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常见的染色体多态性与IVF-ET治疗的效果 被引量:19

Relationship between Chromosome Polymorphisms and the Outcome of Infertile Individuals Undergoing IVF-ET
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摘要 目的:探讨染色体多态性与体外受精-胚胎移植(IVF-ET)治疗结局之间的关系。方法:回顾性分析1768对IVF-ET治疗对象染色体核型,将其分为染色体多态性组与染色体核型正常组,对2组的临床资料进行比较,同时分析染色体多态性在具少弱精症或不良孕产史的特定人群中的检出率。结果:①多态性组与正常组相比,临床妊娠率(45.25% vs 40.85%)、早期流产率(8.39% vs 9.17%)和活产率(34.37%% vs 29.14%)无统计学差异。②在男方少弱精子症、夫妇有不良孕产史的情况下,染色体多态性的检出率与无此类表现者相比无统计学差异(16.95% vs 16.39%,19.42% vs 16.46%)。结论:①染色体多态性对于IVF-ET患者的临床妊娠率、早期流产率、活产率无明显影响。②临床表现为少弱精或具不良孕产史人群的染色体多态性检出率与无此类临床表现者无差异。 Objective: To study the association of chromosome heteromorphism with IVF-ET outcomes. Methods: A total of 1 768 infertile couples underwent chromosome analysis before IVF-ET. Results: 1) There was no statistically significant difference between chromosomal polymorphism group and normal karyotype group in the pregnancy rate (45.25% vs 40.85%), first trimester abortion rate (8.39% vs 9.17%), live birth rate (34.37% vs 29.14%). 2) There was no statistically significant difference in the detected ratio of chromosome polymorphism between those with a history of oligoasthenozoospermia or bad obstetrics history and those without it (16.95% vs 16.39%, 19.42% vs 16.46%). Conclutions: 1) Chromosomal heteromorphisms don't affect clinical pregnancy rate, first trimester abortion rate and live birth rate of IVF-ET patients. 2) There is no significant difference in the detected ratio chromosome polymorphism between those with a history of oligoasthenozoospermia or bad obstetrics history and those without it.
出处 《生殖与避孕》 CAS CSCD 北大核心 2009年第10期637-642,共6页 Reproduction and Contraception
关键词 染色体多态性 体外受精-胚胎移植(IVF-ET) 临床妊娠率 早期流产率 活产率 chromosomal heteromorphisms IVF-ET pregnancy rate first trimester abortion rate live birth rate
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参考文献15

  • 1唐冬生,李晓杰,陈志华,林镇城,杨光,郭晓玲.染色体异态性与早期生殖障碍[J].生殖与避孕,2003,23(1):53-55. 被引量:23
  • 2Madon P F, Athalye AS, Parikh FR. Polymorphic variants on chromosomes probably play a significant role in infertility. Reprod Biomed Online, 2005, 11(6):726-32.
  • 3Sahin FI, Yilmaz Z, Yuregir OO, et al. Chromosome heteromorphisms: an impact on infertility. J Assist Reprod Genet, 2008, 25(5): 191-5.
  • 4Yuce H, Tekedereli I, Elyas H. Cytogenetic results of recurrent spontaneous abortions in Turkey. Med Sci Monit, 2007, 13(6):CR286-9.
  • 5Bhasin M. Human population cytogenetics: a review. Int J Hum Genet, 2005, S(2):83-152.
  • 6Vinci G, Raicu F, Popa L, et al. A deletion of a novel heat shock gene on the Y chromosome associated with azoospermia. Mol Hum Reprod, 2005, 11(4):295-8.
  • 7Nagvenkar P, Desai K, Hinduja I, et al. Chromosomal studies in infertile men with oligozoospermia & non-obstructive azoospermia. Indian J Med Res, 2005, 122:(1):34-42.
  • 8Uehara S, Akai Y, Takeyama Y, et al. Pericentric inversion of chromosome 9 in prenatal diagnosis and infertility. Tohoku J Exp Med, 1992, 166(4):417-27.
  • 9Cortes-Gutierrez EI, Cerda-Flores RM, Daivila-Rodriguez MI, et al. Chromosomal abnormalities and polymorphisms in Mexican infertile men. Arch Androl, 2004, 50(4):261-5.
  • 10Kalantari P, Sepehri H, Behjati F, et al. Chromosomal studies in infertile men. Tsitol Genet, 2001, 35(6):50-4.

二级参考文献7

  • 1Del Porto G, D'Alessandro E, Grammatico P, Coghi IM, Desanctis S, Giambenedette M, Vaccarella C, Fabi R, Marcino MF & Nicotra M. Chromosome heteromorphisms and early recurrent abortions. Hum Reprod, 1993,8(5):755~758.
  • 2Tang DS, Xia JH, Li LY, Dai HP, Jiang SL, Liu CY & Long ZG. Reposity of human chromosomal anomalies in China. Am J Hum Genet, 1997,61(4):A375.
  • 3Lundgren R, Berger R & Kristoffersson U. Constitutive heterchromatin C-band polymorphism in prostatic cancer. Cancer Genet Cytogent, 1991,51:57~62.
  • 4Xia JH & Li LY. G-banded chromosomes of 3 415 liveborn infants. Chin Med J, 1994, 97(12):921-927.
  • 5Patil SR, Lubs HA. Classification of the qh regions in human chromosomes 1,9 and 16 by C-banding. Hum Genet, 1977, 38:35~38.
  • 6Sylvester JE, Whiteman DA, Podolshy R, Pozsgay JM, Respess J & Schmickel RD. The human ribosomal RNA genes: structure and organization of the complete repeating unit. Hum Genet, 1986,3:193~198.
  • 7Buretic-Tomljanovic A, Rodojcic Badovinac A, Vlastelic I, & Randic IJ. Quantitative analysis of constitutive heterochromatin in couples with fetal wastage. Am J Reprod Immunol, 1997,38(3):201~204.

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