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美国囊性纤维化新生儿筛查计划与营养和肺部结局的真实世界关联。

Real-world Associations of US Cystic Fibrosis Newborn Screening Programs With Nutritional and Pulmonary Outcomes.

机构信息

Division of Pulmonary and Sleep Medicine, Seattle Children's Hospital, Seattle, Washington.

Department of Pediatrics, University of Washington, Seattle.

出版信息

JAMA Pediatr. 2022 Oct 1;176(10):990-999. doi: 10.1001/jamapediatrics.2022.2674.

Abstract

IMPORTANCE

Newborn screening (NBS) for cystic fibrosis (CF) has been universal in the US since 2010, but its association with clinical outcomes is unclear.

OBJECTIVE

To describe the real-world effectiveness of NBS programs for CF in the US on outcomes up to age 10 years.

DESIGN, SETTING, AND PARTICIPANTS: This was a retrospective cohort study using CF Foundation Patient Registry data from January 1, 2000, to December 31, 2018. The staggered implementation of NBS programs by state was used to compare longitudinal outcomes among children in the same birth cohort born before vs after the implementation of NBS for CF in their state of birth. Participants included children with an established diagnosis of CF born between January 1, 2000, to December 31, 2018, in any of the 44 states that implemented NBS for CF between 2003 and 2010. Data were analyzed from October 5, 2020, to April 22, 2022.

EXPOSURES

Birth before vs after the implementation of NBS for CF in the state of birth.

MAIN OUTCOMES AND MEASURES

Longitudinal trajectory of height and weight percentiles from diagnosis, lung function (forced expiratory volume in 1 second, [FEV1] percent predicted) from age 6 years, and age at initial and chronic infection with Pseudomonas aeruginosa using linear mixed-effects and time-to-event models adjusting for birth cohort and potential confounders.

RESULTS

A total of 9571 participants (4713 female participants [49.2%]) were eligible for inclusion, with 4510 (47.1%) in the pre-NBS cohort. NBS was associated with higher weight and height percentiles in the first year of life (weight, 6.0; 95% CI, 3.1-8.4; height, 6.6; 95% CI, 3.8-9.3), but these differences decreased with age. There was no association between NBS and FEV1 at age 6 years, but the percent-predicted FEV1 did increase more rapidly with age in the post-NBS cohort. NBS was associated with older age at chronic P aeruginosa infection (hazard ratio, 0.69; 95% CI, 0.54-0.89) but not initial P aeruginosa infection (hazard ratio, 0.88; 95% CI, 0.77-1.01).

CONCLUSIONS AND RELEVANCE

NBS for CF in the US was associated with improved nutritional status up to age 10 years, a more rapid increase in lung function, and delayed chronic P aeruginosa infection. In the future, as highly effective modulator therapies become available for infants with CF, NBS will allow for presymptomatic initiation of these disease-modifying therapies before irreversible organ damage.

摘要

重要性

自 2010 年以来,美国已经全面开展了针对囊性纤维化(CF)的新生儿筛查(NBS),但它与临床结局的关联尚不清楚。

目的

描述美国 CF NBS 计划在 10 岁以下儿童结局方面的真实有效性。

设计、地点和参与者:这是一项回顾性队列研究,使用了 2000 年 1 月 1 日至 2018 年 12 月 31 日期间囊性纤维化基金会患者登记处的数据。利用各州实施 NBS 项目的时间差,比较了在出生州实施 CF NBS 之前和之后出生的同一生育队列中儿童的纵向结局。参与者包括在 2000 年 1 月 1 日至 2018 年 12 月 31 日期间在任何一个实施了 CF NBS 的 44 个州出生的确诊为 CF 的儿童。数据于 2020 年 10 月 5 日至 2022 年 4 月 22 日进行分析。

暴露因素

在出生州实施 CF NBS 之前或之后出生。

主要结局和测量指标

从诊断开始的身高和体重百分位数的纵向轨迹、6 岁时的肺功能(1 秒用力呼气量,[FEV1]预测百分比)以及初始和慢性铜绿假单胞菌感染的时间,使用线性混合效应和时间事件模型进行调整,以纳入出生队列和潜在混杂因素。

结果

共有 9571 名参与者(4713 名女性参与者[49.2%])符合纳入标准,其中 4510 名(47.1%)在 NBS 前队列中。NBS 与生命第一年更高的体重和身高百分位数有关(体重,6.0;95%置信区间,3.1-8.4;身高,6.6;95%置信区间,3.8-9.3),但这些差异随着年龄的增长而减小。NBS 与 6 岁时的 FEV1 无关,但在 NBS 后队列中,FEV1 预测百分比的增长速度随年龄的增长而更快。NBS 与慢性铜绿假单胞菌感染的年龄较大有关(风险比,0.69;95%置信区间,0.54-0.89),但与初始铜绿假单胞菌感染无关(风险比,0.88;95%置信区间,0.77-1.01)。

结论和相关性

美国的 CF NBS 与 10 岁以下儿童营养状况的改善有关,肺功能的增长更快,慢性铜绿假单胞菌感染的时间延迟。在未来,随着针对 CF 婴儿的高度有效的调节剂治疗方法的出现,NBS 将允许在不可逆转的器官损伤之前,对无症状的婴儿进行这些疾病修饰治疗。

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