A retrospective cohort study of isoniazid-resistant tuberculosis treatment outcomes and isoniazid resistance-associated mutations in eastern China from 2013 to 2018. (September 2020)

• Record Type: Journal Article
• Authors: Shao, Yan; Li, Yishu; Song, Honghuan; Li, Guoli; Li, Yan; Zhu, Limei; Lu, Wei; Chen, Cheng
• Is Part Of: Journal of global antimicrobial resistance. Volume 22(2020)
• Page Start: 847
• Page End: 853
• Publication Date: 2020-09
• Subjects: Drug resistance -- Isoniazid -- Treatment outcome -- Genetics -- Tuberculosis; Drug resistance -- Periodicals; Drug resistance -- Periodicals; Drug resistance; Periodicals; 616.9041
• DOI: 10.1016/j.jgar.2020.07.012
• Languages: English
• ISSNs: 2213-7165

Abstract

Highlights: Rate of unfavourable outcomes for isoniazid-resistant, rifampicin-susceptible tuberculosis (Hr-TB) was 17.5%. TB treatment history was associated with poor outcomes for Hr-TB. Current genetic determination of isoniazid resistance is inadequate. Abstract: Objectives: The current situation of isoniazid-resistant, rifampicin-susceptible tuberculosis (Hr-TB) and associated genetic factors is not clear in China. Methods: A retrospective cohort study was conducted from 2013 to 2018 in Jiangsu Province, China. Phenotypic Hr-TB were identified by drug susceptibility testing on Lowenstein–Jensen medium and using a Mycobacterium Growth Indicator Tube 960 (MGIT 960) system, and mutations in the katG 315 codon and inhA promoter nucleotides –8, –15 and –16 were determined by GenoType MTBDR plus and sequencing. All of the Hr-TB patients enrolled were followed up until June 2019. Results: A total of 1416 smear-positive sputum samples were collected, of which 57 were excluded due to the presence of nontuberculous mycobacteria. Finally, 63/1359 (4.6%) were determined as Hr-TB. After follow-up, 11 Hr-TB patients (17.5%) showed an unfavourable outcome, of whom 5 (7.9%) relapsed, 4 (6.3%) had treatment failure and 2 (3.2%) died. A total of 52 isolates (82.5%) were detected with either katG 315 or inhA promoter nucleotide –8, –15 or –16 mutations, whereas no canonical mutations were found in 8 isolates (12.7%); 3 isolates failed in mutation detection. TB history was found to be associated with unfavourable outcomes for Hr-TB (odds ratio = 6.13, 95% confidence interval 1.05–35.82; P = 0.04). However, mutations in katG 315 and the inhA promoter region were not found to be associated with Hr-TB unfavourable outcomes ( P = 0.15). Conclusion: Unfavourable outcomes for Hr-TB are serious in eastern China, especially for previously treated patients. Meanwhile, current genetic determination of Hr-TB is inadequate.