Jagalurappa Kiran, Vrushabaiah Giriraja Kanakapura, Govindaraj Suman
Pristine Hospital and Research Centre Pvt Ltd, Bengaluru, India.
Rajalakshmi Hospital and Research Centre, Bengaluru, India.
Curr Ther Res Clin Exp. 2025 May 17;103:100800. doi: 10.1016/j.curtheres.2025.100800. eCollection 2025.
Dyslipidemia, marked by abnormal lipid levels, significantly increases the risk of cardiovascular diseases. Effective management of these lipid abnormalities is essential for reducing cardiovascular risk. , known as amla in Ayurveda, is traditionally considered the best fruit due to its numerous health benefits.
To evaluate the efficacy and tolerability of amla extract on participants with abnormal lipid levels and compare with the effect of physical activity in reducing atherogenic factors.
Forty-five inactive participants having abnormal lipid levels were selected and instructed to initiate lifestyle changes, including a healthy diet and aerobic exercise for 14 days. Thirty-nine participants who met the study criteria even after exercise were allocated a 500 mg capsule of amla extract (Tri-Low®) twice daily for 90 days. The effect of amla extract on lipid parameters, atherogenic index of plasma (AIP), apolipoprotein (Apo) B/Apo A ratio, high-sensitivity C-reactive protein, coenzyme Q10, and hydroxy methylglutaryl coenzyme A reductase levels was studied and compared with the effect of physical activity or exercise on these parameters. Laboratory parameters, global tolerability, and treatment-emergent adverse events were evaluated for the assessment of safety profile of amla extract.
Amla extract over a period of 90 days significantly reduced triglyceride ( = 0.007), total cholesterol ( < 0.001), LDL ( = 0.006), VLDL ( = 0.014), and AIP ( < 0.001) but reported no significant effect on HDL ( = 0.967) and fasting blood sugar ( = 1.00). Varying the intensity of exercise from low to moderate and high had no significant effect on triglyceride ( = 0.516), total cholesterol ( = 0.676), LDL ( = 0.511), VLDL ( = 0.454), or AIP ( = 0.472). However, LDL exhibited a significant reduction with amla extract, combined with exercise ( < 0.001). Apolipoprotein B/Apo A1 ratio exhibited a trend toward significance ( = 0.061). Weight and reductions were statistically significant with amla extract and exercise, after 45 days ( < 0.001) and 90 days ( = 0.002). Hydroxy methylglutaryl coenzyme A, Apo B, and coenzyme Q10 exhibited no significant changes. Overall, it was evident that the significant changes in lipid parameters are attributable to amla extract rather than physical activity alone. All other factors are not affected by exercise intensity, and the significant changes observed are purely due to the effect of amla extract.
Exercise alone is often insufficient for optimal cardiovascular health. The supplementation of amla extract (Tri-Low®) from this study reported significant potential in improving lipid profiles and other atherogenic factors, thereby providing a comprehensive strategy for cardiovascular health management.
Clinical Trial Registry - India (CTRI/2017/02/007829).
血脂异常以脂质水平异常为特征,显著增加心血管疾病风险。有效管理这些脂质异常对于降低心血管风险至关重要。印度醋栗在阿育吠陀医学中被称为“amla”,由于其诸多健康益处,传统上被认为是最佳水果。
评估印度醋栗提取物对脂质水平异常参与者的疗效和耐受性,并与体育活动在降低致动脉粥样硬化因素方面的效果进行比较。
选取45名脂质水平异常的不活跃参与者,指导他们开始生活方式改变,包括健康饮食和有氧运动,为期14天。39名即使在运动后仍符合研究标准的参与者被分配每天服用两次500毫克印度醋栗提取物胶囊(Tri-Low®),持续90天。研究了印度醋栗提取物对脂质参数、血浆致动脉粥样硬化指数(AIP)、载脂蛋白(Apo)B/Apo A比值、高敏C反应蛋白、辅酶Q10和羟甲基戊二酰辅酶A还原酶水平的影响,并与体育活动或运动对这些参数的影响进行比较。评估实验室参数以及总体耐受性和治疗中出现的不良事件,以评估印度醋栗提取物的安全性。
在90天的时间里,印度醋栗提取物显著降低了甘油三酯(P = 0.007)、总胆固醇(P < 0.001)、低密度脂蛋白(P = 0.006)、极低密度脂蛋白(P = 0.014)和AIP(P < 0.001),但对高密度脂蛋白(P = 0.967)和空腹血糖(P = 1.00)无显著影响。将运动强度从低变到中再到高,对甘油三酯(P = 0.516)、总胆固醇(P = 0.676)、低密度脂蛋白(P = 0.511)、极低密度脂蛋白(P = 0.454)或AIP(P = 0.472)均无显著影响。然而,印度醋栗提取物与运动相结合时,低密度脂蛋白有显著降低(P < 0.001)。载脂蛋白B/Apo A1比值呈现出显著趋势(P = 0.061)。45天后(P < 0.001)和90天后(P = 0.002),印度醋栗提取物和运动使体重减轻具有统计学意义。羟甲基戊二酰辅酶A、Apo B和辅酶Q10无显著变化。总体而言,脂质参数的显著变化显然归因于印度醋栗提取物,而非单纯的体育活动。所有其他因素不受运动强度影响,观察到的显著变化纯粹是由于印度醋栗提取物的作用。
仅靠运动往往不足以实现最佳心血管健康。本研究中补充印度醋栗提取物(Tri-Low®)在改善脂质谱和其他致动脉粥样硬化因素方面显示出显著潜力,从而为心血管健康管理提供了一种全面策略。
印度临床试验注册中心(CTRI/2017/02/007829)