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Epidemiology of anti-tuberculosis drug resistance in a chinese population: current situation and challenges ahead
- Yan Shao†1,
- Dandan Yang†1,
- Weiguo Xu1,
- Wei Lu1,
- Honghuan Song1,
- Yaoyao Dai2,
- Hongbing Shen2 and
- Jianming Wang2Email author
© Shao et al; licensee BioMed Central Ltd. 2011
Received: 31 August 2010
Accepted: 17 February 2011
Published: 17 February 2011
Drug resistance has been a cause of concern for tuberculosis (TB) control in both developed and developing countries. Careful monitoring of the patterns and trends of drug resistance should remain a priority.
Strains were collected from 1824 diagnosed sputum smear positive pulmonary TB patients in Jiangsu province of China and then tested for drug susceptibility against rifampicin, isoniazid, ethambutol and streptomycin. The prevalence and patterns of drug resistance in mycobacterium tuberculosis (MTB) isolates were investigated. Multiple logistic regression analysis was performed to identify the risk factors for multidrug resistant (MDR) bacterial infection. The strength of association was estimated by odds ratio (OR) and 95% confidence interval (95% CI).
The drug susceptibility tests showed that 1077(59.05%) MTB strains were sensitive to all the four antibiotics and the other 747(40.95%) strains were resistant to at least one drug. The proportions of mono-drug resistance were 28.73% for isoniazid, 19.41% for rifampicin, 29.33% for streptomycin, and 13.98% for ethambutol, respectively. The prevalence of MDR-TB was 16.61%, which was significantly different between new cases (7.63%) and those with previous treatment history (33.07%). Geographical variation of drug resistance was observed, where the proportion of MDR-TB among new cases was higher in the central (9.50%) or north part (9.57%) than that in the south area (4.91%) of Jiangsu province. The age of patients was significantly associated with the risk of drug resistance (P < 0.001) and the adjusted OR (95% CI) was 1.88(1.26-2.81) for patients aged 35-44 years when compared with those 65 years or older. Patients with previous treatment history had a more than 5-fold increased risk of MDR-TB (adjusted OR: 6.14, 95% CI: 4.61-8.17), compared with those previously not having been treated.
The high prevalence of drug resistance has been a major challenge for TB control. Prevention and control of drug-resistant TB should be emphasized by the revised DOTS (direct observed therapy, short course) program through prompt case detection, routine and quality-assured drug susceptibility test for patients at high risk of resistance, programmatic treatment with both first and second-line medicines, and systematic treatment observation, with priority for high MDR-TB settings.
Tuberculosis (TB) is a leading cause of death in humans due to an infectious agent (mycobacterium tuberculosis, MTB) and it remains a major public health burden in developing countries . Globally, there were an estimated 8.9-9.9 million incident cases of TB in 2008, most of which occurred in Asia and Africa, with the first two countries being India and China . The current anti-tuberculosis therapies are fraught with problems, predominantly because of the long-term treatment and the increasing occurrence of drug resistance . Drug resistance can be simply defined as the capacity of organisms and their progeny to remain viable or to multiply in the presence of the concentration of the drug that would normally destroy or inhibit cell growth . Drug resistance of MTB was reported soon after the introduction of anti-tuberculosis drugs in the last century and now has been a critical threat to global TB control . One of the particularly dangerous form is multidrug-resistant (MDR) TB, which is defined as resistance to at least isoniazid and rifampicin, the two most powerful anti-tuberculosis drugs, because the treatment of such cases is more complex, lengthy, expensive, frequently less successful and usually produce more severe adverse reactions . In 2008, an estimated 390,000-510,000 cases of MDR-TB have emerged globally . China reported a high proportion of drug resistance with the highest burden of cases in the world, just following the countries of the former Soviet Union . It was estimated that the prevalence of MDR-TB was 5.7% among new cases and 25.6% among those previously treated in China, which confirmed previous estimates that about 100,000 MDR-TB cases emerged annually .
China has reached the global targets for case detection and treatment success now, but careful monitoring of the patterns and trends of drug resistance should remain a priority. In order to obtain insights into the prevalence and distribution of anti-tuberculosis drug resistance, China joined the global surveillance project organized by WHO/IUATLD (World Health Organization/International Union against Tuberculosis and Lung Diseases). By 2007, 13 out of 31 provinces (without Jiangsu) in China have been involved in this surveillance system . As a province located along the eastern coast of China, Jiangsu covers an area of 102.6 thousand square kilometres and contains 13 municipalities and 106 counties (districts), with a total population of 77 million in 2009. DOTS (direct observed therapy, short course) strategy for TB has been introduced in Jiangsu in the 1990s and been 100% available at the county level by now . However, there are still great challenges facing TB control, particularly for the early detection and effective treatment. Unfortunately, until now, no study has been conducted to investigate the current situation and patterns of drug resistance among TB patients at the provincial level in Jiangsu.
Therefore, the aim of the present study was to assess the drug susceptibility patterns of MTB in Jiangsu and explore potential risk factors for MDR-TB in order to provide policy-makers with recommendations for better-organized TB control programs.
The sampling method referred to the "Guidelines for surveillance of drug resistance in tuberculosis" developed by WHO/IUATLD . Thirty counties (districts) from Jiangsu province were selected systematically and the sample size was estimated based on the following parameters: (1) The annual reported new sputum smear positive (SS+) cases were 23603 and previously treated SS+ cases were 5524 (based on the surveillance data in Jiangsu province); (2) The precision was set at 2% for new cases and 4% for previously treated cases; (3) The initial mono-drug resistance rate was set at 6% among new cases and 16% among previously treated cases based on the proportion of rifampicin resistant isolates from a pilot study with small sample size (unpublished); Additionally, the sample size was amplified by taking into account the design effect of the cluster sampling method and potential no-response of study subjects. Finally, the estimated sample size was 2035, which included 1247 new cases and 788 previously treated cases. Sixty-seven SS+ patients from each site were recruited continuously as expected, including 41 new patients and 26 previously treated patients. The period of case recruitment was set between May 1, 2008 and December 31, 2008. All newly registered pulmonary TB patients with sputum smear positive tests in selected study sites were eligible for inclusion. Eligible patients should be continuously recruited since May 1, 2008, until the sampling site reaches a minimum number of cases.
After obtaining informed consent, a standard questionnaire was completed for each recruited patient to collect demographic data and the history of treatment. Cases were classified into new and previously treated ones based on patient's self-reports or available medical documents. The definitions of new/previously treated cases referred to the WHO guidelines [7, 11]. A 'new case' was defined as a newly registered episode of TB in a patient who, in response to direct questioning, denied having had any prior anti-tuberculosis treatment (for up to one month), and in study sites where adequate documentation was available, for whom there was no evidence of such history. A 'previously treated case' was defined as a newly registered episode of TB in a patient who, in response to direct questioning admitted having been treated for TB for one month or more, or, in study sites where adequate documentation was available, there was evidence of such history.
Three sputum smear samples were collected from each subject with labelled plastic bottles. The Ziehl-Neelsen hot staining method was used for sputum smear microscopy test. The two sputum samples with the highest bacterial counts were cultured, and one culture was submitted for drug susceptibility test (DST). Sputum smear microscopy and culture were performed at the level of county (district) laboratory while DST was done at the provincial reference laboratory. The sputum samples were decontaminated with 4% sodium hydroxide (NaOH), centrifuged, and then cultured on Lowenstein-Jensen (LJ) culture media. The LJ culture media were incubated at 37°C and observed on days 3 and 7 to detect contaminations and/or fast growth of atypical mycobacteria and subsequently every week to note the growth and the morphology of the colonies. Identification of MTB was done using the p-nitrobenzoic acid (PNB) and thiophene carboxylic acid hydrazine (TCH) resistance test. Growth in LJ medium containing PNB indicates that the bacilli do not belong to the MTB complex. Species other than MTB were excluded from the current analysis. DST utilizes the same type of LJ medium and inoculation methods as culture techniques. LJ medium was impregnated with isoniazid (INH), rifampicin (RIF), streptomycin (SM), and ethambutol (EMB) according to the proportion method as recommended by WHO/IUATLD [8, 11]. The concentrations of anti-tuberculosis drugs were 0.2 μg/ml for INH, 40 μg/ml for RIF, 4 μg/ml for SM, and 2 μg/ml for EMB. The growth of colonies in the drug-containing plate was compared to the control plate as a proportion. If the bacterial growth on the medium with the specific drug was ≥1% compared to the control, the strain was declared resistant to the specific drug; or it was defined as sensitive when the growth rate was < 1% compared to the control. MDR-TB was defined as isolates being resistant to at least RIF and INH. Internal and external quality controls were conducted through the whole study period. For internal quality assurance on DST, a standard H37Rv laboratory strain was included for each batch of culture. External quality control for sputum smear microscopy and culture was conducted by the provincial TB reference laboratory in Jiangsu and further undertaken by the supranational reference laboratory of Hong Kong.
Data were double entered with EpiData 3.1 (Denmark) and discrepancies were checked against the raw data. The prevalence of mono- and multi- drug resistance among new and previously treated TB cases was calculated. Multiple logistic regression analysis was performed to identify the risk factors for MDR bacterial infection. Variables included in the final model were chosen based on the biological plausibility as well as statistical and epidemiologic criteria. The strength of association was estimated by odds ratio (OR) and 95% confidence interval (95% CI). All tests of significance were two sided and a significant threshold was set at 0.05. All analyses were performed using the STATA statistical software (version 10.0; StataCorp, College Station, TX).
This project has been approved by Institutional Review Board of Nanjing Medical University. Written informed consent was obtained from all participants. Ethics has been respected throughout the whole study period.
Observed mono-drug resistance among tuberculosis cases in Jiangsu Province, China
At least one drug
Previously treated cases
Observed multi-drug resistance among tuberculosis cases in Jiangsu Province, China
Previously treated cases
Observed drug resistance in different areas of Jiangsu Province, China
Area of residence
Previously treated cases
Factors associated with multi-drug resistant tuberculosis
cOR(95% CI) ‡
aOR(95% CI) *
n = 1824
n = 1521, n(%)
n = 303, n(%)
Treatment history #
Area of residence
Cigarette smoking &
As a public health dilemma, drug resistance has been an obstacle to achieve the goal of effective global TB control. Recently, the emergence of MDR and XDR (extensively drug-resistant) TB has incurred a very alarming challenge to global health [5, 12]. Appreciating the importance of documenting the drug susceptibility of MTB, WHO has implemented a worldwide surveillance programme while findings showed regional and national variations in the magnitude and trends of drug-resistance . The high prevalence of MDR recently reported from the expanding number of provinces surveyed in China and Russia is indicative of a larger epidemic than previously suspected . In recent years, the substantial structural transformation of China's economy has contributed to the world's largest ever-peacetime flow of migration. Mobility of population has been proved to strengthen the transmission dynamics of TB as well as antimicrobial drug-resistant organisms [14, 15]. As a more developed eastern province, Jiangsu absorbed a large proportion of migrations within China. Now it has been an area with the highest population density (753 per square kilometre) among all provinces of China. Exploring the prevalence and pattern of drug resistance could substantially facilitate the local and countrywide TB control.
Role of age and sex
In most countries, the majority of TB patients are male . However, male or female TB patients could have different levels of risks for drug resistance due to differences in access to health-care services or exposure to other risk factors . In the present study, the OR of harboring MDR-TB strains for female was 1.43 (95% CI: 0.99-2.06) compared with male, showing a borderline association between MDR-TB and the sex of patients. Discovering gender disparities associated with the risks of MDR-TB could provide insight into the development of targeted measures and improve access to health care and reduce the risk of acquiring drug-resistance. The association between age and the risk of MDR-TB is not well established in the literatures as different studies use different cut-off points for age groups. MDR-TB patients were more likely to be younger than 65 years [17, 18]. A systematic review analysis in Europe revealed the pooled risk of MDR-TB for people younger than 45 was higher than that among older patients (OR: 1.52, 95% CI: 1.13-2.03) . In this study, we found that the frequency of MDR-TB was much higher in young adulthoods and peaked at 35-44 years old, which was similar to the findings from MDR-TB surveillance data in 13 countries of Central and Eastern Europe (CEEUR) . This pattern suggests that MDR-TB epidemic in Jiangsu is a relatively recent phenomenon and bears the highest toll on young adults. We assumed that age-related difference in treatment adherence might be a possible explanation, as patients at 35-44 years old were often occupied by study, work or other activities on a daily basis, in contrast with the more sedentary lifestyle of old patients .
Effect of previous anti-tuberculosis treatment
Drug resistance in MTB isolates arises from spontaneous genetic mutations and can be amplified through selection pressure and further exaggerated by poor adherence of patients . Drug-resistant TB is either acquired due to poor management of treatment or transmission from infectious drug-resistant TB patients . As found in many other studies, the history of anti-tuberculosis treatment has been consistently associated with the risk of MDR-TB . A systematic review on 29 studies in Europe reported the pooled risk of MDR was up to 10 times higher in previously treated cases than in never treated ones . Our study is consistent to the former reports that revealed the importance of previous treatment history in the risk of drug resistance. These previously treated patients often constitute a very heterogeneous group including those who experience relapse after receiving successful treatment, those who return after default, and those who start receiving a re-treatment regimen after having experienced previous treatment failure .
Geographical variation of drug resistance was observed in the present study, where a higher proportion of MDR-TB among new cases was found in the central or north part as compared with that in the south area. Understanding the patterns of transmission is important in TB control because acquired resistance and primary resistance require different control strategies . To prevent primary drug resistance, new technologies for early distinguishing drug resistance and adopting effective measures to block the transmission are important. To reduce acquired drug resistance, development of high-quality drugs and strength of patient management are needed . Lower proportion of primary MDR in the south part indicates that TB control in this region is rather successful and lacks substantial transmission of MDR strains as compared with the central and north part of Jiangsu. However, similar higher proportions of acquired drug resistance among TB patients in these three regions also cause concerns for strengthening drug development and patient management. Another interesting topic in the transmission of MDR-TB is the role of migration, as Jiangsu is a province absorbing a large number of non-permanent residents. In this study, we did not specifically design questions to distinguish the moving population from the native population. However, one question might be associated with this topic: "How long have you been living here"? We analyzed this variable, but found no significant association. One possible explanation might be a large part of moving population preferring to return to their home when they were suspected as TB. A revised epidemiological design is needed to further analyze the role of migration on MDR.
Limitation of this study
Some sources of bias could exist in this study. First, there is a potential bias in estimation of drug resistance in previously treated cases. Although we interviewed the patients, reviewed the medical records and screened the case notification system to check previous episodes of TB, we could not exclude the possibility of misclassification. Second, we did not perform DST for second-line anti-tuberculosis drugs in this study. Thus, the prevalence of XDR is unclear. Third, there are two most useful sampling strategies for the surveillance of drug resistance: 100% sampling of diagnostic centres and cluster sampling . Cluster sampling methods were adopted reasonably in the situations in which it was logistically difficult to cover the entire area and where the number of TB diagnostic centres is high. Cluster sampling is commonly used, rather than simple random sampling, mainly as a means of saving money when, for example, the population is spread out, and the researcher cannot sample from everywhere. The loss of effectiveness by the use of cluster sampling, instead of simple random sampling, should not be neglected. Though in this study, the sample size was multiplied by the design effect, the higher sampling error caused by the cluster sampling method should be taken into account.
The importance of knowing the susceptibility to MTB has become more significant because of the increasing resistance rates, high travel activity of hosts and the limited available anti-tuberculosis agents. Surveillance is a crucial intermediate step to allocate resources and design treatment regimens. However, such population-based surveys are temporary measures until we know the drug-susceptibility profile of each patient, which can be used for prescription of individualized therapy. DST needs to be scaled up so that patients infected with susceptible MTB strains can get DOTS, those with mono-drug resistance can get intensive DOTS to prevent multidrug resistance, and those with MDR can get the life-saving therapy they need . Unfortunately, routine DST of MTB is not available at the country level of China while the laboratories responsible for diagnosing cases have not been strengthened to meet these requirements, despite the drug resistance has captivated the attentions in the past decade. Even in some health facilities with necessary equipments, the results of susceptibility test still take more than several weeks, when the patients with MDR-TB have already been treated with INH and RIF for quite a long time. Therefore, new strategies, rapid diagnostic tools [24, 25] (such as molecular line-probe assay), new anti-tuberculosis therapies, and effective vaccines are urgently needed . A better understanding of the risk factors would help to determine groups of patients who would be more likely to have MDR-TB and thus prioritize the use of rapid diagnostic methods for the identification and determination of drug resistance.
In conclusion, the high prevalence of drug resistance in Jiangsu province has been a major challenge for TB control. Patients with previous treatment history are at higher risk for MDR-TB. Monitoring of drug-resistance should be enhanced by periodic surveys to assess trends and take correct actions when necessary. Prevention and control of drug-resistant TB should be emphasized by the revised DOTS program through prompt case detection, routine and quality-assured DST for those patients at high risk of resistance, programmatic treatment with both first and second-line medicines, and systematic treatment observation, with priority for high MDR-TB settings.
This study is supported by "National S&T Major Project Foundation of China" (2009ZX10004-904) and National Natural Science Foundation of China (81072351).
- Maartens G, Wilkinson RJ: Tuberculosis. Lancet. 2007, 370: 2030-2043. 10.1016/S0140-6736(07)61262-8.View ArticlePubMedGoogle Scholar
- Global Tuberculosis Control: A short update to the 2009 report. [http://whqlibdoc.who.int/publications/2009/9789241598866_eng.pdf]
- Russell DG, Barry CE, Flynn JL: Tuberculosis: what we don't know can, and does, hurt us. Science. 2010, 328: 852-856. 10.1126/science.1184784.View ArticlePubMedPubMed CentralGoogle Scholar
- Kant S, Maurya AK, Kushwaha RA, Nag VL, Prasad R: Multi-drug resistant tuberculosis: an iatrogenic problem. Biosci Trends. 2010, 4: 48-55.PubMedGoogle Scholar
- Yew WW, Leung CC: Management of multidrug-resistant tuberculosis: Update 2007. Respirology. 2008, 13: 21-46. 10.1111/j.1440-1843.2008.01341.x.View ArticlePubMedGoogle Scholar
- Aziz MA, Wright A, Laszlo A, De Muynck A, Portaels F, Van Deun A, Wells C, Nunn P, Blanc L, Raviglione M: Epidemiology of antituberculosis drug resistance (the Global Project on Anti-tuberculosis Drug Resistance Surveillance): an updated analysis. Lancet. 2006, 368: 2142-2154. 10.1016/S0140-6736(06)69863-2.View ArticlePubMedGoogle Scholar
- Multidrug and extensively drug-resistant TB (M/XDR-TB): 2010 global report on surveillance and response. [http://whqlibdoc.who.int/publications/2010/9789241599191_eng.pdf]
- Anti-tuberculosis drug resistance in the world(WHO/HTM/TB/2008.394). [http://whqlibdoc.who.int/hq/2008/WHO_HTM_TB_2008.394_eng.pdf]
- He GX, Zhao YL, Jiang GL, Liu YH, Xia H, Wang SF, Wang LX, Borgdorff MW, van der Werf MJ, van den Hof S: Prevalence of tuberculosis drug resistance in 10 provinces of China. BMC Infect Dis. 2008, 8: 166-10.1186/1471-2334-8-166.View ArticlePubMedPubMed CentralGoogle Scholar
- Xu W, Lu W, Zhou Y, Zhu L, Shen H, Wang J: Adherence to anti-tuberculosis treatment among pulmonary tuberculosis patients: a qualitative and quantitative study. BMC Health Serv Res. 2009, 9: 169-10.1186/1472-6963-9-169.View ArticlePubMedPubMed CentralGoogle Scholar
- Guidelines for surveillance of drug resistance in tuberculosis (WHO/HTM/TB/2009.422). [http://www.who.int/tb/publications/mdr_surveillance/en/index.html]
- Burki T: Tuberculosis-resistance, funding, and drugs. Lancet Infect Dis. 2010, 10: 297-298. 10.1016/S1473-3099(10)70083-9.View ArticlePubMedGoogle Scholar
- Wright A, Zignol M, Van Deun A, Falzon D, Gerdes SR, Feldman K, Hoffner S, Drobniewski F, Barrera L, van Soolingen D, et al: Epidemiology of antituberculosis drug resistance 2002-07: an updated analysis of the Global Project on Anti-Tuberculosis Drug Resistance Surveillance. Lancet. 2009, 373: 1861-1873. 10.1016/S0140-6736(09)60331-7.View ArticlePubMedGoogle Scholar
- MacPherson DW, Gushulak BD, Baine WB, Bala S, Gubbins PO, Holtom P, Segarra-Newnham M: Population mobility, globalization, and antimicrobial drug resistance. Emerg Infect Dis. 2009, 15: 1727-1732.PubMedPubMed CentralGoogle Scholar
- Arguin PM, Marano N, Freedman DO: Globally mobile populations and the spread of emerging pathogens. Emerg Infect Dis. 2009, 15: 1713-1714.View ArticlePubMedPubMed CentralGoogle Scholar
- Neyrolles O, Quintana-Murci L: Sexual inequality in tuberculosis. PLoS Med. 2009, 6: e1000199-10.1371/journal.pmed.1000199.View ArticlePubMedPubMed CentralGoogle Scholar
- Faustini A, Hall AJ, Perucci CA: Risk factors for multidrug resistant tuberculosis in Europe: a systematic review. Thorax. 2006, 61: 158-163. 10.1136/thx.2005.045963.View ArticlePubMedGoogle Scholar
- Law WS, Yew WW, Chiu Leung C, Kam KM, Tam CM, Chan CK, Leung CC: Risk factors for multidrug-resistant tuberculosis in Hong Kong. Int J Tuberc Lung Dis. 2008, 12: 1065-1070.PubMedGoogle Scholar
- Chiang CY, Schaaf HS: Management of drug-resistant tuberculosis. Int J Tuberc Lung Dis. 2010, 14: 672-682.PubMedGoogle Scholar
- Suarez-Garcia I, Rodriguez-Blanco A, Vidal-Perez JL, Garcia-Viejo MA, Jaras-Hernandez MJ, Lopez O, Noguerado-Asensio A: Risk factors for multidrug-resistant tuberculosis in a tuberculosis unit in Madrid, Spain. Eur J Clin Microbiol Infect Dis. 2009, 28: 325-330. 10.1007/s10096-008-0627-y.View ArticlePubMedGoogle Scholar
- Zignol M, Wright A, Jaramillo E, Nunn P, Raviglione MC: Patients with previously treated tuberculosis no longer neglected. Clin Infect Dis. 2007, 44: 61-64. 10.1086/509328.View ArticlePubMedGoogle Scholar
- Gao Q, Li X: Transmission of MDR tuberculosis. Drug Discovery Today: Disease Mechanisms. 2010, 7: e61-e65. 10.1016/j.ddmec.2010.09.006.View ArticleGoogle Scholar
- Borgdorff MW, Small PM: Scratching the surface of ignorance on MDR tuberculosis. Lancet. 2009, 373: 1822-1824. 10.1016/S0140-6736(09)60557-2.View ArticlePubMedGoogle Scholar
- Bwanga F, Hoffner S, Haile M, Joloba ML: Direct susceptibility testing for multi drug resistant tuberculosis: a meta-analysis. BMC Infect Dis. 2009, 9: 67-10.1186/1471-2334-9-67.View ArticlePubMedPubMed CentralGoogle Scholar
- Ling DI, Zwerling AA, Pai M: Rapid diagnosis of drug-resistant TB using line probe assays: from evidence to policy. Expert Rev Respir Med. 2008, 2: 583-588. 10.1586/174763188.8.131.523.View ArticlePubMedGoogle Scholar
- Zhao M, Li X, Xu P, Shen X, Gui X, Wang L, Deriemer K, Mei J, Gao Q: Transmission of MDR and XDR tuberculosis in Shanghai, China. PLoS One. 2009, 4: e4370-10.1371/journal.pone.0004370.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2458/11/110/prepub
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