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囊性纤维化患者气道感染与疾病严重程度的关联

The Association of Airway Infection with Disease Severity in Cystic Fibrosis.

作者信息

Bar-On Ophir, Mei-Zahav Meir, Levine Hagit, Mussaffi Huda, Blau Hannah, Ben Zvi Haim, Prais Dario, Stafler Patrick

机构信息

Graub CF Center, Pulmonary Institute, Schneider Children's Medical Center of Israel, Petach Tikva 4920235, Israel.

School of Medicine, Faculty of Medical and Health Sciences, Tel-Aviv University, Tel Aviv 6997801, Israel.

出版信息

J Clin Med. 2025 Apr 3;14(7):2437. doi: 10.3390/jcm14072437.

DOI:10.3390/jcm14072437
PMID:40217889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11989260/
Abstract

: The prevalence of is increasing in people with Cystic Fibrosis (pwCF), yet its clinical pathogenicity remains controversial. The objective of this study was to chart the longitudinal prevalence and examine clinical associations before and after infection. : This observational, retrospective study was conducted at a single CF center over a 14-year period. Data were collated from patient charts and clinic databases. Patients with sputum cultures were compared to those without the bacterium and analyzed according to whether they had single, intermittent, or chronic infections. : During the study period, an annual average of 124 pwCF were followed up at our clinic, with a median age of 13.6 years (IQR = 7.6-27.7). The detection rate increased from 0 to 6.1%. Twenty-three percent (29/124) of patients had at least one positive culture. The median age at acquisition was 17 years (IQR = 14.5-33). At the time of acquisition, the median FEV was 81% (IQR = 46-94), compared to 90% (IQR = 72-99) for patients without , < 0.001. Patients with tended to demonstrate more chronic (55% vs. 27%, = 0.06) and pancreatic insufficiency (66% vs. 47%, = 0.07). At two years post-acquisition, the median FEV for patients with intermittent and chronically infected decreased by 11.5% (IQR = -3.75-7.5), compared to 1.5% (IQR = -2.5-12.5) for those with a single positive culture, = 0.03. Similarly, pulmonary exacerbations per year became more frequent post-acquisition in intermittent and chronically infected patients: Median (range) 2.5 (0-8) pre-, versus 3.0 (0-9) post-acquisition, = 0.036. : Chronic and intermittent infection with were associated with accelerated lung function decline and increased exacerbation frequency. Larger prospective studies are needed to confirm these findings and examine the effect of eradication on the clinical course.

摘要

在囊性纤维化患者(pwCF)中,[细菌名称]的感染率正在上升,但其临床致病性仍存在争议。本研究的目的是记录其纵向感染率,并检查感染前后的临床关联。:这项观察性回顾性研究在一个单一的囊性纤维化中心进行,为期14年。数据来自患者病历和临床数据库。将有[细菌名称]痰培养结果的患者与没有该细菌的患者进行比较,并根据他们是单次、间歇性还是慢性感染进行分析。:在研究期间,我们诊所每年平均随访124名pwCF患者,中位年龄为13.6岁(四分位间距IQR = 7.6 - 27.7)。[细菌名称]的检出率从0上升到6.1%。23%(29/124)的患者至少有一次阳性培养结果。感染时的中位年龄为17岁(IQR = 14.5 - 33)。感染时,中位第一秒用力呼气容积(FEV)为81%(IQR = 46 - 94),而未感染[细菌名称]的患者为90%(IQR = 72 - 99),P < 0.001。感染[细菌名称]的患者往往表现出更多的慢性[疾病名称](55%对27%,P = 0.06)和胰腺功能不全(66%对47%,P = 0.07)。感染后两年,间歇性和慢性感染患者的中位FEV下降了11.5%(IQR = -3.75 - 7.5),而单次阳性培养结果的患者下降了1.5%(IQR = -2.5 - 12.5),P = 0.03。同样,间歇性和慢性感染患者在感染后每年肺部加重变得更加频繁:感染前中位(范围)为2.5(0 - 8)次,感染后为3.0(0 - 9)次,P = 0.036。:[细菌名称]的慢性和间歇性感染与肺功能加速下降和加重频率增加有关。需要更大规模的前瞻性研究来证实这些发现,并研究根除该细菌对临床病程的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/771a/11989260/0c56396f4c5e/jcm-14-02437-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/771a/11989260/d89d52012c29/jcm-14-02437-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/771a/11989260/0c56396f4c5e/jcm-14-02437-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/771a/11989260/d89d52012c29/jcm-14-02437-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/771a/11989260/0c56396f4c5e/jcm-14-02437-g002.jpg

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本文引用的文献

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Pathogenesis of respiratory infections: colonization, persistence, and transcriptome profiling in synthetic cystic fibrosis sputum medium.呼吸道感染的发病机制:在合成囊性纤维化痰液培养基中的定植、持续存在和转录组分析。
Infect Immun. 2023 Dec 12;91(12):e0041623. doi: 10.1128/iai.00416-23. Epub 2023 Nov 1.
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Clinical outcomes associated with Achromobacter species infection in people with cystic fibrosis.囊性纤维化患者中与无色杆菌属感染相关的临床结局。
J Cyst Fibros. 2023 Mar;22(2):334-343. doi: 10.1016/j.jcf.2022.11.001. Epub 2022 Nov 20.
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Achromobacter spp. prevalence and adaptation in cystic fibrosis lung infection.
无色杆菌属在囊性纤维化肺部感染中的流行情况及适应性
Microbiol Res. 2022 Oct;263:127140. doi: 10.1016/j.micres.2022.127140. Epub 2022 Jul 22.
4
airway infection is associated with lung disease severity in children with cystic fibrosis.气道感染与囊性纤维化患儿的肺部疾病严重程度相关。
ERJ Open Res. 2021 May 31;7(2). doi: 10.1183/23120541.00076-2021. eCollection 2021 Apr.
5
and : Emerging Pathogens Well-Armed for Life in the Cystic Fibrosis Patients' Lung.和:在囊性纤维化患者肺部,新兴病原体为生存做好充分准备。
Genes (Basel). 2021 Apr 21;12(5):610. doi: 10.3390/genes12050610.
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Int J Environ Res Public Health. 2018 Sep 15;15(9):2020. doi: 10.3390/ijerph15092020.
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Effect of respiratory Achromobacter spp. infection on pulmonary function in patients with cystic fibrosis.呼吸道不动杆菌属感染对囊性纤维化患者肺功能的影响。
J Med Microbiol. 2018 Jul;67(7):952-956. doi: 10.1099/jmm.0.000763. Epub 2018 May 22.
8
Impact of High Diversity of Achromobacter Populations within Cystic Fibrosis Sputum Samples on Antimicrobial Susceptibility Testing.囊性纤维化痰液样本中无色杆菌群体的高度多样性对抗菌药物敏感性测试的影响
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Epidemic Achromobacter xylosoxidans strain among Belgian cystic fibrosis patients and review of literature.比利时囊性纤维化患者中流行的木糖氧化无色杆菌菌株及文献综述
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