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# These authors contributed equally to the study and are joint first authors.
Ziang Li
Footnotes
# These authors contributed equally to the study and are joint first authors.
Affiliations
State Key Laboratory of Cardiovascular Disease, Department of Cardiology, Fuwai Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100037, People’s Republic of China
# These authors contributed equally to the study and are joint first authors.
Bin Zhang
Footnotes
# These authors contributed equally to the study and are joint first authors.
Affiliations
State Key Laboratory of Cardiovascular Disease, Department of Cardiology, Fuwai Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100037, People’s Republic of China
Key Laboratory of Cardiovascular Epidemiology & Department of Epidemiology, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100037, China
State Key Laboratory for Oncogenes and Related Genes, Key Laboratory of Gastroenterology and Hepatology, Ministry of Health, Division of Gastroenterology and Hepatology, Shanghai Institute of Digestive Disease, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China
Corresponding author. Address: Fuwai Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Science and Peking Union Medical College, No.167 Beilishi Road, Beijing 100037, China; Tel.: +86 137 0138 7189, fax: +86 10-88396780.
State Key Laboratory of Cardiovascular Disease, Department of Cardiology, Fuwai Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100037, People’s Republic of China
Fatty liver disease has become the most prevalent chronic liver disease globally and is linked to cardiovascular disease, including arrhythmias. However, there have been inconsistent reports on the association between fatty liver disease and atrial fibrillation, while the role of liver stiffness in this association remains unclear.
Non-alcoholic fatty liver disease (NAFLD) and atrial fibrillation (AF) have become the most prevalent diseases in the fields of chronic liver disease and sustained cardiac arrhythmia, respectively, which attract significant interest due to their affiliated morbidity and increased mortality.
The findings, however, were not completely consistent. In a large prospective cohort, Van Kleef et al. discovered that fatty liver disease was not related to prevalent or incident AF.
Observational studies have methodological constraints and are inevitably subject to residual confounding factors. It is still uncertain if NAFLD is a causal factor in AF.
Mendelian randomisation (MR) analysis, which uses genetic variants as instrumental variables, is a powerful statistical tool for investigating causal relationships that have grown in popularity in epidemiology.
Genetic variants, which are unrelated to environmental factors, are randomly distributed at conception, which minimizes confounding and reverse causality. Hence, we used a two-sample MR analysis to assess the potential causal relationship between NAFLD and the risk of AF.
A genome-wide association study (GWAS) analysis in a histologically-characterized cohort of 1,483 biopsied NAFLD cases and 17,781 controls yielded 12 significant single nucleotide polymorphisms (SNPs) as genetically instrumental variables for NAFLD.
Because non-alcoholic steatohepatitis (NASH) and liver fibrosis are clinically important phenotypes in NAFLD and are more closely related to cardiovascular diseases, eight significant SNPs as genetic instrumental variables for NASH and three significant SNPs for advanced fibrosis (fibrosis stage F3 or F4) were extracted from this GWAS study to further investigate whether these severe NAFLD phenotypes lead to the development of AF. Furthermore, 55 significant SNPs (p <5×10−8) were procured from another large-scale GWAS study as genetic instruments of NAFLD for validation analysis, in which NAFLD was proxied by chronic alanine aminotransferase (cALT) elevation.
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.
AF was mainly diagnosed according to ICD-9 and ICD-10 codes. Details of instrumental variable selection and statistical analysis are included in the supplementary information.
To yield an overall estimate of the causal effect of NAFLD, NASH, and advanced fibrosis on AF, the inverse variance weighted method was used. To test the consistency of the results, three sensitivity analyses were performed: MR-Egger regression, weighted median, and MR-PRESSO analysis.
AF risk was not linked with NAFLD (odds ratio [OR] 0.99; 95% CI 0.97–1.01]; p = 0.15), nor NASH (OR 0.99; 95% CI 0.98–1.01; p = 0.43) or advanced fibrosis (OR 0.99; 95% CI 0.98–1.01; p = 0.25) (Fig. 1). If causality between NAFLD or severe NAFLD phenotypes and AF was prevalent at the strength denoted by observational epidemiology
(OR 1.27; 95% CI 1.18–1.37), our study had greater than 99% statistical power to detect a statistically significant effect. All sensitivity analyses produced generally consistent results. The Egger regression intercept analysis revealed no evidence of pleiotropy (intercept p value >0.05). Outliers were determined using the MR-PRESSO method, and their exclusion had no significant effect on the results. The results remained unchanged in the validation analysis (cALT, OR 1.00; 95% CI 0.96–1.04; p = 0.87) (Fig. 1).
There was no causal correlation in this MR study between genetically determined NAFLD or severe NAFLD phenotypes (NASH/advanced fibrosis) and the risk of AF. Although our study had enough statistical power to evaluate the causal relationships, the findings should be interpreted with prudence. The genetic instruments were chosen according to a relatively small-scale GWAS study (NAFLD: n = 1,434; NASH: n = 836; advanced fibrosis: n = 386). The genetic instruments utilized accounted for comparatively little genetic variance of phenotypes (NAFLD: 2.09%; NASH: 1.88%; advanced fibrosis: 1.27%), which could result in weak instrumental variables bias. Although we utilized another large-scale GWAS analysis with more individual SNPs for additional validation, NAFLD was defined in that study by cALT elevation rather than the presence of NAFLD per se. Besides, it did not provide stratification analyses for NASH or liver fibrosis. Given that there have only been a few GWAS studies of NAFLD based on liver biopsy, large-scale GWAS datasets and additional potentially related genetic variants are required for further validation. Furthermore, even though we used several sensitivity analyses to eliminate outlier variants and improve the robustness of the results, horizontal pleiotropy cannot be totally excluded.
In conclusion, our research did not show a causal relationship between genetically determined NAFLD or NAFLD subtypes and the risk of AF. MR analyses based on larger-scale GWAS summary data and more genetic instruments are needed to verify the results of our study.
Financial support
The authors received no financial support to produce this work.
Conflict of interest
All authors declared that no potential conflicts of interest should be disclosed in this study.
Please refer to the accompanying ICMJE disclosure forms for further details.
Authors’ contributions
Z.L and B.Z proposed the idea, performed the MR analyses, and drafted the manuscript. J.L and Z.T checked the integrity and plausibility of data analysis. Y.W revised the manuscript and was responsible for the integrity of data acquisition and statistical analyses.
We gratefully acknowledge the contributions of the Elucidating Pathways of Steatohepatitis consortium, the Million Veteran Program, and the Rotterdam study participants and investigators. Moreover, we thank the participants and investigators for summary statistics making the summary statistics available to the public. We appreciate Dr. Xiaoyi Wang for his helpful suggestions and Enago for the language polishing. Dr. Zhang holds a State Scholarship Fund from China Scholarship Council (No. 201806210439) and a fund from Capital’s Funds for Health Improvement and Research (CFH 2022-4-4037).
Supplementary data
The following are the supplementary data to this article:
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation.
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