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儿童特应性皮炎的纵向控制和持续时间随发病时间而异:一项队列研究。

Longitudinal atopic dermatitis control and persistence vary with timing of disease onset in children: A cohort study.

机构信息

Department of Dermatology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania; Section of Pediatric Dermatology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania; Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.

出版信息

J Am Acad Dermatol. 2019 Dec;81(6):1292-1299. doi: 10.1016/j.jaad.2019.05.016. Epub 2019 May 11.

DOI:10.1016/j.jaad.2019.05.016
PMID:31085263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6892595/
Abstract

BACKGROUND

Wide variation exists in the timing of atopic dermatitis (AD) disease onset among children. Distinct trajectories of early-onset, mid-onset, and late-onset AD have been previously described.

OBJECTIVE

To evaluate longitudinal disease control and persistence with respect to age at onset of AD.

METHODS

A cohort study was performed using the Pediatric Eczema Elective Registry, a prospective observational cohort of subjects with childhood-onset AD. AD control and persistence were assessed biannually for up to 10 years.

RESULTS

A total of 8015 subjects with 41,934 person-years of follow-up were included. In longitudinal analyses using generalized linear latent and mixed modeling, older age at onset of AD was associated with better disease control and less-persistent AD. For each additional year of age at onset of AD, the adjusted odds ratios for poorer AD control and for persistent AD were 0.93 (95% confidence interval, 0.91-0.94) and 0.84 (95% confidence interval, 0.80-0.88), respectively. Differences in AD control and persistence among subjects with early-, mid-, and late-onset AD were most pronounced from early adolescence onward.

LIMITATIONS

Misclassification bias may arise from using self-reported data on age at onset. Attrition and missing data in longitudinal studies may introduce bias.

CONCLUSION

Early-, mid-, and late-onset pediatric AD appear to be clinically distinct subtypes of the disease.

摘要

背景

儿童特应性皮炎(AD)的发病时间存在广泛的差异。先前已经描述了特应性皮炎的早期发病、中期发病和晚期发病的不同轨迹。

目的

评估特应性皮炎发病年龄与疾病控制和持续性的关系。

方法

本研究使用儿科特应性皮炎选择性登记处(一项针对儿童期特应性皮炎患者的前瞻性观察队列研究)进行了一项队列研究。在长达 10 年的时间里,每两年评估一次 AD 的控制和持续性。

结果

共纳入 8015 名患者,随访 41934 人年。使用广义线性潜在和混合模型进行纵向分析,AD 发病年龄越大,疾病控制越好,AD 持续时间越短。AD 发病年龄每增加 1 岁,AD 控制不佳的调整比值比和持续 AD 的调整比值比分别为 0.93(95%置信区间,0.91-0.94)和 0.84(95%置信区间,0.80-0.88)。从青少年早期开始,早发、中发和晚发 AD 患者在 AD 控制和持续性方面的差异最为明显。

局限性

发病年龄的自我报告数据可能存在分类偏倚。纵向研究中的失访和缺失数据可能会产生偏差。

结论

早发、中发和晚发儿童 AD 似乎是该疾病的临床不同亚型。

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