1) Based on analysis of Medicare (CMS) national claims data, we have determined that the epidemiology of mycobacterial disease in the United States has changed over the last 20 years, with a decline in pulmonary tuberculosis and an increase identified in pulmonary nontuberculosis mycobacterial disease. The prevalence of PNTM is increasing significantly across all regions of the United States and among both men and women. Significant racial/ethnic and geographic differences in PNTM prevalence suggest important gene-environment interactions. From 1997-2007, the annual prevalence significantly increased from 20 (95% CI: 18-23) to 47 (95% CI: 44-51) cases/100,000 persons, or 8.2% per year. The period prevalence was 112 (95% CI: 108-116) cases/100,000 persons, although prevalence was two-fold higher among Asians/Pacific Islanders than among whites (228 vs. 116 cases/100,000 persons). One-third of PNTM cases resided in southeastern states, which had a period prevalence of 131 (95% CI: 122-140) cases/100,000 persons;however, western states had the highest period prevalence at 149 (95% CI: 136-163) cases/100,000 persons, with Hawaii having the highest prevalence at 396 (95% CI: 170-211) cases/100,000 persons. PNTM cases had more comorbid conditions than non-cases and were 40% more likely to die than non-cases (OR=1.4 95% CI: 1.3-1.6). Overall, women were 1.4 (95% CI: 1.3-1.5) times more likely to be a PNTM case than men. Relative to whites, Asians/Pacific Islanders were twice as likely to be a case (OR=2.0 95% CI: 1.2-2.5) while blacks were half as likely (OR=0.5 95% CI: 0.4-0.6). Based on geographic differences in NTM prevalence identified, we became interested in further understanding the geographic variability of NTM lung disease and possible gene-environment interactions. The ubiquitous prevalence of the NTM organisms and the rarity of NTM disease support the role for a genetic susceptibility to disease from these organisms. We are currently conducting further analysis of these claims data to identify geographic clusters of disease in the US and to correlate environemental factors with disease prevalence. 2) PNTM risk factors for mortality: Although the disease burden of pulmonary nontuberculous mycobacteria (NTM) is increasing, data are lacking on risk factors for mortality. Predictors of all-cause mortality with pulmonary NTM include low BMI, low pulmonary function, and high levels of inflammation. To estimate the mortality rate among persons with pulmonary NTM and to describe predictors of mortality, we conducted a retrospective review of patient data from the NIH pulmonary NTM natural history cohort. Kaplan-Meier survival curves and Cox Proportional Hazard Models were used to describe survival. The study population for analysis comprised 106 patients, including 26 (25%) who progressed to death and 80 surviving. The mean age at death was 67 years, and the median length of follow-up was 4.9 years. The mortality rate was 4.02 per 100 person-years. Sex, racial/ethnic group, age at entry, and follow-up time were similar between deceased and surviving patients. Pulmonary hypertension and chronic obstructive pulmonary disease (COPD) were more prominent in deceased patients. No significant differences were observed in baseline organism. Mean baseline Body Mass Index (BMI) was 20.0 for deceased patients and 22.2 for surviving patients (p<0.05), with a decrease in BMI observed after one year in patients who died. Deceased patients had significantly lower pulmonary function and higher levels of inflammation at entry (p<0.0005). 3) Effectiveness of inhaled amikacin: Treatment regimens for pulmonary nontuberculous mycobacteria (NTM) disease are complex and may be ineffective. Amikacin is recommended for rapidly growing NTM, cavitary disease, and failed treatments, but systemic use is associated with renal (15%), hearing (37%), and vestibular toxicity (9%). Aerosolized amikacin has the potential for reduced toxicity. In a previous study, 4 of 6 patients on failed treatment for Mycobacterium avium complex (MAC) lung disease were culture negative after 6 months of inhaled amikacin without toxic side effects. The primary purpose of this study was to assess effectiveness and toxicity of inhaled amikacin in patients with treatment refractory NTM lung disease. Records from an IRB-approved natural history study were queried from 2003-2010 to identify NTM patients with aerosolized amikacin added to failing treatment regimens. Patient characteristics and culture results summarized and individual 4-month slope for semi-quantitative culture quantity change estimated using linear regression. Eight patients (38%) had a negative culture during the course of follow-up. Five patients (24%) had no subsequent positive after sequential negative cultures. Patients with an early decrease in culture quantity tended to have negative cultures. Inhaled amikacin appears modestly effective for treating both MAC and M. abscessus pulmonary infections in previously treatment-unresponsive patients. Inhaled amikacin has markedly reduced toxicity as compared to reported systemic (i.v.) amikacin. This retrospective study is limited by variability in dosing, sputum sampling, concomitant organisms, and follow-up. However, early changes in culture quantity at 4 months may be predictive of subsequent culture conversion. 4) Bronchiectasis is a condition characterized by permanent bronchial dilation and repeated infections, particularly with mycobacteria. The Laboratory of Clinical Infectious Diseases, NIAID, is currently conducting clinical studies of bronchiectasis natural history. We sought to describe the trend, associated conditions and risk factors for bronchiectasis among adults 65 years. Bronchiectasis prevalence increased significantly from 2000-2007 in the Medicare outpatient setting and varied by age, sex and race/ethnicity. A 5% sample of the Medicare outpatient claims database was analyzed for bronchiectasis trends among beneficiaries aged 65 years from 2000-2007. Bronchiectasis was identified using the ICD-9-CM claim diagnosis codes for acquired bronchiectasis. Period prevalence was used to describe sex and race/ethnicity specific rates and annual prevalence was used to describe trends and age specific rates. We estimated trends using Poisson regression and odds of bronchiectasis using multivariate logistic regression. From 2000-2007, 22,296 persons had at least one claim for bronchiectasis. The eight year period prevalence of bronchiectasis was 1106 cases/100,000 persons. Bronchiectasis increased by 8.7% per year. We identified an interaction between number of thoracic CT scans and race/ethnicity;there was a significantly greater increase in bronchiectasis period prevalence by number of thoracic CT scans among Asians as compared to whites or blacks. Among persons with one CT scan, Asians had a 2.5 and 3.9 fold higher period prevalence as compared to whites and blacks. This increase could be due to a true increase in the condition or increased recognition of previously undiagnosed cases.

Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
2011
Total Cost
$306,988
Indirect Cost
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Adjemian, Jennifer; Daniel-Wayman, Shelby; Ricotta, Emily et al. (2018) Epidemiology of Nontuberculous Mycobacteriosis. Semin Respir Crit Care Med 39:325-335
Adjemian, Jennifer; Olivier, Kenneth N; Prevots, D Rebecca (2018) Epidemiology of Pulmonary Nontuberculous Mycobacterial Sputum Positivity in Patients with Cystic Fibrosis in the United States, 2010-2014. Ann Am Thorac Soc 15:817-826
van Ingen, Jakko; Wagner, Dirk; Gallagher, Jack et al. (2017) Poor adherence to management guidelines in nontuberculous mycobacterial pulmonary diseases. Eur Respir J 49:
Adjemian, Jennifer; Frankland, Timothy B; Daida, Yihe G et al. (2017) Epidemiology of Nontuberculous Mycobacterial Lung Disease and Tuberculosis, Hawaii, USA. Emerg Infect Dis 23:439-447
Spaulding, Alicen B; Lai, Yi Ling; Zelazny, Adrian M et al. (2017) Geographic Distribution of Nontuberculous Mycobacterial Species Identified among Clinical Isolates in the United States, 2009-2013. Ann Am Thorac Soc :
Prevots, D Rebecca; Loddenkemper, Robert; Sotgiu, Giovanni et al. (2017) Nontuberculous mycobacterial pulmonary disease: an increasing burden with substantial costs. Eur Respir J 49:
Henkle, Emily; Novosad, Shannon A; Shafer, Sean et al. (2017) Long-Term Outcomes in a Population-based Cohort with Respiratory Nontuberculous Mycobacteria Isolation. Ann Am Thorac Soc 14:1120-1128
Henkle, Emily; Aksamit, Timothy; Barker, Alan et al. (2016) Patient-Centered Research Priorities for Pulmonary Nontuberculous Mycobacteria (NTM) Infection. An NTM Research Consortium Workshop Report. Ann Am Thorac Soc 13:S379-84
Fleshner, M; Olivier, K N; Shaw, P A et al. (2016) Mortality among patients with pulmonary non-tuberculous mycobacteria disease. Int J Tuberc Lung Dis 20:582-7
Winthrop, Kevin L; Ku, Jennifer H; Marras, Theodore K et al. (2015) The tolerability of linezolid in the treatment of nontuberculous mycobacterial disease. Eur Respir J 45:1177-9

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