There is only scant evidence that vitamin D supplementation
is of benefit for patients with HIV, according to UK investigators writing in
the January 28th edition of AIDS.
The authors conducted a systematic review of studies
examining the prevalence of vitamin D deficiency in patients with HIV, the
effects of antiretroviral therapy on vitamin D levels, the effects of vitamin D
deficiency and HIV therapy on bone metabolism and fracture risk, and the
benefits of vitamin D supplements.
Both cross-sectional and longitudinal studies showed that
vitamin D deficiency was widespread in HIV-positive patients. Moreover, there
was evidence that starting HIV therapy, especially regimens containing
efavirenz (Sustiva, also in the
combination pill Atripla), was
accompanied by a drop in concentrations of vitamin D. Studies also showed that bone turnover increased in
the early years of antiretroviral therapy.
However, the clinical consequences of vitamin D deficiency
and reduced bone turnover were unclear. Nor was there sufficient evidence to
advocate widespread use of vitamin D supplements by HIV-positive patients.
It is now well established that low bone mineral density and
vitamin D deficiency are both common in patients with HIV. Because of this,
measuring vitamin D levels is becoming a standard component of HIV care and
vitamin D supplements are being widely used.
Despite this, evidence for clinical benefit and cost
effectiveness of this approach to patient management is currently lacking.
Investigators therefore reviewed the findings of recent
published studies looking at the issue of bone loss and its possible causes and
treatment in patients with HIV.
Vitamin D insufficiency was defined as levels between 20-30
ng/dl; deficiency as levels between 10-20 ng/dl; and severe deficiency as a
level below 10 ng/dl.
Prevalence of vitamin
D deficiency
Research in the public domain suggested that between 29% and
73% of HIV-infected patients had vitamin D deficiency.
However, HIV per se
was not the cause.
Rather, risk factors were similar to those seen in the
general population and included black or Hispanic ethnicity, low exposure to
ultraviolet light, measurement in the autumn or winter, increased BMI, high
blood pressure and low levels of exercise.
HIV-related factors associated with vitamin D insufficiency
or deficiency included duration of infection with the virus, a CD4 cell count
below 200 cells/mm3, current use of antiretroviral therapy and viral
load.
The importance of vitamin D to HIV-related outcomes was
unclear, but one study showed that patients with levels below 12 ng/ml at
baseline were more likely to develop AIDS or die.
Vitamin D deficiency
and HIV therapy
Both cross-sectional and longitudinal studies consistently
showed that treatment with efavirenz resulted in reductions in vitamin D
levels. There was little or no evidence that protease inhibitors, NRTIs or
tenofovir (Viread, also in the
combination pills Truvada and Atripla) reduced vitamin D
concentrations.
However, the investigators caution that the clinical
significance of the small reductions in vitamin D seen in patients taking HIV
therapy has not been demonstrated.
Vitamin D deficiency,
antiretroviral treatment and parathyroid hormone levels
Parathyroid hormone helps regulate calcium levels.
Parathyroid disease causes osteoporosis. Elevated parathyroid levels were
common in patients taking HIV therapy and were associated with therapy that
included tenofovir.
Vitamin D deficiency,
antiretrovirals and bone turnover
The available evidence did not show a relationship between
vitamin D deficiency and increased bone turnover. However, it did suggest a
relationship with antiretroviral therapy. Moreover, bone turnover may be
increased in patients taking tenofovir-containing regimens as well as in
individuals with secondary hyperparathyroidism.
Vitamin D deficiency,
HIV therapy and bone mineral density
Longitudinal research showed a relationship between vitamin
D deficiency and lower bone mineral density in the hip.
Reductions in bone mineral density of between 2% and 6%
after starting HIV therapy have been consistently reported, with stabilisation
after six to twelve months of treatment. Tenofovir and ritonavir-boosted
protease inhibitors have been especially associated with bone loss.
The magnitude of this initial loss in bone density is on a
par with that seen in the first year of the menopause. However, its clinical
significance, especially in a relatively young patient population, is unclear.
Furthermore, the role of vitamin D deficiency in antiretroviral-associated bone
loss has yet to be defined.
Vitamin D deficiency,
antiretroviral treatment and fractures
Patients with HIV are approximately 60% more likely to
experience a fracture than HIV-negative individuals.
However, it was unclear if vitamin D deficiency or
treatment-related side-effects were the cause. The majority of these fractures
were due to trauma rather than fragility.
Vitamin D
supplementation
There was some evidence that supplementation resulted in
transient changes in parathyroid hormone levels. However, there was no impact on
bone mineral density or markers of inflammation, or lipid levels.
Recommendations for
vitamin D testing and supplementation
European HIV guidelines recommend monitoring of vitamin D
levels for those with a risk of deficiency, as well as individuals with
osteopenia and osteoperosis. Supplements are recommended for patients with
vitamin levels below 10 ng/ml.
Conclusions
“With the majority of HIV-positive patients receiving
combination antiretroviral therapy below 50 years of age, the benefits of a universal
vitamin D deficiency ‘test and treat’ strategy in terms of fracture prevention
remain to be defined, especially if vitamin D is given without daily calcium
supplements,” comment the authors.
They conclude, “the overall incidence of fragility
fractures, especially in younger HIV-positive patients is low and this should
be taken into consideration when deciding whether to measure [vitamin D0 levels
and recommend vitamin D supplementation.”