Effect of Leptin Therapy on Survival in Generalized and Partial Lipodystrophy: A Matched Cohort Analysis

Author:

Cook Keziah1,Ali Omer1,Akinci Baris2,Foss de Freitas Maria Cristina3,Montenegro Renan Magalhães4,Fernandes Virginia Oliveira4,Gupta Deepshekhar1,Lou Kai-Jye1ORCID,Tuttle Edward1,Oral Elif A5,Brown Rebecca J6ORCID

Affiliation:

1. Analysis Group Inc., Menlo Park, CA 94025, USA

2. Dokuz Eylul University, Izmir, 35220, Turkey

3. University of São Paulo – Ribeirao Preto Medical School, São Paulo, 14049, Brazil

4. Federal University of Ceará, Ceará, 60020, Brazil

5. Metabolism, Endocrine and Diabetes Division, Brehm Center for Diabetes, University of Michigan, Ann Arbor, MI 48109, USA

6. National Institute of Diabetes & Digestive & Kidney Diseases, Bethesda, MD 20814, USA

Abstract

Abstract Context Data quantifying the impact of metreleptin therapy on survival in non-human immunodeficiency virus (HIV)-related generalized lipodystrophy (GL) and partial lipodystrophy (PL) are unavailable. Objective This study aimed to estimate the treatment effect of metreleptin on survival in patients with GL and PL. Design/Setting/Patients Demographic and clinical characteristics were used to match metreleptin-treated and metreleptin-naïve patients with GL and PL. Differences in mortality risk were estimated between matched cohorts of metreleptin-treated and metreleptin-naïve patient cohorts using Cox proportional hazard models. Sensitivity analyses assessed the impact of study assumptions and the robustness of results. Outcome Measures This study assessed time-to-mortality and risk of mortality. Results The analysis evaluated 103 metreleptin-naïve patients with characteristics matched to 103 metreleptin-treated patients at treatment initiation. Even after matching, some metabolic and organ abnormalities were more prevalent in the metreleptin-treated cohort due to bias toward treating more severely affected patients. A Cox proportional hazards model associated metreleptin therapy with an estimated 65% decrease in mortality risk (hazard ratio [HR] 0.348, 95% confidence interval (CI): 0.134–0.900; P = 0.029) even though the actual number of events were relatively small. Results were robust across a broad range of alternate methodological assumptions. Kaplan–Meier estimates of time-to-mortality for the metreleptin-treated and the matched metreleptin-naïve cohorts were comparable. Conclusions Metreleptin therapy was associated with a reduction in mortality risk in patients with lipodystrophy syndromes despite greater disease severity in treated patients, supporting the view that metreleptin can have a positive disease-modifying impact. Confirmatory studies in additional real-world and clinical datasets are warranted.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

University of Michigan

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference32 articles.

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2. Lipodystrophies: genetic and acquired body fat disorders;Garg;J Clin Endocrinol Metab,2011

3. Burden of illness associated with generalized lipodystrophy in leptin replacement therapy-naïve patients: a longitudinal medical chart review study;Akinci;Endocr Rev,2018

4. Leptin controls the fate of fatty acids in isolated rat white adipocytes;William;J Endocrinol,2002

5. Lipodystrophy: pathophysiology and advances in treatment;Fiorenza;Nat Rev Endocrinol,2011

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