Key result
Serum adiponectin levels were significantly lower in NAFLD patients with high-grade liver fibrosis compared to low-grade fibrosis (p=0.000), with a cutoff of 2.31 μg/ml predicting stage 3/4 fibrosis.
Why the study?
The study evaluated the correlation between serum adiponectin level and liver fibrosis degree in NAFLD patients as a potential non-invasive alternative to liver biopsy, and examined its correlation with diabetes mellitus and obesity.
Cross-Sectional (n=50)
No
p-value: p=0.000
Serum adiponectin levels are significantly decreased in NAFLD patients with high-grade liver fibrosis, suggesting its potential as a non-invasive biomarker for assessing fibrosis severity.
Supports adiponectin as potential fibrosis biomarker in NAFLD; hypothesis-generating and requires prospective validation.
Background Non-alcoholic fatty liver disease (NAFLD) is one of the most prevalent chronic liver diseases, particularly in Egypt. It is defined as the accumulation of lipids inside the hepatocytes, in the absence of other etiologies of hepatic damage. It is frequently associated with obesity, diabetes mellitus, and metabolic syndrome. Adiponectin is an abundant adipocyte-derived protein with well-established anti-atherogenic, insulin-sensitizing, and anti-inflammatory properties. The liver is a major target organ for adiponectin especially in fatty liver diseases, and this adipocytokine has the ability to control many liver functions including metabolism, inflammation, and fibrosis. In this study, we aimed to find out the correlation between the degree of liver fibrosis in NAFLD patients and their serum adiponectin level as a future non-invasive method for the assessment of liver fibrosis to substitute liver biopsy to avoid its hazardous complication and also to study the correlation between diabetes mellitus as well as obesity and serum adiponectin level. Results Fifty patients were selected to participate in our study based on our inclusion criteria. They were recruited from the Internal Medicine Department, Gastroenterology Clinic in Al-Demerdash Hospital using a convenient sampling method. Diagnosis of NAFLD was confirmed by laboratory markers: aspartate aminotransferase (AST), alanine aminotransferase (ALT), lipid profile, ultrasound, and FibroScan examination. Analyzing the adiponectin levels showed that besides its significant correlation with body mass index (BMI), hypertension, diabetes mellitus, and dyslipidemia, it was significantly lower in the high-grade fibrosis group compared to the low-grade fibrosis group with a P-value of (0.000) and a cutoff value for stage 3/4 fibrosis of about 2.31 μg/ml which marked a promising hope of adiponectin being of protective value against liver fibrosis. Conclusion Both serum levels and hepatic adiponectin receptor expression are decreased in NAFLD. Therefore, either adiponectin itself or adiponectin-inducing agents might be of key therapeutic interest in the near future in the treatment of NAFLD.
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Mohamed et al. (2021) conducted a cross-sectional in Non-alcoholic fatty liver disease (n=50). Serum adiponectin level vs. Low-grade liver fibrosis was evaluated on Correlation between adiponectin level and degree of liver fibrosis (p=0.000). Serum adiponectin levels were significantly lower in NAFLD patients with high-grade liver fibrosis compared to low-grade fibrosis (p=0.000), with a cutoff of 2.31 μg/ml predicting stage 3/4 fibrosis.
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