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GWAS Study

Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis.

Medina-Gomez C, Mullin BH, Chesi A et al.

37402774 PubMed ID
GWAS Study Type
43832 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MC
Medina-Gomez C
MB
Mullin BH
CA
Chesi A
PV
Prijatelj V
KJ
Kemp JP
SC
Shochat-Carvalho C
TK
Trajanoska K
WC
Wang C
JR
Joro R
ET
Evans TE
SK
Schraut KE
LR
Li-Gao R
AT
Ahluwalia TS
ZM
Zillikens MC
ZK
Zhu K
MD
Mook-Kanamori DO
ED
Evans DS
NM
Nethander M
KM
Knol MJ
TG
Thorleifsson G
PI
Prokic I
ZB
Zemel B
BL
Broer L
MF
McGuigan FE
VS
van Schoor NM
RS
Reppe S
PM
Pawlak MA
RS
Ralston SH
VD
van der Velde N
LM
Lorentzon M
SK
Stefansson K
AH
Adams HHH
WS
Wilson SG
IM
Ikram MA
WJ
Walsh JP
LT
Lakka TA
GK
Gautvik KM
WJ
Wilson JF
OE
Orwoll ES
VD
van Duijn CM
BK
Bønnelykke K
UA
Uitterlinden AG
SU
Styrkársdóttir U
AK
Akesson KE
ST
Spector TD
TJ
Tobias JH
OC
Ohlsson C
FJ
Felix JF
BH
Bisgaard H
GS
Grant SFA
RJ
Richards JB
ED
Evans DM
VD
van der Eerden B
VD
van de Peppel J
AC
Ackert-Bicknell C
KD
Karasik D
KE
Kague E
RF
Rivadeneira F
Chapter II

Abstract

Summary of the research findings

Skull bone mineral density (SK-BMD) provides a suitable trait for the discovery of key genes in bone biology, particularly to intramembranous ossification, not captured at other skeletal sites. We perform a genome-wide association meta-analysis (n ~ 43,800) of SK-BMD, identifying 59 loci, collectively explaining 12.5% of the trait variance. Association signals cluster within gene-sets involved in skeletal development and osteoporosis. Among the four novel loci (ZIC1, PRKAR1A, AZIN1/ATP6V1C1, GLRX3), there are factors implicated in intramembranous ossification and as we show, inherent to craniosynostosis processes. Functional follow-up in zebrafish confirms the importance of ZIC1 on cranial suture patterning. Likewise, we observe abnormal cranial bone initiation that culminates in ectopic sutures and reduced BMD in mosaic atp6v1c1 knockouts. Mosaic prkar1a knockouts present asymmetric bone growth and, conversely, elevated BMD. In light of this evidence linking SK-BMD loci to craniofacial abnormalities, our study provides new insight into the pathophysiology, diagnosis and treatment of skeletal diseases.

38,435 European ancestry individuals, 5,397 individuals

Chapter III

Study Statistics

Key metrics and study information

43832
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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