Evidence map›Paper›PMID 42653024›Full record

ArticleLife (Basel, Switzerland)2026

A Methodological Framework for Non-Invasive Body-Composition Phenotyping in Young Adults: Integrating Bioelectrical Impedance and Patient Similarity Networks.

Róbert László Nagy, Bence Bombera, Csongor István Szepesi, Nóra Horváth, Viktor Rekenyi, László Róbert Kolozsvári

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 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

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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

The trial behind it

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Róbert László NagyDepartment of Family and Occupational Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0009-0000-8150-6051
Bence BomberaDepartment of Family and Occupational Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0009-0007-1727-3119
Csongor István SzepesiDepartment of Family and Occupational Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Nóra HorváthDepartment of Family and Occupational Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0009-0006-7168-1378
Viktor RekenyiDepartment of Family and Occupational Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
László Róbert KolozsváriDepartment of Family and Occupational Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0001-9426-0898

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Body mass index (BMI) does not capture fat distribution or muscle-fat heterogeneity, so adverse patterns go undetected. We present a methodological framework-not a validated prediction tool-combining three laboratory-free constructs: an Office-Based Framingham cardiovascular risk score, a modified proxy-based FINDRISC, and a direct segmental multi-frequency bioelectrical impedance analysis (DSM-BIA)-derived Metabolically Unhealthy Obesity (MUO) index, with a weighted patient similarity network. We tested six predefined hypotheses in 1684 young adults (mean age 22.5 ± 8.3 years; 50.2% female). Framingham was applied off-label below 30 years, so its outputs give only relative within-cohort ordering; unavailable FINDRISC items were scored zero, so standard FINDRISC categories do not apply. BMI-defined obesity occurred in 6.9%, high visceral fat in 21.7%, high MUO in 21.8%, a BIA-defined TOFI (thin outside, fat inside)-like phenotype in 5.2%, and a sarcopenic-obesity-like phenotype in 9.9%. Visceral fat correlated with percent body fat (r = 0.855). The network resolved nine interpretable communities (modularity Q = 0.63; permutation

Indexed as

BIA-defined TOFI-like phenotypebioelectrical impedance analysisBMIbody compositioncardiometabolic riskMetabolically Unhealthy Obesitypatient similarity networkunsupervised clusteringvisceral adiposityyoung adults

Identifiers

PMID42653024
PMCPMC13514111

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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.