北京大学学报(医学版) ›› 2023, Vol. 55 ›› Issue (5): 923-928. doi: 10.19723/j.issn.1671-167X.2023.05.022

• 论著 • 上一篇    下一篇

高原地区不同类型过敏性紫癜藏族患者发病的相关危险因素

魏慧1,次旦央宗2,益西拉姆2,白玛央金2,*()   

  1. 1. 北京大学第三医院风湿免疫科, 北京 100191
    2. 西藏自治区人民医院风湿免疫血液内科, 拉萨 850000
  • 收稿日期:2022-08-02 出版日期:2023-10-18 发布日期:2023-10-09
  • 通讯作者: 白玛央金 E-mail:13518986955@163.com
  • 基金资助:
    西藏自然科学基金(XZ2021ZR-ZY06(Z))

Risk factors associated with different types of Henoch-Schönlein purpura in Tibetan patients at high altitude

Hui WEI1, Ci-dan-yang-zong2, Yi-xi-la-mu2, Bai-ma-yang-jin2,*()   

  1. 1. Department of Rheumatology and Immunology, Peking University Third Hospital, Beijing 100191, China
    2. Department of Rheumatology, Immunology and Hematology, Tibet Autonomous Region People's Hospital, Lhasa 850000, China
  • Received:2022-08-02 Online:2023-10-18 Published:2023-10-09
  • Contact: Bai-ma-yang-jin E-mail:13518986955@163.com
  • Supported by:
    the Natural Science Foundation of Tibet Autonomous Region(XZ2021ZR-ZY06(Z))

RICH HTML

  

摘要:

目的: 分析高原地区不同类型过敏性紫癜(Henoch-Schönlein purpura, HSP)藏族患者发病的相关危险因素, 为高原地区正确识别过敏性紫癜高危患者提供参考。方法: 选择2014年4月至2022年3月西藏自治区人民医院风湿免疫血液内科收治的304例藏族HSP患者的病例资料进行回顾性分析, 收集患者性别、年龄、过敏史、家族史、实验室指标[血红蛋白、血小板计数、嗜酸性粒细胞、C反应蛋白(C-reactive protein, CRP)、白蛋白、免疫球蛋白G、免疫球蛋白A、补体C3、补体C4和红细胞沉降率(erythrocyte sedimentation rate, ESR)]等数据, 采用单因素和多因素Logistic回归分析不同类型过敏性紫癜藏族患者发病的危险因素。结果: 肾型HSP患者表现出较高的IgA[(9.2±1.7) g/L vs. (6.4±2.4) g/L, P=0.015]、较低的补体C3[(203.3±21.6) mg/dL vs. (301.1±19.5) mg/dL, P=0.043]和补体C4[(33.5±2.3) mg/dL vs. (53.0±7.2) mg/dL, P=0.032], 腹型HSP患者表现出较低的血红蛋白[(119.6±19.6) g/L vs. (146.6±47.3) g/L, P=0.038]和血浆白蛋白[24.8 (22.1, 33.9) g/L vs. 32.6 (24.6, 35.1) g/L, P=0.045], 关节型HSP患者表现出更高的CRP[13.5 (0.2, 20.6) g/L vs. 7.5 (0.1, 15.2) g/L, P=0.036]和ESR[24 (5, 40) mm/h vs. 15 (4, 30) mm/h, P=0.049]。IgA升高、补体C4减低是肾型HSP的危险因素, 贫血、血浆白蛋白降低是腹型HSP的危险因素, CRP升高是关节型HSP的危险因素。结论: 高原地区不同类型的HSP临床特点存在差异, 对于高IgA血症、低补体C4、贫血、低白蛋白血症、CRP明显升高的患者应高度警惕, 给予早期有效干预可以提高临床疗效, 避免病情向重症发展, 改善预后。

关键词: 过敏性紫癜, 高原, 临床类型, 危险因素

Abstract:

Objective: To investigate the risk factors of different types of Henoch-Schönlein purpura (HSP) in Tibetan patients at high altitude, as to provide reference for correctly identifying high-risk patients. Methods: A retrospective study was used to analyze the 304 HSP patients admitted to Tibet Autonomous Region People's Hospital from April 2014 to March 2022. The gender, age, allergic history, family history, clinical type, laboratory indexes (hemoglobin, platelet count, eosinophil, C-reactive protein (CRP), albumin, immunoglobulin G, immunoglobulin A, complement C3 and C4) were analyzed retrospectively. Univariate and multivariate Logistic regression analysis to screen for risk factors affecting different types of HSP. Results: Renal HSP patients showed higher IgA [(9.2±1.7) g/L vs. (6.4±2.4) g/L, P=0.015], lower complement C3 [(203.3±21.6) mg/dL vs. (301.1±19.5) mg/dL, P=0.043], and complement C4 [(33.5±2.3) mg/dL vs. (53.0±7.2) mg/dL, P=0.032]. The patients with abdominal HSP showed lower levels of hemoglobin [(119.6±19.6) g/L vs. (146.6±47.3) g/L, P=0.038] and plasma albumin [24.8 (22.1, 33.9) g/L vs. 32.6 (24.6, 35.1) g/L, P=0.045]. The patients with articular HSP exhibited higher CRP [13.5 (0.2, 20.6) g/L vs. 7.5 (0.1, 15.2) g/L, P=0.036] and erythrocyte sedimentation rate (ESR) [24 (5, 40) mm/h vs. 15 (4, 30) mm/h, P=0.049]. Elevated IgA and decreased complement C4 were risk factors for renal HSP, anemia and decreased plasma albumin were risk factors for abdominal HSP, and elevated CRP was a risk factor for articular HSP. Conclusion: The clinical characteristics of different types of HSP in plateau areas were different. Patients with high IgA, low complement C4, anemia, hypoalbuminemia, and significantly elevated CRP should be highly vigilant. Early and effective intervention can improve the clinical efficacy, avoid severe development, and improve the prognosis

Key words: Henoch-Schönlein purpura (HSP), High altitude area, Subclinical manifestations, Risk factors

中图分类号: 

  • R554.6

表1

藏族HSP患者一般资料比较"

Items Renal involvement P Abdominal involvement P Articular involvement P
With Without With Without With Without
Male, n(%) 38 (45.2) 136 (61.8) 0.009 71 (57.7) 103 (56.9) 0.888 21(47.7) 153 (58.8) 0.168
Age/years, M(P25, P75) 27 (18, 41) 28 (18, 20) 0.586 24 (18, 41) 29 (18, 41) 0.045 26 (21, 39) 28 (20, 40) 0.497
Body mass index, ${\bar x}$ ± s 21.1±3.3 22.6±2.9 0.461 20.6±2.7 21.4±3.2 0.373 23.5±5.1 23.6±4.7 0.582
Allergy history, n(%) 30 (35.7) 82 (37.3) 0.801 65 (52.8) 57 (31.5) 0.000 16 (36.4) 96 (36.9) 0.943
Family history, n(%) 17 (20.2) 11 (5.0) 0.000 15 (12.2) 13 (7.2) 0.138 6 (13.6) 22 (8.5) 0.035

表2

肾型过敏性紫癜与非肾型过敏性紫癜实验室结果比较"

Projects Renal HSP (n=84) Without-R HSP (n=220) P
HGB/(g/L), ${\bar x}$ ± s 128.6±23.4 126.6±17.3 0.448
Neutrophils/(×109/L),${\bar x}$ ± s 5.8±3.7 4.9±1.2 0.798
Eosinophils/(×109/L),M(P25, P75) 0.02 (0.00, 0.03) 0.02 (0.00, 0.02) 0.849
Platelets/(×109/L),${\bar x}$ ± s 498.7±80.2 394.2±53.7 0.041
CRP/(g/L), M(P25, P75) 9.4 (0.2, 19.4) 9.5 (0.1, 15.2) 0.737
ESR/(mm/h), M(P25, P75) 15 (4, 31) 15 (4, 30) 0.887
D-dimer/(mg/L), M(P25, P75) 0.27 (0.11, 0.98) 0.28 (0.12, 1.02) 0.053
Albumin/(g/L),M(P25, P75) 30.8 (24.1, 33.9) 30.6 (24.6, 35.1) 0.796
IgG/(g/L),${\bar x}$ ± s 18.9±2.5 18.8±3.4 0.258
IgA/(g/L),${\bar x}$ ± s 9.2±1.7 6.4±2.4 0.015
IgM/(g/L),${\bar x}$ ± s 1.6±0.4 1.5±0.7 0.912
IgE/(g/L),${\bar x}$ ± s 795.1±37.2 577.6±25.3 0.041
Complement C3/(mg/dL),${\bar x}$ ± s 203.3±21.6 301.1±19.5 0.043
Complement C4/(mg/dL),${\bar x}$ ± s 33.5±2.3 53.0±7.2 0.032

表3

腹型过敏性紫癜与非腹型过敏性紫癜实验室结果比较"

Items Abdominal HSP (n=123) Without-A HSP (n=181) P
HGB/(g/L), ${\bar x}$ ± s 119.6±19.6 146.6±47.3 0.038
Neutrophils/(×109/L),${\bar x}$ ± s 7.8±1.7 5.9±1.3 0.049
Eosinophils/(×109/L),M(P25, P75) 0.02 (0.00, 0.03) 0.02 (0.00, 0.02) 0.849
Platelets/(×109/L), ${\bar x}$ ± s 598.7±80.2 394.2±53.7 0.026
CRP/(g/L),M(P25, P75) 9.4 (0.2, 19.4) 9.5 (0.1, 15.2) 0.737
ESR/(mm/h),M(P25, P75) 15 (4, 31) 15 (4, 30) 0.887
D-Dimer/(mg/L),M(P25, P75) 0.27 (0.11, 0.98) 0.28 (0.12, 1.02) 0.053
Albumin/(g/L),M(P25, P75) 24.8 (22.1, 33.9) 32.6 (24.6, 35.1) 0.045
IgG/(g/L), ${\bar x}$ ± s 15.8±2.8 17.2±3.6 0.289
IgA/(g/L), ${\bar x}$ ± s 6.2±3.2 6.4±2.4 0.985
IgM/(g/L), ${\bar x}$ ± s 1.7±0.7 1.6±0.2 0.998
IgE/(g/L), ${\bar x}$ ± s 532.1±31.2 577.6±21.3 0.761
Complement C3 (mg/dL), ${\bar x}$ ± s 403.3±36.6 375.2±27.8 0.998
Complement C4 (mg/dL), ${\bar x}$ ± s 58.5±3.6 53.0±7.2 0.979

表4

关节型过敏性紫癜与非关节型过敏性紫癜实验室结果比较"

Projects Articular HSP (n=44) Withont-Ar HSP (n=260) P
HGB/(g/L), ${\bar x}$ ± s 137.6±13.6 142.6±27.3 0.977
Neutrophils/(×109/L), ${\bar x}$ ± s 7.9±1.7 8.8±2.1 0.599
Eosinophils/(×109/L), M(P25, P75) 0.02 (0.00, 0.03) 0.02 (0.00, 0.02) 0.898
Platelets/(×109/L), ${\bar x}$ ± s 578.7±39.2 533.1±42.3 0.772
CRP/(g/L), M(P25, P75) 13.5 (0.2, 20.6) 7.5 (0.1, 15.2) 0.036
ESR/(mm/h), M(P25, P75) 24 (5, 40) 15 (4, 30) 0.049
D-dimer/(mg/L), M(P25, P75) 0.28 (0.11, 0.98) 0.28 (0.12, 1.02) 0.853
Albumin/(g/L), M(P25, P75) 29.8 (22.1, 33.9) 32.6 (24.6, 35.1) 0.645
IgG/(g/L), ${\bar x}$ ± s 18.8±2.2 17.8±3.0 0.364
IgA/(g/L), ${\bar x}$ ± s 6.2±3.6 6.4±2.5 0.999
IgM/(g/L), ${\bar x}$ ± s 1.2±0.4 1.4±0.3 0.999
IgE/(g/L), ${\bar x}$ ± s 537.1±31.2 575.6±21.3 0.766
Complement C3 (mg/dL), ${\bar x}$ ± s 403.3±37.1 375.2±27.8 0.995
Complement C4 (mg/dL), ${\bar x}$ ± s 50.5±8.8 53.0±9.1 0.980

表5

不同类型HSP患者的易感因素单因素分析"

Predisposing factors Clinical type P OR 95%CI
With Without
Renal involvement
    Male 38 136 0.009 0.764 0.291-1.339
    Family history 17 11 0.000 4.430 1.119-11.257
    Elevate of platelets 74 193 0.930 0.689 0.226-1.385
    Elevate of IgA 80 108 0.000 3.284 1.430-9.884
    Elevate of IgE 77 204 0.511 0.336 0.280-1.332
    Decrease of complement C3 46 119 0.916 3.058 1.066-10.729
    Decrease of complement C4 63 41 0.000 0.223 0.096-0.892
Abdominal involvement
    Age ≤ 20 years old 67 86 0.234 0.778 1.591-19.758
    Allergy history 65 57 0.000 2.469 1.120-15.169
    Anemia 109 65 0.000 3.472 1.984-5.276
    Elevate of neutrophils 103 152 0.956 0.722 0.135-1.398
    Elevate of platelets 112 155 0.156 0.987 1.233-4.920
    Decrease of albumin 88 64 0.000 2.405 1.025-5.647
Articular involvement
    Family history 6 22 0.035 3.059 1.182-7.334
    Elevate of ESR 38 228 0.805 0.382 0.175-3.445
    Elevate of CRP 30 242 0.020 1.973 1.069-4.328

表6

不同类型HSP患者易感因素多因素分析"

Risk factors B SE Wald P OR 95%CI
Renal involvement
    Male 1.329 0.744 3.256 0.986 1.002 0.834-1.017
    Family history 1.466 0.662 4.539 0.634 1.141 1.010-15.169
    Elevate of IgA 1.432 0.661 4.589 0.041 4.132 1.130-15.267
    Decrease of complement C4 1.756 0.823 5.319 0.044 2.405 1.025-5.647
Abdominal involvement
    Allergy history 1.734 0.643 7.195 0.978 5.603 1.591-19.758
    Anemia 1.426 0.663 4.538 0.034 4.132 1.120-15.169
    Decrease of albumin 0.879 0.445 4.067 0.044 2.405 1.025-5.647
Articular involvement
    Family history 1.726 0.784 4.597 0.749 1.382 1.075-3.445
    Elevate of CRP 1.255 0.787 5.203 0.003 4.331 1.357-9.644
1 Wakaki H , Ishikura K . Henoch-Schönlein nephritis with nephrotic state in children: Predictors of poor outcomes[J]. Pediatr Nephrol, 2012, 27 (2): 335.
doi: 10.1007/s00467-011-2052-1
2 Ueda H , Miyazaki Y , Tsuboi N , et al. Clinical and pathological characteristics of elderly Japanese patients with IgA vasculitis with nephritis: A case series[J]. Intern Med, 2019, 58 (1): 31- 38.
doi: 10.2169/internalmedicine.1379-18
3 Cakici EK , Suker EDK , Ozlu SG , et al. MEFV gene mutations in children with Henoch-Schönlein purpura and their correlations-do mutations matter[J]. Clin Rheumatol, 2019, 38 (7): 1947- 1952.
doi: 10.1007/s10067-019-04489-2
4 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.
doi: 10.1016/S0140-6736(02)11279-7
5 Hetland LE , Susrud KS , Lindahl KH , et al. Henoch-Schönlein purpura: A literature review[J]. Acta Derm Venereol, 2017, 97 (10): 1160- 1166.
doi: 10.2340/00015555-2733
6 Wang H , Das L , Hoh SF , et al. Urinalysis monitoring in children with Henoch-Schönlein purpura: Is it time to revise[J]. Int J Rheum Dis, 2019, 22 (7): 1271- 1277.
doi: 10.1111/1756-185X.13552
7 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分析[J]. 现代预防医学, 2018, 45 (12): 2274-2276, 2287.
8 Delbet JD , Hogan J , Aoun B , et al. Clinical outcomes in children with Henoch-Schönlein purpura nephritis without crescents[J]. Pediatr Nephrol, 2017, 32 (7): 1193- 1199.
doi: 10.1007/s00467-017-3604-9
9 Novak J , Vu HL , Novak L , et al. Interactions of human mesangial cells with IgA and IgA-containing immune complexes[J]. Kidney Int, 2002, 62 (2): 465- 475.
doi: 10.1046/j.1523-1755.2002.00477.x
10 Tabel Y , Inanc FC , Dogan DG , et al. Clinical features of children with Henoch-Schönlein purpura: risk factors associated with renal involvement[J]. Iran J Kidney Dis, 2012, 6 (4): 269- 274.
11 Reamy BV , Servey JT , Williams PM . Henoch-Schönlein purpura (IgA vasculitis): Rapid evidence review[J]. Am Fam Physician, 2020, 102 (4): 229- 233.
12 Audemard-Verger A , Pillebout E , Guillevin L , et al. IgA vasculitis (Henoch-Shönlein purpura) in adults: Diagnostic and therapeutic aspects[J]. Autoimmun Rev, 2015, 14 (7): 579- 585.
doi: 10.1016/j.autrev.2015.02.003
13 央珍, 郭琳, 熊昊, 等. 西藏高原地区儿童过敏性紫癜的临床分析[J]. 中国当代儿科杂志, 2014, 16 (12): 1231- 1235.
14 曾传文, 格桑德吉, 达瓦曲珍, 等. 高原藏族儿童过敏性紫癜相关文献因素分析[J]. 中华危重病急救医学, 2019, 31 (6): 742- 745.
15 Tan J , Tang Y , Xu Y , et al. The clinicopathological characteristics of Henoch-Schönlein purpura nephritis with presentation of nephrotic syndrome[J]. Kidney Blood Press Res, 2019, 44 (4): 754- 764.
doi: 10.1159/000501459
16 Buscatti IM , Casella BB , Aikawa NE , et al. Henoch-Schönlein purpura nephritis: Initial risk factors and outcomes in a Latin American tertiary center[J]. Clin Rheumatol, 2018, 37 (5): 1319- 1324.
doi: 10.1007/s10067-017-3972-3
17 Karadag SG , Tanatar A , Sonmez HE , et al. The clinical spectrum of Henoch-Schönlein purpura in children: A single-center study[J]. Clin Rheumatol, 2019, 38 (6): 1707- 1714.
doi: 10.1007/s10067-019-04460-1
18 魏慧, 罗增, 次旦央宗, 等. 高原地区不同海拔高度腹型过敏性紫癜患者临床特征分析[J]. 北京大学学报(医学版), 2021, 53 (6): 1072- 1077.
[1] 魏慧, 张警丰, 姚中强, 赵金霞. 类风湿关节炎合并慢性病贫血患者的临床特征及相关因素[J]. 北京大学学报(医学版), 2026, 58(2): 307-312.
[2] 赵杰, 付春, 赵秀娟, 薛海岩, 李纾, 王振洲, 朱凤雪. 胸部创伤患者在重症监护病房内发生呼吸机相关性肺炎的危险因素[J]. 北京大学学报(医学版), 2026, 58(2): 351-358.
[3] 郭芷均, 俎明, 马超, 张贺军, 张静, 丁士刚. 同时性多发早期胃癌漏诊病灶的临床病理特征[J]. 北京大学学报(医学版), 2026, 58(2): 410-415.
[4] 李博闻, 张强, 孙益鑫. 儿童及青年漏斗胸患者Nuss术后发生脊柱侧弯的风险预测模型建立及验证[J]. 北京大学学报(医学版), 2025, 57(5): 941-946.
[5] 杨小勇, 张帆, 马潞林, 刘承. 前列腺导管腺癌临床特征及腺外侵犯的影响因素[J]. 北京大学学报(医学版), 2025, 57(5): 956-960.
[6] 刘伟, 郭稳, 过哲, 李春艳, 李云龙, 刘思奇, 张亮, 宋慧. 痛风患者放射学阴性骨侵蚀的相关危险因素[J]. 北京大学学报(医学版), 2025, 57(4): 735-739.
[7] 陆梦溪, 刘秋萍, 周恬静, 刘晓非, 孙烨祥, 沈鹏, 林鸿波, 唐迅, 高培. 基于社区人群队列的甘油三酯-葡萄糖指数与心血管病发病和死亡的关联[J]. 北京大学学报(医学版), 2025, 57(3): 430-435.
[8] 杨龙傲, 金旭, 黄文初, 何丽华, 陈娟. 视屏作业人员视疲劳及干眼的流行病学调查[J]. 北京大学学报(医学版), 2025, 57(3): 554-561.
[9] 王紫薇, 李闵, 高慧, 邓芳. 链球菌感染与过敏性紫癜肾炎患儿肾损害的相关性[J]. 北京大学学报(医学版), 2025, 57(2): 284-290.
[10] 郭华秋, 王哲, 杨雪, 白洁. 口腔急诊出血患者的临床特征与危险因素[J]. 北京大学学报(医学版), 2025, 57(1): 142-147.
[11] 邓敏婷, 王楠, 夏斌, 赵玉鸣, 朱俊霞. 儿童及青少年挫入恒前牙自行再萌出的相关影响因素[J]. 北京大学学报(医学版), 2025, 57(1): 148-153.
[12] 李钰锴, 王红彦, 罗靓, 李云, 李春. 抗磷脂抗体在白塞病合并血栓中的临床意义[J]. 北京大学学报(医学版), 2024, 56(6): 1036-1040.
[13] 田杨, 韩永正, 李娇, 王明亚, 曲音音, 房景超, 金辉, 李民, 王军, 徐懋, 王圣林, 郭向阳. 颈椎前路手术后硬膜外血肿的发生率和危险因素[J]. 北京大学学报(医学版), 2024, 56(6): 1058-1064.
[14] 王明瑞, 赖金惠, 姬家祥, 唐鑫伟, 胡浩浦, 王起, 许克新, 徐涛, 胡浩. 使用中文版威斯康星结石生活质量问卷预测肾结石患者生活质量降低的危险因素[J]. 北京大学学报(医学版), 2024, 56(6): 1069-1074.
[15] 李志存, 吴天俣, 梁磊, 范宇, 孟一森, 张骞. 穿刺活检单针阳性前列腺癌术后病理升级的危险因素分析及列线图模型构建[J]. 北京大学学报(医学版), 2024, 56(5): 896-901.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!