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Xuezhikang Therapy Increases miR-33 Expression in Patients with Low HDL-C Levels

机译:血脂康疗法可提高低HDL-C水平患者的miR-33表达

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摘要

Background. MicroRNA-33a and -b (miR-33a/b) have been revealed to be posttranscriptional regulators of HDL metabolism. Xuezhikang (XZK) is a marked natural HDL-raising polypill. We aim to evaluate the effects of XZK on the expression of circulating miR-33a/b in patients with low plasma HDL-C levels. Methods. A total of 42 participating patients with low baseline levels of HDL cholesterol were assigned to receive an XZK capsule, 600 mg twice daily for 6 months. The expression of circulating miR-33a/b was detected at baseline and after XZK therapy measured with quantitative reverse-transcription (RT) polymerase chain reaction (PCR). Results. The mean (SD) HDL-C level after XZK treatment was 1.19 (0.13) mmol/L, representing an increase of 11.2% from baseline (P < 0.001). Q-PCR analysis of plasma miRNAs revealed an increase in relative miR-33a/b expression with XZK treatment. The miR-33a expression was raised from 0.81 to 1.73 (P = 0.012); miR-33b expression was increased from 1.2 to 2.75 (P < 0.001). The changes of miR-33a and miR-33b were inversely related to the posttreatment LDL-C levels (r = −0.37, P = 0.019; r = −0.33, P = 0.035, resp.). Conclusion. In patients with low HDL-C levels, XZK therapy raised plasma levels of miR-33a and miR-33b, which may inhibit cellular cholesterol export and limit the HDL-raising effect of XZK.
机译:背景。 MicroRNA-33a和-b(miR-33a / b)已被证明是HDL代谢的转录后调节剂。血脂康(XZKK)是一种明显的天然HDL升高息肉药。我们旨在评估XZK对低血浆HDL-C水平患者循环miR-​​33a / b表达的影响。方法。共有42名HDL胆固醇基线水平较低的参与患者被分配接受XZK胶囊,每天两次,每次600mg,共6个月。在基线和XZK治疗后,通过定量逆转录(RT)聚合酶链反应(PCR)测定循环miR-​​33a / b的表达。结果。 XZK治疗后HDL-C的平均(SD)水平为1.19(0.13)mmol / L,比基线增加11.2%(P <0.001)。血浆miRNA的Q-PCR分析显示,使用XZK处理后相对miR-33a / b表达增加。 miR-33a表达从0.81升高到1.73(P = 0.012); miR-33b表达从1.2增加到2.75(P <0.001)。 miR-33a和miR-33b的变化与治疗后LDL-C水平成反比(r = -0.37,P = 0.019; r = -0.33,P = 0.035,分别)。结论。在HDL-C水平低的患者中,XZK治疗可升高miR-33a和miR-33b的血浆水平,这可能抑制细胞胆固醇输出并限制XZK的HDL升高作用。

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