Incident asthma and Mycoplasma pneumoniae: A nationwide cohort study - 14/11/15

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Abstract |
Background |
Previous studies investigating the relationship between Mycoplasma pneumoniae and incident asthma in the general population have been inconclusive.
Objective |
We conducted a nationwide cohort study to clarify this relationship.
Methods |
Using the National Health Insurance Research Database of Taiwan, we identified 1591 patients with M pneumoniae infection (International Classification of Diseases, Ninth Revision, Clinical Modification code 4830) given diagnoses between 2000 and 2008. We then frequency matched 6364 patients without M pneumoniae infection from the general population according to age, sex, and index year. Cox proportional hazards regression analysis was performed to determine the adjusted hazard ratio (aHR) of the occurrence of asthma in the M pneumoniae cohort compared with that in the non–M pneumoniae cohort.
Results |
Regardless of comorbidities and the use of antibiotic or steroid therapies, patients with M pneumonia infection had a higher risk of incident asthma than those without it. The aHR of asthma was 3.35 (95% CI, 2.71-4.15) for the M pneumoniae cohort, with a significantly higher risk when patients were stratified by age, sex, follow-up time, and comorbidities, including allergic rhinitis, atopic dermatitis, or allergic conjunctivitis. Patients with M pneumoniae infection had a higher risk of having early-onset (age, <12 years; aHR, 2.87) and late-onset (age, ≥12 years; aHR, 3.95) asthma. The aHR was also higher within the less than 2-year follow-up in the M pneumoniae cohort (aHR, 4.41; 95% CI, 3.40-5.74) than in the cohort without the infection.
Conclusion |
This study found that incident cases of early-onset and late-onset asthma are closely related to M pneumoniae infection, even in nonatopic patients.
Le texte complet de cet article est disponible en PDF.Key words : Mycoplasma pneumoniae, asthma, antibiotic, steroid, cohort study
Abbreviations used : aHR, AC, AD, AR, IRR, LHID
Plan
| Supported in part by the Taiwan Ministry of Health and Welfare Clinical Trial and the Research Center of Excellence (MOHW104-TDU-B-212-113002); the China Medical University Hospital, Academia Sinica Taiwan Biobank, Stroke Biosignature Project (BM104010092); the NRPB Stroke Clinical Trial Consortium (MOST 103-2325-B-039-006); the Tseng-Lien Lin Foundation, Taichung, Taiwan; the Taiwan Brain Disease Foundation, Taipei, Taiwan; the Katsuzo and Kiyo Aoshima Memorial Funds, Japan; and the CMU under the Aim for Top University Plan of the Ministry of Education, Taiwan. |
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| Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest. |
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