Central precocious puberty: clinical and laboratory features

被引:89
作者
Chemaitilly, W
Trivin, C
Adan, L
Gall, V
Sainte-Rose, C
Brauner, R
机构
[1] Hop Necker Enfants Malad, Serv Endocrinol & Croissance, Assistance Publ Hop Paris, F-75743 Paris 15, France
[2] Univ Paris 05, Dept Paediat Endocrinol, F-75270 Paris 06, France
[3] Univ Paris 05, Dept Neurosurg, F-75270 Paris 06, France
[4] Univ Paris 05, Physiol Lab, F-75270 Paris 06, France
关键词
D O I
10.1046/j.1365-2265.2001.01229.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE 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. DESIGN 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). RESULTS 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 < 0.01) 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 <mu>g/l vs. 7.7 +/- 0.5 mug/l, P < 0.01), 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). CONCLUSIONS 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.
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页码:289 / 294
页数:6
相关论文
共 29 条
[1]   Growth, puberty and hypothalamic-pituitary function in children with suprasellar arachnoid cyst [J].
Adan, L ;
Bussières, L ;
Dinand, V ;
Zerah, M ;
Pierre-Kahn, A ;
Brauner, R .
EUROPEAN JOURNAL OF PEDIATRICS, 2000, 159 (05) :348-355
[2]   Leptin [J].
Auwerx, J ;
Staels, B .
LANCET, 1998, 351 (9104) :737-742
[4]  
Blum WF, 1997, J CLIN ENDOCR METAB, V82, P2904, DOI 10.1210/jc.82.9.2904
[5]   Serum leptin levels following hypothalamic surgery [J].
Brabant, G ;
Horn, R ;
Mayr, B ;
vonzurMuhlen, A ;
Honegger, J ;
Buchfelder, M .
HORMONE AND METABOLIC RESEARCH, 1996, 28 (12) :728-731
[6]  
BRAUNER R, 1984, NEW ENGL J MED, V311, P920
[7]   IDIOPATHIC CENTRAL PRECOCIOUS PUBERTY IN GIRLS AS A MODEL OF THE EFFECT OF PLASMA ESTRADIOL LEVEL ON GROWTH, SKELETAL MATURATION AND PLASMA INSULIN-LIKE GROWTH FACTOR-I [J].
BRAUNER, R ;
MALANDRY, F ;
FONTOURA, M ;
PREVOT, C ;
SOUBERBIELLE, JC ;
RAPPAPORT, R .
HORMONE RESEARCH, 1991, 36 (3-4) :116-120
[8]   HOW MANY CASES OF TRUE PRECOCIOUS PUBERTY IN GIRLS ARE IDIOPATHIC [J].
CACCIARI, E ;
FREJAVILLE, E ;
CICOGNANI, A ;
PIRAZZOLI, P ;
FRANK, G ;
BALSAMO, A ;
TASSINARI, D ;
ZAPPULLA, F ;
BERGAMASCHI, R ;
CRISTI, GF .
JOURNAL OF PEDIATRICS, 1983, 102 (03) :357-360
[9]   HYPOTHALAMO-PITUITARY-GONADAL FUNCTION IN MALE CENTRAL PRECOCIOUS PUBERTY [J].
CHAUSSAIN, JL ;
SAVAGE, MO ;
NAHOUL, K ;
BRIJAWI, A ;
CANLORBE, P ;
JOB, JC .
CLINICAL ENDOCRINOLOGY, 1978, 8 (06) :437-444
[10]   A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction [J].
Clément, K ;
Vaisse, C ;
Lahlou, N ;
Cabrol, S ;
Pelloux, V ;
Cassuto, D ;
Gourmelen, M ;
Dina, C ;
Chambaz, J ;
Lacorte, JM ;
Basdevant, A ;
Bougneres, P ;
Lebouc, Y ;
Froguel, P ;
Guy-Grand, B .
NATURE, 1998, 392 (6674) :398-401