Volume 10, Issue 5 (10-2012)                   IJRM 2012, 10(5): 493-0 | Back to browse issues page

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Wiwanitkit V. Semen problem in beta-thalassemia: an interesting focus on tropical reproductive science and hematology. IJRM. 2012; 10 (5) :493-0
URL: http://journals.ssu.ac.ir/ijrmnew/article-1-304-en.html
Viroj Wiwanitkit, Wiwanitkit House, Bangkhae, Bangkok, 10160, Thailand , wviroj@yahoo.com
Full-Text [PDF 165 kb]   (89 Downloads)     |   Abstract (HTML)  (442 Views)
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The problem of congenital hemoglobin disorder is common in tropical Asia. In tropical Southeast Asian countries, very high prevalence of thalassemia disorder especially for beta thalassemia is observed. This tropical hematological problem affects millions of population and cause several health disorders. Of interest, the issue of reproductive health impairment of the population with beta thalassemia disorder is not well mentioned.
Here, the author tried to summarize some important information on the semen problem in beta-thalassemia. In beta-thalassemia major, poor semen quality is observed. It is noted that most patients have “hypogonadotropic hypogonadism state, impairment fertility and growth retardation (1).” Jensen et al proposed that “The causation is multi-factorial, with iron deposition in the pituitary gland resulting from life-long dependence on blood transfusions being a major factor (2).”
It is evidenced that the sperm DNA damage is due to oxidative stress from iron overload (3-4). Nevertheless, it is reported that the spermatogenesis in the patients are also suppressed by chelation therapy, desferrioxamine (5). The degree of sperm DNA damage is interestingly high in the case with low ferritin level (5-6). It seems that the exacts mechanism of semen problem in beta thalassemia patient is very complex and relating to unknown disturbance of iron metabolism impairment in the patients.
Type of Study: Original Article |

References
1. Safarinejad MR. Evaluation of semen quality, endocrine profile and hypothalamus-pituitary-testis axis in male patients with homozygous beta-thalassemia major. Urol 2008; 179: 2327-2332. [DOI:10.1016/j.juro.2008.01.103]
2. Jensen CE, Abdel-Gadir A, Cox C, Tuck SM, Wonke B. Sperm concentrations and quality in beta-thalassaemia major. Int J Androl 1996; 19: 362-364. [DOI:10.1111/j.1365-2605.1996.tb00528.x]
3. Perera D, Pizzey A, Campbell A, Katz M, Porter J, Petrou M, et al. Sperm DNA damage in potentially fertile homozygous beta-thalassaemia patients with iron overload. Hum Reprod 2002; 17: 1820-1825. [DOI:10.1093/humrep/17.7.1820]
4. Carpino A, Tarantino P, Rago V, De Sanctis V, Siciliano L. Antioxidant capacity in seminal plasma of transfusion-dependent beta-thalassemic patients. Exp Clin Endocrinol Diabetes 2004; 112: 131-134. [DOI:10.1055/s-2004-817821]
5. De Sanctis V, Borsari G, Brachi S, Govoni M, Carandina G. Spermatogenesis in young adult patients with beta-thalassaemia major long-term treated with desferrioxamine. Georgian Med News 2008; 156:74-77.
6. De Sanctis V, Perera D, Katz M, Fortini M, Gamberini MR. Spermatozoal DNA damage in patients with B thalassaemia syndromes. Pediatr Endocrinol Rev 2008; 6 (Suppl.): 185-189.

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