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婴儿早期气道功能不佳与22岁时的肺功能:一项非选择性纵向队列研究。

Poor airway function in early infancy and lung function by age 22 years: a non-selective longitudinal cohort study.

作者信息

Stern Debra A, Morgan Wayne J, Wright Anne L, Guerra Stefano, Martinez Fernando D

机构信息

Arizona Respiratory Center, University of Arizona, Tucson, Arizona, USA.

出版信息

Lancet. 2007 Sep 1;370(9589):758-64. doi: 10.1016/S0140-6736(07)61379-8.

Abstract

BACKGROUND

Together with smoking, the lung function attained in early adulthood is one of the strongest predictors of chronic obstructive pulmonary disease. We aimed to investigate whether lung function in early adulthood is, in turn, affected by airway function measured shortly after birth.

METHODS

Non-selected infants were enrolled at birth in the Tucson Children's Respiratory Study between 1980 and 1984. We measured maximal expiratory flows at functional residual capacity (Vmax(FRC)) in 169 of these infants by the chest compression technique at a mean of 2.3 months (SD 1.9). We also obtained measurements of lung function for 123 of these participants at least once at ages 11, 16, and 22 years. Indices were forced expiratory volume in 1 s (FEV1), forced vital capacity (FVC), and forced expiratory flow between 25% and 75% of FVC (FEF25-75), both before and after treatment with a bronchodilator (180 microg of albuterol).

FINDINGS

Participants who had infant Vmax(FRC) in the lowest quartile also had lower values for the FEV1/FVC ratio (-5.2%, p<0.0001), FEF25-75 (-663 mL/s, p<0.0001), and FEV1 (-233 mL, p=0.001) up to age 22, after adjustment for height, weight, age, and sex, than those in the upper three quartiles combined. The magnitude and significance of this effect did not change after additional adjustment for wheeze, smoking, atopy, or parental asthma.

INTERPRETATION

Poor airway function shortly after birth should be recognised as a risk factor for airflow obstruction in young adults. Prevention of chronic obstructive pulmonary disease might need to start in fetal life.

摘要

背景

与吸烟一样,成年早期所达到的肺功能是慢性阻塞性肺疾病最强的预测因素之一。我们旨在研究成年早期的肺功能是否反过来受到出生后不久所测量的气道功能的影响。

方法

1980年至1984年间,图森儿童呼吸研究对非选择性的婴儿进行了出生登记。我们通过胸部按压技术,在这些婴儿平均2.3个月(标准差1.9)时,对其中169名婴儿测量了功能残气量时的最大呼气流量(Vmax(FRC))。我们还对其中123名参与者在11岁、16岁和22岁时至少进行了一次肺功能测量。指标包括1秒用力呼气量(FEV1)、用力肺活量(FVC)以及FVC的25%至75%之间的用力呼气流量(FEF25 - 75),均在使用支气管扩张剂(180微克沙丁胺醇)治疗前后进行测量。

研究结果

在对身高、体重、年龄和性别进行调整后,婴儿期Vmax(FRC)处于最低四分位数的参与者,直至22岁时,其FEV1/FVC比值(-5.2%,p<0.0001)、FEF25 - 75(-663毫升/秒,p<0.0001)和FEV1(-233毫升,p = 0.001)均低于其余三个四分位数合并组。在对喘息、吸烟、特应性或父母哮喘进行额外调整后,这种效应的大小和显著性并未改变。

解读

出生后不久气道功能不佳应被视为年轻人气流阻塞的一个危险因素。慢性阻塞性肺疾病的预防可能需要从胎儿期开始。

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