IL4-589C>T、FCGR2A-166His>Arg、DEFB1-20G>A、DEFB1-52G>A基因多态性对原发性髋关节骨关节病患者TNFα、IL-1β、IL-4、IL-10含量的影响

A. Miromanov, T. Zabello, N. Miromanova
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The exclusion criteria were as follows: close relationship; other types of osteoarthritis (post-traumatic, rheumatoid, metabolic, etc.); dysplastic syndromes and phenotypes; acute and chronic inflammatory diseases at the exacerbation stage; diabetes mellitus; osteoporosis; vascular diseases; obesity; malignant neoplasia; alcohol abuse. Along with clinical examination, the following laboratory methods were applied: immunological techniques, i.e., determination of TNFα, IL-1β, IL-4, IL-10; genetic testing using polymerase chain reaction, e.g., a point mutation of the IL4 gene at the 589(C>T) position, FCGR2A at 166(His>Arg) site, DEFB1 at the 20(G>A) and 52(G>A) positions. DNA from the peripheral blood of patients was used for the molecular genetic analysis. Radiographic examination was also carried out. The data were statistically processed using STATISTICA 6.1 software package (StatSoft, USA), Microsoft Office Excel 2019 for Windows 10. The differences were considered statistically significant at p ≤ 0.05. Results. The -589T/T genotype of IL4-589C>T gene polymorphism indirectly contributes to higher content of TNFα and IL-1β for primary osteoarthritis of the hip joints. The patients with -166Arg/Arg genotype have a 1.3-fold increase of certain cytokine concentrations, e.g., TNFα and IL-1β, as compared with -166His/Arg genotype, and, conversely, lower content of IL-4 and IL-10 (1.3- fold) in comparison with -166His/His genotype. The patients with -20A/A genotype showed higher levels of TNFα and IL-1β, respectively, 1.2 and 1.3 times, compared with -20G/G genotype, and 1.3 times versus the -20G/A genotype. Conclusions: 1. 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引用次数: 0

摘要

我们的目的是研究IL4-589C >t、FCGR2A-166His >arg、DEFB1-20G >a、DEFB1-52G >a基因多态性对原发性髋关节骨关节病患者TNFα、IL-1β、IL-4和IL-10含量的影响。我们对100名居住在贝加尔地区的俄罗斯族(平均年龄61.3±8.5岁)III-IV期原发性关节关节病患者进行了调查。对照组(n = 100)为当地居民,年龄(60±8.3岁)、性别、居住地、民族具有可比性。排除标准为:关系密切;其他类型的骨关节炎(创伤后、类风湿、代谢性等);发育不良综合征和表型;急性加重期急慢性炎性疾病;糖尿病;骨质疏松症;血管疾病;肥胖;恶性肿瘤;酒精滥用。结合临床检查,采用以下实验室方法:免疫学技术,即检测TNFα、IL-1β、IL-4、IL-10;利用聚合酶链反应进行基因检测,例如,il - 4基因在589(C>T)位点、FCGR2A在166(His>Arg)位点、DEFB1在20(G> a)和52(G> a)位点发生点突变。从患者外周血中提取DNA用于分子遗传学分析。同时进行x线检查。使用STATISTICA 6.1软件包(StatSoft, USA)、Microsoft Office Excel 2019 for Windows 10对数据进行统计处理。p≤0.05认为差异有统计学意义。结果。IL4-589C >t基因多态性的-589T/T基因型间接导致原发性髋关节骨关节炎中TNFα和IL-1β含量升高。与- 166his /Arg基因型患者相比,- 166arg /Arg基因型患者某些细胞因子如TNFα和IL-1β浓度增加1.3倍,相反,IL-4和IL-10含量较- 166his /His基因型低(1.3倍)。-20A/A基因型患者的TNFα和IL-1β水平分别比-20G/G基因型高1.2倍和1.3倍,比-20G/A基因型高1.3倍。结论:1。-589T/T基因型的IL4-589C>T基因多态性和-20A/A基因型的DEFB1-20G>A基因多态性的存在导致血清中TNFα和IL-1β含量高,-166His/His FCGR2A-166His>Arg基因多态性的携带与TNFα、IL-1β水平高和IL-4、IL-10浓度低有关。2. 原发性关节关节病患者中携带FCGR2A166HisArg x DEFB152AA x DEFB120AA x IL4589TT基因型的复合携带者,其TNFα、IL-1β细胞因子含量分别增加1.5倍和1.7倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of IL4-589C>T, FCGR2A-166His>Arg, DEFB1-20G>A, DEFB1-52G>A gene polymorphisms on TNFα, IL-1β, IL-4, and IL-10 contents in the patients with primary hip osteoarthrosis
Our objective was to study the effects of IL4-589C>T, FCGR2A-166His>Arg, DEFB1-20G>A, DEFB1-52G>A gene polymorphisms upon content of TNFα, IL-1β, IL-4, and IL-10 in primary osteoarthrosis of the hip joints. We performed a survey of 100 patients of Russian ethnicity (average age 61.3±8.5 years) with primary coxarthrosis at the stage III-IV who lived in the Trans-Baikal region. The control group (n = 100), were local residents, comparable by age (60±8.3 years), gender, habitation place and nationality. The exclusion criteria were as follows: close relationship; other types of osteoarthritis (post-traumatic, rheumatoid, metabolic, etc.); dysplastic syndromes and phenotypes; acute and chronic inflammatory diseases at the exacerbation stage; diabetes mellitus; osteoporosis; vascular diseases; obesity; malignant neoplasia; alcohol abuse. Along with clinical examination, the following laboratory methods were applied: immunological techniques, i.e., determination of TNFα, IL-1β, IL-4, IL-10; genetic testing using polymerase chain reaction, e.g., a point mutation of the IL4 gene at the 589(C>T) position, FCGR2A at 166(His>Arg) site, DEFB1 at the 20(G>A) and 52(G>A) positions. DNA from the peripheral blood of patients was used for the molecular genetic analysis. Radiographic examination was also carried out. The data were statistically processed using STATISTICA 6.1 software package (StatSoft, USA), Microsoft Office Excel 2019 for Windows 10. The differences were considered statistically significant at p ≤ 0.05. Results. The -589T/T genotype of IL4-589C>T gene polymorphism indirectly contributes to higher content of TNFα and IL-1β for primary osteoarthritis of the hip joints. The patients with -166Arg/Arg genotype have a 1.3-fold increase of certain cytokine concentrations, e.g., TNFα and IL-1β, as compared with -166His/Arg genotype, and, conversely, lower content of IL-4 and IL-10 (1.3- fold) in comparison with -166His/His genotype. The patients with -20A/A genotype showed higher levels of TNFα and IL-1β, respectively, 1.2 and 1.3 times, compared with -20G/G genotype, and 1.3 times versus the -20G/A genotype. Conclusions: 1. The presence of -589T/T genotype of the IL4-589C>T gene polymorphism and the -20A/A genotype of the DEFB1-20G>A gene polymorphism contributes to a high content of TNFα and IL-1β in the blood serum, and the carriage of -166His/His FCGR2A-166His>Arg gene polymorphism is associated with both higher level of TNFα, IL-1β, and a low concentration of IL-4, IL-10. 2. Complex carriers of FCGR2A166HisArg x DEFB152AA x DEFB120AA x IL4589TT genotypes in the patients with primary coxarthrosis increases the contents of TNFα, IL-1β cytokines by 1.5 and 1.7 times, respectively.
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