Epidemiology and genetics of rheumatoid arthritis

Alan J Silman, Jacqueline E Pearson, Alan J Silman, Jacqueline E Pearson

Abstract

The prevalence of rheumatoid arthritis (RA) is relatively constant in many populations, at 0.5-1.0%. However, a high prevalence of RA has been reported in the Pima Indians (5.3%) and in the Chippewa Indians (6.8%). In contrast, low occurrences have been reported in populations from China and Japan. These data support a genetic role in disease risk. Studies have so far shown that the familial recurrence risk in RA is small compared with other autoimmune diseases. The main genetic risk factor of RA is the HLA DRB1 alleles, and this has consistently been shown in many populations throughout the world. The strongest susceptibility factor so far has been the HLA DRB1*0404 allele. Tumour necrosis factor alleles have also been linked with RA. However, it is estimated that these genes can explain only 50% of the genetic effect. A number of other non-MHC genes have thus been investigated and linked with RA (e.g. corticotrophin releasing hormone, oestrogen synthase, IFN-gamma and other cytokines). Environmental factors have also been studied in relation to RA. Female sex hormones may play a protective role in RA; for example, the use of the oral contraceptive pill and pregnancy are both associated with a decreased risk. However, the postpartum period has been highlighted as a risk period for the development of RA. Furthermore, breastfeeding after a first pregnancy poses the greatest risk. Exposure to infection may act as a trigger for RA, and a number of agents have been implicated (e.g. Epstein-Barr virus, parvovirus and some bacteria such as Proteus and Mycoplasma). However, the epidemiological data so far are inconclusive. There has recently been renewed interest in the link between cigarette smoking and RA, and the data presented so far are consistent with and suggestive of an increased risk.

Figures

Figure 1
Figure 1
Prevalence of rheumatoid arthritis in various populations. Data from [1-4,6-9,11,12,16,17].
Figure 2
Figure 2
The incidence of rheumatoid arthritis in relation to use of the oral contraceptive pill (OC). Data from the Royal College of General Practioners' oral contraception study [54].
Figure 3
Figure 3
Increased risk of rheumatoid arthritis onset in the postpartum period. * Relative to nonpregnant periods. Data from [59].

References

    1. Carmona L, Villaverde V, Hernandez-Garcia C, Ballina J, Gabriel R, Laffon A. The prevalence of rheumatoid arthritis in the general population of Spain. Rheumatology. 2002;41:88–95. doi: 10.1093/rheumatology/41.1.88.
    1. Riise T, Jacobsen BK, Gran JT. Incidence and prevalence of rheumatoid arthritis in the county of Troms, northern Norway. J Rheumatol. 2000;27:1386–1389.
    1. Aho K, Kaipiainen-Seppanen O, Heliovaara M, Klaukka T. Epidemiology of rheumatoid arthritis in Finland. Semin Arthritis Rheum. 1998;27:325–334.
    1. Cimmino MA, Parisi M, Moggiana G, Mela GS, Accardo S. Prevalence of rheumatoid arthritis in Italy: the Chiavari study. Ann Rheum Dis. 1998;57:315–318.
    1. Kvien TK, Glennas A, Knudsrod OG, Smedstad LM, Mowinckel P, Forre O. The prevalence and severity of rheumatoid arthritis in Oslo: results from a county register and a population survey. Scand J Rheumatol. 1997;26:412–418.
    1. Power D, Codd M, Ivers L, Sant S, Barry M. Prevalence of rheumatoid arthritis in Dublin, Ireland: a population based survey. Ir J Med Sci. 1999;168:197–200.
    1. Saraux A, Guedes C, Allain J, Devauchelle V, Valls I, Lamour A, Guillemin F, Youinou P, Le Goff P. Prevalence of rheumatoid arthritis and spondyloarthropathy in Brittany, France. J Rheumatol. 1999;26:2622–2627.
    1. Simonsson M, Bergman S, Jacobsson LT, Petersson IF, Svensson B. The prevalence of rheumatoid arthritis in Sweden. Scand J Rheumatol. 1999;28:340–343. doi: 10.1080/03009749950155319.
    1. Gabriel SE, Crowson CS, O'Fallon WM. The epidemiology of rheumatoid arthritis in Rochester, Minnesota, 1955–1985. Arthritis Rheum. 1999;42:415–420. doi: 10.1002/1529-0131(199904)42:3<415::AID-ANR4>;2-Z.
    1. Gabriel SE. The epidemiology of rheumatoid arthritis. Rheum Dis Clin North Am. 2001;27:269–281.
    1. del Puente A, Knowler WC, Pettit DJ, Bennett PH. High incidence and prevalence of rheumatoid arthritis in Pima Indians. Am J Epidemiol. 1989;129:1170–1178.
    1. Harvey J, Lotze M, Stevens MB, Lambert G, Jacobson D. Rheumatoid arthritis in a Chippewa band. I. Pilot screening study of disease prevalence. Arthritis Rheum. 1981;24:717–721.
    1. Brighton SW, de la Harpe AL, van Staden DJ, Badenhorst JH, Myers OL. The prevalence of rheumatoid arthritis in a rural African population. J Rheumatol. 1988;15:405–408.
    1. Silman AJ, Ollier W, Holligan S, Birrell F, Adebajo A, Asuzu MC, Thomson W, Pepper L. Absence of rheumatoid arthritis in a rural Nigerian population. J Rheumatol. 1993;20:618–622.
    1. Dans LF, TankehTorres S, Amante CM, Penserga EG. The prevalence of rheumatic diseases in a Filipino urban population: a WHO-ILAR COPCORD study. J Rheumatol. 1997;24:1814–1819.
    1. Shichikawa K, Inoue K, Hirota S, Maeda A, Ota H, Kimura M, Ushiyama T, Tsujimoto M. Changes in the incidence and prevalence of rheumatoid arthritis in Kamitonda, Wakayama, Japan, 1965–1996. Ann Rheum Dis. 1999;58:751–756.
    1. Zeng Q, Huang S, Chen R. 10-year epidemiological study on rheumatic diseases in Shantou area. Zhonghua Nei Ke Za Zhi. 1997;36:193–197.
    1. MacGregor AJ, Riste LK, Hazes JMW, Silman AJ. Low prevalence of rheumatoid arthritis in black-Caribbeans compared with whites in inner city Manchester. Ann Rheum Dis. 1994;53:293–297.
    1. Lau E, Symmons D, Bankhead C, MacGregor A, Donnan S, Silman A. Low prevalence of rheumatoid arthritis in the urbanized Chinese of Hong Kong. J Rheumatol. 1993;20:1133–1137.
    1. Hameed K, Gibson T. A comparison of the prevalence of rheumatoid arthritis and other rheumatic diseases amongst Pakistanis living in England and Pakistan. Br J Rheumatol. 1997;36:781–785. doi: 10.1093/rheumatology/36.7.781.
    1. Lawrence JS, Ball J. Genetic studies on rheumatoid arthritis. Ann Rheum Dis. 1958;17:160–168.
    1. Lawrence JS. Heberden oration, 1969. Rheumatoid arthritis – nature or nurture? Ann Rheum Dis. 1970;29:357–379.
    1. Jones MA, Silman AJ, Whiting S, Barrett EM, Symmons DPM. Occurrence of rheumatoid arthritis is not increased in the first degree relatives of a population based inception cohort of inflammatory polyarthritis. Ann Rheum Dis. 1996;55:89–93.
    1. MacGregor AJ, Snieder H, Rigby AS, Koskenvuo M, Kaprio J, Aho K, Silman AJ. Characterizing the quantitative genetic contribution to rheumatoid arthritis using data from twins. Arthritis Rheum. 2000;43:30–37. doi: 10.1002/1529-0131(200001)43:1<30::AID-ANR5>;2-B.
    1. Silman AJ, Hochberg MC. In: In Epidemiology of the Rheumatic Diseases. Edited by AJ Silman, MC Hochberg, editor. Oxford: Oxford University Press;; 2001. Rheumatoid arthritis. pp. 31–71.
    1. Pascual M, Nieto A, Lopez-Nevot MA, Ramal L, Mataran L, Caballero A, Alonso A, Martin J, Zanelli E. Rheumatoid arthritis in southern Spain – toward elucidation of a unifying role of the HLA class II region in disease predisposition. Arthritis Rheum. 2001;44:307–314. doi: 10.1002/1529-0131(200102)44:2<307::AID-ANR47>;2-B.
    1. Citera G, Padulo LA, Fernandez G, Lazaro MA, Rosemffet MG, Cocco JAM. Influence of HLA-DR alleles on rheumatoid arthritis: susceptibility and severity in Argentine patients. J Rheumatol. 2001;28:1486–1491.
    1. Zanelli E, Breedveld FC, de Vries RRP. HLA class II association with rheumatoid arthritis – facts and interpretations. Hum Immunol. 2000;61:1254–1261. doi: 10.1016/S0198-8859(00)00185-3.
    1. Balsa A, Minaur NJ, Pascual-Salcedo D, McCabe C, Balas A, Fiddament B, Vicario JL, Cox NL, Martin-Mola E, Hall ND. Class II MHC antigens in early rheumatoid arthritis in Bath (UK) and Madrid (Spain). Rheumatology. 2000;39:844–849. doi: 10.1093/rheumatology/39.8.844.
    1. del Rincon I, Escalante A. HLA-DRB1 alleles associated with susceptibility or resistance to rheumatoid arthritis, articular deformities, and disability in Mexican Americans. Arthritis Rheum. 1999;42:1329–1338. doi: 10.1002/1529-0131(199907)42:7<1329::AID-ANR5>;2-1.
    1. Wakitani S, Murata N, Toda Y, Ogawa R, Kaneshige T, Nishimura Y, Ochi T. The relationship between HLA-DRB1 alleles and disease subsets of rheumatoid arthritis in Japanese. Br J Rheumatol. 1997;36:630–636. doi: 10.1093/rheumatology/36.6.630.
    1. Thomson W, Harrison B, Ollier B, Wiles N, Payton T, Barrett J, Symmons D, Silman A. Quantifying the exact role of HLA-DRB1 alleles in susceptibility to inflammatory polyarthritis: results from a large, population-based study. Arthritis Rheum. 1999;42:757–762. doi: 10.1002/1529-0131(199904)42:4<757::AID-ANR20>;2-O.
    1. Gregersen PK. The North American Rheumatoid Arthritis Consortium – bringing genetic analysis to bear on disease susceptibility, severity, and outcome. Arthritis Care Res. 1998;11:1–2.
    1. Meyer JM, Evans TI, Small RE, Redford TW, Han JF, Singh R, Moxley G. HLA-DRB1 genotype influences risk for and severity of rheumatoid arthritis. J Rheumatol. 1999;26:1024–1034.
    1. Mattey DL, Hassell AB, Dawes PT, Ollier WE, Hajeer A. Interaction between tumor necrosis factor microsatellite polymorphisms and the HLA-DRB1 shared epitope in rheumatoid arthritis: influence on disease outcome. Arthritis Rheum. 1999;42:2698–2704. doi: 10.1002/1529-0131(199912)42:12<2698::AID-ANR28>;2-S.
    1. Barton A, John S, Ollier WER, Silman A, Worthington J. Association between rheumatoid arthritis and polymorphism of tumor necrosis factor receptor II, but not tumor necrosis factor receptor I, in Caucasians. Arthritis Rheum. 2001;44:61–65. doi: 10.1002/1529-0131(200101)44:1<61::AID-ANR9>;2-Q.
    1. Hajeer AH, Dababneh A, Makki RF, Thomson W, Poulton K, Gay MA, Garcia-Porrua C, Mattey DL, Ollier WE. Different gene loci within the HLA-DR and TNF regions are independently associated with susceptibility and severity in Spanish rheumatoid arthritis patients. Tissue Antigens. 2000;55:319–325. doi: 10.1034/j.1399-0039.2000.550405.x.
    1. Hajeer AH, Worthington J, Silman AJ, Ollier WER. Association of tumor necrosis factor microsatellite polymorphisms with HLA-DRB1(*)04-bearing haplotypes in rheumatoid arthritis patients. Arthritis Rheum. 1996;39:1109–1114.
    1. Cornelis F, Faure S, Martinez M, Prudhomme JF, Fritz P, Dib C, Alves H, Barrera P, de Vries N, Balsa A, Pascual-Salcedo D, Maenaut K, Westhovens R, Migliorini P, Tran TH, Delaye A, Prince N, Lefevre C, Thomas G, Poirier M, Soubigou S, Alibert O, Lasbleiz S, Fouix S, Bouchier C, Liote F, Loste MN, Lepage V, Charron D, Gyapay G, Lopes-Vaz A, Kuntz D, Bardin T, Weissenbach J. New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study. Proc Natl Acad Sci USA. 1998;95:10746–10750. doi: 10.1073/pnas.95.18.10746.
    1. Shiozawa S, Hayashi S, Tsukamoto Y, Goko H, Kawasaki H, Wada T, Shimizu K, Yasuda N, Kamatani N, Takasugi K, Tanaka Y, Shiozawa K, Imura S. Identification of the gene loci that predispose to rheumatoid arthritis. Int Immunol. 1998;10:1891–1895. doi: 10.1093/intimm/10.12.1891.
    1. Worthington J, Ollier WE, Leach MK, Smith I, Hay EM, Thomson W, Pepper L, Carthy D, Farhan A, Martin S, Dyer P, Davison J, Bamber S, Silman AJ. The Arthritis and Rheumatism Council's National Repository of Family Material: pedigrees from the first 100 rheumatoid arthritis families containing affected sibling pairs. Br J Rheumatol. 1994;33:970–976.
    1. Fife MS, Fisher SA, John S, Worthington J, Shah CJ, Ollier WER, Panayi GS, Lewis CM, Lanchbury JS. Multipoint linkage analysis of a candidate gene locus in rheumatoid arthritis demonstrates significant evidence of linkage and association with the corticotropin-releasing hormone genomic region. Arthritis Rheum. 2000;43:1673–1678. doi: 10.1002/1529-0131(200008)43:8<1673::AID-ANR2>;2-Y.
    1. John S, Myerscough A, Eyre S, Roby P, Hajeer A, Silman AJ, Ollier WE, Worthington J. Linkage of a marker in intron D of the estrogen synthase locus to rheumatoid arthritis. Arthritis Rheum. 1999;42:1617–1620. doi: 10.1002/1529-0131(199908)42:8<1617::AID-ANR8>;2-N.
    1. Khani-Hanjani A, Lacaille D, Hoar D, Chalmers A, Horsman D, Anderson M, Balshaw R, Keown PA. Association between dinucleotide repeat in non-coding region of interferon-gamma gene and susceptibility to, and severity of, rheumatoid arthritis. Lancet. 2000;356:820–825. doi: 10.1016/S0140-6736(00)02657-X.
    1. Ollier WE. Role of interferon-gamma gene in rheumatoid arthritis? Lancet. 2000;356:783–784. doi: 10.1016/S0140-6736(00)02647-7.
    1. Pokorny V, McLean L, McQueen F, Abu-Maree M, Yeoman S. Interferon-gamma microsatellite and rheumatoid arthritis. Lancet. 2001;358:122–123. doi: 10.1016/S0140-6736(01)05342-9.
    1. Hajeer AH, Lazarus M, Turner D, Mageed RA, Vencovsky J, Sinnott P, Hutchinson IV, Ollier WER. IL-10 gene promoter polymorphisms in rheumatoid arthritis. Scand J Rheumatol. 1998;27:142–145. doi: 10.1080/030097498441029.
    1. John S, Myerscough A, Marlow A, Hajeer A, Silman A, Ollier W, Worthington J. Linkage of cytokine genes to rheumatoid arthritis. Evidence of genetic heterogeneity. Ann Rheum Dis. 1998;57:361–365.
    1. John S, Eyre S, Myerscough A, Barrett J, Silman A, Ollier W, Worthington J. Linkage and association analysis of candidate genes in rheumatoid arthritis. J Rheumatol. 2001;28:1752–1755.
    1. Myerscough A, John S, Barrett JH, Ollier WE, Worthington J. Linkage of rheumatoid arthritis to insulin-dependent diabetes mellitus loci: evidence supporting a hypothesis for the existence of common autoimmune susceptibility loci. Arthritis Rheum. 2000;43:2771–2775. doi: 10.1002/1529-0131(200012)43:12<2771::AID-ANR17>;2-V.
    1. Myerscough A, John S, Barrett JH, Eyre S, Barton A, Brintnell B, Ollier WER, Worthington J. Linkage and linkage disequilibrium analysis of chromosome Xp11–p21 microsatellite markers with rheumatoid arthritis (RA) [abstract]. Arthritis Rheum. 2001;44(Suppl):1299.
    1. Barton A, Eyre S, Myerscough A, Brintnell B, Ward D, Ollier WE, Lorentzen JC, Klareskog L, Silman A, John S, Worthington J. High resolution linkage and association mapping identifies a novel rheumatoid arthritis susceptibility locus homologous to one linked to two rat models of inflammatory arthritis. Hum Mol Genet. 2001;10:1901–1906. doi: 10.1093/hmg/10.18.1901.
    1. Heikkila R, Aho K, Heliövaara M, Knekt P, Reunanen A, Aromaa A, Leino A, Palosuo T. Serum androgen-anabolic hormones and the risk of rheumatoid arthritis. Ann Rheum Dis. 1998;57:281–285.
    1. Anonymous. Reduction in incidence of rheumatoid arthritis associated with oral contraceptives. Royal College of General Practioners' oral contraception study. Lancet. 1978;1:569–571.
    1. Brennan P, Bankhead C, Silman A, Symmons D. Oral contraceptives and rheumatoid arthritis: results from primary care-based incident case–control study. Semin Arthritis Rheum. 1997;26:817–823.
    1. Hannaford PC, Kay CR, Hirsch S. Oral contraceptives and rheumatoid arthritis: new data from the Royal College of General Practitioners' oral contraception study. Ann Rheum Dis. 1990;49:744–746.
    1. Silman AJ. Epidemiology of rheumatoid arthritis. APMIS. 1994;102:721–728.
    1. Nelson JL, Ostensen M. Pregnancy and rheumatoid arthritis. Rheum Dis Clin North Am. 1997;23:195–212.
    1. Silman AJ, Kay A, Brennan P. Timing of pregnancy in relation to the onset of rheumatoid arthritis. Arthritis Rheum. 1992;35:152–155.
    1. Brennan P, Silman A. Breast-feeding and the onset of rheumatoid arthritis. Arthritis Rheum. 1994;37:808–813.
    1. Brennan P, Hajeer A, Ong KR, Worthington J, John S, Thomson W, Silman A, Ollier B. Allelic markers close to prolactin are associated with HLA-DRB1 susceptibility alleles among women with rheumatoid arthritis and systemic lupus erythematosus. Arthritis Rheum. 1997;40:1383–1386.
    1. Silman AJ, Ollier WER, Bubel MA. Autoimmune thyroid disease and thyroid autoantibodies in rheumatoid arthritis patients and their families. Br J Rheumatol. 1989;28:18–21.
    1. Oken RJ, Schulzer M. At issue: schizophrenia and rheumatoid arthritis: the negative association revisited. Schizophr Bull. 1999;25:625–638.
    1. Mors O, Mortensen PB, Ewald H. A population-based register study of the association between schizophrenia and rheumatoid arthritis. Schizophr Res. 1999;40:67–74. doi: 10.1016/S0920-9964(99)00030-4.
    1. Rubinstein G. Schizophrenia, rheumatoid arthritis and natural resistance genes. Schizophr Res. 1997;25:177–181. doi: 10.1016/S0920-9964(97)00023-6.
    1. Symmons DPM, Bankhead CR, Harrison BJ, Brennan P, Barrett EM, Scott DGI, Silman AJ. Blood transfusion, smoking, and obesity as risk factors for the development of rheumatoid arthritis: results from a primary care-based incident case-control study in Norfolk, England. Arthritis Rheum. 1997;40:1955–1961.
    1. Uhlig T, Hagen KB, Kvien TK. Current tobacco smoking, formal education, and the risk of rheumatoid arthritis. J Rheumatol. 1999;26:47–54.
    1. Jacobsson LT, Hanson RL, Knowler WC, Pillemer S, Pettitt DJ, McCance DR, Bennett PH. Decreasing incidence and prevalence of rheumatoid arthritis in Pima Indians over a 25 year period. Arthritis Rheum. 1994;37:1158–1165.
    1. Silman AJ, Enzer I, Knowler W, Dunn G, Jacobsson L. Strong influence of period of birth on the occurrence of rheumatoid factor: results from a 30 year follow-up study on Pima Indians [abstract]. Arthritis Rheum. 2000;43(Suppl):605.
    1. Silman AJ, Bankhead C, Rowlingson B, Brennan P, Symmons D, Gatrell A. Do new cases of rheumatoid arthritis cluster in time or in space? Int J Epidemiol. 1997;26:628–634. doi: 10.1093/ije/26.3.628.
    1. Ariza-Ariza R, Mestanza-Peralta M, Cardiel MH. Omega-3 fatty acids in rheumatoid arthritis: an overview. Semin Arthritis Rheum. 1998;27:366–370.
    1. James MJ, Cleland LG. Dietary n-3 fatty acids and therapy for rheumatoid arthritis. Semin Arthritis Rheum. 1997;27:85–97.
    1. Volker D, Fitzgerald P, Major G, Garg M. Efficacy of fish oil concentrate in the treatment of rheumatoid arthritis. J Rheumatol. 2000;27:2343–2346.
    1. Kremer JM. n-3 fatty acid supplements in rheumatoid arthritis. Am J Clin Nutr. 2000;71(Suppl):349S–351S.
    1. Hernandez-Cruz B, Alcocer-Varela J, Cardiel MH. Omega-3 fatty acids supplementation in Mexican patients with rheumatoid arthritis with standard treatment. A blinded, randomized, placebo controlled, one year, clinical trial [abstract]. Arthritis Rheum. 1998;41(Suppl):738.
    1. Albano SA, Santana-Sahagun E, Weisman MH. Cigarette smoking and rheumatoid arthritis. Semin Arthritis Rheum. 2001;31:146–159. doi: 10.1053/sarh.2001.27719.
    1. Harrison BJ, Silman AJ, Wiles NJ, Scott DG, Symmons DP. The association of cigarette smoking with disease outcome in patients with early inflammatory polyarthritis. Arthritis Rheum. 2001;44:323–330. doi: 10.1002/1529-0131(200102)44:2<323::AID-ANR49>;2-3.
    1. Hutchinson D, Shepstone L, Moots R, Lear JT, Lynch MP. Heavy cigarette smoking is strongly associated with rheumatoid arthritis (RA), particularly in patients without a family history of RA. Ann Rheum Dis. 2001;60:223–227. doi: 10.1136/ard.60.3.223.
    1. Karlson EW, Min Lee I, Cook NR, Manson JE, Buring JE, Hennekens CH. A retrospective cohort study of cigarette smoking and risk of rheumatoid arthritis in female health professionals. Arthritis Rheum. 1999;42:910–917. doi: 10.1002/1529-0131(199905)42:5<910::AID-ANR9>;2-4.

Source: PubMed

3
Subscribe