Key result
Elevated serum hsCRP levels in the highest quartile were associated with a significantly increased risk of MAFLD (adjusted OR 2.637) and correlated positively with the severity of liver steatosis and fibrosis in Chinese obese patients.
Why the study?
The association between hsCRP and the severity of liver steatosis and fibrosis among obese patients with MAFLD remained to be elucidated.
Does elevated hsCRP correlate with the risk of MAFLD and the severity of liver steatosis and fibrosis in Chinese obese patients?
Cross-Sectional (n=393)
No
Does elevated hsCRP correlate with the risk of MAFLD and the severity of liver steatosis and fibrosis in Chinese obese patients?
Odds Ratio: 2.637 (95% CI 1.073–6.482)
p-value: p=0.014
Elevated serum hsCRP levels are independently associated with an increased risk of MAFLD and greater severity of liver steatosis and fibrosis in obese patients.
hsCRP may aid risk stratification in obese MAFLD; leaves open whether it improves outcomes beyond imaging in prospective studies.
Background Metabolic dysfunction associated fatty liver disease (MAFLD) is the most common hepatopathy worldwide due to the obesity epidemic and is associated with chronic low-grade inflammation. High-sensitive C-reactive protein (hsCRP) as an inflammatory marker has been used in diagnosing MAFLD. However, the association between hsCRP and the severity of liver steatosis and fibrosis among obese patients with MAFLD remains to be elucidated. Objective To explore the correlation of hsCRP with the severity of liver steatosis and fibrosis among Chinese obese patients with MAFLD. Methods A total of 393 obese patients with mean BMI 34.8 ± 6.6 kg/m 2 were selected and categorized as MAFLD and non-MAFLD groups. Anthropometric data, biochemical indices, and hsCRP were measured. The severity of hepatic steatosis and fibrosis was assessed using FibroScan. Multivariate logistic regression analysis was performed to determine the relationship between hsCRP and the risk of MAFLD and its disease severity. Results Patients with MAFLD showed significantly elevated hsCRP levels and were more likely to have severe steatosis and fibrosis compared to those without MAFLD. The proportions of MAFLD, severe steatosis, and severe fibrosis were significantly increased across the hsCRP quartiles ( P -trend = 0.004, 0.021, and 0.006, respectively). After multivariable adjustments, the adjusted ORs (AORs) and 95%CI for MAFLD were 1.00 (reference), 1.298 (0.587-2.872), 2.407 (1.002-5.781), and 2.637(1.073-6.482) (Q1-Q4, P -trend = 0.014). Likewise, the AORs (95%CI) for severe steatosis and severe fibrosis were remarkably increased with the increment of serum hsCRP quartiles ( P -trend < 0.001, P -trend = 0.021, respectively). Conclusions Elevated serum hsCRP levels were associated with increased risk of MAFLD among Chinese obese patients and correlated positively with the severity of liver steatosis and fibrosis, suggesting that hsCRP can be used as a potential biomarker to monitor and predict disease severity among Chinese obese population with MAFLD.
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Zhu et al. (2022) conducted a cross-sectional in Metabolic Dysfunction Associated Fatty Liver Disease (MAFLD) in obesity (n=393). High-sensitive C-reactive protein (hsCRP) vs. Lowest hsCRP quartile (Q1) was evaluated on Risk of MAFLD (highest vs lowest hsCRP quartile) (OR 2.637, 95% CI 1.073-6.482, p=0.014). Elevated serum hsCRP levels in the highest quartile were associated with a significantly increased risk of MAFLD (adjusted OR 2.637) and correlated positively with the severity of liver steatosis and fibrosis in Chinese obese patients.
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