Vijayan Anoop, Chithra V, Sandhya C
Department of Biosciences, Mar Thoma College, Thiruvalla, Pathanamthitta, Kerala, 689103, India.
Department of Biochemistry, N.S.S College, Pandalam, Pathanamthitta, Kerala, 689501, India.
Mol Biol Rep. 2024 Jul 13;51(1):805. doi: 10.1007/s11033-024-09727-8.
Coronary artery disease (CAD) has been linked to single nucleotide polymorphism (SNP) in superoxide dismutase 2 (SOD 2) gene. Additionally, several modifiable risk factors are also known to influence the CAD risk.
To investigate the association between selected modifiable risk factors and oxidative stress markers with the SOD2 rs4880 SNP in CAD patients.
A cohort of 150 angiographically confirmed CAD patients, and 100 control subjects in the same geographic area were enrolled. SOD levels and lipid peroxidation were assessed in the blood samples using standard protocols. The genotyping of the SOD2 gene was conducted through the PCR-sequencing method.
This study indicated that CAD patients with the rs4880 SNP having heterozygous AG and mutated homozygous GG genotypes have increased oxidative stress, decreased SOD activity, and a positive association with CAD risk (OR 2.85) in comparison with control individuals. The investigation among CAD patients was then carried out based on modifiable risk factors. The risk factors selected were clinical characteristics, physical habits, nutritional status, and body mass index. In all the cases, MDA levels showed a positive association, and SOD activity showed a negative association with the selected polymorphism.
The study suggests that the selected modifiable risk factors have an important role in the higher oxidative stress found in patients, which may lead to SOD2 polymorphism. It also suggests that the SOD2 locus can be identified as a marker gene for CAD susceptibility.
冠状动脉疾病(CAD)与超氧化物歧化酶2(SOD 2)基因中的单核苷酸多态性(SNP)有关。此外,已知几种可改变的危险因素也会影响CAD风险。
研究CAD患者中选定的可改变危险因素和氧化应激标志物与SOD2 rs4880 SNP之间的关联。
招募了一组150例经血管造影证实的CAD患者以及同一地理区域的100名对照受试者。使用标准方案评估血样中的SOD水平和脂质过氧化。通过PCR测序方法对SOD2基因进行基因分型。
本研究表明,与对照个体相比,具有杂合AG和突变纯合GG基因型的rs4880 SNP的CAD患者氧化应激增加,SOD活性降低,且与CAD风险呈正相关(OR 2.85)。然后根据可改变的危险因素对CAD患者进行调查。选定的危险因素为临床特征、生活习惯、营养状况和体重指数。在所有病例中,MDA水平与选定的多态性呈正相关,SOD活性与选定的多态性呈负相关。
该研究表明,选定的可改变危险因素在患者中发现的较高氧化应激中起重要作用,这可能导致SOD2多态性。研究还表明,SOD2基因座可被确定为CAD易感性的标记基因。