There is a high
prevalence of low bone mineral density among patients with HIV, Spanish investigators
report in the online edition of AIDS.
The researchers also found evidence during follow-up of deterioration of bone
health in many patients.
“Our…study revealed a
marked incidence of low BMD [bone mineral density] in a large number of
patients with long-term HIV infection and prolonged antiretroviral therapy,”
comment the researchers.
They believe that
their findings have immediate clinical significance, and write: “Clinical
monitoring of BMD by DXA scan should be a priority in HIV-infected patients,
specifically in those at risk of fracture.”
HIV infection has been
firmly linked with an increased risk of low bone density. However, the exact causes
are unclear.
Traditional risk
factors for this condition include smoking, heavy alcohol consumption,
malnutrition, low body weight, and lack of physical activity.
HIV itself can cause
loss of bone mineral, and treatment with some anti-HIV drugs has also been
associated with loss of bone mineral density.
Spanish researchers
wanted to gain a better understanding of the prevalence, risks and progression
of bone loss in their HIV-positive patients.
They therefore
designed a retrospective study involving 671 patients who received HIV care
between 2000 and 2009 in Barcelona. All the patients had at least one DXA scan.
Progression of bone loss was assessed in 391 individuals who had two or more
scans.
Most (72%) of the
patients were male, 6% were aged over 55, the median age was 42 years (interquartile range 37 to 47), 67% had a body mass index (BMI)
within the normal range, 62% had an adequate calcium intake, and 35% were
co-infected with hepatitis B or C.
CD4 cell count at the
time of entry to the study was 496 cells/mm3, 93% had experience of
antiretroviral therapy, and 61% had an undetectable viral load.
The patients had been
taking anti-HIV drugs for a median of seven years, 53% were taking a protease
inhibitor, and the same proportion of patients took tenofovir (Viread, also in the combination pills Truvada and Atripla).
Osteopenia – mild bone
loss – was diagnosed in 47% of patients and osteoporosis – porous bone with an
increased risk of fractures – in
23%.
Factors associated
with low bone mineral density were increasing age (p < 0.001), low BMI (p
< 0.001), male sex (p = 0.0078), high creatinine levels (p = 0.0047), taking
HIV therapy at the time of DXA scan (p = 0.007), longer duration of
antiretroviral treatment (p = 0.004), and increased amount of time taking a
protease inhibitor (p = 0.0001).
Next the investigators
looked at the progression of bone loss. Their analysis included the patients
who had two or more DXA scans.
The median time
between the first and last scan was 2.5 years, but in 27% of patients it was
more than five years.
At the first scan, 49%
of patients had osteopenia and 22% osteoporosis. At the second scan this had
increased to 50% and 27%.
Overall, 29% of patients
experienced progression to low bone mineral density, including 13% progressed
to osteopenia, and 16% from osteopenia to osteoporosis.
When analysis was
restricted to the 105 patients with five or more years of follow-up, 47% lost
bone mineral density, including 18% who developed osteopenia and 29% who
developed osteoporosis.
Factors associated
with bone loss during follow-up included increasing age (p < 0.0001), male
sex (p < 0.0001), low BMI (p < 0.0001), longer duration of treatment with
a protease inhibitor (p < 0.0001) or tenofovir (p < 0.0001), and taking a
protease inhibitor at the time the DXA scan was performed (p < 0.0001).
“We reveal a high
prevalence of low BMD in our cohort. The longitudinal analysis – more than five
years of follow-up in some cases – revealed rapid progression to demineralization,”
comment the investigators.
The investigators
stress the need “for close monitoring of BMD, specifically in at-risk patients
who are taking antiretroviral therapy that affect bone demineralization”.