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

• Published in: PloS one Vol. 8; no. 2; p. e55258
• Main Authors: Spencer, Kylee L., Malinowski, Jennifer, Carty, Cara L., Franceschini, Nora, Fernández-Rhodes, Lindsay, Young, Alicia, Cheng, Iona, Ritchie, Marylyn D., Haiman, Christopher A., Wilkens, Lynne, ChunyuanWu, Matise, Tara C., Carlson, Christopher S., Brennan, Kathleen, Park, Amy, Rajkovic, Aleksandar, Hindorff, Lucia A., Buyske, Steven, Crawford, Dana C.
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 12.02.2013; Public Library of Science (PLoS)
• Subjects: Adolescent; African American women; African Americans; Apolipoprotein E; Architecture; Arteriosclerosis; Atherosclerosis; Biology; Black or African American - genetics; Black or African American - statistics & numerical data; Breast cancer; Cancer; Cardiovascular disease; Cardiovascular diseases; Epidemiologic Studies; Epidemiology; Female; Genetic aspects; Genetic diversity; Genetic variance; Genetic Variation; Genome-wide association studies; Genomes; Genomics; Health promotion; Health risk assessment; Hormone replacement therapy; Humans; KCNQ1 protein; Life span; Lipoprotein (low density) receptors; Medical research; Medicine; Menarche; Menarche - ethnology; Menarche - genetics; Menarche - physiology; Menopause; Menopause - ethnology; Menopause - genetics; Menopause - physiology; Middle Aged; Obesity; Populations; Potassium channels (voltage-gated); Reproduction - genetics; Single-nucleotide polymorphism; Type 2 diabetes; Women's health; North Carolina; Los Angeles California; United States > US; Tennessee; Hawaii; California; Maryland; Nashville Tennessee; New Jersey
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0055258

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.