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GWAS Study

Translational genomics of osteoarthritis in 1,962,069 individuals.

Hatzikotoulas K, Southam L, Stefansdottir L et al.

40205036 PubMed ID
GWAS Study Type
1962069 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HK
Hatzikotoulas K
SL
Southam L
SL
Stefansdottir L
BC
Boer CG
MM
McDonald ML
PJ
Pett JP
PY
Park YC
TM
Tuerlings M
MR
Mulders R
BA
Barysenka A
AA
Arruda AL
TV
Tragante V
RA
Rocco A
BN
Bittner N
CS
Chen S
HS
Horn S
SV
Srinivasasainagendra V
TK
To K
KG
Katsoula G
KP
Kreitmaier P
TA
Tenghe AMM
GA
Gilly A
AL
Arbeeva L
CL
Chen LG
DP
de Pins AM
DD
Dochtermann D
HC
Henkel C
HJ
Höijer J
IS
Ito S
LP
Lind PA
LB
Lukusa-Sawalena B
MA
Minn AKK
MM
Mola-Caminal M
NA
Narita A
NC
Nguyen C
RE
Reimann E
SM
Silberstein MD
SA
Skogholt AH
TH
Tiwari HK
YM
Yau MS
YM
Yue M
ZW
Zhao W
ZJ
Zhou JJ
AG
Alexiadis G
BK
Banasik K
BS
Brunak S
CA
Campbell A
CJ
Cheung JTS
DJ
Dowsett J
FT
Faquih T
FJ
Faul JD
FL
Fei L
FA
Fenstad AM
FT
Funayama T
GM
Gabrielsen ME
GC
Gocho C
GK
Gromov K
HT
Hansen T
HG
Hudjashov G
IT
Ingvarsson T
JJ
Johnson JS
JH
Jonsson H
KS
Kakehi S
KJ
Karjalainen J
KE
Kasbohm E
LS
Lemmelä S
LK
Lin K
LX
Liu X
LM
Loef M
MM
Mangino M
MD
McCartney D
MI
Millwood IY
RJ
Richman J
RM
Roberts MB
RK
Ryan KA
SD
Samartzis D
SM
Shivakumar M
SS
Skou ST
SS
Sugimoto S
SK
Suzuki K
TH
Takuwa H
TM
Teder-Laving M
TL
Thomas L
TK
Tomizuka K
TC
Turman C
WS
Weiss S
WT
Wu TT
ZE
Zengini E
ZY
Zhang Y
FM
Ferreira MAR
BG
Babis G
BA
Baras A
BT
Barker T
CD
Carey DJ
CK
Cheah KSE
CZ
Chen Z
CJ
Cheung JP
DM
Daly M
DM
de Mutsert R
EC
Eaton CB
EC
Erikstrup C
FO
Furnes ON
GY
Golightly YM
GD
Gudbjartsson DF
HN
Hailer NP
HC
Hayward C
HM
Hochberg MC
HG
Homuth G
HL
Huckins LM
HK
Hveem K
IS
Ikegawa S
IM
Ishijima M
IM
Isomura M
JM
Jones M
KJ
Kang JH
KS
Kardia SLR
KM
Kloppenburg M
KP
Kraft P
KN
Kumahashi N
KS
Kuwata S
LM
Lee MTM
LP
Lee PH
LR
Lerner R
LL
Li L
LS
Lietman SA
LL
Lotta L
LM
Lupton MK
MR
Mägi R
MN
Martin NG
MT
McAlindon TE
MS
Medland SE
MK
Michaëlsson K
MB
Mitchell BD
MD
Mook-Kanamori DO
MA
Morris AP
NT
Nabika T
NF
Nagami F
NA
Nelson AE
OS
Ostrowski SR
PA
Palotie A
PO
Pedersen OB
RF
Rosendaal FR
SM
Sakurai-Yageta M
SC
Schmidt CO
SP
Sham PC
SJ
Singh JA
SD
Smelser DT
SJ
Smith JA
SY
Song YQ
SE
Sørensen E
TG
Tamiya G
TY
Tamura Y
TC
Terao C
TG
Thorleifsson G
TA
Troelsen A
TA
Tsezou A
UY
Uchio Y
UA
Uitterlinden AG
UH
Ullum H
VA
Valdes AM
VH
van Heel DA
WR
Walters RG
WD
Weir DR
WJ
Wilkinson JM
WB
Winsvold BS
YM
Yamamoto M
ZJ
Zwart JA
SK
Stefansson K
MI
Meulenbelt I
TS
Teichmann SA
VM
van Meurs JBJ
SU
Styrkarsdottir U
ZE
Zeggini E
Chapter II

Abstract

Summary of the research findings

Osteoarthritis is the third most rapidly growing health condition associated with disability, after dementia and diabetes1. By 2050, the total number of patients with osteoarthritis is estimated to reach 1 billion worldwide2. As no disease-modifying treatments exist for osteoarthritis, a better understanding of disease aetiopathology is urgently needed. Here we perform a genome-wide association study meta-analyses across up to 489,975 cases and 1,472,094 controls, establishing 962 independent associations, 513 of which have not been previously reported. Using single-cell multiomics data, we identify signal enrichment in embryonic skeletal development pathways. We integrate orthogonal lines of evidence, including transcriptome, proteome and epigenome profiles of primary joint tissues, and implicate 700 effector genes. Within these, we find rare coding-variant burden associations with effect sizes that are consistently higher than common frequency variant associations. We highlight eight biological processes in which we find convergent involvement of multiple effector genes, including the circadian clock, glial-cell-related processes and pathways with an established role in osteoarthritis (TGFβ, FGF, WNT, BMP and retinoic acid signalling, and extracellular matrix organization). We find that 10% of the effector genes express a protein that is the target of approved drugs, offering repurposing opportunities, which can accelerate translation.

441,288 European ancestry cases, 1,271,822 European ancestry controls, 10,408 East Asian ancestry cases, 128,633 East Asian ancestry controls, 25,698 African or African American cases, 34,718 African or African American controls, 2,422 South Asian ancestry cases, 18,894 South Asian ancestry controls, 8,128 Hispanic cases, 9,759 Hispanic controls, 2,031 Admixed ancestry cases, 8,268 Admixed ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1962069
Total Participants
GWAS
Study Type
No
Replicated
European, East Asian, African unspecified, African American or Afro-Caribbean, South Asian, Hispanic or Latin American, Other admixed ancestry
Ancestry
Iceland, Greece, Netherlands, Sweden, U.S., Norway, Finland, Denmark, U.K., Australia, Germany, Estonia, Japan, China
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.