Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1996 Feb;58(2):371–383.

Sex influences on the penetrance of HLA shared-epitope genotypes for rheumatoid arthritis.

J M Meyer 1, J Han 1, R Singh 1, G Moxley 1
PMCID: PMC1914550  PMID: 8571964

Abstract

The association between rheumatoid arthritis (RA) and HLA DRB1 alleles may arise through linkage disequilibrium with a disease locus or the direct involvement of HLA alleles in RA. In support of the latter possibility, the shared-epitope hypothesis has been postulated, stating that conformationally similar DR beta chains encoded by several DRB1 alleles confer disease susceptibility. To examine these alternative hypotheses of marker-disease association and to investigate gender differences in RA susceptibility, we analyzed the distributions of PCR-based DRB1 genotypes of 309 Caucasian RA patients and 283 Caucasian controls. Initially, the marker-association-segregation chi 2 method was used to evaluate evidence for linkage disequilibrium and the direct involvement of markers DR4 Dw4, DR4 Dw14, and DR1 in RA susceptibility. Additional shared-epitope models that grouped DRB1 alleles into five classes (*0401, *0404/*0102, *0405/*0408/*0101, *1001, and all others) and postulated relationships between genotypes and RA susceptibility were also fitted to observed genotypic distributions by the method of minimal chi 2. For females, a linkage-disequilibrium model provided a good fit to the data, as did a shared-epitope model with RA most penetrant among individuals with the *0401,*0401 genotype. For males, the best model indicated highest RA penetrance among shared-epitope compound heterozygotes. Clinically, male RA patients had more subcutaneous nodules and greater use of slowly acting antirheumatic drugs, while female RA patients had earlier disease onset. This study therefore suggests that sex-related factors influence the RA penetrance associated with DRB1 shared-epitope genotypes and that DRB1 effects on RA prognosis and pathogenesis should be considered separately for men and women.

Full text

PDF
371

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Arnett F. C., Edworthy S. M., Bloch D. A., McShane D. J., Fries J. F., Cooper N. S., Healey L. A., Kaplan S. R., Liang M. H., Luthra H. S. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988 Mar;31(3):315–324. doi: 10.1002/art.1780310302. [DOI] [PubMed] [Google Scholar]
  2. Bidwell J. L., Jarrold E. A. HLA-DR allogenotyping using exon-specific cDNA probes and application of rapid minigel methods. Mol Immunol. 1986 Oct;23(10):1111–1116. doi: 10.1016/0161-5890(86)90009-x. [DOI] [PubMed] [Google Scholar]
  3. Bidwell J. DNA-RFLP analysis and genotyping of HLA-DR and DQ antigens. Immunol Today. 1988 Jan;9(1):18–23. doi: 10.1016/0167-5699(88)91351-5. [DOI] [PubMed] [Google Scholar]
  4. Boki K. A., Panayi G. S., Vaughan R. W., Drosos A. A., Moutsopoulos H. M., Lanchbury J. S. HLA class II sequence polymorphisms and susceptibility to rheumatoid arthritis in Greeks. The HLA-DR beta shared-epitope hypothesis accounts for the disease in only a minority of Greek patients. Arthritis Rheum. 1992 Jul;35(7):749–755. doi: 10.1002/art.1780350706. [DOI] [PubMed] [Google Scholar]
  5. Carthy D., Ollier W., Papasteriades C., Pappas H., Thomson W. A shared HLA-DRB1 sequence confers RA susceptibility in Greeks. Eur J Immunogenet. 1993 Oct;20(5):391–398. doi: 10.1111/j.1744-313x.1993.tb00158.x. [DOI] [PubMed] [Google Scholar]
  6. Clerget-Darpoux F., Babron M. C., Prum B., Lathrop G. M., Deschamps I., Hors J. A new method to test genetic models in HLA associated diseases: the MASC method. Ann Hum Genet. 1988 Jul;52(Pt 3):247–258. doi: 10.1111/j.1469-1809.1988.tb01102.x. [DOI] [PubMed] [Google Scholar]
  7. Cutolo M., Accardo S. Sex hormones, HLA and rheumatoid arthritis. Clin Exp Rheumatol. 1991 Nov-Dec;9(6):641–646. [PubMed] [Google Scholar]
  8. Deighton C. M., Kelly P. J., Walker D. J. Linkage of rheumatoid arthritis with HLA. Ann Rheum Dis. 1993 Sep;52(9):638–642. doi: 10.1136/ard.52.9.638. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Deighton C. M., Walker D. J., Griffiths I. D., Roberts D. F. The contribution of HLA to rheumatoid arthritis. Clin Genet. 1989 Sep;36(3):178–182. doi: 10.1111/j.1399-0004.1989.tb03185.x. [DOI] [PubMed] [Google Scholar]
  10. Dizier M. H., Eliaou J. F., Babron M. C., Combe B., Sany J., Clot J., Clerget-Darpoux F. Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation chi-square (MASC) method: rejection of the unifying-shared-epitope hypothesis. Am J Hum Genet. 1993 Sep;53(3):715–721. [PMC free article] [PubMed] [Google Scholar]
  11. Eberhardt K., Grubb R., Johnson U., Pettersson H. HLA-DR antigens, Gm allotypes and antiallotypes in early rheumatoid arthritis--their relation to disease progression. J Rheumatol. 1993 Nov;20(11):1825–1829. [PubMed] [Google Scholar]
  12. Gao X. J., Olsen N. J., Pincus T., Stastny P. HLA-DR alleles with naturally occurring amino acid substitutions and risk for development of rheumatoid arthritis. Arthritis Rheum. 1990 Jul;33(7):939–946. doi: 10.1002/art.1780330704. [DOI] [PubMed] [Google Scholar]
  13. Gao X., Gazit E., Livneh A., Stastny P. Rheumatoid arthritis in Israeli Jews: shared sequences in the third hypervariable region of DRB1 alleles are associated with susceptibility. J Rheumatol. 1991 Jun;18(6):801–803. [PubMed] [Google Scholar]
  14. Go R. C., Alarcón G. S., Acton R. T., Koopman W. J., Vittor V. J., Barger B. O. Analyses of HLA linkage in white families with multiple cases of seropositive rheumatoid arthritis. Arthritis Rheum. 1987 Oct;30(10):1115–1123. doi: 10.1002/art.1780301005. [DOI] [PubMed] [Google Scholar]
  15. Goronzy J. J., Weyand C. M. Interplay of T lymphocytes and HLA-DR molecules in rheumatoid arthritis. Curr Opin Rheumatol. 1993 Mar;5(2):169–177. doi: 10.1097/00002281-199305020-00008. [DOI] [PubMed] [Google Scholar]
  16. Gough A., Faint J., Salmon M., Hassell A., Wordsworth P., Pilling D., Birley A., Emery P. Genetic typing of patients with inflammatory arthritis at presentation can be used to predict outcome. Arthritis Rheum. 1994 Aug;37(8):1166–1170. doi: 10.1002/art.1780370809. [DOI] [PubMed] [Google Scholar]
  17. Gregersen P. K., Silver J., Winchester R. J. The shared epitope hypothesis. An approach to understanding the molecular genetics of susceptibility to rheumatoid arthritis. Arthritis Rheum. 1987 Nov;30(11):1205–1213. doi: 10.1002/art.1780301102. [DOI] [PubMed] [Google Scholar]
  18. Hasstedt S. J., Clegg D. O., Ingles L., Ward R. H. HLA-linked rheumatoid arthritis. Am J Hum Genet. 1994 Oct;55(4):738–746. [PMC free article] [PubMed] [Google Scholar]
  19. Hillarby M. C., Hopkins J., Grennan D. M. A re-analysis of the association between rheumatoid arthritis with and without extra-articular features, HLA-DR4, and DR4 subtypes. Tissue Antigens. 1991 Jan;37(1):39–41. doi: 10.1111/j.1399-0039.1991.tb01842.x. [DOI] [PubMed] [Google Scholar]
  20. Jaraquemada D., Ollier W., Awad J., Young A., Silman A., Roitt I. M., Corbett M., Hay F., Cosh J. A., Maini R. N. HLA and rheumatoid arthritis: a combined analysis of 440 British patients. Ann Rheum Dis. 1986 Aug;45(8):627–636. doi: 10.1136/ard.45.8.627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Jawaheer D., Ollier W. E., Thomson W. Multiplex ARMS-RFLP: a simple and rapid method for HLA-DR4 subtyping. Eur J Immunogenet. 1993 Jun;20(3):175–187. doi: 10.1111/j.1744-313x.1993.tb00108.x. [DOI] [PubMed] [Google Scholar]
  22. Khan M. A., Khan M. K. HLA studies in familial and sporadic rheumatoid arthritis. Dis Markers. 1986 Jun;4(1-2):67–76. [PubMed] [Google Scholar]
  23. Kidd K. K. Associations of disease with genetic markers: déjà vu all over again. Am J Med Genet. 1993 Jul 15;48(2):71–73. doi: 10.1002/ajmg.1320480202. [DOI] [PubMed] [Google Scholar]
  24. Lawrence J. S. Heberden Oration, 1969. Rheumatoid arthritis--nature or nurture? Ann Rheum Dis. 1970 Jul;29(4):357–379. doi: 10.1136/ard.29.4.357. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Legrand L., Lathrop G. M., Marcelli-Barge A., Dryll A., Bardin T., Debeyre N., Poirier J. C., Schmid M., Ryckewaert A., Dausset J. HLA-DR genotype risks in seropositive rheumatoid arthritis. Am J Hum Genet. 1984 May;36(3):690–699. [PMC free article] [PubMed] [Google Scholar]
  26. Lewis R. B., Sanders L. L., Lipsmeyer E. Characteristics of rheumatoid arthritis in a male population. J Rheumatol. 1980 Jul-Aug;7(4):559–562. [PubMed] [Google Scholar]
  27. Martens H. F., Sheets P. K., Tenover J. S., Dugowson C. E., Bremner W. J., Starkebaum G. Decreased testosterone levels in men with rheumatoid arthritis: effect of low dose prednisone therapy. J Rheumatol. 1994 Aug;21(8):1427–1431. [PubMed] [Google Scholar]
  28. Moxley G. DNA polymorphism of immunoglobulin kappa confers risk of rheumatoid arthritis. Arthritis Rheum. 1989 May;32(5):634–637. doi: 10.1002/anr.1780320518. [DOI] [PubMed] [Google Scholar]
  29. Nelson J. L., Hughes K. A., Smith A. G., Nisperos B. B., Branchaud A. M., Hansen J. A. Maternal-fetal disparity in HLA class II alloantigens and the pregnancy-induced amelioration of rheumatoid arthritis. N Engl J Med. 1993 Aug 12;329(7):466–471. doi: 10.1056/NEJM199308123290704. [DOI] [PubMed] [Google Scholar]
  30. Nelson J. L., Mickelson E., Masewicz S., Barrington R., Dugowson C., Koepsell T., Hansen J. A. Dw14(DRB1*0404) is a Dw4-dependent risk factor for rheumatoid arthritis. Rethinking the "shared epitope" hypothesis. Tissue Antigens. 1991 Oct;38(4):145–151. doi: 10.1111/j.1399-0039.1991.tb01888.x. [DOI] [PubMed] [Google Scholar]
  31. Nepom B. S., Nepom G. T., Mickelson E., Schaller J. G., Antonelli P., Hansen J. A. Specific HLA-DR4-associated histocompatibility molecules characterize patients with seropositive juvenile rheumatoid arthritis. J Clin Invest. 1984 Jul;74(1):287–291. doi: 10.1172/JCI111413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Nepom G. T., Byers P., Seyfried C., Healey L. A., Wilske K. R., Stage D., Nepom B. S. HLA genes associated with rheumatoid arthritis. Identification of susceptibility alleles using specific oligonucleotide probes. Arthritis Rheum. 1989 Jan;32(1):15–21. doi: 10.1002/anr.1780320104. [DOI] [PubMed] [Google Scholar]
  33. Rigby A. S., Silman A. J., Voelm L., Gregory J. C., Ollier W. E., Khan M. A., Nepom G. T., Thomson G. Investigating the HLA component in rheumatoid arthritis: an additive (dominant) mode of inheritance is rejected, a recessive mode is preferred. Genet Epidemiol. 1991;8(3):153–175. doi: 10.1002/gepi.1370080303. [DOI] [PubMed] [Google Scholar]
  34. Rigby A. S., Voelm L., Silman A. J. Epistatic modeling in rheumatoid arthritis: an application of the Risch theory. Genet Epidemiol. 1993;10(5):311–320. doi: 10.1002/gepi.1370100504. [DOI] [PubMed] [Google Scholar]
  35. Rossen R. D., Brewer E. J., Sharp R. M., Ott J., Templeton J. W. Familial rheumatoid arthritis: linkage of HLA to disease susceptibility locus in four families where proband presented with juvenile rheumatoid arthritis. J Clin Invest. 1980 Mar;65(3):629–642. doi: 10.1172/JCI109708. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Rønningen K. S., Ploski R., Hansen T., Thorsby E. Dw14 is a Dw4-independent risk factor for rheumatoid arthritis among Norwegians. Tissue Antigens. 1992 May;39(5):280–280. doi: 10.1111/j.1399-0039.1992.tb01949.x. [DOI] [PubMed] [Google Scholar]
  37. Rønningen K. S., Spurkland A., Egeland T., Iwe T., Munthe E., Vartdal F., Thorsby E. Rheumatoid arthritis may be primarily associated with HLA-DR4 molecules sharing a particular sequence at residues 67-74. Tissue Antigens. 1990 Nov;36(5):235–240. doi: 10.1111/j.1399-0039.1990.tb01834.x. [DOI] [PubMed] [Google Scholar]
  38. Salmon M. The immunogenetic component of susceptibility to rheumatoid arthritis. Curr Opin Rheumatol. 1992 Jun;4(3):342–347. doi: 10.1097/00002281-199206000-00011. [DOI] [PubMed] [Google Scholar]
  39. Salmon M., Wordsworth P., Emery P., Tunn E., Bacon P. A., Bell J. I. The association of HLA DR beta alleles with self-limiting and persistent forms of early symmetrical polyarthritis. Br J Rheumatol. 1993 Jul;32(7):628–630. doi: 10.1093/rheumatology/32.7.628. [DOI] [PubMed] [Google Scholar]
  40. Scharf S. J., Griffith R. L., Erlich H. A. Rapid typing of DNA sequence polymorphism at the HLA-DRB1 locus using the polymerase chain reaction and nonradioactive oligonucleotide probes. Hum Immunol. 1991 Mar;30(3):190–201. doi: 10.1016/0198-8859(91)90034-7. [DOI] [PubMed] [Google Scholar]
  41. Silman A. J., MacGregor A. J., Thomson W., Holligan S., Carthy D., Farhan A., Ollier W. E. Twin concordance rates for rheumatoid arthritis: results from a nationwide study. Br J Rheumatol. 1993 Oct;32(10):903–907. doi: 10.1093/rheumatology/32.10.903. [DOI] [PubMed] [Google Scholar]
  42. Stastny P. Mixed lymphocyte cultures in rheumatoid arthritis. J Clin Invest. 1976 May;57(5):1148–1157. doi: 10.1172/JCI108382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Strotzer M., Menninger H., Scholz S., Albert E. D. HLA typing in families with multiple cases of rheumatoid arthritis. Ann Rheum Dis. 1991 May;50(5):298–300. doi: 10.1136/ard.50.5.298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Taneja V., Mehra N. K., Kailash S., Anand C., Malaviya A. N. Protective & risk DR phenotypes in Asian Indian patients with rheumatoid arthritis. Indian J Med Res. 1992 Feb;96:16–23. [PubMed] [Google Scholar]
  45. Thomson W., Pepper L., Payton A., Carthy D., Scott D., Ollier W., Silman A., Symmons D. Absence of an association between HLA-DRB1*04 and rheumatoid arthritis in newly diagnosed cases from the community. Ann Rheum Dis. 1993 Jul;52(7):539–541. doi: 10.1136/ard.52.7.539. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Toda Y., Minamikawa Y., Akagi S., Sugano H., Mori Y., Nishimura H., Arita S., Sugino Y., Ogawa R. Rheumatoid-susceptible alleles of HLA-DRB1 are genetically recessive to non-susceptible alleles in the progression of bone destruction in the wrists and fingers of patients with RA. Ann Rheum Dis. 1994 Sep;53(9):587–592. doi: 10.1136/ard.53.9.587. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Walker D. J., Burn J., Griffiths I. D., Roberts D. F., Stephenson A. M. Linkage studies of HLA and rheumatoid arthritis in multicase families. Arthritis Rheum. 1987 Jan;30(1):31–35. doi: 10.1002/art.1780300104. [DOI] [PubMed] [Google Scholar]
  48. Weyand C. M., Hicok K. C., Conn D. L., Goronzy J. J. The influence of HLA-DRB1 genes on disease severity in rheumatoid arthritis. Ann Intern Med. 1992 Nov 15;117(10):801–806. doi: 10.7326/0003-4819-117-10-801. [DOI] [PubMed] [Google Scholar]
  49. Weyand C. M., Xie C., Goronzy J. J. Homozygosity for the HLA-DRB1 allele selects for extraarticular manifestations in rheumatoid arthritis. J Clin Invest. 1992 Jun;89(6):2033–2039. doi: 10.1172/JCI115814. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Winchester R. The molecular basis of susceptibility to rheumatoid arthritis. Adv Immunol. 1994;56:389–466. doi: 10.1016/s0065-2776(08)60456-3. [DOI] [PubMed] [Google Scholar]
  51. Wordsworth B. P., Lanchbury J. S., Sakkas L. I., Welsh K. I., Panayi G. S., Bell J. I. HLA-DR4 subtype frequencies in rheumatoid arthritis indicate that DRB1 is the major susceptibility locus within the HLA class II region. Proc Natl Acad Sci U S A. 1989 Dec;86(24):10049–10053. doi: 10.1073/pnas.86.24.10049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Wordsworth B. P., Stedeford J., Rosenberg W. M., Bell J. I. Limited heterogeneity of the HLA class II contribution to susceptibility to rheumatoid arthritis is suggested by positive associations with HLA-DR4, DR1 and DRw10. Br J Rheumatol. 1991 Jun;30(3):178–180. doi: 10.1093/rheumatology/30.3.178. [DOI] [PubMed] [Google Scholar]
  53. Wordsworth P., Pile K. D., Buckely J. D., Lanchbury J. S., Ollier B., Lathrop M., Bell J. I. HLA heterozygosity contributes to susceptibility to rheumatoid arthritis. Am J Hum Genet. 1992 Sep;51(3):585–591. [PMC free article] [PubMed] [Google Scholar]
  54. de Vries N., Rønningen K. S., Tilanus M. G., Bouwens-Rombouts A., Segal R., Egeland T., Thorsby E., van de Putte L. B., Brautbar C. HLA-DR1 and rheumatoid arthritis in Israeli Jews: sequencing reveals that DRB1*0102 is the predominant HLA-DR1 subtype. Tissue Antigens. 1993 Jan;41(1):26–30. doi: 10.1111/j.1399-0039.1993.tb01973.x. [DOI] [PubMed] [Google Scholar]
  55. del Junco D., Luthra H. S., Annegers J. F., Worthington J. W., Kurland L. T. The familial aggregation of rheumatoid arthritis and its relationship to the HLA-DR4 association. Am J Epidemiol. 1984 May;119(5):813–829. doi: 10.1093/oxfordjournals.aje.a113802. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES