Impaired pubertal development and testicular hormone function in males with sickle cell anemia

Impaired pubertal development and testicular hormone function in males with sickle cell anemia

Author Juliano Martins, Paulo Roberto Google Scholar
Kerbauy, Jose Autor UNIFESP Google Scholar
Moraes-Souza, Helio Google Scholar
Pereira, Gilberto de Araujo Google Scholar
Figueiredo, Maria Stella Autor UNIFESP Google Scholar
Verreschi, Ieda Therezinha Autor UNIFESP Google Scholar
Institution Univ Fed Triangulo Mineiro
Universidade Federal de São Paulo (UNIFESP)
Abstract Changes in weight/height ratio, delayed sexual maturation, hypogonadism and impaired fertility have been demonstrated in sickle cell disease (SCD). This study aimed to evaluate the clinical and laboratory views of the Leydig cells function after stimulation with hCG in adults with sickle cell disease. We studied 15 patients with SCD (18 to 40 years; median = 27 years old), fourteen homozygous S, and one with SC disease. the control group, composed by adult males, was divided into two groups: I-10 relatives (18-39 years, median = 26 years) with the same socioeconomic level of the patients, and II-9 normal individuals (23-28, median = 31 years) randomly chosen. Clinically it was observed a slight degree of malnutrition, important puberty delay, rarefaction of chest, underarm and pubic hair, and important reduction of the testis and penis size, featuring a mild hypogonadism in patients with SCD. the hormonal level assessment of testosterone at baseline and at 24,48 and 72 h after hCG stimulation showed no significant differences between the groups studied. We can presume that adult men with SCD showed clinical hypoandrogenism with normal testicular hormonal function, a fact inconsistent with the hypothesis of primary hypogonadism. (C) 2014 Elsevier Inc. All rights reserved.
Keywords Sickle cell disease
Pubertal development
Testicular hormonal function
Language English
Date 2015-01-01
Published in Blood Cells Molecules and Diseases. San Diego: Academic Press Inc Elsevier Science, v. 54, n. 1, p. 29-32, 2015.
ISSN 1079-9796 (Sherpa/Romeo, impact factor)
Publisher Elsevier B.V.
Extent 29-32
Access rights Closed access
Type Article
Web of Science ID WOS:000345539300006

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