European mitochondrial DNA haplogroups and metabolic changes during antiretroviral therapy in AIDS Clinical Trials Group Study A5142

被引:41
作者
Hulgan, Todd [1 ]
Haubrich, Richard [2 ]
Riddler, Sharon A. [3 ]
Tebas, Pablo [4 ]
Ritchie, Marylyn D. [1 ]
McComsey, Grace A. [5 ]
Haas, David W. [1 ]
Canter, Jeffrey A. [1 ]
机构
[1] Vanderbilt Univ, Nashville, TN USA
[2] Univ Calif San Diego, San Diego, CA 92103 USA
[3] Univ Pittsburgh, Pittsburgh, PA USA
[4] Univ Penn, Philadelphia, PA 19104 USA
[5] Case Western Reserve Univ, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
antiretroviral therapy; DNA; dyslipidemias; highly active; HIV-associated; lipodystrophy syndrome; metabolic diseases; mitochondrial; mitochondrial genome; TYPE-2; DIABETES-MELLITUS; INSULIN-RESISTANCE; MYOCARDIAL-INFARCTION; PERIPHERAL NEUROPATHY; JAPANESE POPULATION; GENE POLYMORPHISMS; SPARING REGIMENS; LIPID LEVELS; ASSOCIATION; LIPODYSTROPHY;
D O I
10.1097/QAD.0b013e32833f9d02
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Mitochondrial DNA (mtDNA) influences metabolic diseases and perhaps antiretroviral therapy (ART) complications. We explored associations between European mtDNA haplogroups and metabolic changes among A5142 participants. Methods: Seven hundred and fifty-seven ART-naive patients were randomized to one of three class-sparing ART regimens including efavirenz and/or lopinavir/ritonavir with or without nucleoside reverse transcriptase inhibitors (NRTIs). Nonrandomized NRTIs included stavudine, tenofovir, or zidovudine, each with lamivudine. Fasting lipid profiles and whole-body dual-energy X-ray absorptiometry (DEXA) were performed. Nine European mtDNA haplogroups were determined for 231 self-identified non-Hispanic white individuals. Metabolic changes from baseline to 96 weeks were analyzed by haplogroup. Results: Median age was 39 years, 9% were women, and 37, 32, and 30 were randomized to NRTI-containing regimens with either efavirenz or lopinavir/ritonavir, and an NRTI-sparing regimen, respectively. Among NRTI-containing regimens, 51% included zidovudine, 28% tenofovir, and 21% stavudine. Compared with other haplogroups, mtDNA haplogroup I (N - 10) had higher baseline non-HDL cholesterol [160 mg/dl (interquartile range 137-171) vs. 120 mg/dl (104-136); P = 0.005], a decrease in non-HDL cholesterol over 96 weeks [-14% (-20 to 6) vs. +25% (8 to 51); P < 0.001], tended to have more baseline extremity fat, and had more extremity fat loss by DEXA [-13% (-13 to 12) vs. +9%(-13 to 26); P = 0.08] and lipoatrophy (50 vs. 20%; P = 0.04). Haplogroup W (N 5; all randomized to NRTI-sparing regimens) had the greatest increase in extremity fat [+35.5% (26.8 to 54.9); P = 0.02]. Conclusions: Lipids and extremity fat were associated with European mtDNA haplogroups in this HIV-infected population. These preliminary results suggest that mitochondrial genomics may influence metabolic parameters before and during ART. (C) 2011 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:37 / 47
页数:11
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