Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patien...
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| Vydané v: | Nature genetics Ročník 50; číslo 12; s. 1681 - 1687 |
|---|---|
| Hlavní autori: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
New York
Nature Publishing Group US
01.12.2018
Nature Publishing Group |
| Predmet: | |
| ISSN: | 1061-4036, 1546-1718, 1546-1718 |
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| Abstract | Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes
SMO
(rs143083812, frequency 0.11%, odds ratio (OR) = 2.8,
P
= 7.9 × 10
−12
, p.Arg173Cys) and
IL11
(rs4252548, frequency 2.08%, OR = 1.30,
P
= 2.1 × 10
−11
, p.Arg112His). A common missense variant in the
COL11A1
gene also associates with hip osteoarthritis (rs3753841, frequency 61%,
P
= 5.2 × 10
–10
, OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of
CHADL
1
(rs117018441,
P
= 1.8 × 10
−25
, OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis.
Genome-wide association meta-analysis of data sets from Iceland and the UK identifies 16 new risk loci for osteoarthritis, including missense variants in
SMO
,
IL11
, and
COL11A1
. |
|---|---|
| AbstractList | Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes SMO (rs143083812, frequency 0.11%, odds ratio (OR) = 2.8, P = 7.9 × 10.sup.-12, p.Arg173Cys) and IL11 (rs4252548, frequency 2.08%, OR = 1.30, P = 2.1 × 10.sup.-11, p.Arg112His). A common missense variant in the COL11A1 gene also associates with hip osteoarthritis (rs3753841, frequency 61%, P = 5.2 × 10.sup.-10, OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of CHADL.sup.1 (rs117018441, P = 1.8 × 10.sup.-25, OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis. Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes SMO (rs143083812, frequency 0.11%, odds ratio (OR) = 2.8, P = 7.9x10-12, p.Arg173Cys) and IL11 (rs4252548, frequency 2.08%, OR = 1.30, P = 2.1x10-11, p.Arg112His). A common missense variant in the COL11A1 gene also associates with hip osteoarthritis (rs3753841, frequency 61%, P = 5.2 x 10-10, OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of CHADL1 (rs117018441, P = 1.8 x 10-25, OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis. Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes SMO (rs143083812, frequency 0.11%, odds ratio (OR) = 2.8, P = 7.9 × 10 −12 , p.Arg173Cys) and IL11 (rs4252548, frequency 2.08%, OR = 1.30, P = 2.1 × 10 −11 , p.Arg112His). A common missense variant in the COL11A1 gene also associates with hip osteoarthritis (rs3753841, frequency 61%, P = 5.2 × 10 –10 , OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of CHADL 1 (rs117018441, P = 1.8 × 10 −25 , OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis. Genome-wide association meta-analysis of data sets from Iceland and the UK identifies 16 new risk loci for osteoarthritis, including missense variants in SMO , IL11 , and COL11A1 . Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes SMO (rs143083812, frequency 0.11%, odds ratio (OR) = 2.8, P = 7.9 × 10.sup.-12, p.Arg173Cys) and IL11 (rs4252548, frequency 2.08%, OR = 1.30, P = 2.1 × 10.sup.-11, p.Arg112His). A common missense variant in the COL11A1 gene also associates with hip osteoarthritis (rs3753841, frequency 61%, P = 5.2 × 10.sup.-10, OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of CHADL.sup.1 (rs117018441, P = 1.8 × 10.sup.-25, OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis. Genome-wide association meta-analysis of data sets from Iceland and the UK identifies 16 new risk loci for osteoarthritis, including missense variants in SMO, IL11, and COL11A1. Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes SMO (rs143083812, frequency 0.11%, odds ratio (OR) = 2.8, P = 7.9 × 10 , p.Arg173Cys) and IL11 (rs4252548, frequency 2.08%, OR = 1.30, P = 2.1 × 10 , p.Arg112His). A common missense variant in the COL11A1 gene also associates with hip osteoarthritis (rs3753841, frequency 61%, P = 5.2 × 10 , OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of CHADL (rs117018441, P = 1.8 × 10 , OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis. Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes SMO (rs143083812, frequency 0.11%, odds ratio (OR) = 2.8, P = 7.9 × 10-12, p.Arg173Cys) and IL11 (rs4252548, frequency 2.08%, OR = 1.30, P = 2.1 × 10-11, p.Arg112His). A common missense variant in the COL11A1 gene also associates with hip osteoarthritis (rs3753841, frequency 61%, P = 5.2 × 10-10, OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of CHADL1 (rs117018441, P = 1.8 × 10-25, OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis.Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest meta-analysis so far of osteoarthritis of the hip and the knee in samples from Iceland and the UK Biobank (including 17,151 hip osteoarthritis patients, 23,877 knee osteoarthritis patients, and more than 562,000 controls). We found 23 independent associations at 22 loci in the additive meta-analyses, of which 16 of the loci were novel: 12 for hip and 4 for knee osteoarthritis. Two associations are between rare or low-frequency missense variants and hip osteoarthritis, affecting the genes SMO (rs143083812, frequency 0.11%, odds ratio (OR) = 2.8, P = 7.9 × 10-12, p.Arg173Cys) and IL11 (rs4252548, frequency 2.08%, OR = 1.30, P = 2.1 × 10-11, p.Arg112His). A common missense variant in the COL11A1 gene also associates with hip osteoarthritis (rs3753841, frequency 61%, P = 5.2 × 10-10, OR = 1.08, p.Pro1284Leu). In addition, using a recessive model, we confirm an association between hip osteoarthritis and a variant of CHADL1 (rs117018441, P = 1.8 × 10-25, OR = 5.9). Furthermore, we observe a complex relationship between height and risk of osteoarthritis. |
| Audience | Academic |
| Author | Oddsson, Asmundur Masson, Gisli Ingvarsson, Thorvaldur Norddahl, Gudmundur L. Thorleifsson, Gudmar Bjornsdottir, Gyda Jonsson, Helgi Gudmundsson, Reynir L. Sveinbjornsson, Gardar Thorsteinsdottir, Unnur Sigurbjornsdottir, Sara Halldorsson, Gisli H. Rafnar, Thorunn Lund, Sigrun H. Sigurdsson, Jon K. Norland, Kristjan Stefansdottir, Lilja Gudbjartsson, Daniel F. Stefansson, Kari Sulem, Patrick Jonsdottir, Ingileif Bjarnadottir, Kristbjörg Steingrimsson, Eirikur Styrkarsdottir, Unnur Zink, Florian Sigurdsson, Asgeir Jonsson, Stefan Juliusson, Kristinn Stefansson, Olafur A. |
| Author_xml | – sequence: 1 givenname: Unnur orcidid: 0000-0001-8146-8278 surname: Styrkarsdottir fullname: Styrkarsdottir, Unnur email: unnur.styrkarsdottir@decode.is organization: deCODE genetics/Amgen, Inc – sequence: 2 givenname: Sigrun H. orcidid: 0000-0002-3806-2296 surname: Lund fullname: Lund, Sigrun H. organization: deCODE genetics/Amgen, Inc., Faculty of Medicine, University of Iceland – sequence: 3 givenname: Gudmar surname: Thorleifsson fullname: Thorleifsson, Gudmar organization: deCODE genetics/Amgen, Inc – sequence: 4 givenname: Florian surname: Zink fullname: Zink, Florian organization: deCODE genetics/Amgen, Inc – sequence: 5 givenname: Olafur A. surname: Stefansson fullname: Stefansson, Olafur A. organization: deCODE genetics/Amgen, Inc – sequence: 6 givenname: Jon K. surname: Sigurdsson fullname: Sigurdsson, Jon K. organization: deCODE genetics/Amgen, Inc – sequence: 7 givenname: Kristinn surname: Juliusson fullname: Juliusson, Kristinn organization: deCODE genetics/Amgen, Inc – sequence: 8 givenname: Kristbjörg surname: Bjarnadottir fullname: Bjarnadottir, Kristbjörg organization: deCODE genetics/Amgen, Inc – sequence: 9 givenname: Sara surname: Sigurbjornsdottir fullname: Sigurbjornsdottir, Sara organization: Biochemistry and Molecular Biology, BioMedical Center, Faculty of Medicine, University of Iceland – sequence: 10 givenname: Stefan orcidid: 0000-0001-5401-8589 surname: Jonsson fullname: Jonsson, Stefan organization: deCODE genetics/Amgen, Inc – sequence: 11 givenname: Kristjan surname: Norland fullname: Norland, Kristjan organization: deCODE genetics/Amgen, Inc – sequence: 12 givenname: Lilja surname: Stefansdottir fullname: Stefansdottir, Lilja organization: deCODE genetics/Amgen, Inc – sequence: 13 givenname: Asgeir surname: Sigurdsson fullname: Sigurdsson, Asgeir organization: deCODE genetics/Amgen, Inc – sequence: 14 givenname: Gardar surname: Sveinbjornsson fullname: Sveinbjornsson, Gardar organization: deCODE genetics/Amgen, Inc – sequence: 15 givenname: Asmundur orcidid: 0000-0002-4606-5163 surname: Oddsson fullname: Oddsson, Asmundur organization: deCODE genetics/Amgen, Inc – sequence: 16 givenname: Gyda surname: Bjornsdottir fullname: Bjornsdottir, Gyda organization: deCODE genetics/Amgen, Inc – sequence: 17 givenname: Reynir L. surname: Gudmundsson fullname: Gudmundsson, Reynir L. organization: deCODE genetics/Amgen, Inc – sequence: 18 givenname: Gisli H. orcidid: 0000-0001-7067-9862 surname: Halldorsson fullname: Halldorsson, Gisli H. organization: deCODE genetics/Amgen, Inc – sequence: 19 givenname: Thorunn orcidid: 0000-0003-0491-7046 surname: Rafnar fullname: Rafnar, Thorunn organization: deCODE genetics/Amgen, Inc – sequence: 20 givenname: Ingileif orcidid: 0000-0001-8339-150X surname: Jonsdottir fullname: Jonsdottir, Ingileif organization: deCODE genetics/Amgen, Inc., Faculty of Medicine, University of Iceland, Department of Immunology, Landspitali–The National University Hospital of Iceland – sequence: 21 givenname: Eirikur surname: Steingrimsson fullname: Steingrimsson, Eirikur organization: Biochemistry and Molecular Biology, BioMedical Center, Faculty of Medicine, University of Iceland – sequence: 22 givenname: Gudmundur L. surname: Norddahl fullname: Norddahl, Gudmundur L. organization: deCODE genetics/Amgen, Inc – sequence: 23 givenname: Gisli surname: Masson fullname: Masson, Gisli organization: deCODE genetics/Amgen, Inc – sequence: 24 givenname: Patrick orcidid: 0000-0001-7123-6123 surname: Sulem fullname: Sulem, Patrick organization: deCODE genetics/Amgen, Inc – sequence: 25 givenname: Helgi surname: Jonsson fullname: Jonsson, Helgi organization: Faculty of Medicine, University of Iceland, Department of Medicine, Landspitali–The National University Hospital of Iceland – sequence: 26 givenname: Thorvaldur surname: Ingvarsson fullname: Ingvarsson, Thorvaldur organization: Faculty of Medicine, University of Iceland, Department of Orthopedic Surgery, Akureyri Hospital, Institution of Health Science, University of Akureyri – sequence: 27 givenname: Daniel F. orcidid: 0000-0002-5222-9857 surname: Gudbjartsson fullname: Gudbjartsson, Daniel F. organization: deCODE genetics/Amgen, Inc., School of Engineering and Natural Sciences, University of Iceland – sequence: 28 givenname: Unnur surname: Thorsteinsdottir fullname: Thorsteinsdottir, Unnur organization: deCODE genetics/Amgen, Inc., Faculty of Medicine, University of Iceland – sequence: 29 givenname: Kari orcidid: 0000-0003-1676-864X surname: Stefansson fullname: Stefansson, Kari email: kstefans@decode.is organization: deCODE genetics/Amgen, Inc., Faculty of Medicine, University of Iceland |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30374069$$D View this record in MEDLINE/PubMed |
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| ContentType | Journal Article |
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| Snippet | Osteoarthritis has a highly negative impact on quality of life because of the associated pain and loss of joint function. Here we describe the largest... |
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| Title | Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis |
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