Isolated follicle-stimulating hormone (FSH) deficiency in a young man with normal virilization who did not have mutations in the FSHβ gene

Giovanna Mantovani, Stefano Borgato, Paolo Beck-Peccoz, Roberto Romoli, Giorgio Borretta, Luca Persani

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Objective: To determine the cause of isolated FSH deficiency in a young infertile man. Design: Case report. Setting: Clinical and genetic studies in an academic research environment. Patient(s): A 19-year-old man with normal virilization, azoospermia, and isolated FSH deficiency. Intervention(s): Pituitary and gonadal functions were evaluated at baseline and after repeated GnRH stimulation. FSH was tested with both immunological and biological methods. The FSHβ gene was sequenced in the patient and in a series of 50 controls. Main Outcome Measure(s): Clinical, endocrine, and genetic characterization of an infertile patient with isolated FSH deficiency. Result(s): LH and T secretions were normal. No interference in FSH measurement was detected, and serum FSH concentrations were very low and completely unresponsive to repeated GnRH stimulation. No circulating FSH-like bioactivity was detected by means of rat Sertoli cell bioassay. Other pituitary functions were unaffected, and no lesions were seen at pituitary nuclear magnetic resonance (NMR). Inhibin B and activin levels were normal, but a progressive decrease of activin concentrations was seen during GnRH stimulation. The coding sequence of the FSHβ gene was normal, but the patient was homozygous for a novel G/T substitution in the promoter region within a P response element. This substitution was present in heterozygosity in eight out of 50 controls and in homozygosity in one man with normal FSH levels. Conclusion(s): We report an infertile male with isolated FSH deficiency but no evidence of mutations in the FSHβ gene. The G/T substitution in the FSHβ promoter represents a novel silent polymorphism, indicating that other defects in factors involved in FSH-specific expression should be taken into account.

Original languageEnglish
Pages (from-to)434-436
Number of pages3
JournalFertility and Sterility
Volume79
Issue number2
DOIs
Publication statusPublished - Feb 1 2003

Fingerprint

Virilism
Follicle Stimulating Hormone
Mutation
Genes
Gonadotropin-Releasing Hormone
Isolated Follicle-stimulating hormone deficiency
Activins
Azoospermia
Sertoli Cells
Response Elements
Genetic Promoter Regions
Biological Assay
Magnetic Resonance Spectroscopy
Outcome Assessment (Health Care)

Keywords

  • Activin
  • Azoospermia
  • FSH deficiency
  • FSHβ gene
  • Hypogonadism
  • Inhibin
  • Sertoli cell aromatase bioassay

ASJC Scopus subject areas

  • Obstetrics and Gynaecology

Cite this

Isolated follicle-stimulating hormone (FSH) deficiency in a young man with normal virilization who did not have mutations in the FSHβ gene. / Mantovani, Giovanna; Borgato, Stefano; Beck-Peccoz, Paolo; Romoli, Roberto; Borretta, Giorgio; Persani, Luca.

In: Fertility and Sterility, Vol. 79, No. 2, 01.02.2003, p. 434-436.

Research output: Contribution to journalArticle

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