Ramalingam Sekar and Manoharan Mythreyee*
Department of Microbiology, Faculty of Medicine, Government Theni Medical College, The Tamilnadu Dr. MGR Medical University, Theni, India
Received Date: December 08, 2011; Accepted Date: January 01, 2012; Published Date: January 07, 2012
Citation: Sekar R, Mythreyee M (2012) Tuberculosis, HIV/AIDS and Diabetes – Is it Time to Think Together? J Medical Microbiol Diagnosis 1:e103. doi: 10.4172/2161-0703.1000e103
Copyright: © 2012 Sekar R, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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HIV; Tuberculosis; Diabetes; Incidence; Risk; Control
Human Immunodeficiency Virus (HIV)/Acquired Immunodeficiency Syndrome (AIDS), Tuberculosis (TB) and Diabetes mellitus (DM) were individually one of the top ten causes of mortality all over the world . Annual deaths caused by these diseases were 1.78 million, 1.34 million and 1.26 million respectively. Dreadfully, all together these three killers claim 4.38 million lives, which correspond to 7.7% of total deaths/annum. Among the three killers two are chronic communicable disease i.e., HIV and TB; and the other is chronic noncommunicable disease i.e., DM. The association between communicable and noncommunicable diseases were known for centuries but are neglected until recently . Intriguingly, in the recent past evidences were accumulating on the association between TB and DM, as well as HIV/ AIDS and DM, which gained importance to the communicable – noncommunicable disease association . Nevertheless, the HIV-TB link was well recognized since the beginning of HIV epidemic. Hence, this editorial is attempted to review the evidence and counter-evidence stating the association between these three deadly diseases in relation to aetiopathogenesis, diagnosis and management.
Tuberculosis holding a persistent top position among the fatal infections of bacterial diseases all over the world [1,4]. According to the World Health Organization (WHO) report, there are about 8.8 million new TB cases and 1.45 million deaths owing to TB in the year of 2010 . However, in recent past, TB incidence has declined in developed countries, but the incidence remains high in developing and underdeveloped countries. Awfully, it is estimated that 1/3 of the world population i.e., ~ 2 billion were latently infected with Mycobacteriumtuberculosis and may get progressed to active TB at any time of life, especially during the immunosuppression. At the same time, the prevalence of diabetes mellitus is increasing globally in an alarming manner. As estimated by Wild et al.  the prevalence of DM was 171 million or 2.8% in the year of 2000. Shockingly, the estimated prevalence was more than doubled within the short period of 10 years. According to International Diabetes Federation report, the global prevalence of DM was estimated to be 366 million or 8.3% in the year of 2011 and is expected to surge to 552 million or 9.9% people, by 2030 [6,7].
The relationship between TB and DM has been recognized for centuries . In the middle of twentieth century, there were reports on the association between TB and DM, stating that, merging the management of these diseases could improve the patient outcome [9-11]. However, until recent years , there was a lack of strong evidence on the strength of the association between TB and DM. Presently the association between the TB and DM are poorly acknowledged. The link was not even mentioned in many global and national TB control strategies yet it is plausible that diabetes is a major threat to effective TB control [3,5].
According to a recent meta-analysis, diabetes patients have three times the risk of contracting TB as non-diabetics  and studies report the portion of TB cases ascribable to diabetes to be between 15% and 25% [13,14]. The WHO suspects that the TB control could become difficult, as there is alarming rise in the prevalence of DM patients across the globe . The biological mechanism for the association between TB and DM is not fully understood but studies suggest that diabetes depresses the immune response , which in turn facilitates the progression of latently infected Mycobacterium tuberculosis to active TB disease.
Furthermore, the incidence of multi-drug resistant TB (MDR-TB) was also reported to be high among DM patients owing to the impaired absorption of anti-TB drugs in the gastrointestinal mucosa, which resulted in the sub-lethal dose achievement at the tissue level where the bacteria exist, and facilitate the development of drug resistance [17-19]. However, it was not supported by other studies [20,21] and uncertainty remains.
Although the many number of studies evaluated the presence of diabetes as a risk factor for TB [12,22], the connection between DM and TB is suggested to be bidirectional. According to the reports by Nichols et al.  and Karachunskii et al. , TB could increase the risk of developing diabetes. However, ambiguity remains around whether TB is a risk factor for DM.
Therefore, it is obvious that patients with diabetes are at higher risk of developing active TB than non-diabetic patients [2,12]. Integrating TB and diabetes control programs worldwide would facilitate TB prevention among diabetes patients. Such a strategy would provide a way to earlier case detection and improve the management of both TB and diabetes.
According to the recent UNAIDS report, 33.3 million people were estimated to be living with HIV/AIDS . Sub-Saharan Africa sustained to hold a maximum share of the global burden of HIV patients and AIDS related deaths.
The association between HIV infection and DM is poorly understood. According to Butt et al.  HIV infection is not having direct association with DM; however, the intake of anti-retroviral therapy (ART) increases the risk of developing DM. According to Brown et al. [27,28] the incidence of DM was 4 times higher among the persons taking highly active ART (HAART), than that of HIV uninfected persons.
ART is the only approved tool for the management and control of HIV/AIDS disease progression. It consists of a number of drugs that suppresses viral multiplication and decreases the viral load. HAART is the gold standard for the management of AIDS, where three or more drugs are combined together in order to prevent the development of drug resistance in HIV. According to recent report of UNAIDS, ART was currently put on more than 5 million HIV infected persons .
Patients living with HIV/AIDS (PLHA) are increasing in number, partly owing to improved screening strategy (earlier diagnosis of HIV), better treatment and monitoring options (management of opportunistic infections and monitoring of CD4 cell count at regular intervals), and greater accessibility to ART at government centers with free of cost - altogether help improve the survival of these patients. Consequently, HIV/AIDS associated mortality was reported to be significantly declining in the recent past. Addition of newer cases and the endurance of previously diagnosed cases, results in the increasing number of PLHA .
However, the major problem with ART is, once started it should be continued for entire life. This resulted in an augmented exposure to ART and caused chronic complications due to drug toxicity among them. Hence, PLHA taking ART frequently presents with diabetes and other metabolic complaints . The prevalence of hyperglycemia and diabetes mellitus is significantly higher in PLHA being treated with ART, as compared with the general population [29-32]. Therefore, as number of PLHA increases, the incidence of HIV-associated diabetes is also bound to grow. There are three subgroups of diabetes among PLHA: the most important subgroup in relation to HIV associated diabetes is developing hyperglycemia after the initiation of ART, other two subgroups were, patients with preexisting diabetes, and those who are diagnosed to have diabetes at the time of HIV diagnosis. The management of diabetes in these three PLHA subgroups were different, since the mechanisms of metabolic dysregulation vary in them .
The aetiopathogenesis of DM in PLHA were mainly insulin resistance, rather than insulin deficiency. Reportedly, insulin resistance is common in HIV-infected people, particularly among those being treated with protease inhibitor. It is hypothesized that, protease inhibitor (PI) confer acute metabolic risks, while nucleoside reverse transcriptase inhibitor (NRTI) confers cumulative risks of diabetes in exposed, predisposed persons. Exposure to a combination of NRTI and PI has synergistic effect on the onset of diabetes . Takarabe and Rokukawa  recently reported the autoimmune mechanism of DM among the HIV infected persons during the restoration of immunity after the initiation of HAART.
Therefore, it is strongly recommended that, the patients with HIV should be screened for diabetes at the time of HIV diagnosis, at the initiation of HAART, and three to six months after HAART.
The association between TB and HIV was well recognized, since the early years of HIV epidemic. Their dangerous synergy affects all aspects of both the diseases, from pathogenesis and epidemiology; to clinical manifestation, treatment, and prevention. The greatest burden of the TB-HIV co-infection was observed in sub-Saharan Africa.
Individually, both HIV and TB were the two leading causes of infectious disease associated mortality worldwide . Additionally, TB is the leading cause of death among PLHA. Nearly one in four deaths among people with HIV is owing to TB. According to the recent WHO report [5,35], 1.1 million new TB cases were estimated among the HIV patients in 2010. Among them around 82% of patients was living in sub-Saharan Africa.
At least one-third of the 33.3 million people living with HIV worldwide are latently infected with TB. The HIV-TB co-infected persons are 21-34 times more likely to develop active TB disease, than the persons without HIV . The HIV-TB co-infection can occur in two forms: person with latent TB acquire HIV infection or HIV infected person acquire new TB infection. In both the cases, the risk of developing active TB increases several fold. According to Chaisson et al.  the risk of reactivation of latent TB infection, increases to 100- fold, when a person acquires HIV infection. More importantly, PLHA need early diagnosis and treatment of active TB disease; and if TB was not present, they should receive Isoniazid preventive therapy [5,35].
The increasing incidence of MDR-TB and the emerging problem of extensively drug-resistant TB (XDR-TB), were reported to be more common in HIV infected and are most problematic for the management (Table 1). The drug resistant forms worsen the management of active TB cases, and are responsible for very high mortality rate among PLHA and may undermine the current TB control strategies especially in low and middle-income countries [37,38].
|Adverse Outcomes||HIV – TB||DM – TB||(HIV & DM) – TB|
|Increased TB cases||++||+||? (+++)|
|More difficult to diagnose TB cases||Yes||Yes||? (Yes)|
|Increased Death||Yes||Yes||? (Yes)|
|Increased Recurrent TB||Yes||Yes||? (Yes)|
|Increased incidence of MDR - TB||Yes||Yes||? (Yes)|
HIV – Human Immunodeficiency Virus Infection
TB – Tuberculosis
DM – Diabetes mellitus
MDR-TB – Multi-Drug resistant TB
Results inside the parenthesis were hypothesized.
Table 1: Assessment of each condition in association with Tuberculosis.
HIV-TB co-infection complicates both the diagnosis and treatment of tuberculosis. Because the sputum smear microscopy in HIV infected persons were, reportedly having reduced sensitivity than that of HIV uninfected persons. The treatment of HIV-TB co-infection includes the concomitant administration of both anti-tuberculosis therapy (ATT) and ART. The most common treatment challenges include, pill burden and overlapping toxic effects of ATT and ART, drug interactions, patient compliance and immune reconstitution inflammatory syndrome. Current treatment guideline for the HIV-TB co-infection is starting ART within a few weeks of ATT for patients with CD4 cell count <350 cells/μL; however, when to start ART and what to start remain ambiguous in HIV-TB management .
It has long been recognized that infective agents may predispose to, or trigger, some chronic noncommunicable diseases . Now, it has become evident that two of the most common infectious diseases, TB and HIV, may also be closely related to chronic noncommunicable disease . Based on the available evidence, it is clearly understood that, diabetes predisposes to TB [2,13], whereas with limited evidence TB may also predispose to diabetes . ART for HIV/AIDS may increase the risk of metabolic syndrome and thus predispose to DM (Figure 1) [27,30]. Hence, we call for the action of considering all the three diseases together for diagnosis and management to improve the case detection, early treatment and possible prevention.
Although, the current evidences suggest the strong association between HIV, TB and DM much research is needed to arrive conclusion, especially the combined effect of HIV and DM on TB is yet to be unveiled (Table 1). Nevertheless, integrating HIV/AIDS, TB and diabetes control programs in low and middle-income countries would have a great public health impact in preventing TB among HIV and/ or DM patients; and DM among HIV patients. Such a strategy would lead to earlier case detection, improve the management of all the three deadly diseases, and reduce the mortality significantly.
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