REPRODUCTIVE BIOMEDICINE ONLINE | 卷:22 |
Genome-wide analysis shows no genomic predictors of ovarian response to stimulation by exogenous FSH for IVF | |
Article | |
van Disseldorp, Jeroen1  Franke, Lude2  Eijkemans, Rene1,3  Broekmans, Frank1  Macklon, Nick1,4  Wijmenga, Cisca2  Fauser, Bart1  | |
[1] Univ Med Ctr Utrecht, Dept Reprod Med & Gynaecol, NL-3508 GA Utrecht, Netherlands | |
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, NL-9700 RB Groningen, Netherlands | |
[3] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, NL-3508 GA Utrecht, Netherlands | |
[4] Univ Southampton, Princess Anne Hosp, Div Dev Origins Hlth & Dis, Southampton, Hants, England | |
关键词: genes; genome-wide association study; IVF; ovarian response; ovarian stimulation; | |
DOI : 10.1016/j.rbmo.2010.12.006 | |
来源: Elsevier | |
【 摘 要 】
The current proof of principle study explores the possibility that a genetic single-nucleotide polymorphism (SNP) profile is associated with ovarian response to standardized stimulation for IVF using exogenous FSH. Such a pharmacogenomic approach could aid in rendering ovarian stimulation for IVF more tailored to the patient, potentially improving the delicate balance between efficacy, side effects and chances for complications. Genome-wide association (GWA) analysis using Illumina Human 610-Quad Bead-Chips was used in a homogeneous group of 102 healthy, Caucasian, regularly cycling, non-smoking women aged 38 years or less with a body mass index <30 kg/m(2) with a regular indication for IVF in a tertiary referral University Hospital. Genetic profiles were associated with the number of oocytes obtained. Ovarian response varied widely, ranging from cancellation (less than three follicles) to more than 20 oocytes. After correction for multiple testing, no SNPs were observed to be significantly correlated to ovarian response, embryo quality or pregnancy. Restricting the information to SNPs involved in granulosa cell function, cell cycle regulation or apoptosis also did not yield significant associations for ovarian response. A study in a larger cohort is warranted, aiming to further explore subtle genetic variants with greater power. (C) 2010, Reproductive Healthcare Ltd. Published by Elsevier Ltd. All rights reserved.
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