The metabolic influence of duodenal mucosal resurfacing for nonalcoholic fatty liver disease

Author:

Chuang Te-Jung12ORCID,Ko Chung-Wang3,Shiu Sz-Iuan34

Affiliation:

1. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Tri Service General Hospital, Taipei, Taiwan

2. Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan

3. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan

4. Department of Critical Care Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.

Abstract

Background: Nonalcoholic fatty liver disease (NAFLD) or nonalcoholic steatohepatitis (NASH) is a leading cause of chronic liver disease worldwide with decreased life expectancy. Duodenal mucosal resurfacing (DMR) has been associated with metabolic improvement in glycemic and hepatic parameters of type 2 diabetes, but the metabolic impact of DMR for NAFLD/NASH remains inconclusive. We conducted a meta-analysis to investigate metabolic effects of DMR in patients with NAFLD/NASH. Methods: Three major bibliographic databases were reviewed for enrollment of trials prior to January 28, 2022. We included adults with biopsy-proven NAFLD/NASH or liver magnetic resonance imaging proton density fat fraction (MRI-PDFF) >5% at baseline and focused on the metabolic difference of MRI-PDFF at 12 weeks, and HbA1c or homeostatic model assessment index for insulin resistance (HOMA-IR) at 24 weeks. Results: Two studies involved a total of 67 participants for analysis. When compared with pre-intervention status, mean difference of MRI-PDFF, HbA1c, and HOMA-IR after DMR were −2.22 (95% CI: −12.79~8.34), −0.32% (95% CI: −0.80~0.16), and 0.15 (95% CI: −5.11~5.41) without statistical significance. Conclusions: For patients with NAFLD/NASH, DMR has the trend to improve liver fat at 12 weeks, and glycemic control in terms of HbA1c level at 24 weeks based on a very low quality of evidence.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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