Why the study?
Do cardiometabolic risk factors and HbA1c levels predict disease severity in patients with metabolic dysfunction-associated steatotic liver disease?
Observational (n=2,882)
Yes
Do cardiometabolic risk factors and HbA1c levels predict disease severity in patients with metabolic dysfunction-associated steatotic liver disease?
Answers are grounded in this paper and cite their sources.
Cardiometabolic risk factors and elevated HbA1c levels are significantly associated with advanced fibrosis in patients with metabolic dysfunction-associated steatotic liver disease, highlighting the importance of diabetes control in this population.
The impacts of cardiometabolic risk factors (CMRFs) and the biomarkers on disease severity in metabolic dysfunction‐associated steatotic liver disease (MASLD) remain elusive. Accordingly, a multicenter study by recruiting MASLD patients from a nationwide registry database was conducted with a total of 2882 MASLD patients (54.1% males, mean age = 55.6 ± 13.9 years, mean body mass index [BMI] = 28.1 ± 4.9 kg/m 2 ) being recruited. The proportions of patients carrying CMRFs of overweight/obesity, hypertension, hypertriglyceridemia, low high‐density lipoprotein cholesterol level, and diabetes/prediabetes were 91.2%, 74.5%, 54.8%, 59.6%, and 74.5%, respectively. There was a significant linear trend between significant fibrosis and CMRFs (5.1%, 27%, and 54.6% in patients with one CMRF, 3 CMRFs, and ≥ 4 CMRFs, respectively, p = 0.009). The adjusted odds ratios (aOR) with 95% confidence intervals (CIs) for advanced fibrosis in patients of hemoglobin A1c (HbA1c) 5.7%–6.5%, 6.5%–8.0%, and > 8.0% were 1.02 (95% CI = 0.68–1.53, p = 0.93), 1.83 (95% CI = 1.16–2.88, p = 0.01), and 2.78 (95% CI = 1.45–5.34, p = 0.002), respectively. The significant risk factors for advanced fibrosis in MASLD were age > 60 years (aOR = 12.08, 95% CI = 6.23–23.46, p < 0.001), elevated transaminase level (aOR = 1.06, 95% CI = 1.05–1.09, p < 0.001), and diabetes (aOR = 1.51, 95% CI = 1.02–2.26, p = 0.04). In conclusion, there was a significant linear association between advanced fibrosis and the items of CMRFs. The HbA1c level could serve as a predictive biomarker for advanced fibrosis in MASLD with the implication that diabetes control is mandatory for patients with MASLD.
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Huang et al. (2026) conducted an observational in Metabolic dysfunction-associated steatotic liver disease (MASLD) (n=2,882). Elevated HbA1c (> 8.0%) and cardiometabolic risk factors vs. Lower HbA1c levels and fewer cardiometabolic risk factors was evaluated on Advanced fibrosis (aOR 2.78, 95% CI 1.45-5.34, p=0.002).
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