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The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis.

Fernández-Rhodes L, Malinowski JR, Wang Y et al.

30044860 PubMed ID
GWAS Study Type
17730 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

FL
Fernández-Rhodes L
MJ
Malinowski JR
WY
Wang Y
TR
Tao R
PN
Pankratz N
JJ
Jeff JM
YS
Yoneyama S
CC
Carty CL
SV
Setiawan VW
LM
Le Marchand L
HC
Haiman C
CS
Corbett S
DE
Demerath E
HG
Heiss G
GM
Gross M
BP
Buzkova P
CD
Crawford DC
HS
Hunt SC
RD
Rao DC
SK
Schwander K
CA
Chakravarti A
GO
Gottesman O
AN
Abul-Husn NS
BE
Bottinger EP
LR
Loos RJF
RL
Raffel LJ
YJ
Yao J
GX
Guo X
BS
Bielinski SJ
RJ
Rotter JI
VD
Vaidya D
CY
Chen YI
CS
Castañeda SF
DM
Daviglus M
KR
Kaplan R
TG
Talavera GA
RK
Ryckman KK
PU
Peters U
AJ
Ambite JL
BS
Buyske S
HL
Hindorff L
KC
Kooperberg C
MT
Matise T
FN
Franceschini N
NK
North KE
Chapter II

Abstract

Summary of the research findings

Current knowledge of the genetic architecture of key reproductive events across the female life course is largely based on association studies of European descent women. The relevance of known loci for age at menarche (AAM) and age at natural menopause (ANM) in diverse populations remains unclear. We investigated 32 AAM and 14 ANM previously-identified loci and sought to identify novel loci in a trans-ethnic array-wide study of 196,483 SNPs on the MetaboChip (Illumina, Inc.). A total of 45,364 women of diverse ancestries (African, Hispanic/Latina, Asian American and American Indian/Alaskan Native) in the Population Architecture using Genomics and Epidemiology (PAGE) Study were included in cross-sectional analyses of AAM and ANM. Within each study we conducted a linear regression of SNP associations with self-reported or medical record-derived AAM or ANM (in years), adjusting for birth year, population stratification, and center/region, as appropriate, and meta-analyzed results across studies using multiple meta-analytic techniques. For both AAM and ANM, we observed more directionally consistent associations with the previously reported risk alleles than expected by chance (p-valuesbinomial≤0.01). Eight densely genotyped reproductive loci generalized significantly to at least one non-European population. We identified one trans-ethnic array-wide SNP association with AAM and two significant associations with ANM, which have not been described previously. Additionally, we observed evidence of independent secondary signals at three of six AAM trans-ethnic loci. Our findings support the transferability of reproductive trait loci discovered in European women to women of other race/ethnicities and indicate the presence of additional trans-ethnic associations both at both novel and established loci. These findings suggest the benefit of including diverse populations in future studies of the genetic architecture of female growth and development.

7,928 African American, 5,271 Hispanic, 4,347 Asian American, 184 Native American ancestry women

Chapter III

Study Statistics

Key metrics and study information

17730
Total Participants
GWAS
Study Type
No
Replicated
Hispanic or Latin American, African American or Afro-Caribbean, Asian unspecified, Native American
Ancestry
U.S.
Recruitment Country
Chapter IV

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