Evidence map›Paper›PMID 40434639›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2025

Manifold fitting reveals metabolomic heterogeneity and disease associations in UK Biobank populations.

Bingjie Li, Jiaji Su, Runyu Lin, Shing-Tung Yau, Zhigang Yao

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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

5 authors.

Bingjie Li *Department of Statistics and Data Science, National University of Singapore, Singapore 117546, Singapore.
Jiaji Su *Department of Statistics and Data Science, National University of Singapore, Singapore 117546, Singapore.ORCID 0000-0003-3675-1407
Runyu Lin *Department of Statistics and Data Science, National University of Singapore, Singapore 117546, Singapore.ORCID 0009-0006-6604-5350
Shing-Tung YauYau Mathematical Sciences Center, Tsinghua University, Jingzhai, Beijing 100084, China.ORCID 0000-0003-3394-2187
Zhigang YaoDepartment of Statistics and Data Science, National University of Singapore, Singapore 117546, Singapore.ORCID 0000-0001-5927-6958

Funding

Singapore MOE Tier 1 A-8000987-00-00Singapore MOE Tier 1 A-8002931-00-00Singapore MOE Tier 2 A-0008520-00-00Singapore MOE Tier 2 A-8001562-00-00
6 · The paper itself

Abstract

NMR-based metabolic biomarkers provide comprehensive insights into human metabolism; however, extracting biologically meaningful patterns from such high-dimensional data remains a significant challenge. In this study, we propose a manifold-fitting-based framework to analyze metabolic heterogeneity within the UK Biobank population, utilizing measurements of 251 NMR biomarkers from 212,853 participants. Initially, our method clusters these biomarkers into seven distinct metabolic categories that reflect the modular organization of human metabolism. Subsequent manifold fitting to each category unveils underlying low-dimensional structures, elucidating fundamental variations from basic energy metabolism to hormone-mediated regulation. Importantly, three of these manifolds clearly stratify the population, identifying subgroups with distinct metabolic profiles and associated disease risks. These subgroups exhibit consistent links with specific diseases, including severe metabolic dysregulation and its complications, as well as cardiovascular and autoimmune conditions, highlighting the intricate relationship between metabolic states and disease susceptibility. Supported by strong correlations with demographic factors, clinical measurements, and lifestyle variables, these findings validate the biological relevance of the identified manifolds. By utilizing a geometrically informed approach to dissect metabolic heterogeneity, our framework enhances the accuracy of population stratification and deepens our understanding of metabolic health, potentially guiding personalized interventions and preventive healthcare strategies.

Indexed as

Biological Specimen BanksMetabolomeMetabolomicsAgedBiomarkersFemaleHumansMagnetic Resonance SpectroscopyMaleMiddle AgedUK BiobankUnited KingdomBiomarkersdisease risk predictiongeometric decompositionmanifold fittingmetabolic manifoldspopulation heterogeneity

Identifiers

PMID40434639
PMCPMC12146735

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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.