Antiretroviral treatment-induced dyslipidemia in HIV-infected patients is influenced by the <it>APOC3</it>-related rs10892151 polymorphism

<p>Abstract</p> <p>Background</p> <p>The recently observed association between the APOC3-related rs10892151 polymorphism and serum triglyceride levels has prompted us the possibility to explore whether this genetic variant may play a major role in human immunodeficiency...

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Main Authors: Fernández-Sender Laura (Author), Rodríguez-Gallego Esther (Author), Beltrán-Debón Raúl (Author), Rull Anna (Author), Pardo-Reche Pedro (Author), Alonso-Villaverde Carlos (Author), Aragonès Gerard (Author), Camps Jordi (Author), Joven Jorge (Author)
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Published: BMC, 2011-09-01T00:00:00Z.
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001 doaj_a2dccd42d69b460a836b6965e4ac323b
042 |a dc 
100 1 0 |a Fernández-Sender Laura  |e author 
700 1 0 |a Rodríguez-Gallego Esther  |e author 
700 1 0 |a Beltrán-Debón Raúl  |e author 
700 1 0 |a Rull Anna  |e author 
700 1 0 |a Pardo-Reche Pedro  |e author 
700 1 0 |a Alonso-Villaverde Carlos  |e author 
700 1 0 |a Aragonès Gerard  |e author 
700 1 0 |a Camps Jordi  |e author 
700 1 0 |a Joven Jorge  |e author 
245 0 0 |a Antiretroviral treatment-induced dyslipidemia in HIV-infected patients is influenced by the <it>APOC3</it>-related rs10892151 polymorphism 
260 |b BMC,   |c 2011-09-01T00:00:00Z. 
500 |a 10.1186/1471-2350-12-120 
500 |a 1471-2350 
520 |a <p>Abstract</p> <p>Background</p> <p>The recently observed association between the APOC3-related rs10892151 polymorphism and serum triglyceride levels has prompted us the possibility to explore whether this genetic variant may play a major role in human immunodeficiency virus (HIV)/antiretroviral therapy-induced dyslipidemia.</p> <p>Methods</p> <p>We determined the rs10892151 genotype distribution and serum apolipoprotein (apo) C-III concentration in a group of HIV-infected patients (<it>n </it>= 208) and in a group of age and sex-matched healthy volunteers (<it>n </it>= 200). Circulating lipid and lipoprotein levels were followed for 12 months after antiretroviral treatment initiation in the HIV-infected group.</p> <p>Results</p> <p>There were no significant variations in the frequency of the A allele between the healthy and HIV-infected groups (7.5 vs. 8.6%, respectively; p = 0.7); additionally, the A allele was not related to serum apo C-III concentration. However, among patients receiving protease inhibitor (PI) treatment, carriers of the A allele had significantly increased serum triglyceride (5.76 ± 2.54 mmol/L) and total cholesterol (6.63 ± 2.85 mmol/L) concentrations together with depressed levels of HDL-cholesterol (0.75 ± 0.3 mmol/L) when compared with patients not carrying the allele (2.43 ± 1.32, 5.2 ± 2.17 and 1.24 ± 0.4 mmol/L, respectively) at the end of the study. This effect was only evident for HDL-cholesterol concentration when patients were treated with non-nucleoside reverse transcriptase inhibitors (1.05 ± 0.4 vs. 1.28 ± 0.4 mmol/L).</p> <p>Conclusions</p> <p>The A allelic variant of the rs10892151 polymorphism is not associated with serum apo C-III concentration, but predisposes HIV-infected patients to less favorable lipid profile, particularly in those patients treated with PIs.</p> 
546 |a EN 
690 |a Internal medicine 
690 |a RC31-1245 
690 |a Genetics 
690 |a QH426-470 
655 7 |a article  |2 local 
786 0 |n BMC Medical Genetics, Vol 12, Iss 1, p 120 (2011) 
787 0 |n http://www.biomedcentral.com/1471-2350/12/120 
787 0 |n https://doaj.org/toc/1471-2350 
856 4 1 |u https://doaj.org/article/a2dccd42d69b460a836b6965e4ac323b  |z Connect to this object online.