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Vitamin D and Nonalcoholic Fatty Liver Disease: Bi-directional Mendelian Randomization Analysis

BACKGROUND: Vitamin D deficiency is associated with nonalcoholic fatty liver disease (NAFLD) in many cross-sectional studies. However, the causality between them has not been established. We used bi-directional mendelian randomization (MR) analysis to explore the causal relationship between 25-hydro...

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Autores principales: Wang, Ningjian, Chen, Chi, Zhao, Li, Chen, Yi, Han, Bing, Xia, Fangzhen, Cheng, Jing, Li, Qin, Lu, Yingli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835542/
https://www.ncbi.nlm.nih.gov/pubmed/29339098
http://dx.doi.org/10.1016/j.ebiom.2017.12.027
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author Wang, Ningjian
Chen, Chi
Zhao, Li
Chen, Yi
Han, Bing
Xia, Fangzhen
Cheng, Jing
Li, Qin
Lu, Yingli
author_facet Wang, Ningjian
Chen, Chi
Zhao, Li
Chen, Yi
Han, Bing
Xia, Fangzhen
Cheng, Jing
Li, Qin
Lu, Yingli
author_sort Wang, Ningjian
collection PubMed
description BACKGROUND: Vitamin D deficiency is associated with nonalcoholic fatty liver disease (NAFLD) in many cross-sectional studies. However, the causality between them has not been established. We used bi-directional mendelian randomization (MR) analysis to explore the causal relationship between 25-hydroxyvitamin D [25(OH)D] and NAFLD. METHODS: 9182 participants were included from a survey in East China from 2014 to 2016. We calculated weighted genetic risk scores (GRS) for 25(OH)D concentration and NAFLD based on 25(OH)D-related and NAFLD-related single nucleotide polymorphisms. Presence of liver steatosis was assessed using ultrasound. Instrumental variable was used to measure the causal relationship between them. RESULTS: An SD increase in the 25(OH)D GRS was significantly associated with 25(OH)D (β 1.29, 95%CI − 1.54, − 1.04, P < 0.05) but not with NAFLD (OR 0.97, 95%CI 0.92, 1.01). An SD increase in NAFLD GRS was also strongly associated with NAFLD (OR 1.09, 95%CI 1.04, 1.15, P < 0.05) but not with 25(OH)D (β − 0.15, 95%CI − 0.41, 0.10). Using an instrumental variable estimator, no associations were found for genetically instrumented 25(OH)D with NAFLD and for genetically instrumented NAFLD with 25(OH)D. CONCLUSION: Our results support the conclusion that there is no causal association between vitamin D and NAFLD using a bi-directional MR approach in a Chinese population.
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spelling pubmed-58355422018-03-06 Vitamin D and Nonalcoholic Fatty Liver Disease: Bi-directional Mendelian Randomization Analysis Wang, Ningjian Chen, Chi Zhao, Li Chen, Yi Han, Bing Xia, Fangzhen Cheng, Jing Li, Qin Lu, Yingli EBioMedicine Research Paper BACKGROUND: Vitamin D deficiency is associated with nonalcoholic fatty liver disease (NAFLD) in many cross-sectional studies. However, the causality between them has not been established. We used bi-directional mendelian randomization (MR) analysis to explore the causal relationship between 25-hydroxyvitamin D [25(OH)D] and NAFLD. METHODS: 9182 participants were included from a survey in East China from 2014 to 2016. We calculated weighted genetic risk scores (GRS) for 25(OH)D concentration and NAFLD based on 25(OH)D-related and NAFLD-related single nucleotide polymorphisms. Presence of liver steatosis was assessed using ultrasound. Instrumental variable was used to measure the causal relationship between them. RESULTS: An SD increase in the 25(OH)D GRS was significantly associated with 25(OH)D (β 1.29, 95%CI − 1.54, − 1.04, P < 0.05) but not with NAFLD (OR 0.97, 95%CI 0.92, 1.01). An SD increase in NAFLD GRS was also strongly associated with NAFLD (OR 1.09, 95%CI 1.04, 1.15, P < 0.05) but not with 25(OH)D (β − 0.15, 95%CI − 0.41, 0.10). Using an instrumental variable estimator, no associations were found for genetically instrumented 25(OH)D with NAFLD and for genetically instrumented NAFLD with 25(OH)D. CONCLUSION: Our results support the conclusion that there is no causal association between vitamin D and NAFLD using a bi-directional MR approach in a Chinese population. Elsevier 2018-01-09 /pmc/articles/PMC5835542/ /pubmed/29339098 http://dx.doi.org/10.1016/j.ebiom.2017.12.027 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Wang, Ningjian
Chen, Chi
Zhao, Li
Chen, Yi
Han, Bing
Xia, Fangzhen
Cheng, Jing
Li, Qin
Lu, Yingli
Vitamin D and Nonalcoholic Fatty Liver Disease: Bi-directional Mendelian Randomization Analysis
title Vitamin D and Nonalcoholic Fatty Liver Disease: Bi-directional Mendelian Randomization Analysis
title_full Vitamin D and Nonalcoholic Fatty Liver Disease: Bi-directional Mendelian Randomization Analysis
title_fullStr Vitamin D and Nonalcoholic Fatty Liver Disease: Bi-directional Mendelian Randomization Analysis
title_full_unstemmed Vitamin D and Nonalcoholic Fatty Liver Disease: Bi-directional Mendelian Randomization Analysis
title_short Vitamin D and Nonalcoholic Fatty Liver Disease: Bi-directional Mendelian Randomization Analysis
title_sort vitamin d and nonalcoholic fatty liver disease: bi-directional mendelian randomization analysis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835542/
https://www.ncbi.nlm.nih.gov/pubmed/29339098
http://dx.doi.org/10.1016/j.ebiom.2017.12.027
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