Prevalence of silent cerebral small-vessel disease (SCSVD) – an important precursor to more serious neurocognitive conditions – is significantly higher among middle-aged HIV-positive patients compared to controls in the general population, according to French research published in Clinical Infectious Diseases.
After controlling for age, blood pressure and other traditional risk factors, the investigators found that HIV was associated with a doubling in the risk of SCSVD. HIV-positive patients aged between 50 and 54 years had an especially elevated risk of the condition compared to their HIV-negative peers.
“Our study results revealed a high CSVD prevalence among middle-aged PLWHIVs, despite cART-sustained immunovirological control,” comment the authors. “We confirmed classical risk factors, e.g. hypertension and advancing age, and identified a specific HIV-associated factor, the nadir CD4-cell count.”
CSVD covers a range of abnormalities affecting blood vessels in the brain. In the general population, it is a major cause of cognitive impairment, frailty, altered gait, and is the second most important cause of dementia in the elderly.
Age and hypertension are known risk factors, but its association with HIV is unclear.
Investigators in France therefore designed a cross-sectional study involving middle-aged HIV-positive patients, all of whom were doing well on antiretroviral therapy, and matched HIV-negative controls.
The aim was to compare the prevalence of CSVD and severe CSVD according to HIV infection status. MRI scanning – the acknowledged gold standard – was used to diagnose CSVD.
All the HIV-positive patients were aged 50 years or older, were taking long-term antiretroviral therapy and had sustained virological suppression. Exclusion criteria included HCV co-infection, drug or alcohol abuse and diagnosed neurological disease.
The final study population consisted of 456 patients with HIV and 156 controls. Recruitment took place between 2013 and 2016.
Patients with HIV were younger than the controls (median age 56 vs. 58 years, p = 0.001) and were also more likely to be male (85% vs. 77%, p = 0.03).
Approximately two-thirds of the HIV-positive sample had been diagnosed before the introduction of effective antiretroviral treatment in 1996. Median nadir and current CD4 cell counts were 196 and 665 cells/mm3, respectively.
CSVD was detected in 52% of patients with HIV compared to 36% of the controls. Severe CSVD was present in a fifth of the HIV-positive sample and 14% of HIV-negative patients.
After adjustment for age, sex, alcohol use, blood pressure, lipids and history of cardiovascular disease, the investigators found that CSVD was significantly more frequent in patients with HIV than controls (aOR = 2.3; 95% CI, 1.5-3.6); however, there was no association between HIV and the risk of severe CSVD.
Overall, the risk of CSVD increased with age.
Despite this, younger HIV-positive patients (50 to 54 years) had a five-fold increase in the risk of CSVD compared to age-matched controls; the risk was three-fold higher for HIV-positive individuals aged between 54 and 60.
Risk factors for CSVD in patients with HIV included a nadir CD4 cell count below 200 cells/mm3 (aOR = 1.5; 95% CI, 1.0-2.3).
“Recent study results showing links between CSVD and cognitive and gait impairments, frailty and stroke in the general population and PLHIVs should prompt medical providers to search for CSVD in PLHIVs, using a brief MRI,” conclude the authors, who recommend that screening should be especially targeted at the over-60s.