Gürkan Ali, Emingil Gülnur, Saygan Buket Han, Atilla Gül, Cinarcik Serhat, Köse Timur, Berdeli Afig
Department of Periodontology, School of Dentistry, Ege University, Izmir, Turkey.
Arch Oral Biol. 2008 Apr;53(4):337-45. doi: 10.1016/j.archoralbio.2007.11.002. Epub 2007 Dec 21.
Matrix metalloproteinases (MMPs) are involved in periodontal tissue remodeling and degradation. MMP polymorphisms could alter transcription and function of these enzymes. The aim of this study was to investigate MMP-2, MMP-9 and MMP-12 gene polymorphisms in relation to susceptibility to severe chronic periodontitis (CP).
Genomic DNA was obtained from peripheral blood of 87 severe CP patients and 107 periodontally healthy subjects. MMP-2 -735C/T, MMP-9 -1562C/T and MMP -12357Asn/Ser gene polymorphisms were genotyped by polymerase chain reaction and restriction fragment length polymorphism. Probing depth, clinical attachment loss, supragingival plaque accumulation and bleeding on probing were recorded. The data were analyzed by chi-square, logistic regression and Mann-Whitney-U-tests.
The genotype distributions and allele frequencies of MMP-2, MMP-9 and MMP-12 genes were similar in CP and healthy subjects (p>0.05). Differences between rare allele carriage rates of CP and healthy groups regarding MMP-2, MMP-9 and MMP-12 gene polymorphisms were not significant (p>0.05). However, T allele carriers of MMP-9 -1562 gene had less risk for CP (OR=0.36; 95% CI=0.16-0.81).
These data suggest that MMP-2 -735C/T, MMP-9 -1562C/T and MMP-12 357Asn/Ser polymorphisms are not associated with susceptibility to severe CP in Turkish population. However, T allele of MMP-9 -1562 gene might be associated with decreased susceptibility to severe CP.
基质金属蛋白酶(MMPs)参与牙周组织重塑和降解。MMP基因多态性可能会改变这些酶的转录和功能。本研究旨在调查MMP - 2、MMP - 9和MMP - 12基因多态性与重度慢性牙周炎(CP)易感性之间的关系。
从87例重度CP患者和107例牙周健康受试者的外周血中获取基因组DNA。采用聚合酶链反应和限制性片段长度多态性技术对MMP - 2 - 735C/T、MMP - 9 - 1562C/T和MMP - 12 357Asn/Ser基因多态性进行基因分型。记录探诊深度、临床附着丧失、龈上菌斑堆积和探诊出血情况。采用卡方检验、逻辑回归和曼 - 惠特尼 - U检验对数据进行分析。
CP患者和健康受试者中MMP - 2、MMP - 9和MMP - 12基因的基因型分布和等位基因频率相似(p>0.05)。CP组和健康组在MMP - 2、MMP - 9和MMP - 12基因多态性的罕见等位基因携带率方面的差异不显著(p>0.05)。然而,MMP - 9 - 1562基因的T等位基因携带者患CP的风险较低(OR = 0.36;95% CI = 0.16 - 0.81)。
这些数据表明,在土耳其人群中,MMP - 2 - 735C/T、MMP - 9 - 1562C/T和MMP - 12 357Asn/Ser多态性与重度CP易感性无关。然而,MMP - 9 - 1562基因的T等位基因可能与重度CP易感性降低有关。