皮肤t细胞吸引趋化因子在儿童特应性皮炎不同表型发展中的作用

V. Dytiatkovsky, O. Abaturov, N. Naumenko, O. Alifirenko, I. Filatova, S. Taran
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引用次数: 0

摘要

本研究的目的是检测儿童发生不同特应性皮炎(AD)表型(单独或合并其他共病特应性疾病(AtD))的风险,这取决于血清中皮肤t细胞吸引趋化因子(CTACK)/CCL27的浓度。主要组包括39名患有不同AD表型的3至18岁儿童-单独(18例)和合并AtD - AR/ARC和/或支气管哮喘(21例)。对照组为47例3 ~ 18岁的胃肠道疾病(GIT)患儿。检测所有患儿血清CTACK/CCL 27浓度。在全主组中,CTACK/CCL27的平均水平显著高于对照组患者:4403.6 pg/ml (95% CI: 3726.2;5148.7, p<0.001)和3495.9 pg/ml (95% CI: 3197.8;4186.8, p<0.001)。不同AD表型主组患者的平均血清CTACK/CCL27水平高于完全主组:分离AD - 4549.4 pg/ml (LQ;总部:3923.5;5175.2, p<0.05), AD与其他AtD相关- 5116.6 pg/ml (LQ, HQ: 4062.8;6170.5, p < 0.05)。在整体AD和孤立AD的表型中,血清CTACK/ CCL27的临界值为3586.5 pg/ml(分别为76.9%和77.8%,对照组为38.3%)。该浓度下的发展风险为5.37 (95% CI: 2.05;14.07, p<0.001), 5.64 (95% 1.56;20.32, p<0.05)。在AD表型合并合并AtD时,血清CTACK/CCL27的临界值为4308.8 pg/ml(占主组的66.7%,对照组的21.3%)。在该浓度下发生这种AD表型的风险为7.40 (95% CI: 2.30;23.76, p < 0.001)。血清CTACK/CCL27水平是儿童发生不同AD表型风险的可靠生物标志物。血清CTACK/CCL27=3658.5 pg/ml时,发生总AD表型的显著风险为5.37,分离性- AD=5.64。血清CTACK/CCL27浓度=4308.8 pg/ml时,AD表型合并AtD的显著风险为7.40。
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The role of cutaneous T-cell attracting chemokine in the development of different phenotypes of atopic dermatitis in children
The goal of this study was to detect the risk of developing different atopic dermatitis (AD) phenotypes in children (isolated or combined with other comorbid atopic diseases (AtD)) depending on serum concentrations of cutaneous T-cell attracting chemokine (CTACK)/CCL27. The main group comprised 39 children aged 3 to 18 years old suffering from different AD phenotypes – isolated (18 patients) and combined with comorbid AtD – AR/ARC and/or bronchial asthma (21 patients). The control group comprised 47 children aged 3 to 18 years old, suffering from diseases of the gastrointestinal tract (GIT). Serum CTACK/CCL 27 concentrations were detected in all children. In the full main group, the average level of CTACK/CCL27 was significantly higher compared to the patients of the control group: 4403.6 pg/ml (95% CI: 3726.2; 5148.7, p<0.001) and 3495.9 pg/ml (95% CI: 3197.8; 4186.8, p<0.001), respectively. Mean serum CTACK/CCL27 levels in patients of the main group with different AD phenotypes were higher than those in the full main group: with isolated AD – 4549.4 pg/ml (LQ; HQ: 3923.5; 5175.2, p<0.05), with AD associated with other AtD – 5116.6 pg/ml (LQ, HQ: 4062.8; 6170.5, p<0.05). In phenotypes of overall and isolated AD, the cut-off value of serum CTACK/ CCL27 is 3586.5 pg/ml (76.9% and 77.8%, respectively, and 38.3% in the control group). The risk of development at this concentration is 5.37 (95% CI: 2.05; 14.07, p<0.001) for the total AD phenotype and 5.64 (95% 1.56; 20.32, p<0.05) for the isolated AD phenotype. In AD phenotype combined with comorbid AtD, the cut-off value of serum CTACK/CCL27 is 4308.8 pg/ml (66.7% of the main and 21.3% in the control group). The risk of developing this AD phenotype at this concentration is 7.40 (95% CI: 2.30; 23.76, p<0.001). Serum CTACK/CCL27 levels are the reliable biomarker of the risk for developing different AD phenotypes in children. In the serum level of CTACK/CCL27=3658.5 pg/ml, the significant risk of developing total AD phenotype is 5.37, and isolated – AD=5.64. In the serum concentration of CTACK/CCL27=4308.8 pg/ml, the significant risk of developing AD phenotype combined with comorbid AtD is 7.40.
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