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嗜麦芽窄食单胞菌抗体水平与囊性纤维化患者预后的纵向研究

Longitudinal study of Stenotrophomonas maltophilia antibody levels and outcomes in cystic fibrosis patients.

作者信息

Wettlaufer Jillian, Klingel Michelle, Yau Yvonne, Stanojevic Sanja, Tullis Elizabeth, Ratjen Felix, Waters Valerie

机构信息

Division of Infectious Diseases, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, 555 University Avenue, Toronto, Canada M5G 1X8.

Division of Respiratory Medicine, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto.

出版信息

J Cyst Fibros. 2017 Jan;16(1):58-63. doi: 10.1016/j.jcf.2016.06.007. Epub 2016 Jun 23.

Abstract

BACKGROUND

Previous studies have shown an association between higher Stenotrophomonas maltophilia antibody levels and decreased lung function in patients with cystic fibrosis (CF). The purpose of this study was to assess the serologic response to S. maltophilia over time and to determine whether changes in antibody levels could predict clinical outcomes.

METHODS

Changes in S. maltophilia antibody levels in adult and pediatric patients with CF from 2008 to 2014 were assessed between groups of infection patterns. Regression models accounting for repeated measures were used to assess whether antibody levels could predict subsequent S. maltophilia microbiological status, and whether they are associated with lung function and subsequent pulmonary exacerbation.

RESULTS

A total of 409 S. maltophilia antibody samples from 135 CF patients showed that antibody levels did not change significantly between study visits, regardless of infection group. Higher antibody levels were independently associated with future culture positivity (OR 1.62; 95% CI 1.09, 2.41; p=0.02). While higher antibody levels were not independently associated with decreases in FEV% predicted, they were associated with an increased hazard ratio for subsequent pulmonary exacerbation (HR 1.3; 95% CI 1.1, 1.6; p<0.001).

CONCLUSIONS

S. maltophilia antibody levels may be helpful to identify individuals at risk of exacerbation who may benefit from earlier antimicrobial treatment.

摘要

背景

既往研究表明,在囊性纤维化(CF)患者中,嗜麦芽窄食单胞菌抗体水平升高与肺功能下降之间存在关联。本研究的目的是评估随时间推移对嗜麦芽窄食单胞菌的血清学反应,并确定抗体水平的变化是否可以预测临床结局。

方法

评估了2008年至2014年成年和儿科CF患者中嗜麦芽窄食单胞菌抗体水平在不同感染模式组之间的变化。使用考虑重复测量的回归模型来评估抗体水平是否可以预测随后的嗜麦芽窄食单胞菌微生物学状态,以及它们是否与肺功能和随后的肺部加重相关。

结果

来自135例CF患者的总共409份嗜麦芽窄食单胞菌抗体样本显示,无论感染组如何,研究访视之间抗体水平均无显著变化。较高的抗体水平与未来培养阳性独立相关(比值比1.62;95%置信区间1.09,2.41;p=0.02)。虽然较高的抗体水平与预测的第一秒用力呼气容积(FEV%)下降无独立相关性,但它们与随后肺部加重的风险比增加相关(风险比1.3;95%置信区间1.1,1.6;p<0.001)。

结论

嗜麦芽窄食单胞菌抗体水平可能有助于识别有加重风险的个体,这些个体可能从早期抗菌治疗中获益。

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