Affiliation:
1. Department of Pediatric Endocrinology and Center for Rare Diseases in Hormonal Receptivity (R.C., N.B.-N., F.G., S.D., S.R.), Angers University Hospital, 49033 Angers, France;
2. Department of Pediatrics (E.B.-D.), General Hospital, 83600 Frejus, France;
3. Department of Pediatric Endocrinology and Center for Rare Disorders of Sex Development (C.B.), St. Vincent de Paul Hospital and René Descartes University, 75014 Paris, France
4. Department of Pediatric Hormonology and Metabolic Diseases (N.L.), St. Vincent de Paul Hospital and René Descartes University, 75014 Paris, France
Abstract
Context: The diagnosis of isolated hypogonadotropic hypogonadism (IHH) in boys with delayed puberty is challenging, as may be the diagnosis of hypogonadotropic hypogonadism (HH) in boys with combined pituitary hormone deficiency (CPHD). Yet, the therapeutic choices for puberty induction depend on accurate diagnosis and may influence future fertility.
Objective: The aim was to assess the utility of baseline inhibin B (INHB) and anti-Mullerian hormone (AMH) measurements to discriminate HH from constitutional delay of puberty (CDP). Both hormones are produced by Sertoli cells upon FSH stimulation. Moreover, prepubertal AMH levels are high as a reflection of Sertoli cell integrity.
Patients: We studied 82 boys aged 14 to 18 yr with pubertal delay: 16 had IHH, 15 congenital HH within CPHD, and 51 CDP, as confirmed by follow-up. Subjects were genital stage 1 (testis volume <3 ml; 9 IHH, 7 CPHD, and 23 CDP) or early stage 2 (testis volume, 3–6 ml; 7 IHH, 8 CPHD, and 28 CDP).
Results: Age and testis volume were similar in the three groups. Compared with CDP subjects, IHH and CPHD subjects had lower INHB, testosterone, FSH, and LH concentrations (P < 0.05), whereas AMH concentration was lower only in IHH and CPHD subjects with genital stage 1, likely reflecting a smaller pool of Sertoli cells in profound HH. In IHH and CPHD boys with genital stage 1, sensitivity and specificity were 100% for INHB concentration of 35 pg/ml or less. In IHH and CPHD boys with genital stage 2, sensitivities were 86 and 80%, whereas specificities were 92% and 88%, respectively, for an INHB concentration of 65 pg/ml or less. The performance of testosterone, AMH, FSH, and LH measurements was lower. No combination or ratio of hormones performed better than INHB alone.
Conclusion: Discrimination of HH from CDP with baseline INHB measurement was excellent in subjects with genital stage 1 and fair in subjects with genital stage 2.
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference42 articles.
1. Puberty: ontogeny, neuroendocrinology, physiology, and disorders;Grumbach;In: Larsen PR, Kronenberg HM, Melmed S, Polonsky KS, eds. Williams textbook of endocrinology. 10th ed. Philadelphia: Saunders;,2003
2. Kallmann’s syndrome: is it always for life?;Quinton;Clin Endocrinol (Oxf),1999
3. Clinical and molecular characterization of a large sample of patients with hypogonadotropic hypogonadism.;Bhagavath;Fertil Steril,2006
4. Digenic mutations account for variable phenotypes in isolated hypogonadotropic hypogonadism.;Pitteloud;J Clin Invest,2007
5. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.;Dodé;Nat Genet,2003
Cited by
116 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献