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确立儿童湿疹的亚类、其危险因素和预后。

Establishing subclasses of childhood eczema, their risk factors and prognosis.

机构信息

Allergy and Lung Health Unit, The University of Melbourne, Melbourne, Victoria, Australia.

Department of Medical Education, The University of Melbourne, Melbourne, Victoria, Australia.

出版信息

Clin Exp Allergy. 2022 Sep;52(9):1079-1090. doi: 10.1111/cea.14139. Epub 2022 Apr 4.

Abstract

BACKGROUND

The heterogeneity of development and progression of eczema suggests multiple underlying subclasses for which aetiology and prognosis may vary. A better understanding may provide a comprehensive overview of eczema development and progression in childhood. Thus, we aimed to determine longitudinal eczema subclasses based on assessments and identify their associations with risk factors and allergic outcomes.

METHODS

A total of 619 participants with a family history of allergic disease were assessed at 24 time-points from birth to 12 years. At each time, eczema was defined as the report of current rash treated with topical steroid-based preparations. Longitudinal latent class analysis was used to determine eczema subclasses. Subsequent analyses using regression models assessed the associations between eczema subclasses and potential risk factors and allergic outcomes at 18- and 25-year follow-ups (eczema, allergic rhinitis, asthma and allergic sensitization).

RESULTS

We identified five eczema subclasses 'early-onset persistent', 'early-onset resolving', 'mid-onset persistent', 'mid-onset resolving' and 'minimal eczema'. Filaggrin null mutations were associated with the early-onset persistent (OR = 2.58 [1.09-6.08]) and mid-onset persistent class (OR = 2.58 [1.32-5.06]). Compared with 'minimal eczema', participants from early-onset persistent class had higher odds of eczema (OR = 11.8 [5.20-26.6]) and allergic rhinitis (OR = 3.13 [1.43-6.85]) at 18 and at 25 years eczema (OR = 9.37 [3.17-27.65]), allergic rhinitis (OR = 3.26 [1.07-9.93]) and asthma (OR = 2.91 [1.14-7.43]). Likewise, mid-onset persistent class had higher odds of eczema (OR = 2.59 [1.31-5.14]), allergic rhinitis (OR = 1.70 [1.00-2.89]) and asthma (OR = 2.00 [1.10-3.63]) at 18 and at 25 years eczema (OR = 6.75 [3.11-14-65]), allergic rhinitis (OR = 2.74 [1.28-5.88]) and asthma (OR = 2.50 [1.25-5.00]). Allergic and food sensitization in early life was more common in those in the persistent eczema subclasses.

CONCLUSION

We identified five distinct eczema subclasses. These classes were differentially associated with risk factors, suggesting differences in aetiology, and also with the development of allergic outcomes, highlighting their potential to identify high-risk groups for close monitoring and intervention.

摘要

背景

湿疹的发展和进展存在异质性,这表明可能存在多种潜在的亚类,其病因和预后可能有所不同。更好的了解可能会提供对儿童期湿疹发展和进展的全面概述。因此,我们旨在根据评估确定基于时间的湿疹亚类,并确定其与危险因素和过敏结局的关联。

方法

共有 619 名具有过敏疾病家族史的参与者在出生到 12 岁之间进行了 24 次评估。每次评估时,湿疹均定义为报告当前皮疹并使用基于局部类固醇的制剂进行治疗。使用纵向潜在类别分析确定湿疹亚类。使用回归模型进行的后续分析评估了湿疹亚类与潜在危险因素和 18 岁和 25 岁随访时的过敏结局(湿疹、过敏性鼻炎、哮喘和过敏致敏)之间的关联。

结果

我们确定了五个湿疹亚类,即“早发性持续性”、“早发性缓解性”、“中发性持续性”、“中发性缓解性”和“轻度湿疹”。丝聚蛋白基因突变与早发性持续性(OR=2.58[1.09-6.08])和中发性持续性类别(OR=2.58[1.32-5.06])相关。与“轻度湿疹”相比,来自早发性持续性类别的参与者发生湿疹(OR=11.8[5.20-26.6])和过敏性鼻炎(OR=3.13[1.43-6.85])的几率更高18 岁和 25 岁时的湿疹(OR=9.37[3.17-27.65])、过敏性鼻炎(OR=3.26[1.07-9.93])和哮喘(OR=2.91[1.14-7.43])。同样,中发性持续性类别发生湿疹(OR=2.59[1.31-5.14])、过敏性鼻炎(OR=1.70[1.00-2.89])和哮喘(OR=2.00[1.10-3.63])的几率更高)在 18 岁和 25 岁时,湿疹(OR=6.75[3.11-14-65])、过敏性鼻炎(OR=2.74[1.28-5.88])和哮喘(OR=2.50[1.25-5.00])。生命早期的过敏和食物致敏在持续性湿疹亚类中更为常见。

结论

我们确定了五个不同的湿疹亚类。这些类别与危险因素的相关性不同,提示病因不同,也与过敏结局的发展相关,这突出了它们识别高危人群进行密切监测和干预的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fc8/9546228/1f13ad592705/CEA-52-1079-g002.jpg

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