZE, ERIC J · 2014 to 2019
$15.6M
1/3-Incomplete Response in Late-Life Depression: Getting to RemissionR01MH083660 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REYNOLDS, CHARLES F. · 2009 to 2013
$2.7M
EVALUATION OF MOLECULAR MECHANISMS OF TREATMENT RESPONSE IN LATE LIFE DEPRESSIONR01MH118311 · NIMH · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI DINIZ, BRENO SATLER, TSENG, GEORGE C. · 2019 to 2022
$2.0M
NIA NIH HHS R01 AG049369NIMH NIH HHS R01 MH083660NIMH NIH HHS R01 MH118311
6 · The paper itself

Abstract

objectiveIn older adults, major depressive disorder (MDD) is associated with accelerated physiological and cognitive aging, generating interest in uncovering biological pathways that may be targetable by interventions. Growth differentiation factor-15 (GDF-15) plays a significant role in biological aging via multiple biological pathways relevant to age and age-related diseases. Elevated levels of GDF-15 correlate with increasing chronological age, decreased telomerase activity, and increased mortality risk in older adults. We sought to evaluate the circulating levels of GDF-15 in older adults with MDD and its association with depression severity, physical comorbidity burden, age of onset of first depressive episode, and cognitive performance.

designThis study assayed circulating levels of GDF-15 in 393 older adults (mean ± SD age 70 ± 6.6 years, male:female ratio 1:1.54), 308 with MDD and 85 non-depressed comparison individuals.

resultsAfter adjusting for confounding variables, depressed older adults had significantly higher GDF-15 serum levels (640.1 ± 501.5 ng/mL) than comparison individuals (431.90 ± 223.35 ng/mL) (t=3.75, d.f.= 391, p=0.0002). Among depressed individuals, those with high GDF-15 had higher levels of comorbid physical illness, lower executive cognitive functioning, and higher likelihood of having late-onset depression.

conclusionOur results suggest that depression in late life is associated with GDF-15, a marker of amplified age-related biological changes. GDF-15 is a novel and potentially targetable biological pathway between depression and accelerated aging, including cognitive aging.

Indexed as

Growth Differentiation Factor 15Major Depressive DisorderAgedAgingBiomarkersComorbidityDepressionFemaleHumansMaleBiomarkersGrowth Differentiation Factor 15Agingbiological markersGDF-15GeroscienceLate life depression

Identifiers

PMID36153290
PMCPMC9701166
OpenAlexW4293216803

What OpenQuestion holds

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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.