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Association between nonalcoholic fatty liver disease and left ventricular diastolic dysfunction: A 7-year retrospective cohort study of 3,380 adults using serial echocardiography - 21/04/24

Doi : 10.1016/j.diabet.2024.101534 
Gyuri Kim a, 1, Tae Yang Yu b, 1, Jae Hwan Jee c, Ji Cheol Bae d, Mira Kang c, , Jae Hyeon Kim a, e, f,
a Division of Endocrinology and Metabolism, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea 
b Division of Endocrinology and Metabolism, Department of Medicine, Wonkwang Medical Center, Wonkwang University School of Medicine, Iksan, Republic of Korea 
c Department of Health Promotion Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea 
d Division of Endocrinology and Metabolism, Department of Medicine, Samsung Changwon Hospital, Sungkyunkwan University School of Medicine, Changwon, Republic of Korea 
e Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Republic of Korea 
f Department of Clinical Research Design & Evaluation, SAIHST, Sungkyunkwan University, Republic of Korea 

Corresponding authors: Department of Health Promotion Center, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81, Irwon-ro, Gangnam-gu, Seoul 06351, Republic of Korea.Department of Health Promotion CenterSamsung Medical CenterSungkyunkwan University School of Medicine81, Irwon-ro, Gangnam-guSeoul06351Republic of Korea⁎⁎Corresponding authors: Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81, Irwon-ro, Gangnam-gu, Seoul 06351, Republic of Korea.Department of MedicineSamsung Medical CenterSungkyunkwan University School of Medicine81, Irwon-ro, Gangnam-guSeoul06351Republic of Korea

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Abstract

Aim

Left ventricular diastolic dysfunction (LVDD) has been observed in people with nonalcoholic fatty liver disease (NAFLD) in cross-sectional studies but the causal relationship is unclear. This study aimed to investigate the impact of NAFLD and the fibrotic progression of the disease on the development of LVDD, assessed by serial echocardiography, in a large population over a 7-year longitudinal setting.

Methods

This retrospective cohort study included the data of 3,380 subjects from a medical health check-up program. We defined subjects having NAFLD by abdominal ultrasonography and assessed significant liver fibrosis by the aspartate transaminase (AST) to platelet ratio index (APRI), the NAFLD fibrosis score (NFS), and the fibrosis-4 (FIB-4) index. LVDD was defined using serial echocardiography. A parametric Cox proportional hazards model was used.

Results

During 11,327 person-years of follow-up, there were 560 (16.0 %) incident cases of LVDD. After adjustment for multiple risk factors, subjects with NAFLD showed an increased adjusted hazard ratio (aHR) of 1.21 (95 % confidence interval [CI]=1.02–1.43) for incident LVDD compared to those without. The risk of LV diastolic dysfunction increased progressively with increasing degree of hepatic steatosis (P < 0.001). Compared to subjects without NAFLD, the multivariable-aHR (95 % CI) for LVDD in subjects with APRI < 0.5 and APRI ≥ 0.5 were 1.20 (1.01–1.42) and 1.36 (0.90–2.06), respectively (P = 0.036), while other fibrosis prediction models (NFS and FIB-4 index) showed insignificant results.

Conclusions

This study demonstrated that NAFLD was associated with an increased risk of LVDD in a large cohort. More severe forms of hepatic steatosis and/or significant liver fibrosis may increase the risk of developing LVDD.

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Keywords : Diastolic heart failure, Longitudinal study, Nonalcoholic fatty liver disease

Abbreviations : ALT, APRI, AST, BMI, CI, EF, FIB-4, FLI, FPG, HF, HFpEF, HFrEF, HR, LV, LVDD, NAFLD, NASH, NFS, TTE, US


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Vol 50 - N° 3

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