Sensitisation to staphylococcal enterotoxins and asthma severity: a longitudinal study in the EGEA cohort

被引:49
作者
Sintobin, Ina [1 ]
Siroux, Valerie [2 ]
Holtappels, Gabriele [1 ]
Pison, Christophe [3 ,4 ]
Nadif, Rachel [5 ,6 ]
Bousquet, Jean [5 ,6 ,7 ,8 ,9 ,10 ,11 ]
Bachert, Claus [1 ,12 ]
机构
[1] Univ Ghent, Upper Airways Res Lab, C Heymanslaan 10, B-9000 Ghent, Belgium
[2] Univ Grenoble Alpes, Team Environm Epidemiol Appl Reprod & Resp Hlth, INSERM, CNRS,IAB,U1209,Joint Res Ctr, Grenoble, France
[3] Univ Grenoble Alpes, Grenoble, France
[4] CHU Grenoble, Inserm 1055, Pole Thorax & Vaisseaux, Clin Univ Pneumol, Grenoble, France
[5] INSERM, VIMA Aging & Chron Diseases Epidemiol & Publ Hlt, U1168, Villejuif, France
[6] Univ Versailles St Quentin En Yvelines, UMR S 1168, Montigny Le Bretonneux, France
[7] Charite Univ Med Berlin, Berlin, Germany
[8] Free Univ Berlin, Berlin, Germany
[9] Humboldt Univ, Berlin, Germany
[10] Berlin Inst Hlth, Comprehens Allergy Ctr, Dept Dermatol & Allergy, Berlin, Germany
[11] MACVIA France, Fdn Partenariale FMC VIA LR, Montpellier, France
[12] Univ Stockholm, Karolinska Inst, CLINTEC, Div ENT Dis, Stockholm, Sweden
关键词
BRONCHIAL HYPERRESPONSIVENESS; AUREUS ENTEROTOXINS; IGE SENSITIZATION; ALLERGIC-ASTHMA; ENVIRONMENT; GENETICS; ATOPY; RHINOSINUSITIS; COLONIZATION; POPULATION;
D O I
10.1183/13993003.00198-2019
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction: Evidence is accumulating that Staphylococcus aureus plays an important role as disease modifier in upper and lower airway diseases. Sensitisation to S. aureus enterotoxins (SEs) was associated with an increased risk of severe asthma in previous cross-sectional studies, but evidence from longitudinal studies is lacking. We aimed to assess associations between SE-sensitisation and the subsequent risk for asthma severity and exacerbations. Methods: This is a nested case-control study from the 20-year Epidemiological Study of the Genetics and Environment of Asthma (EGEA) cohort, including 225 adults (75 without asthma, 76 with mild asthma and 74 with severe asthma) in EGEA2 (2003-2007). For 173 of these individuals, SE-sensitisation was measured on samples collected 11 years earlier (EGEA1). Cross-sectional associations were conducted for EGEA1 and EGEA2. Longitudinal analyses estimated the association between SE-sensitisation in EGEA1 and the risk of severe asthma and asthma exacerbations assessed in the follow-up. Models were adjusted for sex, age, smoking, parental asthma/allergy and skin-prick test to house dust mite. Results: SE-sensitisation varied between 39% in controls to 58% and 76% in mild and severe asthma, respectively, in EGEA1. An adjusted cross-sectional association showed that SE-sensitisation was associated with an increased risk of severe, but not for mild asthma. SE-sensitisation in EGEA1 was associated with severe asthma (adjusted OR 2.69, 95% CI 1.18-6.15) and asthma exacerbations (adjusted OR 4.59, 95% CI 1.40-15.07) assessed 10-20 years later. Conclusion: For the first time, this study shows that being sensitised to SEs is associated with an increased subsequent risk of severe asthma and asthma exacerbations.
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页数:10
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