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. Author manuscript; available in PMC: 2014 Sep 1.
Published in final edited form as: J Acquir Immune Defic Syndr. 2013 Sep 1;64(1):10.1097/QAI.0b013e31829ed726. doi: 10.1097/QAI.0b013e31829ed726

Table 4.

Multivariate Regression Analysis of IMT Change and CAC Progression.

A. IMTa Progression, Internal carotid
Risk Factor Beta-coefficient (μm) (SE) p-value
Intercept -0.24 ± 0.1 0.05
Age 0.008 ± 0.003 0.002
Baseline high triglycerides (≥150mg/dL) 0.14 ± 0.04 <0.001
Pack-years tobacco 0.003 ± 0.001 0.03
B. IMTa Progression, Common carotid
Risk Factor Beta-coefficient (μm) ± SE p-value
Intercept -0.03 ± 0.03 0.35
Cholesterol (mg/dL) 0.0002 ± 0.0001 0.005
Age 0.002 ± 0.0006 <0.001
Nadir CD4+ (100 cells/mm3) 0.005 ± 0.002 0.03
PIb use at baseline 0.02 ± 0.008 0.05
C. CACc progression
Risk Factor Odds Ratio (Confidence Interval) p-value
Baseline diabetes 7.4 (2.5,21.5) <0.001
HIV viral load (log 10 copies/mL) 1.7 (1.2,2.4) 0.001
HAARTd duration (months) 1.02 (1.01,1.03) 0.004
a

IMT, carotid intima-media thickness

b

PI, protease inhibitor

c

CAC, coronary artery calcium

d

HAART, highly active antiretroviral therapy.