Abstract

BackgroundDyslipidemia is one of the most frequently implicated risk factors for development of atherosclerosis. This study evaluated the efficacy of amla (Emblica officinalis) extract (composed of polyphenols, triterpenoids, oils etc. as found in the fresh wild amla fruit) in patients with dyslipidemia.MethodsA total of 98 dyslipidemic patients were enrolled and divided into amla and placebo groups. Amla extract (500 mg) or a matching placebo capsule was administered twice daily for 12 weeks to the respective group of patients. The patients were followed up for 12 weeks and efficacy of study medication was assessed by analyzing lipid profile. Other parameters evaluated were apolipoprotein B (Apo B), apolipoprotein A1 (Apo A1), Coenzyme Q10 (CoQ10), high-sensitive C-reactive protein (hsCRP), fasting blood sugar (FBS), homocysteine and thyroid stimulating hormone (TSH).ResultsIn 12 weeks, the major lipids such as total cholesterol (TC) (p = 0.0003), triglyceride (TG) (p = 0.0003), low density lipoprotein cholesterol (LDL-C) (p = 0.0064) and very low density lipoprotein cholesterol (VLDL-C) (p = 0.0001) were significantly lower in amla group as compared to placebo group. Additionally, a 39% reduction in atherogenic index of the plasma (AIP) (p = 0.0177) was also noted in amla group. The ratio of Apo B to Apo A1 was reduced more (p = 0.0866) in the amla group as compared to the placebo. There was no significant change in CoQ10 level of amla (p = 0.2942) or placebo groups (p = 0.6744). Although there was a general trend of FBS reduction, the numbers of participants who may be classified as pre-diabetes and diabetes groups (FBS > 100 mg/dl) in the amla group were only 8. These results show that the amla extract used in the study is potentially a hypoglycaemic as well. However, this needs reconfirmation in a larger study.ConclusionsThe Amla extract has shown significant potential in reducing TC and TG levels as well as lipid ratios, AIP and apoB/apo A-I in dyslipidemic persons and thus has scope to treat general as well as diabetic dyslipidemia. A single agent to reduce cholesterol as well as TG is rare. Cholesterol reduction is achieved without concomitant reduction of Co Q10, in contrast to what is observed with statins.Trial registrationRegistered with Clinical Trials Registry- India at www.ctri.nic.in (Registration number: CTRI/2015/04/005682) on 8 April 2015 (retrospectively registered).

Highlights

  • Dyslipidemia is one of the most frequently implicated risk factors for development of atherosclerosis

  • Cholesterol reduction is achieved without concomitant reduction of Co Q10, in contrast to what is observed with statins

  • atherogenic index of the plasma (AIP) is associated with prediction of type 2 diabetes mellitus (T2DM)

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Summary

Introduction

Dyslipidemia is one of the most frequently implicated risk factors for development of atherosclerosis. Dyslipidemia is one of the major risk factors for development of atherosclerosis and other heart disorders [1] This indicates a high level of lipids in the blood, of which includes triglycerides (TGs) and total cholesterol (TC). It is apparent that for effective management of dyslipidemia, several of the individual parameters need to be controlled simultaneously This is amply demonstrated by the observation that people whose cholesterol has been brought to normal levels are not free from CVD risk. AIP is increased in people at higher risk for coronary heart disease and has recently been identified as a marker of plasma atherogenicity This simple ratio reflects the balance between atherogenic versus antiatherogenic lipids and is inversely correlated with LDL-C particle size. Almost all the studies reported in the meta-analysis reported positive associations between AIP and T2DM [4]

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