Association of APOC3 polymorphisms with both dyslipidemia and lipoatrophy in HAART-receiving patients

被引:21
作者
Bonnet, Eric [1 ,4 ,5 ]
Bernard, Jacques [1 ]
Fauvel, Josette [2 ,4 ,5 ]
Massip, Patrice [1 ]
Ruidavets, Jean-Bernard [3 ]
Perret, Bertrand [2 ,4 ,5 ]
机构
[1] Hop Purpan, CHU Toulouse, Dept Infect Dis, Serv Malad Infect, F-31059 Toulouse 9, France
[2] Hop Purpan, CHU Toulouse, Dept Biochem, F-31059 Toulouse, France
[3] INSERM, U558, F-31300 Toulouse, France
[4] Ctr Physiopathol Toulouse Purpan, INSERM, U563, F-31300 Toulouse, France
[5] Univ Toulouse 3, IFR30, F-31300 Toulouse, France
关键词
D O I
10.1089/aid.2007.0076
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The incidence and the magnitude of lipodystrophy and dyslipidemia in HIV-treated people reported in previous studies are very variable. Several predisposing factors have been identified, but there are few data on genetic factors. To search for a correlation between APOC3 polymorphisms and lipid disorders and lipodystrophy in HIV patients under d4T and protease inhibitors (PI)-containing HAART, we designed a monocenter, cross-sectional study in a University Hospital in Southern France during the period 2001-2004. Forty patients under HAART were included, with d4T for >= 2 years and PI for >= 1 year. We determined body mass composition by DXA, lipoprotein markers, and the -455/-482 apo C3 genotypes. Carriers of APOC3 variant alleles (-455 1/-482 1) displayed higher levels of triglycerides (3.72 vs. 2.57 mmol/liter), apo C3 (45.3 vs. 34.5 mg/liter), and apo E (130.2 vs. 66.5 mg/liter) and a lower fat mass (13.9 vs. 19.7%) than patients with nonvariant alleles (-455 0/- 482 0). APOC3 polymorphisms might be associated with both dyslipidemia and lipoatrophy in HAART-treated patients.
引用
收藏
页码:169 / 171
页数:3
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