Pharmacogenetics of controlled ovarian hyperstimulation

被引:22
作者
de Castro, F
Morón, FJ
Montoro, L
Real, LM
Ruiz, A
机构
[1] Hosp Univ Principe Asturias, Unidad Reprod Humana Asistida, Madrid, Spain
[2] Neocodex, Dept Genom Estructural, Seville 41092, Spain
关键词
assisted reproductive techniques; clomifene citrate; controlled ovarian hyperstimulation; estrogen; follicle-stimulating hormone; follicle-stimulating hormone receptor; gonaclotropin-releasing hormone analogues; human menopausal gonadotropin; pharmacogenctics; single nucleotide polymorphism;
D O I
10.2217/14622416.6.6.629
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Controlled ovarian hyperstimulation (COH) is a routine treatment employed in most assisted reproductive techniques (ARTs). The existence of genetic factors involved in COH has been suspected. The main challenge for clinicians involved in ART is COH cycle cancellation, which usually occurs due to two opposing situations. On the one hand, there is the presence of a poor response during COH treatment, and on the other there is the presentation of a side effect related to gonadotropin hypersensitivity (ovarian hyperstimulation syndrome [OHSS]). Evidence for an association between single nuclecitide polymorphisms and COH outcome has been obtained during the last decade. The genetic dissection of both extreme phenotypes of COH will be the main objective of this review. The development of predictive panels useful for the clinical management of COH is currently underway, and will improve the clinical management of patients undergoing ART.
引用
收藏
页码:629 / 637
页数:9
相关论文
共 51 条
[1]   MUTATION IN THE FOLLICLE-STIMULATING-HORMONE RECEPTOR GENE CAUSES HEREDITARY HYPERGONADOTROPIC OVARIAN FAILURE [J].
AITTOMAKI, K ;
LUCENA, JLD ;
PAKARINEN, P ;
SISTONEN, P ;
TAPANAINEN, J ;
GROMOLL, J ;
KASKIKARI, R ;
SANKILA, EM ;
LEHVASLAIHO, H ;
ENGEL, AR ;
NIESCHLAG, E ;
HUHTANIEMI, I ;
DELACHAPELLE, A .
CELL, 1995, 82 (06) :959-968
[2]  
ANDERSEN TI, 1994, HUM GENET, V94, P665
[3]  
Bachvarova R, 1985, Dev Biol (N Y 1985), V1, P453
[4]   Significance of a common single nucleotide polymorphism in exon 10 of the follicle-stimulating hormone (FSH) receptor gene for the ovarian response to FSH:: a pharmacogenetic approach to controlled ovarian hyperstimulation [J].
Behre, HM ;
Greb, RR ;
Mempel, A ;
Sonntag, B ;
Kiesel, L ;
Kaltwasser, P ;
Seliger, E ;
Röpke, F ;
Gromoll, J ;
Nieschlag, E ;
Simoni, M .
PHARMACOGENETICS AND GENOMICS, 2005, 15 (07) :451-456
[5]   The agony and ecstasy of "OMIC" technologies in drug development [J].
Bilello, JA .
CURRENT MOLECULAR MEDICINE, 2005, 5 (01) :39-52
[6]   PVUII RFLP INSIDE THE HUMAN ESTROGEN-RECEPTOR GENE [J].
CASTAGNOLI, A ;
MAESTRI, I ;
BERNARDI, F ;
DELSENNO, L .
NUCLEIC ACIDS RESEARCH, 1987, 15 (02) :866-866
[7]   NUCLEAR FACTOR RIP140 MODULATES TRANSCRIPTIONAL ACTIVATION BY THE ESTROGEN-RECEPTOR [J].
CAVAILLES, V ;
DAUVOIS, S ;
LHORSET, F ;
LOPEZ, G ;
HOARE, S ;
KUSHNER, PJ ;
PARKER, MG .
EMBO JOURNAL, 1995, 14 (15) :3741-3751
[8]   Endometrial volume and thickness measurements predict pituitary suppression and non-suppression during IVF [J].
Child, TJ ;
Sylvestre, C ;
Tan, SL .
HUMAN REPRODUCTION, 2002, 17 (12) :3110-3113
[9]   Prediction of severity of symptoms in iatrogenic ovarian hHyperstimulation syndrome by follicle-stimulating hormone receptor Ser680 Asn polymorphism [J].
Daelemans, C ;
Smits, G ;
de Maertelaer, V ;
Costagliola, S ;
Englert, Y ;
Vassart, G ;
Delbaere, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (12) :6310-6315
[10]  
De Castro F, 2005, JNCI-J NATL CANCER I, V97, P152, DOI 10.1093/jnci/dji029