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. 2006 Sep;65(9):1163-7.
doi: 10.1136/ard.2005.049676. Epub 2006 Aug 3.

Smoking interacts with genetic risk factors in the development of rheumatoid arthritis among older Caucasian women

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Smoking interacts with genetic risk factors in the development of rheumatoid arthritis among older Caucasian women

L A Criswell et al. Ann Rheum Dis. 2006 Sep.

Abstract

Objective: To determine whether the impact of tobacco exposure on rheumatoid arthritis (RA) risk is influenced by polymorphisms at the HLA-DRB1 and glutathione S-transferase M1 (GSTM1) loci.

Methods: Subjects were participants from a case-control study nested within the Iowa Women's Health Study, a population based, prospective cohort study of postmenopausal women. Incident RA cases (n = 115) were identified and medical records reviewed to confirm RA diagnosis. Controls without RA (n = 466) were matched with RA cases by age and ethnic background. HLA-DRB1 typing classified subjects according to the presence of alleles encoding the RA "shared epitope" (SE) sequence. GSTM1 was genotyped using a multiplex polymerase chain reaction assay. Conditional logistic regression was used to estimate the odds ratios (ORs) and 95% confidence intervals.

Results: Strong positive associations of smoking (OR = 6.0, p = 0.004), SE positivity (OR = 4.6, p = 0.0006), and GSTM1 null genotype (OR = 3.4, p = 0.007) with risk of RA, and significant gene-environment interactions (smoking by SE interaction p = 0.034; smoking by GSTM1 interaction p = 0.047) were observed. Stratified analyses indicated that exposure to tobacco smoke primarily increased the risk of RA among subjects who lacked genetic risk factors for the disease (that is, SE negative or GSTM1 present).

Conclusions: Although these findings require confirmation in other groups, the results support the importance of considering both genetic and environmental factors, and also their interaction, in studies of complex diseases like RA.

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Conflict of interest statement

Competing interests: None.

References

    1. Seldin M F, Amos C I, Ward R, Gregersen P K. The genetics revolution and the assault on rheumatoid arthritis. Arthritis Rheum 1999421071–1079. - PubMed
    1. Cornelis F, Faure S, Martinez M, Prud'homme J ‐ F, Fritz P, Dib C.et al New susceptibility locus for rheumatoid arthritis suggested by a genome‐wide linkage study. Proc Natl Acad Sc USAi 19989510746–10750. - PMC - PubMed
    1. Jawaheer D, Seldin M F, Amos C I, Chen W V, Shigeta R, Etzel C.et al Screening the genome for rheumatoid arthritis susceptibility genes. A replication study and combined analysis of 512 multicase families. Arthritis Rheum 200348906–916. - PubMed
    1. John S, Shephard N, Liu G, Zeggini E, Cao M, Chen W.et al Whole‐genome scan, in a complex disease, using 11,245 single‐nucleotide polymorphisms: comparison with microsatellites. Am J Hum Genet 20047554–64. - PMC - PubMed
    1. Amos C I, Chen W V, Lee A, Li W, Kern M, Lundsten R.et al High‐density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33. Genes Immun 20067277–286. - PubMed

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