2017
DOI: 10.1038/s41598-017-08061-3
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Transmission is a Noticeable Cause of Resistance Among Treated Tuberculosis Patients in Shanghai, China

Abstract: It is generally believed that drug resistance among treated tuberculosis (TB) patients is as a result of acquired drug resistance due to inappropriate treatment. Previous studies have shown that primary drug resistance caused by transmission also plays a role among treated cases. Differentiating the two types of drug resistance will help in developing appropriate strategies for control of drug resistant tuberculosis. In this study, we tested the hypothesis that drug resistance among treated TB patients is main… Show more

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Cited by 17 publications
(19 citation statements)
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“…This decline may be due to the improvement of TB treatment and management in Hangzhou City, as it has implemented the DOTS Plus program—a DOTS program with components for MDR TB diagnosis, management, and treatment. A recent study in Shanghai showed the primary resistance due to exogenous reinfection was the major cause of drug resistance among treated TB patients [ 16 ], and this observation was also confirmed in other parts of China [ 17 ]. Another study found that 60% MRD patients had primary drug resistance attributable to transmission [ 18 ].…”
Section: Discussionmentioning
confidence: 78%
“…This decline may be due to the improvement of TB treatment and management in Hangzhou City, as it has implemented the DOTS Plus program—a DOTS program with components for MDR TB diagnosis, management, and treatment. A recent study in Shanghai showed the primary resistance due to exogenous reinfection was the major cause of drug resistance among treated TB patients [ 16 ], and this observation was also confirmed in other parts of China [ 17 ]. Another study found that 60% MRD patients had primary drug resistance attributable to transmission [ 18 ].…”
Section: Discussionmentioning
confidence: 78%
“…Studies reported stepwise acquisition of resistance to INH and RIF (i.e., multidrug resistance [MDR]) over a period of 12 to 13 months (20,21) and increases of resistance from para-aminosalicylic acid (PAS) monoresistance to XDR within 42 months (22) and from full susceptibility or MDR to XDR within 12 to 60 months (23,24). Two other studies also reported drug resistance levels increasing from susceptible to MDR and from MDR to XDR, respectively, but without indicating the exact time lapse (25,26). In the remaining 31 studies, no increase or a one-step increase in drug resistance level was observed during treatment.…”
Section: Within-host Evolution Of Drug Resistancementioning
confidence: 99%
“…While there are likely many compensatory mechanisms, maybe as many as there are drug resistanceconferring mutations, our understanding of compensatory mutations in M. tuberculosis remains limited to the rpoC/rpoA and ahpC promoter mutations (47,85,86). As MDR-TB and XDR-TB are mainly transmitted rather than acquired (26,87,88), large data sets from MDR strains evolving to pre-XDR and XDR within a patient are difficult to obtain. Yet studies of serial isolates would provide stronger evidence of causality than mere association studies, as the chronology of events can be studied, and compensatory mutations can be distinguished from hitchhiking ones.…”
Section: Knowledge Gapsmentioning
confidence: 99%
“…As a result, MDR-TB has become a major focus for TB research in recent years [ 1 , 2 ], with 480,000 new MDR-TB cases recorded in 2015 [ 1 ], comprising 5% of the total global TB burden [ 5 ]. Current evidence suggests that MDR-TB will increase globally as a proportion of total TB cases, not only due to transmission of MDR-TB [ 6 , 7 ], but also poor adherence to TB treatment leading to the emergence of MDR-TB [ 1 , 8 – 11 ]. World Health Organization (WHO) global targets for MDR-TB treatment success and adherence are currently 75%, which is lower than the 85% target for drug-sensitive TB [ 1 , 12 ], reflecting both the higher rates of mortality and barriers to treatment adherence.…”
Section: Introductionmentioning
confidence: 99%