HIV disease, metabolic dysfunction and atherosclerosis: A three year prospective study.
Hann LowAnh HoangTatiana PushkarskyLarisa DubrovskyElizabeth DewarMaria-Silvana Di YacovoNigora MukhamedovaLesley ChengCatherine DownsGary SimonMaria SaumoyAndrew F HillMichael L FitzgeraldPaul NestelAnthony DartJennifer HoyMichael BukrinskyDmitri SviridovPublished in: PloS one (2019)
HIV infection is known to be associated with cardiometabolic abnormalities; here we investigated the progression and causes of these abnormalities. Three groups of participants were recruited: HIV-negative subjects and two groups of treatment-naïve HIV-positive subjects, one group initiating antiretroviral treatment, the other remaining untreated. Intima-media thickness (cIMT) increased in HIV-positive untreated group compared to HIV-negative group, but treatment mitigated the difference. We found no increase in diabetes-related metabolic markers or in the level of inflammation in any of the groups. Total cholesterol, low density lipoprotein cholesterol and apoB levels were lower in HIV-positive groups, while triglyceride and Lp(a) levels did not differ between the groups. We found a statistically significant negative association between viral load and plasma levels of total cholesterol, LDL cholesterol, HDL cholesterol, apoA-I and apoB. HIV-positive patients had hypoalphalipoproteinemia at baseline, and we found a redistribution of sub-populations of high density lipoprotein (HDL) particles with increased proportion of smaller HDL in HIV-positive untreated patients, which may result from increased levels of plasma cholesteryl ester transfer protein in this group. HDL functionality declined in the HIV-negative and HIV-positive untreated groups, but not in HIV-positive treated group. We also found differences between HIV-positive and negative groups in plasma abundance of several microRNAs involved in lipid metabolism. Our data support a hypothesis that cardiometabolic abnormalities in HIV infection are caused by HIV and that antiretroviral treatment itself does not influence key cardiometabolic parameters, but mitigates those affected by HIV.
Keyphrases
- hiv positive
- antiretroviral therapy
- men who have sex with men
- south africa
- hiv infected
- human immunodeficiency virus
- hiv testing
- hiv aids
- hiv infected patients
- low density lipoprotein
- end stage renal disease
- newly diagnosed
- oxidative stress
- cardiovascular disease
- chronic kidney disease
- ejection fraction
- radiation therapy
- metabolic syndrome
- optical coherence tomography
- skeletal muscle
- adipose tissue
- fatty acid
- deep learning
- mass spectrometry
- electronic health record
- high speed
- big data
- replacement therapy