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高加索人群中Fcγ受体IIa基因型与慢性牙周炎的关联

Association of Fcgamma receptor IIa genotype with chronic periodontitis in Caucasians.

作者信息

Yamamoto Kouji, Kobayashi Tetsuo, Grossi Sara, Ho Alex W, Genco Robert J, Yoshie Hiromasa, De Nardin Ernesto

机构信息

Division of Periodontology, Department of Oral Biological Science, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

出版信息

J Periodontol. 2004 Apr;75(4):517-22. doi: 10.1902/jop.2004.75.4.517.

Abstract

BACKGROUND

Functional polymorphisms of immunoglobulin G (IgG) Fc receptors IIIa and IIIb (FcgammaRIIIa and FcgammaRIIIb) have been shown as risk factors for periodontitis. The aim of this study is to examine whether FcgammaRIIa polymorphism is associated with a disease risk as well.

METHODS

Baseline periodontal and general health examinations were carried out on 1,221 Caucasian adults. From these, 422 subjects with moderate to severe, or little or no periodontal disease were assigned to two groups according to their mean clinical attachment loss (CAL). Subjects with mean CAL > or = 2.94 mm were diagnosed with chronic periodontitis (n = 213, 62 never-smokers and 151 smokers). Subjects with mean CAL < or = 1.77 mm were considered as having little or no periodontal disease and designated as controls (n = 209, 125 never-smokers and 84 smokers). The FcgammaRIIa genotype for three bi-allelic polymorphisms (FcgammaRIIa-R/ R131, R/H131, and H/H131) was determined by means of allele-specific polymerase chain reactions.

RESULTS

The distribution of FcgammaRIIa genotype between the patient and control groups was significantly different, with enrichment of the high ligand-binding genotype FcgammaRIIa-H/H131 in the patients (patients versus controls: 36.6% versus 25.4%; P = 0.04). Multivariate logistic regression model demonstrated that subject age and gender, smoking, and the FcgammaRIIa genotype were significantly associated with severity of chronic periodontitis. For smokers, a significant over-representation of FcgammaRIIa-H/H131 in the patient group compared to the control group (patients versus controls: 35.1% versus 19.0%; P = 0.03). Additionally, smokers with FcgammaRIIa-H/H131 exhibited significantly greater mean CAL (mean +/- SE: 3.44 +/- 0.16 mm) than those with FcgammaRIIa-R/H131 (2.91 +/- 0.14 mm) and R/R131 (2.82 +/- 0.16 mm) (P = 0.04). There was no association between FcgammaRIIa genotype and the disease susceptibility or severity in subjects who had never smoked.

CONCLUSIONS

Our results suggest that the FcgammaRIIa-H/H131 genotype may be associated with chronic periodontitis risk (and disease severity) in Caucasian smokers. Further studies with families and studies of mechanisms are necessary to help establish the extent to which this is a genetic determinant of periodontal diseases.

摘要

背景

免疫球蛋白G(IgG)Fc受体IIIa和IIIb(FcγRIIIa和FcγRIIIb)的功能多态性已被证明是牙周炎的危险因素。本研究的目的是检验FcγRIIa多态性是否也与疾病风险相关。

方法

对1221名白种成年人进行了基线牙周和全身健康检查。从这些人中,根据平均临床附着丧失(CAL)将422名患有中度至重度或轻度或无牙周疾病的受试者分为两组。平均CAL≥2.94mm的受试者被诊断为慢性牙周炎(n = 213,62名从不吸烟者和151名吸烟者)。平均CAL≤1.77mm的受试者被认为几乎没有或没有牙周疾病,并被指定为对照组(n = 209,125名从不吸烟者和84名吸烟者)。通过等位基因特异性聚合酶链反应确定三种双等位基因多态性(FcγRIIa-R/R131、R/H131和H/H131)的FcγRIIa基因型。

结果

患者组和对照组之间FcγRIIa基因型的分布存在显著差异,患者中高配体结合基因型FcγRIIa-H/H131富集(患者与对照组:36.6%对25.4%;P = 0.04)。多变量逻辑回归模型表明,受试者的年龄和性别、吸烟以及FcγRIIa基因型与慢性牙周炎的严重程度显著相关。对于吸烟者,与对照组相比,患者组中FcγRIIa-H/H131的比例显著过高(患者与对照组:35.1%对19.0%;P = 0.03)。此外,FcγRIIa-H/H131的吸烟者的平均CAL(平均值±标准误:3.44±0.16mm)显著高于FcγRIIa-R/H131(2.91±0.14mm)和R/R131(2.82±0.16mm)的吸烟者(P = 0.04)。在从不吸烟的受试者中,FcγRIIa基因型与疾病易感性或严重程度之间没有关联。

结论

我们的结果表明,FcγRIIa-H/H131基因型可能与白种吸烟者的慢性牙周炎风险(和疾病严重程度)相关。需要对家庭进行进一步研究并研究其机制,以帮助确定这在多大程度上是牙周疾病的遗传决定因素。

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