The
specifics
The study was a substudy of the
PIVOT trial, a randomised controlled trial of protease inhibitor
monotherapy versus standard combination therapy taking place at 40
centres in the UK.
This substudy included 560 patients,
382 (68%) of white ethnicity and the rest African. The researchers, at the start of the study while they were all still on combination therapy,
gave all patients five neurocognitive performance tests: the grooved
pegboard test, a measure of fine motor skills, two memory tests
(sort-term and delayed recall) and two 'trailmaking' tests that
involve a combination of fast motor and executive (decision-making)
skills.
Three-quarters of the white patients
were men and 40% of the Africans. The average CD4 nadir was
moderately low, at 177 cells/mm3
in white patients and
146 in black, but current CD4 counts were good at 554 and 511
cells/mm3
respectively, reflecting the fact that patients regardless of
ethnicity had been on combination therapy for an average of five
years and with a viral load uner 50 copies/ml for four.
There were substantial differences
in rates of smoking in the group, with 62% of white patients and 28%
of black ever having smoked and of cardiovascular risk, with 48% of
white patients at a more than 10% risk of a cardiovascular even in
the next ten years compared with only 18% of black patients, which
probably reflects smoking habits and gender in the two groups. The
age of the two ethnic groups was the same and so was their
psychological health as measured by anxiety scores.
In the general population, one would
expect 16% of people given the five psychological tests to have a
global performance score more than one standard deviation lower than
the mean score. In the unadjusted figures, 17% of white patients fell
into this category, thus having the same score as the general
population, but far higher rates of black patients – 66%.
The general-population scores are in
fact derived from studies of patients mainly in the US and Canada.
The researchers adjusted these 'normative' comparison scores by using
the quite limited data of NC performance in African-Americans to
derive comparison scores more reflective of the ethnic balance of the
UK patient group (though this assumes African-Americans and people
born in Africa will tend to resemble each other in NC results). In
these adjusted normative scores, 20% rather than 16% of HIV-negative
people would, on average, have NC performance more than one standard
deviation worse than mean.
They found that using these adjusted
scores more than doubled the proportion of white patients with global
NC impairment – from 17% to 38% - and reduced
impairment in black patients, from 66% to 55%.
The researchers did the same
analysis for impairment in at least two of the five tests measured.
Unsurprisingly, if you defined NC impairment in this way, it was more
common, seen in 38% of white patients and no less than 81% of black.
If the adjusted normative scores were used, however, this increased
to 64% in white patients and decreased to 69% in black, so the difference became
statistically non-significant.
The researchers did a multivariate
analysis of factors associated with NC impairment in the unadjusted
normative figures. They found
that white patients with hepatitis C were 33% more likely to have NC
impairment. They also found that white patients on nevirapine were
34% more likely to have it too, but this is thought to be a
'channelling bias' whereby patients with pre-existing NC symptoms are
more likely to be prescribed nevirapine than efavirenz. Oddly, black
patients who smoked were 66% less
likely to have NC than average, but this may reflect demographic
differences not picked up in the study (e.g. black smokers might be
more likely to be gay men, or born in the UK).
This study should not necessarily be
taken to indicate more reliably than previous studies what the 'real'
relative rates of NC impairment are in people with HIV in the UK
compared to the general population, but it does illustrate that the
results of all studies depend crucially on how we estimate
neurocognitive impairment in general.
Researcher Alan Winston of Imperial
College in London told the conference that the question of the
relative rates of NC impairment in the HIV positive population would
not be settled until more studies were done with matched control
groups of HIV-negative peers, matched for more variables like
sexuality, drug use, STI history and so on.