Suppr超能文献

砷诱导的心血管疾病易感性与遗传多态性的关联。

Association of arsenic-induced cardiovascular disease susceptibility with genetic polymorphisms.

机构信息

Department of Genetic Engineering and Biotechnology, Faculty of Biological Sciences, University of Chittagong, Chittagong, 4331, Bangladesh.

Department of Biochemistry and Biotechnology, University of Science and Technology, Chittagong (USTC), Foy's Lake, Chittagong, 4202, Bangladesh.

出版信息

Sci Rep. 2021 Mar 18;11(1):6263. doi: 10.1038/s41598-021-85780-8.

Abstract

Inorganic arsenic (iAs) exposure has been reported to have an impact on cardiovascular diseases (CVD). However, there is not much known about the cardiac tissue injury of CVD patients in relation to iAs exposure and potential role of single nucleotide polymorphisms (SNPs) of genes related to iAs metabolism, oxidative stress, endothelial dysfunction and inflammation which may play important roles in such CVD cases. In this dual center cross-sectional study, based on the exclusion and inclusion criteria, we have recruited 50 patients out of 270, who came from known arsenic-affected and- unaffected areas of mainly Chittagong, Dhaka and Rajshahi divisions of Bangladesh and underwent open-heart surgery at the selected centers during July 2017 to June 2018. We found that the patients from arsenic affected areas contained significantly higher average iAs concentrations in their urine (6.72 ± 0.54 ppb, P = 0.028), nail (529.29 ± 38.76 ppb, P < 0.05) and cardiac tissue (4.83 ± 0.50 ppb, P < 0.05) samples. Patients' age, sex, BMI, hypertension and diabetes status adjusted analysis showed that patients from arsenic-affected areas had significantly higher iAs concentration in cardiac tissue (2.854, 95%CI 1.017-8.012, P = 0.046) reflecting higher cardiac tissue injury among them (1.831, 95%CI 1.032-3.249, P = 0.039), which in turn allowed the analysis to assume that the iAs exposure have played a vital role in patients' disease condition. Adjusted analysis showed significant association between urinary iAs concentration with AA (P = 0.012) and AG (P = 0.034) genotypes and cardiac iAs concentration with AA (P = 0.017) genotype of AS3MT rs10748835. The AG genotype of AS3MT rs10748835 (13.333 95%CI 1.280-138.845, P = 0.013), AA genotype of NOS3 rs3918181 (25.333 95%CI 2.065-310.757, P = 0.002), GG genotype of ICAM1 rs281432 (12.000 95%CI 1.325-108.674, P = 0.010) and AA genotype of SOD2 rs2758331 (13.333 95%CI 1.280-138.845, P = 0.013) were found significantly associated with CVD patients from arsenic-affected areas. Again, adjusted analysis showed significant association of AA genotype of AS3MT rs10748835 with CVD patients from arsenic affected areas. In comparison to the reference genotypes of the selected SNPs, AA of AS3MT 10748835, AG of NOS3 rs3918181 and AC of rs3918188, GG of ICAM1 rs281432, TT of VCAM1 rs3176867, AA of SOD2 rs2758331 and GT of APOE rs405509 significantly increased odds of cardiac tissue injury of CVD patients from arsenic affected areas. The results showed that the selected SNPs played a susceptibility role towards cardiac tissue iAs concentration and injury among CVD patients from iAs affected areas.

摘要

无机砷(iAs)暴露已被报道对心血管疾病(CVD)有影响。然而,对于与 iAs 暴露相关的 CVD 患者的心脏组织损伤以及与 iAs 代谢、氧化应激、内皮功能障碍和炎症相关的基因的单核苷酸多态性(SNP)的潜在作用知之甚少,这些基因可能在这种 CVD 情况下发挥重要作用。在这项双中心横断面研究中,根据排除和纳入标准,我们从主要来自吉大港、达卡和拉杰沙希地区的已知受砷影响和不受影响的地区招募了 270 名患者中的 50 名,并在 2017 年 7 月至 2018 年 6 月期间在选定的中心接受了心脏手术。我们发现来自砷污染地区的患者尿液(6.72 ± 0.54 ppb,P = 0.028)、指甲(529.29 ± 38.76 ppb,P < 0.05)和心脏组织(4.83 ± 0.50 ppb,P < 0.05)样本中的 iAs 浓度明显更高。对患者年龄、性别、BMI、高血压和糖尿病状况进行调整分析显示,来自砷污染地区的患者心脏组织中的 iAs 浓度显著更高(2.854,95%CI 1.017-8.012,P = 0.046),反映出他们的心脏组织损伤更高(1.831,95%CI 1.032-3.249,P = 0.039),这反过来又使得分析可以假设 iAs 暴露在患者的病情中发挥了重要作用。调整分析显示,尿液 iAs 浓度与 AA(P = 0.012)和 AG(P = 0.034)基因型和心脏 iAs 浓度与 AS3MT rs10748835 的 AA(P = 0.017)基因型之间存在显著关联。AS3MT rs10748835 的 AG 基因型(13.333 95%CI 1.280-138.845,P = 0.013)、NOS3 rs3918181 的 AA 基因型(25.333 95%CI 2.065-310.757,P = 0.002)、ICAM1 rs281432 的 GG 基因型(12.000 95%CI 1.325-108.674,P = 0.010)和 SOD2 rs2758331 的 AA 基因型(13.333 95%CI 1.280-138.845,P = 0.013)与来自砷污染地区的 CVD 患者显著相关。同样,调整分析显示,AS3MT rs10748835 的 AA 基因型与来自砷污染地区的 CVD 患者显著相关。与所选 SNP 的参考基因型相比,AS3MT 10748835 的 AA、NOS3 rs3918181 的 AG 和 rs3918188 的 AC、ICAM1 rs281432 的 GG、VCAM1 rs3176867 的 TT、SOD2 rs2758331 的 AA 和 APOE rs405509 的 GT 显著增加了来自砷污染地区的 CVD 患者心脏组织损伤的几率。结果表明,所选 SNP 对来自 iAs 污染地区的 CVD 患者的心脏组织 iAs 浓度和损伤具有易感性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d65/7973792/0461fa29ee44/41598_2021_85780_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验