Title of article :
Age and sex modulate metabolic and cardiovascular risk markers of patients after 1 year of highly active antiretroviral therapy (HAART)
Author/Authors :
Judith Maria Leitner، نويسنده , , Heidemarie Pernerstorfer-Schoen، نويسنده , , Alina Weiss، نويسنده , , Karin Schindler، نويسنده , , Armin Rieger، نويسنده , , Bernd Jilma، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
9
From page :
177
To page :
185
Abstract :
Objective Primary aim: To evaluate the modulating effects of age and sex on changes in plasma lipid levels in the response to highly active antiretroviral therapy (HAART). Secondary aim: To study insulin, leptin, adiponectin, E-selectin and P-selectin levels and their relation to demographics. Design Comparative, longitudinal, open cohort-study. Setting Tertiary care center at a University Hospital. Methods Eighty-two consecutive HIV-seropositive patients of either sex were enrolled in the study. Subjects were between 19 and 60 years of age and naive to HAART. Patients were treated with nucleoside reverse transcriptase inhibitors (NRTIs) and protease inhibitor(s) (PIs) or reverse transcriptase inhibitors (RTIs) only. Subjects were evaluated at baseline and after 3, 6 and 12 months. Results Total cholesterol levels increased in all patients. The greatest increase was seen in patients of older age treated with PI. Male gender was another risk factor for higher cholesterol but also for higher triglyceride levels. Therapy with protease inhibitors and/or stavudine had a negative influence on plasma triglyceride levels. Selectins, adipokines and insulin were less influenced by HAART. Conclusion Based on the results of this study selection of therapy regimen according to the demographic risk factors sex and age can offer an easy strategy to help to minimize lipid elevations.
Keywords :
age , HIV , Adipocytokines , Selectins , sex , hyperlipidemia , atherosclerosis
Journal title :
Atherosclerosis
Serial Year :
2006
Journal title :
Atherosclerosis
Record number :
632041
Link To Document :
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