Subclinical reduced G6PD activity in rheumatoid arthritis and Sjogren's Syndrome patients: Relation to clinical characteristics, disease activity and metabolic syndrome

被引:33
作者
Gheita, Tamer Atef [1 ]
Kenawy, Sanaa Abdel Baky [2 ]
El Sisi, Rehab Wafik [3 ]
Gheita, Heba Atef [4 ]
Khalil, Hossam [5 ]
机构
[1] Cairo Univ, Fac Med, Dept Rheumatol, Giza 12613, Egypt
[2] Cairo Univ, Fac Med, Dept Pharmacol, Giza 12613, Egypt
[3] Cairo Univ, Fac Oral & Dent Med, Giza 12613, Egypt
[4] Atom Energy Authorizat, Dept Pharmacol, Cairo, Egypt
[5] Beni Sweif Univ, Fac Med, Dept Ophthalmol, Beni Sweif, Egypt
关键词
DAS28; G6PD activity; Metabolic syndrome; Rheumatoid arthritis; Sjogren's Syndrome; GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY; OXIDATIVE STRESS; CLASSIFICATION CRITERIA; GENETIC ABNORMALITIES; RISK; FREQUENCY;
D O I
10.3109/14397595.2013.851639
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 Sjogren'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.
引用
收藏
页码:612 / 617
页数:6
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