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伊朗西部系统性红斑狼疮患者血管紧张素转换酶(ACE) I/D 变异与生化参数和氧化应激标志物的关系。

Association of angiotensin-converting enzyme (ACE) I/D variation with biochemical parameters and oxidative stress markers in systemic lupus erythematosus patients in west of Iran.

机构信息

Regenerative Medicine Research Center (RMRC), Kermanshah University of Medical Sciences, Kermanshah, Iran.

Institute of Allergology, Charité - Universitätsmedizin Berlin, Corporate member of Freie Universität Berlin and Humboldt-Universität Zu Berlin, Berlin, Germany.

出版信息

Mol Biol Rep. 2023 Oct;50(10):8201-8212. doi: 10.1007/s11033-023-08685-x. Epub 2023 Aug 10.

Abstract

PURPOSE

We aimed to study insertion/deletion (I/D) variation (rs4646994) of ACE gene in a group of SLE patients in west of Iran and its possible relationship with oxidative stress.

METHOD AND RESULTS

Genotypes and allele frequencies related to ACE (I/D) variation were determined in 108 SLE patients and 110 gender and age-matched healthy controls using PCR. Neopterin, malondialdehyde (MDA), and serum lipid concentrations were determined by HPLC and enzyme assay respectively. The overall distribution of ACE I/D genotypes in SLE patients was different from that of the control group (P = 0.005). DD genotype compared to ID genotype increased the risk of SLE (OR = 2.57, 95% CI 1.4-4.8, P = 0.003). ID genotype compared to the II genotype decreased the risk of disease (OR = 0.45, 95% CI 0.2-0.99, p = 0.042). SLE patients with DD, ID, and II genotypes had lower paraoxonase (PON) activity and higher serum levels of MDA and neopterin versus control patients. We also detected a significant protective effect against SLE in presence of ACE I alleles and lack of angiotensin II receptor, type 1 (AGTR1) A1166C (NCBI reference SNP id: rs5186), C alleles in this study (OR = 0.31, 95% CI 0.14-0.68, P = 0.002).

CONCLUSIONS

Carriers of the DD genotype of ACE gene with higher serum concentrations of neopterin and MDA, and lower PON activity had a high risk to develop SLE, while ID genotype decreased the risk of disease development by 2.22 times compared to II genotype.

摘要

目的

我们旨在研究伊朗西部一组系统性红斑狼疮(SLE)患者 ACE 基因插入/缺失(I/D)变异(rs4646994)及其与氧化应激的可能关系。

方法与结果

采用 PCR 法检测 108 例 SLE 患者和 110 名性别和年龄匹配的健康对照者 ACE(I/D)变异的基因型和等位基因频率。采用 HPLC 和酶法分别测定新蝶呤、丙二醛(MDA)和血清脂质浓度。SLE 患者 ACE I/D 基因型的总体分布与对照组不同(P=0.005)。与 ID 基因型相比,DD 基因型增加了 SLE 的发病风险(OR=2.57,95%CI 1.4-4.8,P=0.003)。与 II 基因型相比,ID 基因型降低了疾病的发病风险(OR=0.45,95%CI 0.2-0.99,P=0.042)。与对照组相比,DD、ID 和 II 基因型的 SLE 患者的对氧磷酶(PON)活性降低,血清 MDA 和新蝶呤水平升高。此外,我们还发现 ACE I 等位基因的存在和缺乏血管紧张素 II 受体 1(AGTR1)A1166C(NCBI 参考 SNP id:rs5186)C 等位基因对 SLE 有显著的保护作用(OR=0.31,95%CI 0.14-0.68,P=0.002)。

结论

携带 ACE 基因 DD 基因型、血清新蝶呤和 MDA 浓度较高、PON 活性较低的患者发生 SLE 的风险较高,而与 II 基因型相比,ID 基因型使疾病发病风险降低 2.22 倍。

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