Evidence map›Paper›PMID 42315653›Full record

ArticleScientific reports2026

Abdominal fat distribution phenotypes and metabolic risk in premenopausal Asian women: insights beyond general adiposity measures.

Yeshe M Kway, Navin Michael, Narasimhan Kothandaraman, Jadegoud Yaligar, Mya Thway Tint, Kok Hian Tan, Keith M Godfrey, Peter D Gluckman, Yap Seng Chong, Melvin Khee-Shing Leow and 9 more

Abstract read
In one paragraph

Article in Scientific reports, 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
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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

19 authors.

Yeshe M KwayInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore. yeshekway@u.nus.edu.
Navin MichaelInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Narasimhan KothandaramanInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Jadegoud YaligarInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Mya Thway TintInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Kok Hian TanGraduate Medical School, Duke-National University of Singapore, Singapore, Singapore.
Keith M GodfreyMRC Lifecourse Epidemiology Centre & NIHR Southampton Biomedical Research Centre, University of Southampton & University Hospital Southampton NHS Foundation Trust, Southampton, UK.
Peter D GluckmanInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Yap Seng ChongInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Melvin Khee-Shing LeowInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Jerry K Y ChanDepartment of Reproductive Medicine, KK Women's and Children's Hospital, Singapore, Singapore.
Shiao-Yng ChanInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Marielle V FortierInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Johan G ErikssonInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Jonathan HuangInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Yung Seng LeeInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Mengling FengInstitute of Data Science, National University of Singapore, Singapore, Singapore.
S Sendhil VelanInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.
Suresh Anand SadananthanInstitute for Human Development and Potential, Agency for Science, Technology and Research, Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The rising prevalence of metabolic syndrome (MetS) and gestational diabetes mellitus (GDM) in women of reproductive age highlights their growing susceptibility to future cardiometabolic diseases. Both conditions signal early metabolic dysfunction tied to abdominal adiposity. We investigated whether relative abdominal adipose tissue (AAT) distribution characterises metabolic risk beyond general adiposity. Using magnetic resonance imaging, we quantified superficial (SSAT) and deep (DSAT) subcutaneous, intraperitoneal (IPAT), and retroperitoneal (RPAT) adipose tissue compartments to derive AAT distribution phenotypes from their relative contributions. These phenotypes were characterized with respect to MetS, GDM risk, ectopic fat accumulation, and metabolic profiles. The relative AAT distribution of higher %IPAT and lower %DSAT was a significant determinant for MetS. Women with both lower %IPAT and higher %DSAT exhibited the most favourable metabolic profiles, whereas women with higher %IPAT and lower %DSAT showed increased prevalence of MetS, hepatic steatosis, elevated high-sensitivity C-reactive protein, and 5.36-fold higher odds of developing GDM (95% CI 1.12-27.85). Notably, metabolic differences were observed despite similar overall adiposity including total AAT, body fat percentage, body mass index, and waist circumference. This suggests that AAT accumulation, particularly preferential DSAT over IPAT, captures metabolic heterogeneity and may support precision risk stratification of cardiometabolic disease in women.

Indexed as

Abdominal FatAdiposityMetabolic SyndromePremenopauseAdultAsian PeopleBody Mass IndexDiabetes, GestationalFemaleHumansMagnetic Resonance ImagingPhenotypePregnancyRisk FactorsSingaporeAbdominal adipose tissue distributionMetabolic risk phenotypesMetabolic syndrome

Identifiers

PMID42315653
PMCPMC13547274

What Socratic holds

Textmetadata
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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 Socratic graph.