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GWAS Study

New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.

Springelkamp H, Iglesias AI, Mishra A et al.

28073927 PubMed ID
GWAS Study Type
29817 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SH
Springelkamp H
IA
Iglesias AI
MA
Mishra A
HR
Höhn R
WR
Wojciechowski R
KA
Khawaja AP
NA
Nag A
WY
Wang YX
WJ
Wang JJ
CG
Cuellar-Partida G
GJ
Gibson J
BJ
Bailey JN
VE
Vithana EN
GP
Gharahkhani P
BT
Boutin T
RW
Ramdas WD
ZT
Zeller T
LR
Luben RN
YE
Yonova-Doing E
VA
Viswanathan AC
YS
Yazar S
CA
Cree AJ
HJ
Haines JL
KJ
Koh JY
SE
Souzeau E
WJ
Wilson JF
AN
Amin N
MC
Müller C
VC
Venturini C
KL
Kearns LS
KJ
Kang JH
TY
Tham YC
ZT
Zhou T
VL
van Leeuwen EM
NS
Nickels S
SP
Sanfilippo P
LJ
Liao J
VD
van der Linde H
ZW
Zhao W
VK
van Koolwijk LM
ZL
Zheng L
RF
Rivadeneira F
BM
Baskaran M
VD
van der Lee SJ
PS
Perera S
DJ
de Jong PT
OB
Oostra BA
UA
Uitterlinden AG
FQ
Fan Q
HA
Hofman A
TE
Tai ES
VJ
Vingerling JR
SX
Sim X
WR
Wolfs RC
TY
Teo YY
LH
Lemij HG
KC
Khor CC
WR
Willemsen R
LK
Lackner KJ
AT
Aung T
JN
Jansonius NM
MG
Montgomery G
WP
Wild PS
YT
Young TL
BK
Burdon KP
HP
Hysi PG
PL
Pasquale LR
WT
Wong TY
KC
Klaver CC
HA
Hewitt AW
JJ
Jonas JB
MP
Mitchell P
LA
Lotery AJ
FP
Foster PJ
VV
Vitart V
PN
Pfeiffer N
CJ
Craig JE
MD
Mackey DA
HC
Hammond CJ
WJ
Wiggs JL
CC
Cheng CY
VD
van Duijn CM
MS
MacGregor S
Chapter II

Abstract

Summary of the research findings

Primary open-angle glaucoma (POAG), the most common optic neuropathy, is a heritable disease. Siblings of POAG cases have a ten-fold increased risk of developing the disease. Intraocular pressure (IOP) and optic nerve head characteristics are used clinically to predict POAG risk. We conducted a genome-wide association meta-analysis of IOP and optic disc parameters and validated our findings in multiple sets of POAG cases and controls. Using imputation to the 1000 genomes (1000G) reference set, we identified 9 new genomic regions associated with vertical cup-disc ratio (VCDR) and 1 new region associated with IOP. Additionally, we found 5 novel loci for optic nerve cup area and 6 for disc area. Previously it was assumed that genetic variation influenced POAG either through IOP or via changes to the optic nerve head; here we present evidence that some genomic regions affect both IOP and the disc parameters. We characterized the effect of the novel loci through pathway analysis and found that pathways involved are not entirely distinct as assumed so far. Further, we identified a novel association between CDKN1A and POAG. Using a zebrafish model we show that six6b (associated with POAG and optic nerve head variation) alters the expression of cdkn1a. In summary, we have identified several novel genes influencing the major clinical risk predictors of POAG and showed that genetic variation in CDKN1A is important in POAG risk.

20,353 European ancestry individuals, 2,131 Erasmus Rucphen (founder/genetic isolate) individuals

Chapter III

Study Statistics

Key metrics and study information

29817
Total Participants
GWAS
Study Type
Yes
Replicated
7,333 Asian ancestry individuals
Replication Participants
South Asian, South East Asian, East Asian, European
Ancestry
China, Singapore, U.S., Australia, Germany, Netherlands, U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.