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   <subfield code="a">Effect of hCG or hCG + treatments in young thalassemic patients with hypogonadotropic hypogonadism</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[R. Balducci, Vincenzo Toscano, G. Finocchi, G. Municchi, A. Mangiantini, B. Boscherini]</subfield>
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   <subfield code="a">Hypogonadotropic hypogonadism (HH) is common (40%) in beta-thalassemic patients. Taking into consideration that in HH non-thalassemic patients we obtained good results in pubertal development using hCG treatment (1500 IU every 6 days), 10 HH thalassemic subjects (14 5/12 -17 yr, all with bone age greater than 13 6/12) were treated with the same regimen. In 5 of these patients purified FSH (75 IU every 3 days) was added to hCG in order to evaluate the FSH effect on testosterone (T) response (Group 1 was given hCG alone, Group 2 hCG + FSH: Profasi HP and Metrodin Serono). To evaluate the kinetics of testosterone response, plasma level of T was determined basally and 1, 2, 4 and 6 days after hCG injection. This dynamic study and a clinical examination were carried out at the beginning of treatment and at the 4th and 12th month after. Results obtained in the first group confirmed our previous data from non-thalassemic HH patients: in fact, after 12 months of therapy a stage G2-G3 was reached. In the second group, however, testis size and testosterone secretion were significantly higher than in the first group. At the 4th month, in Group 1 and in Group 2 testis size and the area under the T response curve were 3.18 ± 0.18ml and 13,364 ± 1047 ng/dl vs 4.62 ± 0.25 ml (p &lt; 0.02) and 18,045 ±1110 ng/dl (p &lt; 0.016), respectively. At the 12th month testis size and area under T response curve were increased to 6.12 ± 0.25 ml and 24,017 + 1176 ng/dl in Group 1 and 8.12 ± 0.6 ml (p &lt; 0.01) and 33,924 ± 2181 ng/dl (p &lt; 0.01) in Group 2. After 12 months, a significant comparable increase in growth velocity, without bone age acceleration, was observed in both groups. Our results demonstrate that hCG or hCG + FSH treatments are able to induce a satisfactory sexual development in thalassemic HH patients; moreover FSH in addition to hCG seems to improve not only testis size as expected, but also testosterone production.</subfield>
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