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Genetically predicted body fat mass and distribution with diabetic kidney disease: A two-sample Mendelian randomization study

The aim of this study is to apply a Mendelian randomization (MR) design to investigate the potential causal associations between the body mass index (BMI), body fat mass such as trunk fat mass and waist circumference (WC), and diabetic kidney disease (DKD). A two-sample MR study was conducted to obt...

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Autores principales: Wang, Min, Li, Xin, Mei, Hang, Huang, Zhao-Hui, Liu, Yue, Zhu, Yong-Hong, Ma, Tian-Kui, Fan, Qiu-Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557077/
https://www.ncbi.nlm.nih.gov/pubmed/36246637
http://dx.doi.org/10.3389/fgene.2022.872962
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author Wang, Min
Li, Xin
Mei, Hang
Huang, Zhao-Hui
Liu, Yue
Zhu, Yong-Hong
Ma, Tian-Kui
Fan, Qiu-Ling
author_facet Wang, Min
Li, Xin
Mei, Hang
Huang, Zhao-Hui
Liu, Yue
Zhu, Yong-Hong
Ma, Tian-Kui
Fan, Qiu-Ling
author_sort Wang, Min
collection PubMed
description The aim of this study is to apply a Mendelian randomization (MR) design to investigate the potential causal associations between the body mass index (BMI), body fat mass such as trunk fat mass and waist circumference (WC), and diabetic kidney disease (DKD). A two-sample MR study was conducted to obtain exposure and outcome data from previously published studies. The instrumental variables for BMI, trunk fat mass, and WC were selected from genome-wide association study datasets based on summary-level statistics. The random-effects inverse-variance weighted (IVW) method was used for the main analyses, and the weighted median and MR-Egger approaches were complementary. In total, three MR methods suggested that genetically predicted BMI, trunk fat mass, and WC were positively associated with DKD. Using IVW, we found evidence of causal relationships between BMI [odds ratio (OR) = 1.99; 95% confidence interval (CI), 1.47–2.69; p = 7.89 × 10(−6)], trunk fat mass (OR = 1.80; 95% CI, 1.28–2.53; p = 6.84 × 10(−4)), WC (OR = 2.48; 95% CI, 1.40–4.42; p = 1.93 × 10(−3)), and DKD. MR-Egger and weighted median regression also showed directionally similar estimates. Both funnel plots and MR-Egger intercepts showed no directional pleiotropic effects involving the aforementioned variables and DKD. Our MR analysis supported the causal effect of BMI, trunk fat mass, and WC on DKD. Individuals can substantially reduce DKD risk by reducing body fat mass and modifying their body fat distribution.
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spelling pubmed-95570772022-10-14 Genetically predicted body fat mass and distribution with diabetic kidney disease: A two-sample Mendelian randomization study Wang, Min Li, Xin Mei, Hang Huang, Zhao-Hui Liu, Yue Zhu, Yong-Hong Ma, Tian-Kui Fan, Qiu-Ling Front Genet Genetics The aim of this study is to apply a Mendelian randomization (MR) design to investigate the potential causal associations between the body mass index (BMI), body fat mass such as trunk fat mass and waist circumference (WC), and diabetic kidney disease (DKD). A two-sample MR study was conducted to obtain exposure and outcome data from previously published studies. The instrumental variables for BMI, trunk fat mass, and WC were selected from genome-wide association study datasets based on summary-level statistics. The random-effects inverse-variance weighted (IVW) method was used for the main analyses, and the weighted median and MR-Egger approaches were complementary. In total, three MR methods suggested that genetically predicted BMI, trunk fat mass, and WC were positively associated with DKD. Using IVW, we found evidence of causal relationships between BMI [odds ratio (OR) = 1.99; 95% confidence interval (CI), 1.47–2.69; p = 7.89 × 10(−6)], trunk fat mass (OR = 1.80; 95% CI, 1.28–2.53; p = 6.84 × 10(−4)), WC (OR = 2.48; 95% CI, 1.40–4.42; p = 1.93 × 10(−3)), and DKD. MR-Egger and weighted median regression also showed directionally similar estimates. Both funnel plots and MR-Egger intercepts showed no directional pleiotropic effects involving the aforementioned variables and DKD. Our MR analysis supported the causal effect of BMI, trunk fat mass, and WC on DKD. Individuals can substantially reduce DKD risk by reducing body fat mass and modifying their body fat distribution. Frontiers Media S.A. 2022-09-29 /pmc/articles/PMC9557077/ /pubmed/36246637 http://dx.doi.org/10.3389/fgene.2022.872962 Text en Copyright © 2022 Wang, Li, Mei, Huang, Liu, Zhu, Ma and Fan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Wang, Min
Li, Xin
Mei, Hang
Huang, Zhao-Hui
Liu, Yue
Zhu, Yong-Hong
Ma, Tian-Kui
Fan, Qiu-Ling
Genetically predicted body fat mass and distribution with diabetic kidney disease: A two-sample Mendelian randomization study
title Genetically predicted body fat mass and distribution with diabetic kidney disease: A two-sample Mendelian randomization study
title_full Genetically predicted body fat mass and distribution with diabetic kidney disease: A two-sample Mendelian randomization study
title_fullStr Genetically predicted body fat mass and distribution with diabetic kidney disease: A two-sample Mendelian randomization study
title_full_unstemmed Genetically predicted body fat mass and distribution with diabetic kidney disease: A two-sample Mendelian randomization study
title_short Genetically predicted body fat mass and distribution with diabetic kidney disease: A two-sample Mendelian randomization study
title_sort genetically predicted body fat mass and distribution with diabetic kidney disease: a two-sample mendelian randomization study
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9557077/
https://www.ncbi.nlm.nih.gov/pubmed/36246637
http://dx.doi.org/10.3389/fgene.2022.872962
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