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Impact of GLP-1 Receptor Agonist Use in Patients With Steatotic Liver Disease and Type 2 Diabetes: A Retrospective Cohort Study.
Wood, Marci; Kennedy, Amanda G; Khan, Sidra; Hitt, Juvena R; Davis, Kayla; Reddy, Sheela S; Gilbert, Matthew P.
Afiliação
  • Wood M; The University of Vermont Medical Center, Burlington, VT, USA.
  • Kennedy AG; Department of Medicine Quality Program, University of Vermont Larner College of Medicine, Burlington, VT, USA.
  • Khan S; The University of Vermont Medical Center, Burlington, VT, USA.
  • Hitt JR; Department of Medicine Quality Program, University of Vermont Larner College of Medicine, Burlington, VT, USA.
  • Davis K; Ambulatory Clinical Pharmacist- Endocrinology, Yale New Haven Hospital, New Haven, CT, USA.
  • Reddy SS; Division of Gastroenterology and Hepatology, Harvard Medical School, Boston, Beth Israel Deaconess Medical Center, MA, USA.
  • Gilbert MP; Division of Endocrinology, Diabetes and Osteoporosis, The University of Vermont Larner College of Medicine, Burlington, VT USA.
J Pharm Pract ; : 8971900241253661, 2024 May 08.
Article em En | MEDLINE | ID: mdl-38720191
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.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Pharm Pract Assunto da revista: FARMACIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: J Pharm Pract Assunto da revista: FARMACIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos