Chemaitilly W, Trivin C, Adan L, Gall V, Sainte-Rose C, Brauner R
Paediatric Endocrinology, Université René Descartes and Hôpital Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, France.
Clin Endocrinol (Oxf). 2001 Mar;54(3):289-94. doi: 10.1046/j.1365-2265.2001.01229.x.
To determine whether the initial presentation of patients with central precocious puberty (CPP) varies according to the aetiology, whether this permits the differentiation between idiopathic and organic forms, and whether the body mass index (BMI) and plasma leptin concentrations are linked to gonadotrophin secretion.
The clinical and laboratory features of 256 patients (26 boys and 230 girls) with CPP were studied separately in boys and girls. We compared patients with idiopathic CPP (seven boys and 186 girls) to those with organic CPP, whose pubertal development revealed a central nervous system (CNS) lesion (five boys and 11 girls), and to patients with organic CPP associated with a previously treated CNS lesion (14 boys and 33 girls).
Boys with organic CPP, having revealed or treated CNS lesions, started their puberty earlier (3.0 +/- 1.0 years and 6.7 +/- 0.5 years) than boys with idiopathic CPP (8.5 +/- 0.2 years, P < 0.01 and < 0.05). Boys with organic CPP associated with a treated CNS lesion had lower luteinizing hormone (LH)/follicle stimulating hormone (FSH) peaks ratio after stimulation with gonadotrophin releasing hormone (GnRH) (1.6 +/- 0.5) than did boys with idiopathic CPP (2.2 +/- 0.3, P < 0.05). Girls with organic CPP revealing a CNS lesion started their puberty earlier (3.6 +/- 0.9 years) than girls with idiopathic CPP (6.6 +/- 0.1 years, P < 0.0 l) and had higher LH (P < 0.01) and FSH peaks (< 0.05). Girls with organic CPP associated with a treated CNS lesion had higher BMI (1.8 +/- 0.2 z-score) than did girls with idiopathic CPP (1.3 +/- 0.1 zs, P < 0.05), higher leptin concentrations (11.7 +/- 1.8 microg/l vs. 7.7 +/- 0.5 microg/l, P < 0.0 l), LH peak (P < 0.01), FSH peak (P < 0.05) and LH/FSH peaks ratio (1 +/- 0.1 vs. 0.8 +/- 0.1, P < 0.05). Only 12.4% of the girls with idiopathic CPP had BMI-zs < 0, and their plasma leptins were positively correlated with BMI (P < 0.0001).
The features of central precocious puberty vary according to the aetiology, but it is impossible to exclude a central nervous system lesion in a given patient with central precocious puberty without performing central nervous system imaging. This imaging remains necessary in all cases of central precocious puberty. Most of the girls with idiopathic central precocious puberty had increased BMI, but we found no correlation between plasma leptin concentrations and gonadotrophin secretion.
确定中枢性性早熟(CPP)患者的初始表现是否因病因不同而有所差异,这是否有助于区分特发性和器质性类型,以及体重指数(BMI)和血浆瘦素浓度是否与促性腺激素分泌有关。
分别对256例CPP患者(26例男孩和230例女孩)的临床和实验室特征进行研究。我们将特发性CPP患者(7例男孩和186例女孩)与器质性CPP患者进行比较,后者的青春期发育显示有中枢神经系统(CNS)病变(5例男孩和11例女孩),并与先前接受过CNS病变治疗的器质性CPP患者(14例男孩和33例女孩)进行比较。
已发现或接受过CNS病变治疗的器质性CPP男孩比特发性CPP男孩青春期开始得更早(分别为3.0±1.0岁和6.7±0.5岁,而特发性CPP男孩为8.5±0.2岁,P<0.01和<0.05)。与接受过CNS病变治疗的器质性CPP男孩相比,特发性CPP男孩在促性腺激素释放激素(GnRH)刺激后黄体生成素(LH)/卵泡刺激素(FSH)峰值比更低(1.6±0.5)(特发性CPP男孩为2.2±0.3,P<0.05)。显示有CNS病变的器质性CPP女孩比特发性CPP女孩青春期开始得更早(3.6±0.9岁,而特发性CPP女孩为6.6±0.1岁,P<0.01),且LH峰值更高(P<0.01),FSH峰值更高(<0.05)。与接受过CNS病变治疗的器质性CPP女孩相比,特发性CPP女孩的BMI更高(1.8±0.2标准差评分)(特发性CPP女孩为1.3±0.1标准差评分,P<0.05),瘦素浓度更高(11.7±1.8μg/L对7.7±0.5μg/L,P<0.01),LH峰值更高(P<0.01),FSH峰值更高(P<0.05),LH/FSH峰值比更高(1±0.1对0.8±0.1,P<0.05)。特发性CPP女孩中只有12.4%的BMI标准差评分<0,且她们的血浆瘦素与BMI呈正相关(P<0.0001)。
中枢性性早熟的特征因病因不同而有所差异,但在未进行中枢神经系统成像的情况下,不可能排除某一中枢性性早熟患者存在中枢神经系统病变。在所有中枢性性早熟病例中,这种成像检查仍然是必要的。大多数特发性中枢性性早熟女孩的BMI有所增加,但我们发现血浆瘦素浓度与促性腺激素分泌之间没有相关性。