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Risk of Periodontitis in Systemic Lupus Erythematosus Is Associated with Fcγ Receptor Polymorphisms
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Background: Leukocyte Fc receptors for immunoglobulin G (FcγR) play a major role in the handling of immune complexes and pathogens in systemic lupus erythematosus (SLE) and periodontitis. Both diseases have been shown to be partly influenced by genetic components including FcγR genotype. The aim of this study was therefore to evaluate whether FcγR gene polymorphisms are associated with periodontitis risk in SLE patients.Methods: The study subjects consisted of 42 SLE patients with periodontitis (SLE/P), 18 SLE patients without periodontitis (SLE/H), 42 healthy subjects with periodontitis (H/P), and 42 healthy subjects without periodontitis (H/H), who were all unrelated Japanese non‐smokers. Genomic DNA was isolated from peripheral blood, and FcγR genotypes for 3 biallelic polymorphisms (FcγRIIa‐R131/H131, FcγRIIIa‐158V/158F, FcγRIIIb‐NA1/NA2) were determined by allele‐specific polymerase chain reactions.Results: The SLE/P group was found to have more mild levels of periodontal destruction than the H/P group (P < 0.01). There was a significant difference in the distribution of FcγRIIa genotypes between SLE/P and H/H groups (P = 0.004). A significant overrepresentation of the FcγRIIa‐R131 allele was found in the SLE/P group compared to the H/H group (SLE/P versus H/H: odds ratio [OR] 3.13, 95% confidence interval [CI] 1.46‐6.77, P = 0.0013). Furthermore, the prevalence of periodontitis was found to be 70% in SLE patients. The FcγRIIa‐R131 allele was also found to be overrepresented in the SLE/P group compared to the SLE/H group (SLE/P versus SLE/H: OR 3.40, 95% CI 1.18‐10.25, P = 0.011).Conclusion:These results show the FcγRIIa‐R131 allele to be associated with periodontitis risk in SLE patients. J Periodontol 2003;74:378‐384.
Title: Risk of Periodontitis in Systemic Lupus Erythematosus Is Associated with Fcγ Receptor Polymorphisms
Description:
Background: Leukocyte Fc receptors for immunoglobulin G (FcγR) play a major role in the handling of immune complexes and pathogens in systemic lupus erythematosus (SLE) and periodontitis.
Both diseases have been shown to be partly influenced by genetic components including FcγR genotype.
The aim of this study was therefore to evaluate whether FcγR gene polymorphisms are associated with periodontitis risk in SLE patients.
Methods: The study subjects consisted of 42 SLE patients with periodontitis (SLE/P), 18 SLE patients without periodontitis (SLE/H), 42 healthy subjects with periodontitis (H/P), and 42 healthy subjects without periodontitis (H/H), who were all unrelated Japanese non‐smokers.
Genomic DNA was isolated from peripheral blood, and FcγR genotypes for 3 biallelic polymorphisms (FcγRIIa‐R131/H131, FcγRIIIa‐158V/158F, FcγRIIIb‐NA1/NA2) were determined by allele‐specific polymerase chain reactions.
Results: The SLE/P group was found to have more mild levels of periodontal destruction than the H/P group (P < 0.
01).
There was a significant difference in the distribution of FcγRIIa genotypes between SLE/P and H/H groups (P = 0.
004).
A significant overrepresentation of the FcγRIIa‐R131 allele was found in the SLE/P group compared to the H/H group (SLE/P versus H/H: odds ratio [OR] 3.
13, 95% confidence interval [CI] 1.
46‐6.
77, P = 0.
0013).
Furthermore, the prevalence of periodontitis was found to be 70% in SLE patients.
The FcγRIIa‐R131 allele was also found to be overrepresented in the SLE/P group compared to the SLE/H group (SLE/P versus SLE/H: OR 3.
40, 95% CI 1.
18‐10.
25, P = 0.
011).
Conclusion:These results show the FcγRIIa‐R131 allele to be associated with periodontitis risk in SLE patients.
J Periodontol 2003;74:378‐384.
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