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Pubertal Height Growth and Adult Height in Cystic Fibrosis After Newborn Screening.新生儿筛查后囊性纤维化患者的青春期身高增长及成人身高
Pediatrics. 2016 May;137(5). doi: 10.1542/peds.2015-2907. Epub 2016 Apr 5.
2
Growth and the Growth Hormone-Insulin Like Growth Factor 1 Axis in Children With Chronic Inflammation: Current Evidence, Gaps in Knowledge, and Future Directions.慢性炎症患儿的生长和生长激素-胰岛素样生长因子 1 轴:现有证据、知识空白和未来方向。
Endocr Rev. 2016 Feb;37(1):62-110. doi: 10.1210/er.2015-1026. Epub 2015 Dec 31.
3
Standardization of Research-Quality Anthropometric Measurement of Infants and Implementation in a Multicenter Study.婴儿研究质量人体测量标准化及其在多中心研究中的实施
Clin Transl Sci. 2015 Aug;8(4):330-3. doi: 10.1111/cts.12283. Epub 2015 Jun 5.
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Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.鲁马卡托-依伐卡托用于携带苯丙氨酸508位缺失CFTR基因纯合突变的囊性纤维化患者。
N Engl J Med. 2015 Jul 16;373(3):220-31. doi: 10.1056/NEJMoa1409547. Epub 2015 May 17.
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Early respiratory infection is associated with reduced spirometry in children with cystic fibrosis.早期呼吸道感染与囊性纤维化患儿肺功能检测降低有关。
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Inflammation and growth in young children with obstructive sleep apnea syndrome before and after adenotonsillectomy.阻塞性睡眠呼吸暂停综合征幼儿腺样体扁桃体切除术前和术后的炎症与生长情况
Mediators Inflamm. 2014;2014:146893. doi: 10.1155/2014/146893. Epub 2014 Aug 24.
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新生儿筛查诊断囊性纤维化对生命第一年体重和身长的影响。

Effects of Diagnosis by Newborn Screening for Cystic Fibrosis on Weight and Length in the First Year of Life.

作者信息

Leung Daniel H, Heltshe Sonya L, Borowitz Drucy, Gelfond Daniel, Kloster Margaret, Heubi James E, Stalvey Michael, Ramsey Bonnie W

机构信息

Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.

Cystic Fibrosis Foundation Therapeutics Development Network Coordinating Center, Seattle Children's Research Institute, Seattle, Washington3Division of Pulmonary and Sleep Medicine, Department of Pediatrics, University of Washington, Seattle.

出版信息

JAMA Pediatr. 2017 Jun 1;171(6):546-554. doi: 10.1001/jamapediatrics.2017.0206.

DOI:10.1001/jamapediatrics.2017.0206
PMID:28437538
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5731827/
Abstract

IMPORTANCE

Since the implementation of universal newborn screening (NBS) for cystic fibrosis (CF), the timing and magnitude of growth deficiency or its association with correlates of disease among infants with CF who underwent NBS has not been well described.

OBJECTIVE

To examine incremental weight gain, linear growth, and clinical features in the first year of life among infants with CF who underwent NBS.

DESIGN, SETTING, AND PARTICIPANTS: The Baby Observational and Nutrition Study (BONUS), a multicenter, longitudinal, observational cohort study, was conducted during regular CF clinic visits in the first 12 months of life at 28 US Cystic Fibrosis Foundation-accredited Care Centers from January 7, 2012, through May 31, 2015. Participants included 231 infants younger than 3.5 months who underwent NBS and had confirmed CF, with a gestational age of at least 35 weeks, birth weight of at least 2.5 kg, and toleration of full oral feeds. Of these, 222 infants (96.1%) had follow-up beyond 6 months of age and 215 (93.1%) completed 12 months of follow-up.

EXPOSURE

Cystic fibrosis.

MAIN OUTCOME AND MEASURES

Attained weight and length for age and World Health Organization normative z scores at ages 1 to 6 and 8, 10, and 12 months (defined a priori).

RESULTS

Of the 231 infants enrolled, 110 infants (47.6%) were female and 121 (52.4%) were male, with a mean (SD) age of 2.58 (0.69) months. BONUS infants had lower than mean birth weights (mean z score, -0.15; 95% CI, -0.27 to -0.04) and higher birth lengths (mean z score, 0.44; 95% CI, 0.26 to 0.62). They achieved normal weight by 12 months, a significant improvement over a prescreening cohort of newborns with CF from 20 years before the contemporary cohort (mean z score increase, 0.57; 95% CI, 0.37-0.77). However, length was lower than the mean at 12 months (mean z score, -0.56; 95% CI, -0.70 to -0.42). Only 30 infants (13.6%) were at less than the 10th percentile of weight for age, whereas 53 (23.9%) were at less than the 10th percentile of length for age at more than half their visits. Male sex, pancreatic insufficiency, meconium ileus, histamine blocker use, and respiratory Pseudomonas aeruginosa infection were associated with lower weight or length during the first year. Insulinlike growth factor 1 levels were significantly lower among low-length infants. Persistently low-weight infants consumed significantly more calories, and weight and length z scores were negatively correlated with caloric intake.

CONCLUSIONS AND RELEVANCE

Since initiation of universal NBS for CF, significant improvement has occurred in nutritional status, with normalization of weight in the first year of life. However, length stunting remains common.

摘要

重要性

自从实施针对囊性纤维化(CF)的新生儿普遍筛查(NBS)以来,接受NBS的CF婴儿生长发育不足的时间和程度,或其与疾病相关因素之间的关联尚未得到充分描述。

目的

研究接受NBS的CF婴儿在出生后第一年的体重增加、线性生长及临床特征。

设计、地点和参与者:婴儿观察与营养研究(BONUS)是一项多中心、纵向、观察性队列研究,于2012年1月7日至2015年5月31日在美国28家经囊性纤维化基金会认可的护理中心,在婴儿出生后的前12个月定期进行的CF门诊就诊期间开展。参与者包括231名年龄小于3.5个月且接受了NBS并确诊为CF的婴儿,其胎龄至少35周,出生体重至少2.5kg,且能耐受完全经口喂养。其中,222名婴儿(96.1%)随访至6个月以上,215名(93.1%)完成了12个月的随访。

暴露因素

囊性纤维化。

主要结局和指标

1至6个月以及8、10和12个月时的年龄别体重和身长以及世界卫生组织标准z评分(预先定义)。

结果

在纳入的231名婴儿中,110名婴儿(47.6%)为女性,121名(52.4%)为男性,平均(标准差)年龄为2.58(0.69)个月。BONUS婴儿的出生体重低于平均水平(平均z评分,-0.15;95%置信区间,-0.27至-0.04),出生身长高于平均水平(平均z评分,0.44;95%置信区间,0.26至0.62)。他们在12个月时体重达到正常水平,相较于当代队列20年前的CF新生儿预筛查队列有显著改善(平均z评分增加,0.57;95%置信区间,0.37 - 0.77)。然而,12个月时的身长低于平均水平(平均z评分,-0.56;95%置信区间,-0.70至-0.42)。只有30名婴儿(13.6%)年龄别体重低于第10百分位数,而在超过半数的访视中,53名(23.9%)婴儿年龄别身长低于第10百分位数。男性、胰腺功能不全、胎粪性肠梗阻、使用组胺阻滞剂以及呼吸道铜绿假单胞菌感染与第一年体重或身长较低有关。低身长婴儿的胰岛素样生长因子1水平显著较低。持续低体重婴儿摄入的热量显著更多,体重和身长z评分与热量摄入呈负相关。

结论与意义

自开始对CF进行新生儿普遍筛查以来,营养状况有了显著改善,婴儿在出生后第一年体重恢复正常。然而,身长发育迟缓仍然很常见。