Your browser doesn't support javascript.
loading
Long-term effectiveness and safety of metreleptin in the treatment of patients with generalized lipodystrophy.
Brown, Rebecca J; Oral, Elif A; Cochran, Elaine; Araújo-Vilar, David; Savage, David B; Long, Alison; Fine, Gregory; Salinardi, Taylor; Gorden, Phillip.
Afiliação
  • Brown RJ; National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA. brownrebecca@niddk.nih.gov.
  • Oral EA; Department of Internal Medicine, University of Michigan Medical School and Health Systems, Ann Arbor, MI, USA.
  • Cochran E; National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Araújo-Vilar D; Department of Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.
  • Savage DB; The University of Cambridge Metabolic Research Laboratories, Wellcome Trust-MRC Institute of Metabolic Science, Cambridge, UK.
  • Long A; Aegerion Pharmaceuticals, Cambridge, MA, USA.
  • Fine G; Aegerion Pharmaceuticals, Cambridge, MA, USA.
  • Salinardi T; Aegerion Pharmaceuticals, Cambridge, MA, USA.
  • Gorden P; National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
Endocrine ; 60(3): 479-489, 2018 06.
Article em En | MEDLINE | ID: mdl-29644599
ABSTRACT

PURPOSE:

The purpose of this study is to summarize the effectiveness and safety of metreleptin in patients with congenital or acquired generalized lipodystrophy.

METHODS:

Patients (n = 66) aged ≥6 months had lipodystrophy, low circulating leptin, and ≥1 metabolic abnormality (diabetes mellitus, insulin resistance, or hypertriglyceridemia). Metreleptin dose (once or twice daily) was titrated to a mean dose of 0.10 mg/kg/day with a maximum of 0.24 mg/kg/day. Means and changes from baseline to month 12 were assessed for glycated hemoglobin (HbA1c), fasting triglycerides (TGs), and fasting plasma glucose (FPG). Additional assessments included the proportions of patients achieving target decreases in HbA1c or fasting TGs at months 4, 12, and 36, medication changes, and estimates of liver size. Treatment-emergent adverse events (TEAEs) were recorded.

RESULTS:

Significant mean reductions from baseline were seen at month 12 for HbA1c (-2.2%, n = 59) and FPG (-3.0 mmol/L, n = 59) and mean percent change in fasting TGs (-32.1%, n = 57) (all p ≤ 0.001). Reductions from baseline over time in these parameters were also significant at month 36 (all p < 0.001, n = 14). At month 4, 34.8% of patients had a ≥1% reduction in HbA1c and 62.5% had a ≥30% reduction in fasting TGs; at month 12, 80% of patients had a ≥1% decrease in HbA1c or ≥30% decrease in TGs, and 66% had a decrease of ≥2% in HbA1c or ≥40% decrease in TGs. Of those on medications, 41%, 22%, and 24% discontinued insulin, oral antidiabetic medications, or lipid-lowering medications, respectively. Mean decrease in liver volume at month 12 was 33.8% (p < 0.001, n = 12). Most TEAEs were of mild/moderate severity.

CONCLUSIONS:

In patients with generalized lipodystrophy, long-term treatment with metreleptin was well tolerated and resulted in sustained improvements in hypertriglyceridemia, glycemic control, and liver volume.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipertrigliceridemia / Leptina / Lipodistrofia Generalizada Congênita Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hipertrigliceridemia / Leptina / Lipodistrofia Generalizada Congênita Idioma: En Ano de publicação: 2018 Tipo de documento: Article