Familial aggregation of arthritis-related diseases in seropositive and seronegative rheumatoid arthritis: a register-based case-control study in Sweden

被引:66
作者
Frisell, Thomas [1 ]
Hellgren, Karin [1 ,2 ]
Alfredsson, Lars [3 ]
Raychaudhuri, Soumya [4 ,5 ,6 ,7 ]
Klareskog, Lars [2 ]
Askling, Johan [1 ,2 ]
机构
[1] Karolinska Inst, Dept Med, Clin Epidemiol Unit, Solna, Sweden
[2] Karolinska Inst, Dept Med, Rheumatol Unit, Solna, Sweden
[3] Karolinska Inst, Inst Environm Med, S-10401 Stockholm, Sweden
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Rheumatol Allergy & Immunol, Boston, MA 02115 USA
[5] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Genet, Boston, MA 02115 USA
[6] Broad Inst, Program Med & Populat Genet, Cambridge, MA USA
[7] Univ Manchester, Ctr Musculoskeletal Res, Inst Inflammat & Repair, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
基金
英国医学研究理事会; 瑞典研究理事会;
关键词
AUTOIMMUNE-DISEASES; PROTEIN ANTIBODIES; RISK; HERITABILITY; SEX;
D O I
10.1136/annrheumdis-2014-206133
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objectives Our objective was to estimate the risk of developing rheumatoid arthritis (RA) associated with a family history of non-RA arthritis-related diseases. This familial co-aggregation is of clinical interest since it is often encountered when assessing family history of RA specifically, but also informative on the genetic overlap between these diseases. Since anticitrullinated peptide antibodies/rheumatoid factor (RF)-positive and RF-negative RA have both specific and shared genetic factors, the familial co-aggregation was assessed separately for seropositive and seronegative disease. Methods Nested case-control study in prospectively recorded Swedish total population data. The Multi-Generation Register identified first-degree relatives. RA and arthritis-related diseases were ascertained through the nationwide patient register. RA serology was based on International Classification of Diseases tenth revision coded diagnoses, mainly reflecting RF. Familial risks were calculated using conditional logistic regression. Results were replicated using the Swedish rheumatology register. Results Familial co-aggregation was found between RA and every studied arthritis-related disease, but the magnitude varied widely, from juvenile idiopathic arthritis (JIA) (seropositive RA OR=3.98 (3.01 to 5.26); seronegative RA OR=5.70 (3.47 to 9.36)) to osteoarthritis (seropositive RA OR=1.03 (1.00 to 1.06); seronegative RA OR=1.05 (1.00 to 1.09)). The familial co-aggregation pattern of non-RA arthritis-related diseases was overall similar for seropositive and seronegative RA. Among those with family history of RA, relatives' other arthritis-related diseases conferred little or no additional risk. Conclusions Although family history of several arthritis-related diseases may be useful to predict RA (eg, lupus and JIA), others (eg, osteoarthritis and arthralgia) are less useful. Seropositive and seronegative RA had rather similar familial co-aggregation patterns with arthritis-related diseases, suggesting that the two RA subsets are similar in the genetic factors that overlap with these diseases.
引用
收藏
页码:183 / 189
页数:7
相关论文
共 23 条
[1]
Association of chronic inflammation, not its treatment, with increased lymphoma risk in rheumatoid arthritis [J].
Baecklund, E ;
Iliadou, A ;
Askling, J ;
Ekborn, A ;
Backlin, C ;
Granath, F ;
Catrina, AT ;
Rosenquist, R ;
Feltelius, N ;
Sundström, C ;
Klareskog, L .
ARTHRITIS AND RHEUMATISM, 2006, 54 (03) :692-701
[2]
The genetics of autoimmune diseases: a networked perspective [J].
Baranzini, Sergio E. .
CURRENT OPINION IN IMMUNOLOGY, 2009, 21 (06) :596-605
[3]
Non-participation in EIRA: a population-based case-control study of rheumatoid arthritis [J].
Bengtsson, C. ;
Berglund, A. ;
Serra, M-L ;
Nise, L. ;
Nordmark, B. ;
Klareskog, L. ;
Alfredsson, L. .
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2010, 39 (04) :344-346
[4]
How do autoimmune diseases cluster in families? A systematic review and meta-analysis [J].
Cardenas-Roldan, Jorge ;
Rojas-Villarraga, Adriana ;
Anaya, Juan-Manuel .
BMC MEDICINE, 2013, 11
[5]
Ekbom A, 2011, METHODS MOL BIOL, V675, P215, DOI 10.1007/978-1-59745-423-0_10
[6]
High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis [J].
Eyre, Steve ;
Bowes, John ;
Diogo, Dorothee ;
Lee, Annette ;
Barton, Anne ;
Martin, Paul ;
Zhernakova, Alexandra ;
Stahl, Eli ;
Viatte, Sebastien ;
McAllister, Kate ;
Amos, Christopher I. ;
Padyukov, Leonid ;
Toes, Rene E. M. ;
Huizinga, Tom W. J. ;
Wijmenga, Cisca ;
Trynka, Gosia ;
Franke, Lude ;
Westra, Harm-Jan ;
Alfredsson, Lars ;
Hu, Xinli ;
Sandor, Cynthia ;
de Bakker, Paul I. W. ;
Davila, Sonia ;
Khor, Chiea Chuen ;
Heng, Khai Koon ;
Andrews, Robert ;
Edkins, Sarah ;
Hunt, Sarah E. ;
Langford, Cordelia ;
Symmons, Deborah ;
Concannon, Pat ;
Onengut-Gumuscu, Suna ;
Rich, Stephen S. ;
Deloukas, Panos ;
Gonzalez-Gay, Miguel A. ;
Rodriguez-Rodriguez, Luis ;
Arlsetig, Lisbeth ;
Martin, Javier ;
Rantapaa-Dahlqvist, Solbritt ;
Plenge, Robert M. ;
Raychaudhuri, Soumya ;
Klareskog, Lars ;
Gregersen, Peter K. ;
Worthington, Jane .
NATURE GENETICS, 2012, 44 (12) :1336-1340
[7]
Familial Risks and Heritability of Rheumatoid Arthritis Role of Rheumatoid Factor/Anti-Citrullinated Protein Antibody Status, Number and Type of Affected Relatives, Sex, and Age [J].
Frisell, Thomas ;
Holmqvist, Marie ;
Kallberg, Henrik ;
Klareskog, Lars ;
Alfredsson, Lars ;
Askling, Johan .
ARTHRITIS AND RHEUMATISM, 2013, 65 (11) :2773-2782
[8]
Grant SFA, 2001, ARTHRITIS RHEUM-US, V44, P2247, DOI 10.1002/1529-0131(200110)44:10<2247::AID-ART387>3.0.CO
[9]
2-Y
[10]
Fine Mapping Seronegative and Seropositive Rheumatoid Arthritis to Shared and Distinct HLA Alleles by Adjusting for the Effects of Heterogeneity [J].
Han, Buhm ;
Diogo, Dorothee ;
Eyre, Steve ;
Kallberg, Henrik ;
Zhernakova, Alexandra ;
Bowes, John ;
Padyukov, Leonid ;
Okada, Yukinori ;
Gonzalez-Gay, Miguel A. ;
Rantapaa-Dahlqvist, Solbritt ;
Martin, Javier ;
Huizinga, Tom W. J. ;
Plenge, Robert M. ;
Worthington, Jane ;
Gregersen, Peter K. ;
Klareskog, Lars ;
de Bakker, Paul I. W. ;
Raychaudhuri, Soumya .
AMERICAN JOURNAL OF HUMAN GENETICS, 2014, 94 (04) :522-532