Evidence map›Paper›PMID 41193036›Full record

ArticleThe American journal of clinical nutrition2025

Cross-sectional analysis of visceral adipose tissue associations with obesity-related disease.

Adam W Potter, Karl E Friedl

Abstract read
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Article in The American journal of clinical nutrition, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

13 citing papers in PubMed.

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  7. Low testosterone is a phenotype of visceral adiposity.Journal of the Endocrine Society · 2026
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  13. Clinical Thresholds for Visceral Adiposity Accumulation: A Comparative Analysis in Sex-, Age-, and BMI-Matched Black and White Adults.American journal of human biology : the official journal of the Human Biology Council · 2025
    Article
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

2 authors.

Adam W PotterU.S. Army Research Institute of Environmental Medicine, Natick, MA, United States. Electronic address: adam.w.potter.civ@health.mil.
Karl E FriedlU.S. Army Research Institute of Environmental Medicine, Natick, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBody mass index (BMI) and waist circumference (WC) have served as primary metrics of obesity disease risk for the past 50+ y, but visceral adipose tissue (VAT) is the more direct etiological basis of obesity-related metabolic disease. Increasing availability of technologies for VAT estimation now makes it possible to practically apply this more precise assessment of individual risk.

objectivesWe hypothesized that VAT is a stronger predictor of metabolic syndrome, type 2 diabetes mellitus (T2DM), and insulin resistance [as measured by homeostasis model assessment of insulin resistance (HOMA-IR)] in United States adults than BMI, percent body fat (%BF), or WC. This hypothesis was tested using data from the National Health and Nutrition Examination Survey (NHANES).

methodsCross-sectional data from 4139 men and 4147 women, aged 18-59 y, from NHANES survey years 2011-2018, were analyzed for BMI, %BF, WC, WC/height, and VAT determined by dual-energy X-ray absorptiometry, compared with MetS disease risk outcomes classified as ≥3 markers, T2DM (glycated hemoglobin ≥6.5), insulin resistance (by HOMA-IR ≥2.0).

resultsReceiver operating characteristic curves and area under the curve (AUC) revealed high classification performance for VAT to MetS [AUC 0.84 ± 0.01 standard error (SE)], T2DM (AUC 0.80 ± 0.01 SE), and HOMA-IR (AUC 0.79 ± 0.01 SE). VAT risk thresholds for MetS were observed at 103 cm

conclusionsThese data suggest that VAT estimates may improve individual obesity risk management although this analysis did not demonstrate a clear advantage of VAT or a simple WC or WC/height. These data suggest a sex-independent threshold could be set for metabolic disease risk at approximately VAT ≥ 100 cm

Indexed as

Diabetes Mellitus, Type 2Intra-Abdominal FatMetabolic SyndromeObesityAdolescentAdultBody Mass IndexCross-Sectional StudiesFemaleHumansInsulin ResistanceMaleMiddle AgedNutrition SurveysWaist CircumferenceYoung Adultbody fatbody mass index (BMI)metabolic syndromeVATvisceral fat

Identifiers

PMID41193036
PMCPMC12799386

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Registered trials

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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.