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GWAS Study

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.

Warrington NM, Shevroja E, Hemani G et al.

29659830 PubMed ID
GWAS Study Type
12636 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WN
Warrington NM
SE
Shevroja E
HG
Hemani G
HP
Hysi PG
JY
Jiang Y
AA
Auton A
BC
Boer CG
MM
Mangino M
WC
Wang CA
KJ
Kemp JP
MG
McMahon G
MC
Medina-Gomez C
HM
Hickey M
TK
Trajanoska K
WD
Wolke D
IM
Ikram MA
MG
Montgomery GW
FJ
Felix JF
WM
Wright MJ
MD
Mackey DA
JV
Jaddoe VW
MN
Martin NG
TJ
Tung JY
DS
Davey Smith G
PC
Pennell CE
ST
Spector TD
VM
van Meurs J
RF
Rivadeneira F
MS
Medland SE
ED
Evans DM
Chapter II

Abstract

Summary of the research findings

The ratio of the length of the index finger to that of the ring finger (2D:4D) is sexually dimorphic and is commonly used as a non-invasive biomarker of prenatal androgen exposure. Most association studies of 2D:4D ratio with a diverse range of sex-specific traits have typically involved small sample sizes and have been difficult to replicate, raising questions around the utility and precise meaning of the measure. In the largest genome-wide association meta-analysis of 2D:4D ratio to date (N = 15 661, with replication N = 75 821), we identified 11 loci (9 novel) explaining 3.8% of the variance in mean 2D:4D ratio. We also found weak evidence for association (β = 0.06; P = 0.02) between 2D:4D ratio and sensitivity to testosterone [length of the CAG microsatellite repeat in the androgen receptor (AR) gene] in females only. Furthermore, genetic variants associated with (adult) testosterone levels and/or sex hormone-binding globulin were not associated with 2D:4D ratio in our sample. Although we were unable to find strong evidence from our genetic study to support the hypothesis that 2D:4D ratio is a direct biomarker of prenatal exposure to androgens in healthy individuals, our findings do not explicitly exclude this possibility, and pathways involving testosterone may become apparent as the size of the discovery sample increases further. Our findings provide new insight into the underlying biology shaping 2D:4D variation in the general population.

12,636 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

12636
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Australia, Netherlands, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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