Skip to main content
Indian Journal of Endocrinology and Metabolism logoLink to Indian Journal of Endocrinology and Metabolism
letter
. 2017 Jul-Aug;21(4):636–637. doi: 10.4103/ijem.IJEM_73_17

Does Testosterone Replacement Therapy Promote an Augmented Risk of Thrombotic Events in Thalassemia Major Male Patients with Hypogonadism?

Vincenzo De Sanctis 1, Shahina Daar 2, Ashraf T Soliman 3,, Heba Elsedfy 4, Doaa Khater 5,6, Salvatore Di Maio 7
PMCID: PMC5477457  PMID: 28670553

Sir,

Hypogonadotropic hypogonadism (HH) is the most frequent endocrinopathy in transfused patients with thalassemia major (TM). Hypogonadism is likely to be caused by iron deposits in the gonads, pituitary gland, or both. The treatment of pubertal disorders in thalassaemia is a complex issue due to the frequent coexistence of other factors such as severity of iron overload, chronic liver disease, insulin-dependent diabetes, and/or the identification of a hypercoagulable state.[1,2] In addition, splenectomy can contribute to, and increase, the risk of thrombosis.

As the current literature is very limited regarding the potential risks of venous thromboembolism and cardiovascular in TM patients with hypogonadism, the main aim of the present retrospective study was to investigate the incidence of venous thromboembolism (deep venous thrombosis and pulmonary embolism) in three cohorts of hypogonadal men with TM treated with depot testosterone, in Muscat (Oman), Doha (Qatar), and Ferrara (Italy).

The registry database included 424 male patients followed regularly or occasionally in Muscat (96 patients), in Doha (56 patients), and in Ferrara (272 patients). In the latter group, all patients were of Italian ethnic origin. Forty-one of 96 TM patients in Muscat (42.7%), 22 of 56 TM in Doha (43%), and 95 of 272 TM patients in Ferrara (34.9%) developed a pubertal disorder: delayed puberty (1.8%), arrested puberty (1.7%), HH (91.1%), or acquired HH (5.4%).

One of the coauthors (ATS) observed the development of left atrial thrombosis in a 19-year-old adolescent male with TM and diabetes mellitus, who had been on testosterone replacement therapy (100 mg testosterone enanthate, monthly) for 1 year. His laboratory and hormonal profile is reported in Table 1.

Table 1.

Laboratory and hormonal levels of our patient who developed a left atrial thrombosis

graphic file with name IJEM-21-636-g001.jpg

Diabetes mellitus (blood glucose at 2 h oral glucose tolerance test = 220 mg/dl) developed 7 months after starting testosterone therapy. He was on insulin therapy with HbA1c = 8%, and he did not show any of the side effects of testosterone therapy apart from this acute incidence. The hormone replacement therapy (HRT) with testosterone was stopped. Unfortunately, no further information was available after his admission to the Cardiac Intensive Care Unit.

No cases of thrombosis were reported in our thalassaemic patients with spontaneous pubertal development.

In conclusion, male hypogonadism and its treatment is a rapidly evolving area. Much of the controversy surrounding testosterone therapy stems from intense attention on recent reports suggesting increased risk of venous thromboembolism or cardiovascular events in young and aging men.[3,4,5] HRT has numerous benefits that can greatly enhance a patient's quality of life. Before prescribing testosterone, physicians should be aware of the potential side effects of testosterone therapy and how best to address them. Particular attention should be made in TM patients with a clinical history of splenectomy and/or thrombophilia before administration of exogenous testosterone. Patients receiving testosterone therapy should be followed according to a standardized monitoring plan to ensure any potential side effects are detected early. Therefore, we urge health-care professionals to report side effects involving prescription testosterone products and to encourage a regular endocrine follow-up of multitransfused TM patients on HRT.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

Acknowledgments

We wish to express our sincere thanks to Prof. Charles J. Glueck, Cholesterol Center, Suite 430, 2135 Dana Avenue, Cincinnati, OH 45207, USA, for his thoughtful advice in the course of manuscript preparation.

REFERENCES

  • 1.De Sanctis V, Soliman AT, Elsedfy H, Yaarubi SA, Skordis N, Khater D, et al. The ICET-A recommendations for the diagnosis and management of disturbances of glucose homeostasis in thalassemia major patients. Mediterr J Hematol Infect Dis. 2016;8:e2016058. doi: 10.4084/MJHID.2016.058. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Moratelli S, De Sanctis V, Gemmati D, Serino ML, Mari R, Gamberini MR, et al. Thrombotic risk in thalassemic patients. J Pediatr Endocrinol Metab. 1998;11(Suppl 3):915–21. [PubMed] [Google Scholar]
  • 3.Martinez C, Suissa S, Rietbrock S, Katholing A, Freedman B, Cohen AT, et al. Testosterone treatment and risk of venous thromboembolism: Population based case-control study. BMJ. 2016;355:i5968. doi: 10.1136/bmj.i5968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Glueck CJ, Prince M, Patel N, Patel J, Shah P, Mehta N, et al. Thrombophilia in 67 patients with thrombotic events after starting testosterone therapy. Clin Appl Thromb Hemost. 2016;22:548–53. doi: 10.1177/1076029615619486. [DOI] [PubMed] [Google Scholar]
  • 5.Vigen R, O'Donnell CI, Barón AE, Grunwald GK, Maddox TM, Bradley SM, et al. Association of testosterone therapy with mortality, myocardial infarction, and stroke in men with low testosterone levels. JAMA. 2013;310:1829–36. doi: 10.1001/jama.2013.280386. [DOI] [PubMed] [Google Scholar]

Articles from Indian Journal of Endocrinology and Metabolism are provided here courtesy of Wolters Kluwer -- Medknow Publications

RESOURCES