Literature DB >> 17018446

beta-thalassemia and gonadal axis: a cross-sectional, clinical study in a Greek population.

John Papadimas1, Dimitrios G Goulis, Eudokia Mandala, George Georgiadis, Vassiliki Zournatzi, Basil C Tarlatzis, John N Bontis.   

Abstract

beta-thalassemia (beta-thal) is characterized by disturbances of the reproductive system. The aim of the present study was: 1) to assess the hypothalamic- pituitary-gonadal axis in patients with beta-thal in relation to their phenotype and 2) to determine prognostic features of current gonadal status. We studied 135 patients (67 males and 68 females) with beta-thal through history, physical examination, spermiograms and GnRH test. These patients were divided into beta-thal major (51 males and 62 females) and beta-thal intermedia phenotypes (16 males and 6 females). Male patients with beta-thal major were subdivided into three groups a) eugonadal (35%, Tanner's stage V, normal testicular volume, normal spermiograms, normal basal and stimulated hormone values), b) patients with hypogonadotrophic hypogonadism (HH) of late onset (24%, Tanner's stage II-V, low-normal testicular volume, abnormal spermiograms, normal basal gonadotrophin values and abnormal response to GnRH test) and c) patients with HH of early onset (41%, Tanner's stage I, small testicular volume, abnormal spermiograms, abnormal basal and stimulated hormone values). Female patients with beta-thal major were subdivided into: a) eugonadal (32%, Tanner's stage V, regular menstruation, normal basal and stimulated hormone values), b) patients with hypogonadotrophic hypogonadism (HH) of late onset (34%, Tanner's stage II-V, secondary amenorrhea, subnormal basal and stimulated gonadotrophin values) and c) patients with HH of early onset (34%, Tanner's stage I, primary amenorrhea, subnormal basal and stimulated hormone values). Patients with beta-thal intermedia were subdivided into eugonadal (75% of males, 33% of females) and hypogonadal (25% of males, 67% of females). Current gonadal status could not be predicted by means of transfusion or chelation parameters. In conclusion, beta-thal patients could be eugonadal or develop early or late onset HH. trade mark-thal intermedia patients have a more favorable profile than beta-thal major individuals. Current gonadal status of beta-thal patients cannot be predicted by means of history, clinical or laboratory parameters.

Entities:  

Year:  2002        PMID: 17018446     DOI: 10.14310/horm.2002.1166

Source DB:  PubMed          Journal:  Hormones (Athens)        ISSN: 1109-3099            Impact factor:   2.885


  6 in total

Review 1.  Iron and a Man's Reproductive Health: the Good, the Bad, and the Ugly.

Authors:  J Scott Gabrielsen; Dolores J Lamb; Larry I Lipshultz
Journal:  Curr Urol Rep       Date:  2018-06-01       Impact factor: 3.092

2.  Reproductive capacity in iron overloaded women with thalassemia major.

Authors:  Sylvia T Singer; Elliott P Vichinsky; Ginny Gildengorin; Jereon van Disseldorp; Mitchell Rosen; Marcelle I Cedars
Journal:  Blood       Date:  2011-07-14       Impact factor: 22.113

3.  Fertility potential in thalassemia major women: current findings and future diagnostic tools.

Authors:  Sylvia T Singer; Nancy Sweeters; Olivia Vega; Annie Higa; Elliott Vichinsky; Marcelle Cedars
Journal:  Ann N Y Acad Sci       Date:  2010-08       Impact factor: 5.691

Review 4.  Endocrine and bone complications in β-thalassemia intermedia: current understanding and treatment.

Authors:  Adlette Inati; MohammadHassan A Noureldine; Anthony Mansour; Hussein A Abbas
Journal:  Biomed Res Int       Date:  2015-03-05       Impact factor: 3.411

5.  Beta-thalassaemia intermedia: evaluation of endocrine and bone complications.

Authors:  M Baldini; A Marcon; R Cassin; F M Ulivieri; D Spinelli; M D Cappellini; G Graziadei
Journal:  Biomed Res Int       Date:  2014-07-07       Impact factor: 3.411

Review 6.  Thalassaemia is a tropical disease.

Authors:  T R Kotila
Journal:  Ann Ib Postgrad Med       Date:  2012-12
  6 in total

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