Background: Non-alcoholic fatty liver disease (NAFLD) and cardiovascular diseases frequently
coincide due to shared risk factors. Cardiovascular events are the most common causes
of death in NAFLD patients.
Objectives: To investigate whether established cardiovascular risk scores such as
the Framingham risk score (FRS) and the Heart Score of the European Society of Cardiology
(HS) are associated with the degree of fibrosis in NAFLD in a large screening cohort.
Material and Methods: We investigated 2138 asymptomatic subjects (59.6 ± 10.2 years, 50% males, BMI 27.2
± 4.6 kg/m2). NAFLD was diagnosed if 1. (Significantly increased echogenicity in relation to
the renal parenchyma present in ultrasound) and 2. (Exclusion of viral, autoimmune,
and hereditary liver disease and excess alcohol consumption) were fulfilled. The FRS
(ten-year risk of coronary heart disease), the HS (ten-year risk of fatal cardiovascular
disease) and the NAFLD Fibrosis Score (NFS) were calculated for each subject. Subsequently,
NFS, FRS and HS were correlated.
Results: Of 2138 subjects, 829 (38.7%) had NAFLD. Patients with NAFLD had a significantly
higher cardiovascular risk: FRS: no NAFLD: 5.5 ± 5.2%; NAFLD: 8.8 ± 6.5% (p < 0.001);
HS: no NAFLD: 2.9 ± 3.8%; NAFLD: 3.7 ± 4.1% (p = 0.002). In NAFLD subjects, NFS correlated
significantly with FRS (r = 0.18, p < 0.001) and HS (r = 0.27, p < 0.001) in Spearman
rank correlation. Patients with NAFLD were grouped into three groups according their
NFS: F0-F2 (n = 663); indifferent (n = 155); F3-F4 (n = 11). In patients with F0-F2,
FRS was 8.0 ± 6.1%; with indifferent NFS, 10.8 ± 6.4%; and in F3-F4: 11.5 ± 5.2%,
respectively. HS showed a similar pattern: F0-F2: 3.0 ± 3.4%; with indifferent NFS,
5.4 ± 4.5%, and in F3-F4: 7.0 ± 5.7%, respectively.
Conclusions: In this large asymptomatic screening cohort, subjects with non-invasive indicators
of advanced stages of NAFLD had an increased risk of coronary heart disease and cardiovascular
outcomes. A multidisciplinary approach including hepatologists and cardiologists is
important to ensure optimal care for these patients at high risk of CVD and liver-related
endpoints.