The effect of gonadotropin-releasing hormone analog treatment on the endocrine system in central precocious puberty patients: a meta-analysis

Author:

Guo Na12,Zhou Fei23,Jiang Xiaolan12,Yang Linlin24,Ma Huijuan5

Affiliation:

1. Graduate School of Hebei North University , Zhangjiakou , Hebei , P.R. China

2. Key Laboratory of Metabolic Diseases , Hebei General Hospital , Shijiazhuang , Hebei , P.R. China

3. Department of Internal Medicine , Hebei Medical University , Shijiazhuang , Hebei , P.R. China

4. Data Center , The First Hospital of Hebei Medical University , Hebei , 050031 , P.R. China

5. Department of Endocrinology , The First Hospital of Hebei Medical University , Shijiazhuang , Hebei , P.R. China

Abstract

Abstract Objectives Gonadotropin-releasing hormone (GnRHa) is the first choice for the treatment of patients with central precocious puberty (CPP). However, the effects of GnRHa on the endocrine system of CPP patients, including insulin sensitivity, lipid level, thyroid function, bone mineral density (BMD), and testosterone (T) level, are currently contradictory. Therefore, the long-term safety of GnRHa therapy remains controversial. Content A systematic literature search was performed using PubMed, Embase, Cochrane Library, and CNKI databases. The changes in HOMA-IR, TG, LDL-C, HDL-C, TSH, FT3, FT4, T, and BMD in CPP patients before and after GnRHa treatment were compared by meta-analysis. As the heterogeneity between studies, we estimated standard deviation mean differences (SMDs) and 95 % confidence intervals (CIs) using a random-effects model. Egger’s test was used to assess publication bias. Summary A total of 22 studies were included in our meta-analysis. Compared with before GnRHa treatment, there were no statistically significant differences in endocrine indicators including HOMA-IR, TG, LDL-C, HDL-C, TSH, FT4, FT3, T, and BMD of CPP patients treated with GnRHa. Outlook Treatment with GnRHa for central precocious puberty will not increase the adverse effect on the endocrine system.

Publisher

Walter de Gruyter GmbH

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