Evidence map›Paper›PMID 42090348›Full record

ArticleNeuroimmunomodulation2026

Depressive Symptoms in Obese Individuals Accompanied by Greater Basal Inflammation but Lower Monocyte Inflammatory Responses to LPS: A Quest to Uncover Immunologic Links between Depression and Obesity.

Suzi Hong, Jordan Kohn, Stoyan Dimitrov, Christopher S Pruitt, Tiefu Cheng, Farah Shaikh

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

6 authors.

Suzi HongHerbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego, San Diego, California, USA, s1hong@health.ucsd.edu.
Jordan KohnHerbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego, San Diego, California, USA.
Stoyan DimitrovDepartment of Psychiatry, University of California San Diego, San Diego, California, USA.
Christopher S PruittHerbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego, San Diego, California, USA.
Tiefu ChengDepartment of Psychiatry, University of California San Diego, San Diego, California, USA.
Farah ShaikhDepartment of Psychiatry, University of California San Diego, San Diego, California, USA.

Funding

SAN DIEGO CLINICAL AND TRANSLATIONAL RESEARCH INSTITUTEUL1RR031980 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S · 2010 to 2011
$14.0M
Autonomic and Immuno-vascular Mechanisms of Antihypertensive Effects of TaichiR01HL126056 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HONG, SUZI, REDWINE, LAURA S · 2015 to 2019
$3.6M
Role of obesity on vascular inflammation and immune cell activation in prehyperteR01HL090975 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HONG, SUZI · 2009 to 2013
$2.2M
NCRR NIH HHS UL1 RR031980NHLBI NIH HHS R01 HL090975NHLBI NIH HHS R01 HL126056
6 · The paper itself

Abstract

introductionDespite the high prevalence of co-occurring conditions between obesity and depression, the knowledge of the underlying mechanisms remains limited. Given the existing evidence of obesity being an inflammatory condition and the association between elevated inflammation and treatment-resistant depression, investigations to uncover immune pathways underlying the obesity-depression link will shed light on the mechanisms and therapeutic options. We investigated whether depressive symptoms and adiposity are associated with greater inflammation and with suppressed innate immune responses to an immune challenge.

methodsImmune activities and depressive symptoms using the Beck Depression Inventory (BDI) were assessed in 96 participants of a weight range (normal weight, overweight, or obesity). Percent adiposity was measured by dual-energy X-ray absorptiometry. Plasma C-reactive protein (CRP), tumor necrosis factor (TNF), interleukin (IL)-1β, and IL-6 levels were determined by immunoassay. Lipopolysaccharides (LPSs)-stimulated intracellular TNF in peripheral blood monocytes was assessed by flow cytometry, which was also examined after incubation with recombinant TNF (rTNF) in 10 healthy participants of normal body mass index (BMI).

resultsObese, but not overweight, participants showed significantly higher BDI scores (T

conclusionOur findings provide the evidence that greater adiposity is associated with depressive symptoms and that obese individuals even without clinical depression experience elevated depressive symptoms. Whether immunologic dysregulation underlies this depressive mood-adiposity association is inconclusive despite greater CRP and lower monocyte reactivity among the obese, but low-grade inflammation in obesity may contribute to impaired innate immune responses to immunological challenge. Additional mechanistic investigations of obesity-related immune dysregulation underlying mood disorders would inform effective therapeutics.

Indexed as

DepressionInflammationMonocytesObesityAdultC-Reactive ProteinFemaleHumansLipopolysaccharidesMaleMiddle AgedTumor Necrosis Factor-alphaYoung AdultC-Reactive ProteinLipopolysaccharidesTumor Necrosis Factor-alphaDepressionInflammationMonocytesObesityTumor necrosis factor

Identifiers

PMID42090348
PMCPMC13348235

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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.