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Arquivos Brasileiros de Endocrinologia & Metabologia

On-line version ISSN 1677-9487

Arq Bras Endocrinol Metab vol.54 no.2 São Paulo Mar. 2010

http://dx.doi.org/10.1590/S0004-27302010000200006 

REVIEW

 

Vitamin D deficiency in HIV-infected individuals: one more risk factor for bone loss and cardiovascular disease?

 

Deficiência de vitamina D em indivíduos infectados pelo HIV: mais um fator de risco para perda óssea e doença cardiovascular?

 

 

Tereza ConradoI; Demócrito de Barros Miranda-FilhoI; Francisco BandeiraII

IDepartamento de Medicina Interna, Divisão de Doenças Infecciosas, Universidade de Pernambuco (UPE), Recife, PE, Brasil
IIDivisão de Endocrinologia, Departamento de Medicina, Hospital Agamenon Magalhães, Sistema Único de Saúde (SUS), UPE, Faculdade de Ciências Médicas, Recife, PE, Brasil

Correspondence

 

 


SUMMARY

The epidemiological profile of the HIV virus has undergone substantial modifications with advances in antiretroviral therapy. There has been a sharp decline in morbi-mortality levels of HIV-infected patients, which has resulted in higher survival rates. The HIV seropositive population is living longer and more exposed to chronic complications caused by the disease itself and the prolonged use of antiretrovirals. Initially, metabolic alterations were reported, increasing cardiovascular disease risk. Subsequently, damage on bone metabolism was related. Vitamin D insufficiency has now reached epidemic proportions, even in healthy individuals living in the tropics. Recent data suggest the hypovitaminosis D association with metabolic syndrome, immune diseases, diabetes and hypertension. Little is known regarding the effects of HIV/Aids and its treatment on the metabolism of vitamin D. In HIV-positive patients, factors linked to the virus itself and the use of antiretrovirals may be added to the other causes of hypovitaminosis D.

Keywords: Vitamin D deficiency; HIV; vitamin D; ART


SUMÁRIO

O perfil epidemiológico da infecção pelo vírus HIV vem sofrendo grandes modificações com os avanços na terapia antirretroviral. Houve uma queda expressiva na morbi-mortalidade do paciente infectado pelo HIV e, por conseguinte, aumento da sobrevida. A população soropositiva está envelhecendo e mais exposta às complicações da cronificação da doença e ao uso prolongado dos antirretrovirais. Inicialmente foram descritas alterações metabólicas que contribuem para um aumento no risco de doença cardiovascular. Em seguida, surgiram relatos de danos ao metabolismo ósseo. A deficiência de vitamina D tem atingido proporções epidêmicas envolvendo até mesmo indivíduos saudáveis em regiões tropicais. Dados recentes sugerem sua associação com síndrome metabólica, doenças imunes, diabetes e hipertensão. A doença HIV/Aids e a ação dos antirretrovirais no metabolismo da vitamina D ainda permanecem pouco conhecidas. Em pacientes HIV positivos, fatores ligados ao próprio vírus e ao uso dos antirretrovirais podem estar adicionados às demais causas de hipovitaminose D.

Descritores: Deficiência de vitamina D; HIV; vitamina D; TARV


 

 

INTRODUCTION

Throughout the world, 33 million people have been infected to date by the human immunodeficiency virus (HIV) and, in 2007 alone, 2 million people died as a result of Aids. In Brazil, there are an estimated 730 thousand HIV-positive patients, representing one third of all registered cases in Latin America (1,2). However, the sociodemographic profile of this infection has undergone a number of modifications. Over the previous few years there has been an increase in the number of cases amongst heterosexual men and a predominance of this form of transmission amongst women (3). Currently, the chances of men contracting this disease are 1.5 time greater than women, as compared to the last decade, when it was 15 times greater. This tendency of Aids towards gender parity has had a profound impact on the health of women all over the world (1,2).

Apart from affecting more women, HIV-positive patients have also experienced a greater chance of survival due to the advent of ART (antiretroviral therapy), coupled with an increased knowledge of the infection. The female seropositive population is now growing older and is consequently more exposed to chronic degenerative diseases brought on by prolonged exposure to the HIV virus and antiretroviral therapy. Initially, metabolic abnormalities were reported such as dyslipidemia, insulin resistance and lipodystrophy, which all contribute to the increased risk of cardiovascular disease (CVD). Subsequently, reports emerged of damage to the bone metabolism (4-7).

In association with these factors, menopausal women experience a period of hormone decline, progressively reducing the effects of estrogen protection on bone metabolism and CVD (8,9). According to Pernerstorfer, metabolic abnormalities resulting from ART are more pronounced in women, suggesting that, after they begin treatment, infected patients lose part of their natural protection against atherosclerosis (9).

The introduction of ART has had a profound impact by reducing the viral load and reconstituting the immune system of HIV/Aids patients. Thus, a significant impact has been observed on the natural history of the infection, represented by the considerable decline in morbi-mortality associated with the disease. The treatment is a complex therapeutic regimen made up of a combination of at least 3 drugs that include the use of two nucleoside-analogue reverse-transcriptase inhibitors (NRTI) and one from another class, which is usually a non-nucleoside reverse-transcriptase inhibitor (NNRTI) or a (PI) protease inhibitor (10).

Another important issue has been the growing pauperization of this epidemic and its consequent importance regarding nutritional deficiency. Currently, more than 2/3 of the most recently infected individuals live in extremely poor regions of the world, where there is a high prevalence of nutritional deficiency. A lack of macronutrients has been associated with an increasing number of clinical manifestations and a rise in Aids-related mortality (1,11). Furthermore, studies have also revealed how the beneficial effects of being well-nourished with the necessary vitamin supplements can lead to an improvement in the immune systems of HIV-positive patients (11,12).

With regard specifically to vitamin D deficiency, much attention has been focused on its importance as a steroid hormone and its properties as an immunomodulator since the vitamin D nuclear receptor (VDR) was discovered, during the 1980s, in various cells, especially those in the immune system such as T and B lymphocytes, monocytes and dendritic cells. Before the advent of antibiotics, vitamin D was used in the treatment of bacterial infections (11-15). Many in vitro experiments confirm the action of its active form, 1,25(OH)2 D, as a potent modulator of the immune system as well as its important role in calcium homeostasis. In addition, in vivo, a lack of vitamin D is associated with macrophage dysfunction and bacterial infection (11,13). Despite these advances, much remains to be clarified regarding the role of vitamin D in HIV infection and how its deficiency may affect the progression of the disease (11-13). Low levels of vitamin D and vitamin D receptor (VDR) polymorphism have been associated with low CD4, immune activity and the progression of Aids (11,13,16).

Currently, vitamin D is recognized as a complex, pluripotent hormone, and its deficiency has now gone beyond the simple concept of causing rickets and osteomalacia. Much evidence has associated it to the metabolic syndrome, diabetes, immune diseases, high blood pressure and cancer (14,15,17-20). Recently, vitamin D has been suggested as an emergent biomarker for CVD (21). However, the exact mechanism that would explain the multiple effects of vitamin D on different tissues is still unknown. The only common factor is that the vitamin D receptor has been discovered in various tissues such as those of the pancreas, the smooth muscle of the blood vessels and the cardiac cells, and in the renin-angiotensin axis (17,20).

Vitamin D is obtained in its natural form by exposing the skin to sun rays that converts 7-dehydrocholesterol (pro-vitamin D3) into cholecalciferol (vitamin D3) through which the bloodstream passes, where it joins the D-binding protein (VDBP) and is transported to the liver. The second source of vitamin D is via oral intake, through the transformation of ergosterol (vitamin D2) in plants and fungi. Vitamins D3 and D2, are both metabolized in the liver to 25-hydroxicholecalciferol [(25(OH)D] and are transformed in the kidneys into its active form, 1,25 dihydroxyvitamin D [1,25(OH)2D], which is a steroid hormone vital for calcium and bone metabolism (Figure 1). Other factors such as the seasons of the year, latitude, time of day, skin pigmentation, aging and the use of sun blocks may all influence the cutaneous production of vitamin D (14,15,22,23).

 

 

In healthy adults, vitamin D deficiency sets in in a subtle manner, with mild hypocalcemia, and secondary hyperparathyroidism, causing trabecular bone loss and a thinning of the cortical bone, leading to an increased risk of osteoporosis and fractures (15,22). Before antiretroviral treatment was introduced, few studies had indicated that bone metabolism was affected in HIV-positive patients, although it has recently been confirmed that infected patients present a higher risk of low bone mass and osteoporosis. Despite the fact that that was initially attributed to the use of these medications, it was later confirmed that its origins were due to a series of factors, one of the main ones being metabolic dysfunction of vitamin D (7,8,24).

In HIV-positive patients, other factors linked to the virus itself and to the use of antiretrovirals can be considered as additional causes of hypovitaminosis D, and therefore regarded as a threat to the general population, such as poor nutrition, skin pigmentation, aging and inadequate sun exposure. A number of mechanisms are proposed to explain this deficiency in HIV-positive patients (Figure 2): a) the virus itself decreases vitamin D levels through the action of proinflammatory cytokines such as TNF-α (Tumor necrosis factor-α), inhibiting renal hydroxylation; b) the consumption of 25(OH)D by the macrophages and lymphocytes as the disease progresses; and c) the type of antiretrovirals used. PIs (protease inhibitors) block the hydroxylation of 25(OH)D (25-hydroxycholecalciferol) and the bioactivation of 1,25(OH)2 (1,25 dihydroxyvitamin D) in the kidneys (11,16,17), while NNRTIs (non-nucleoside reverse-transcriptase inhibitors) increase the catabolism of 25 (OH)D and 1,25 (OH)2D (25).

 

 

A study carried out in the Netherlands with HIV-positive patients of both sexes reported a 58.1% prevalence of vitamin D deficiency in women with a mean age of 36.5 years, using reference levels for serum 25(OH)D of 10-14 ng/mL for winter and summer, respectively (25). Similar results were reported in a US population of seropositive teenagers and young adults, employing a cut-off for serum 25(OH)D of 15 ng/mL, demonstrating a prevalence of 87% of hypovitaminosis D (12). Seminari, in Italy, found serum 25(OH)D levels of less than 18 ng/mL in 81,25% of the patients, aged 41 years, who were on ART and had been losing bone (24). Similar prevalence (86%) was described by Aparicio and cols. (26) when evaluating Spanish infected males, using reference levels of serum 25(OH)D less than 10ng/mL (26). Rodriguez, in the US, also reported hypovitaminosis D in 74.4% of infected adults aged 46 years, using reference levels of serum 25(OH)D less than 32 ng/mL (27).

There is no consensus on the ideal serum concentration of 25(OH)D and there are many suggested values for setting the lower limit of normality from 20 to as much 37 ng/mL (14,15,22,23). Therefore the level of vitamin D should be the one that does not induce a rise in parathyroid hormone (PTH), and the optimal serum 25(OH)D concentrations have yet to be established (14,15,22,23). It is not surprising that discordant results are obtained because these laboratories use substantially different methodology for measurement of 25(OH)D, which, to this time, has not been standardized (14,15,22,23).

In healthy populations, clinical evidence based on epidemiological studies has demonstrated an association between vitamin D deficiency and an overall increased risk of mortality, based on NHANES-III " Third National Health and Nutrition Examination Survey (18). Further evidence that hypovitaminosis D increases the risk of CVD has appeared in a recent nested case-control study, in which men and couples were studied over a ten-year period for classical risk factors of CVD, with detected levels less than 30 ng/mL of serum 25(OH)D being associated with a significant increase in myocardial infarction (19).

There are very few reports for seropositive patients on the consequences of hypovitaminosis D on the lipid and glucose metabolism, although it is known that there is an association between ART and complications of fat redistribution (loss of peripheral fat and increased central obesity), insulin resistance and dyslipidemia (4,5). Recently, similar alterations have also been described in healthy patients with vitamin D deficiency (14,15,17,20,28).

In NHANES-III, Ford followed-up 8,421 healthy men and women and described an inverse association between serum 25(OH)D levels and the metabolic syndrome, caused mainly by hyperglycemia, hypertriglyceridemia and abdominal obesity (28). In a UK study, 524 randomized, healthy individuals were followed-up for a 10-year period. A negative association was observed between the serum levels of 25(OH)D and an increase in glycemia and insulin resistance, possibly explained by the action of VDR in the pancreatic β cells and in the insulin activation receptors, or indirectly by the increased number of inflammatory cytokines resulting from the decreased levels of vitamin D (29).

Current data from the Framingham Offspring Study cohort evaluated 1,739 patients without renal disease or previous CVD and described an association between vitamin D deficiency and an increased risk of CVD, especially in hypertensive individuals with serum 25(OH)D levels of less than 15 ng/mL, who had a two-fold risk of a cardiovascular event (17).

The results of the DAD study, which enrolled more than 22,000 HIV-positive patients, indicated a high frequency of hypertension, smoking, dyslipidemia and diabetes, in which ART was associated with a 26% increase in the relative risk levels of myocardial infarction for each year it was taken (6). Besides the traditional risk factors for CVD, these individuals are also exposed to other risk factors, including the disease itself, the direct effect of the virus on blood vessels, inflammation and complications from the prolonged use of antiretroviral therapy (5,6).

Together with this chain of possible events, vitamin D deficiency may also be included as one more cause of bone loss, the metabolic syndrome, dyslipidemia and an increased risk of CVD. These results are of particular relevance for HIV-positive women on ART. Not only are they likely to stimulate the progression of the disease through vitamin D deficiency, but also add one more risk factor to the prolonged use of antiretroviral therapy.

In conclusion, considering that vitamin D deficiency has been suggested as a possible risk condition for metabolic and cardiovascular events, the increased prevalence of this clinical condition in this population indicates the need for prevention. It is too early to identify the groups at greatest risk for which these measures would be required. In this context, vitamin D supplementation becomes necessary and/or sun exposure when the measurement of serum 25(OH)D is not feasible. Additional observational studies are needed to confirm the associations between vitamin D status and HIV disease progression and intervention studies will be necessary to define the benefits of vitamin D in the cardiovascular system and endocrine metabolism in the HIV-infected patient.

Disclosure: no potential conflict of interest relevant to this article was reported.

 

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Correspondence to:
Tereza Conrado
Rua Frei Leandro, 70/502
51011-600 - Recife, PE, Brasil
terezaconrado@hotmail.com

Received on Nov/16/2009
Accepted on Feb/28/2010

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