Estimated rates of progression to tuberculosis disease for persons infected with Mycobacterium tuberculosis in the United States

肺结核 结核分枝杆菌 医学 疾病 病毒学 免疫学 内科学 病理
作者
Mina Ekramnia,Yunfei Li,Maryam B. Haddad,Suzanne M. Marks,J. Steve Kammerer,Nicole A. Swartwood,Ted Cohen,Jeffrey W. Miller,C. Robert Horsburgh,Joshua A. Salomon,Nicolas A Menzies
出处
期刊:Epidemiology [Ovid Technologies (Wolters Kluwer)]
卷期号:35 (2): 164-173
标识
DOI:10.1097/ede.0000000000001707
摘要

Background: In the United States, over 80% of tuberculosis (TB) disease cases are estimated to result from reactivation of latent TB infection (LTBI) acquired more than 2 years previously (“reactivation TB”). We estimated reactivation TB rates for the US population with LTBI, overall, by age, sex, race–ethnicity, and US-born status, and for selected comorbidities (diabetes, end-stage renal disease, and HIV). Methods: We collated nationally representative data for 2011–2012. Reactivation TB incidence was based on TB cases reported to the National TB Surveillance System that were attributed to LTBI reactivation. Person–years at risk of reactivation TB were calculated using interferon-gamma release assay (IGRA) positivity from the National Health and Nutrition Examination Survey, published values for interferon-gamma release assay sensitivity and specificity, and population estimates from the American Community Survey. Results: For persons aged ≥6 years with LTBI, the overall reactivation rate was estimated as 0.072 (95% uncertainty interval: 0.047, 0.12) per 100 person-years. Estimated reactivation rates declined with age. Compared to the overall population, estimated reactivation rates were higher for persons with diabetes (adjusted rate ratio [aRR] = 1.6 [1.5, 1.7]), end-stage renal disease (aRR = 9.8 [5.4, 19]), and HIV (aRR = 12 [10, 13]). Conclusions: In our study, individuals with LTBI faced small, non-negligible risks of reactivation TB. Risks were elevated for individuals with medical comorbidities that weaken immune function.
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