Arrigo Teresa, De Luca Filippo, Antoniazzi Franco, Galluzzi Fiorella, Segni Maria, Rosano Maria, Messina Maria Francesca, Lombardo Fortunato
Department of Pediatrics, University of Messina, Italy.
Eur J Endocrinol. 2004 Apr;150(4):533-7. doi: 10.1530/eje.0.1500533.
To investigate longitudinally body mass index (BMI) evolution and obesity prevalence in a large and very homogeneous study population consisting only of girls with non-organic central precocious puberty (CPP) who were treated with gonadotropin-releasing hormone agonists (GnRHa) for at least two years.
The 101 girls with idiopathic CPP who were selected for this study fulfilled the following inclusion criteria: (a) suppression of gonadotropin and gonadal sex steroid secretion during the overall GnRHa treatment period; (b) adequate compliance with the therapy regimen. All the girls were treated for 44+/-14 months and were followed-up for 15.7+/-7.8 months after therapy withdrawal.
At the start of therapy, 23.8% of the girls had a BMI exceeding 2 standard deviation scores (SDS) and were therefore classified as obese; both average BMI-SDS and obesity prevalence significantly decreased during the treatment period (chi(2)=16.6, P<0.0005) and only 4% of the patients, all with pre-existing obesity, were still obese at the end of therapy; during the therapy period, BMI-SDS increased in none of the patients. Both average BMI-SDS and obesity prevalence (from 4 to 0%; chi(2)=4.0, P<0.05) further decreased during the period that followed therapy withdrawal.
(a) girls with idiopathic CPP are frequently obese at the onset of GnRHa therapy (23.8%), probably due to the hormonal changes which accompany the start of puberty; (b) their obesity is neither long-lasting nor related to GnRHa administration; (c) on the contrary, GnRHa therapy may have a favourable effect on BMI decrease, provided that treatment is performed for at least two years and is accompanied by a complete suppression of gonadotropin secretion; (d) this unexpected effect, which has never been reported hitherto, might represent a further indication for GnRHa administration in idiopathic CPP.
在一个仅由接受促性腺激素释放激素激动剂(GnRHa)治疗至少两年的非器质性中枢性性早熟(CPP)女孩组成的大型且高度同质的研究人群中,纵向研究体重指数(BMI)的演变和肥胖患病率。
本研究选取的101例特发性CPP女孩符合以下纳入标准:(a)在整个GnRHa治疗期间促性腺激素和性腺甾体激素分泌受到抑制;(b)充分依从治疗方案。所有女孩接受了44±14个月的治疗,并在停药后随访了15.7±7.8个月。
治疗开始时,23.8%的女孩BMI超过2个标准差评分(SDS),因此被归类为肥胖;治疗期间平均BMI-SDS和肥胖患病率均显著下降(χ²=16.6,P<0.0005),治疗结束时只有4%的患者(均为原有肥胖者)仍为肥胖;治疗期间,无一例患者的BMI-SDS升高。停药后的随访期间,平均BMI-SDS和肥胖患病率(从4%降至0%;χ²=4.0,P<0.05)进一步下降。
(a)特发性CPP女孩在GnRHa治疗开始时经常肥胖(23.8%),可能是由于青春期开始时伴随的激素变化;(b)她们的肥胖既不是持久的,也与GnRHa给药无关;(c)相反,GnRHa治疗可能对BMI降低有有利影响,前提是治疗至少进行两年并伴有促性腺激素分泌的完全抑制;(d)这种此前从未报道过的意外效果可能代表了GnRHa用于特发性CPP治疗的另一个指征。