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Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study

BACKGROUND: A bidirectional association between atopic dermatitis and chronic kidney disease (CKD) has been revealed in observational studies, whereas the causality of this association was unclear. We conducted a Mendelian randomization study to determine the bidirectional causal association between...

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Autores principales: Zhang, Han, Yuan, Shuai, Li, Yong, Li, Doudou, Yu, Zengli, Hu, Lidan, Li, Xue, Wang, Yuming, Larsson, Susanna C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333750/
https://www.ncbi.nlm.nih.gov/pubmed/37441684
http://dx.doi.org/10.3389/fmed.2023.1180596
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author Zhang, Han
Yuan, Shuai
Li, Yong
Li, Doudou
Yu, Zengli
Hu, Lidan
Li, Xue
Wang, Yuming
Larsson, Susanna C.
author_facet Zhang, Han
Yuan, Shuai
Li, Yong
Li, Doudou
Yu, Zengli
Hu, Lidan
Li, Xue
Wang, Yuming
Larsson, Susanna C.
author_sort Zhang, Han
collection PubMed
description BACKGROUND: A bidirectional association between atopic dermatitis and chronic kidney disease (CKD) has been revealed in observational studies, whereas the causality of this association was unclear. We conducted a Mendelian randomization study to determine the bidirectional causal association between atopic dermatitis and CKD. METHODS: Independent genetic instruments associated with atopic dermatitis and CKD at the genome-wide significance level were chosen from corresponding meta-analyses of genome-wide association studies. Summary-level data for atopic dermatitis were obtained from the EAGLE Eczema consortium (30,047 cases and 40,835 controls) and FinnGen consortium (7,024 cases and 198,740 controls). Summary-level data for CKD were derived from CKDGen consortium (64,164 cases and 625,219 controls) and FinnGen consortium (3,902 cases and 212,841 controls). The inverse-variance weighted method was used in the main analysis and supplemented with three sensitivity analyses. RESULTS: Genetic predisposition to atopic dermatitis was associated with an increased risk of CKD. For a one-unit increase in the prevalence of atopic dermatitis, the odds ratio of CKD was 1.07 (95% confidence interval: 1.01–1.12). In the reverse Mendelian randomization analysis, the odds ratio of atopic dermatitis was 1.14 (95% confidence interval: 1.03–1.26) for a one-unit increase in the prevalence of CKD. The associations persisted in sensitivity analyses and no pleiotropy was detected. CONCLUSION: This Mendelian randomization study suggests a bidirectional positive association between atopic dermatitis and CKD.
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spelling pubmed-103337502023-07-12 Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study Zhang, Han Yuan, Shuai Li, Yong Li, Doudou Yu, Zengli Hu, Lidan Li, Xue Wang, Yuming Larsson, Susanna C. Front Med (Lausanne) Medicine BACKGROUND: A bidirectional association between atopic dermatitis and chronic kidney disease (CKD) has been revealed in observational studies, whereas the causality of this association was unclear. We conducted a Mendelian randomization study to determine the bidirectional causal association between atopic dermatitis and CKD. METHODS: Independent genetic instruments associated with atopic dermatitis and CKD at the genome-wide significance level were chosen from corresponding meta-analyses of genome-wide association studies. Summary-level data for atopic dermatitis were obtained from the EAGLE Eczema consortium (30,047 cases and 40,835 controls) and FinnGen consortium (7,024 cases and 198,740 controls). Summary-level data for CKD were derived from CKDGen consortium (64,164 cases and 625,219 controls) and FinnGen consortium (3,902 cases and 212,841 controls). The inverse-variance weighted method was used in the main analysis and supplemented with three sensitivity analyses. RESULTS: Genetic predisposition to atopic dermatitis was associated with an increased risk of CKD. For a one-unit increase in the prevalence of atopic dermatitis, the odds ratio of CKD was 1.07 (95% confidence interval: 1.01–1.12). In the reverse Mendelian randomization analysis, the odds ratio of atopic dermatitis was 1.14 (95% confidence interval: 1.03–1.26) for a one-unit increase in the prevalence of CKD. The associations persisted in sensitivity analyses and no pleiotropy was detected. CONCLUSION: This Mendelian randomization study suggests a bidirectional positive association between atopic dermatitis and CKD. Frontiers Media S.A. 2023-06-27 /pmc/articles/PMC10333750/ /pubmed/37441684 http://dx.doi.org/10.3389/fmed.2023.1180596 Text en Copyright © 2023 Zhang, Yuan, Li, Li, Yu, Hu, Li, Wang and Larsson. 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 Medicine
Zhang, Han
Yuan, Shuai
Li, Yong
Li, Doudou
Yu, Zengli
Hu, Lidan
Li, Xue
Wang, Yuming
Larsson, Susanna C.
Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study
title Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study
title_full Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study
title_fullStr Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study
title_full_unstemmed Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study
title_short Atopic dermatitis and chronic kidney disease: a bidirectional Mendelian randomization study
title_sort atopic dermatitis and chronic kidney disease: a bidirectional mendelian randomization study
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10333750/
https://www.ncbi.nlm.nih.gov/pubmed/37441684
http://dx.doi.org/10.3389/fmed.2023.1180596
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