Sestan Mario, Kifer Nastasia, Frkovic Marijan, Sapina Matej, Srsen Sasa, Batnozic Varga Mateja, Ovuka Aleksandar, Held Martina, Gudelj Gracanin Ana, Kozmar Ana, Bulimbasic Stela, Coric Marijana, Laskarin Gordana, Gagro Alenka, Jelusic Marija
Department of Paediatrics, University of Zagreb School of Medicine, University Hospital Centre Zagreb, Zagreb, Croatia.
Department of Paediatrics, Josip Juraj Strossmayer University of Osijek, Medical Faculty and Faculty of Dental Medicine and Health Osijek, University Hospital Centre Osijek, Osijek, Croatia.
Ther Adv Musculoskelet Dis. 2021 Jun 30;13:1759720X211024828. doi: 10.1177/1759720X211024828. eCollection 2021.
We analysed clinical and biochemical parameters in predicting severe gastrointestinal (GI) manifestations in childhood IgA vasculitis (IgAV) and the risk of developing renal complications.
A national multicentric retrospective study included children with IgAV reviewed in five Croatian University Centres for paediatric rheumatology in the period 2009-2019.
Out of 611 children, 281 (45.99%) had at least one GI manifestation, while 42 of 281 (14.95%) had the most severe GI manifestations. Using logistic regression several clinical risk factors for the severe GI manifestations were identified: generalized rash [odds ratio (OR) 2.09 (95% confidence interval (CI) 1.09-4.01)], rash extended on upper extremities (OR 2.77 (95% CI 1.43-5.34)] or face [OR 3.69 (95% CI 1.42-9.43)] and nephritis (IgAVN) [OR 4.35 (95% CI 2.23-8.50)], as well as lower values of prothrombin time (OR 0.05 (95% CI 0.01-0.62)], fibrinogen [OR 0.45 (95% CI 0.29-0.70)] and IgM [OR 0.10 (95% I 0.03-0.35)]] among the laboratory parameters. Patients with severe GI involvement more frequently had relapse of the disease [OR 2.14 (CI 1.04-4.39)] and recurrent rash [OR 2.61 (CI 1.27-5.38)]. Multivariate logistic regression found that the combination of age, GI symptoms at the beginning of IgAV and severity of GI symptoms were statistically significant predictors of IgAVN. Patients in whom IgAV has started with GI symptoms [OR 6.60 (95% CI 1.67-26.06)], older children [OR 1.22 (95% CI 1.02-1.46)] with severe GI form of IgAV (OR 5.90 (95% CI 1.12-31.15)] were particularly high-risk for developing IgAVN.
We detected a group of older children with the onset of GI symptoms before other IgAV symptoms and severe GI form of the IgAV, with significantly higher risk for acute and chronic complications of IgAV.
我们分析了临床和生化参数,以预测儿童IgA血管炎(IgAV)的严重胃肠道(GI)表现以及发生肾脏并发症的风险。
一项全国多中心回顾性研究纳入了2009年至2019年期间在克罗地亚五个大学儿科风湿病中心接受评估的IgAV患儿。
在611名儿童中,281名(45.99%)至少有1种胃肠道表现,其中281名中的42名(14.95%)有最严重的胃肠道表现。通过逻辑回归确定了几种严重胃肠道表现的临床危险因素:全身性皮疹[比值比(OR)2.09(95%置信区间(CI)1.09 - 4.01)]、皮疹累及上肢(OR 2.77(95% CI 1.43 - 5.34)]或面部[OR 3.69(95% CI 1.42 - 9.43)]以及肾炎(IgAVN)[OR 4.35(95% CI 2.23 - 8.50)],以及实验室参数中凝血酶原时间较低值[OR 0.05(95% CI 0.01 - 0.62)]、纤维蛋白原[OR 0.45(95% CI 0.29 - 0.70)]和IgM[OR 0.10(95% CI 0.03 - 0.35)]。严重胃肠道受累的患者疾病复发[OR 2.14(CI 1.04 - 4.39)]和皮疹复发[OR 2.61(CI 1.27 - 5.38)]更为频繁。多因素逻辑回归发现年龄、IgAV开始时的胃肠道症状以及胃肠道症状严重程度的组合是IgAVN的统计学显著预测因素。IgAV以胃肠道症状开始的患者[OR 6.60(95% CI 1.67 - 26.06)]、年龄较大的儿童[OR 1.22(95% CI 1.02 - 1.46)]以及具有严重胃肠道形式的IgAV患者(OR 5.90(95% CI 1.12 - 31.15)]发生IgAVN的风险特别高。
我们发现一组年龄较大的儿童,在出现其他IgAV症状之前先出现胃肠道症状,且具有严重胃肠道形式的IgAV,其发生IgAV急性和慢性并发症的风险显著更高。