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- Publisher Website: 10.1186/s12916-021-01972-z
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Article: Shared genetic etiology and causality between body fat percentage and cardiovascular diseases: a large-scale genome-wide cross-trait analysis
Title | Shared genetic etiology and causality between body fat percentage and cardiovascular diseases: a large-scale genome-wide cross-trait analysis |
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Authors | |
Keywords | Body fat percentage Cardiovascular diseases Shared genetics Genetic correlation Mendelian randomization |
Issue Date | 2021 |
Publisher | BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcmed/ |
Citation | BMC Medicine, 2021, v. 19 n. 1, p. article no. 100 How to Cite? |
Abstract | Background:
Accumulating evidences have suggested that high body fat percentage (BF%) often occurs in parallel with cardiovascular diseases (CVDs), implying a common etiology between them. However, the shared genetic etiology underlying BF% and CVDs remains unclear.
Methods:
Using large-scale genome-wide association study (GWAS) data, we investigated shared genetics between BF% (N = 100,716) and 10 CVD-related traits (n = 6968-977,323) with linkage disequilibrium score regression, multi-trait analysis of GWAS, and transcriptome-wide association analysis, and evaluated causal associations using Mendelian randomization.
Results:
We found strong positive genetic correlations between BF% and heart failure (HF) (Rg = 0.47, P = 1.27 × 10− 22) and coronary artery disease (CAD) (Rg = 0.22, P = 3.26 × 10− 07). We identified 5 loci and 32 gene-tissue pairs shared between BF% and HF, as well as 16 loci and 28 gene-tissue pairs shared between BF% and CAD. The loci were enriched in blood vessels and brain tissues, while the gene-tissue pairs were enriched in the nervous, cardiovascular, and exo-/endocrine system. In addition, we observed that BF% was causally related with a higher risk of HF (odds ratio 1.63 per 1-SD increase in BF%, P = 4.16 × 10–04) using a MR approach.
Conclusions:
Our findings suggest that BF% and CVDs have shared genetic etiology and targeted reduction of BF% may improve cardiovascular outcomes. This work advances our understanding of the genetic basis underlying co-morbid obesity and CVDs and opens up a new way for early prevention of CVDs. |
Persistent Identifier | http://hdl.handle.net/10722/305893 |
ISSN | 2023 Impact Factor: 7.0 2023 SCImago Journal Rankings: 2.711 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Zhuang, Z | - |
dc.contributor.author | Yao, M | - |
dc.contributor.author | Wong, JYY | - |
dc.contributor.author | Liu, Z | - |
dc.contributor.author | Huang, T | - |
dc.date.accessioned | 2021-10-20T10:15:50Z | - |
dc.date.available | 2021-10-20T10:15:50Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | BMC Medicine, 2021, v. 19 n. 1, p. article no. 100 | - |
dc.identifier.issn | 1741-7015 | - |
dc.identifier.uri | http://hdl.handle.net/10722/305893 | - |
dc.description.abstract | Background: Accumulating evidences have suggested that high body fat percentage (BF%) often occurs in parallel with cardiovascular diseases (CVDs), implying a common etiology between them. However, the shared genetic etiology underlying BF% and CVDs remains unclear. Methods: Using large-scale genome-wide association study (GWAS) data, we investigated shared genetics between BF% (N = 100,716) and 10 CVD-related traits (n = 6968-977,323) with linkage disequilibrium score regression, multi-trait analysis of GWAS, and transcriptome-wide association analysis, and evaluated causal associations using Mendelian randomization. Results: We found strong positive genetic correlations between BF% and heart failure (HF) (Rg = 0.47, P = 1.27 × 10− 22) and coronary artery disease (CAD) (Rg = 0.22, P = 3.26 × 10− 07). We identified 5 loci and 32 gene-tissue pairs shared between BF% and HF, as well as 16 loci and 28 gene-tissue pairs shared between BF% and CAD. The loci were enriched in blood vessels and brain tissues, while the gene-tissue pairs were enriched in the nervous, cardiovascular, and exo-/endocrine system. In addition, we observed that BF% was causally related with a higher risk of HF (odds ratio 1.63 per 1-SD increase in BF%, P = 4.16 × 10–04) using a MR approach. Conclusions: Our findings suggest that BF% and CVDs have shared genetic etiology and targeted reduction of BF% may improve cardiovascular outcomes. This work advances our understanding of the genetic basis underlying co-morbid obesity and CVDs and opens up a new way for early prevention of CVDs. | - |
dc.language | eng | - |
dc.publisher | BioMed Central Ltd. The Journal's web site is located at http://www.biomedcentral.com/bmcmed/ | - |
dc.relation.ispartof | BMC Medicine | - |
dc.rights | BMC Medicine. Copyright © BioMed Central Ltd. | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Body fat percentage | - |
dc.subject | Cardiovascular diseases | - |
dc.subject | Shared genetics | - |
dc.subject | Genetic correlation | - |
dc.subject | Mendelian randomization | - |
dc.title | Shared genetic etiology and causality between body fat percentage and cardiovascular diseases: a large-scale genome-wide cross-trait analysis | - |
dc.type | Article | - |
dc.identifier.email | Liu, Z: zhhliu@hku.hk | - |
dc.identifier.authority | Liu, Z=rp02429 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1186/s12916-021-01972-z | - |
dc.identifier.pmid | 33910581 | - |
dc.identifier.pmcid | PMC8082910 | - |
dc.identifier.scopus | eid_2-s2.0-85104939441 | - |
dc.identifier.hkuros | 327203 | - |
dc.identifier.volume | 19 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | article no. 100 | - |
dc.identifier.epage | article no. 100 | - |
dc.identifier.isi | WOS:000647037600001 | - |
dc.publisher.place | United Kingdom | - |