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与儿童起病系统性红斑狼疮内皮失调相关的生物标志物。

Biomarkers associating endothelial Dysregulation in pediatric-onset systemic lupus erythematous.

机构信息

Division of Allergy, Asthma, and Rheumatology, Department of Pediatrics, Chang Gung Memorial Hospital Linko branch, Taoyuan, Taiwan.

Chang Gung University, College of Medicine, Taoyuan, Taiwan.

出版信息

Pediatr Rheumatol Online J. 2019 Oct 24;17(1):69. doi: 10.1186/s12969-019-0369-7.

Abstract

BACKGROUND/PURPOSE: Endothelium is a key element in the regulation of vascular homeostasis and its alteration can lead to the development of vascular diseases. Systemic lupus erythematosus (SLE) is a systemic autoimmune disease with potential extensive vascular lesions, involving skin vessels, renal glomeruli, cardiovascular system, brain, lung alveoli, gastrointestinal tract vessels and more. We aimed to assess endothelial dysregulation related biomarkers in pediatric-onset SLE (pSLE) patient serum and elucidate its correlation with their clinical features, laboratory parameters, and the overall disease activity.

METHODS

Disease activities were evaluated by SLE disease activity index (SLEDAI). Patient characteristics were obtained by retrospective chart review. Six biomarkers associated with endothelial dysregulation, including Angiopoietin-1 (Ang-1), Angiopoietin-2 (Ang-2), Tie2, Vascular endothelial growth factor (VEGF), thrombomodulin, and a disintegrin-like and metalloprotease with thrombospondin type 1 motif (ADAMTS13) were tested through enzyme-linked immunosorbent assay (ELISA) measurement.

RESULTS

This study comprised 118 pSLE patients. Data from 40 age-matched healthy controls were also obtained. The mean diagnostic age was 13 ± 4.12 years-old and 90.7% are females. Serum levels of VEGF, Tie2, thrombomodulin were significantly higher while serum ADAMTS13 was lower in active pSLE patients when compared to those with inactive diseases (all p < 0.05). In organ specific association, serum thrombomodulin level was higher in pSLE patient with renal involvement, and serum ADAMTS13 levels was negatively associated with neurological involvement (p < 0.05). A cutoff of thrombomodulin at 3333.6 pg/ml best correlated renal involvement. (AUC = 0.752, p < 0.01).

CONCLUSION

Endothelial dysregulation associating proteins seems to be potent biomarkers for pSLE activity as well as organ involvement in pSLE patients. These biomarkers may be beneficial in understanding of the vascular pathogenesis and disease monitoring.

摘要

背景/目的:内皮细胞是调节血管稳态的关键因素,其改变可导致血管疾病的发生。系统性红斑狼疮(SLE)是一种全身性自身免疫性疾病,具有潜在的广泛血管病变,涉及皮肤血管、肾小球、心血管系统、大脑、肺肺泡、胃肠道血管等。我们旨在评估儿科发病的系统性红斑狼疮(pSLE)患者血清中的内皮功能障碍相关生物标志物,并阐明其与临床特征、实验室参数和整体疾病活动的相关性。

方法

通过 SLE 疾病活动指数(SLEDAI)评估疾病活动。通过回顾性图表审查获取患者特征。通过酶联免疫吸附试验(ELISA)测量,测试了 6 种与内皮功能障碍相关的生物标志物,包括血管生成素-1(Ang-1)、血管生成素-2(Ang-2)、Tie2、血管内皮生长因子(VEGF)、血栓调节蛋白和 a disintegrin-like and metalloprotease with thrombospondin type 1 motif (ADAMTS13)。

结果

本研究纳入了 118 例 pSLE 患者。还获得了 40 名年龄匹配的健康对照者的数据。平均诊断年龄为 13±4.12 岁,90.7%为女性。与疾病不活动的患者相比,活动期 pSLE 患者的血清 VEGF、Tie2、血栓调节蛋白水平显著升高,而 ADAMTS13 水平较低(均 p<0.05)。在器官特异性关联方面,有肾脏受累的 pSLE 患者血清血栓调节蛋白水平较高,而 ADAMTS13 水平与神经系统受累呈负相关(p<0.05)。血栓调节蛋白截断值为 3333.6 pg/ml 时与肾脏受累相关性最佳。(AUC=0.752,p<0.01)。

结论

与内皮功能障碍相关的蛋白似乎是 pSLE 活动以及 pSLE 患者器官受累的有效生物标志物。这些生物标志物可能有助于了解血管发病机制和疾病监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c9e/6814049/24a873ed8cc1/12969_2019_369_Fig1_HTML.jpg

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