Multivariable regression models improve accuracy and sensitive grading of antibiotic resistance mutations in Mycobacterium tuberculosis Article Swipe
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· 2025
· Open Access
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· DOI: https://doi.org/10.1038/s41467-025-57174-1
Rapid genotype-based drug susceptibility testing for the Mycobacterium tuberculosis complex (MTBC) relies on a comprehensive knowledgebase of the genetic determinants of resistance. Here we present a catalogue of resistance-associated mutations using a regression-based approach and benchmark it against the 2nd edition of the World Health Organisation (WHO) mutation catalogue. We train multivariate logistic regression models on over 52,000 MTBC isolates to associate binary resistance phenotypes for 15 antitubercular drugs with variants extracted from candidate resistance genes. Regression detects 450/457 (98%) resistance-associated variants identified using the existing method (a.k.a, SOLO method) and grades 221 (29%) more total variants than SOLO. The regression-based catalogue achieves higher sensitivity on average (+3.2 percentage points, pp) than SOLO with smaller average decreases in specificity (-1.0 pp) and positive predictive value (-1.6 pp). Sensitivity gains are highest for ethambutol, clofazimine, streptomycin, and ethionamide as regression graded considerably more resistance-associated variants than SOLO for these drugs. There is no difference between SOLO and regression with regards to meeting the target product profiles set by the WHO for genetic drug susceptibility testing, except for rifampicin, for which regression specificity is below the threshold of 98% at 97%. The regression pipeline also detects isoniazid resistance compensatory mutations in ahpC and variants linked to bedaquiline and aminoglycoside hypersusceptibility. These results inform the continued development of targeted next generation sequencing, whole genome sequencing, and other commercial molecular assays for diagnosing resistance in the MTBC.
Related Topics
- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1038/s41467-025-57174-1
- https://www.nature.com/articles/s41467-025-57174-1.pdf
- OA Status
- gold
- Cited By
- 6
- References
- 37
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W4408110940
Raw OpenAlex JSON
- OpenAlex ID
-
https://openalex.org/W4408110940Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.1038/s41467-025-57174-1Digital Object Identifier
- Title
-
Multivariable regression models improve accuracy and sensitive grading of antibiotic resistance mutations in Mycobacterium tuberculosisWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2025Year of publication
- Publication date
-
2025-03-03Full publication date if available
- Authors
-
Sanjana G. Kulkarni, Sacha Laurent, Paolo Miotto, A Sarah Walker, Leonid Chindelevitch, Carl‐Michael Nathanson, Nazir Ismail, Timothy C. Rodwell, Maha FarhatList of authors in order
- Landing page
-
https://doi.org/10.1038/s41467-025-57174-1Publisher landing page
- PDF URL
-
https://www.nature.com/articles/s41467-025-57174-1.pdfDirect link to full text PDF
- Open access
-
YesWhether a free full text is available
- OA status
-
goldOpen access status per OpenAlex
- OA URL
-
https://www.nature.com/articles/s41467-025-57174-1.pdfDirect OA link when available
- Concepts
-
Mycobacterium tuberculosis, Tuberculosis, Antibiotics, Antibiotic resistance, Multivariable calculus, Microbiology, Regression, Medicine, Biology, Pathology, Statistics, Mathematics, Control engineering, EngineeringTop concepts (fields/topics) attached by OpenAlex
- Cited by
-
6Total citation count in OpenAlex
- Citations by year (recent)
-
2025: 6Per-year citation counts (last 5 years)
- References (count)
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37Number of works referenced by this work
- Related works (count)
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10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.450/457 | 78 |
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| institutions_distinct_count | 9 |
| corresponding_institution_ids | https://openalex.org/I4210087915 |
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| citation_normalized_percentile.is_in_top_10_percent | True |