Evidence map›Paper›PMID 41582473›Full record

ArticleClinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology2026

Sex-specific Serum Biomarker Associations with Antidepressant Treatment Outcomes in Depressive Disorders.

Jae-Min Kim, Hee-Ju Kang, Ju-Wan Kim, Min Jhon, Min-Gon Kim, Ju-Yeon Lee, Sung-Wan Kim, Il-Seon Shin

Abstract read
In one paragraph

Article in Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology, 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.

Jae-Min KimDepartment of Psychiatry, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0001-7409-6306
Hee-Ju KangDepartment of Psychiatry, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0002-4784-4820
Ju-Wan KimDepartment of Psychiatry, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0002-9888-1090
Min JhonDepartment of Psychiatry, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0002-0408-768X
Min-Gon KimGwangju Institute of Science and Technology, Gwangju, Korea.ORCID https://orcid.org/0000-0002-3525-0048
Ju-Yeon LeeDepartment of Psychiatry, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0003-0653-7223
Sung-Wan KimDepartment of Psychiatry, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0002-6739-2163
Il-Seon ShinDepartment of Psychiatry, Chonnam National University Medical School, Gwangju, Korea.ORCID https://orcid.org/0000-0001-5370-7649

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study examined whether baseline levels of 14 serum biomarkers predicted antidepressant remission differently by sex at 12 weeks and 12 months. Methods: In a prospective cohort, 1,086 outpatients with depressive disorders received stepwise antidepressant treatment following a naturalistic protocol. Baseline serum samples were analyzed for biomarkers from six systems: immune (high-sensitivity C-reactive protein, tumor necrosis factor-alpha, interleukin-1 beta, interleukin-6, interleukin-4, interleukin-10), metabolic (leptin, ghrelin, total cholesterol), neurotrophic (brain-derived neurotrophic factor), neurotransmitter (serotonin), endocrine (cortisol), and nutritional (folate, homocysteine). Remission, defined as a Hamilton Depression Rating Scale scores ≤ 7, was assessed at 12 weeks and 12 months. Logistic regression models with biomarker-by-sex interaction and stratified analyses were used, adjusting for clinical covariates. Results: Higher baseline serotonin predicted 12-week remission in males but not in females. At 12 months, lower leptin and higher folate predicted remission only in males, while lower cortisol predicted remission only in females. These showed significant biomarker-sex interactions. No sex-specific interactions were found for immune markers. Conclusion: Baseline serum biomarkers across biological systems showed sex-specific associations with treatment outcomes. Neurotransmitter, metabolic, endocrine, and nutritional markers may offer predictive value for sex-tailored, biomarker-informed treatment strategies in depression.

Indexed as

BiomarkerDepressionDrug therapyRemissionSex characteristics

Identifiers

PMID41582473
PMCPMC12854124

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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.