Return to search

Identification of Copy Number Variants in a Cohort of Women with Premature Ovarian Insufficiency

Premature ovarian failure (POF), or premature ovarian insufficiency (POI), is characterized by the absence or early cessation of menstruation before the age of 40. Clinically this can be seen as primary amenorrhea, the complete absence of menstruation, or secondary amenorrhea, the development of amenorrhea due to cessation of ovarian function. POI affects approximately 1% of women under the age of 40 years and 0.1% of women under the age of 30. Most cases of POI are idiopathic, as only 10% have a known cause. We utilized SNP array technology to identify novel copy number variations (CNVs) in 89 women with POI. Illuminas (San Diego, CA, USA) HumanCNV370-Duo DNA Analysis BeadChip and Human660W-Quad v1 DNA Analysis BeadChip were used to identify microdeletions and microduplications on autosomal chromosomes. A total of 198 autosomal CNVs were identified ranging from 0.1 Mb to 3.4 Mb. The Database of Genomic Variants (DGV) was used as a control population. We identified seven novel microdeletions in our POI cohort, six of which contained gene-coding regions: 8q24.13, 10p15-p14, 10q23.31, 10q26.3, 15q25.2, and 18q21.32. Two of the novel microdeletions contained genes known to cause ovarian failure in knockout mice models, SYCE1 and CPEB1. Seventeen novel microduplications were also detected, with the majority of CNVs detected being on autosomal chromosomes rather than the X chromosome. This pilot study demonstrates an association between specific CNVs and POI and highlights the importance for studies with larger samples sizes to confirm the findings and further support the hypothesis. Furthermore, array technology may be a useful addition to conventional karyotyping when evaluating women with POI. Studies on the genetic factors of POI have public health significance because they search for genomic imbalances in a disease that affects 1% of the American population. Finding the genetic causes may lead to effective treatment methods and earlier recognition of those at risk, particularly before the onset of amenorrhea.

Identiferoai:union.ndltd.org:PITT/oai:PITTETD:etd-04052011-152145
Date29 June 2011
CreatorsEngel, Natalie Joy
ContributorsAleksandar Rajkovic, MD, PhD, Elizabeth Gettig, MS, CGC, M. Michael Barmada, PhD, John W. Wilson, PhD
PublisherUniversity of Pittsburgh
Source SetsUniversity of Pittsburgh
LanguageEnglish
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.library.pitt.edu/ETD/available/etd-04052011-152145/
Rightsunrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to University of Pittsburgh or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.

Page generated in 0.0025 seconds