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doi:10.22028/D291-40975
Title: | Discovery and validation of a personalized risk predictor for incident tuberculosis in low transmission settings |
Author(s): | Gupta, Rishi K. Calderwood, Claire J. Yavlinsky, Alexei Krutikov, Maria Quartagno, Matteo Aichelburg, Maximilian C. Altet, Neus Diel, Roland Dobler, Claudia C. Dominguez, Jose Doyle, Joseph S. Erkens, Connie Geis, Steffen Haldar, Pranabashis Hauri, Anja M. Hermansen, Thomas Johnston, James C. Lange, Christoph Lange, Berit van Leth, Frank Muñoz, Laura Roder, Christine Romanowski, Kamila Roth, David Sester, Martina Sloot, Rosa Sotgiu, Giovanni Woltmann, Gerrit Yoshiyama, Takashi Zellweger, Jean-Pierre Zenner, Dominik Aldridge, Robert W. Copas, Andrew Rangaka, Molebogeng X. Lipman, Marc Noursadeghi, Mahdad Abubakar, Ibrahim |
Language: | English |
Title: | Nature Medicine |
Volume: | 26 |
Issue: | 12 |
Pages: | 1941-1949 |
Publisher/Platform: | Springer Nature |
Year of Publication: | 2020 |
Free key words: | Biomarkers Diseases Medical research Risk factors |
DDC notations: | 610 Medicine and health |
Publikation type: | Journal Article |
Abstract: | The risk of tuberculosis (TB) is variable among individuals with latent Mycobacterium tuberculosis infection (LTBI), but validated estimates of personalized risk are lacking. In pooled data from 18 systematically identified cohort studies from 20 countries, including 80,468 individuals tested for LTBI, 5-year cumulative incident TB risk among people with untreated LTBI was 15.6% (95% confidence interval (CI), 8.0–29.2%) among child contacts, 4.8% (95% CI, 3.0–7.7%) among adult contacts, 5.0% (95% CI, 1.6–14.5%) among migrants and 4.8% (95% CI, 1.5–14.3%) among immunocompromised groups. We confirmed highly variable estimates within risk groups, necessitating an individualized approach to risk stratification. Therefore, we developed a personalized risk predictor for incident TB (PERISKOPE-TB) that combines a quantitative measure of T cell sensitization and clinical covariates. Internal–external cross-validation of the model demonstrated a random effects meta-analysis C-statistic of 0.88 (95% CI, 0.82–0.93) for incident TB. In decision curve analysis, the model demonstrated clinical utility for targeting preventative treatment, compared to treating all, or no, people with LTBI. We challenge the current crude approach to TB risk estimation among people with LTBI in favor of our evidence-based and patient-centered method, in settings aiming for pre-elimination worldwide. |
DOI of the first publication: | 10.1038/s41591-020-1076-0 |
URL of the first publication: | https://www.nature.com/articles/s41591-020-1076-0 |
Link to this record: | urn:nbn:de:bsz:291--ds-409757 hdl:20.500.11880/36790 http://dx.doi.org/10.22028/D291-40975 |
ISSN: | 1546-170X 1078-8956 |
Date of registration: | 7-Nov-2023 |
Description of the related object: | Supplementary information |
Related object: | https://static-content.springer.com/esm/art%3A10.1038%2Fs41591-020-1076-0/MediaObjects/41591_2020_1076_MOESM1_ESM.pdf https://static-content.springer.com/esm/art%3A10.1038%2Fs41591-020-1076-0/MediaObjects/41591_2020_1076_MOESM2_ESM.pdf |
Faculty: | M - Medizinische Fakultät |
Department: | M - Infektionsmedizin |
Professorship: | M - Prof. Dr. Martina Sester |
Collections: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
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