Aging, COPD, and Other Risk Factors Do Not Explain the Increased Prevalence of Pulmonary Mycobacterium avium Complex in Ontario

被引:49
作者
Al-Houqani, Mohammed [1 ]
Jamieson, Frances [4 ,5 ]
Mehta, Mauli [2 ,3 ]
Chedore, Pamela [5 ]
May, Kevin [5 ]
Marras, Theodore K. [2 ,3 ]
机构
[1] United Arab Emirates Univ, Fac Med & Hlth Sci, Al Ain, U Arab Emirates
[2] Univ Toronto, Mt Sinai Hosp, Toronto, ON, Canada
[3] Univ Hlth Network, Dept Med, Div Respirol, Toronto, ON, Canada
[4] Univ Hlth Network, Dept Lab Med & Pathohiol, Publ Hlth Lab, Publ Hlth Ontario, Toronto, ON, Canada
[5] Univ Hlth Network, TB & Mycobacteriol Lab, Toronto, ON, Canada
关键词
NONTUBERCULOUS MYCOBACTERIA; CLINICAL-SIGNIFICANCE; DISEASE PREVALENCE; WALKERTON TRAGEDY; BCG-VACCINATION; UNITED-STATES; INTRACELLULARE; EPIDEMIOLOGY; INFECTION; NETHERLANDS;
D O I
10.1378/chest.11-0089
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: The cause of observed increases in pulmonary Mycobacterium avium complex (pMAC) isolation and disease is unexplained. To explore possible causes of the increase in pMAC isolation and disease prevalence in Ontario, Canada, we studied age and other population-level risk factors. Methods: We determined age and sex of patients with pMAC disease between 2003 and 2008. We then estimated whether the potential effect of population aging and changes in prevalence of HIV infection, solid organ transplant, COPD, and tumor necrosis factor-alpha (TNF-alpha) inhibition have contributed to the observed increase in pMAC disease. Results: During 2003 to 2008, pMAC isolation and disease prevalence (per 100,000) both increased (8.44 to 12.62 and 4.35 to 6.81, respectively). The total number of cases of disease increased by 348 (2.46 per 100,000). Based on actual contemporary population changes, aging could explain 70 additional cases (increase of 0.57 per 100,000). The increase in self-reported COPD prevalence could potentially explain 11 (95% CI, 0-42) additional cases (increase of 0.09 per 100,000 [95% CI, 0-0.34 per 100,000]). HIV infection, solid organ transplant, and TNF-alpha inhibition combined could potentially explain no more than 73 additional cases (increase of 0.60 per 100,000). Conclusions: Although population aging appears to be a major risk factor, the increase in pMAC disease in Ontario could be only partly explained by aging, increases in COPD, HIV, solid organ transplantation, and TNF-alpha inhibition therapy. The increase in pMAC is likely multifactorial and may be affected by environmental or pathogen factors not addressed in this study. CHEST 2012; 141(1):190-197
引用
收藏
页码:190 / 197
页数:8
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