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Differential Subcutaneous Adipose Tissue Gene Expression Patterns in a Randomized Clinical Trial of Efavirenz or Lopinavir-Ritonavir in Antiretroviral-Naive Patients

机译:依法韦仑或洛匹那韦-利托那韦在抗逆转录病毒初治患者中的随机临床试验中的差异皮下脂肪组织基因表达模式

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摘要

Gene expression studies of subcutaneous adipose tissue may help to better understand the mechanisms behind body fat changes in HIV-infected patients who initiate antiretroviral therapy (ART). Here, we evaluated early changes in adipose tissue gene expression and their relationship to fat changes in ART-naive HIV-infected patients randomly assigned to initiate therapy with emtricitabine/tenofovir plus efavirenz (EFV) or ritonavir-boosted lopinavir (LPV/r). Patients had abdominal subcutaneous adipose tissue biopsies at baseline and week 16 and dual-energy-X-ray absorptiometry at baseline and weeks 16 and 48. mRNA changes of 11 genes involved in adipogenesis, lipid and glucose metabolism, mitochondrial energy, and inflammation were assessed through reverse transcription-quantitative PCR (RT-qPCR). Additionally, correlations between gene expression changes and fat changes were evaluated. Fat increased preferentially in the trunk with EFV and in the limbs with LPV/r (P < 0.05). After 16 weeks of exposure to the drug regimen, transcripts of CEBP/A, ADIPOQ, GLUT4, LPL, and COXIV were significantly down-regulated in the EFV arm compared to the LPV/r arm (P < 0.05). Significant correlations were observed between LPL expression change and trunk fat change at week 16 in both arms and between CEBP/A or COXIV change and trunk fat change at the same time point only in the EFV arm and not in the LPV/r arm. When combined with emtricitabine/tenofovir as standard backbone therapy, EFV and LPV/r induced differential early expression of genes involved in adipogenesis and energy metabolism. Moreover, these mRNA expression changes correlated with trunk fat change in the EFV arm. (This was a substudy of a randomized clinical trial [LIPOTAR study] registered at under identifier .)
机译:皮下脂肪组织的基因表达研究可能有助于更好地了解发起抗逆转录病毒疗法(ART)的HIV感染患者体内脂肪变化的机制。在这里,我们评估了随机分配开始使用恩曲他滨/替诺福韦+依非韦韦联合依法韦仑(EFV)或利托那韦增强洛匹那韦(LPV / r)治疗的未感染ART的HIV感染患者中脂肪组织基因表达的早期变化及其与脂肪变化的关系。患者在基线和第16周进行腹部皮下脂肪组织活检,在基线以及第16和48周进行双能X线吸收法。评估了11个与脂肪形成,脂质和葡萄糖代谢,线粒体能量和炎症有关的基因的mRNA变化。通过逆转录定量PCR(RT-qPCR)。另外,评估了基因表达变化和脂肪变化之间的相关性。 EFV的躯干和LPV / r的四肢脂肪优先增加(P <0.05)。暴露于该药物方案16周后,与LPV / r组相比,EFV组的CEBP / A,ADIPOQ,GLUT4,LPL和COXIV的转录产物显着下调(P <0.05)。仅在EFV组而非LPV / r组中,观察到LPL表达变化与第16周的躯干脂肪变化之间存在显着相关性,并且CEBP / A或COXIV变化与躯干脂肪变化在同一时间点存在显着相关性。当与恩曲他滨/替诺福韦联合用作标准的骨干疗法时,EFV和LPV / r诱导脂肪形成和能量代谢相关基因的早期差异表达。此外,这些mRNA表达的变化与EFV组的躯干脂肪变化相关。 (这是在标识符下注册的随机临床试验[LIPOTAR研究]的子研究。)

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