Copy number variants on the X chromosome in women with primary ovarian insufficiency


Autoria(s): KNAUFF, Erik A. H.; BLAUW, Hylke M.; PEARSON, Peter L.; KOK, Klaas; WIJMENGA, Cisca; VELDINK, Jan H.; BERG, Leonard H. van den; BOUCHARD, Philippe; FAUSER, Bart C. J. M.; FRANKE, Lude; Dutch Primary Ovarian Insufficienc
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Objective: To investigate whether submicroscopic copy number variants (CNVs) on the X chromosome can be identified in women with primary ovarian insufficiency (POI), defined as spontaneous secondary amenorrhea before 40 years of age accompanied by follicle-stimulating hormone levels above 40 IU/L on at least two occasions. Design: Analysis of intensity data of single nucleotide polymorphism (SNP) probes generated by genomewide Illumina 370k CNV BeadChips, followed by the validation of identified loci using a custom designed ultra-high-density comparative genomic hybridization array containing 48,325 probes evenly distributed over the X chromosome. Setting: Multicenter genetic cohort study in the Netherlands. Patient(s): 108 Dutch Caucasian women with POI, 97 of whom passed quality control, who had a normal karyogram and absent fragile X premutation, and 235 healthy Dutch Caucasian women as controls. Intervention(s): None. Main Outcome Measure(s): Amount and locus of X chromosomal microdeletions or duplications. Result(s): Intensity differences between SNP probes identify microdeletions and duplications. The initial analysis identified an overrepresentation of deletions in POI patients. Moreover, CNVs in two genes on the Xq21.3 locus (i.e., PCDH11X and TGIF2LX) were statistically significantly associated with the POI phenotype. Mean size of identified CNVs was 262 kb. However, in the validation study the identified putative Xq21.3 deletions samples did not show deviations in intensities in consecutive probes. Conclusion(s): X chromosomal submicroscopic CNVs do not play a major role in Caucasian POI patients. We provide guidelines on how submicroscopic cytogenetic POI research should be conducted. (Fertil Steril (R) 2011;95:1584-8. (C) 2011 by American Society for Reproductive Medicine.)

Netherlands Genomics Initiative

Netherlands Genomics Initiative[93519031]

NWO (ZonMW)[916.10.135]

Netherlands Organisation for Scientific Research (NWO)

Identificador

FERTILITY AND STERILITY, v.95, n.5, p.1584-U74, 2011

0015-0282

http://producao.usp.br/handle/BDPI/27475

10.1016/j.fertnstert.2011.01.018

http://dx.doi.org/10.1016/j.fertnstert.2011.01.018

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE INC

Relação

Fertility and Sterility

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE INC

Palavras-Chave #Copy number variation #premature ovarian failure #primary ovarian insufficiency #X chromosome #AMYOTROPHIC-LATERAL-SCLEROSIS #GENOME-WIDE ASSOCIATION #LONG ARM #INTERSTITIAL DELETION #MENOPAUSAL AGE #FAILURE POF #YOUNG-WOMEN #DISEASE #GENE #SUSCEPTIBILITY #Obstetrics & Gynecology #Reproductive Biology
Tipo

article

original article

publishedVersion