Source:http://linkedlifedata.com/resource/pubmed/id/12826700
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2003-6-26
|
pubmed:abstractText |
A multicenter, open-label, randomized efficacy and safety study was performed with combined human chorionic gonadotropin (hCG) and recombinant follicle-stimulating hormone (recFSH) (Puregon(R)) treatment to induce spermatogenesis in hypogonadotropic hypogonadal male patients. Patients were pretreated for 16 weeks with hCG to normalize testosterone levels. A total of 30 of 49 (61%) subjects had normalized testosterone levels but were still azoospermic after the hCG-alone phase. These patients were randomized into 2 treatment schemes with recFSH (2 x 225 IU recFSH per week [group A] or 3 x 150 IU recFSH per week [group B]), in combination with hCG for a period of 48 weeks. Total testosterone increased during the hCG-alone period from 1.08 and 1.22 ng/mL to 6.26 and 4.52 ng/mL for groups A and B, respectively. Combined gonadotropin treatment was effective in inducing spermatogenesis (sperm count >/=1 x 10(6)/mL) in 14 of 30 subjects (47%) and this was achieved after a median duration of treatment of approximately 5.5 months. Treatment time necessary for first sperm cells to appear in the ejaculate was related to the initial testicular volume. Subjects with a history of maldescended testes (11 of 30 subjects, 37%) showed a lower mean response to treatment as indicated by the relatively lower number of subjects reaching levels of at least 1 x 10(6) sperm cells per milliliter. Combined testicular volume increased during combined gonadotropin treatment from 11.4 to 24.0 mL. Although subjects with a history of maldescended testes had a lower starting testicular volume, subjects with and without a history of maldescended testes showed approximately the same relative increase in testicular volume. Total testosterone levels showed only a minor further increase during the combined gonadotropin treatment period. In conclusion, a weekly dose of 450 IU (3 x 150 IU or 2 x 225 IU) recFSH, in addition to hCG, was able to induce spermatogenesis in many hypogonadotropic azoospermic men who failed to respond to treatment with hCG alone.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
0196-3635
|
pubmed:author |
pubmed-author:BakerGordon H WGH,
pubmed-author:BoulouxPierre-Marc GPM,
pubmed-author:BurgerHenry GHG,
pubmed-author:ConwayAnn JAJ,
pubmed-author:GiwercmanAleksanderA,
pubmed-author:HandelsmanDavid JDJ,
pubmed-author:McLachlanRobert IRI,
pubmed-author:NieschlagEberhardE,
pubmed-author:OchsenkuehnRobertR,
pubmed-author:SkakkebaekNiels ENE,
pubmed-author:SyskaAnnemarieA,
pubmed-author:TurnerLeoL,
pubmed-author:VoortmanGerritG,
pubmed-author:WuFrederick C WFC,
pubmed-author:van KuijkJacqueline H MJH
|
pubmed:issnType |
Print
|
pubmed:volume |
24
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
604-11
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:12826700-Adult,
pubmed-meshheading:12826700-Chorionic Gonadotropin,
pubmed-meshheading:12826700-Drug Therapy, Combination,
pubmed-meshheading:12826700-Follicle Stimulating Hormone, Human,
pubmed-meshheading:12826700-Humans,
pubmed-meshheading:12826700-Hypogonadism,
pubmed-meshheading:12826700-Male,
pubmed-meshheading:12826700-Oligospermia,
pubmed-meshheading:12826700-Recombinant Proteins,
pubmed-meshheading:12826700-Spermatogenesis,
pubmed-meshheading:12826700-Testis,
pubmed-meshheading:12826700-Testosterone,
pubmed-meshheading:12826700-Treatment Outcome
|
pubmed:articleTitle |
Induction of spermatogenesis by recombinant follicle-stimulating hormone (puregon) in hypogonadotropic azoospermic men who failed to respond to human chorionic gonadotropin alone.
|
pubmed:affiliation |
Department of Endocrinology, The Royal Free Hospital, London, United Kingdom.
|
pubmed:publicationType |
Journal Article,
Clinical Trial,
Randomized Controlled Trial,
Multicenter Study,
Clinical Trial, Phase III
|