Data underlying the publication "Fatty Liver Index and mortality after myocardial infarction: A prospective analysis in the Alpha Omega Cohort"

doi: 10.4121/2949ab36-4860-4c96-a751-52eeb6e8022d.v2
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doi: 10.4121/2949ab36-4860-4c96-a751-52eeb6e8022d
Datacite citation style:
Heerkens, L. (2024): Data underlying the publication "Fatty Liver Index and mortality after myocardial infarction: A prospective analysis in the Alpha Omega Cohort" . Version 2. 4TU.ResearchData. dataset.
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version 2 - 2024-02-03 (latest)
version 1 - 2023-08-10

Data in this repository consists of the metadata, a read-me file, and the codebook, but not the minimal dataset to reproduce the results of the corresponding manuscript. The dataset is secured at the Division of Human Nutrition and Health, Wageningen University and Research, Wageningen, The Netherlands.

Accumulating evidence shows that NAFLD might play a role in the etiology and progression of CVD, but little is known on the association of NAFLD and CVD mortality in patients with a history of a myocardial infarction (MI). Therefore, we studied the relationship of Fatty Liver Index (FLI), as indicator for non-alcoholic fatty liver disease (NAFLD), with 12-year risk of cardiovascular disease (CVD) and all-cause mortality in post-MI patients. We included 4165 Dutch patients from the Alpha Omega Cohort aged 60-80 years who had an MI ≤10 years prior to study enrolment. NAFLD was defined as FLI ≥60. Patients were followed for cause-specific mortality from enrolment (2002-2006) through December 2018. Hazard ratios for CVD and all-cause mortality were obtained by multivariable Cox regression using FLI <30 (indicating absence of NAFLD) as the reference. Baseline FLI as a continuous measure were studied with mortality using restricted cubic splines analyses. The median (IQR) FLI was 68 (48-84). Sixty percent of the patients had FLI ≥60, who were more likely to be male and more often had diabetes, high blood pressure and high serum cholesterol levels. During 12 years of follow-up, 2042 deaths occurred of which 846 from CVD. Patients with NAFLD were at increased risk of CVD mortality (HR: 1.55 [1.19, 2.03]) and all-cause mortality (HR: 1.21 [1.03; 1.41]) compared to patients without NAFLD. Results remained consistent after excluding patients with obesity and diabetes. To conclude, the adverse association of FLI with CVD mortality were stronger in female than in male patients with conventional cut-off points. FLI ≥60, indicating NAFLD, was a predictor for CVD and all-cause mortality in post-MI patients, independent of other cardiometabolic risk factors. However, cut-off points might differ between male and female patients for predicting CVD mortality.

  • 2023-08-10 first online
  • 2024-02-03 published, posted
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Wageningen University & Research, Nutrition and Disease


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