Xpert MTB/RIF Assay Shows Faster Clearance of Mycobacterium tuberculosis DNA with Higher Levels of Rifapentine Exposure

Author:

Jayakumar A.1,Savic R. M.2,Everett C. K.1,Benator D.3,Alland D.4,Heilig C. M.5,Weiner M.6,Friedrich S. O.7,Martinson N. A.8,Kerrigan A.9,Zamudio C.10,Goldberg S. V.5,Whitworth W. C.5,Davis J. L.11,Nahid P.1

Affiliation:

1. University of California, San Francisco, Division of Pulmonary and Critical Care Medicine, San Francisco, California, USA

2. University of California, San Francisco, School of Pharmacy, San Francisco, California, USA

3. Washington DC VA Medical Center and the George Washington University, Washington, DC, USA

4. Rutgers-New Jersey Medical School, Newark, New Jersey, USA

5. Division of Tuberculosis Elimination, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

6. Veterans Administration Medical Center and University of Texas Health Science Center, San Antonio, Texas, USA

7. Division of Medical Physiology, MRC Centre for Tuberculosis Research, DST/NRF Centre of Excellence for Biomedical Tuberculosis Research, Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa

8. Perinatal HIV Research Unit (PHRU), MRC Soweto Matlosana Collaborating Centre for HIV/AIDS and TB, University of the Witwatersrand, Johannesburg, South Africa

9. Vanderbilt University School of Medicine, Nashville, Tennessee, USA

10. Universidad Peruana Cayetano Heredia, Lima, Peru

11. Yale School of Public Health, New Haven, Connecticut, USA

Abstract

ABSTRACT The Xpert MTB/RIF assay is both sensitive and specific as a diagnostic test. Xpert also reports quantitative output in cycle threshold ( C T ) values, which may provide a dynamic measure of sputum bacillary burden when used longitudinally. We evaluated the relationship between Xpert C T trajectory and drug exposure during tuberculosis (TB) treatment to assess the potential utility of Xpert C T for treatment monitoring. We obtained serial sputum samples from patients with smear-positive pulmonary TB who were consecutively enrolled at 10 international clinical trial sites participating in study 29X, a CDC-sponsored Tuberculosis Trials Consortium study evaluating the tolerability, safety, and antimicrobial activity of rifapentine at daily doses of up to 20 mg/kg of body weight. Xpert was performed at weeks 0, 2, 4, 6, 8, and 12. Longitudinal C T data were modeled using a nonlinear mixed effects model in relation to rifapentine exposure (area under the concentration-time curve [AUC]). The rate of change of C T was higher in subjects receiving rifapentine than in subjects receiving standard-dose rifampin. Moreover, rifapentine exposure, but not assigned dose, was significantly associated with rate of change in C T ( P = 0.02). The estimated increase in C T slope for every additional 100 μg · h/ml of rifapentine drug exposure (as measured by AUC) was 0.11 C T /week (95% confidence interval [CI], 0.05 to 0.17). Increasing rifapentine exposure is associated with a higher rate of change of Xpert C T , indicating faster clearance of Mycobacterium tuberculosis DNA. These data suggest that the quantitative outputs of the Xpert MTB/RIF assay may be useful as a dynamic measure of TB treatment response.

Funder

HHS | National Institutes of Health

HHS | NIH | National Institute of Allergy and Infectious Diseases

HHS | Centers for Disease Control and Prevention

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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