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血清铁水平与囊性纤维化患者使用抗生素的时间相关。

Serum Iron Level Is Associated with Time to Antibiotics in Cystic Fibrosis.

作者信息

Gifford Alex H, Dorman Dana B, Moulton Lisa A, Helm Jennifer E, Griffin Mary M, MacKenzie Todd A

机构信息

Department of Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.

Translational Research Core, Dartmouth Lung Biology Center, Lebanon, New Hampshire, USA.

出版信息

Clin Transl Sci. 2015 Dec;8(6):754-8. doi: 10.1111/cts.12358. Epub 2015 Dec 8.

Abstract

BACKGROUND

Serum levels of hepcidin-25, a peptide hormone that reduces blood iron content, are elevated when patients with cystic fibrosis (CF) develop pulmonary exacerbation (PEx). Because hepcidin-25 is unavailable as a clinical laboratory test, we questioned whether a one-time serum iron level was associated with the subsequent number of days until PEx, as defined by the need to receive systemic antibiotics (ABX) for health deterioration.

METHODS

Clinical, biochemical, and microbiological parameters were simultaneously checked in 54 adults with CF. Charts were reviewed to determine when they first experienced a PEx after these parameters were assessed. Time to ABX was compared in subgroups with and without specific attributes. Multivariate linear regression was used to identify parameters that significantly explained variation in time to ABX.

RESULTS

In univariate analyses, time to ABX was significantly shorter in subjects with Aspergillus-positive sputum cultures and CF-related diabetes. Multivariate linear regression models demonstrated that shorter time to ABX was associated with younger age, lower serum iron level, and Aspergillus sputum culture positivity.

CONCLUSIONS

Serum iron, age, and Aspergillus sputum culture positivity are factors associated with shorter time to subsequent PEx in CF adults.

摘要

背景

囊性纤维化(CF)患者发生肺部加重(PEx)时,一种可降低血液铁含量的肽类激素——铁调素-25的血清水平会升高。由于铁调素-25无法作为临床实验室检测项目,我们质疑单次血清铁水平是否与后续直至发生PEx的天数相关,PEx定义为因健康状况恶化而需要接受全身用抗生素(ABX)治疗。

方法

对54名成年CF患者同时检查临床、生化和微生物学参数。查阅病历以确定在评估这些参数后他们首次发生PEx的时间。比较具有和不具有特定特征的亚组中至使用ABX的时间。采用多元线性回归来确定能显著解释至使用ABX时间变化的参数。

结果

在单因素分析中,痰培养曲霉菌阳性和患有CF相关糖尿病的受试者至使用ABX的时间显著更短。多元线性回归模型表明,至使用ABX的时间较短与年龄较小、血清铁水平较低以及痰培养曲霉菌阳性有关。

结论

血清铁、年龄和痰培养曲霉菌阳性是与成年CF患者后续发生PEx时间较短相关的因素。

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本文引用的文献

1
Measurement of serum calprotectin in stable patients predicts exacerbation and lung function decline in cystic fibrosis.
Am J Respir Crit Care Med. 2015 Jan 15;191(2):233-6. doi: 10.1164/rccm.201407-1365LE.
3
What is hepcidin telling us about the natural history of cystic fibrosis?
J Cyst Fibros. 2015 Jan;14(1):155-7. doi: 10.1016/j.jcf.2014.03.012. Epub 2014 Apr 30.
4
Plasma sCD14 as a biomarker to predict pulmonary exacerbations in cystic fibrosis.
PLoS One. 2014 Feb 20;9(2):e89341. doi: 10.1371/journal.pone.0089341. eCollection 2014.
5
Candidate markers associated with the probability of future pulmonary exacerbations in cystic fibrosis patients.
PLoS One. 2014 Feb 12;9(2):e88567. doi: 10.1371/journal.pone.0088567. eCollection 2014.
6
Iron supplementation does not worsen respiratory health or alter the sputum microbiome in cystic fibrosis.
J Cyst Fibros. 2014 May;13(3):311-8. doi: 10.1016/j.jcf.2013.11.004. Epub 2013 Dec 13.
7
Incidence and clinical impact of respiratory viruses in adults with cystic fibrosis.
Thorax. 2014 Mar;69(3):247-53. doi: 10.1136/thoraxjnl-2013-204000. Epub 2013 Oct 14.
8
Treatment of pulmonary exacerbations in cystic fibrosis.
Eur Respir Rev. 2013 Sep 1;22(129):205-16. doi: 10.1183/09059180.00006512.
9
Systematic review of blood biomarkers in cystic fibrosis pulmonary exacerbations.
Chest. 2013 Nov;144(5):1659-1670. doi: 10.1378/chest.13-0693.
10
Iron accumulates in the lavage and explanted lungs of cystic fibrosis patients.
J Cyst Fibros. 2013 Jul;12(4):390-8. doi: 10.1016/j.jcf.2012.10.010. Epub 2012 Nov 22.

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