Abstract
We investigated the prevalence of vitamin D deficiency among individuals who have a history of tuberculosis (TB) diagnosis in Korea. Using the 5th Korean National Health and Nutrition Examination Survey, we selected 805 individuals with a history of TB diagnosis and 16,049 controls without a history of TB. Vitamin D deficiency was defined as a 25(OH)D level less than 20 ng/mL. Vitamin D deficiency was revealed in 71.7% of the individuals with a history of TB diagnosis and in 72.1% of the controls. Vitamin D deficiency was more likely in women than in men, in people who engaged in other jobs or were unemployed than in people who engaged in skilled agricultural, forestry, and fishery jobs, and in people who walked 3–5 days per week than in people who walked 6–7 days per week. Vitamin D deficiency was highly prevalent in the TB group. Regular examination and strategies to increase vitamin D levels in individuals with a history of TB are needed, as vitamin D is associated with TB conditions and bone disease.
Keywords: nutrition surveys, tuberculosis, vitamin D, vitamin D deficiency
1. Introduction
Tuberculosis (TB) is an infectious disease caused by Mycobacterium tuberculosis and is a serious problem around the world. In 2014, the total number of TB cases in the world stood at 9.6 million, and the number of TB-related deaths was 1.5 million [1]. According to the World Health Organization’s 2015 Global Tuberculosis Report, the Korean incidence of TB in 2014 was 86/100,000 individuals, and that incidence of TB takes the top spot among the member nations of the Organization for Economic Cooperation and Development. TB remains the highest public health priority in Korea [2,3].
Vitamin D is an important hormone for skeletal growth and maintenance. It maintains mineral homeostasis and plays an important role in various tissues [4]. Vitamin D is produced naturally from the skin if the skin is exposed to the sun. Vitamin D produced from the skin is prone to deficiency nowadays due to modern lifestyles. Vitamin D deficiency has been reported to be associated with cancer [5] as well as chronic diseases like hypertension [6], autoimmune disease [7], and diabetes [8]. Hence, there has recently been a growing interest in vitamin D around the globe. Few reports have examined the prevalence of vitamin D deficiency among TB patients. A case-control study of 105 TB patients and 255 controls reported that vitamin D deficiency was found in 57% of TB patients and 33% of controls [9]. In a different case-control study in Pakistan, vitamin D deficiency was common among TB patients (118/260, 45%) and was independently associated with susceptibility to TB (adjusted odds ratio (aOR) =1.87, 95% confidence interval (CI) = 1.15–3.04) [10]. In another cross-sectional study in northern India, patients with pulmonary TB had significantly lower mean vitamin D levels (11.2 ± 6.5 ng/mL) and had the highest prevalence of vitamin D deficiency (92%) compared with other groups [11].
The prevalence of vitamin D deficiency has not been adequately determined among Korean subjects with a history of TB. Therefore, we investigated the prevalence of vitamin D deficiency among individuals who have a history of TB diagnosis in Korea. We also investigated the difference between subjects with TB history and controls and identified the factors associated with vitamin D deficiency among TB patients.
2. Materials and Methods
2.1. Data Source
This study was based on data acquired in the 5th (2010–2012) Korean National Health and Nutrition Examination Survey (KNHANES). The KNHANES is a nationwide survey that investigates the health status, health behavior, and nutritive conditions of the Korean people. KNHANES consisted of three components: health interview, health examination and nutrition survey. A stratified, multistage probability sampling design was used to interview household units. The KNHANES response rates were 81.9% (8958 of 10,938) in 2010, 80.4% (8518 of 10,589) in 2011, and 80.0% (8058 of 10,069) in 2012. Among a total of 25,534 participants, 24,173 subjects participated in health interview and health examination. Among them, participants ≤19 years of age (n = 5602), participants with missing data of TB status or serum 25(OH)D level (n = 1474) and covariates (n = 243) were excluded. Finally, a total of 16,854 adults with recorded serum 25(OH)D levels were included in the study. All data were approved by the Institutional Review Board of the Korea Centers for Disease Control (2010-02CON-21-C, 2011-02CON-06-C and 2012-01EXP-01-2C). Informed consent was received from each participant before the survey [12].
2.2. History of Tuberculosis Diagnosis
Participants with a history of TB diagnosis were defined as those who answered “yes” to the question, “Have you ever heard from a doctor that you had TB?” Those who had a history of TB diagnosis were asked about their age at diagnosis. The time since diagnosis was calculated from the difference between the age at diagnosis and the age at survey participation. Controls were defined as subjects who reported no history of TB diagnosis.
2.3. Vitamin D Deficiency
Blood samples were separated and refrigerated. 25(OH)D levels were measured by radioimmunoassay methods using a 1470 WIZARD gamma-Counter (PerkinElmer, Turku, Finland). Vitamin D deficiency was defined as a 25(OH)D level <20 ng/mL as per the guideline proposed by the Institute of Medicine.
2.4. Covariates
Several variables such as sex, age (19–44, 45–64, ≥65 years), education (≤high school, ≥college), monthly income (low, middle, high), occupation type (skilled agricultural, forestry, fishery workers; others; unemployed (e.g., housewife, student)), smoking status (current smoker, ex-smoker, non-smoker), drinking status (current drinker, ex-drinker, non-drinker), subjective health status (good, fair, bad), body mass index (underweight, normal, overweight), walking in a week (0–2, 3–5, 6–7 days), and the use of dietary supplements (yes, no) were used.
2.5. Statistical Analysis
Statistical analysis was conducted using SAS Version 9.3 (SAS Institute INC, Cary, NC, USA). All analyses were conducted using survey weighting to account for the multistage probability sampling design. The general characteristics of the subjects by history of TB diagnosis were shown as the number and percentage and compared using chi-square tests. The prevalence of vitamin D deficiency by the subjects’ characteristics in the TB and control groups was tested with chi-square tests. Multiple logistic regression analyses were used to identify factors associated with vitamin D deficiency in the subjects with a history of TB diagnosis and in the non-TB controls. Numbers were expressed as crude numbers, and all other values were expressed as weighted values.
3. Results
3.1. General Characteristics of Subjects by History of TB Diagnosis
The general characteristics of the TB group and the controls were substantially different. The proportions of participants ≥65 years of age in the TB and control groups were 20.9% and 12.6%, respectively (p < 0.001). The most common age at diagnosis among those with a history of TB diagnosis was 19–44 years (55.8%), and the time since diagnosis was 20–39 years for 46.1% of the TB group (Table 1).
Table 1.
General characteristics of subjects by history of TB diagnosis.
| Characteristics | Self-Reported History of TB (n = 805) | No-Reported History of TB (n = 16,049) | p-Value |
|---|---|---|---|
| Sex | <0.0001 | ||
| Male | 442 (58.5) | 6775 (49.5) | |
| Female | 363 (41.5) | 9274 (50.5) | |
| Age (years) | <0.0001 | ||
| 19–44 | 180 (30.5) | 6592 (52.5) | |
| 45–64 | 350 (48.6) | 5941 (34.9) | |
| ≥65 | 275 (20.9) | 3516 (12.6) | |
| Education | 0.375 | ||
| ≤High school | 576 (69.3) | 11,112 (67.3) | |
| ≥College | 229 (30.7) | 4930 (32.7) | |
| Monthly income | 0.913 | ||
| Low | 191 (27.4) | 3819 (26.6) | |
| Middle | 394 (49.6) | 8025 (50.3) | |
| High | 206 (23.0) | 4050 (23.2) | |
| Occupation | 0.006 | ||
| Skilled agricultural, forestry, and fishery workers | 61 (5.9) | 1348 (6.7) | |
| Others | 373 (53.0) | 8301 (59.0) | |
| Unemployed | 370 (41.0) | 6355 (34.3) | |
| Smoking status | <0.0001 | ||
| Current smoker | 163 (27.2) | 3337 (26.8) | |
| Ex-smoker | 249 (29.5) | 3174 (19.4) | |
| Non-smoker | 393 (43.3) | 9538 (53.8) | |
| Drinking status | 0.124 | ||
| Current drinker | 136 (14.6) | 2255 (12.0) | |
| Ex-drinker | 565 (75.8) | 11,638 (77.9) | |
| Non-drinker | 104 (9.6) | 2156 (10.0) | |
| Subjective health status | <0.0001 | ||
| Good | 223 (28.6) | 5393 (34.9) | |
| Fair | 380 (48.1) | 7663 (48.4) | |
| Bad | 202 (23.3) | 2993 (16.7) | |
| Body mass index | <0.0001 | ||
| Underweight | 49 (7.2) | 676 (4.5) | |
| Normal | 585 (72.2) | 10,103 (62.7) | |
| Overweight | 170 (20.6) | 5177 (32.8) | |
| Walking days per week | 0.175 | ||
| 0–2 | 299 (37.5) | 5500 (33.6) | |
| 3–5 | 240 (29.3) | 4932 (30.1) | |
| 6–7 | 266 (33.3) | 5614 (36.2)) | |
| Dietary supplements | 0.101 | ||
| Yes | 349 (46.5) | 6564 (42.7) | |
| No | 372 (53.5) | 7685 (57.3) | |
| Age at diagnosis (years) | |||
| 19–29 | 327 (55.8) | - | |
| 30–39 | 142 (18.4) | - | |
| ≥40 | 197 (25.7) | - | |
| Time since diagnosis (years) | |||
| <10 | 130 (19.9) | - | |
| 10–19 | 133 (20.2) | - | |
| 20–39 | 373 (46.1) | - | |
| ≥40 | 169 (13.9) | - |
Data are expressed as crude numbers (weighted %).
3.2. Prevalence of Vitamin D Deficiency in the TB and Control Groups
The mean vitamin D levels were 17.5 ng/mL, 17.6 ng/mL, and 17.5 ng/mL in the total sample, the TB group, and the controls, respectively. The rate of vitamin D deficiency (<20 ng/mL) was 72.0% among all the subjects. Vitamin D deficiency was found in 71.7% of the TB group and in 72.1% of the controls. Multiple logistic regression analysis showed that the prevalence of vitamin D deficiency was similar between the TB group and the controls after controlling for several covariates (aOR = 0.97, 95% CI = 0.79–1.18).
3.3. Factors Associated with Vitamin D deficiency in the TB and Control Groups
The prevalence of vitamin D deficiency was significantly higher among women (80.4%), younger subjects (79.2%), subjects whose type of job was “other” (75.8%), and non-smokers (77.0%). These figures were similar to those identified in the non-TB controls (Table 2).
Table 2.
Prevalence of vitamin D deficiency by subject characteristics in the TB and control groups.
| Characteristics | Self-Reported History of TB | No Reported History of TB | ||
|---|---|---|---|---|
| % with Vitamin D Deficiency | p-Value | % with Vitamin D Deficiency | p-Value | |
| Total | 71.7 | 72.1 | ||
| Sex | <0.001 | <0.001 | ||
| Male | 65.6 | 66.2 | ||
| Female | 80.4 | 77.8 | ||
| Age (years) | <0.001 | <0.001 | ||
| 19–44 | 79.2 | 79.6 | ||
| 45–64 | 73.2 | 65.4 | ||
| ≥65 | 57.6 | 58.8 | ||
| Education | 0.109 | <0.001 | ||
| ≤High school | 69.7 | 69.3 | ||
| ≥College | 76.3 | 77.8 | ||
| Monthly income | 0.829 | 0.163 | ||
| Low | 71.3 | 70.9 | ||
| Middle | 72.3 | 73.0 | ||
| High | 69.1 | 71.2 | ||
| Occupation | <0.001 | <0.001 | ||
| Skilled agricultural, forestry, and fishery workers | 37.2 | 41.1 | ||
| Others | 75.8 | 73.7 | ||
| Unemployed | 71.5 | 75.2 | ||
| Smoking status | 0.016 | <0.001 | ||
| Current smoker | 72.9 | 70.7 | ||
| Ex-smoker | 63.0 | 63.3 | ||
| Non-smoker | 77.0 | 75.9 | ||
| Drinking status | 0.651 | 0.027 | ||
| Current drinker | 75.9 | 73.5 | ||
| Ex-drinker | 71.1 | 72.3 | ||
| Non-drinker | 70.8 | 68.5 | ||
| Subjective health status | 0.356 | 0.429 | ||
| Good | 71.0 | 71.3 | ||
| Fair | 74.3 | 72.6 | ||
| Bad | 67.3 | 72.3 | ||
| Body mass index | 0.575 | <0.001 | ||
| Underweight | 72.9 | 79.9 | ||
| Normal | 70.5 | 72.0 | ||
| Overweight | 75.7 | 70.9 | ||
| Walking days per week | 0.062 | <0.001 | ||
| 0–2 | 73.8 | 72.3 | ||
| 3–5 | 76.3 | 74.4 | ||
| 6–7 | 65.4 | 69.9 | ||
| Dietary supplements | 0.674 | <0.001 | ||
| Yes | 69.7 | 68.6 | ||
| No | 71.6 | 73.8 | ||
| Age at diagnosis (years) | 0.183 | |||
| 19–29 | 73.7 | |||
| 30–39 | 66.8 | |||
| ≥40 | 64.9 | |||
| Time since diagnosis (years) | 0.289 | |||
| <10 | 78.5 | |||
| 10–19 | 67.9 | |||
| 20–39 | 71.8 | |||
| ≥40 | 67.6 | |||
Data are expressed as weighted %.
Multiple logistic regression analysis showed that women had a significantly higher aOR for vitamin D deficiency within the TB group (aOR = 2.37, 95% CI = 1.04–5.40). TB subjects whose type of job was ”other” (aOR = 3.40, 95% CI = 1.51–7.66), were unemployed (aOR = 2.89, 95% CI = 1.34–6.23), and who walked 3–5 days per week (aOR = 1.80, 95% CI = 1.05–3.10) were more likely to have vitamin D deficiency. The use of dietary supplements and the time since TB diagnosis were not associated with vitamin D deficiency (Table 3).
Table 3.
Odds ratios (95% confidence interval) for vitamin D deficiency in the TB and control groups.
| Characteristics | Self-Reported History of Tuberculosis | No-Reported History of Tuberculosis |
|---|---|---|
| Sex (Male) | ||
| Female | 2.37 (1.04–5.40) | 1.93 (1.68–2.23) |
| Age (≥65) | ||
| 19–44 | 2.14 (0.84–5.47) | 2.28 (1.93–2.71) |
| 45–64 | 1.57 (0.88–2.77) | 1.30 (1.13–1.50) |
| Education (≤High school) | ||
| ≥College | 1.08 (0.60–1.97) | 1.18 (1.04–1.34) |
| Monthly income (High) | ||
| Low | 0.95 (0.47–1.94) | 0.94 (0.80–1.11) |
| Middle | 1.11 (0.61–2.02) | 1.07 (0.93–1.22) |
| Occupation/(Skilled agricultural, forestry, and fishery workers) | ||
| Others | 3.40 (1.51–7.66) | 2.97 (2.35–3.75) |
| Unemployed | 2.89 (1.34–6.23) | 2.98 (2.36–3.77) |
| Smoking status (Current smoker) | ||
| Ex-smoker | 0.72 (0.36–1.46) | 0.82 (0.70–0.96) |
| Non-smoker | 0.64 (0.26–1.54) | 0.94 (0.80–1.12) |
| Drinking status (Current drinker) | ||
| Ex-drinker | 0.94 (0.47–1.88) | 0.85 (0.73–0.99) |
| Non-drinker | 0.98 (0.41–2.32) | 0.81 (0.65–0.99) |
| Body mass index (Normal) | ||
| Underweight | 1.10 (0.39–3.05) | 1.05 (0.82–1.34) |
| Overweight | 1.55 (0.84–2.89) | 1.02 (0.91–1.14) |
| Walking days per week (6–7) | ||
| 0–2 | 1.38 (0.82–2.32) | 1.12 (0.99–1.26) |
| 3–5 | 1.80 (1.05–3.10) | 1.19 (1.05–1.36) |
| Dietary supplements (Yes) | ||
| No | 1.47 (0.91–2.36) | 1.49 (1.34–1.66) |
| Time since diagnosis (≥40 years) | ||
| <10 | 1.11 (0.50–2.44) | |
| 10–19 | 0.47 (0.21–1.07) | |
| 20–39 | 0.64 (0.35–1.17) |
Among the non-TB controls, sex, age, education, occupation, smoking status, drinking status, walking in a week, and the use of dietary supplements were associated with vitamin D deficiency (Table 3).
4. Discussion
A meta-analysis of in vivo studies showed that low serum vitamin D levels were associated with a higher risk of active TB [13]. Decreased vitamin D levels in patients with latent TB were associated with a 5-fold increased risk of progression to TB [14,15]. We investigated the prevalence of vitamin D deficiency and examined the factors associated with vitamin D deficiency among individuals with TB in Korea. Approximately 71.7% and 72.1% of the TB group and the controls, respectively, exhibited vitamin D deficiency. The prevalence and associated factors were also compared in subjects without a history of TB. Sex, occupation, and number of days of walking per week were associated with vitamin D deficiency in the TB group in multiple analyses.
Vitamin D deficiency can be associated with TB due to its essential functions in the immune system. Vitamin D can influence on TB through the regulation of cathelicidin which has a direct antibacterial effect on TB [16] and vitamin D receptor gene polymorphisms was associated with susceptibility to TB [17]. Vitamin D modulates immune functions mediated by monocytes, macrophages, dendritic cells, T cells, B cells [18].
In our study, the prevalence of vitamin D deficiency was high in both the TB group and the controls (71.7% and 72.1%, respectively). A previous case-control study of 362 TB patients and 494 controls revealed that vitamin D deficiency was more common in TB patients (46.0% vs. 39%) [19]. The high prevalence of vitamin D deficiency that we found in both groups suggests that vitamin D deficiency is not a problem limited to individuals with specific conditions such as TB but is rather a general public health burden in Korea. Recent reviews emphasizing the high prevalence of vitamin D deficiency is a global problem [20,21]. The prevalence of vitamin D deficiency (<20 ng/mL) was estimated to be 36% in USA, 61% in Canada, 57%–64% in Europe and 78%–98% in Asia [20]. Vitamin D deficiency is prevalent in Asia including Korea. Latitude of the countries, attitudes and behavior toward sunlight exposure were the major determinants of vitamin D status [22].
A high prevalence of vitamin D deficiency in women than in men was revealed (80.4% vs. 65.6%) in the TB group. Vitamin D deficiency was most prevalent in subjects 19–44 years of age (79.2%) and was least prevalent in subjects over 65 years of age (57.6%). Vitamin D deficiency is highly prevalent and greatly contributes to women’s health [23] and young and middle-aged adults have high risks for vitamin D deficiency worldwide because of lifestyle changes such as decreased outdoor activity and the avoidance of sun exposure [22,24]. Generally, men seem to be more affected than women by TB [25]. But according to age group there was a higher risk for younger women than men [26,27]. Our high prevalence of vitamin D deficiency in women and younger subjects who were high risk groups for TB suggested that management of vitamin D status and further studies on the association between TB and vitamin D are needed in these group.
In terms of occupation, unemployed subjects had relatively high rates of vitamin D deficiency in TB group. In our study, the unemployment rate in TB groups was higher than controls (41.0% vs. 34.3%). Unemployment among TB patients was associated with poor course of the disease and was a serious problem [28,29]. Strategies and efforts are needed to improve the occupational status among TB subjects. Due to the nature of KNHANES, we did not directly assess sun exposure or outdoor activities. We considered skilled agricultural, forestry, and fishery work as outdoor activities and other jobs or unemployment as indoor activities. Outdoor activities were associated with lower risk of vitamin D deficiency [30,31].
The use of dietary supplements was associated with a lower risk of vitamin D deficiency among the controls but not among the subjects with a history of TB diagnosis. Vitamin D supplementation is usually prescribed for osteoporosis prevention, yet guidelines for its use to prevent TB are deficient, despite the rarity of adverse effects [32]. Experts recommend the maintenance of an appropriate vitamin D concentration (30–44 ng/mL) to prevent vitamin D-related illness [33,34] and suggest taking vitamin D 800–1000 International Unit/day [35]. In a recent review, several studies reported that vitamin D supplementation has benefited TB patients by several means including the shortening of the sputum conversion period and improved inhibitory effects on monocyte counts and inflammatory cytokines. However, several other studies reported no significant associations. It is possible that the association could be influenced by the vitamin D dose and seasonality [16]. Unfortunately, the KNHANES did not record the type and amount of supplements. Further studies with sufficient vitamin D supplementation are needed to define the role of vitamin D in TB.
Our study has some limitations. First, we used a cross-sectional design, so we could not identify a causal relationship between vitamin D deficiency and TB. Second, the KNHANES did not record the current status of TB and associated clinical data, and it excluded institutionalized individuals and TB patients who were admitted to the hospital or were convalescing. Therefore, the TB group in our study might not be representative of all individuals who have a history of TB diagnosis in Korea. Also, KNHANES could not distinguish between latent or active TB. The history of TB was measured by self-reported method, and positive TB history could be interpreted as having active or latent TB. Clinical significance and its health burden are substantially different according to TB status (active or latent). Previous studies reported that vitamin D associated with both active or latent TB infection and vitamin D deficiency was associated with the risk of active TB in subjects with latent TB infection [36,37]. On the other hand, vitamin D level was not different between latent TB and controls groups [38]. TB status (active or latent) should be considered in further study about the effect of vitamin D on TB. Third, the serum vitamin D level is influenced by seasonality, and we could not use the information about the survey time. The KNHANES data are collected throughout the year, however, which should solve the problem of seasonal variations [12]. Fourth, history of TB diagnosis was based on self-report and there was a risk of recall bias. Fifth, there were significant differences in general characteristics (such as gender, age group, occupation, etc.) of TB groups and controls. These differences can compromise the comparison between TB group and controls. Matched controls or subgroup analysis according to covariates might be needed to solve these differences.
Vitamin D deficiency was highly prevalent in the TB group, and the prevalence was similar to that among the non-TB controls in Korea. Regular examination and strategies to elevate vitamin D levels in individuals with a history of TB diagnosis are needed, because vitamin D is associated with TB conditions and bone disease.
5. Conclusions
Vitamin D deficiency was highly prevalent in the TB group, and the prevalence was similar to that among the non-TB controls in Korea. Regular examination and strategies to elevate vitamin D levels in individuals with a history of TB diagnosis are needed, because vitamin D is associated with TB conditions and bone disease.
Author Contributions
Mi Hyun Joo and Mi Ah Han conceived and designed the experiments; Mi Hyun Joo and Sum Mi Park performed the experiments; Mi Hyun Joo and Hwan Ho Shin analyzed the data; Mi Hyun Joo and Mi Ah Han contributed reagents/materials/analysis tools; Mi Hyun Joo and Mi Ah Han wrote the paper.
Conflicts of Interest
The authors declare no conflict of interest.
References
- 1.Raviglione M., Sulis G. Tuberculosis 2015: Burden, challenges and strategy for control and elimination. Infect. Dis. Rep. 2016;8:8. doi: 10.4081/idr.2016.6570. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Kim J.H., Yim J.J. Achievements in and challenges of tuberculosis control in South Korea. Emerg. Infect. Dis. 2015;21:1913–1920. doi: 10.3201/eid2111.141894. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Kang H.Y., Yoo H., Park W., Go U., Jeong E., Jung K.S., Son H. Tuberculosis notification completeness and timeliness in the Republic of Korea during 2012–2014. Osong Public Health Res. Perspect. 2016;7:320–326. doi: 10.1016/j.phrp.2016.08.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Holick M.F. Sunlight and vitamin D for bone health and prevention of autoimmune diseases, cancers, and cardiovascular disease. Am. J. Clin. Nutr. 2004;80:1678s–1688s. doi: 10.1093/ajcn/80.6.1678S. [DOI] [PubMed] [Google Scholar]
- 5.Gandini S., Boniol M., Haukka J., Byrnes G., Cox B., Sneyd M.J., Mullie P., Autier P. Meta-analysis of observational studies of serum 25-hydroxyvitamin D levels and colorectal, breast and prostate cancer and colorectal adenoma. Int. J. Cancer. 2011;128:1414–1424. doi: 10.1002/ijc.25439. [DOI] [PubMed] [Google Scholar]
- 6.Wang T.J., Pencina M.J., Booth S.L., Jacques P.F., Ingelsson E., Lanier K., Benjamin E.J., D’Agostino R.B., Wolf M., Vasan R.S. Vitamin D deficiency and risk of cardiovascular disease. Circulation. 2008;117:503–511. doi: 10.1161/CIRCULATIONAHA.107.706127. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Song G.G., Bae S.C., Lee Y.H. Association between vitamin D intake and the risk of rheumatoid arthritis: A meta-analysis. Clin. Rheumatol. 2012;31:1733–1739. doi: 10.1007/s10067-012-2080-7. [DOI] [PubMed] [Google Scholar]
- 8.Zhang F.F., Al Hooti S., Al Zenki S., Alomirah H., Jamil K.M., Rao A., Al Jahmah N., Saltzman E., Ausman L.M. Vitamin D deficiency is associated with high prevalence of diabetes in Kuwaiti adults: Results from a national survey. BMC Public Health. 2016;16 doi: 10.1186/s12889-016-2758-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Iftikhar R., Kamran S.M., Qadir A., Haider E., Bin Usman H. Vitamin D deficiency in patients with tuberculosis. J. Coll. Physicians Surg. Pak. 2013;23:780–783. [PubMed] [Google Scholar]
- 10.Junaid K., Rehman A., Jolliffe D.A., Saeed T., Wood K., Martineau A.R. Vitamin D deficiency associates with susceptibility to tuberculosis in Pakistan, but polymorphisms in VDR, DBP and CYP2R1 do not. BMC Pulm. Med. 2016;16 doi: 10.1186/s12890-016-0240-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Manhar M. Vitamin D deficiency in medical patients at a teaching hospital in North India. J. Assoc. Physicians India. 2015;63:35–39. [PubMed] [Google Scholar]
- 12.Kweon S., Kim Y., Jang M.J., Kim Y., Kim K., Choi S., Chun C., Khang Y.H., Oh K. Data resource profile: The Korea national health and nutrition examination survey (KNHANES) Int. J. Epidemiol. 2014;43:69–77. doi: 10.1093/ije/dyt228. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Nnoaham K.E., Clarke A. Low serum vitamin D levels and tuberculosis: A systematic review and meta-analysis. Int. J. Epidemiol. 2008;37:113–119. doi: 10.1093/ije/dym247. [DOI] [PubMed] [Google Scholar]
- 14.Talat N., Perry S., Parsonnet J., Dawood G., Hussain R. Vitamin D deficiency and tuberculosis progression. Emerg. Infect. Dis. 2010;16:853–855. doi: 10.3201/eid1605.091693. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Zuberi L.M., Habib A., Haque N., Jabbar A. Vitamin D Deficiency in ambulatory patients. J. Pak. Med. Assoc. 2008;58:482–484. [PubMed] [Google Scholar]
- 16.Hejazi M.E., Modarresi-Ghazani F., Entezari-Maleki T. A review of vitamin D effects on common respiratory diseases: Asthma, chronic obstructive pulmonary disease, and tuberculosis. J. Res. Pharm. Pract. 2016;5:7–15. doi: 10.4103/2279-042X.176542. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Cao Y., Wang X., Cao Z., Cheng X. Association of vitamin D receptor gene TaqI polymorphisms with tuberculosis susceptibility: A meta-analysis. Int. J. Clin. Exp. Med. 2015;8:10187–10203. [PMC free article] [PubMed] [Google Scholar]
- 18.Selvaraj P., Afsal K., Harishankar M. Vitamin D and macrophage functions in tuberculosis. Macrophage. 2015;2:e756. [Google Scholar]
- 19.Wejse C., Olesen R., Rabna P., Kaestel P., Gustafson P., Aaby P., Andersen P.L., Glerup H., Sodemann M. Serum 25-hydroxyvitamin D in a West African population of tuberculosis patients and unmatched healthy controls. Am. J. Clin. Nutr. 2007;86:1376–1383. doi: 10.1093/ajcn/86.5.1376. [DOI] [PubMed] [Google Scholar]
- 20.Hossein-nezhad A., Holick M.F. Vitamin D for health: A global perspective. Mayo Clin. Proc. 2013;88:720–755. doi: 10.1016/j.mayocp.2013.05.011. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Palacios C., Gonzalez L. Is vitamin D deficiency a major global public health problem? J. Steroid. Biochem. Mol. Biol. 2014;144:138–145. doi: 10.1016/j.jsbmb.2013.11.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Nimitphong H., Holick M.F. Vitamin D status and sun exposure in Southeast Asia. Dermatoendocrinol. 2013;5:34–37. doi: 10.4161/derm.24054. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Khadilkar S.S. The emerging role of vitamin D3 in women’s health. J. Obstet. Gynaecol. India. 2013;63:147–150. doi: 10.1007/s13224-013-0420-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Nair R., Maseeh A. Vitamin D: The “sunshine” vitamin. J. Pharmacol. Pharmacother. 2012;3:118–126. doi: 10.4103/0976-500X.95506. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Neyrolles O., Quintana-Murci L. Sexual inequality in tuberculosis. PLoS Med. 2009;6:e1000199. doi: 10.1371/journal.pmed.1000199. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Nyirenda T. Epidemiology of tuberculosis in Malawi. Malawi Med. J. 2006;18:147–159. doi: 10.4314/mmj.v18i3.10919. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Boum Y., Atwine D., Orikiriza P., Assimwe J., Page A.L., Mwanga-Amumpaire J., Bonnet M. Male gender is independently associated with pulmonary tuberculosis among sputum and non-sputum producers people with presumptive tuberculosis in Southwestern Uganda. BMC Infect. Dis. 2014;14 doi: 10.1186/s12879-014-0638-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Przybylski G., Dabrowska A., Pilaczynska-Cemel M., Krawiecka D. Unemployment in TB patients—Ten-year observation at regional center of pulmonology in Bydgoszcz, Poland. Med. Sci. Monit. 2014;20:2125–2131. doi: 10.12659/MSM.890709. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Mishra P., Hansen E.H., Sabroe S., Kafle K.K. Socio-economic status and adherence to tuberculosis treatment: A case-control study in a district of Nepal. Int. J. Tuberc. Lung Dis. 2005;9:1134–1139. [PubMed] [Google Scholar]
- 30.Jeong H., Hong S., Heo Y., Chun H., Kim D., Park J., Kang M.Y. Vitamin D status and associated occupational factors in Korean wage workers: Data from the 5th Korea national health and nutrition examination survey (KNHANES 2010–2012) Ann. Occup. Environ. Med. 2014;26 doi: 10.1186/s40557-014-0028-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Wacker M., Holick M.F. Sunlight and vitamin D: A global perspective for health. Dermatoendocrinol. 2013;5:51–108. doi: 10.4161/derm.24494. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Turnbull E.R., Drobniewski F. Vitamin D supplementation: A comprehensive review on supplementation for tuberculosis prophylaxis. Expert Rev. Respir. Med. 2015;9:269–275. doi: 10.1586/17476348.2015.1042458. [DOI] [PubMed] [Google Scholar]
- 33.Bischoff-Ferrari H.A., Shao A., Dawson-Hughes B., Hathcock J., Giovannucci E., Willett W.C. Benefit-risk assessment of vitamin D supplementation. Osteoporos. Int. 2010;21:1121–1132. doi: 10.1007/s00198-009-1119-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Choi H.S., Oh H.J., Choi H., Choi W.H., Kim J.G., Kim K.M., Kim K.J., Rhee Y., Lim S.K. Vitamin D insufficiency in Korea—A greater threat to younger generation: The Korea national health and nutrition examination survey (KNHANES) 2008. J. Clin. Endocrinol. Metab. 2011;96:643–651. doi: 10.1210/jc.2010-2133. [DOI] [PubMed] [Google Scholar]
- 35.Holick M.F. Vitamin D deficiency. N. Engl. J. Med. 2007;357:266–281. doi: 10.1056/NEJMra070553. [DOI] [PubMed] [Google Scholar]
- 36.Huang S.J., Wang X.H., Liu Z.D., Cao W.L., Han Y., Ma A.G., Xu S.F. Vitamin D deficiency and the risk of tuberculosis: A meta-analysis. Drug Des. Dev. Ther. 2016;11:91–102. doi: 10.2147/DDDT.S79870. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Zeng J., Wu G., Yang W., Gu X., Liang W., Yao Y., Song Y. A serum vitamin D level <25 nmol/L pose high tuberculosis risk: A meta-analysis. PLoS ONE. 2015;10:e0126014. doi: 10.1371/journal.pone.0126014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Arnedo-Pena A., Juan-Cerdán J.V., Romeu-Garcia A., Garcia-Ferrer D., Holguín-Gómez R., Iborra-Millet J., Herrero-Carot C., Piñana M.J., Bellido-Blasco J., Ferrero-Vega J.A., et al. Latent tuberculosis infection, tuberculin skin test and vitamin D status in contacts of tuberculosis patients: A cross-sectional and case-control study. BMC Infect. Dis. 2011;11 doi: 10.1186/1471-2334-11-349. [DOI] [PMC free article] [PubMed] [Google Scholar]