دورية أكاديمية

Leptin replacement therapy for the treatment of non-HAART associated lipodystrophy syndromes: a meta-analysis into the effects of leptin on metabolic and hepatic endpoints

التفاصيل البيبلوغرافية
العنوان: Leptin replacement therapy for the treatment of non-HAART associated lipodystrophy syndromes: a meta-analysis into the effects of leptin on metabolic and hepatic endpoints
المؤلفون: Rodríguez, Alexander J., Neeman, Teresa, Giles, Aaron G., Mastronardi, Claudio A., Paz Filho, Gilberto
المصدر: Arquivos Brasileiros de Endocrinologia & Metabologia. November 2014 58(8)
بيانات النشر: Sociedade Brasileira de Endocrinologia e Metabologia, 2014.
سنة النشر: 2014
مصطلحات موضوعية: Leptin, lipodystrophy, meta-analysis, metreleptin, nonalcoholic fatty liver disease
الوصف: The clinical manifestations of lipodystrophy syndromes (LS) are hypoleptinemia, hyperglycemia, insulin resistance, dyslipidemia and hepatic steatosis. Leptin replacement therapy (LRT) is effective at improving these pathologies. Currently, there are no data compiling the evidence from the literature, and demonstrating the effect of LRT in LS patients. A systematic review of the MEDLINE and Cochrane Library databases was conducted to identify studies assessing the effect of LRT on metabolic and hepatic endpoints in patients with LS not associated with highly active antiretroviral therapy (HAART) use. Standardized mean differences (SMD) and 95% confidence intervals of pooled results were calculated for overall changes in glucose homeostasis, lipid profile, and hepatic physiology, using an inverse-variance random-effects model. After screening, 12 studies were included for review. Meta-analysis of results from 226 patients showed that LRT decreased fasting glucose [0.75 SMD units (range 0.36‐1.13), p=0.0001], HbA1c [0.49 (0.17‐0.81), p=0.003], triglycerides [1.00 (0.69‐1.31), p<0.00001], total cholesterol [0.62 (0.21‐1.02), p=0.003], liver volume [1.06 (0.51‐1.61), p=0.0002] and AST [0.41 (0.10‐0.73) p=0.01]. In patients with non-HAART LS, LRT improves the outcome of several metabolic and hepatic parameters. Studies were limited by small populations and therefore large prospective trials are needed to validate these findings.
نوع الوثيقة: article
وصف الملف: text/html
اللغة: English
تدمد: 0004-2730
DOI: 10.1590/0004-2730000003174
URL الوصول: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302014000800783
حقوق: info:eu-repo/semantics/openAccess
رقم الأكسشن: edssci.S0004.27302014000800783
قاعدة البيانات: SciELO
الوصف
تدمد:00042730
DOI:10.1590/0004-2730000003174