Table 4.
Year (reference) | Study design | Total participants analysed (n) | Baseline method of assessment of NAFLD | Cardiovascular disease study outcome | Adjusted risk (95% CI) for study outcome comparing presence versus absence of NAFLD |
---|---|---|---|---|---|
200614 | Cross-sectional analysis | 7526 | Elevated serum ALT >43 IU/l | 10-y coronary heart disease (CHD) risk by Framingham Risk Score | • adjusted HR men 1.3 (1.2 to 1.5) |
20076 | Prospective cohort study | 1439 | Upper tertileserum ALT | • 10-y all-cause mortality | • HR women 2.1 (1.5 to 3.0) |
• Fatal and non-fatal CVD | • HR 1.3 (0.92 to 1.8) | ||||
• Fatal and non-fatal CHD | • HR 1.4 (1.1 to 1.8) | ||||
• HR 2.0 (1.4 to 3.1) | |||||
200515 | Prospective nested case-control study | 744 | Ultrasound findings of hepatic steatosis | Incidence of CVD event within 5-year follow-up in patients with DM2 | OR 1.6 (1.2 to 1.9) |
200716 | Prospective observational cohort study | 1221 | Ultrasound findings of hepatic steatosis | Incidence of CVD within a 5-year follow-up without DM2 | OR 4.1 (1.6 to 10.8) |
200817 | Prospective cohort study | 37085 | Elevated serum ALT >31 IU/l | CVD- or diabetes-related mortality | RR 2.3 (1.0 to 5.1) |
201118 | Cross-sectional study | 303 | Elevated serum ALT ≥95th centile | Acute ischemic stroke | OR 3.3 (1.3 to 8.4) |
Current | Prospective cohort study | 528 | Elevated serum ALT ≥90th centile | • Maximum measured cardiac troponin concentration at 24 h | • OR 7.1 (1.8 to 27.4) |
• All-cause mortality in-hospital | • OR 10.8 (3.6 to 32.4) | ||||
• All-cause mortality in-hospital and ≤6 months | • OR 9.0 (3.3 to 24.5) | ||||
• Composite of myocardial infarction, stroke, re-hospitalisation or all-cause mortality ≤6 months | • OR 2.7 (1.1 to 6.6) |
CHD, coronary heart disease; CVD, cardiovascular disease; DM2, type 2 diabetes mellitus; RR, adjusted relative risk.