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首页> 外文期刊>Modern rheumatology >Subclinical reduced G6PD activity in rheumatoid arthritis and Sj?gren's Syndrome patients: Relation to clinical characteristics, disease activity and metabolic syndrome
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Subclinical reduced G6PD activity in rheumatoid arthritis and Sj?gren's Syndrome patients: Relation to clinical characteristics, disease activity and metabolic syndrome

机译:类风湿关节炎和干燥综合征患者的亚临床G6PD活性降低:与临床特征,疾病活动性和代谢综合征的关系

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Objective. Glucose-6-phosphate dehydrogenase (G6PD) is an important site of metabolic control in the pentose phosphate pathway. The purpose of this study was to investigate the enzyme activity of G6PD in Rheumatoid Arthritis (RA) and Sj?gren's Syndrome (SS) patients not known to be deficient in this enzyme. It was also within the scope of the aim to find the relation of G6PD to the presence of metabolic syndrome (MetS) in these patients. Methods. Erythrocyte G6PD activity was evaluated in 40 RA patients, 30 SS patients and in 30 age-and sex-matched control. The clinical characteristics, disease activity score (DAS28), SS disease activity (SSDAI) and damage (SSDDI) indices and presence of MetS of the included patients were analyzed in relation to the enzyme level. Results. The G6PD activity in RA patients (7.72 ± 3.57 U/g Hb) was significantly reduced compared to that in the SS patients (11.55 ± 3.14 U/g Hb) and control (13.23 ± 3.34 U/g Hb) especially those with MetS (4.61 ± 1.84 U/g Hb) (p < 0.001). There was a significant negative correlation of the G6PD activity with the disease duration and DAS28 (p < 0.001). Conclusion. The results of this study, suggest that G6PD not only does not protect against MetS in RA, but may even be considered a risk factor for the development of this disorder. The identification of regulatory tools for G6PD activity may prove promising for treating the associated metabolic disorders and chronic inflammation in RA.
机译:目的。 6-磷酸葡萄糖脱氢酶(G6PD)是磷酸戊糖途径中代谢控制的重要部位。这项研究的目的是调查G6PD在类风湿性关节炎(RA)和干燥综合征(SS)患者中的酶活性,这些患者尚缺乏这种酶。在这些患者中发现G6PD与代谢综合征(MetS)的关系也在目的范围之内。方法。在40例RA患者,30例SS患者以及30例年龄和性别匹配的对照中评估了红细胞G6PD活性。分析患者的临床特征,疾病活动评分(DAS28),SS疾病活动(SSDAI)和损伤(SSDDI)指标以及MetS的存在与酶水平的关系。结果。与SS患者(11.55±3.14 U / g Hb)和对照组(13.23±3.34 U / g Hb)相比,RA患者的G6PD活性(7.72±3.57 U / g Hb)显着降低,特别是MetS( 4.61±1.84 U / g Hb)(p <0.001)。 G6PD活性与疾病持续时间和DAS28呈显着负相关(p <0.001)。结论。这项研究的结果表明,G6PD不仅不能预防RA中的MetS,而且甚至可能被认为是发展这种疾病的危险因素。对于G6PD活性的调节工具的鉴定可能有望用于治疗RA中相关的代谢紊乱和慢性炎症。

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