Longitudinal Evaluation of the Hypothalamic-Pituitary-Testicular Function in 8 Boys with Adrenal Hypoplasia Congenita (AHC) Due to NR0B1 Mutations

被引:10
作者
Galeotti, Caroline [1 ,2 ]
Lahlou, Zineb [1 ,2 ]
Goullon, Domitille [1 ,2 ]
Sarda-Thibault, Helene [3 ]
Cahen-Varsaux, Juliette [4 ]
Bignon-Topalovic, Joelle [5 ]
Bashamboo, Anu [5 ]
McElreavey, Ken [5 ]
Brauner, Raja [1 ,2 ]
机构
[1] Univ Paris 05, Sorbonne Paris Cite, France
[2] Hop Bicetre, AP HP, Unite Endocrinol Pediat, Le Kremlin Bicetre, France
[3] Ctr Hosp Rene Dubos, Serv Pediat, Pontoise, France
[4] Ctr Hosp Victor Dupuy, Serv Diabetol Endocrinol, Argenteuil, France
[5] Inst Pasteur, Human Dev Genet Unit, Paris, France
来源
PLOS ONE | 2012年 / 7卷 / 06期
关键词
FOLLICLE-STIMULATING-HORMONE; SERUM INHIBIN-B; INCOMPLETE HYPOGONADOTROPIC HYPOGONADISM; NONSENSE MUTATION; GONADAL-FUNCTION; DAX-1; GENE; INSUFFICIENCY; MEN; SPERMATOGENESIS; EXPERIENCE;
D O I
10.1371/journal.pone.0039828
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Boys carrying mutations in the NR0B1 gene develop adrenal hypoplasia congenita (AHC) and impaired sexual development due to the combination of hypogonadotropic hypogonadism (HH) and primary defects in spermatogenesis. Methods: We analysed the evolution of hypothalamic-pituitary-testicular function of 8 boys with AHC due to NR0B1 mutations. Our objective was to characterize and monitor the progressive deterioration of this function. Results: The first symptoms appeared in the neonatal period (n = 5) or between 6 months and 8.7 years (n = 3). Basal plasma adrenocorticotrophic hormone (ACTH) concentrations increased in all boys, whilst cortisol levels decreased in one case. The natremia was equal or below 134 mmol/L and kaliemia was over 5 mmol/L. All had increased plasma renin. In 3 of 4 patients diagnosed in the neonatal period and evaluated during the first year, the basal plasma gonadotropins concentrations, and their response to gonadotropin releasing hormone (GnRH) test (n = 2), and those of testosterone were normal. The plasma inhibin B levels were normal in the first year of life. With the exception of two cases these concentrations decreased to below the normal for age. Anti-Mullerian hormone concentrations were normal for age in all except one case, which had low concentrations before the initiation of testosterone treatment. In 3 of the 8 cases the gene was deleted and the remaining 5 cases carried frameshift mutations that are predicted to introduce a downstream nonsense mutation resulting in a truncated protein. Conclusions: The decreases in testosterone and inhibin B levels indicated a progressive loss of testicular function in boys carrying NR0B1 mutations. These non-invasive examinations can help to estimate the age of the testicular degradation and cryopreservation of semen may be considered in these cases as investigational procedure with the aim of restoring fertility.
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页数:8
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