Murthykumar Karthikeyan, Varghese Sheeja, Jayaseelan Vijayashree Priyadharsini
Department of Periodontics, Saveetha Dental College, Chennai, Tamil Nadu, India.
Department of Clinical Genetics Lab, Centre for Cellular and Molecular Research, Saveetha Dental College, Chennai, Tamil Nadu, India.
Contemp Clin Dent. 2022 Oct-Dec;13(4):363-368. doi: 10.4103/ccd.ccd_309_21. Epub 2022 Nov 3.
Emerging evidence suggests that oxidative stress forms a key component in the etiopathogenesis of periodontitis. Literature evidence have shown potential antioxidants responsible for combating the pro-oxidants which stress the periodontium, but the peroxiredoxin-sulfiredoxin system is explored very minimally in periodontal disease. Thus, the present study was aimed to evaluate the genetic association of SRXN1 receptor gene polymorphism (rs6053666).
A total of 100 subjects were recruited for this study, which included 50 Periodontitis patients (Stage II and above based on the criteria of American Association of Periodontology-2018) and 50 periodontally healthy or mild gingivitis. Genomic DNA was extracted from the whole blood collected from the subjects. DNA was amplified using specific primers flanking the BtgI region of the SRXN1 receptor gene. The amplicon was further subjected to genotyping using restriction fragment length using BtgI enzyme. The genotype obtained based on the restriction fragment length polymorphism pattern was recorded and used for statistical analysis. The distribution of genotypes and allele frequencies in the periodontitis and control groups were compared using the Chi-square test. The risk associated with individual alleles or genotypes was calculated as the odds ratio with 95% confidence intervals. Statistical significance in all tests was determined at < 0.05.
The genotype frequency and distributions of SRXN1 receptor BtgI polymorphism did not differ significantly at ꭕ2df ( = 0.557). Our study results showed that homozygous and heterozygous mutant genotypes had no significant difference (CC vs. CT + TT) between the periodontitis patients and control group with a = 0.4266. The detected frequency of CT (38% vs. 34%) and TT (42% vs. 52%) genotype showed no significant difference between control and test group. There was no significant difference in C allele (39% vs. 31%) and T allele (61% vs. 69%) between the test and control group.
The present study denotes that SRXN1 receptor gene polymorphism is not associated with periodontitis in the study group analyzed.
新出现的证据表明,氧化应激是牙周炎发病机制的关键组成部分。文献证据显示了潜在的抗氧化剂可对抗使牙周组织产生应激的促氧化剂,但过氧化物酶-硫氧还蛋白系统在牙周疾病中的研究非常少。因此,本研究旨在评估SRXN1受体基因多态性(rs6053666)的遗传关联。
本研究共招募了100名受试者,其中包括50名牙周炎患者(根据美国牙周病学会2018年标准为II期及以上)和50名牙周健康或患有轻度牙龈炎的患者。从受试者采集的全血中提取基因组DNA。使用位于SRXN1受体基因BtgI区域侧翼的特异性引物对DNA进行扩增。扩增产物进一步使用BtgI酶通过限制性片段长度进行基因分型。记录基于限制性片段长度多态性模式获得的基因型,并用于统计分析。使用卡方检验比较牙周炎组和对照组中基因型和等位基因频率的分布。将与个体等位基因或基因型相关的风险计算为具有95%置信区间的优势比。所有检验的统计学显著性均确定为P<0.05。
SRXN1受体BtgI多态性的基因型频率和分布在χ2df(=0.557)时无显著差异。我们的研究结果表明,纯合和杂合突变基因型在牙周炎患者和对照组之间无显著差异(CC与CT+TT),P=0.4266。检测到的CT(38%对34%)和TT(42%对52%)基因型频率在对照组和试验组之间无显著差异。试验组和对照组之间的C等位基因(39%对31%)和T等位基因(61%对69%)无显著差异。
本研究表明,在所分析的研究组中,SRXN1受体基因多态性与牙周炎无关。