Link to the University of Pittsburgh Homepage
Link to the University Library System Homepage Link to the Contact Us Form

Genetic Variation and Reproductive Timing: African American Women from the Population Architecture Using Genomics and Epidemiology (PAGE) Study

Spencer, KL and Malinowski, J and Carty, CL and Franceschini, N and Fernández-Rhodes, L and Young, A and Cheng, I and Ritchie, MD and Haiman, CA and Wilkens, L and ChunyuanWu, and Matise, TC and Carlson, CS and Brennan, K and Park, A and Rajkovic, A and Hindorff, LA and Buyske, S and Crawford, DC (2013) Genetic Variation and Reproductive Timing: African American Women from the Population Architecture Using Genomics and Epidemiology (PAGE) Study. PLoS ONE, 8 (2).

[img]
Preview
PDF
Published Version
Available under License : See the attached license file.

Download (628kB) | Preview
[img] Plain Text (licence)
Available under License : See the attached license file.

Download (1kB)

Abstract

Age at menarche (AM) and age at natural menopause (ANM) define the boundaries of the reproductive lifespan in women. Their timing is associated with various diseases, including cancer and cardiovascular disease. Genome-wide association studies have identified several genetic variants associated with either AM or ANM in populations of largely European or Asian descent women. The extent to which these associations generalize to diverse populations remains unknown. Therefore, we sought to replicate previously reported AM and ANM findings and to identify novel AM and ANM variants using the Metabochip (n = 161,098 SNPs) in 4,159 and 1,860 African American women, respectively, in the Women's Health Initiative (WHI) and Atherosclerosis Risk in Communities (ARIC) studies, as part of the Population Architecture using Genomics and Epidemiology (PAGE) Study. We replicated or generalized one previously identified variant for AM, rs1361108/CENPW, and two variants for ANM, rs897798/BRSK1 and rs769450/APOE, to our African American cohort. Overall, generalization of the majority of previously-identified variants for AM and ANM, including LIN28B and MCM8, was not observed in this African American sample. We identified three novel loci associated with ANM that reached significance after multiple testing correction (LDLR rs189596789, p = 5×10-08; KCNQ1 rs79972789, p = 1.9×10-07; COL4A3BP rs181686584, p = 2.9×10-07). Our most significant AM association was upstream of RSF1, a gene implicated in ovarian and breast cancers (rs11604207, p = 1.6×10-06). While most associations were identified in either AM or ANM, we did identify genes suggestively associated with both: PHACTR1 and ARHGAP42. The lack of generalization coupled with the potentially novel associations identified here emphasize the need for additional genetic discovery efforts for AM and ANM in diverse populations. © 2013 Spencer et al.


Share

Citation/Export:
Social Networking:
Share |

Details

Item Type: Article
Status: Published
Creators/Authors:
CreatorsEmailPitt UsernameORCID
Spencer, KL
Malinowski, J
Carty, CL
Franceschini, N
Fernández-Rhodes, L
Young, A
Cheng, I
Ritchie, MD
Haiman, CA
Wilkens, L
ChunyuanWu,
Matise, TC
Carlson, CS
Brennan, K
Park, A
Rajkovic, Aalr110@pitt.eduALR110
Hindorff, LA
Buyske, S
Crawford, DC
Date: 12 February 2013
Date Type: Publication
Journal or Publication Title: PLoS ONE
Volume: 8
Number: 2
DOI or Unique Handle: 10.1371/journal.pone.0055258
Schools and Programs: School of Medicine > Obstetrics, Gynecology, and Reproductive Sciences
Refereed: Yes
Other ID: NLM PMC3570525
PubMed Central ID: PMC3570525
PubMed ID: 23424626
Date Deposited: 20 Mar 2013 19:55
Last Modified: 05 Feb 2019 15:55
URI: http://d-scholarship.pitt.edu/id/eprint/17835

Metrics

Monthly Views for the past 3 years

Plum Analytics

Altmetric.com


Actions (login required)

View Item View Item