Literature DB >> 19184397

Optimization of IVF pregnancy outcomes with donor spermatozoa.

Jeff G Wang1, Nataki C Douglas, Robert Prosser, Daniel Kort, Janet M Choi, Mark V Sauer.   

Abstract

PURPOSE: To identify risk factors for suboptimal IVF outcomes using insemination with donor spermatozoa and to define a lower threshold that may signal a conversion to fertilization by ICSI rather than insemination.
METHOD: Retrospective, age-matched, case-control study of women undergoing non-donor oocyte IVF cycles using either freshly ejaculated (N=138) or cryopreserved donor spermatozoa (N=69). Associations between method of fertilization, semen sample parameters, and pregnancy rates were analyzed.
RESULTS: In vitro fertilization of oocytes with donor spermatozoa by insemination results in equivalent fertilization and pregnancy rates compared to those of freshly ejaculated spermatozoa from men with normal semen analyses when the post-processing motility is greater than or equal to 88%. IVF by insemination with donor spermatozoa when the post-processing motility is less than 88% is associated with a 5-fold reduction in pregnancy rates when compared to those of donor spermatozoa above this motility threshold. When the post-processing donor spermatozoa motility is low, fertilization by ICSI is associated with significantly higher pregnancy rates compared to those of insemination.
CONCLUSION: While ICSI does not need to be categorically instituted when using donor spermatozoa in IVF, patients should be counseled that conversion from insemination to ICSI may be recommended based on low post-processing motility.

Entities:  

Mesh:

Year:  2009        PMID: 19184397      PMCID: PMC2654931          DOI: 10.1007/s10815-008-9291-5

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  23 in total

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Authors:  A Ahmadi; S C Ng
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2.  Interrelationships between seminal parameters and sperm nuclear DNA damage before and after density gradient centrifugation: implications for assisted conception.

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3.  Sperm DNA fragmentation decreases the pregnancy rate in an assisted reproductive technique.

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4.  Human gene expression first occurs between the four- and eight-cell stages of preimplantation development.

Authors:  P Braude; V Bolton; S Moore
Journal:  Nature       Date:  1988-03-31       Impact factor: 49.962

5.  The spectrum of DNA damage in human sperm assessed by single cell gel electrophoresis (Comet assay) and its relationship to fertilization and embryo development.

Authors:  I D Morris; S Ilott; L Dixon; D R Brison
Journal:  Hum Reprod       Date:  2002-04       Impact factor: 6.918

6.  Cryopreservation of human semen and prepared sperm: effects on motility parameters and DNA integrity.

Authors:  E T Donnelly; N McClure; S E Lewis
Journal:  Fertil Steril       Date:  2001-11       Impact factor: 7.329

7.  Evaluation of chromatin integrity in human sperm using acridine orange staining with different fixatives and after cryopreservation.

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8.  Successful use of human semen cryobanking for in vitro fertilization.

Authors:  M M Mahadevan; A O Trounson; J F Leeton
Journal:  Fertil Steril       Date:  1983-09       Impact factor: 7.329

9.  In vitro fertilization using cryopreserved donor semen in cases where both partners are infertile.

Authors:  J Cohen; R G Edwards; C B Fehilly; S B Fishel; J Hewitt; G F Rowland; P C Steptoe; D E Walters; J Webster
Journal:  Fertil Steril       Date:  1985-04       Impact factor: 7.329

10.  Influence of deoxyribonucleic acid damage on fertilization and pregnancy.

Authors:  Ralf Henkel; Marjam Hajimohammad; Thomas Stalf; Christiaan Hoogendijk; Claas Mehnert; Roelof Menkveld; Holger Gips; Wolf-Bernhard Schill; Thinus F Kruger
Journal:  Fertil Steril       Date:  2004-04       Impact factor: 7.329

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