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Expression of Matrix Metalloproteinases and Their Tissue Inhibitors in Peripheral Blood Leukocytes and Plasma of Children with Nonalcoholic Fatty Liver Disease. | LitMetric

AI Article Synopsis

  • The study examined gene expression profiles of matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in blood leukocytes of children with nonalcoholic fatty liver disease (NAFLD).
  • Results showed increased levels of certain gene expressions, plasma MMP-9, TIMP-1, and the MMP-9/TIMP-1 ratio in children with NAFLD, along with elevated liver injury markers like AST, ALT, and GGT.
  • The findings suggest that early changes in leukocyte gene expression may play a role in the initial stages of NAFLD before more widespread inflammatory responses occur.

Article Abstract

Gene expression profiles of matrix metalloproteinases () and their tissue inhibitors () were evaluated in peripheral blood leukocytes of children with nonalcoholic fatty liver disease (NAFLD). Gene expression patterns were correlated with their plasma protein counterparts, systemic parameters of liver injury, and selected markers of inflammation. The -, -, -, -, -, -, -, and - transcripts levels were tested by the real-time PCR. Plasma concentrations of MMP-9, TIMP-1, MMP-9/TIMP-1 ratio, MMP-2/TIMP-2 ratio, sCD14, leptin, resistin, IL-1 beta, and IL-6 and serum markers of liver injury were estimated by ELISA. The -, - expression levels, plasma amounts of MMP-9, TIMP-1, and the MMP-9/TIMP-1 ratio were increased in children with NAFLD. Concentrations of AST, ALT, GGT, and leptin were elevated in serum patients with NAFLD, while concentration of other inflammatory or liver injury markers was unchanged. The - and - levels correlated with serum liver injury parameters (ALT and GGT concentrations, respectively); there were no other correlations between gene expression profiles, their plasma counterparts, and serum inflammatory markers. Association of - and -9 expression with serum liver injury parameters (ALT, GGT) may suggest leukocyte engagement in the early stages of NAFLD development which possibly precedes subsequent systemic inflammatory responses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501567PMC
http://dx.doi.org/10.1155/2020/8327945DOI Listing

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