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. 2020 Jun 4;20:854. doi: 10.1186/s12889-020-08856-6

Effect of smoking on treatment outcome among tuberculosis patients in Malaysia; a multicenter study

Amer Hayat Khan 1,, Syed Azhar Syed Sulaiman 1, Mohamed Azmi Hassali 2, Kashif Ullah Khan 1, Long Chiau Ming 3,4, Omer Mateen 1, Malik Obaid Ullah 5
PMCID: PMC7273674  PMID: 32498682

Abstract

Background

Smoking plays a key role in the development of tuberculosis (TB) infection and is also a predictor of poor TB treatment prognosis and outcomes. The current study was conducted to determine the prevalence of smoking and to assess the effects of smoking on treatment outcomes among TB patients.

Methods

A multi-center retrospective study design was used to collect data from TB patients in four different states of Malaysia, namely Penang, Sabah, Sarawak, and Selangor. The study included medical records of TB patients admitted to the selected hospitals in the period from January 2006 to March 2009. Medical records with incomplete data were not included. Patient demographics and clinical data were collected using a validated data collection form.

Results

Of all patients with TB (9337), the prevalence of smokers was 4313 (46.2%). Among smokers, 3584 (83.1%) were associated with pulmonary TB, while 729 (16.9%) were associated with extrapulmonary TB. Male gender (OR = 1.43, 95% CI 1.30–1.58), Chinese ethnicity (OR = 1.23, 95% CI 1.02–1.49), Sarawak indigenous ethnicity (OR = 0.74, 95% CI 0.58–0.95), urban residents (OR = 1.46, 95% CI 1.33–1.61), employed individuals (OR = 1.21, 95% CI 1.09–1.34), alcoholics (OR = 4.91, 95% CI 4.04–5.96), drug abusers (OR = 7.43, 95% CI 5.70–9.60) and presence of co-morbid condition (OR = 1.27, 95% CI 1.16–1.40) all showed significant association with smoking habits. This study found that 3236 (75.0%) patients were successfully treated in the smokers’ group, while 4004 (79.7%) patients were non-smokers. The proportion of deaths (6.6%, n = 283), defaulters (6.6%, n = 284) and treatment interruptions (4.7%, n = 204) was higher in the smokers’ group.

Conclusions

Smoking has a strong influence on TB and is a major barrier towards treatment success (OR = 0.76, 95% CI 0.69–0.84, p < 0.001). Therefore, the findings indicate that smoking cessations are an effective way to decrease treatment failure and drug resistance.

Keywords: Smoking, Treatment outcome, Tuberculosis

Background

Global data on tuberculosis (TB) provided by the World Health Organization revealed that 10.0 million people (range, 9.0–11.1 million) were ill with TB in 2018. In addition, in 2018, there were 1.2 million TB fatalities among people who are HIV negative and 251,000 deaths among those who are HIV positive. Since 2007, TB has been the leading cause of death from a single infectious agent, ranking above HIV/AIDS [1]. Smoking and tuberculosis remain two major health concerns worldwide [2]. Some studies from China and India reported that smoking increases the severity and mortality rate of tuberculosis [2, 3]. In 2010, the WHO suggested a stronger focus on preventing exposures to tuberculosis [4]. In addition to cancer and coronary heart disease, numerous studies have identified smoking as a risk factor in the development of TB [5, 6]. Tobacco-associated deaths are projected to increase to 8.4 million by 2020 [7], along with TB, both of which are major sources of mortality and morbidity. Various components of the cigarette smoke such as free radicals of oxygen, acrolein, formaldehyde and carbon monoxide increase the oxidative stress in smokers, thus affecting the bronchial mucosa and increasing the threat of Mycobacterium tuberculosis infection [8]. This might be the reason for less effective TB treatment outcomes among specific populations [9, 10]. Although the prevalence of TB in Malaysia decreased significantly compared to the early 1990s, Malaysia was still ranked as an intermediate burden country by the World Health Organization (WHO) in 2018 with an incidence rate of 92/100,000 and estimated mortality rate of 4.9/100,000 population [1].

Despite increasing pieces of evidence showing a strong association between tobacco smoking and TB [1, 11], there are only a few observational studies highlighting the association between smoking and TB treatment outcomes with limited study population [7] and or single-center studies [12, 13] which are difficult to generalize. Previous studies have typically identified potential risk factors for poor results of TB treatment [7, 9, 10]. In this study, the prevalence of smoking in TB patients in Malaysia was determined and the impact that smoking has on the outcomes of tuberculosis treatment was investigated.

Methods

Study design and location

A multicenter retrospective study was conducted among the TB patients in four states of Malaysia (Sabah, Sarawak, Selangor, and Penang) — two representative states from west Malaysia and two from peninsular Malaysia — selected based on the highest burden of TB patients [14].

Inclusion & exclusion criteria

All TB patients (new, relapse, treatment failure and treatment defaulters) of both genders, either with or without co-morbidity, who presented at the chest clinic of Penang hospital from January 2006 to March 2009 were included in the study. Patients with incomplete medical records were removed from the study. Disease classification, treatment protocol and treatment outcomes were defined as per the Malaysian tuberculosis treatment guidelines [15], which are aiming to meet World Health Organization criteria. Sputum smear examinations were done at the end of two, four and 6 months of treatment in new cases and at the end of two, three, five and 8 months in retreatment cases. Sputum examination was repeated again after 1 month if positive at 2 months of treatment. Treatment outcomes initially recorded as cured, treatment completed, defaulted, transferred out, expired and treatment continued were then classified into two categories: successful or unsuccessful treatment. Cured and treatment-completed patients were placed in the successful treatment category, and the remainder was placed in the unsuccessful treatment category. Owing to the main objective of the study, patients were grouped into either ever smokers (those who smoked cigarettes at the time of TB diagnosis or who had previously smoked) or never smokers (those who had never smoked or had smoked less than 100 cigarettes in their lifetime).

Data collection

A purpose-developed pre-validated data collection form was used to collect demographic and clinical data. Demographic data included patients’ gender, age, weight, ethnicity, residential area, marital status, and smoking and alcohol consumption status. Clinical data collected included clinical presentation, serum biochemistry results, nature of TB case (new, retreatment - failure, default and relapse), site of TB infection (pulmonary or extrapulmonary), presence of the co-morbid condition along with respective medications, results of sputum cultures, and treatment outcomes.

Statistical analysis

The data were analyzed using the Statistical Package for Social Sciences (SPSS), version 20.0 (SPSS, Inc., Chicago, IL, USA). Percentages and frequencies were used for categorical variables, while means ± standard deviations were calculated for continuous variables. Univariate and multivariate binary regression analyses were used to examine whether tobacco smoking had contributed to poor treatment outcomes in TB patients. The results are presented as P-value, odds ratio (OR) and 95% confidence interval (CI). A P-value ≤0.05 was considered statistically significant.

Results

Out of 9337 TB patients, the prevalence of smokers was 4313 (46.2%) while 5024 (53.8%) were non-smokers. The mean age of patients among smokers and non-smokers was 42.18 ± 15.97 and 41.12 ± 17.05 years old, respectively, while the mean weight was 42.02 ± 10.48 and 41.53 ± 9.77 kg, respectively. The male gender was more predominant among both smokers and non-smokers: 3261 (75.6%) and 3181 (63.3%) patients, respectively. There was a high male-to-female ratio in the smoker’s group (3:1). Most of the cases in the smoker group lie in the age group 26–55 years. Malay ethnicity (28.6%, n = 1232) followed by Chinese ethnicity (26.7%, n = 1153) were in a higher proportion in the smokers’ group. About 2958 (68.6%), 3159 (73.2%) and 3010 (69.8%) smoker patients belong to urban areas, were unmarried and were unemployed, respectively. The prevalence of alcohol and drug abusers was also higher in the smokers’ group than non-smokers’ group: 18.6% (n = 802) and 14% (n = 602), respectively. The majority of the smoker patients (83.1%, n = 3584) had PTB while co-morbidity was observed in 44.2% (n = 1907) of patients (Table 1).

Table 1.

Sociodemographic distribution of TB patients according to smoking habit

Patient Variables Total
N = 9337
Never smoked
N = 5024
Ever smoked
N = 4313
Weight (mean ± SD) 41.75 ± 10.11 41.53 ± 9.77 42.02 ± 10.48
Gender
 Male 6442 (69) 3181 (63.3) 3261 (75.6)
 Female 2895 (31) 1843 (36.7) 1052 (24.4)
Age (mean ± SD) 41.61 ± 16.57 41.12 ± 17.05 42.18 ± 15.97
  < 15 265 (2.8) 172 (3.4) 93 (2.2)
 16–25 1472 (15.8) 876 (17.4) 596 (13.8)
 26–35 1878 (20.1) 1001 (19.9) 877 (20.3)
36–45 1754 (18.8) 872 (17.4) 882 (20.4)
 46–55 1674 (17.9) 880 (17.5) 794 (18.4)
 56–65 1279 (13.7) 673 (13.4) 606 (14.1)
  > 65 1015 (10.9) 550 (10.9) 465 (10.8)
Race
 Malay 2504 (26.8) 1272 (25.3) 1232 (28.6)
 Chinese 2211 (23.7) 1058 (21.1) 1153 (26.7)
 Indian 671 (7.2) 350 (7) 321 (7.4)
 Indigenous Sarawak 976 (10.5) 614 (12.2) 362 (8.4)
 Indigenous Sabah 1702 (18.2) 1003 (20) 699 (16.2)
 Indonesian immigrants 631 (6.8) 372 (7.4) 259 (6)
 Philippine immigrants 493 (5.3) 287 (5.7) 206 (4.8)
 Others 149 (1.6) 68 (1.4) 81 (1.9)
Area
 Urban 5959 (63.8) 3001 (59.7) 2958 (68.6)
 Rural 3378 (36.2) 2023 (40.3) 1355 (31.4)
Marital status
 Single 6706 (71.8) 3547 (70.6) 3159 (73.2)
 Married 2631 (28.2) 1477 (29.4) 1154 (26.8)
Employment status
 Employed 2531 (27.1) 1228 (24.4) 1303 (30.2)
 Unemployed 6806 (72.9) 3796 (75.6) 3010 (69.8)
Alcohol drinkers
 Yes 941 (10.1) 139 (2.8) 802 (18.6)
 No 8396 (89.9) 4885 (97.2) 3511 (81.4)
Intravenous drug user (IVDU)
 Yes 670 (7.2) 68 (1.4) 602 (14)
 No 8667 (92.8) 4956 (98.6) 3711 (86)
TB-type
 PTB 7781 (83.3) 4197 (83.5) 3584 (83.1)
 EPTB 1556 (16.7) 827 (16.5) 729 (16.9)
Co-morbidity
 Yes 3414 (36.6) 1507 (30) 1907 (44.2)
 No 5923 (63.4) 3517 (70) 2406 (55.8)

Patient variables were further analyzed based on smoking habits using univariate and multivariate analysis. Multivariate binary logistic regression in Table 2 shows that the odds of smoking showed a significant association with male gender (OR = 1.43, 95% CI 1.30–1.58), Chinese ethnicity (OR = 1.23, 95% CI 1.02–1.49), and Sarawak indigenous ethnicity (OR = 0.74, 95% CI 0.58–0.95). The odds were high and statistically significant with urban residents (OR = 1.46, 95% CI 1.33–1.61), employed individuals (OR = 1.21, 95% CI 1.09–1.34), alcoholics (OR = 4.91, 95% CI 4.04–5.96), drug abusers (OR = 7.43, 95% CI 5.70–9.60) and those with a co-morbid condition (OR = 1.27, 95% CI 1.16–1.40).

Table 2.

Distribution of TB patients according to smoking habit based on multivariate analysis

Patient variables Univariate analysis Multivariate analysis
Crude OR 95% CI p-Value aOR 95% CI p-Value
Gender
 Male 1.79 1.64–1.96 < 0.001 1.43 1.30–1.58 < 0.001
 Female 1.00 1.00
Age
  < 15 0.62 0.48–0.80 < 0.001 0.86 0.66–1.14 0.31
 16–25 0.75 0.67–0.85 < 0.001 0.92 0.81–1.04 0.22
 26–35 1.02 0.92–1.13 0.62
 36–45 1.22 1.10–1.35 < 0.001 1.02 0.91–1.15 0.65
 46–55 1.06 0.95–1.18 0.26
 56–65 1.05 0.93–1.18 0.35
  > 65 0.98 0.86–1.12 0.79
Race
 Malay 1.17 1.07–1.29 < 0.001 1.10 0.91–1.32 0.31
 Chinese 1.36 1.24–1.50 < 0.001 1.23 1.02–1.49 0.02
 Indian 1.07 0.91–1.25 0.37
 Indigenous Sarawak 0.65 0.57–0.75 < 0.001 0.74 0.58–0.95 0.02
 Indigenous Sabah 0.77 0.69–0.86 < 0.001 1.01 0.83–1.23 0.91
 Indonesian immigrants 0.79 0.67–0.94 0.007 0.91 0.72–1.16 0.47
 Philippine immigrants 0.82 0.68–0.99 0.04 0.97 0.75–1.25 0.83
 Others 1.39 1.00–1.93 0.04 1.30 0.89–1.90 0.16
Area
 Urban 1.47 1.35–1.60 < 0.001 1.46 1.33–1.61 < 0.001
 Rural 1.00 1.00
Marital status
 Single 1.14 1.04–1.24 0.005 0.97 0.88–1.07 0.63
 Married 1.00 1.00
Employment status
 Employed 1.33 1.22–1.46 < 0.001 1.21 1.09–1.34 < 0.001
 Unemployed 1.00 1.00
Alcohol drinkers
 Yes 8.02 6.67–9.66 < 0.001 4.91 4.04–5.96 < 0.001
 No 1.00 1.00
Intravenous drug user (IVDU)
 Yes 11.82 9.16–15.24 < 0.001 7.43 5.70–9.60 < 0.001
 No 1.00 1.00
TB type
 PTB 0.96 0.86–1.08 0.56
 EPTB 1.00
Co-morbidity
 Yes 1.85 1.69–2.01 < 0.001 1.27 1.16–1.40 < 0.001
 No 1.00 1.00

Table 3 is based on the clinical signs and symptoms and shows that significant differences exist among both the smokers’ and non-smokers’ groups. Despite this, data analysis indicated that the prevalence of night sweats (1462, 33.9%), coughs (3579, 83%), shortness of breath (1911, 44.3%), fever (2794, 64.8%), weight loss (2969, 68.8%) and loss of appetite (3181, 73.8%) was significantly higher in the smokers’ group.

Table 3.

Clinical signs & symptoms among smokers and non-smokers patient groups

Symptoms Total
N = 9337
Never smoked
N = 5024
Ever smoked
N = 4313
p-Value
Night sweats
 Yes 2962 (31.7) 1500 (29.9) 1462 (33.9) < 0.001
 No 6164 (66) 3382 (67.3) 2782 (64.5)
 Unknown 211 (2.3) 142 (2.8) 69 (1.6)
Cough
 Yes 7365 (78.9) 3786 (75.4) 3579 (83) < 0.001
 No 1944 (20.8) 1225 (24.4) 719 (16.7)
 Unknown 28 (0.3) 13 (0.3) 15 (0.3)
Sputum
 Yes 5139 (55) 2947 (58.7) 2192 (50.8) < 0.001
 No 4035 (43.2) 2000 (39.8) 2035 (47.2)
 Unknown 163 (1.7) 77 (1.5) 86 (2)
Shortening of breath
 Yes 3944 (42.2) 2033 (40.5) 1911 (44.3) 0.001
 No 5298 (56.7) 2942 (58.6) 2356 (54.6)
 Unknown 95 (1) 49 (1) 46 (1.1)
Fever
 Yes 5940 (63.6) 3146 (62.6) 2794 (64.8) 0.002
 No 3377 (36.2) 1873 (37.3) 1504 (34.9)
 Unknown 20 (0.2) 5 (0.1) 15 (0.3)
Weight loss
 Yes 6203 (66.4) 3234 (64.4) 2969 (68.8) < 0.001
 No 3037 (32.5) 1705 (33.9) 1332 (30.9)
 Unknown 97 (1) 85 (1.7) 12 (0.3)
Loss of appetite
 Yes 6528 (69.9) 3347 (66.6) 3181 (73.8) < 0.001
 No 2694 (28.9) 1575 (31.3) 1119 (25.9)
 Unknown 115 (1.2) 102 (2) 13 (0.3)
Hemoptysis
 Yes 2381 (25.5) 1295 (25.8) 1086 (25.2) < 0.001
 No 6842 (73.3) 3637 (72.4) 3205 (74.3)
 Unknown 114 (1.2) 92 (1.8) 22 (0.5)

This study revealed that the overall success rate was 77.5% (n = 7240) patients out of which 75% (3236) patients were successfully treated in the smokers’ group while 4004 (79.7%) patients belonged to non-smokers group. The rates of mortality (6.6%, n = 283), defaulters (6.6%, n = 284) and treatment interruption (4.7%, n = 204) were high in the smokers’ group. In multivariate analysis, treatment completion (aOR 0.87, 95% CI 0.78–0.96, p < 0.01), death rate (aOR 1.57, 95% CI 1.31–1.89, p < 0.001), defaulters (aOR 1.57, 95% CI 1.31–1.89, p < 0.001) and treatment interruption (aOR 1.49, 95% CI 1.21–1.84, p < 0.001) showed significant associations with smoking habit. The chances of treatment success rate were less for smokers (aOR 0.76, 95% CI 0.69–0.84, p < 0.001), as shown in Table 4.

Table 4.

Unsuccessful treatment outcomes among smokers and non-smokers patients groups with Binary logistic regression

Treatment outcome Total
N = 9337
Never smoked
N = 5024
Ever smoked
N = 4313
Univariate analysis Multivariate analysis
Crude OR 95% CI p-Value aOR 95% CI p-Value
Cured
 Yes

5319

(57)

2900

(57.5)

2419

(56.1)

0.93 0.86–1.01 0.111
 No

4018

(43)

2124

(42.3)

1894

(43.9)

1.00
Treatment completed
 Yes

1924

(20.6)

1117

(22.2)

807

(18.7)

0.80 0.72–0.89 < 0.001 0.87 0.78–0.96 0.01
 No

7413

(79.4)

3907

(77.8)

3506

(81.3)

1.00 1.00
Expired
 Yes

500

(5.4)

217

(4.3)

283

(6.6)

1.55 1.29–1.86 < 0.001 1.57 1.31–1.89 < 0.001
 No

8837

(94.6)

4807

(95.7)

4030

(93.4)

1.00 1.00
Defaulters
 Yes

502

(5.4)

218

(4.3)

284

(6.6)

1.55 1.29–1.86 < 0.001 1.57 1.31–1.89 < 0.001
 No

8835

(94.6)

4806

(95.7)

4029

(93.4)

1.00 1.00
Treatment interrupted
 Yes

369

(4)

165

(3.3)

204

(4.7)

1.46 1.18–1.80 < 0.001 1.49 1.21–1.84 < 0.001
 No

8968

(96)

4859

(96.7)

4109

(95.3)

1.00 1.00
Treatment continued
 Yes

723

(7.7)

407 (8.1)

316

(7.3)

0.89 0.77–1.04 0.163
 No

8614

(92.3)

4617

(91.9)

3997

(92.7)

1.00
Overall treatment success
 Yes

7240

(77.5)

4004

(79.7)

3236

(75)

0.76 0.69–0.84 < 0.001
 No

2097

(22.5)

1020

(20.3)

1077

(25)

1.00

Discussion

Based on the National Health and Morbidity Surveys in 2006, the prevalence of smoking in Malaysia was 46.5%, as revised in 2015 [12]. The current study reported the same prevalence of smoking, i.e. 46.2%. Previously published studies conducted in Malaysia reported a higher prevalence of smokers than non-smokers among TB patients [11, 13]. The tobacco-tuberculosis association worldwide has been documented with different types of studies [1]. While the exact mechanism is not understood, nicotine may interfere with the host’s immune reaction to M. tuberculosis [16].

The present study found that the male gender has a significant association with smoking habits. This could account for the observed differences in TB rates between men and women. A study from China reported that intravenous drug users (IVDUs) were found to be significantly associated with the smokers’ group [17]. An additional study found that excessive intake of alcohol meant a greater chance of M. tuberculosis infection [18]. Chronic ethanol intake causes changes in the immune system and an increased risk of bacterial infections [19]. Consistent with the previous findings, the present study found that alcohol use and IVDUs were significantly associated with smoker TB patients.

If smoking is responsible for a decrease in cure rates and an increase in the risk of rapid disease progression and severity then there is a clear immunopathological association between smoking and TB [20, 21]. In the current study, the treatment success rate was low among the smokers’ group. A person who smokes one packet of cigarettes daily inhales 1.12 μg of iron; iron-loading in the alveolar macrophages makes them more susceptible to the growth of Mycobacterium tuberculosis [22]. Cigarette smoke increases the threat of Mycobacterium tuberculosis infection in multiple ways: declined activity of alveolar macrophage, impairment of mucociliary clearance, decrease in the immune response of pulmonary lymphocytes, modified pulmonary dendritic cells activity, and reduction in the cytotoxic activity of natural killer cells [8]. Smoking also produces an alteration in both natural and acquired cell immunity, affecting macrophages and leukocytes. The effect of oxidative stress is important, as it induces apoptosis in both activated and non-activated macrophages, favoring the multiplication of the bacilli and making the process chronic [23, 24]. This is why tobacco smoking leads to severe clinical illness and eventually death. The current study showed that smokers were more likely to die. A previous study in China reported that the mortality rate was nine times higher among tuberculosis patients who smoked [25] while other studies from South Africa and India concluded that the higher odds of mortality were among smokers [26, 27]. Previous studies had also proved that tobacco smoking as one predictor and risk factors significantly associated with poor adherence and higher default rate in TB care settings [9, 28, 29]. A study from Hong Kong also showed that a smoking habit is a good indicator to evaluate the risk of defaulters from TB treatment under DOTS (OR = 3.00, 95% CI 1.41–6.39, p = 0.004) [9]. Patients who default treatment are at greatest risk of developing drug resistance and spreading TB in the community [30]. A recent study from Malaysia recommends that interventions are necessary to improve treatment compliance in TB patients [11]. Improving compliance among smoking TB patients is a great challenge and should be addressed by securing support from families and social organizations as well as providing smoking cessation interventions [11]. Tachfounti et al. studied the association of smoking among TB patients and reported that the TB treatment failure rate was higher among smokers compared to non-smokers (9.1% vs 4.5%, p < 0.01) [31]. A few studies tested the effect of smoking on treatment outcomes and concluded that treatment failure was higher among current and ex-smokers, and smoking was significantly associated with low treatment success [2, 32, 33]. Fahrettin Talay et al. evaluated the treatment outcomes among TB patients and identified multiple patient factors that affect TB treatment outcomes [34]. The current study showed that patient mortality is higher among smokers [OR 1.57 (91.31–1.89); p < 0.01]. The reason might be due to drug addiction (OR 5.7) and co-morbidities (OR 1.27). The same picture can be drawn from the published articles [33, 35]. Smoking cessation seems to be an essential means of controlling TB epidemics, improving outcomes and drug resistance particularly in high-burden developing countries, as published elsewhere [3335].

Conclusion

In conclusion, smoking is a risk factor for the occurrence of tuberculosis. Additionally, this study shows that the treatment effects are also poor. Tobacco also poses a strong risk factor in terms of poor adherence and higher mortality as well as defaulter rate. Therefore, proper public awareness campaigns and smoking cessation interventions should be presented to all smoking TB patients undergoing DOTS treatment to avoid the severity and progression of the disease and to avoid drug resistance.

Limitation of the study

A number of TB patients were excluded from the analysis due to a lack of / incomplete smoking-related data.

Acknowledgments

We would like to thank the director general of Health Malaysia for his permission to publish this study. The researchers are grateful to all the paramedic staff who helped them out with data collection in the centers.

Abbreviations

TB

tuberculosis

WHO

World Health Organization

OR

odds ratio

CI

Confidence interval

MREC

Medical Research Ethics Committee

DOTS

Direct Observed Treatment Short course

Authors’ contributions

AHK: collected, analyzed, and interpreted the data. SASS, MOU and AHK: participated in conception and design of the study. MAH and AHK: drafted the manuscript. KUK: Article review, draft review & formatting. LCM: Revised the manuscript critically after analysis. OM: Analysis & Drafted the manuscript. MOU: Revised the manuscript critically after analysis and English editing. All the authors have read and approved the final manuscript.

Funding

This study received no funding from any organization.

Availability of data and materials

The datasets generated and/or analyzed during the current study are not publicly available as institutional permission is required, but are available from the corresponding author upon reasonable request.

Ethics approval and consent to participate

Ethical approval was granted from all relevant local authorities and obtained from the Medical Research Ethics Committee (MREC), registration number NMRR (National Medical Research Registration) # (2) KKM/NIHSEC/08/0804/P 67–177. Due to the study nature, patient consent was not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets generated and/or analyzed during the current study are not publicly available as institutional permission is required, but are available from the corresponding author upon reasonable request.


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