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Journal of Zhejiang University SCIENCE B

ISSN 1673-1581(Print), 1862-1783(Online), Monthly

Genetic polymorphisms of CYP2D6*10 and the effectiveness of combined tamoxifen citrate and testosterone undecanoate treatment in infertile men with idiopathic oligozoospermia

Abstract: Tamoxifen citrate, as the first line of treatment for infertile men with idiopathic oligozoospermia, was proposed by the World Health Organization (WHO), and testosterone undecanoate has shown benefits in semen values. Our objective was to assess the effectiveness of treatment with tamoxifen citrate and testosterone undecanoate in infertile men with idiopathic oligozoospermia, and whether the results would be affected by polymorphisms of CYP2D6*10. A total of 230 infertile men and 147 controls were included in the study. Patients were treated with tamoxifen citrate and testosterone undecanoate. Sex hormone, sperm parameters, and incidence of spontaneous pregnancy were detected. There were no significant differences between the control and patient groups with respect to CYP2D6*10 genotype frequencies (P>0.05). The follicle-stimulation hormone (FSH), luteinizing hormone (LH), and testosterone (T) levels were raised, and sperm concentration and motility were increased at 3 months and became significant at 6 months, and they were higher in the wild-type allele (C/C) than in the heterozygous variant allele (C/T) or homozygous variant allele (T/T) subgroups (P<0.05). In addition, the percentage of normal morphology was raised at 6 months, and represented the highest percentage in the C/C subgroup (P<0.05). The incidence of spontaneous pregnancy in the C/C subgroup was higher than that in the C/T or T/T subgroups (P<0.01). This study showed that the CYP2D6*10 variant genotype demonstrated worse clinical effects in infertile men with idiopathic oligozoospermia.

Key words: Infertility, Cytochrome P450, Oligozoospermia, Tamoxifen, Testosterone

Chinese Summary  <24> CYP2D6*10基因多æ€æ€§å¯¹ä»–莫昔芬è”åˆå一酸ç¾é…®æ²»ç–—特å‘性少精男性ä¸è‚²ç—‡çš„疗效影å“

中文概è¦ï¼š
目的:探讨细胞色素P4502D6*10(CYP2D6*10)基因é—传多æ€æ€§ï¼Œå¹¶è¯„估其对他莫昔芬è”åˆå一酸ç¾é…®æ²»ç–—特å‘性少精男性ä¸è‚²ç—‡æ‚£è€…血清性激素ã€ç²¾æ¶²å‚æ•°åŠè‡ªç„¶å¦Šå¨ çŽ‡çš„å½±å“。
方法:该病例对照研究包括230例特å‘性少精男性ä¸è‚²æ‚£è€…å’Œ147例正常对照。病例组æœç”¨æž¸æ©¼é…¸ä»–莫昔芬20mg/då’Œå一酸ç¾é…®40mg/d,疗程共6个月。采用HphI内切酶对CYP2D6*10基因èšåˆé…¶é“¾å¼å应(PCR)产物进行内切åŽï¼Œä»Žè€Œå¯¹å…¶åˆ†åž‹ã€‚分别于研究开始时ã€3月åŠ6月分别检测研究对象性激素水平ã€ç²¾æ¶²å‚æ•°åŠé…å¶è‡ªç„¶å¦Šå¨ çŽ‡ã€‚
结论: CYP2D6*10基因çªå˜åž‹ç‰¹å‘性少精男性ä¸è‚²æ‚£è€…接å—他莫昔芬è”åˆå一酸ç¾é…®ç–—效较基因野生型组差。

关键è¯ç»„:男性ä¸è‚²ç—‡ï¼›ç»†èƒžè‰²ç´ P450;少精å­ç—‡ï¼›ä»–莫昔芬;性激素


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DOI:

10.1631/jzus.B1400282

CLC number:

R698.2

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On-line Access:

2015-03-05

Received:

2014-10-21

Revision Accepted:

2015-01-01

Crosschecked:

2015-02-22

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