TY - JOUR
T1 - Coronary aging in HIV-infected patients
AU - Guaraldi, Giovanni
AU - Zona, Stefano
AU - Alexopoulos, Nikolaos
AU - Orlando, Gabriella
AU - Carli, Federica
AU - Ligabue, Guido
AU - Fiocchi, Federica
AU - Lattanzi, Antonella
AU - Rossi, Rosario
AU - Modena, Maria Grazia
AU - Esposito, Roberto
AU - Palella, Frank
AU - Raggi, Paolo
N1 - Funding Information:
We thank Dr Bruno Guidetti for database management and query construction. We thank Drs Giulia Nardini and Barbara Beghetto for their support during the organization and conduct of the trial. Financial support. N.A. was supported by a scholarship from the Hellenic Cardiological Society. The Metabolic Clinic staff was supported by an unrestricted research grant from Gilead Sciences. Potential conflicts of interest. All authors: no conflicts.
PY - 2009/12
Y1 - 2009/12
N2 - Background: Human immunodeficiency virus (HIV)-infected patients often demonstrate accelerated aging processes. We investigated whether the vascular age of a cohort of stable HIV-infected patients receiving antiretroviral therapy (ART) was increased and sought out predictors of increased vascular age. Methods: In this cross-sectional study, 400 HIV-infected patients (mean age, 48 years) attending a cardiometabolic clinic underwent cardiac computed tomography imaging to identify coronary artery calcium (CAC).Vascular age was estimated on the basis of the extent of CAC by means of previously published equations. Results: Increased vascular age was observed in 162 patients (40.5%), with an average increase of 15 years (range, 1-43 years) over the chronological age. In univariable analyses, chronological age, male sex, systolic blood pressure, duration of ART, fasting glucose level, fasting serum triglyceride level, total cholesterol level, low-density and high-density lipoprotein cholesterol levels, hypertension, and the presence of the metabolic syndrome were associated with increased vascular age. In multivariable linear regression analyses, current CD4+ cell count was the only predictor of increased vascular age (β = 0.51; P = .005). Conclusions: Increased vascular age is frequent among HIV-infected patients and appears to be associated with CD4+ cell count. If these findings were to be confirmed in prospective trials, a positive response to ART with an increase in CD4+ cell count may become a marker of increased risk of atherosclerosis development.
AB - Background: Human immunodeficiency virus (HIV)-infected patients often demonstrate accelerated aging processes. We investigated whether the vascular age of a cohort of stable HIV-infected patients receiving antiretroviral therapy (ART) was increased and sought out predictors of increased vascular age. Methods: In this cross-sectional study, 400 HIV-infected patients (mean age, 48 years) attending a cardiometabolic clinic underwent cardiac computed tomography imaging to identify coronary artery calcium (CAC).Vascular age was estimated on the basis of the extent of CAC by means of previously published equations. Results: Increased vascular age was observed in 162 patients (40.5%), with an average increase of 15 years (range, 1-43 years) over the chronological age. In univariable analyses, chronological age, male sex, systolic blood pressure, duration of ART, fasting glucose level, fasting serum triglyceride level, total cholesterol level, low-density and high-density lipoprotein cholesterol levels, hypertension, and the presence of the metabolic syndrome were associated with increased vascular age. In multivariable linear regression analyses, current CD4+ cell count was the only predictor of increased vascular age (β = 0.51; P = .005). Conclusions: Increased vascular age is frequent among HIV-infected patients and appears to be associated with CD4+ cell count. If these findings were to be confirmed in prospective trials, a positive response to ART with an increase in CD4+ cell count may become a marker of increased risk of atherosclerosis development.
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U2 - 10.1086/648080
DO - 10.1086/648080
M3 - Article
C2 - 19886793
AN - SCOPUS:72849128722
SN - 1058-4838
VL - 49
SP - 1756
EP - 1762
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 11
ER -