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Efficacy and Safety of Glucagon-Like Peptide 1 Agonists in a Retrospective Study of Patients With Familial Partial Lipodystrophy

Overview
Journal Diabetes Care
Specialty Endocrinology
Date 2024 Feb 1
PMID 38300898
Authors
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Abstract

Objective: Glucagon-like peptide 1 receptor agonists (GLP-1RA) are widely used for the management of diabetes mellitus (DM), but their efficacy in familial partial lipodystrophy (FPLD) is unknown. In this retrospective study, we evaluated the effect of GLP-1RA in patients with FPLD.

Research Design And Methods: We analyzed data, reported with SDs, from 14 patients with FPLD (aged 58 ± 12 years; 76.47% female) and 14 patients with type 2 DM (aged 58 ± 13 years; 71% female) before and 6 months after starting GLP-1RA.

Results: We observed reduction in weight (95 ± 23 to 91 ± 22 kg; P = 0.002), BMI (33 ± 6 to 31 ± 6 kg/m2; P = 0.001), HbA1c (8.2% ± 1.4% to 7.7% ± 1.4%; P = 0.02), and fasting glucose (186 ± 64 to 166 ± 53 mg/dL; P = 0.04) in patients with FPLD. The change in triglycerides after treatment was greater in the FPLD group compared with the DM group (P = 0.02). We noted acute pancreatitis in two case subjects with FPLD with longer therapy.

Conclusions: Our study demonstrates the relative safety and effectiveness of GLP-1RA in patients with FPLD.

Citing Articles

Response to Comment on Foss-Freitas et al. Efficacy and Safety of Glucagon-Like Peptide 1 Agonists in a Retrospective Study of Patients With Familial Partial Lipodystrophy. Diabetes Care 2024;47:653-659.

Foss-Freitas M, Broome D, Oral E Diabetes Care. 2025; 48(3):e32.

PMID: 39977641 PMC: 11870280. DOI: 10.2337/dci24-0080.


Safety and effectiveness in an uncontrolled setting of glucagon-like-peptide-1 receptor agonists in patients with familial partial lipodystrophy: Real-life experience from a national reference network.

Lamothe S, Belalem I, Vantyghem M, Nobecourt E, Mosbah H, Beliard S Diabetes Obes Metab. 2025; 27(4):1815-1825.

PMID: 39829337 PMC: 11885082. DOI: 10.1111/dom.16175.


Familial partial lipodystrophy resulting from loss-of-function PPARγ pathogenic variants: phenotypic, clinical, and genetic features.

Soares R, da Silva M, de Melo Campos J, Lima J Front Endocrinol (Lausanne). 2024; 15:1394102.

PMID: 39398333 PMC: 11466747. DOI: 10.3389/fendo.2024.1394102.

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