A double-blind clinical study of Rokkaku Reishi essence in women

Y. Yonei, Yoko Takahashi, H. Takahashi, Miwako Watanabe, T. Mochizuki, H. Bando
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引用次数: 6

Abstract

A double-blind, randomized and placebo controlled study was carried out to examine the anti-aging efficacy and safety of Rokkaku Reishi in 22 overweight Japanese women (46.5±7.9 years old, BMI 26.8±2.7) consisting of 11 in the Analyte Group and 11 in the Placebo Group. Total cholesterol, LDL cholesterol and neutral fat values in the blood, which had been checked as background factors of the subjects, were mismatched, significantly higher respectively in the Analyte Group than in the Placebo Group. Evaluation of efficacy for lipid profiles was inevitable. In the Analyte Group the values of Hematocrit (-3.5%) and γ-GTP (-15.0%) significantly declined while HbAlc (2.3%) and K (5.4%) significantly increased after supplementation. The rate of increase of HbAlc in the Analyte Group was significantly higher than that in the Placebo Group. NK-cell activity showed no difference pre- and post-supplementation in either group. Oxidative-stress markers showed no significant difference pre- and post-supplementation for either group. A Common questionnaire on physical symptoms showed that the categories “Coughing and sputum” and “Grey hair” significantly declined after supplementation in the Analyte Group while no difference was found in the Placebo Group. For skin age scores measured using a Roboskinanalyzer, the scores for the categories “Noticeable pores”, “Large noticeable pores” and “Dusky noticeable pores” were significantly lower in the Analyte Group compared to the Placebo Group. A significant correlation was found between 8-OHdG in terms of its level, creatinine-corrected value and generation rate, and the number of “Noticeable pores”. No adverse reaction was found during the study. These results suggest that the four weeks supplementation of Rokkaku Reishi showed favorable effects on skin condition.
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六甲灵芝精对女性的双盲临床研究
本研究采用双盲、随机、安慰剂对照的方法,对22名体重超重的日本女性(46.5±7.9岁,BMI 26.8±2.7),其中Analyte组11名,placebo组11名,进行了六加灵芝抗衰老疗效和安全性的研究。作为受试者背景因素的血液中总胆固醇、低密度脂蛋白胆固醇和中性脂肪值不匹配,分析物组显著高于安慰剂组。评估脂质谱的疗效是不可避免的。在Analyte组中,添加后红细胞压积(-3.5%)和γ-GTP(-15.0%)显著降低,HbAlc(2.3%)和K(5.4%)显著升高。分析物组的HbAlc升高率明显高于安慰剂组。两组的nk细胞活性均无差异。两组的氧化应激指标在补充前后均无显著差异。一份常见的身体症状问卷显示,在补充后,分析物组的“咳嗽、痰”和“白发”类别明显下降,而安慰剂组无差异。对于使用Roboskinanalyzer测量的皮肤年龄得分,与安慰剂组相比,Analyte组的“明显毛孔”,“明显毛孔大”和“暗沉明显毛孔”类别得分明显较低。8-OHdG在其水平、肌酐校正值和生成率与“明显毛孔”数量之间存在显著相关性。研究过程中未发现不良反应。这些结果表明,补充四周的六甲灵芝对皮肤状况有良好的影响。
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