Introduction
Patients with diabetes mellitus (DM) are at an increased risk of developing cardiovascular disease (CVD). Hepatic steatosis is common among patients with DM, but its impact on CVD risk remains unclear.
Aims & Methods
This study aimed to prospectively assess the association between a reduction in hepatic steatosis and a lower risk of CVD in patients with DM.
A total of 323 patients with DM were prospectively enrolled from January 2022, after excluding those with viral hepatitis, overt cirrhosis, and cancer. Clinical measurements and CVD history were recorded. The following parameters were assessed: body weight (BW), body mass index (BMI), waist circumference (WC), laboratory data (aspartate aminotransferase, alanine aminotransferase, gamma-glutamyl transferase, platelet count, hemoglobin A1C, cholesterol, and triglycerides), presence of hypertension (HTN), dyslipidemia, alcohol consumption, smoking status, liver stiffness measurement (LSM by FibroScan®), and current anti-DM medications. Hepatic steatosis was quantified using the controlled attenuation parameter (CAP) measured by FibroScan® at baseline and after two years. CVD was defined as ischemic heart disease or ischemic/hemorrhagic stroke.
Results
A total of 277 patients completed the two-year follow-up and underwent repeat CAP assessment. The mean age was 57±12 years, and 56.3% were male. The baseline mean CAP was 274±18 dB/m. A history of CVD was present in 86 (31%) patients, while 6 (3.2%) developed new CVD events during follow-up. Among the new CVD cases, 3 were cardiac events, and 3 were neurovascular events. CAP scores decreased in 176 patients (d-CAP group) and increased in 101 patients (i-CAP group). The mean CAP change was -33±29 dB/m in the d-CAP group and +24±18 dB/m in the i-CAP group. The mean age was higher in the d-CAP group than in the i-CAP group (58±12 vs. 55±12 years, p=0.012). The baseline mean CAP was higher in the d-CAP group than in the i-CAP group (284±50 vs. 255±47 dB/m, p<0.001). There were no significant differences in male proportion (58% vs. 53.5%, p=0.468), BW (71±14 vs. 73±17 kg, p=0.258), BMI (26.1±4.2 vs. 27±4.9 kg/m2, p=0.14), WC (89±10 vs. 90±12 cm, p=0.397), laboratory data, HTN (56.8% vs. 48.5%, p=0.182), dyslipidemia (66.5% vs. 64.4%, p=0.72), alcohol consumption (24.4% vs. 21.8%, p=0.616), smoking status (48.9% vs. 43.6%, p=0.395), or baseline LSM (6.9±3.8 vs. 6.9±3.5 kPa, p=0.988) between the two groups. The use of metformin (93.2% vs. 93.1%, p=0.972) and pioglitazone (2.3% vs. 2%, p=1.0) did not differ significantly, but insulin use was lower in the d-CAP group than in the i-CAP group (5.1% vs. 12.9%, p=0.022). When stratified by CAP change, the incidence of new CVD was 0% (0/55) in patients with CAP reduction of ≤-40 dB/m, 2% (4/201) in those with changes between -40 and +40 dB/m, and 9.5% (2/21) in those with CAP increases of ≥+40 dB/m (p=0.037).
Conclusion
Hepatic steatosis, as measured by CAP, can change dynamically in patients with DM. Although this was an observational study, a marked decrease in CAP score was associated with a lower risk of CVD in patients with DM. Therefore, CAP monitoring may be a valuable tool for assessing CVD risk. Efforts to reduce hepatic steatosis, as reflected by CAP reduction, may contribute to CVD prevention in this population.