Evidence map›Paper›PMID 42417024›Full record

ArticlePsychological medicine2026

Peripheral transcriptomic aging acceleration in major depressive disorder: the mediating role of insular cortex alterations.

Yushun Yan, Min Wang, Yuanmei Tao, Jinxue Wei, Liansheng Zhao, Rongjun Ni, Xiao Yang, Xiaohong Ma

Abstract read
In one paragraph

Article in Psychological medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Yushun YanMental Health Center and Institute of Psychiatry, https://ror.org/007mrxy13National Center for Mental Disorders, West China Hospital, Sichuan University, Chengdu, China.
Min WangMental Health Center and Institute of Psychiatry, https://ror.org/007mrxy13National Center for Mental Disorders, West China Hospital, Sichuan University, Chengdu, China.
Yuanmei TaoMental Health Center and Institute of Psychiatry, https://ror.org/007mrxy13National Center for Mental Disorders, West China Hospital, Sichuan University, Chengdu, China.
Jinxue WeiMental Health Center and Institute of Psychiatry, https://ror.org/007mrxy13National Center for Mental Disorders, West China Hospital, Sichuan University, Chengdu, China.
Liansheng ZhaoMental Health Center and Institute of Psychiatry, https://ror.org/007mrxy13National Center for Mental Disorders, West China Hospital, Sichuan University, Chengdu, China.
Rongjun NiMental Health Center and Institute of Psychiatry, https://ror.org/007mrxy13National Center for Mental Disorders, West China Hospital, Sichuan University, Chengdu, China.ORCID 0000-0001-7421-136X
Xiao YangMental Health Center and Institute of Psychiatry, https://ror.org/007mrxy13National Center for Mental Disorders, West China Hospital, Sichuan University, Chengdu, China.ORCID 0000-0003-4717-6276
Xiaohong MaMental Health Center and Institute of Psychiatry, https://ror.org/007mrxy13National Center for Mental Disorders, West China Hospital, Sichuan University, Chengdu, China.ORCID 0000-0003-2627-9946

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiological aging may contribute to the pathogenesis of major depressive disorder (MDD). However, whether and how peripheral transcriptomic aging increases the risk of MDD onset remains unclear.

methodsTranscriptomic age was estimated using peripheral blood RNA sequencing data from 141 individuals with MDD and 134 healthy controls. The residuals of transcriptomic age regressed on chronological age were calculated to indicate transcriptomic aging acceleration. Enrichment analysis was performed to explore potential biological mechanisms underlying aging- and MDD-associated transcriptomic alterations. Associations between transcriptomic aging and clinical, neurocognitive, environmental, genetic, and neuroimaging phenotypes were examined.

resultsParticipants with MDD exhibited significantly accelerated transcriptomic aging both before (

conclusionsTranscriptomic aging may represent a novel risk factor for MDD. Disruption in the insular cortex may serve as a critical neural substrate through which accelerated transcriptomic aging increases vulnerability to MDD.

Indexed as

AgingInsular CortexMajor Depressive DisorderTranscriptomeAdultFemaleHumansMagnetic Resonance ImagingMaleMiddle Agedbiological aging accelerationinsular cortexmajor depressive disorderperipheral transcriptome

Identifiers

PMID42417024
PMCPMC13370190

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.