Genetically predicted basal metabolic rate and venous thromboembolism risk: a Mendelian randomization study

BackgroundBasal metabolic rate (BMR) is the minimum amount of energy needed by the body to carry out essential physiological functions. The goal of this study was to evaluate whether BMR causally influences venous thromboembolism (VTE) and its subtypes in European individuals.MethodsA two-sample Men...

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Main Authors: Jian Huang, Yubo Xie
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-12-01
Series:Frontiers in Nutrition
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnut.2023.1263804/full
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author Jian Huang
Yubo Xie
Yubo Xie
author_facet Jian Huang
Yubo Xie
Yubo Xie
author_sort Jian Huang
collection DOAJ
description BackgroundBasal metabolic rate (BMR) is the minimum amount of energy needed by the body to carry out essential physiological functions. The goal of this study was to evaluate whether BMR causally influences venous thromboembolism (VTE) and its subtypes in European individuals.MethodsA two-sample Mendelian randomization (MR) was performed. Within a genome-wide association study (GWAS) involving 454,874 people, genetic variants were chosen as instrumental variables based on their significant associations (p < 5 × 10−8) with BMR and their limited linkage disequilibrium (r2 < 0.001). The FinnGen project served as sources for summary statistics of VTE, encompassing different subtypes.ResultsUsing the multiplicative random-effect inverse variance weighted method, our investigation revealed that one standard deviation higher BMR was associated with VTE (odds ratio [OR] = 1.684, 95% confidence interval [CI]: 1.465–1.936, p = 2.339 × 10−13), PE (OR = 1.824, 95% CI: 1.512–2.200, p = 3.399 × 10−10), and DVT of lower extremities (OR = 1.887, 95% CI: 1.562–2.280, p = 4.778 × 10−11). The consistency of these associations was observed in sensitivity analyses using various MR techniques like Mendelian randomization pleiotropy residual sum and outlier, MR-Egger, weighted median, and contamination mixture method. In addition, multivariable MR revealed direct effects of BMR on VTE and its subtypes when taking body mass index and current tobacco smoking into account.ConclusionHigher BMR may increase the risk of VTE and its subtypes including PE and DVT of lower extremities.
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spelling doaj.art-339edaaf1ac844f49c73f8a3a15e9e2d2023-12-21T04:29:07ZengFrontiers Media S.A.Frontiers in Nutrition2296-861X2023-12-011010.3389/fnut.2023.12638041263804Genetically predicted basal metabolic rate and venous thromboembolism risk: a Mendelian randomization studyJian Huang0Yubo Xie1Yubo Xie2Clinical Laboratory Center, The First Affiliated Hospital of Guangxi Medical University, Nanning, ChinaDepartment of Anesthesiology, The First Affiliated Hospital of Guangxi Medical University, Nanning, ChinaGuangxi Key Laboratory of Enhanced Recovery After Surgery for Gastrointestinal Cancer, The First Affiliated Hospital of Guangxi Medical University, Nanning, ChinaBackgroundBasal metabolic rate (BMR) is the minimum amount of energy needed by the body to carry out essential physiological functions. The goal of this study was to evaluate whether BMR causally influences venous thromboembolism (VTE) and its subtypes in European individuals.MethodsA two-sample Mendelian randomization (MR) was performed. Within a genome-wide association study (GWAS) involving 454,874 people, genetic variants were chosen as instrumental variables based on their significant associations (p < 5 × 10−8) with BMR and their limited linkage disequilibrium (r2 < 0.001). The FinnGen project served as sources for summary statistics of VTE, encompassing different subtypes.ResultsUsing the multiplicative random-effect inverse variance weighted method, our investigation revealed that one standard deviation higher BMR was associated with VTE (odds ratio [OR] = 1.684, 95% confidence interval [CI]: 1.465–1.936, p = 2.339 × 10−13), PE (OR = 1.824, 95% CI: 1.512–2.200, p = 3.399 × 10−10), and DVT of lower extremities (OR = 1.887, 95% CI: 1.562–2.280, p = 4.778 × 10−11). The consistency of these associations was observed in sensitivity analyses using various MR techniques like Mendelian randomization pleiotropy residual sum and outlier, MR-Egger, weighted median, and contamination mixture method. In addition, multivariable MR revealed direct effects of BMR on VTE and its subtypes when taking body mass index and current tobacco smoking into account.ConclusionHigher BMR may increase the risk of VTE and its subtypes including PE and DVT of lower extremities.https://www.frontiersin.org/articles/10.3389/fnut.2023.1263804/fullbasal metabolic ratevenous thromboembolismdeep vein thrombosis of lower extremitiespulmonary embolismMendelian randomization
spellingShingle Jian Huang
Yubo Xie
Yubo Xie
Genetically predicted basal metabolic rate and venous thromboembolism risk: a Mendelian randomization study
Frontiers in Nutrition
basal metabolic rate
venous thromboembolism
deep vein thrombosis of lower extremities
pulmonary embolism
Mendelian randomization
title Genetically predicted basal metabolic rate and venous thromboembolism risk: a Mendelian randomization study
title_full Genetically predicted basal metabolic rate and venous thromboembolism risk: a Mendelian randomization study
title_fullStr Genetically predicted basal metabolic rate and venous thromboembolism risk: a Mendelian randomization study
title_full_unstemmed Genetically predicted basal metabolic rate and venous thromboembolism risk: a Mendelian randomization study
title_short Genetically predicted basal metabolic rate and venous thromboembolism risk: a Mendelian randomization study
title_sort genetically predicted basal metabolic rate and venous thromboembolism risk a mendelian randomization study
topic basal metabolic rate
venous thromboembolism
deep vein thrombosis of lower extremities
pulmonary embolism
Mendelian randomization
url https://www.frontiersin.org/articles/10.3389/fnut.2023.1263804/full
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AT yuboxie geneticallypredictedbasalmetabolicrateandvenousthromboembolismriskamendelianrandomizationstudy
AT yuboxie geneticallypredictedbasalmetabolicrateandvenousthromboembolismriskamendelianrandomizationstudy