Diencephalic syndrome due to hypothalamic tumor: A model of the relationship between weight and puberty onset

被引:30
作者
Brauner, Raja
Trivin, Christine
Zerah, Michel
Souberbielle, Jean-Claude
Doz, Francois
Kalifa, Chantal
Sainte-Rose, Christian
机构
[1] Univ Paris 05, APHP, Hop Bicetre, Unite Endocrinol Pediat, F-94270 Le Kremlin Bicetre, France
[2] Hop Necker Enfants Malad, APHP, Ser Explorat Fonct, F-75743 Paris, France
[3] Hop Necker Enfants Malad, APHP, Serv Neurochirurg Pediat, F-75743 Paris, France
[4] Univ Paris 05, Inst Curie, Dept Pediat Oncol, F-75248 Paris, France
[5] Inst Gustave Roussy, Dept Pediat Oncol, F-94805 Villejuif, France
关键词
D O I
10.1210/jc.2006-0322
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Changes in body weight, statural growth rate, and puberty may be the presenting symptoms of hypothalamic-pituitary tumors. Objective: The objective of the study was to assess the relationship between the tumor and its treatment and the weight, growth rate, and onset of puberty, using the diencephalic syndrome of emaciation as model. Patients: Eleven patients seen before 1 yr of age, except one aged 9 yr, for diencephalic syndrome of emaciation due to hypothalamic pilocytic astrocytoma, were treated by surgical resection (n = 9), cranial irradiation (n = 7), and/or chemotherapy (n = 10). Results: At diagnosis, growth rate was normal, despite the emaciation, and there was no hypothalamic-pituitary deficiency, except in the oldest patient. After tumor treatment, all had GH and thyroid-stimulating hormone deficiencies, but only three, who underwent major surgical resection, also had ACTH deficiency and diabetes insipidus. Eight became obese, and all but the oldest had transient precocious puberty. Plasma leptin concentrations were very low at diagnosis, increased after tumor treatment, and decreased transiently in one boy when the testosterone increased. The plasma soluble leptin receptor concentrations changed in the opposite direction, leading to an increase in the free leptin index, including in the three patients whose tumor was reduced without surgery. The body mass index was correlated positively with plasma leptin (rho = 0.73, P = 0.0004) and free leptin index (rho = 0.63, P < 0.004) and negatively with ghrelin (rho = -0.49, P < 0.03) concentrations. Conclusions: The obesity that occurs after treatment of hypothalamic tumors is not due to dysregulation of leptin secretion because it and plasma soluble leptin receptor remain regulated by factors like testosterone. This study also shows the influence of weight, possibly via leptin secretion, on the transient hypothalamic-pituitary-gonadal activation that occurs during the first year of life.
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页码:2467 / 2473
页数:7
相关论文
共 28 条
[1]   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
[2]   DIENCEPHALIC SYNDROME REVISITED [J].
BURR, IM ;
SLONIM, AE ;
DANISH, RK ;
GADOTH, N ;
BUTLER, IJ .
JOURNAL OF PEDIATRICS, 1976, 88 (03) :439-444
[3]   Serum leptin through childhood and adolescence [J].
Clayton, PE ;
Gill, MS ;
Hall, CM ;
Tillmann, V ;
Whatmore, AJ ;
Price, DA .
CLINICAL ENDOCRINOLOGY, 1997, 46 (06) :727-733
[4]   Obesity in childhood craniopharyngioma: Relation to post-operative hypothalamic damage shown by magnetic resonance imaging [J].
DeVile, CJ ;
Grant, DB ;
Hayward, RD ;
Kendall, BE ;
Neville, BGR ;
Stanhope, R .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (07) :2734-2737
[5]   INAPPROPRIATE GROWTH-HORMONE RELEASE IN THE DIENCEPHALIC SYNDROME OF CHILDHOOD - CASE-REPORT AND 4-YEAR ENDOCRINOLOGICAL FOLLOW-UP [J].
DROP, SLS ;
GUYDA, HJ ;
COLLE, E .
CLINICAL ENDOCRINOLOGY, 1980, 13 (02) :181-187
[6]   Effects of recombinant leptin therapy in a child with congenital leptin deficiency [J].
Farooqi, IS ;
Jebb, SA ;
Langmack, G ;
Lawrence, E ;
Cheetham, CH ;
Prentice, AM ;
Hughes, IA ;
McCamish, MA ;
O'Rahilly, S .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (12) :879-884
[7]  
FISHMAN MA, 1970, PEDIATRICS, V45, P973
[8]   Diencephalic syndrome: A cause of failure to thrive and a model of partial growth hormone resistance [J].
Fleischman, A ;
Brue, C ;
Poussaint, TY ;
Kieran, M ;
Pomeroy, SL ;
Goumnerova, L ;
Scott, RM ;
Cohen, LE .
PEDIATRICS, 2005, 115 (06) :E742-E748
[9]  
Gropman AL, 1998, CANCER-AM CANCER SOC, V83, P166, DOI 10.1002/(SICI)1097-0142(19980701)83:1<166::AID-CNCR22>3.0.CO
[10]  
2-U