Impact of GLP-1 Receptor Agonist Use in Patients With Steatotic Liver Disease and Type 2 Diabetes: A Retrospective Cohort Study

Author:

Wood Marci1ORCID,Kennedy Amanda G.2ORCID,Khan Sidra1,Hitt Juvena R.2,Davis Kayla3,Reddy Sheela S.4,Gilbert Matthew P.5

Affiliation:

1. The University of Vermont Medical Center, Burlington, VT, USA

2. Department of Medicine Quality Program, University of Vermont Larner College of Medicine, Burlington, VT, USA

3. Ambulatory Clinical Pharmacist- Endocrinology, Yale New Haven Hospital, New Haven, CT, USA

4. Division of Gastroenterology and Hepatology, Harvard Medical School, Boston, Beth Israel Deaconess Medical Center, MA, USA

5. Division of Endocrinology, Diabetes and Osteoporosis, The University of Vermont Larner College of Medicine, Burlington, VT USA

Abstract

Background: Glucagon-like peptide 1 receptor agonists (GLP-1 RAs) help manage type 2 diabetes (T2DM) and may have efficacy in steatotic liver disease. Objective: To determine the prevalence and clinical impact of GLP-1 RA use in patients with T2DM and liver disease. Methods: This was a retrospective study of adult patients with T2DM and nonalcoholic fatty liver disease (NAFLD), nonalcoholic fatty liver (NAFL), or nonalcoholic steatohepatitis (NASH) between 1/1/21-12/31/21. Patients with hepatitis B or C, or on pioglitazone were excluded. Eligible patients treated with a GLP-1 RA were compared to controls. The primary outcome was change in Fibrosis-4 (FIB-4) score, with NAFLD Fibrosis Score (NFS) as a secondary outcome. Follow-up scores were calculated from labs within 3 to 15 months after baseline. Results: Of 242 eligible patients, 79 patients (32.6%) were treated with a GLP-1 RA. At baseline, FIB-4 score was lower and NFS was higher in the GLP-1 RA group vs controls (1.80 vs 2.33; P = .101, .36 vs −.47, P < .001; respectively). At follow up, FIB-4 score decreased to 1.77 in the GLP-1 RA group and increased to 2.71 in controls (P = .045). Follow up NFS was stable in the GLP-1 RA group and increased in the control group (.36 vs −.43; P = .308). Conclusion: Patients treated with GLP-1 RAs had less evidence of liver fibrosis progression compared to no treatment, although the differences were small. These results suggest that treatment with GLP-1 RAs may have clinical impact on slowing liver fibrosis, however results should be confirmed in a larger, more diverse sample.

Publisher

SAGE Publications

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