Malíčková Karin, Duricová Dana, Bortlík Martin, Hrušková Zdenka, Svobodová Barbora, Machková Naděžda, Komárek Viktor, Fučíková Terezie, Janatková Ivana, Zima Tomáš, Lukáš Milan
Institute of Clinical Biochemistry and Laboratory Diagnostics, General University Hospital in Prague, First Faculty of Medicine, Charles University in Prague, Karlovo nam. 32, 121 11 Prague 2, Czech Republic.
Autoimmune Dis. 2011;2011:945861. doi: 10.4061/2011/945861. Epub 2011 May 29.
Background and Aims. Deoxyribonuclease I (DNaseI) is an endonuclease that facilitates chromatin breakdown and promotes susceptibility to autoimmune disorders. The aim of current study was to investigate serum DNase I activity in patients with inflammatory bowel diseases (IBD). Patients and Methods. A cohort of 110 IBD patients was evaluated, aged 35 ± 12 years, 77 with Crohn's disease (CD) and 33 with ulcerative colitis (UC). 50 SLE patients and 50 healthy blood donors were examined as control groups. Results. DNase I activity in IBD patients was significantly lower than in healthy individuals, but higher than in SLE patients (P < .0001). Patients with UC showed higher DNase I activity than CD patients, P = .21. DNase I activity in female patients with IBD was significantly lower than in males, P = .024; however, no differences in DNase I activity were found in relation to gender in healthy individuals. DNase I activity has shown a strong negative correlation with the serum concentration of anti-nucleosomal antibodies in the autoimmune (SLE + IBD) cohort, as well as in the separate IBD cohort. Conclusions. Reduced serum DNase I activity probably has pathogenetic consequences in IBD. Induction of autoantibodies towards nucleosomes could be a reflection of impaired DNase I activity.
背景与目的。脱氧核糖核酸酶I(DNaseI)是一种核酸内切酶,可促进染色质分解并增加自身免疫性疾病的易感性。本研究旨在调查炎症性肠病(IBD)患者的血清DNase I活性。
患者与方法。对110名IBD患者进行了评估,年龄为35±12岁,其中77例为克罗恩病(CD),33例为溃疡性结肠炎(UC)。50名系统性红斑狼疮(SLE)患者和50名健康献血者作为对照组进行检查。
结果。IBD患者的DNase I活性显著低于健康个体,但高于SLE患者(P <.0001)。UC患者的DNase I活性高于CD患者,P =.21。IBD女性患者的DNase I活性显著低于男性,P =.024;然而,健康个体中未发现DNase I活性与性别有关的差异。在自身免疫(SLE + IBD)队列以及单独的IBD队列中,DNase I活性与抗核小体抗体的血清浓度呈强烈负相关。
结论。血清DNase I活性降低可能在IBD中具有致病后果。针对核小体的自身抗体诱导可能反映了DNase I活性受损。