切换至 "中华医学电子期刊资源库"

中华妇幼临床医学杂志(电子版) ›› 2019, Vol. 15 ›› Issue (02) : 143 -149. doi: 10.3877/cma.j.issn.1673-5250.2019.02.004

所属专题: 文献

论著

初发过敏性紫癜患儿发病早期肾脏受累危险因素分析
孙小妹1, 曹杨1, 戴亮1, 孙飞扬1, 董丽群1,()   
  1. 1. 四川大学华西第二医院儿科、出生缺陷与相关妇儿疾病教育部重点实验室,成都 610041
  • 收稿日期:2018-10-30 修回日期:2019-03-15 出版日期:2019-04-01
  • 通信作者: 董丽群

Risk factors of renal involvement in children with primary Henoch-Schönlein purpura in the early stage

Xiaomei Sun1, Yang Cao1, Liang Dai1, Feiyang Sun1, Liqun Dong1,()   

  1. 1. Department of Pediatrics, Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu 610041, Sichuan Province, China
  • Received:2018-10-30 Revised:2019-03-15 Published:2019-04-01
  • Corresponding author: Liqun Dong
  • About author:
    Corresponding author: Dong Liqun, Email:
  • Supported by:
    Scientific Research Project of Health and Family Planning Commission of Sichuan Province(16P238); Project of Pediatric Clinical Medical Research Center of Sichuan Province(2017-46-4); the Forth Baili Scientific Research Project of Chinese Journal of Pediatrics(B2016-C-3); Clinical Medical Research Project of West China Second University Hospital, Sichuan University(K012)
引用本文:

孙小妹, 曹杨, 戴亮, 孙飞扬, 董丽群. 初发过敏性紫癜患儿发病早期肾脏受累危险因素分析[J]. 中华妇幼临床医学杂志(电子版), 2019, 15(02): 143-149.

Xiaomei Sun, Yang Cao, Liang Dai, Feiyang Sun, Liqun Dong. Risk factors of renal involvement in children with primary Henoch-Schönlein purpura in the early stage[J]. Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition), 2019, 15(02): 143-149.

目的

探讨初发过敏性紫癜(HSP)患儿发病早期肾脏受累的危险因素,为合并肾脏受累危险因素的HSP患儿的临床早期干预提供参考。

方法

选择2011年1月至2015年12月,于四川大学华西第二医院儿科接受住院治疗的1 402例初发HSP患儿为研究对象。根据HSP患儿发病早期是否合并肾脏受累,将其分为肾脏受累组(n=423)与对照组(n=979,肾脏未受累)。采用回顾性分析方法,收集所有患儿的临床病例资料。2组患儿性别、发病年龄、居住地区、发病季节、发病至确诊时间的构成比,发病早期皮疹、胃肠道症状、关节肿痛、肾脏受累、血管神经性水肿、神经系统受累发生率等比较,采用χ2检验。采用多因素非条件logistic回归分析,评估HSP患儿发病早期肾脏受累的独立危险因素。本研究遵循的程序符合2013年修订的《世界医学协会赫尔辛基宣言》要求,并与所有受试儿监护人签署临床研究知情同意书。

结果

①本研究1 402例患儿中,发病早期合并肾脏受累为423例(30.17%),合并胃肠道症状为937例(66.84%),合并关节肿痛症状为609例(43.33%),合并血管神经性水肿为352例(25.11%),合并神经系统受累为31例(2.21%),所有患儿合并皮疹。②发病早期肾脏受累影响因素的单因素分析结果显示,2组HSP患儿的发病年龄、发病季节、发病至确诊时间的构成比比较,差异均有统计学意义(χ2=53.682,P<0.001;χ2=11.990,P=0.007;χ2=14.635,P<0.001)。肾脏受累组患儿居住于农村、无关节肿痛症状、合并血管神经性水肿所占比例,均显著高于对照组,并且差异均有统计学意义(χ2=10.032,P=0.002;χ2=6.514,P=0.011;χ2=6.362,P=0.012)。③多因素非条件logistic回归分析结果显示,HSP患儿的发病年龄为≥5~7岁(OR=2.23,95%CI:1.42~3.51,P<0.001),≥7~9岁(OR=2.38,95%CI:1.51~3.76,P<0.001),≥9岁(OR=4.11,95%CI:2.65~6.36,P<0.001),以及于秋季发病(OR=1.61,95%CI:1.09~2.37,P=0.014)与冬季发病(OR=1.79,95%CI:1.09~2.37,P=0.001),发病至确诊时间≥8 d(OR=1.59,95%CI:1.17~2.17,P=0.004),居住于农村(OR=1.37,95%CI:1.07~1.76,P=0.012)及合并血管神经性水肿(OR=1.74,95%CI:1.32~2.31,P<0.001),均为HSP患儿发病早期肾脏受累的独立危险因素;而合并关节肿痛(OR=0.77,95%CI:0.60~0.99,P=0.038),则为HSP患儿发病早期肾脏受累的独立保护因素。

结论

本研究第一次提出合并血管神经性水肿,是初发HSP患儿发病早期肾脏受累的独立危险因素。HSP患儿发病年龄≥5岁、于秋季或者冬季发病、发病至确诊时间≥8 d、居住于农村等,亦均为该病患儿发病早期肾脏受累的独立危险因素。

Objective

To explore the risk factors of renal involvement in children with primary Henoch-Sch?nlein purpura (HSP) in the early stage, and provide clinical references for early intervention of HSP these children with risk factors of renal involvement.

Methods

A total of 1 402 children with primary HSP who hospitalized in Department of Pediatrics, West China Second University Hospital, Sichuan University from January 2011 to December 2015 were included in this study. According to whether combined with renal involvement or not in the early stage of HSP, these children were divided into the renal involvement group (n=423) and control group (n=979, without renal involvement). Their demographic data and clinical manifestation were collected by retrospective method. Constituent ratios of gender, age of onset, residential area, season of onset and duration from symptoms onset to diagnosis, and incidences of skin rash, gastrointestinal symptoms, joint swelling and pain, renal involvement, angioneurotic edema, and nervous system involvement in the early stage were compared between two groups by chi-square test. Multivariate unconditional logistic regression analysis was used to assess the risk factors of renal involvement in children with HSP in the early stage. This study was in line with the World Medical Association Declaration of Helsinki revised in 2013. The guardians of all children signed the clinical research informed consents.

Results

①Among the 1 402 children with HSP, 423 cases (30.17%) occurred renal involvement in the early stage of onset, 937 cases (66.84%) with gastrointestinal symptoms, 609 cases (43.33%) with joint swelling and pain, 352 cases (25.11%) with angioneurotic edema, 31 cases (2.21%) with nervous system involvement, and all cases (100%) with skin rash. ②Univariate analysis of the influencing factors of renal involvement in the early stage of HSP showed that there were statistically significant differences between two groups in constituent ratios of age of onset, season of onset, and duration from symptoms onset to diagnosis (χ2=53.682, P<0.001; χ2=11.990, P=0.007; χ2=14.635, P<0.001). And the proportions of children lived in rural areas, without joint swelling or pain and with angioneurotic edema in renal involvement group all were statistically higher than those in control group, and all the differences were statistically significant (χ2=10.032, P=0.002; χ2=6.514, P=0.011; χ2=6.362, P=0.012). ③Multivariate unconditional logistic regression analysis results showed that the onset age of HSP≥5 years old (≥5-7 years old, OR=2.23, 95%CI: 1.42-3.51, P<0.001; ≥7-9 years old, OR=2.38, 95%CI: 1.51-3.76, P<0.001; ≥9 years old, OR=4.11, 95%CI: 2.65-6.36, P<0.001), onset in the autumn (OR=1.61, 95%CI: 1.09-2.37, P=0.014) and winter (OR=1.79, 95%CI: 1.09-2.37, P=0.001), the duration from symptoms onset to diagnosis ≥8 d (OR=1.59, 95%CI: 1.17-2.17, P=0.004), living in rural areas (OR=1.37, 95%CI: 1.07-1.76, P=0.012) and combined with angioneurotic edema (OR=1.74, 95%CI: 1.32-2.31, P<0.001) were independent risk factors for renal involvement in children with HSP in the early stage. While combined with joint swelling and pain (OR=0.77, 95%CI: 0.60-0.99, P=0.038) was independent protective factors for renal involvement in children with HSP in the early stage.

Conclusions

Results in this study first show that HSP children combined with angioneurotic edema have high risk of renal involvement in the early stage of HSP and reconfirm that onset age of HSP ≥5 years old, onset in autumn or winter, duration from symptoms onset to diagnosis ≥8 d, and residence in rural areas all are the independent risk factors for renal involvements in children with primary HSP in the early stage.

表1 1 402例过敏性紫癜患儿发病早期的临床资料分析[例数(%)]
表2 2组过敏性紫癜患儿发病早期肾脏受累影响因素的单因素分析结果[例数(%)]
表3 过敏性紫癜患儿发病早期肾脏受累影响因素的多因素非条件logistic回归分析的变量含义及赋值情况
表4 过敏性紫癜患儿发病早期肾脏受累影响因素的多因素非条件logistic回归分析结果
[1]
Gardner-Medwin JM, Dolezalova P, Cummins C, et al. Incidence of Henoch-Schönlein purpura, Kawasaki disease, and rare vasculitides in children of different ethnic origins[J]. Lancet, 2002, 360(9341): 1197-1202.
[2]
Yang YH, Hung CF, Hsu CR, et al. A nationwide survey on epidemiological characteristics of childhood Henoch-Schönlein purpura in Taiwan[J]. Rheumatology, 2005, 44(5): 618-622.
[3]
李克莉,刘大卫,武文娣,等. 中国六个市2007~2009年过敏性紫癜住院病例发病情况分析[J]. 中国疫苗和免疫,2011, 17(2): 128-132.
[4]
Davin JC, Coppo R. Henoch-Schönlein purpura nephritis in children[J]. Nat Rrev Nephrol, 2014, 10(10): 563-573.
[5]
吴小川. 儿童过敏性紫癜循证诊治建议解读[J]. 中华儿科杂志,2013, 51(7): 508-511.
[6]
Jauhola O, Ronkainen J, Koskimies O, et al. Renal manifestations of Henoch-Schonlein purpura in a 6-month prospective study of 223 children[J]. Arch Dis Child, 2010, 95(11): 877-882.
[7]
Chan H, Tang YL, Lv XH, et al. Risk Factors associated with renal involvement in childhood Henoch-Schönlein purpura: a Meta-analysis[J]. PLoS One, 2016, 11(11): e0167346.
[8]
Sano H, Izumida M, Shimizu H, et al. Risk factors of renal involvement and significant proteinuria in Henoch-Schönlein purpura[J]. Eur J Pediatr, 2002, 161(4): 196-201.
[9]
Ronkainen J, Nuutinen M, Koskimies O. The adult kidney 24 years after childhood Henoch-Schönlein purpura: a retrospective cohort study[J]. Lancet, 2002, 360(9334): 666-670.
[10]
Bogdanović R. Henoch-Schönlein purpura nephritis in children: risk factors, prevention and treatment[J]. Acta Paediatr, 2009, 98(12): 1882-1889.
[11]
Ozen S, Pistorio A, Iusan SM, et al. EULAR/ PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part Ⅱ:Final classification criteria[J]. Ann Rheum Dis, 2010, 69(5): 798-806.
[12]
Chen JY, Mao JH. Henoch-Schönlein purpura nephritis in children: incidence, pathogenesis and management[J]. World J Pediatr, 2015, 11(1): 29-34.
[13]
Rostoker G. Schönlein-henoch purpura in children and adults: diagnosis, pathophysiology and management[J]. BioDrugs, 2001, 15(2): 99-138.
[14]
Rigante D, Candelli M, Federico G, et al. Predictive factors of renal involvement or relapsing disease in children with Henoch-Schönlein purpura[J]. Rheumatol Int, 2005, 25(1): 45-48.
[15]
孙小妹,戴亮,孙飞扬,等. 成都地区与川西高原地区过敏性紫癜患儿临床特征比较[J]. 现代预防医学,2018, 45(12): 2274-2276, 2287.
[16]
Zhao YL, Liu ZJ, Bai XM, et al. Obesity increases the risk of renal involvement in children with Henoch-Schonlein purpura[J]. Eur J Pediatr, 2015, 174(10): 1357-1363.
[17]
Shin JI, Park JM, Shin YH, et al. Predictive factors for nephritis, relapse, and significant proteinuria in childhood Henoch-Schönlein purpura[J]. Scand J Rheumatol, 2006, 35(1): 56-60.
[18]
de Almeida JL, Campos LM, Paim LB, et al. Renal involvement in Henoch-Schönlein purpura: a multivariate analysis of initial prognostic factors[J]. J Pediatr (Rio J), 2007, 83(3): 259-266.
[19]
Narchi H. Risk of long term renal impairment and duration of follow up recommended for Henoch-Schonlein purpura with normal or minimal urinary findings: a systematic review[J]. Arch Dis Child, 2005, 90(9): 916-920.
[20]
Gupta V, Aggarwal A, Gupta R, et al. Differences between adult and pediatric onset Henoch-Schonlein purpura from North India[J]. Int J Rheum Dis, 2018, 21(1): 292-298.
[21]
Algoet C, Proesmans W. Renal biopsy 2-9 years after Henoch Schönlein purpura[J]. Pediatr Nephrol, 2003, 18(5): 471-473.
[22]
Yang YH, Hung CF, Hsu CR, et al. A nationwide survey on epidemiological characteristics of childhood Henoch-Schönlein purpura in Taiwan[J]. Rheumatology (Oxford), 2005, 44(5): 618-622.
[23]
Wang XH, Zhu YM, Gao LQ, et al. Henoch-Schönlein purpura with joint swelling and involvement: analysis of 71 cases[J]. Pediatr Rheumatol Online J, 2016, 14(1): 20.
[24]
Wang K, Sun X, Cao Y, et al. Risk factors for renal involvement and severe kidney disease in 2 731 Chinese children with Henoch-Schönlein purpura: a retrospective study[J]. Medicine (Baltimore), 2018, 97(38): e12520.
[25]
Lee YH, Kim YB, Koo JW, et al. Henoch-Schonlein purpura in children hospitalized at a tertiary hospital during 2004-2015 in Korea: epidemiology and clinical management[J]. Pediatr Gastroenterol Hepatol Nutr, 2016, 19(3): 175-185.
[26]
Mao YY, Yin L, Huang H, et al. Henoch-Schönlein purpura in 535 Chinese children: clinical features and risk factors for renal involvement[J]. J Int Med Res, 2014, 42(4): 1043-1049.
[27]
刘雄彪,汪晓红,刘璐苑,等. 过敏性紫癜伴发血管神经性水肿7例[J]. 中国皮肤性病学杂志,2017, 31(8): 927.
[28]
Duman MA, Duru NS, Çalışkan B, et al. Lumbar swelling as the unusual presentation of Henoch-Schonlein purpura in a child[J]. Balkan Med J, 2016, 33(3): 360-362.
[29]
王佳佩,吴菱,王天波,等. 伴血管神经性水肿的过敏性紫癜患儿预后及治疗[J]. 临床荟萃,2017, 32(1): 68-70.
[1] 张璇, 马宇童, 苗玉倩, 张云, 吴士文, 党晓楚, 陈颖颖, 钟兆明, 王雪娟, 胡淼, 孙岩峰, 马秀珠, 吕发勤, 寇海燕. 超声对Duchenne肌营养不良儿童膈肌功能的评价[J]. 中华医学超声杂志(电子版), 2023, 20(10): 1068-1073.
[2] 张宝富, 俞劲, 叶菁菁, 俞建根, 马晓辉, 刘喜旺. 先天性原发隔异位型肺静脉异位引流的超声心动图诊断[J]. 中华医学超声杂志(电子版), 2023, 20(10): 1074-1080.
[3] 韩丹, 王婷, 肖欢, 朱丽容, 陈镜宇, 唐毅. 超声造影与增强CT对儿童肝脏良恶性病变诊断价值的对比分析[J]. 中华医学超声杂志(电子版), 2023, 20(09): 939-944.
[4] 刘婷婷, 林妍冰, 汪珊, 陈幕荣, 唐子鉴, 代东伶, 夏焙. 超声衰减参数成像评价儿童代谢相关脂肪性肝病的价值[J]. 中华医学超声杂志(电子版), 2023, 20(08): 787-794.
[5] 周钰菡, 肖欢, 唐毅, 杨春江, 周娟, 朱丽容, 徐娟, 牟芳婷. 超声对儿童髋关节暂时性滑膜炎的诊断价值[J]. 中华医学超声杂志(电子版), 2023, 20(08): 795-800.
[6] 刘欢颜, 华扬, 贾凌云, 赵新宇, 刘蓓蓓. 颈内动脉闭塞病变管腔结构和血流动力学特征分析[J]. 中华医学超声杂志(电子版), 2023, 20(08): 809-815.
[7] 唐旭, 韩冰, 刘威, 陈茹星. 结直肠癌根治术后隐匿性肝转移危险因素分析及预测模型构建[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 16-20.
[8] 李建美, 邓静娟, 杨倩. 两种术式联合治疗肝癌合并肝硬化门静脉高压的安全性及随访评价[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 41-44.
[9] 吴方园, 孙霞, 林昌锋, 张震生. HBV相关肝硬化合并急性上消化道出血的危险因素分析[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 45-47.
[10] 逄世江, 黄艳艳, 朱冠烈. 改良π形吻合在腹腔镜全胃切除消化道重建中的安全性和有效性研究[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 66-69.
[11] 杨体飞, 杨传虎, 陆振如. 改良无充气经腋窝入路全腔镜下甲状腺手术对喉返神经功能的影响研究[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 74-77.
[12] 陈旭渊, 罗仕云, 李文忠, 李毅. 腺源性肛瘘经手术治疗后创面愈合困难的危险因素分析[J]. 中华普外科手术学杂志(电子版), 2024, 18(01): 82-85.
[13] 陆猛桂, 黄斌, 李秋林, 何媛梅. 蜂蛰伤患者发生多器官功能障碍综合征的危险因素分析[J]. 中华临床医师杂志(电子版), 2023, 17(9): 1010-1015.
[14] 刘笑笑, 张小杉, 刘群, 马岚, 段莎莎, 施依璐, 张敏洁, 王雅晳. 中国学龄前儿童先天性心脏病流行病学研究进展[J]. 中华临床医师杂志(电子版), 2023, 17(9): 1021-1024.
[15] 李达, 张大涯, 陈润祥, 张晓冬, 黄士美, 陈晨, 曾凡, 陈世锔, 白飞虎. 海南省东方市幽门螺杆菌感染现状的调查与相关危险因素分析[J]. 中华临床医师杂志(电子版), 2023, 17(08): 858-864.
阅读次数
全文


摘要