Sputum neutrophil elastase and its relation to pediatric bronchiectasis severity: A cross-sectional study

被引:9
作者
Ali, Heba A. [1 ]
Fouda, Eman M. [1 ]
Salem, Mona A. [2 ]
Abdelwahad, Marwa A. [3 ]
Radwan, Heba H. [4 ]
机构
[1] Ain Shams Univ Childrens Hosp, Fac Med, Dept Pediat, Pulmonol Div, Cairo, Egypt
[2] Ain Shams Univ Hosp, Dept Radiol, Cairo, Egypt
[3] Ain Shams Univ Hosp, Dept Clin Pathol, Cairo, Egypt
[4] Minist Hlth Cairo, Cairo, Egypt
关键词
colonization; exacerbations; cystic fibrosis; non-CF bronchiectasis; neutrophil elastase; severity scores; CYSTIC FIBROSIS BRONCHIECTASIS; LUNG-FUNCTION DECLINE; PULMONARY-FUNCTION; LONG-TERM; CHILDREN; INFLAMMATION; DISEASE; AIRWAY; EXACERBATIONS; VALIDATION;
D O I
10.1002/hsr2.581
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background and Aims Sputum neutrophil elastase (NE) is a marker of neutrophilic airway inflammation in bronchiectasis. Yet, not much is known about its role in pediatric bronchiectasis severity. This study aimed to assess the sputum NE value as a biomarker of clinical and radiological severity in pediatric bronchiectasis. Methods This was a cross-sectional study assessing sputum NE in a total of 50 bronchiectasis patients under the age of 18 years-30 patients with cystic fibrosis (CF) and 20 patients with non-CF bronchiectasis were included. Bronchiectasis severity was assessed using Shwachman-Kulczycki (SK) score, CF-ABLE score, and CF risk of disease progression score, among CF patients, and bronchiectasis severity index (BSI) and FACED criteria among non-CF bronchiectasis patients, associations between sputum NE and bronchiectasis severity were assessed in both patient groups. Results Sputum NE was directly correlated with C-reactive protein (r = 0.914, p < 0.001), (r = 0.786, p < 0.001), frequency of exacerbations (r = 0.852, p < 0.001) (r = 0.858, p < 0.001), exacerbations severity (r = 0.735, p = 0.002), (r = 0.907, p < 0.001), and the number of hospital admissions (r = 0.813, p < 0.001), (r = 0.612, p =0.004) in the last year among CF, and non-CF bronchiectasis patients, respectively. Additional linear correlations were found between sputum NE, CF risk of disease progression score (p < 0.001), CF-ABLE score (p < 0.001), and lower forced expiratory volume 1% of predicted (p = 0.017; rho = -0.8) among CF patients. Moreover, sputum NE was positively correlated with the neutrophil count (p = 0.018), and BSI severity score (p = 0.039; rho = 0.465) among non-CF bronchiectasis patients. Conclusions Sputum NE may be considered a good biomarker of bronchiectasis severity in both CF and non-CF bronchiectasis patients, as confirmed by the exacerbations rate, CF risk of disease progression, and BSI scores.
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页数:10
相关论文
共 37 条
[21]   The CF-ABLE Score A Novel Clinical Prediction Rule for Prognosis in Patients With Cystic Fibrosis [J].
McCarthy, Cormac ;
Dimitrov, Borislav D. ;
Meurling, Imran J. ;
Gunaratnam, Cedric ;
McElvaney, Noel G. .
CHEST, 2013, 143 (05) :1358-1364
[22]   Standardisation of spirometry [J].
Miller, MR ;
Hankinson, J ;
Brusasco, V ;
Burgos, F ;
Casaburi, R ;
Coates, A ;
Crapo, R ;
Enright, P ;
van der Grinten, CPM ;
Gustafsson, P ;
Jensen, R ;
Johnson, DC ;
MacIntyre, N ;
McKay, R ;
Navajas, D ;
Pedersen, OF ;
Pellegrino, R ;
Viegi, G ;
Wanger, J .
EUROPEAN RESPIRATORY JOURNAL, 2005, 26 (02) :319-338
[23]  
Moustaki Maria, 2017, World J Clin Pediatr, V6, P132, DOI 10.5409/wjcp.v6.i3.132
[24]   ALPHA(1)-PROTEINASE INHIBITOR, ELASTASE ACTIVITY, AND LUNG-DISEASE SEVERITY IN CYSTIC-FIBROSIS [J].
OCONNOR, CM ;
GAFFNEY, K ;
KEANE, J ;
SOUTHEY, A ;
BYRNE, N ;
OMAHONEY, S ;
FITZGERALD, MX .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 148 (06) :1665-1670
[25]   British Thoracic Society guideline for non-CF bronchiectasis [J].
Pasteur, M. C. ;
Bilton, D. ;
Hill, A. T. .
THORAX, 2010, 65 :I1-I58
[26]   Inflammatory lung secretions inhibit dendritic cell maturation and function via neutrophil elastase [J].
Roghanian, Ali ;
Drost, Ellen M. ;
MacNee, William ;
Howie, Sarah E. M. ;
Sallenave, Jean-Michel .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 174 (11) :1189-1198
[27]   The CF-Sputum Induction Trial (CF-SpIT) to assess lower airway bacterial sampling in young children with cystic fibrosis: a prospective internally controlled interventional trial [J].
Ronchetti, Katherine ;
Tame, Jo-Dee ;
Paisey, Christopher ;
Thia, Lena P. ;
Doull, Iolo ;
Howe, Robin ;
Mahenthiralingam, Eshwar ;
Forton, Julian T. .
LANCET RESPIRATORY MEDICINE, 2018, 6 (06) :461-471
[28]   Sputum Biomarkers of Inflammation and Lung Function Decline in Children with Cystic Fibrosis [J].
Sagel, Scott D. ;
Wagner, Brandie D. ;
Anthony, Margaret M. ;
Emmett, Peggy ;
Zemanick, Edith T. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2012, 186 (09) :857-865
[29]   Induced sputum matrix metalloproteinase-9 correlates with lung function and airway inflammation in children with cystic fibrosis [J].
Sagel, SD ;
Kapsner, RK ;
Osberg, I .
PEDIATRIC PULMONOLOGY, 2005, 39 (03) :224-232
[30]   LONG-TERM STUDY OF 105 PATIENTS WITH CYSTIC FIBROSIS [J].
SHWACHMAN, H ;
KULCZYCKI, LL .
AMA JOURNAL OF DISEASES OF CHILDREN, 1958, 96 (01) :6-15