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血清免疫球蛋白E水平:与 Gianotti-Crosti 综合征的临床病程是否存在关联?

The Serum Immunoglobulin E Level: Is There a Relationship With the Clinical Course of the Gianotti-Crosti Syndrome?

作者信息

Bassi Andrea, Pedaci Fausto, Oranges Teresa, Azzari Chiara, Galli Luisa, Ricci Silvia, Filippeschi Cesare, Venturini Elisabetta

机构信息

Department of Health Sciences, Anna Meyer Children University Hospital, University of Florence, Florence, Italy.

出版信息

Front Pediatr. 2021 Feb 25;9:643341. doi: 10.3389/fped.2021.643341. eCollection 2021.

Abstract

Gianotti Crosti syndrome (GCS) is a self-healing condition with a spontaneous resolution in 2-6 weeks but, even if rarely, recurrent episodes have been reported. The aim of this observational study is to investigate serum Immunoglobulin E (IgE) level in children with GCS, evaluating if there is a relationship between IgE level and clinical course of the disease. Children with GCS diagnosed at a tertiary care children's university hospital between June 2018 and November 2019 were prospectively enrolled. Demographic, clinical and hematochemical data of children investigated were collected. In particular, IgE level were investigated at symptoms onset and, if available, at the following blood tests. Patients were divided in 2 groups on the bases of the clinical course: children with a chronic relapsing course and children who did not present any relapse. Among 29 patients enrolled in this study, 14 (48.3%) children had a chronic relapsing course and 15 (51.7%) did not present any relapse. A statistically significant difference was present considering the length of the disease: 210 days (IQR: 161.25-255) for patients with a chronic relapsing course compared to 40 days (IQR: 30-75) for the other group ( < 0.0001). About the median IgE level in the 2 groups, a value about 10 time higher was found in children with chronic course compared to the other group (1,144 vs. 116 U/mL) with a statistically significant difference ( < 0.0001). Despite the study limitations, a significant correlation between higher IgE levels and chronic-relapsing course of the GCS can be assumed.

摘要

詹诺蒂-克罗西综合征(GCS)是一种可自愈的疾病,通常在2 - 6周内自行缓解,但即便极为罕见,也有复发病例的报道。本观察性研究旨在调查GCS患儿的血清免疫球蛋白E(IgE)水平,评估IgE水平与该疾病临床病程之间是否存在关联。2018年6月至2019年11月期间,在一家三级儿童大学医院确诊为GCS的患儿被前瞻性纳入研究。收集了所调查患儿的人口统计学、临床和血液生化数据。特别地,在症状出现时以及如有可能,在后续血液检查时检测IgE水平。根据临床病程将患者分为两组:慢性复发病程患儿和未出现任何复发的患儿。在本研究纳入的29例患者中,14例(48.3%)患儿为慢性复发病程,15例(51.7%)未出现任何复发。考虑到疾病持续时间,两组之间存在统计学显著差异:慢性复发病程患者为210天(四分位间距:161.25 - 255),而另一组为40天(四分位间距:30 - 75)(<0.0001)。关于两组的IgE水平中位数,慢性病程患儿的值比另一组高约10倍(1144 vs. 116 U/mL),差异具有统计学显著性(<0.0001)。尽管本研究存在局限性,但可以推测较高的IgE水平与GCS的慢性复发病程之间存在显著相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f8d/7947791/6e3531aba3fc/fped-09-643341-g0001.jpg

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