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白细胞介素-1(IL-1)基因分型用于重度慢性牙周炎遗传易感性检测时的批判性评估。

A critical assessment of interleukin-1 (IL-1) genotyping when used in a genetic susceptibility test for severe chronic periodontitis.

作者信息

Greenstein Gary, Hart Thomas C

机构信息

University of Medicine and Dentistry of New Jersey, Newark, USA.

出版信息

J Periodontol. 2002 Feb;73(2):231-47. doi: 10.1902/jop.2002.73.2.231.

Abstract

BACKGROUND

This review addresses the ability of a commercially available genetic susceptibility test to determine the risk of developing severe chronic periodontitis. The test is used to detect the simultaneous occurrence of allele 2 at the IL-1A+4845 and IL-1B+3954 loci. If both of these polymorphisms are present, patients are referred to as being genotype-positive and considered predisposed to becoming afflicted with severe chronic periodontitis. A basic premise of this test is the assumption that individuals who are genotype-positive produce increased amounts of IL-beta in response to microbial lipopolysaccharides, which allegedly predisposes them to an exaggerated inflammatory response and an increased incidence of chronic periodontitis.

METHODS

Controlled clinical trials were selected that evaluated the ability of the genetic test to predict which patients were susceptible to bleeding upon probing, periodontitis, peri-implantitis, and tooth loss.

RESULTS

Comparison of results from test (genotype-positive) and control groups (genotype-negative) revealed that there is ambiguity with regard to predicting which patients will manifest elevated sub-gingival levels of IL-beta. Similarly, it is questionable if the test is able to forecast which individuals will demonstrate an increased occurrence of bleeding upon probing, diminished clinical attachment, decreased osseous support, or loss of teeth.

CONCLUSIONS

There are many unanswered questions concerning the utility of detecting allele 2 at the IL-1A+4845 and IL-IB+3954 loci to foretell which patients will develop severe chronic periodontitis. Therefore, clinicians must cautiously interpret results obtained with the commercially available genetic susceptibility test before they alter maintenance schedules or treatment regimens of symptomatic or asymptomatic patients.

摘要

背景

本综述探讨了一种市售基因易感性检测方法用于确定发生重度慢性牙周炎风险的能力。该检测用于检测白细胞介素 -1A +4845和白细胞介素 -1B +3954位点等位基因2的同时出现。如果这两种多态性均存在,则患者被称为基因型阳性,并被认为易患重度慢性牙周炎。该检测的一个基本前提是假设基因型阳性个体在接触微生物脂多糖时会产生更多的白细胞介素 -β,据称这会使他们易于出现过度的炎症反应和慢性牙周炎发病率增加。

方法

选择对照临床试验来评估基因检测预测哪些患者易出现探诊出血、牙周炎、种植体周围炎和牙齿缺失的能力。

结果

检测组(基因型阳性)和对照组(基因型阴性)结果的比较显示,在预测哪些患者龈下白细胞介素 -β水平会升高方面存在不确定性。同样,该检测能否预测哪些个体探诊出血发生率增加、临床附着丧失、骨支持减少或牙齿缺失也值得怀疑。

结论

关于检测白细胞介素 -1A +4845和白细胞介素 -1B +3954位点的等位基因2以预测哪些患者会发生重度慢性牙周炎的实用性,存在许多未解决的问题。因此,临床医生在改变有症状或无症状患者的维护计划或治疗方案之前,必须谨慎解释通过市售基因易感性检测获得的结果。

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