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成人类风湿关节炎患者颈动脉斑块;与对氧磷酶 1 酶活性和 Q192R 对氧磷酶 1 基因多态性的关系。

Carotid plaques in adult rheumatoid arthritis patients; association with paroxonase 1 enzymatic activity and Q192R paroxonase 1 gene polymorphism.

机构信息

Faculty of Medicine, Zagazig University, Zagazig, Egypt.

出版信息

Mol Biol Rep. 2020 Jun;47(6):4255-4262. doi: 10.1007/s11033-020-05558-5. Epub 2020 May 30.

Abstract

Paroxonase 1 (PON 1) enzymatic activity and Q192R PON polymorphism has been implicated with greater cardiovascular risk in general population. Rheumatoid arthritis (RA) is a systemic autoimmune disease characterized with increased inflammatory markers leading to increased cardiovascular morbidity. The aim of the work was to study association between PON1 enzymatic activity & gene polymorphism with carotid plaques in RA patients. This case-control study was carried out at Zagazig University Hospitals on 99 subjects divided randomly into two groups; 48 RA patients and 51 controls. RA patients fulfilled the revised 2010 EULAR/ACR classification criteria of RA. All patients were subjected to history taking, clinical evaluation, laboratory investigations & plain X-rays. Carotid intima-media thickness (CIMT) and PON1 enzyme assay & genotyping were done for both groups. PON1 enzyme levels were significantly higher in patients than controls. Also, there was a significant negative correlation of PON1 enzyme activity with increased CIMT & plaques. The cut-off value of PON1 enzyme level that had the highest CVD prediction was 4.2 U/ml. Although PON1 genotyping was insignificantly different between patients and controls, patients with QQ genotype had the lowest PON1 activity then patients with QR genotype then RR genotype. In RA patients, decreased serum PON1 enzymatic activity and QQ genotyping of Q192R PON polymorphism was associated with increased CIMT & plaques. Serum PON1 could be a good marker for atherosclerosis prediction in RA patients at cutoff 4.2 U/ml.

摘要

对氧磷酶 1(PON1)酶活性和 Q192R PON 多态性与一般人群的心血管风险增加有关。类风湿关节炎(RA)是一种系统性自身免疫性疾病,其特征是炎症标志物增加,导致心血管发病率增加。本研究旨在探讨 PON1 酶活性和基因多态性与 RA 患者颈动脉斑块的关系。这项病例对照研究在宰加济格大学医院进行,共纳入 99 例患者,随机分为两组:48 例 RA 患者和 51 例对照组。RA 患者符合 2010 年 EULAR/ACR 修订的 RA 分类标准。所有患者均接受了病史采集、临床评估、实验室检查和普通 X 线检查。对两组患者进行颈动脉内膜中层厚度(CIMT)、PON1 酶测定和基因分型。结果显示,与对照组相比,RA 患者的 PON1 酶水平显著升高。此外,PON1 酶活性与 CIMT 和斑块的增加呈显著负相关。PON1 酶水平的截断值为 4.2U/ml,对 CVD 的预测价值最高。虽然 PON1 基因分型在患者和对照组之间无显著差异,但 QQ 基因型患者的 PON1 活性最低,QR 基因型患者次之,RR 基因型患者最高。在 RA 患者中,血清 PON1 酶活性降低和 Q192R PON 多态性的 QQ 基因型与 CIMT 和斑块的增加有关。血清 PON1 可能是 RA 患者动脉粥样硬化预测的一个良好标志物,截断值为 4.2U/ml。

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