Amla
Summary
Amla is the fruit of Phyllanthus emblica. In nine small trials, 500–1,500 mg/day of fruit or extract modestly lowered LDL cholesterol, triglycerides and CRP (grade C), and one add-on trial lowered blood pressure. Most trials were short and small and used different products. Amla also reduced platelet aggregation.
Key facts
- LDL about 15 mg/dL lower than placebo across 9 RCTs (535 people), with high heterogeneity[1]
- As an add-on to medicines, 1,500 mg/day lowered systolic pressure 15.6% vs 6.3% with placebo over 8 weeks[5]
- 500 mg reduced platelet aggregation alone and with clopidogrel or aspirin in a 10-person crossover[7][8]
- 500–1,500 mg/day of fruit or extract for 2–12 weeks[1]
- Five RCTs pooled showed lower CRP, fasting glucose, LDL, total cholesterol and triglycerides and higher HDL[2]
- 5 graded human outcomes on this page
- October 13, 2026
How it works
ProposedAmla is rich in hydrolyzable tannins (such as emblicanins) and vitamin C. Trial authors propose antioxidant and anti-inflammatory effects on blood vessels and lipid metabolism; the mechanism in people is not established.[6][7]
What the human research says
Human trials only, one row per outcome. The form column shows what each trial actually tested. Grades follow our evidence-grading policy.
At a glance: strongest evidence per outcome
| Outcome | Grade | Effect | Strongest evidence | Rows |
|---|---|---|---|---|
| Cholesterol | Grade C | Improved | Meta-analysis of 9 trials · n = 535 · 2023 | 2 rows |
| Blood pressure | Grade C | Improved | RCT · n = 81 · 2020 | 1 row |
| Endothelial function | Grade D | Improved | RCT · n = 80 · 2013 | 2 rows |
Every graded row
| Outcome | Effect | Grade | Best evidence | PMID |
|---|---|---|---|---|
| LDL cholesterol, triglycerides and hsCRP | Improved | Grade C | Meta-analysis · n = 535 · 2023 Adults in 9 RCTs (healthy, dyslipidemia, diabetes and other groups) Form: Amla fruit or fruit extract · Dose: 500–1,500 mg/day · Duration: 14–84 days LDL fell 15.1 mg/dL, triglycerides 22.4 mg/dL and hsCRP 1.7 mg/L vs placebo. Heterogeneity was high and prediction intervals crossed zero for LDL and triglycerides. | 37296402 (opens PubMed)Source [1] |
| Lipids in dyslipidemia | Improved | Grade C | RCT · n = 98 · 2019 Adults with dyslipidemia (India, multicenter) Form: Amla fruit extract · Dose: 500 mg twice daily (1,000 mg/day) · Duration: 12 weeks Total cholesterol, triglycerides, LDL and VLDL were significantly lower than placebo; the atherogenic index fell 39%. CoQ10 did not change. | 30670010 (opens PubMed)Source [3] |
| Blood pressure as add-on to blood pressure medicines | Improved | Grade C | RCT · n = 81 · 2020 Adults with uncontrolled hypertension on standard drugs (Iran) Form: Amla (Emblica officinalis) · Dose: 500 mg three times daily (1,500 mg/day) · Duration: 8 weeks Systolic pressure fell 15.6% vs 6.3% with placebo and diastolic 12.3% vs 3.9% (both P<0.001). No side effects were reported. | 33082832 (opens PubMed)Source [5] |
| Endothelial function and oxidative stress in type 2 diabetes | Improved | Grade D | RCT · n = 80 · 2013 Adults with type 2 diabetes (India) Form: Aqueous amla extract standardized to hydrolyzable tannins · Dose: 250 mg or 500 mg twice daily · Duration: 12 weeks Both amla doses improved the reflection index (endothelial function) from baseline, similar to atorvastatin 10 mg; oxidative stress markers, hsCRP, lipids and HbA1c improved versus baseline and placebo. | 23935377 (opens PubMed)Source [6] |
| Blood fluidity, endothelial markers and lipids in healthy adults | Improved | Grade D | Crossover RCT · n = 15 · 2020 Healthy adults (Japan) Form: Amla extract · Dose: 500 mg/day · Duration: 18-week crossover study Blood fluidity improved, von Willebrand factor and an oxidative DNA marker fell, HDL rose and LDL fell. No adverse events or liver changes. | 31890983 (opens PubMed)Source [4] |
Forms
| Form | Elemental % | Absorption (human data) | GI tolerance | Studied for |
|---|---|---|---|---|
| Standardized amla fruit extract capsules | Varies[1] | No head-to-head human absorption data.[1] | Well tolerated in the cited trials; no liver, kidney or blood-count changes in a 12-week diabetes trial or an 18-week crossover.[4][6] | Lipid, blood pressure and endothelial trials (500–1,500 mg/day) |
| Dried amla fruit powder | Varies[1] | No head-to-head human absorption data.[1] | Included among the fruit preparations in the 9-trial meta-analysis; tolerance was not summarized in its abstract.[1] | Cardiovascular risk-factor trials |
Studied doses
Doses studied in human trials ranged from 500 mg/day to 1,500 mg/day of amla fruit or extract, for 14 days up to 12 weeks in most trials and 18 weeks in one crossover.[1][3][4][5]
Interactions
Published interactions only: each row cites a source. No row means none was found in our sources, not that a combination is safe.
Who should be careful
Talk to your pharmacist or clinician before starting a supplement, especially if you take prescription medicines.
How to read the label
- Label dose vs studied doseTrials used 500 mg once to three times daily of fruit or extract; extracts were standardized differently, so mg are not directly comparable between products.[1][3][5][6]
- StandardizationOne diabetes trial used an extract standardized to hydrolyzable tannins (emblicanin A and B, pedunculagin, punigluconin).[6]
Cost per studied dose, without the sales pitch
Compare any product you already have by the amount it delivers, not by capsule count or front-of-pack weight.
Cost per studied dose
Enter the price, servings and the amount per serving from your label.
Frequently asked questions
Does amla lower cholesterol?
Modestly in small trials. Pooled across 9 RCTs, LDL fell about 15 mg/dL and triglycerides about 22 mg/dL versus placebo, but results varied widely.[1]
Does amla lower blood pressure?
One 8-week trial in 81 people with uncontrolled hypertension found 1,500 mg/day added to medicines lowered systolic pressure 15.6% vs 6.3% with placebo.[5]
Does amla help blood sugar?
In a 12-week trial in type 2 diabetes, 250–500 mg twice daily improved HbA1c and lipids versus placebo and endothelial function from baseline; a 5-trial meta-analysis also found lower fasting glucose.[2][6]
Is amla safe with blood thinners?
Amla extract reduced platelet aggregation and lengthened bleeding time, including when combined with clopidogrel or aspirin, in a 10-person study.[7]
How much amla was used in studies?
Trials used 500–1,500 mg/day of fruit or extract, usually for 2–12 weeks.[1]
Sources
- [1]Clinical effects of Emblica officinalis fruit consumption on cardiovascular disease risk factors: a systematic review and meta-analysis.. BMC Complement Med Ther, 2023. meta-analysis
- [2]The impact of Emblica Officinalis (Amla) on lipid profile, glucose, and C-reactive protein: A systematic review and meta-analysis of randomized controlled trials.. Diabetes Metab Syndr, 2023. meta-analysis
- [3]A randomized, double blind, placebo controlled, multicenter clinical trial to assess the efficacy and safety of Emblica officinalis extract in patients with dyslipidemia.. BMC Complement Altern Med, 2019. RCT
- [4]Clinical evaluation of Emblica Officinalis Gatertn (Amla) in healthy human subjects: Health benefits and safety results from a randomized, double-blind, crossover placebo-controlled study.. Contemp Clin Trials Commun, 2020. crossover-RCT
- [5]A Randomized, Triple-Blind, Placebo-Controlled, Add-On Clinical Trial to Evaluate the Efficacy of Emblica officinalis in Uncontrolled Hypertension.. Evid Based Complement Alternat Med, 2020. RCT
- [6]Effects of Phyllanthus emblica extract on endothelial dysfunction and biomarkers of oxidative stress in patients with type 2 diabetes mellitus: a randomized, double-blind, controlled study.. Diabetes Metab Syndr Obes, 2013. RCT
- [7]Study of pharmacodynamic interaction of Phyllanthus emblica extract with clopidogrel and ecosprin in patients with type II diabetes mellitus.. Phytomedicine, 2014. crossover-RCT
- [8]Supplementation of a standardized extract from Phyllanthus emblica improves cardiovascular risk factors and platelet aggregation in overweight/class-1 obese adults.. J Med Food, 2015. open-label
What changed
- First draft. Every PMID checked against NCBI E-utilities esummary (title and year taken from the record) and abstracts read for the cited rows. Abstracts read for all 8 PMIDs. Page set indexable.
