Young men
participating in a pre-exposure prophylaxis (PrEP) demonstration project
experienced modest but significant bone loss after starting Truvada, according to findings presented
yesterday to a joint session of the 15th European
AIDS Conference and the 17th International Workshop on Co-morbidities and Adverse Drug
Reactions in HIV.
Presenter Kathleen
Mulligan of the University of California at San Francisco reported that bone mineral
density (BMD) declines were seen in men who had tenofovir blood levels shown to
be highly protective against HIV infection; in contrast, bone density increased
in men with undetectable drug levels, as expected for young men of their age.
Tenofovir
disoproxil fumarate (Viread, also in
several single-tablet regimens) is one of the most widely used antiretrovirals,
and the Truvada (tenofovir/emtricitabine)
coformulation is increasingly used for HIV prevention. The iPrEx study showed
that daily Truvada reduced the risk
of HIV infection by 92% among gay men with measurable blood drug levels.
Tenofovir is
considered to be generally safe and well-tolerated, but it is known to cause a
small amount of bone loss soon after starting therapy. Bone loss has been seen
in HIV-positive adults taking tenofovir-containing antiretroviral therapy and in
infants exposed to tenofovir during gestation. Tenofovir-related bone loss has
not yet been studied extensively in HIV-negative people or in adolescents and
young adults – the age at which peak bone density occurs.
This analysis looked at bone density changes among participants
in ATN 110, an open-label
demonstration project investigating the safety and feasibility of PrEP for
young gay men age 18-22 years. Results of the main study were presented at the International AIDS Society
Conference this summer.
Bone mass generally
peaks during early adulthood – typically around age 20 – after which it begins
to gradually decline. Peak bone mass is an important predictor of fracture risk
later in life, Mulligan noted as background.
ATN 110 enrolled 200
at-risk HIV-negative young men who have sex with men in 12 US cities. The
median age was 20 years, nearly half were African American and about a quarter
were Latino. Overall body weight was normal, but with a wide variation (median
body mass index 23.6; range 17.3-58.9 kg/m2).
All participants were
offered PrEP using once-daily Truvada
for 48 weeks, along with a full package of HIV prevention services including
risk reduction and adherence counselling, testing and treatment for sexually
transmitted infections and free condoms. Drug levels were measured throughout
the study and dosing frequency was estimated based on tenofovir concentrations
in dried blood spots.
The bone sub-study
performed dual X-ray absorptiometry (DXA) scans of the hip, spine and whole
body at baseline and at weeks 24 and 48. The four participants who became
HIV-positive during the study were excluded from the bone analysis.
Bone mineral density
levels were lower than expected at baseline, falling below norms for age and
race/ethnicity; 8.1% of participants had spine BMD, 6.1% had hip BMD and 3.7%
had whole body BMD below standard international thresholds for low bone mass.
Mulligan noted that low bone mass has previously been reported in other studies
of at-risk HIV-negative men.
At week 24 after
starting Truvada, bone density
decreased at the spine (by about -0.2%), hip (by about -0.4%) and whole body (by
about -0.8%), with the latter two changes being statistically significant. At
48 weeks, hip BMD continued to decrease steeply (falling by about -1.0%) and
whole body BMD further decreased by a small amount, but spine BMD started to increase
and in fact rose above the baseline level.
Z-scores – a measure
of deviation from the norm for people of the same age and race/ethnicity – decreased
for the spine, hip and whole body at both week 24 and week 48; all these
changes were significant.
The researchers then
looked at the relationship between bone loss and tenofovir concentrations in
dried blood spots. More than half of participants had drug levels shown to
confer a high level of protection – indicating that Truvada was taken at least four times a week – for the first 12
weeks. Adherence declined over time, however, and by week 48 only about a third
of participants still had highly protective drug levels.
This allowed the
researchers to compare bone density changes between men who had highly protective
tenofovir levels and those with lower levels, showing that bone loss at the
spine and hip through week 48 was correlated with tenofovir exposure.
Men with highly
protective tenofovir levels showed spine bone loss of about -0.5% at week 24
and about -1.5% at week 48, while those with undetectable drug levels saw their
bone density rise by approximately the same amount. Hip bone density decreased
by smaller amounts at weeks 24 and 48 in men with protective drug levels, while
remaining unchanged in those with undetectable drug levels.
Mulligan noted that differences
in bone loss between men who took Truvada
seven days a week and those who took it four times a week were not significant,
so it is not clear whether taking PrEP less
often – perhaps using an intermittent or 'on demand' dosing schedule like the
one used in the Ipergay
study – would be protective against bone
loss.
Looking at bone
fractures, about a quarter of participants reported that they had sustained
fractures prior to the study. During the study period, five participants experienced
eight fractures, all due to trauma (slamming fingers in a door, a vehicle
accident, a fall and a fight). None of the men with fractures had Z-scores
indicating low bone mass.
"Although the BMD
losses were generally modest, their occurrence before attainment of peak bone
mass in young men who already have low bone mass may increase their risk of
fragility in adulthood," the researchers concluded.
In response to an audience question, Mulligan
said there was "very little evidence" of kidney toxicity among PrEP
recipients, with very few cases of protein or glucose in the urine and little
change in serum creatinine.
The study will
continue to follow participants for a year to determine whether bone loss is
reversible after stopping Truvada.