Evidence map›Paper›PMID 37498361›Full record

ArticleMolecular genetics and genomics : MGG2023

Identification of potential genetic causal variants for obesity-related traits using statistical fine mapping.

Rui Gong, Jonathan Greenbaum, Xu Lin, Yan Du, Kuan-Jui Su, Yun Gong, Jie Shen, Hong-Wen Deng

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Article in Molecular genetics and genomics : MGG, 2023. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Rui GongEndocrinology Cadre Ward, Gansu Provincial Hospital, Lanzhou, 730000, Gansu, China.
Jonathan GreenbaumTulane Center for Biomedical Informatics and Genomics, Deming Department of Medicine, School of Medicine, Tulane University, New Orleans, LA, 70112, USA.
Xu LinShunde Hospital of Southern Medical University (The First People's Hospital of Shunde), Foshan, 528000, China.
Yan DuSchool of Nursing, The University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229, USA.
Kuan-Jui SuTulane Center for Biomedical Informatics and Genomics, Deming Department of Medicine, School of Medicine, Tulane University, New Orleans, LA, 70112, USA.
Yun GongTulane Center for Biomedical Informatics and Genomics, Deming Department of Medicine, School of Medicine, Tulane University, New Orleans, LA, 70112, USA.
Jie ShenShunde Hospital of Southern Medical University (The First People's Hospital of Shunde), Foshan, 528000, China.
Hong-Wen DengTulane Center for Biomedical Informatics and Genomics, Deming Department of Medicine, School of Medicine, Tulane University, New Orleans, LA, 70112, USA. hdeng2@tulane.edu.ORCID http://orcid.org/0000-0002-0387-8818

Funding

Trans-omics Integration of Multi-omics Studies for OsteoporosisU19AG055373 · NIA · TULANE UNIVERSITY OF LOUISIANA · PI HUI SHEN · 2017 to 2026
$24.3M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon · 2015 to 2026
$14.1M
Decoding Methylation Mediated Epigenomic Contributions to Male OsteoporosisR01AR069055 · NIAMS · TULANE UNIVERSITY OF LOUISIANA · PI DENG, HONG-WEN · 2017 to 2021
$2.9M
Foundation for the National Institutes of Health R01AR069055Foundation for the National Institutes of Health U19AG05537301Innovative Research Group Project of the National Natural Science Foundation of China 81770878Key Discipline Program of Gansu Provincial Hospital 20GSSY1-17NIAMS NIH HHS R01 AR069055NIA NIH HHS P30 AG044271NIA NIH HHS U19 AG055373Science and Technology Program of Chengguan district of Lanzhou 2020-2-2-13
6 · The paper itself

Abstract

backgroundObesity is highly influenced by heritability and variant effects. While previous genome-wide association studies (GWASs) have successfully identified numerous genetic loci associated with obesity-related traits [body mass index (BMI) and waist-to-hip ratio (WHR)], most causal variants remain unidentified. The high degree of linkage disequilibrium (LD) throughout the genome makes it extremely difficult to distinguish the GWAS-associated SNPs that exert a true biological effect.

objectiveThis study was to identify the potential causal variants having a biological effect on obesity-related traits.

methodsWe used Probabilistic Annotation INTegratOR, a Bayesian fine-mapping method, which incorporated genetic association data (GWAS summary statistics), LD structure, and functional annotations to calculate a posterior probability of causality for SNPs across all loci of interest. Moreover, we performed gene expression analysis using the available public transcriptomic data to validate the corresponding genes of the potential causal SNPs partially.

resultsWe identified 96 SNPs for BMI and 43 SNPs for WHR with a high posterior probability of causality (> 99%), including 49 BMI SNPs and 24 WHR SNPs which did not reach genome-wide significance in the original GWAS. Finally, we partially validated some genes corresponding to the potential causal SNPs.

conclusionUsing a statistical fine-mapping approach, we identified a set of potential causal variants to be prioritized for future functional validation and also detected some novel trait-associated variants. These results provided novel insight into our understanding of the genetics of obesity and also demonstrated that fine mapping may improve upon the results identified by the original GWASs.

Indexed as

Genome-Wide Association StudyObesityBayes TheoremChromosome MappingHumansLinkage DisequilibriumBMIFine mappingGenetic casual variantsObesityWHR

Identifiers

PMID37498361
PMCPMC11829812

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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.