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Increased vegetable and fruit intake is associated with reduced failure rate of tuberculosis treatment: a hospital-based cohort study in China

Published online by Cambridge University Press:  02 September 2020

Lei Xu
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
Jinyu Wang
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
Shanliang Zhao
Affiliation:
Department of Respiratory Medicine, Linyi People’s Hospital East Branch, Linyi, Shandong, 276000, People’s Republic of China
Jianwen Zhang
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
Ke Xiong
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
Jing Cai
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
Qiuzhen Wang
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
Song Lin
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
Yan Ma
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
Aiguo Ma*
Affiliation:
Institute of Nutrition and Health, School of Public Health, Qingdao University, Qingdao, Shandong, 266021, People’s Republic of China
*
* Corresponding author: Professor Aiguo Ma, email [email protected]
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Abstract

Increased intake of vegetables and fruits has been associated with reduced risk of tuberculosis infection. Vegetables and fruits exert immunoregulatory effects; however, it is not clear whether vegetables and fruits have an adjuvant treatment effect on tuberculosis. Between 2009 and 2013, a hospital-based cohort study was conducted in Linyi, Shandong Province, China. Treatment outcome was ascertained by sputum smear and chest computerised tomography, and dietary intake was assessed by a semi-quantitative FFQ. The dietary questionnaire was conducted at the end of month 2 of treatment initiation. Participants recalled their dietary intake of the previous 2 months. A total of 2309 patients were enrolled in this study. After 6 months of treatment, 2099 patients were successfully treated and 210 were uncured. In multivariate models, higher intake of total vegetables and fruits (OR 0·70; 95 % CI 0·49, 0·99), total vegetables (OR 0·68; 95 % CI 0·48, 0·97), dark-coloured vegetables (OR 0·61; 95 % CI 0·43, 0·86) and light-coloured vegetables (OR 0·67; 95 % CI 0·48, 0·95) were associated with reduced failure rate of tuberculosis treatment. No association was found between total fruit intake and reduced failure rate of tuberculosis treatment (OR 0·98; 95 % CI 0·70, 1·37). High intake of total vegetables and fruits, especially vegetables, is associated with lower risk of failure of tuberculosis treatment in pulmonary tuberculosis patients. The results provide important information for dietary guidelines during tuberculosis treatment.

Type
Full Papers
Copyright
© The Author(s), 2020. Published by Cambridge University Press on behalf of The Nutrition Society

Pulmonary tuberculosis is an infectious disease caused by Mycobacterium tuberculosis, and it is also a chronic wasting disease. M. tuberculosis bacilli are characterised by induction of chronic inflammation and intracellular survival(Reference Huang, Nazarova and Russell1). In 2018, there were approximately 10 million new cases of tuberculosis and 1·24 million HIV-negative tuberculosis-associated deaths worldwide. China accounted for 9 % of the global tuberculosis incidence(2). Although many countries have reduced their tuberculosis prevalence in the past few decades, the burdens are still high. Preventing and treating pulmonary tuberculosis remain to be crucial public health issues(Reference Shah, Abbas and Hanif3).

Epidemiological studies have indicated that malnutrition is associated with the occurrence and development of pulmonary tuberculosis(Reference Sinha, Davis and Saag4,Reference Bhargava5) and can be a predictor for tuberculosis treatment failure(6). The association between malnutrition and tuberculosis may be mediated by impaired immune function, increased oxidative stress, altered inflammation levels and dysfunctional gut microbiota(Reference Kant, Gupta and Ahluwalia7Reference Wang, Xiong and Zhao9). During tuberculosis chemotherapy, excessive pro-inflammatory mediators can lead to T-cell signalling defects and immune effector dysfunction, and this hyper-inflammatory reaction may continue through treatment completion, thereby adversely affecting treatment outcome(Reference Zumla, Rao and Parida10Reference Kumar, Fukutani and Shruthi13). Additionally, foods rich in fibre promote SCFA production and can control the intestinal immune response by increasing transforming growth factor-β, reducing proinflammatory cytokines(Reference Wallace, Bailey and Blumberg14,Reference De Rosa, Galgani and Santopaolo15) . Several studies have indicated that micronutrient deficiencies are relatively common in tuberculosis patients and that they can delay sputum smear conversion, exacerbate tuberculosis symptoms and affect tuberculosis treatment(Reference Oh, Choi and Park16Reference Wang, Xiong and Wang18). Vegetables and fruits are important components of a balanced diet, and they are as a source of vitamins, especially vitamins C and E, minerals, fibre and phytochemicals(Reference Alissa and Ferns19). Vegetables and fruits exert anti-inflammatory effects, play a role in immunoregulation(Reference Zhu, Du and Xu20,Reference Lampe21) and may be beneficial for treating pulmonary tuberculosis.

However, several observational studies have indicated that inadequate intake of vegetables and fruits is associated with increased risk of tuberculosis infection(Reference Fox, Lee and Lucas22Reference Hemila, Kaprio and Pietinen24). To the authors’ knowledge, limited research has been conducted on the dietary effect on tuberculosis treatment outcome. Consequently, the purpose of this study was to investigate the effect of vegetable and fruit intake on tuberculosis treatment outcome.

Methods

Ethics

The study was approved by the Medical Ethic Committee of Qingdao Municipal Center for Disease Control and Prevention, and all aspects of this study complied with the Declaration of Helsinki. This study was registered as ChiCTR-OCC-10000994 in the Chinese Clinical Trial Registry.

Study design and population

Between 2009 and 2013, a hospital-based cohort study was conducted in Linyi, Shandong Province, China. Seven hospitals or tuberculosis clinics were randomly selected for the study including Lanshan, Yishui, Tancheng, Yinan, Cangshan, Feixian and Pingyi. Each site had a defined catchment area including approximately 0·9 million residents. The three-tier health care delivery system constituted the existing health care system, and the tuberculosis control programme was centralised. The basic units of the tuberculosis health care system were the hospitals or tuberculosis clinics which were responsible for tuberculosis diagnosis, treatment and patient management guided by the national tuberculosis control programme(Reference Ying, Wang and Gong25). This was a post hoc analysis. In this study, study staff screened 2716 potential participants. A total of 407 participants were excluded due to (1) declining to participate (n 97); (2) meeting exclusion criteria (n 212) or (3) having incomplete data or implausible values from the diet history questionnaires (n 98). The final analytic population to evaluate associations with diet included 2309 participants. The flow chart of the study population is shown in Fig. 1.

Fig. 1. Flow chart of the study population.

The inclusion criteria were (1) being 18 years of age or older and (2) diagnosed as having pulmonary tuberculosis. Patients with clinical and radiographic abnormalities consistent with pulmonary tuberculosis and those suspected to have pulmonary tuberculosis were examined by sputum smear. If the sputum smear was positive, the patient was diagnosed with smear-positive pulmonary tuberculosis; if the sputum specimen was negative and the computerised tomography scan of the chest was compatible with active pulmonary tuberculosis, the patient was diagnosed with smear-negative pulmonary tuberculosis after discussion of the radiographic and clinical doctors(26). The final inclusion criterion was (3) providing informed consent. The exclusion criteria were (1) clinical evidence of extra-pulmonary tuberculosis, drug-resistant tuberculosis, organ dysfunction or neoplasm or being HIV positive; (2) having diseases that impaired eating; (3) having cognitive dysfunction or mental disorder and (4) being pregnant or lactating.

Ascertainment of regimens and treatment outcome

Patients diagnosed with pulmonary tuberculosis were followed up prospectively until completion of the standard 6-month tuberculosis treatment. Tuberculosis treatments used in this study were in line with the China Tuberculosis Control Collaboration strategy(27). To be specific, the standard regimen was used which consisted of four drugs (e.g. isoniazid, rifampicin, ethambutol and pyrazinamide) during the initial 2 months followed by isoniazid and rifampicin for the next 4 months(26). During the first month of hospitalisation, participants purchased meals by themselves according to their normal dietary habits. Subsequently, the patients were discharged from the hospital for home treatment and periodic re-examination.

The National Tuberculosis Control Programme Guidelines in China(26) were based on the definitions and reporting framework for tuberculosis organised by the WHO(28). Treatment success was defined as patients who were cured and those who completed treatment. The criteria patients with successful treatment were received all treatments, had two consecutive negative sputum smear results, one of which was obtained at the end of the treatment and had no active lesions detected by computerised tomography scan. The treatment outcomes were obtained from the patients’ medical records.

Dietary assessment

Dietary intake was assessed with a semi-quantitative FFQ. The questionnaire was formulated based on the foods with higher intake frequency according to the 2002 national nutrition survey in China that was developed and previously locally validated(Reference Li, Rao and Kong29,Reference Zhang, Zhao and Cai30) . All the participants were surveyed face to face by trained medical staff and project investigators to ensure good compliance of the respondents and quality of the questionnaire. The dietary questionnaire was conducted at the end of month two of treatment initiation. Participants recalled their dietary intake of the previous 2 months. The frequency options for vegetables and fruits included ‘three times a day’, ‘twice a day’, ‘once a day’, ‘four to five times a week’, ‘two to three times a week’, ‘once a week’, ‘once every 2 weeks’, ‘once a month’, ‘once every 2 months’ and ‘almost never’. A standard portion size was specified for vegetables and fruits, and participants were asked to denote their usual portion size from several options (<0·5 times, standard, >1·5 times or other). Vegetable and fruit intake was calculated by multiplying the portion size of a single serving of each food by its reported frequency of intake and then dividing by the time corresponding to the frequency of intake. Tools for data collection were a structured questionnaire, medical records, food-model booklets and locally available bowls, plates and cups for measuring or estimating the amount of food consumed.

In the study, total vegetables were divided into dark-coloured vegetables and light-coloured vegetables(31). Dark-coloured vegetables refer to those that are dark green, red, orange and purple. Light-coloured vegetables refer to those that are white, yellowish and slightly green. In view of the residents’ dietary habits in Linyi city, the researchers selected fifteen specific types of vegetables for qualitative research. Then participants were asked to recall whether they often ate one of the fifteen specific types of vegetables; if they responded ‘several times a month or a week’, the status of regular consumption was assessed. On the contrary, participants responded ‘never or infrequently’ if they seldom ate the vegetable, and the status of little consumption was assessed.

Covariates

Information was collected on age, sex, height and weight. BMI (kg/m2) was calculated as body weight in kg divided by the square of height in m. The physique was classified as underweight, normal weight, overweight or obese according to the BMI values for the Chinese population (<18·5, 18·5–23·9 and ≥24 kg/m2)(32). Other information collected included education completed (none, primary school, class VII–IX, class X–XII, diploma or higher), occupation (unskilled farmer or worker, student, professional, retired or other), marital status (single, divorced, widowed or married), lifestyle parameters including history of smoking, drinking and regular exercise, geographic location (Lanshan, Yishui, Tancheng, Yinan, Cangshan, Feixian or Pingyi), season of FFQ return (winter (December–February), spring (March–May), summer (June–August), autumn (September–November)) and total energy intake (kcal/d).

Statistical analysis

The survey data were analysed with SPSS version 19.0. In this study, qualitative data are expressed as numbers and percentages. Quantitative data are described as medians and inter-quartile ranges because of their non-normal distributions based on the Kolmogorov–Smirnov normality test. The statistical difference for the characteristics between the treatment success and the treatment failure groups was assessed with a χ 2 test for categorical variables and a Mann–Whitney U test for non-normal continuous variables. The intake of vegetables and fruits was categorised with tertiles according to their distributions in the study population. The associations between total vegetables and fruits, total vegetables, total fruits, dark-coloured vegetables, light-coloured vegetables, specific types of vegetables (regular consumption v. little consumption) and the failure rate of tuberculosis treatment were appraised by binary logistic regression. The lowest tertile of intake or little consumption was used as the reference category. Through univariate analysis, we determined the variables (BMI, marital status) related to treatment outcome. Additionally, variables previously reported to be associated with outcome (age(Reference Cardoso, do Brasil and Schmaltz33), sex(Reference Cardoso, do Brasil and Schmaltz33), education completed(Reference Wang, Yin and Du34), occupation(Reference Cai, Wang and Ma35), smoking(Reference Thomas, Thiruvengadam and Kadam36), drinking(Reference Thomas, Thiruvengadam and Kadam36), regular exercise(Reference Qiu, Shi and Li37) and total energy intake(Reference Ren, Zhao and Chen38)) were considered potential confounders. The crude model was unadjusted; model 1 was adjusted for age and sex; model 2 was adjusted for age, sex, BMI, education completed, occupation, marital status, smoking, drinking, regular exercise and total energy intake. Furthermore, stratified analyses were performed based on sex and smoking status to evaluate the relationship between total vegetable and fruit intake and the risk of failure of tuberculosis treatment.

The Box–Tidwell procedure was utilised to test the linearity between the continuous independent variables and the dependent variables(Reference Box and Tidwell39). The interactions of the continuous independent variables and their natural logarithm conversion values were incorporated into the regression model. To protect against type I error, Bonferroni’s correction was used. The tolerance and variance expansion factor was used to test the collinearity among the independent variables. Tolerance <0·1 or variance expansion factor > 10 meant that collinearity existed. The linear trend for the vegetable and fruit variables was tested by using the median values of each category and including them as continuous variables in the logistic regression model. Adjusted OR and 95 % CI were reported to indicate the strength and direction of associations. For all analyses, P < 0·05 or P < 0·01 was considered statistically significant (* P < 0·05, ** P < 0·01). All P values were two sided. The data were verified after collection, and confidentiality was maintained.

Results

The characteristics of the 2309 participants are shown in Table 1. After 6 months of treatment, 2099 patients were successfully treated and 210 were uncured. The success rate was 90·91 %. No significant difference was detected between the successful treatment and failed treatment groups for age, sex, education completed, marital status, occupation, smoking, drinking, regular exercise, geographic location, season of FFQ return or total energy intake. However, the successful treatment and failed treatment groups showed significant differences in BMI (P = 0·02) and marital status (P = 0·01).

Table 1. Baseline characteristics of study subjects (n 2309)*

(Numbers and percentages; median values and interquartile ranges (IQR))

* Categorical variables are presented as n and % while non-normal continuous variables are presented as medians and IQR. P values derived from χ 2 tests for categorical variables and Mann–Whitney U tests for non-normal continuous variables.

To convert kcal to kJ, multiply by 4·184.

As shown in Table 2, compared with the failed treatment group, the successful treatment group showed higher intake of total vegetables and fruits (200·00 v. 175·00 g/d, P = 0·007), total vegetables (142·86 v. 109·59 g/d, P = 0·004), dark-coloured vegetables (64·29 v. 42·86 g/d, P < 0·001) and light-coloured vegetables (85·71 v. 64·29 g/d, P = 0·02).

Table 2. Comparison with daily vegetable and fruit intake between the successful treatment and failed treatment groups*

(Median values and interquartile ranges (IQR))

* Non-normal continuous variables are presented as medians and IQR. P values derived from Mann–Whitney U tests for non-normal continuous variables.

The OR of treatment outcome according to tertiles of total vegetables and fruits, total vegetables, dark-coloured vegetables, light-coloured vegetables and total fruits are shown in Table 3. Compared with the lowest tertile, total vegetable and fruit intake for the highest tertile was inversely associated with the risk of failure of tuberculosis treatment; the OR was 0·70 (95 % CI 0·49, 0·99) in multivariate model 2. The intake of total vegetables was significantly associated with reduced risk of failure of tuberculosis treatment in the multivariate analysis (OR 0·68, 95 % CI 0·48, 0·97). Moreover, when we examined the association between vegetables according to colour categories and tuberculosis treatment outcome after adjustment for multiple confounders, compared with the lowest tertile, the OR of tuberculosis treatment outcome for the highest tertile intakes of dark-coloured vegetables and light-coloured vegetables were 0·61 (95 % CI 0·43, 0·86) and 0·67 (95 % CI 0·48, 0·95), respectively. No association was found between total fruit intake and reduced failure rate of tuberculosis treatment (OR 0·98, 95 % CI 0·70, 1·37).

Table 3. Association of vegetable and fruit intake with the failure rate of tuberculosis treatment

(Odds ratios and 95 % confidence intervals)

*P < 0·05, ** P < 0·01.

Crude model unadjusted.

Model 1 adjusted for age and sex.

§ Model 2 adjusted for age, sex, smoking, drinking, BMI, education completed, marital status, occupation, regular exercise and total energy intake.

|| Tests for linear trend were carried out by logistic regression, using a median value of each exposure intake category as a single.

The association between total vegetable and fruit intake and the failure rate of tuberculosis treatment in stratified analyses are shown in Table 4. In stratified analyses by sex, compared with the lowest tertile, total vegetable and fruit intake in males for the highest tertile was inversely associated with the risk of failure of tuberculosis treatment with an OR of 0·65 (95 % CI 0·43, 0·98) in model 2. In stratified analyses by smoking, no association was found between total vegetable and fruit intake and reduced failure rate of tuberculosis treatment.

Table 4. Association of total vegetable and fruit intake with the failure rate of tuberculosis treatment, stratified by sex and smoking status

(Odds ratios and 95 % confidence intervals)

* P < 0·05, ** P < 0·01.

Crude model unadjusted.

Model 2 adjusted for age, sex, smoking, drinking, BMI, education completed, marital status, occupation, regular exercise and total energy intake. The corresponding stratified variables were excluded from the adjusted model.

The OR of treatment outcome according to regular or little consumption of specific types of vegetables are shown in Table 5. After adjustment (model 2), the OR of tuberculosis treatment outcome for eating Chinese cabbage, spinach, radish, oilseed rape, eggplant, carob, tomato, cucumber, cauliflower and scallion were 0·52 (95 % CI 0·38, 0·71), 0·52 (95 % CI 0·39, 0·70), 0·65 (95 % CI 0·46, 0·92), 0·70 (95 % CI 0·50, 0·96), 0·55 (95 % CI 0·40, 0·76), 0·65 (95 % CI 0·48, 0·87), 0·53 (95 % CI 0·39, 0·71), 0·49 (95 % CI 0·36, 0·66), 0·61 (95 % CI 0·39, 0·94) and 0·56 (95 % CI 0·41, 0·76), respectively.

Table 5. Association of specific types of vegetables consumption with the failure rate of tuberculosis treatment

(Odds ratios and 95 % confidence intervals)

* P < 0·05, ** P < 0·01.

Crude model unadjusted.

Model 2 adjusted for age, sex, smoking, drinking, BMI, education completed, marital status, occupation, regular exercise and total energy intake.

§ The little consumption group was used as the reference group.

Discussion

In the present study, we found that sufficient intake of total vegetables and fruits, total vegetables, dark-coloured vegetables and light-coloured vegetables is associated with lower risk of failure of tuberculosis treatment. Regular consumption of Chinese cabbage, spinach, radish, oilseed rape, eggplant, carob, tomato, cucumber, cauliflower and scallion is inversely associated with the risk of failure of tuberculosis treatment.

Several previous studies have indicated a protective effect of vegetable and fruit intake on tuberculosis infection(Reference Fox, Lee and Lucas22Reference Hemila, Kaprio and Pietinen24). Sarita Aguirre found individuals with limited vegetables in their diet had an increased risk of respiratory symptoms related to tuberculosis(Reference Aguirre, Cuellar and Herrero40). He et al.(Reference He, Zhang and Wei41) found that vitamin C, vitamin E and superoxide dismutase in fresh vegetables and fruits constitute an antioxidant network during dietary intervention for patients with pulmonary tuberculosis complicated with type 2 diabetes, contributing to reducing malondialdehyde content, scavenging free radicals and reducing the proportion of patients with sputum positive for bacilli. These studies provided epidemiological evidence between vegetable and fruit intake and tuberculosis, supporting our findings to a certain extent. M. tuberculosis induces reactive oxygen species and reactive nitrogen species, and the equilibrium of pulmonary function between oxidant and antioxidant status is disturbed, thus provoking an inflammatory state and giving rise to immune suppression(Reference Golubovic, Stankovic and Ristic42). Vegetables and fruits may maintain this balance through anti-inflammatory and antioxidant effects, thus having beneficial effects on tuberculosis treatment. Nonetheless, the association between total fruit intake and reduced failure rate of tuberculosis treatment was not statistically significant. This may have been due to low intake of fruits by local people. Household income, fruit prices and regional dietary habits may be important constraints. Thus, the results indicate possible evidence for a relationship between fruit intake and treatment outcome that warrants further investigation.

Importantly, a large body of epidemiological evidence suggests that certain types of vegetables, particularly cruciferous vegetables (e.g. cauliflower, radish), dark-green leafy vegetables (e.g. celery(Reference Kooti and Daraei43), oilseed rape, spinach(Reference Roberts and Moreau44), swamp cabbage) have substantial health-promoting activities. Although not yet completely understood, phytochemicals and antioxidants within these vegetables can have multiple effects including decreasing activity of pro-inflammatory cytokines, reducing oxidative damage and even stimulating the immune system(Reference Wallace, Bailey and Blumberg14,Reference Lampe21) . Overall, most cell and animal studies supported a potential role for certain types of vegetables and their ingredients in tuberculosis prevention and treatment.

Several advantages of this study should be mentioned. First, to the authors’ knowledge, this was the first study to explore the association of vegetable and fruit intake on the outcome of tuberculosis treatment. Second, this study subdivided vegetables into dark-coloured vegetables and light-coloured vegetables, which greatly enhanced the practicality, and the colour categories were beneficial for menu planning(Reference Slavin and Lloyd45). Third, certain kinds of vegetables may affect tuberculosis treatment. Therefore, this was the first study to qualitatively investigate the relationship between specific types of vegetables and reduced failure rate of tuberculosis treatment. Awareness of the intake, colour category and specific types of vegetables provides context into how people with tuberculosis select food and may enhance intervention strategies aimed at improving dietary practice to promote health in this growing portion of the population living with a chronic wasting disease.

Nevertheless, some limitations of this study need to be acknowledged. First, there was a potential risk of recall bias regarding dietary intake, as this information relied on the participants’ ability to recall their dietary intake(Reference Naska, Lagiou and Lagiou46). Moreover, dietary information was not measured repeatedly, and measurement error in the FFQ might occur if the participants changed their diet over time. In this study, however, it was expected that dietary patterns among adults were relatively stable over time, based on other longitudinal studies that showed minimal temporal changes(Reference Batis, Sotres-Alvarez and Gordon-Larsen47,Reference Bacelo, do Brasil and Cople-Rodrigues48) . Second, although many potential confounders were controlled, household income and other socio-economic factors(Reference Li, Wang and Liu49,Reference Miller, Yusuf and Chow50) were not considered and could have affected the results. Third, different cooking methods and storage methods can lead to different nutritional values of vegetables and fruits. The information was not accounted in this study.

Conclusion

In conclusion, high intake of total vegetables and fruits, especially vegetables, is associated with lower risk of failure of tuberculosis treatment in pulmonary tuberculosis patients. The results provide important information for dietary guidelines during tuberculosis treatment.

Acknowledgements

The authors would like to thank the medical staff of Linyi People’s Hospital East Branch and county hospitals or tuberculosis clinics for their support.

The study was supported by the National Natural Science Foundation of China (grant no. 81872610 to Aiguo Ma).

The authors’ contributions were as follows: conceptualisation: A. M. and S. Z.; data curation: J. C.; investigation: Q. W. and J. C.; formal analysis: L. X. and J. Z.; funding acquisition: A. M.; methodology: A. M.; project administration: S. Z.; resources: S. Z. and A. M.; supervision: Y. M.; validation: J. W. and S. L.; writing - original draft: L. X.; writing - review and editing: J. W., K. X. and A. M.. All authors approved the final manuscript.

The authors declared no conflicts of interest.

References

Huang, L, Nazarova, EV & Russell, DG (2019) Mycobacterium tuberculosis: bacterial fitness within the host macrophage. Microbiol Spectr 2, BAI-0001-2019.Google Scholar
World Health Organization (2019) Global tuberculosis report. https://www.who.int/tb/publications/global_report/en/ (accessed October 2019).Google Scholar
Shah, S, Abbas, G, Hanif, M, et al. (2019) Increased burden of disease and role of health economics: Asia-pacific region. Expert Rev Pharmacoecon Outcomes Res 19, 517528.CrossRefGoogle ScholarPubMed
Sinha, P, Davis, J, Saag, L, et al. (2019) Undernutrition and tuberculosis: public health implications. J Infect Dis 219, 13561363.CrossRefGoogle ScholarPubMed
Bhargava, A (2016) Undernutrition, nutritionally acquired immunodeficiency, and tuberculosis control. BMJ 355, i5407.CrossRefGoogle ScholarPubMed
World Health Organization (2013) Nutritional care and support for patients with tuberculosis. https://www.who.int/nutrition/publications/guidelines/nutcare_support_patients_with_tb/en/ (accessed October 2019).Google Scholar
Kant, S, Gupta, H & Ahluwalia, S (2015) Significance of nutrition in pulmonary tuberculosis. Crit Rev Food Sci Nutr 55, 955963.CrossRefGoogle ScholarPubMed
Vidhya, R, Rathnakumar, K, Balu, V, et al. (2019) Oxidative stress, antioxidant status and lipid profile in pulmonary tuberculosis patients before and after anti-tubercular therapy. Indian J Tuberc 66, 375381.CrossRefGoogle ScholarPubMed
Wang, J, Xiong, K, Zhao, S, et al. (2020) Long-term effects of multi-drug-resistant tuberculosis treatment on gut microbiota and its health consequences. Front Microbiol 11, 53.CrossRefGoogle ScholarPubMed
Zumla, A, Rao, M, Parida, SK, et al. (2015) Inflammation and tuberculosis: host-directed therapies. J Intern Med 277, 373387.CrossRefGoogle ScholarPubMed
Mattos, AM, Almeida Cde, S, Franken, KL, et al. (2010) Increased IgG1, IFN-gamma, TNF-alpha and IL-6 responses to Mycobacterium tuberculosis antigens in patients with tuberculosis are lower after chemotherapy. Int Immunol 22, 775782.CrossRefGoogle ScholarPubMed
Sutherland, JS, Hill, PC, Adetifa, IM, et al. (2011) Identification of probable early-onset biomarkers for tuberculosis disease progression. PLoS ONE 6, e25230.CrossRefGoogle ScholarPubMed
Kumar, NP, Fukutani, KF, Shruthi, BS, et al. (2019) Persistent inflammation during anti-tuberculosis treatment with diabetes comorbidity. Elife 8, e46477.CrossRefGoogle ScholarPubMed
Wallace, TC, Bailey, RL, Blumberg, JB, et al. (2019) Fruits, vegetables, and health: a comprehensive narrative, umbrella review of the science and recommendations for enhanced public policy to improve intake. Crit Rev Food Sci Nutr 3, 138.Google Scholar
De Rosa, V, Galgani, M, Santopaolo, M, et al. (2015) Nutritional control of immunity: balancing the metabolic requirements with an appropriate immune function. Semin Immunol 27, 300309.CrossRefGoogle ScholarPubMed
Oh, J, Choi, R, Park, HD, et al. (2017) Evaluation of vitamin status in patients with pulmonary tuberculosis. J Infect 74, 272280.CrossRefGoogle ScholarPubMed
Karyadi, E, Schultink, W, Nelwan, R, et al. (2000) Poor micronutrient status of active pulmonary tuberculosis patients in Indonesia. J Nutr 130, 29532958.CrossRefGoogle ScholarPubMed
Wang, J, Xiong, K, Wang, Q, et al. (2020) Adjunctive vitamin A and D during pulmonary tuberculosis treatment: a randomized controlled trial with a 2 × 2 factorial design. Food Funct 5, 46724681.CrossRefGoogle Scholar
Alissa, EM & Ferns, GA (2017) Dietary fruits and vegetables and cardiovascular diseases risk. Crit Rev Food Sci Nutr 57, 19501962.Google ScholarPubMed
Zhu, F, Du, B & Xu, B (2018) Anti-inflammatory effects of phytochemicals from fruits, vegetables, and food legumes: a review. Crit Rev Food Sci Nutr 58, 12601270.CrossRefGoogle ScholarPubMed
Lampe, JW (1999) Health effects of vegetables and fruit: assessing mechanisms of action in human experimental studies. Am J Clin Nutr 70, 475S490S.CrossRefGoogle ScholarPubMed
Fox, GJ, Lee, RS, Lucas, M, et al. (2015) Inadequate diet is associated with acquiring Mycobacterium tuberculosis infection in an inuit community: a case–control study. Ann Am Thorac Soc 12, 11531162.Google Scholar
Fan, Y, Liu, H, Jiang, H, et al. (2014) A case-control study of the effect of vegetables and fruits on the risk of tuberculosis pathogenesis. Shenzhen J Integr Tradit Chin West Med 24, 2123.Google Scholar
Hemila, H, Kaprio, J, Pietinen, P, et al. (1999) Vitamin C and other compounds in vitamin C rich food in relation to risk of tuberculosis in male smokers. Am J Epidemiol 150, 632641.CrossRefGoogle ScholarPubMed
Ying, T, Wang, Y, Gong, Y, et al. (2015) Non-adherence to anti-tuberculosis treatment among internal migrants with pulmonary tuberculosis in Shenzhen, China: a cross-sectional study. BMC Public Health 15, 474.Google Scholar
Chinese Ministry of Health and Chinese Centre on TB Control and Prevention (2009) National Tuberculosis Control Programme Guidelines (2008 version). Beijing: Peking Union Medical College Publishing House.Google Scholar
China Tuberculosis Control Collaboration (1996) Results of directly observed short-course chemotherapy in 112842 Chinese patients with smear-positive tuberculosis. Lancet 347, 358362.CrossRefGoogle Scholar
World Health Organization (2006) Revised TB recording and reporting forms and registers. https://www.who.int/tb/dots/r_and_r_forms/en/ (accessed June 2020).Google Scholar
Li, L, Rao, K, Kong, L, et al. (2005) Technical Working Group of China National Nutrition and Health Survey. A description on the Chinese national nutrition and health survey in 2002. Chin. J Epidemiol 26, 478484.Google Scholar
Zhang, J, Zhao, S, Cai, J, et al. (2019) Analysis of dietary and nutritional status of elderly pulmonary tuberculosis patients in Linyi city, Shandong province. Acta Nutrimenta Sinica 41, 135138.CrossRefGoogle Scholar
Chinese Nutrition Society (2016) Chinese Dietary Guidelines. Beijing: People’s Medical Publishing House.Google Scholar
Working Group on Obesity in China (2004) Guidelines for prevention and control of overweight and obesity in Chinese adults. Acta Nutrimenta Sinica 26, 14.Google Scholar
Cardoso, MA, do Brasil, PEAA, Schmaltz, CAS, et al. (2017) Tuberculosis treatment outcomes and factors associated with each of them in a cohort followed up between 2010 and 2014. Biomed Res Int 2017, 3974651.CrossRefGoogle Scholar
Wang, X, Yin, S, Du, J, et al. (2017) Risk factors for the treatment outcome of retreated pulmonary tuberculosis patients in China: an optimized prediction model. Epidemiol Infect 145, 18051814.CrossRefGoogle ScholarPubMed
Cai, J, Wang, X, Ma, A, et al. (2015) Factors associated with patient and provider delays for tuberculosis diagnosis and treatment in Asia: a systematic review and meta-analysis. PLOS ONE 10, e0120088.CrossRefGoogle Scholar
Thomas, BE, Thiruvengadam, K, Kadam, D, et al. (2019) Smoking, alcohol use disorder and tuberculosis treatment outcomes: a dual co-morbidity burden that cannot be ignored. PLOS ONE 7, e0220507.CrossRefGoogle Scholar
Qiu, H, Shi, Y, Li, Y, et al. (2017) Incident rate and risk factors for tuberculosis among patients with type 2 diabetes: retrospective cohort study in Shanghai, China. Trop Med Int Health 7, 830838.CrossRefGoogle Scholar
Ren, Z, Zhao, F, Chen, H, et al. (2019) Nutritional intakes and associated factors among tuberculosis patients: a cross-sectional study in China. BMC Infect Dis 19, 907.CrossRefGoogle ScholarPubMed
Box, GEP & Tidwell, PW (1962) Transformation of the independent variables. Technometrics 4, 531550.CrossRefGoogle Scholar
Aguirre, S, Cuellar, CM, Herrero, MB, et al. (2017) Prevalence of tuberculosis respiratory symptoms and associated factors in the indigenous populations of Paraguay (2012). Mem Inst Oswaldo Cruz 112, 474484.CrossRefGoogle ScholarPubMed
He, L, Zhang, G, Wei, M, et al. (2019) Effect of individualized dietary intervention on oxidative stress in patients with type 2 diabetes complicated by tuberculosis in Xinjiang. China. Diabetes Ther 10, 20952105.CrossRefGoogle ScholarPubMed
Golubovic, S, Stankovic, I, Ristic, L, et al. (2010) Antioxidant enzymes and lipid peroxidation products in patients with pulmonary tuberculosis. Med Pregl 63, 450453.CrossRefGoogle ScholarPubMed
Kooti, W & Daraei, N (2017) A review of the antioxidant activity of celery (Apium graveolens L). J Evid Based Complementary Altern Med 22, 10291034.CrossRefGoogle ScholarPubMed
Roberts, JL & Moreau, R (2016) Functional properties of spinach (Spinacia oleracea L.) phytochemicals and bioactives. Food Funct 7, 3337–53.CrossRefGoogle ScholarPubMed
Slavin, JL & Lloyd, B (2012) Health benefits of fruits and vegetables. Adv Nutr 3, 506516.CrossRefGoogle ScholarPubMed
Naska, A, Lagiou, A & Lagiou, P (2017) Dietary assessment methods in epidemiological research: current state of the art and future prospects. F1000Res 6, 926.CrossRefGoogle ScholarPubMed
Batis, C, Sotres-Alvarez, D, Gordon-Larsen, P, et al. (2014) Longitudinal analysis of dietary patterns in Chinese adults from 1991 to 2009. Br J Nutr 8, 14411451.CrossRefGoogle Scholar
Bacelo, AC, do Brasil, PE, Cople-Rodrigues, CD, et al. (2017) Dietary counseling adherence during tuberculosis treatment: a Longitudinal Study. Clin Nutr ESPEN 17, 4453.CrossRefGoogle ScholarPubMed
Li, Y, Wang, L, Liu, X, et al. (2018) Structure and characteristics of food consumption of rural households in Shandong Province based on household tracking survey. J Nat Resour 6, 978991.Google Scholar
Miller, V, Yusuf, S, Chow, CK, et al. (2016) Availability, affordability, and consumption of fruits and vegetables in 18 countries across income levels: findings from the Prospective Urban Rural Epidemiology (PURE) study. Lancet Glob Health 10, e695e703.CrossRefGoogle Scholar
Figure 0

Fig. 1. Flow chart of the study population.

Figure 1

Table 1. Baseline characteristics of study subjects (n 2309)*(Numbers and percentages; median values and interquartile ranges (IQR))

Figure 2

Table 2. Comparison with daily vegetable and fruit intake between the successful treatment and failed treatment groups*(Median values and interquartile ranges (IQR))

Figure 3

Table 3. Association of vegetable and fruit intake with the failure rate of tuberculosis treatment(Odds ratios and 95 % confidence intervals)

Figure 4

Table 4. Association of total vegetable and fruit intake with the failure rate of tuberculosis treatment, stratified by sex and smoking status(Odds ratios and 95 % confidence intervals)

Figure 5

Table 5. Association of specific types of vegetables consumption with the failure rate of tuberculosis treatment(Odds ratios and 95 % confidence intervals)