Why the study?
Are newly described adipokines associated with liver histology in patients with biopsy-proven NAFLD?
Are newly described adipokines associated with liver histology in patients with biopsy-proven NAFLD?
Newly described adipokines such as chemerin, resistin, and adipocyte-fatty-acid-binding protein may play a role in NAFLD pathogenesis, but standardized assays and larger studies are needed to confirm these associations.
Adipokines should not guide NAFLD care; leaves open their pathogenic role pending consistent studies.
The prevalence of non-alcoholic fatty liver disease (NAFLD) is rising, as is the prevalence of obesity and type 2 diabetes. It is increasingly recognized that an impaired pattern in adipokine secretion could play a pivotal role in the development of NAFLD. We performed a systematic review to evaluate the potential link between newly described adipokines and liver histology in biopsy-proven NAFLD patients. A computerized literature search was performed in PubMed, EMBASE and Web of Science electronic databases. Thirty-one cross-sectional studies were included, resulting in a total of seven different investigated adipokines. Studies included in this review mainly had a good methodological quality. Most adipokines were suggested to be involved in the inflammatory response that develops within the context of NAFLD, either at hepatic or systemic level, and/or hepatic insulin resistance. Based on literature, clinical studies suggest that chemerin, resistin and adipocyte-fatty-acid-binding protein potentially are involved in NAFLD pathogenesis and/or progression. However, major inconsistency still exists, and there is a high need for larger studies, together with the need of standardized assays to determine adipokine levels.
No takes yet. Share an insight, caveat, or question.
Bekaert et al. (2015) studied this question.
Synapse has enriched one closely related paper. Consider it for comparative context: