Conventional and genetic evidence on the association between adiposity and CKD

<p><strong>Background </strong>The size of any causal contribution of central and general adiposity to CKD risk and the underlying mechanism of mediation are unknown.</p> <p><strong>Methods</strong> Data from 281,228 UK Biobank participants were used to est...

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Main Authors: Zhu, P, Herrington, WG, Haynes, R, Emberson, J, Landray, MJ, Sudlow, CLM, Woodward, M, Baigent, C, Lewington, S, Staplin, N
格式: Journal article
語言:English
出版: American Society of Nephrology 2020
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author Zhu, P
Herrington, WG
Haynes, R
Emberson, J
Landray, MJ
Sudlow, CLM
Woodward, M
Baigent, C
Lewington, S
Staplin, N
author_facet Zhu, P
Herrington, WG
Haynes, R
Emberson, J
Landray, MJ
Sudlow, CLM
Woodward, M
Baigent, C
Lewington, S
Staplin, N
author_sort Zhu, P
collection OXFORD
description <p><strong>Background </strong>The size of any causal contribution of central and general adiposity to CKD risk and the underlying mechanism of mediation are unknown.</p> <p><strong>Methods</strong> Data from 281,228 UK Biobank participants were used to estimate the relevance of waist-to-hip ratio and body mass index (BMI) to CKD prevalence. Conventional approaches used logistic regression. Genetic analyses used Mendelian randomization (MR) and data from 394 waist-to-hip ratio and 773 BMI-associated loci. Models assessed the role of known mediators (diabetes mellitus and BP) by adjusting for measured values (conventional analyses) or genetic associations of the selected loci (multivariable MR).</p> <p><strong>Results</strong> Evidence of CKD was found in 18,034 (6.4%) participants. Each 0.06 higher measured waist-to-hip ratio and each 5-kg/m2 increase in BMI were associated with 69% (odds ratio, 1.69; 95% CI, 1.64 to 1.74) and 58% (1.58; 1.55 to 1.62) higher odds of CKD, respectively. In analogous MR analyses, each 0.06–genetically-predicted higher waist-to-hip ratio was associated with a 29% (1.29; 1.20 to 1.38) increased odds of CKD, and each 5-kg/m2 genetically-predicted higher BMI was associated with a 49% (1.49; 1.39 to 1.59) increased odds. After adjusting for diabetes and measured BP, chi-squared values for associations for waist-to-hip ratio and BMI fell by 56%. In contrast, mediator adjustment using multivariable MR found 83% and 69% reductions in chi-squared values for genetically-predicted waist-to-hip ratio and BMI models, respectively.</p> <p><strong>Conclusions</strong> Genetic analyses suggest that conventional associations between central and general adiposity with CKD are largely causal. However, conventional approaches underestimate mediating roles of diabetes, BP, and their correlates. Genetic approaches suggest these mediators explain most of adiposity-CKD–associated risk.</p>
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spelling oxford-uuid:f13c73d1-0acb-4aba-822e-f2ee4e7f345f2022-03-27T11:54:33ZConventional and genetic evidence on the association between adiposity and CKDJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:f13c73d1-0acb-4aba-822e-f2ee4e7f345fEnglishSymplectic ElementsAmerican Society of Nephrology2020Zhu, PHerrington, WGHaynes, REmberson, JLandray, MJSudlow, CLMWoodward, MBaigent, CLewington, SStaplin, N<p><strong>Background </strong>The size of any causal contribution of central and general adiposity to CKD risk and the underlying mechanism of mediation are unknown.</p> <p><strong>Methods</strong> Data from 281,228 UK Biobank participants were used to estimate the relevance of waist-to-hip ratio and body mass index (BMI) to CKD prevalence. Conventional approaches used logistic regression. Genetic analyses used Mendelian randomization (MR) and data from 394 waist-to-hip ratio and 773 BMI-associated loci. Models assessed the role of known mediators (diabetes mellitus and BP) by adjusting for measured values (conventional analyses) or genetic associations of the selected loci (multivariable MR).</p> <p><strong>Results</strong> Evidence of CKD was found in 18,034 (6.4%) participants. Each 0.06 higher measured waist-to-hip ratio and each 5-kg/m2 increase in BMI were associated with 69% (odds ratio, 1.69; 95% CI, 1.64 to 1.74) and 58% (1.58; 1.55 to 1.62) higher odds of CKD, respectively. In analogous MR analyses, each 0.06–genetically-predicted higher waist-to-hip ratio was associated with a 29% (1.29; 1.20 to 1.38) increased odds of CKD, and each 5-kg/m2 genetically-predicted higher BMI was associated with a 49% (1.49; 1.39 to 1.59) increased odds. After adjusting for diabetes and measured BP, chi-squared values for associations for waist-to-hip ratio and BMI fell by 56%. In contrast, mediator adjustment using multivariable MR found 83% and 69% reductions in chi-squared values for genetically-predicted waist-to-hip ratio and BMI models, respectively.</p> <p><strong>Conclusions</strong> Genetic analyses suggest that conventional associations between central and general adiposity with CKD are largely causal. However, conventional approaches underestimate mediating roles of diabetes, BP, and their correlates. Genetic approaches suggest these mediators explain most of adiposity-CKD–associated risk.</p>
spellingShingle Zhu, P
Herrington, WG
Haynes, R
Emberson, J
Landray, MJ
Sudlow, CLM
Woodward, M
Baigent, C
Lewington, S
Staplin, N
Conventional and genetic evidence on the association between adiposity and CKD
title Conventional and genetic evidence on the association between adiposity and CKD
title_full Conventional and genetic evidence on the association between adiposity and CKD
title_fullStr Conventional and genetic evidence on the association between adiposity and CKD
title_full_unstemmed Conventional and genetic evidence on the association between adiposity and CKD
title_short Conventional and genetic evidence on the association between adiposity and CKD
title_sort conventional and genetic evidence on the association between adiposity and ckd
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