Evidence map›Paper›PMID 40017018›Full record

ArticleDiabetes, obesity & metabolism2025

Machine learning approach on plasma proteomics identifies signatures associated with obesity in the KORA FF4 cohort.

Jiefei Niu, Jonathan Adam, Thomas Skurk, Jochen Seissler, Qiuling Dong, Esienanwan Efiong, Christian Gieger, Annette Peters, Sapna Sharma, Harald Grallert

Abstract read
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Article in Diabetes, obesity & metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Jiefei NiuResearch Unit of Molecular Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.ORCID 0000-0003-4104-1426
Jonathan AdamResearch Unit of Molecular Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.
Thomas SkurkSchool of Medicine, Technical University of Munich, Munich, Germany.
Jochen SeisslerGerman Center for Diabetes Research (DZD), Neuherberg, Germany.
Qiuling DongResearch Unit of Molecular Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.ORCID 0000-0002-3369-4120
Esienanwan EfiongResearch Unit of Molecular Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.
Christian GiegerResearch Unit of Molecular Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.
Annette PetersInstitute of Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.
Sapna SharmaResearch Unit of Molecular Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.
Harald GrallertResearch Unit of Molecular Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.

Funding

Bavarian State Ministry of Health, Care and PreventionGerman Federal Ministry of Education and Research (BMBF)Helmholtz Zentrum München - German Research Center for Environmental HealthUniversity Hospital of Augsburg
6 · The paper itself

Abstract

aimsThis study investigated the role of plasma proteins in obesity to identify predictive biomarkers and explore underlying biological mechanisms.

methodsIn the Cooperative Health Research in the Region of Augsburg (KORA) FF4 study, 809 proteins were measured in 2045 individuals (564 obese and 1481 non-obese). Multivariate logistic regression adjusted for confounders (basic and full models) was used to identify obesity-associated proteins. Priority-Lasso was applied for feature selection, followed by machine learning models (support vector machine [SVM], random forest [RF], k-nearest neighbour [KNN] and adaptive boosting [Adaboost]) for prediction. Correlation and enrichment analyses were performed to elucidate relationships between protein biomarkers, obesity risk factors and perturbed pathways. Mendelian randomisation (MR) assessed causal links between proteins and obesity.

resultsA total of 16 proteins were identified as significantly associated with obesity through multivariable logistic regression in the basic model and subsequent Priority-Lasso analysis. Enrichment analyses highlighted immune response, lipid metabolism and inflammation regulation were linked to obesity. Machine learning models demonstrated robust predictive performance with area under the curves (AUC) of 0.820 (SVM), 0.805 (RF), 0.791 (KNN) and 0.819 (Adaboost). All 16 proteins correlated with obesity-related risk factors such as blood pressure and lipid levels. MR analysis identified AFM, CRP and CFH as causal and potentially modifiable proteins.

conclusionsThe protein signatures identified in our study showed promising predictive potential for obesity. These findings warrant further investigation to evaluate their clinical applicability, offering insights into obesity prevention and treatment strategies.

Indexed as

Blood ProteinsMachine LearningObesityProteomicsAdultAgedBiomarkersCohort StudiesFemaleHumansMaleMendelian Randomization AnalysisMiddle AgedRisk FactorsBiomarkersBlood Proteinscohort studymachine learningobesityproteomics

Identifiers

PMID40017018
PMCPMC11965001

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