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儿童喘息表型在整个青春期的 FEV1 增长低于预期。

Childhood wheeze phenotypes show less than expected growth in FEV1 across adolescence.

机构信息

1 Centre for Epidemiology and Biostatistics, School of Population and Global Health, University of Melbourne, Melbourne, Australia.

出版信息

Am J Respir Crit Care Med. 2014 Jun 1;189(11):1351-8. doi: 10.1164/rccm.201308-1487OC.

Abstract

RATIONALE

Better characterization of childhood wheeze phenotypes using newer statistical methods provides a basis for addressing the heterogeneity of childhood asthma. Outcomes of these phenotypes beyond childhood are unknown.

OBJECTIVES

To determine if adolescent respiratory symptoms, lung function, and changes in lung function over adolescence differ by childhood wheeze phenotypes defined through latent class analysis.

METHODS

A prospective birth cohort (Melbourne Atopy Cohort Study) followed 620 high allergy-risk children, recording respiratory symptoms and spirometry at 12 and 18 years. Regression analyses identified relationships between wheeze phenotypes (never/infrequent, early transient, early persistent, intermediate onset, and late onset) and lung function, change in lung function (12-18 yr), respiratory symptoms, and asthma. The baseline classification was never/infrequent wheeze.

MEASUREMENTS AND MAIN RESULTS

Deficits in expected growth of lung function, measured by change in prebronchodilator FEV1 between 12 and 18 years, were found for early persistent (reduced 290 ml; 95% confidence interval [CI], 82-498), intermediate-onset (reduced 210 ml; 95% CI, 62-359), and late-onset wheeze (reduced 255 ml; 95% CI, 69-442). Intermediate-onset wheezers had persistent FEV1 deficit after bronchodilator at 18 years (reduced 198 ml; 46,350). Current asthma risk was increased for all phenotypes except early transient, which was also not associated with lung function deficits at 12 or 18 years.

CONCLUSIONS

Persistent wheeze phenotypes in childhood were associated with reduced growth in prebronchodilator FEV1 over adolescence. Intermediate-onset wheezers showed irreversible airflow limitation by 18 years. Conversely, early transient wheeze was a benign condition with no sequelae for respiratory health by age 18.

摘要

背景

使用新的统计方法更好地描述儿童喘息表型,为解决儿童哮喘的异质性提供了基础。这些表型在儿童期后的结果尚不清楚。

目的

通过潜在类别分析确定儿童喘息表型是否与青少年呼吸症状、肺功能以及青少年时期肺功能的变化不同。

方法

前瞻性出生队列(墨尔本过敏队列研究)随访了 620 名高过敏风险儿童,在 12 岁和 18 岁时记录呼吸症状和肺活量。回归分析确定了喘息表型(从未/不频繁、早期一过性、早期持续性、中间起病和晚期起病)与肺功能、肺功能变化(12-18 岁)、呼吸症状和哮喘之间的关系。基线分类为从未/不频繁喘息。

测量和主要结果

12 至 18 年间,使用支气管扩张剂前 FEV1 的变化来衡量,发现早期持续性(减少 290ml;95%置信区间[CI],82-498)、中间起病(减少 210ml;95%CI,62-359)和晚期起病(减少 255ml;95%CI,69-442)的肺功能预期增长受损。中间起病的喘息者在 18 岁时仍有支气管扩张剂后 FEV1 不足(减少 198ml;46,350)。除了早期一过性,所有表型的哮喘风险都增加,而早期一过性与 12 岁或 18 岁时的肺功能不足无关。

结论

儿童期持续性喘息表型与青少年时期支气管扩张剂前 FEV1 生长减少有关。中间起病的喘息者在 18 岁时出现不可逆的气流受限。相反,早期一过性喘息是一种良性疾病,到 18 岁时对呼吸健康没有后遗症。

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