ArticleCommunications medicine2026
Metabolic hormone and adipokine alterations in major depressive disorder in relation to the acute-phase inflammatory response and early-life adversity.
Article in Communications 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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundMajor depressive disorder (MDD) involves dysregulated neuroimmune, metabolic, and inflammatory pathways. This study characterized metabolic hormone and adipokine profiles in Chinese MDD patients stratified for metabolic syndrome (MetS), and examined associations with depression severity (OSOD), suicidal ideation (SI), illness recurrence (ROI), and physiosomatic symptoms.
methodsWe enrolled 125 MDD inpatients (age 18-70 years) and 40 healthy controls (age 20-65 years). Fasting serum insulin, glucose, glucagon, GIP, GLP‑1, leptin, secretin, PAI‑1, resistin, ghrelin, and adiponectin were measured. The acute‑phase inflammatory (API) response was assessed using albumin, transferrin, and monomeric CRP. Group comparisons used ANOVA or general linear models (adjusted for age, BMI, MetS) with false discovery rate correction. Associations were tested with Pearson correlations, stepwise multiple regression, and binary logistic regression. Discriminatory performance was evaluated by ROC‑AUC.
resultsMDD showed significantly lower insulin, glucagon, and PAI‑1, along with a higher API index (all adjusted). A composite GAP index (ghrelin, adiponectin, PAI‑1) correlated negatively with OSOD, SI, ROI, physiosomatic symptoms, and adverse childhood experiences (ACEs). A model combining GAP index, API index, and ACEs discriminated MDD from controls with AUC = 0.864 and 80% accuracy.
conclusionSevere MDD in this Chinese inpatient sample is characterized by suppressed anabolic hormones and lower adipokines coupled with mild chronic inflammation, independent of MetS. This hormonal‑immune‑metabolic signature is integral to MDD pathophysiology.
Identifiers
What Socratic holds
Registered trials
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.