类风湿关节炎患者CXCL2和自噬基因表达的评价及其与心血管疾病的关系

Mona Elhelaly, D. Nassar, M. Nassar, Khaled AbdElAlim, S. Tharwat
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引用次数: 0

摘要

背景:心血管疾病是类风湿性关节炎(RA)患者最常见的合并症之一,也是导致患者死亡的主要原因。本研究的目的是评估RA患者CXCL2和自噬基因如轻链(LC3)和beclin1的水平及其与临床表现和颈动脉内膜厚度的关系。患者和方法:本横断面研究包括RA患者。记录社会人口学特征及临床和治疗数据。通过全面的医学和临床检查来评估疾病状况,包括肿胀和压痛关节的数量,视觉模拟量表,疾病活动评分28。每位参与者采集约5ml全血,评估CXCL2、LC3和beclin1的表达水平。双超声系统评估颈动脉内膜中膜厚度(CIMT)。选取年龄、性别相匹配的健康个体79例作为对照组。结果:共纳入79例RA患者,平均±SD年龄45.24±10.07岁。其中以女性居多(87.3%),RA中位病程为7年。类风湿因子阳性约85%,抗ccp抗体阳性约70.9%。CXCL2与LC3中强度呈正相关(P < 1 / 4 0.026)。CXCL2与皮下类风湿结节存在显著正相关,而CXCL2低强度与收缩压、舒张压、健康评估问卷评分呈正相关。LC3基因表达与关节畸形呈显著正相关,与高胆固醇血症呈显著负相关。在控制(调整)患者年龄后,病程大于等于7年的患者中强度LC3与CIMT呈正相关,有统计学意义。结论:CXCL2及自噬基因表达水平(LC3、beclin1)与RA患者临床表现及CIMT呈正相关。这些基因可能作为类风湿关节炎患者心血管疾病的预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of CXCL2 and autophagy genes expression in rheumatoid arthritis patients and its relation to cardiovascular diseases
Background: Cardiovascular disease is among the most common comorbidity and the leading cause of mortality in patients with rheumatoid arthritis (RA). The aim of this study was to assess the levels of CXCL2 and autophagy genes such light chain (LC3) and beclin1 in patients with RA and how they relate to the clinical manifestations and carotid intimalemedial thickness. Patients and methods: This cross-sectional study included patients with RA. Sociodemographic characteristics and clinical and therapeutic data were recorded. Thorough medical and clinical examination was conducted to evaluate the disease status, including the number of swollen and tender joints, visual analog scale, and disease activity score 28. Approximately 5 ml of whole blood was collected from each participant, and CXCL2, LC3, and beclin1 expression levels were evaluated. The carotid intimaemedia thickness (CIMT) was assessed by a duplex ultrasound system. As a control group, 79 healthy individuals of matching age and sex were included. Results: A total of 79 patients with RA were included in the study, with mean ± SD age of 45.24 ± 10.07 years. Most of them were females (87.3%), and the median duration of RA was 7 years. Approximately 85% had positive rheumatoid factor, whereas 70.9% had positive anti-CCP antibody. CXCL2 and LC3 had a statistically significant positive correlation of medium strength (P 1⁄4 0.026). CXCL2 showed a significant positive correlation with presence of subcutaneous rheumatoid nodules, whereas there was a positive correlation of low strength between CXCL2 and systolic blood pressure, diastolic blood pressure, and health assessment questionnaire score. For LC3 gene expression, it was significantly correlated positively with presence of joint deformities and negatively with hypercholesterolemia. There was a statistically significant positive correlation of medium strength between LC3 and CIMT in those with disease duration more than or equal to 7 years after controlling (adjusting) for patient's age. Conclusions: CXCL2 and autophagy gene expression levels (LC3 and beclin1) are positively correlated with the clinical manifestations and CIMT in patients with RA. These genes may serve as predictors for cardiovascular disease in patients with RA.
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