Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Overt diabetes mellitus among newly diagnosed Ugandan tuberculosis patients: a cross sectional study

BMC Infectious Diseases volume 13, Article number: 122 (2013) Cite this article

Abstract

Background

There is a documented increase of diabetes mellitus in Sub Saharan Africa, a region where tuberculosis is highly endemic. Currently, diabetes mellitus is one of the recognised risk factors of tuberculosis. No study has reported the magnitude of diabetes mellitus among tuberculosis patients in Uganda, one of the countries with a high burden of tuberculosis.

Methods

This was a cross-sectional study conducted among 260 consenting adult patients with a confirmed diagnosis of tuberculosis admitted on the pulmonology wards of Mulago national referral and teaching hospital in Kampala, Uganda to determine the prevalence of diabetes mellitus and associated clinical factors. Laboratory findings as well as the socio-demographic and clinical data collected using a validated questionnaire was obtained. Point of care random blood sugar (RBS) testing was performed on all the patients prior to initiation of anti tuberculosis treatment. Diabetes mellitus was diagnosed if the RBS level was ≥ 200mg/dl in the presence of the classical symptoms of diabetes mellitus.

Results

The prevalence of diabetes mellitus among the admitted patients with tuberculosis was 8.5%. Only 5 (1.9%) patients with TB had a known diagnosis of diabetes mellitus at enrolment. Majority of the study participants with TB-DM co-infection had type 2 diabetes mellitus (n=20, 90.9%).

At bivariate analysis, raised mean ALT concentrations of ≥80 U/L were associated with DM (OR-6.1, 95% CI 1.4-26.36, p=0.032) and paradoxically, HIV co-infection was protective of DM (OR-0.32, 95% CI 0.13-0.79, P=0.016). The relationship between DM and HIV as well as that with ALT remained statistically significant at multivariate analysis (HIV: OR- 0.17 95%CI 0.06-0.51, p=0.002 and ALT: OR-11.42 95%CI 2.15-60.59, p=0.004).

Conclusion

This study demonstrates that diabetes mellitus is common among hospitalized tuberculosis patients in Uganda. The significant clinical predictors associated with diabetes mellitus among tuberculosis patients were HIV co-infection and raised mean serum alanine transaminase concentrations.

Peer Review reports

Background

In 2011, the International Diabetes Federation (IDF) estimated that about 366 million people worldwide have diabetes mellitus (DM). 80% of these people live in the low and middle income countries where tuberculosis (TB) is highly prevalent [1]. According to the World Health Organisation (WHO), there were an estimated 8.8 million incident cases of TB globally in 2010 [2].

Currently, both TB and DM are of great public health importance globally especially in Sub Saharan Africa (SSA) due to the converging epidemics of both communicable and non communicable diseases. With a prevalence rate of TB of 193/100,000 in 2010, Uganda is one of the high burden TB countries in SSA [3]. There is also an observed trend of increasing prevalence of DM in Uganda. The estimated prevalence according to the International Diabetes Federation in 2010 was 2.2% [4].

Recent evidence advocates for bi-directional screening and care of TB and DM patients. This is because both morbidities adversely affect each other [5] and currently, there is plausible evidence from different studies to support the strong association between DM and TB [6, 7]. Diabetic patients have impaired cell mediated immunity, renal failure, micronutrient deficiency and pulmonary microangiopathy, all of which increase their propensity to develop TB [8]. DM is also known to alter the clinical presentation of TB and its outcomes in terms of delayed sputum/culture conversion, case fatality and treatment failure [9].

TB co-infection is associated with poor glycemic control among DM patients. Reactionary hyperglycemia often accompanies chronic infections like TB due to the increased pro-inflammatory state and release of counter-regulatory stress hormones like epinephrine, cortisol and glucagon that are antagonistic of insulin [10]. Rifampicin, a very potent anti TB drug has also been shown to induce a transient early phase hyperglycemia owing to augmentation of intestinal glucose absorption [11].

This study sought to determine the prevalence of DM and the associated clinical factors among the adult TB patients admitted on the pulmonology wards of Mulago national referral and teaching hospital, Uganda.

Methods

Study site description

Mulago national referral and teaching hospital is located in Kampala, the capital city of Uganda and serves a population of about 2 million people. It is a 1,500 bed facility serving as a national referral hospital and teaching hospital for Makerere University College of Health Sciences, Uganda. The hospital has two adult pulmonology wards primarily for admission of patients with the varied pulmonary medical conditions like TB.

Study methods

This was a cross sectional study in which adult patients with a confirmed diagnosis of TB admitted on the pulmonology wards of Mulago hospital were consecutively recruited during weekdays of the study period of September 2011 up to February 2012.

Patients enrolled into the study were ≥18 years of age, admitted on the pulmonology wards during the study periods and had a confirmed diagnosis of TB. All patients who were on anti TB drugs and those who could not offer informed consent were excluded from the study.

A confirmed diagnosis of TB was made if the patient presented with clinical symptoms suggestive of TB and at least one of the following: a positive sputum smear on Ziehl Nielsen or flourochrome (Auramine-O) stain for acid fast bacilli (AFB), a positive Xpert/RIF-TB test result, a positive sputum culture for TB and a histological diagnosis of TB on lymph node or pleural biopsy.

Data collection

All patients gave informed consent prior to enrolment into the study. Information on the socio-demographic characteristics, medical history and laboratory variables of the consented eligible study participants was collected using pre-coded questionnaire forms. All patients underwent anthropometric measurements for estimation of the body mass index (BMI).

A capillary blood sample was obtained for measurement of the random blood sugar (RBS) level using a One Touch Ultra® glucometer from Johnson and Johnson Company, United Kingdom. Blood was also drawn for measurement of the serum albumin, renal function tests (serum urea and creatinine) for calculation of the glomerular filtration rate (GFR), liver function tests (alanine transaminase (ALT) and alkaline phosphatase (ALP) levels), HIV serology and CD4 counts. The normal values for the above tests were: serum albumin: 35–50 g/L, GFR: 90–120 ml/min/1.73 m [2], ALT: 0-80U/L and ALP: 30–129 U/L. All the above tests were done prior to initiation of anti TB drugs. The cockroft Gault formula below was used to estimate the glomerular filtration rate (GFR). Normal GFR was defined as an estimated GFR of ≥ 90 ml/min/1.73 m [2].

GFR = [(140-Age in years) × body weight in kg/ serum creatinine in mg/dl × 72] × 0.85 if female.

The diagnosis of DM was made basing on the recent American Diabetes Association (ADA) guidelines of a random or casual blood sugar level ≥ 200mg/dl in the presence of the classical symptoms of DM [12]. The classical symptoms of DM include: polyuria, polydipsia, polyphagia, generalised body weakness and progressive weight loss. Type 2 diabetic patients were defined as patients aged ≥30 years on oral hypoglycaemic drugs and/or insulin therapy while type 1 diabetic patients were those aged < 30 years on insulin monotherapy.

Statistical analysis

Data was entered into EPI-INFO Version 6 and analysed using SPSS version 14. Patient’s characteristics were summarised with proportions and the continuous variables expressed in mean and standard deviation for normally distributed variables.

To determine associations between the different factors and RBS levels, the outcome variable, bivariate analyses using chi-square test was performed. For variables in which the cell values were less than 5, the Fischer’s exact test was used instead. Continuous variables were categorised into 2 groups based on the normal cut off values and then compared. Age was categorised into 2 groups using the cut of value of the average age.

Binary logistic regression analysis was performed to determine which factors were independently associated with DM among the study participants. Multivariate analysis was then performed and variables considered were those which had a conservatively set cut off p-value of <0.3 on bivariate analysis. A p-value of <0.05 and confidence intervals not including 1 were considered to be statistically significant.

Using the prevalence of 13.2% of DM among TB patients in Indonesia [13], with 80% power and a two-sided α < 0.05, a sample size of 176 study subjects was obtained. However, we enrolled 260 patients for the study.

Ethical consideration

This study was approved by the department of Internal Medicine, Makerere College of Health Sciences and the Makerere University School of Medicine research and ethics committee, Uganda.

Results

Socio-demographic, clinical and laboratory characteristics of the patients

Of the 260 study participants enrolled, majority were male (n=146, 56.2%). The mean age of the study participants was 34.5 years (S.D 9.5). The youngest participant was 18 years and the eldest was 65 years. HIV co-infection was documented in 280 (80%) participants with 78% of them having CD4 counts < 200 cells/mm [3]. The mean BMI was 17.4 kg/m [2]. Sixty three (23.2%) and 197 (75.8%) participants had extra pulmonary TB (EPTB) and pulmonary TB (PTB) respectively. Fifty (19.2%) of the participants had TB relapse (Tables 1 and 2).

Table 1 Baseline socio-demographic factors and clinical characteristics of the study participants
Full size table
Table 2 Laboratory findings of the study participants
Full size table

Prevalence of DM and the clinical characteristics of the TB-DM co-infected participants

DM was diagnosed in 22 study participants giving a prevalence of 8.5%. Twenty participants had type 2 DM while 2 had type 1 DM. Of the 22 participants, 5 (22.7%) had a known diagnosis of DM and all had poor glycemic control (defined as RBS level > 180 mg/dl) at baseline despite being on glucose lowering therapy. The background prevalence of DM on the medical units in the hospital during the study period was 6.4%.

The most frequent symptoms among the study participants with DM-TB co-infection were polyuria (90.9%), polydipsia (77.3%) and progressive weight loss (68.2%). The socio-demographic characteristics, category and episode of TB of the study participants did not significantly differ between the diabetic and non diabetic TB patients (Table 3).

Table 3 Bivariate analysis for the characteristics of the study participants
Full size table

At bivariate analysis, HIV co-infection was protective of DM (OR-0.32, 95% CI 0.13-0.79, P=0.016) and raised mean ALT concentrations were associated with DM (OR-6.1, 95% CI 1.4-26.36, p=0.032). For every unit change in the ALT category there was a 1.8 unit increase in the RBS (95% CI 0.35-3.3, p=0.02).

The relationship between DM and HIV as well as that with ALT remained statistically significant on multivariate analysis (HIV: OR- 0.17 95%CI 0.06-0.51, p=0.002 and ALT: OR-11.42 95%CI 2.15-60.59, p=0.004). On multivariate analysis, for every unit change in the ALT category, there was a 2.4 unit change in the random blood sugar (95%CI=0.77-4.1, p=0.04). Other variables considered in the multivariate analysis included age, sex, episode of TB infection (relapse or new infection), BMI, category of TB and smoking, though were not statistically significant.

The diabetic TB-HIV co-infected patients had lower baseline mean CD4 counts compared to non diabetic TB-HIV co-infected patients, although this was not statistically significant (Table 4).

Table 4 Predictor variables considered for association with DM at multivariate analysis
Full size table

Discussion

This study demonstrates that DM is highly frequent among admitted TB patients in Mulago hospital, Uganda. To our knowledge, this is the first study to examine this association in Uganda, one of the high burden TB countries in SSA. The reported prevalence of DM among the TB patients of 8.5% is significantly higher than the estimated prevalence of DM among the general population in Uganda (2.2%) [4] and the back ground prevalence of DM on the medical units in the hospital during the study period (6.4%).

The documented prevalence of DM among TB patients in the African studies published between 1980 and 2006 varies between 2.1%-6.7% [14–17]. The observed prevalence of DM among TB patients in our study is comparable to that reported from Nigeria [16] and Tanzania [17] but higher than what was noted in South Africa [14] and Guinea Conakry [15].

This heterogeneity in the above results could probably be explained by the varied techniques used to diagnose DM among the TB patients and the probable effects of co morbidities like HIV. Largely, an oral glucose tolerance test (OGTT) was used in diagnosing DM in most African studies [14, 16, 17]. Balde et al. used a fasting capillary blood test to diagnose DM among TB patients in Guinea Conakry [15]. In our study, the diagnosis of DM was made basing on a random or casual capillary blood test. No particular method of diagnosing DM among TB patients has been advocated for. Either a random blood sugar (RBS), fasting blood sugar (FBS), OGTT or glycated haemoglobin (HbA1c) test can be used alone or in combination [5].

Similar studies from other parts of the world have reported remarkably higher prevalence of DM among TB patients. In Asia and the Middle East, the documented prevalence varies from 9.5%-44% [13, 18–23] and 11.9%-27% [24–26] respectively. A multi centre study done in Texas, USA and Mexico reported prevalence of 39% and 36% respectively [27]. This higher prevalence could probably be due to the higher background prevalence of DM in the general population in those respective countries.

Type 2 DM was the most frequent type of DM encountered among the study participants with DM-TB co-infection (90.9%). A similar observation has been documented in most similar studies [13, 15, 18]. This could probably be due to the higher proportions of people with type 2 DM compared to type 1 DM in most general populations.

Five (1.9%) of the study participants at enrolment had a prior diagnosis of DM and on assessment to determine the extent of glycemic control, they all had poor glycemic control which we defined as a RBS level ≥ 180 mg/dl. TB infection is often associated with a transient stress induced hyperglycemia which results into suboptimal glycemic control among diabetic patients. It usually resolves following TB therapy [28].

This form of reactionary hyperglycemia can also lead to over diagnosis of DM among TB patients. Studies by Alisjahbana et al. [13], Oluboyo et al. [16] and Mugusi et al. [17] demonstrated improvement in the glycemic status of some patients following TB treatment. However in our study, we did not perform a repeat assessment of the glycemic status among the newly diagnosed DM patients during the course of TB therapy.

HIV co-infection and raised mean serum ALT concentrations were noted to be independently associated with DM among TB patients in our study. In contrast to available literature and findings from other studies [29–33], HIV infection appeared protective in our study. A probable explanation for this is that most of our HIV positive patients were taking cotrimoxazole prophylaxis, a drug which has been found to cause hypoglycaemic effects in some patients [34]. However, this relationship between HIV and DM in our study needs to be interpreted with caution. This is because a study done in this similar setting to determine glycemic levels in patients with severe sepsis (80% of whom also had HIV infection and were on cotrimoxazole prophylaxis) revealed no statistically significant association between HIV infection and hyperglycemia (OR-0.97, 95%CI 0.57-1.62) [35].

Raised mean serum ALT concentrations in TB/DM patients have not been described in any similar studies. However, since majority of the study participants had HIV co-infection, an elevated mean ALT concentration of >66 U/L prior to diagnosis of DM was noted to be significantly associated with DM among HIV infected patients in one case control study performed in an urban HIV clinic in the USA [33].

A raised mean serum ALT concentration is a strong predictor of insulin resistance [36]. It also principally reflects direct hepatocellular damage or liver dysfunction. Liver dysfunction secondary to underlying hepatitis C and hepatosteatosis have been demonstrated to be associated with DM [37–40].

Hepatitis C infection is associated with insulin resistance owing to an increased pro-inflammatory state and production of cytokines especially tumour necrosis factor α and interleukin 6. These inhibit transcription of the glucose transporter-4 and peroxisome proliferator –activated receptor γ. Insulin resistance results into alteration in lipid metabolism and deposition in the hepatocytes. Hepatosteatosis often develops later. Hepatitis C co-infection is also associated with autoimmune pancreatic beta cell damage leading to DM [37–40]. In addition to hepatitis C infection, human herpes virus type 8 (HHV-8), a highly prevalent virus among HIV infected patients that causes with kaposi sarcoma has also been demonstrated to be linked to ketosis prone type 2 DM, an atypical form of DM commonest among black Africans [41]. In our study however, we did not assess for presence of hepatosteatosis, hepatitis C or HHV-8 co-infection among the study participants.

Majority of the similar studies have reported increasing age, overweight or obesity [15, 19, 20, 27] and male gender [20] as the clinical factors associated with DM among TB patients. Sedentary lifestyle and family history of DM and obesity were also noted to be independently associated with DM in the study done in Guinea Conakry [15]. These clinical factors were not significantly associated with DM among our study participants.

Study limitations

We acknowledge important limitations in our study. Only one RBS estimation was used to diagnose DM hence leading to a possibility of overestimating of the prevalence of DM among our study participants since patients with reactive hyperglycemia could have been included. Use of an OGTT could have diagnosed more patients with borderline DM.

Although the study adjusted for some of the confounding factors, the role of residual confounding factors for the association between DM and TB cannot be ruled out. In addition, due to the cross sectional nature of the study, the temporality between the TB and DM could not be ascertained.

As similar findings have been documented among TB patients in other parts of the world, we believe that our findings are generalisable and hence we recommend that patients diagnosed with TB should routinely have their blood sugar levels assessed in order to enable timely diagnosis and optimal management of DM.

Conclusion

DM is a frequent co morbid condition among TB patients in Uganda. HIV co-infection and raised mean serum ALT concentrations are independently associated with DM among TB patients. We recommend routine screening for DM among TB patients in Uganda especially those with raised mean serum ALT concentrations of ≥80 U/L. Further prospective studies to examine the effects of DM on the clinical outcomes among TB-DM co-infected patients in Uganda are warranted.

Abbreviations

DK:

Davis Kibirige

RS:

Richard Ssekitoleko

EM:

Edrisa Mutebi

WW:

William Worodria

References

  1. International Diabetes Federation Diabetes Atlas. http://wwwidforg/diabetesatlas/5e/ Accessed CIon 26/06/2012.

  2. Global tuberculosis control: WHO report. 2011

  3. http://www whoint/tb/data Accessed on 6/6/2012

  4. The International Diabetes Federation Atlas. 2010, 4

  5. Ottmani S, Murray M, Jeon C: Consultation meeting on tuberculosis and diabetes mellitus: meeting summary and recommendations. Int J Tuberc Lung Dis. 2010, 14 (12): 1513-1517.

    PubMed  Google Scholar 

  6. Faurholt-Jepsen D, Range N, PrayGod G: Diabetes Is a Risk Factor for Pulmonary Tuberculosis: A Case–control Study from Mwanza, Tanzania. PLoS One. 2011, 6 (8): e24215-

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Jeon C, Murray M: Diabetes Mellitus Increases the Risk of Active Tuberculosis: A Systematic Review of 13 Observational Studies. PLoS Med. 2008, 5 (7): 1091-1101.

    Article  Google Scholar 

  8. Harriesa A, Billo N, Kapurc A: Links between diabetes mellitus and tuberculosis: should we integrate screening and care?. Trans R Soc Trop Med Hyg. 2009, 103: 1-2.

    Article  Google Scholar 

  9. Stevenson C, Forouhi N, Roglic G, Williams B, Lauer J, Dye C: Diabetes and tuberculosis: the impact of the diabetes epidemic on tuberculosis incidence. BMC Publ Health. 2007, 7: 234-

    Article  Google Scholar 

  10. Van-Cromphaut S, Vanhorebeek I, Van-den-Berghe G: Glucose metabolism and insulin resistance in sepsis. Curr Pharm Des. 2008, 14: 1887-1899.

    Article  CAS  PubMed  Google Scholar 

  11. Takasu N, Yamada T, Miura H: Rifampicin-induced early phase hyperglycemia in humans. Am Rev Respir Dis. 1982, 125: 23-27.

    CAS  PubMed  Google Scholar 

  12. American Diabetes Association Position statement- Standards of Medical Care in Diabetes. Diabetes Care. 2012, 35: S11-S63.

  13. Alisjahbana B, Van-Crevel R, Sahiratmadja E: Diabetes mellitus is strongly associated with tuberculosis in Indonesia. Int J Tuberc Lung Dis. 2006, 10 (6): 696-700.

    CAS  PubMed  Google Scholar 

  14. Marais R: Diabetes Mellitus in Black and Coloured Tuberculosis patients. S Afr Med J. 1980, 57: 483-484.

    CAS  PubMed  Google Scholar 

  15. Baldé N, Camara A, Camara L, Diallo M, Kaké A, Bah-Sow O: Associated tuberculosis and diabetes in Conakry, Guinea: prevalence and clinical characteristics. Int J Tuberc Lung Dis. 2006, 10 (9): 1036-1040.

    PubMed  Google Scholar 

  16. Oluboyo P, Erasmus R: The significance of glucose intolerance in pulmonary tuberculosis. Tubercle. 1990, 71: 135-138.

    Article  CAS  PubMed  Google Scholar 

  17. Mugusi F, Swai A, Alberti K, McLarty D: Increased prevalence of diabetes mellitus in patients with pulmonary tuberculosis in Tanzania. Tubercle. 1990, 71: 271-276.

    Article  CAS  PubMed  Google Scholar 

  18. Zhang Q, Xiao H, Sugawara I: Tuberculosis complicated by diabetes mellitus at Shangai Pulmonary hospital China. Jpn J Infect Dis. 2009, 62: 390-391.

    PubMed  Google Scholar 

  19. Wang P, Lin R: Epidemiological features of diabetics among tuberculosis patients in Taiwan. J Infect Dis Antimicrob Agents. 2000, 17: 101-105.

    Google Scholar 

  20. Suleiman S, Aweis D, Mohamed A, RazakMuttalif A, Moussa M: Role of Diabetes in the Prognosis and Therapeutic Outcome of Tuberculosis. Int J Endocrinol. 2012, 10: 1-6.

    Google Scholar 

  21. Li L, Lin Y, Mi F: Screening of patients with tuberculosis for diabetes mellitus in China. Trop Med Int Health. 2012, 17 (10): 1294-1301.

    Article  PubMed  Google Scholar 

  22. Viswanathan V, Kumpatla S, Aravindalochanan V: Prevalence of Diabetes and Pre-Diabetes and Associated Risk Factors among Tuberculosis Patients in India. PLoS One. 2012, 7 (7): e41367-

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Balakrishnan S, Vijayan S, Nair S: High Diabetes Prevalence among Tuberculosis Cases in Kerala, India. PLoS One. 2012, 7 (10): e46502-

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Golsha R, Shiraz R, Shafiee A, Najafi L, Dashti M, Roshandel G: Pulmonary Tuberculosis And Some Underlying Conditions In Golestan Province Of Iran, During 2001–2005. J Clin Diagn Res. 2009, 3: 1302-1306.

    Google Scholar 

  25. Singla R, Khan N, Al-Sharif N, Al-Sayegh M, Shaikh M, Osman M: Influence of diabetes on manifestations and treatment outcome of pulmonary TB patients. Int J Tuberc Lung Dis. 2006, 10 (1): 74-79.

    CAS  PubMed  Google Scholar 

  26. Jabbar A, Hussain S, Khan A: Clinical characteristics of pulmonary tuberculosis in adult Pakistani patients with co-existing diabetes mellitus. East Mediterr Health J. 2006, 12 (5): 522-527.

    CAS  PubMed  Google Scholar 

  27. Restrepo B, Camerlin A, Rahbar M: Cross-sectional assessment reveals high diabetes prevalence among newly-diagnosed tuberculosis cases. Bull World Health Organ. 2011, 89: 352-359.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Shamoon M, Hendlei R, Sherwin R: Synergistic interaction among anti-insulin hormones in the pathogcncsis of stress hyperglyccmia in humans. J Clin Endo Metab. 1981, 52: 1235-1240.

    Article  CAS  Google Scholar 

  29. Kalra S, Kalra B, Agrawal N, Unnikrishnan A: Understanding diabetes in patients with HIV/AIDS. Diabetol Metab Syndr. 2011, 3: 2-

    Article  PubMed  PubMed Central  Google Scholar 

  30. Petoumenos K, Worm S, Fontas E: Predicting the short-term risk of diabetes in HIV-positive patients: the Data Collection on Adverse Events of Anti-HIV Drugs (D:A:D) study. J Int AIDS Soc. 2012, 15: 17426-

    Article  PubMed  PubMed Central  Google Scholar 

  31. El-Sadr W, Mullin C, Carr A: Effects of HIV disease on lipid, glucose and insulin levels: Results from a large antiretroviral-naive cohort. HIV Med. 2005, 6: 114-121.

    Article  CAS  PubMed  Google Scholar 

  32. Kilby J, Tabereaux P: Severe hyperglycemia in an HIV clinic: Pre-existing versus drug-associated diabetes mellitus. J Acquir Immune Defic Syndr Hum Retrovirol. 1998, 17: 46-50.

    Article  CAS  PubMed  Google Scholar 

  33. Yoon C, Gulick R, Hoover D: Case–control study of diabetes mellitus in HIV-infected patients. J Acquir Immune Defic Syndr. 2004, 37: 1464-1469.

    Article  PubMed  Google Scholar 

  34. Strevel E, Kuper A, Gold W: Severe and protracted hypoglycaemia associated with co-trimoxazole use. Lancet Infect Dis. 2006, 6 (3): 178-182.

    Article  PubMed  Google Scholar 

  35. Ssekitoleko R, Jacob S, Banura P: Hypoglycemia at admission is associated with inhospital mortality in Ugandan patients with severe sepsis. Crit Care Med. 2011, 39: 2271-2276.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Chung R, Casson D, Murray G: Alanine aminotransferase levels predict insulin resistance in HIV lipodystrophy. J Acquir Immune Defic Syndr. 2003, 34: 534-536.

    Article  PubMed  Google Scholar 

  37. Mason A, Lau J, Hoang N: Association of diabetes mellitus and chronic hepatitis C virus infection. Hepatology. 1999, 29: 328-333.

    Article  CAS  PubMed  Google Scholar 

  38. Ali S, Abera S, Mihret A, Abebe T: Association of Hepatitis C Virus Infection with Type II Diabetes in Ethiopia: A Hospital-Based Case–control Study. Interdiscip Perspect Infect Dis. 2012, 10: 1155-

    Google Scholar 

  39. Naing C, Mak J, Ahmed S, Maung M: Relationship between hepatitis C virus infection and type 2 diabetes mellitus: Meta-analysis. World J Gastroenterol. 2012, 18 (14): 1642-1651.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Masini M, Campani D, Boggi U: Hepatitis C Virus Infection and Human Pancreatic beta-Cell Dysfunction. Diabetes Care. 2005, 28 (4): 940-941.

    Article  PubMed  Google Scholar 

  41. Sobngwi E, Choukem S, Agbalika F: Ketosis-Prone Type 2 Diabetes Mellitus and Human Herpes virus 8 Infection in Sub-Saharan Africans. JAMA. 2008, 299 (23): 2770-2776.

    Article  CAS  PubMed  Google Scholar 

Pre-publication history

Download references

Acknowledgements

We would like to acknowledge all the study participants and the Clinical Operational and Health Services Research (COHRE) training program under the Joint Clinical Research Centre (JCRC), Uganda for funding this study.

Author information

Authors and Affiliations

  1. Department of Medicine, St. Raphael of St. Francis hospital Nsambya, P.O.BOX 7146, Kampala, Uganda

    Davis Kibirige

  2. Department of Medicine, Makerere University College of Health Sciences, Kampala, Uganda

    Richard Ssekitoleko, Edrisa Mutebi & William Worodria

  3. Infectious diseases unit, Mulago National referral and Teaching Hospital, Kampala, Uganda

    Richard Ssekitoleko

  4. Endocrine unit, Mulago National referral and Teaching Hospital, Kampala, Uganda

    Edrisa Mutebi

  5. Pulmonology unit, Mulago National referral and Teaching Hospital, Kampala, Uganda

    William Worodria

Authors
  1. Davis Kibirige
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Richard Ssekitoleko
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Edrisa Mutebi
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. William Worodria
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Davis Kibirige.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

Concept development: DK, EM, RS and WW, Data collection: DK, Supervision of the study: EM and WW, Data interpretation and revision of the all the drafts: DK, EM, RS and WW. All authors read and approved the final manuscript.

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Kibirige, D., Ssekitoleko, R., Mutebi, E. et al. Overt diabetes mellitus among newly diagnosed Ugandan tuberculosis patients: a cross sectional study. BMC Infect Dis 13, 122 (2013). https://doi.org/10.1186/1471-2334-13-122

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1471-2334-13-122

Keywords

BMC Infectious Diseases

ISSN: 1471-2334

Contact us