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Effects of metabolic traits, lifestyle factors, and pharmacological interventions on liver fat: mendelian randomisation study

OBJECTIVE: To investigate the effects of metabolic traits, lifestyle factors, and drug interventions on liver fat using the mendelian randomisation paradigm. DESIGN: Mendelian randomisation study. SETTING: Publicly available summary level data from genome-wide association studies. PARTICIPANTS: Geno...

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Detalles Bibliográficos
Autores principales: Yuan, Shuai, Chen, Jie, Vujkovic, Marijana, Chang, Kyong-Mi, Li, Xue, Larsson, Susanna C, Gill, Dipender
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978690/
https://www.ncbi.nlm.nih.gov/pubmed/36936593
http://dx.doi.org/10.1136/bmjmed-2022-000277
Descripción
Sumario:OBJECTIVE: To investigate the effects of metabolic traits, lifestyle factors, and drug interventions on liver fat using the mendelian randomisation paradigm. DESIGN: Mendelian randomisation study. SETTING: Publicly available summary level data from genome-wide association studies. PARTICIPANTS: Genome-wide association studies of 32 974 to 1 407 282 individuals who were predominantly of European descent. EXPOSURES: Genetic variants predicting nine metabolic traits, six lifestyle factors, four lipid lowering drug targets, three antihypertensive drug targets, and genetic association estimates formagnetic resonance imaging measured liver fat. MAIN OUTCOME MEASURES: Mendelian randomisation analysis was used to investigate the effects of these exposures on liver fat, incorporating sensitivity analyses that relaxed the requisite modelling assumptions. RESULTS: Genetically predicted liability to obesity, type 2 diabetes, elevated blood pressure, elevated triglyceride levels, cigarette smoking, and sedentary time watching television were associated with higher levels of liver fat. Genetically predicted lipid lowering drug effects were not associated with liver fat; however, β blocker and calcium channel blocker antihypertensive drug effects were associated with lower levels of liver fat. CONCLUSION: These analyses provide evidence of a causal effect of various metabolic traits, lifestyle factors, and drug targets on liver fat. The findings complement existing epidemiological associations, further provide mechanistic insight, and potentially supports a role for drug interventions in reducing the burden of hepatic steatosis and related disease. Further clinical study is now warranted to investigate the relevance of these genetic analyses for patient care.