Volume 64, Issue 3 pp. 655-664
Rheumatoid Arthritis

Impact of interactions of cigarette smoking with NAT2 polymorphisms on rheumatoid arthritis risk in African Americans

Ted R. Mikuls

Corresponding Author

Ted R. Mikuls

University of Nebraska Medical Center and Omaha VA Medical Center, Omaha, Nebraska

Department of Medicine, University of Nebraska Medical Center, 986270 Nebraska Medical Center, Omaha, NE 68198-6270Search for more papers by this author
Tricia LeVan

Tricia LeVan

University of Nebraska Medical Center, Omaha

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Karen A. Gould

Karen A. Gould

University of Nebraska Medical Center, Omaha

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Fang Yu

Fang Yu

University of Nebraska Medical Center, Omaha

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Geoffrey M. Thiele

Geoffrey M. Thiele

University of Nebraska Medical Center and Omaha VA Medical Center, Omaha, Nebraska

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Kimberly K. Bynote

Kimberly K. Bynote

University of Nebraska Medical Center, Omaha

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Doyt Conn

Doyt Conn

Emory University, Atlanta, Georgia

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Beth L. Jonas

Beth L. Jonas

University of North Carolina, Chapel Hill

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Leigh F. Callahan

Leigh F. Callahan

University of North Carolina, Chapel Hill

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Edwin Smith

Edwin Smith

Medical University of South Carolina, Charleston

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Richard Brasington

Richard Brasington

Washington University Medical Center, St. Louis, Missouri

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Larry W. Moreland

Larry W. Moreland

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania

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Richard Reynolds

Richard Reynolds

University of Alabama at Birmingham

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Angelo Gaffo

Angelo Gaffo

University of Alabama at Birmingham

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S. Louis Bridges Jr.

S. Louis Bridges Jr.

University of Alabama at Birmingham

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First published: 11 October 2011
Citations: 26

Abstract

Objective

To examine whether polymorphisms in genes coding for drug-metabolizing enzymes (DMEs) have an impact on rheumatoid arthritis (RA) risk due to cigarette smoking in African Americans.

Methods

Smoking status was evaluated in African American patients with RA compared with non-RA controls, with smoking exposure categorized as heavy smoker (≥10 pack-years) versus never smoker/<10 pack-years. Individuals were genotyped for a homozygous deletion polymorphism in the M1 gene loci of glutathione S-transferase (GSTM1-null) in addition to tagging single-nucleotide polymorphisms (SNPs) in N-acetyltransferase 1 (NAT1), NAT2, and epoxide hydrolase 1 (EPXH1). Associations of these genotypes with RA risk were examined using logistic regression, and gene–smoking interactions were assessed.

Results

There were no significant associations of any DME genotype with RA. After adjustment for multiple comparisons, there were significant additive interactions between heavy smoking and the NAT2 SNPs rs9987109 (Padditive = 0.000003) and rs1208 (Padditive = 0.00001); the attributable proportion due to interaction ranged from 0.61 to 0.67. None of the multiplicative gene–smoking interactions examined remained significant with regard to overall disease risk, after adjustment for multiple testing. There was no evidence of significant gene–smoking interactions in analyses of GSTM1-null, NAT1, or EPXH1. DME gene–smoking interactions were similar when cases were limited to those patients who were positive for anti–citrullinated protein antibodies.

Conclusion

Among African Americans, RA risk imposed by heavy smoking appears to be mediated in part by genetic variation in NAT2. While further studies are needed to elucidate the mechanisms underpinning these interactions, these SNPs appear to identify African American smokers at a much higher risk for RA, in whom the relative risk is at least 2-fold higher when compared to nonsmokers lacking these risk alleles.

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