目的 分析过敏性紫癜(Henoch-Sch?nlein purpura,HSP)患儿血清降解单糖的水平变化特点,并探讨其临床意义。 方法 前瞻性选取2019年9月至2022年1月诊断为HSP的132例患儿为研究对象,另选取健康儿童132例为对照组,利用高效液相色谱技术分析2组血清降解单糖的含量。通过受试者工作特征曲线分析降解单糖的诊断效果。 结果 HSP患儿血清降解甘露糖、氨基葡萄糖、氨基半乳糖和半乳糖浓度均高于对照组(P<0.001),4种降解单糖的曲线下面积分别为0.919、0.913、0.832、0.932(P<0.05),对HSP具有诊断价值。 结论 HSP患儿血清中降解甘露糖、氨基葡萄糖、氨基半乳糖和半乳糖的含量高,其水平对HSP的诊断可能具有重要价值。
Abstract
Objective To examine the serum levels of degraded monosaccharides in children with Henoch-Sch?nlein purpura (HSP) and to study the clinical significance of degraded monosaccharides in HSP. Methods A prospective analysis was performed on 132 children who were diagnosed with HSP from September 2019 to January 2022, and 132 healthy children were enrolled as the control group. High-performance liquid chromatography was used to determine the content of degraded monosaccharides in serum in both groups. The receiver operating characteristic (ROC) curve was used to evaluate the efficiency of degraded monosaccharides for the diagnosis of HSP. Results Compared with the control group, the HSP group had significantly higher serum levels of mannose, glucosamine, aminogalactose, and galactose (P<0.001). The four degraded monosaccharides had an area under the ROC curve of 0.919, 0.913, 0.832, and 0.932 respectively for the diagnosis of HSP (P<0.05). Conclusions Children with HSP have higher serum levels of mannose, glucosamine, aminogalactose, and galactose than the healthy population. The levels of degraded monosaccharides may have an important value for the diagnosis of HSP.
关键词
过敏性紫癜 /
单糖 /
诊断 /
儿童
Key words
Henoch-Sch?nlein purpura /
Monosaccharide /
Diagnosis /
Child
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
1 尹薇, 陈晶. 儿童过敏性紫癜免疫机制研究[J]. 中华实用儿科临床杂志, 2017, 32(21): 1604-1607. DOI: 10.3760/cma.j.issn.2095-428X.2017.21.002.
2 刘丽君, 于静, 李宇宁. 儿童过敏性紫癜325例回顾性分析[J]. 中国当代儿科杂志, 2015, 17(10): 1079-1083. PMID: 26483228. DOI: 10.7499/j.issn.1008-8830.2015.10.012.
3 高春林, 夏正坤. 从过敏性紫癜到IgA血管炎——发病机制新认识[J]. 中国实用儿科杂志, 2022, 37(1): 12-16. DOI: 10.19538/j.ek2022010603.
4 Nakazawa S, Imamura R, Kawamura M, et al. Evaluation of IgA1 O-glycosylation in Henoch-Sch?nlein purpura nephritis using mass spectrometry[J]. Transplant Proc, 2019, 51(5): 1481-1487. PMID: 31084922. DOI: 10.1016/j.transproceed.2019.01.122.
5 Hastings MC, Moldoveanu Z, Suzuki H, et al. Biomarkers in IgA nephropathy: relationship to pathogenetic hits[J]. Expert Opin Med Diagn, 2013, 7(6): 615-627. PMID: 24175678. PMCID: PMC4557957. DOI: 10.1517/17530059.2013.856878.
6 王晓龙, 王秀然, 卢天成. 蛋白质糖基化修饰的研究进展[J]. 基因组学与应用生物学, 2017, 36(10): 4380-4384. DOI: 10.13417/j.gab.036.004380.
7 Zhang M, Zhang Y, Ma X, et al. Using a PCR instrument to hydrolyze polysaccharides for monosaccharide composition analyses[J]. Carbohydr Polym, 2020, 240: 116338. PMID: 32475593. DOI: 10.1016/j.carbpol.2020.116338.
8 Hu M, Lan Y, Lu A, et al. Glycan-based biomarkers for diagnosis of cancers and other diseases: past, present, and future[J]. Prog Mol Biol Transl Sci, 2019, 162: 1-24. PMID: 30905444. DOI: 10.1016/bs.pmbts.2018.12.002.
9 中华医学会儿科学分会免疫学组, 《中华儿科杂志》编辑委员会. 儿童过敏性紫癜循证诊治建议[J]. 中华儿科杂志, 2013, 51(7): 502-507. DOI:10.3760/cma.j.issn.0578-1310.2013.07.006.
10 Varki A. Biological roles of glycans[J]. Glycobiology, 2017, 27(1): 3-49. PMID: 27558841. PMCID: PMC5884436. DOI: 10.1093/glycob/cww086.
11 章晓联. 蛋白糖基化与免疫[J]. 中国免疫学杂志, 2004, 20(4): 290-293.
12 中华医学会儿科学分会肾脏学组. 紫癜性肾炎诊治循证指南(2016)[J]. 中华儿科杂志, 2017, 55(9): 647-651. PMID: 28881507. DOI: 10.3760/cma.j.issn.0578-1310.2017.09.003.
13 康志娟, 刘波, 李志辉. 半乳糖缺陷IgA1在儿童紫癜性肾炎早期诊断中的意义[J]. 中国当代儿科杂志, 2019, 21(2): 172-175. PMID: 30782282. PMCID: PMC7389824. DOI: 10.7499/j.issn.1008-8830.2019.02.013.
14 尹晶, 胡坚. 半乳糖缺陷IgA1及其在紫癜性肾炎和IgA肾病中的作用[J]. 海南医学, 2016, 27(5): 795-797. DOI: 10.3969/j.issn.1003-6350.2016.05.037.