<abstract xmlns="http://www.w3.org/1999/xhtml"><sec id="j_1905-7415.0902.385_s_005_w2aab3b7b8b1b6b1aab1c17b1Aa"><h3>Background</h3><p>Regular blood transfusion and iron chelation therapy have improved the quality of life of patients with thalassemia and increased their longevity, but transfusion also increases the frequency of endocrine complications, possibly because of iron deposition in the pituitary gland or the gonads, or both.</p></sec><sec id="j_1905-7415.0902.385_s_006_w2aab3b7b8b1b6b1aab1c17b2Aa"><h3>Objective</h3><p>To evaluate testicular function in patients with thalassemia major by basal hormonal study, and identify risk factors for dysfunction.</p></sec><sec id="j_1905-7415.0902.385_s_007_w2aab3b7b8b1b6b1aab1c17b3Aa"><h3>Methods</h3><p>We performed a cross-sectional study of 28 patients with thalassemia major aged 11.7 ± 1.8 (8–14.9) years (15 in prepuberty, 13 in puberty with no delayed puberty) who had regular blood transfusions. A normal control group comprised 64 boys who were matched for age and Tanner genital stage.</p></sec><sec id="j_1905-7415.0902.385_s_008_w2aab3b7b8b1b6b1aab1c17b4Aa"><h3>Results</h3><p>The mean level of serum ferritin in the previous year was 1,575 ± 642 ng/mL, and the onset of blood transfusion was at 3.8 ± 2.3 years and iron chelation therapy was 6.6 ± 2.8 years. The trend for anti-Müllerian hormone levels in patients and controls was similar with age, and although higher in the patients, particularly at Tanner stage II, was not significantly different. Testosterone levels were lower in the patients compared with controls; particularly at Tanner stages IV–V (290.88 vs. 537.4 ng/dL, <italic>P</italic> &lt; 0.05). Serum follicle-stimulating hormone and luteinizing hormone levels were not significantly different between the groups at any Tanner stage.</p></sec><sec id="j_1905-7415.0902.385_s_009_w2aab3b7b8b1b6b1aab1c17b5Aa"><h3>Conclusion</h3><p>Patients who received regular blood transfusions had normal Sertoli cell function. Leydig cell dysfunction may occur, even though the patients had a normal pubertal onset.</p></sec></abstract>

BackgroundRegular blood transfusion and iron chelation therapy have improved the quality of life of patients with thalassemia and increased their longevity, but transfusion also increases the frequency of endocrine complications, possibly because of iron deposition in the pituitary gland or the gonads, or both.ObjectiveTo evaluate testicular function in patients with thalassemia major by basal hormonal study, and identify risk factors for dysfunction.MethodsWe performed a cross-sectional study of 28 patients with thalassemia major aged 11.7 ± 1.8 (8–14.9) years (15 in prepuberty, 13 in puberty with no delayed puberty) who had regular blood transfusions. A normal control group comprised 64 boys who were matched for age and Tanner genital stage.ResultsThe mean level of serum ferritin in the previous year was 1,575 ± 642 ng/mL, and the onset of blood transfusion was at 3.8 ± 2.3 years and iron chelation therapy was 6.6 ± 2.8 years. The trend for anti-Müllerian hormone levels in patients and controls was similar with age, and although higher in the patients, particularly at Tanner stage II, was not significantly different. Testosterone levels were lower in the patients compared with controls; particularly at Tanner stages IV–V (290.88 vs. 537.4 ng/dL, P < 0.05). Serum follicle-stimulating hormone and luteinizing hormone levels were not significantly different between the groups at any Tanner stage.ConclusionPatients who received regular blood transfusions had normal Sertoli cell function. Leydig cell dysfunction may occur, even though the patients had a normal pubertal onset.

Testicular function in patients with regular blood transfusion for thalassemia major

Division of Endocrinology, Department of Pediatrics

Division of Hematology and Oncology, Department of Pediatrics

Asian Biomedicine

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

BackgroundRegular blood transfusion and iron chelation therapy have improved the quality of life of patients with thalassemia and increased their longevity,...

Testicular function in patients with regular blood transfusion for thalassemia major

Article Category: Brief communication (Original)

Publicado en línea: 31 ene 2017

Páginas: 185 - 191

DOI: https://doi.org/10.5372/1905-7415.0902.385

Palabras clave
Anti-Müllerian hormone, follicle stimulating hormone, hypogonadism, luteinizing hormone, regular blood transfusion, thalassemia major

© 2017 Sukumarn Siripunthana, Taninee Sahakitrungruang, Suttipong Wacharasindhu, Darintr Sosothikul, Vichit Supornsilchai

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Testicular function in patients with regular blood transfusion for thalassemia major

Article Category: Brief communication (Original)

Publicado en línea: 31 ene 2017

Páginas: 185 - 191

DOI: https://doi.org/10.5372/1905-7415.0902.385

Palabras claveAnti-Müllerian hormone, follicle stimulating hormone, hypogonadism, luteinizing hormone, regular blood transfusion, thalassemia major

© 2017 Sukumarn Siripunthana, Taninee Sahakitrungruang, Suttipong Wacharasindhu, Darintr Sosothikul, Vichit Supornsilchai

This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Palabras clave
Anti-Müllerian hormone, follicle stimulating hormone, hypogonadism, luteinizing hormone, regular blood transfusion, thalassemia major