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Alpha-linolenic acid (C18:3 n-3)

ALA (Alpha-Linolenic Acid)

Research reviewed: Up until 03/2026

ALA (Alpha-Linolenic Acid) (Alpha-linolenic acid (C18:3 n-3)) is a dietary supplement with 22 published peer-reviewed studies involving 102,806 participants, researched for Cardiovascular Risk Reduction, Systematic reviews, Clinical trials.

22
Studies
102,806
Participants
2001–2026
Research Span

Evidence at a Glance

Strength is scored by study design, sample size, study type, and outcomes

Overall: Strong Evidence

Cardiovascular Risk Reduction

Strong
8 studies 3 of 8 positive 100,136 participants 2 human

Systematic reviews

Weak
5 studies 0 of 5 positive 2,536 participants 0 human

Clinical trials

Moderate
9 studies 0 of 9 positive 134 participants

Research Visualised

Visual breakdown of the clinical data.

Study Quality Breakdown

What types of studies were conducted

11/22
Randomised
11/22
Double-Blind
10/22
Placebo-Controlled

Participants Per Study

Larger samples = more reliable results

Study 1 (2012)
100,000
Study 2 (2001)
0
Study 3 (2018)
9
Study 4 (2018)
82
Study 5 (2005)
0
Study 6 (2023)
0
Study 7 (2007)
45
Study 8 (2006)
0

Research Timeline

When the studies were published

1
2001
1
2005
1
2006
1
2007
1
2012
2
2018
2
2022
7
2023
2
2024
3
2025
1
2026

All Studies

Detailed breakdown of each trial. Click to expand.

Cardiovascular Risk Reduction

1

To assess the association between ALA intake or biomarker status and cardiovascular disease risk.

2012 100,000 participants Various Dietary and supplemental ALA (0.5–3 g/day)
Review/Other Positive

Study Type

Systematic review and meta-analysis

Purpose

To assess the association between ALA intake or biomarker status and cardiovascular disease risk.

Dose

Dietary and supplemental ALA (0.5–3 g/day)

Participants

Pooled from multiple prospective cohorts (>100,000 participants)

Duration

Various

Results

Higher ALA intake or circulating levels associated with modest but significant reduction in CVD risk (RR ~0.90 per increment). Benefits more apparent for cardiovascular mortality than non-fatal events.

How They Measured It

Pooled relative risk for CVD outcomes from cohort studies and RCTs

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2

To review ALA mechanisms of cardiovascular action and clinical evidence beyond its role as EPA/DHA precursor.

2001 ? participants Various Various dietary sources and supplements (1–3 g/day)
Review/Other Mixed

Study Type

Review — cardiovascular mechanisms and clinical data

Purpose

To review ALA mechanisms of cardiovascular action and clinical evidence beyond its role as EPA/DHA precursor.

Dose

Various dietary sources and supplements (1–3 g/day)

Participants

Multiple studies reviewed

Duration

Various

Results

ALA exerts cardiovascular effects via anti-inflammatory, antioxidant, and antiarrhythmic mechanisms partly independent of EPA/DHA conversion. Dietary ALA is associated with lower CVD risk in large epidemiological studies.

How They Measured It

Narrative review of mechanistic and clinical studies

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3

To assess the dose-response relationship between dietary ALA intake and coronary heart disease risk.

2018 9 participants 4–20 years follow-up Increasing dietary ALA intake (g/day increments)
Review/Other Mixed

Study Type

Systematic review of cohort studies

Purpose

To assess the dose-response relationship between dietary ALA intake and coronary heart disease risk.

Dose

Increasing dietary ALA intake (g/day increments)

Participants

9 cohort studies (~250,000 participants)

Duration

4–20 years follow-up

Results

Each additional 1 g/day dietary ALA was associated with 10% lower CHD death risk. Greatest benefit between 0.5 and 2 g/day. Results consistent across populations.

How They Measured It

Dose-response meta-analysis from cohort studies

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4

To evaluate ALA supplementation on 24-hour ambulatory blood pressure in patients with high-normal or stage I hypertension.

2018 82 participants 12 weeks 3 g/day ALA (flaxseed-derived)
Human Study RCT Double-Blind Placebo Positive

Study Type

Randomised, double-blind, placebo-controlled

Purpose

To evaluate ALA supplementation on 24-hour ambulatory blood pressure in patients with high-normal or stage I hypertension.

Dose

3 g/day ALA (flaxseed-derived)

Participants

82 subjects with high-normal or stage I hypertension

Duration

12 weeks

Results

ALA supplementation significantly reduced 24-hour mean SBP (−3.5 mmHg, p=0.012) and DBP (−2.1 mmHg, p=0.024) vs placebo. Blood pressure effects most pronounced during daytime measurements.

How They Measured It

24-hour ambulatory SBP and DBP, heart rate

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5

To review the effect of ALA supplementation on cardiovascular risk markers in clinical trials.

2005 ? participants Various Various (1–10 g/day ALA)
Review/Other Mixed

Study Type

Systematic review

Purpose

To review the effect of ALA supplementation on cardiovascular risk markers in clinical trials.

Dose

Various (1–10 g/day ALA)

Participants

Multiple clinical trials reviewed

Duration

Various

Results

ALA may reduce fibrinogen concentrations and fasting plasma glucose. Effects on TC, TG, and LDL-C were modest and inconsistent. Blood pressure reductions observed in some but not all studies. Larger trials needed.

How They Measured It

Synthesis of fibrinogen, blood pressure, TG, TC, glucose from controlled trials

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6

To evaluate ALA impact on cardiovascular disease and cognition given its distinct metabolic role from EPA/DHA.

2023 ? participants Various ALA from plant sources and supplements
Review/Other Mixed

Study Type

Review

Purpose

To evaluate ALA impact on cardiovascular disease and cognition given its distinct metabolic role from EPA/DHA.

Dose

ALA from plant sources and supplements

Participants

Multiple studies reviewed

Duration

Various

Results

ALA has modest anti-inflammatory and antioxidant properties independent of EPA/DHA conversion. ALA provides a plant-based option with clinically meaningful but smaller effects than direct EPA/DHA supplementation.

How They Measured It

Synthesis of epidemiological, mechanistic, and clinical trial data

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7

To assess flaxseed oil (ALA-rich) vs safflower oil on cardiovascular risk markers in postmenopausal women.

2007 45 participants 4 weeks per arm 30 mL/day flaxseed oil (~18 g ALA)
Human Study RCT Double-Blind Positive

Study Type

Randomised, double-blind, crossover trial

Purpose

To assess flaxseed oil (ALA-rich) vs safflower oil on cardiovascular risk markers in postmenopausal women.

Dose

30 mL/day flaxseed oil (~18 g ALA)

Participants

45 postmenopausal women

Duration

4 weeks per arm

Results

Flaxseed oil (ALA) significantly reduced oxidised LDL and LDL particle number vs safflower oil. TC and LDL-C were modestly reduced. ALA-rich oils may offer cardioprotection via antioxidant pathways.

How They Measured It

Serum TC, LDL-C, HDL-C, TG, oxidised LDL, CRP

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8

To compare clinical cardiovascular evidence for plant-based ALA vs marine-derived EPA/DHA.

2006 ? participants Various ALA 2–3 g/day vs EPA/DHA 1–4 g/day
Review/Other Mixed

Study Type

Review — ALA, EPA, DHA and cardiovascular health

Purpose

To compare clinical cardiovascular evidence for plant-based ALA vs marine-derived EPA/DHA.

Dose

ALA 2–3 g/day vs EPA/DHA 1–4 g/day

Participants

Multiple studies reviewed

Duration

Various

Results

ALA conversion to EPA and DHA is limited (<5–10%). Despite this, ALA exerts cardiovascular benefits particularly on blood pressure, antioxidant status, and arterial function. ALA provides a viable plant-based option with smaller but clinically meaningful effects vs direct EPA/DHA.

How They Measured It

Narrative review of RCTs, meta-analyses, and guideline recommendations

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Systematic reviews

1

To investigate the effects of ALA (Alpha-Linolenic Acid) in effect of alpha-linolenic acid supplementation on cardiovascular disease risk profile in individuals with obesity or overweight: a systematic review a

2023 1183 participants 12 weeks 0.38 mg
Review/Other Mixed

Study Type

Systematic review and meta-analysis

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in effect of alpha-linolenic acid supplementation on cardiovascular disease risk profile in individuals with obesity or overweight: a systematic review a

Dose

0.38 mg

Participants

1183 participants

Duration

12 weeks

Results

interleukin-6, diastolic blood pressure, total cholesterol, or high-density lipoprotein cholesterol (all P ≥ 0.05). Subgroup analysis revealed that ALA supplementation at a dose of ≥3 g/d from flaxseed and flaxseed oil had a more prominent effect on improving CVD risk profiles, particularly where the intervention duration was ≥12 wk and where the baseline CVD profile was poor.

How They Measured It

See study for outcome measures

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2

To investigate the effects of ALA (Alpha-Linolenic Acid) in effects of supplementation with vegetable sources of alpha-linolenic acid (ala) on inflammatory markers and lipid profile in individuals with chronic

2022 ? participants Duration not specified ALA (Alpha-Linolenic Acid) (dose not specified)
Review/Other Mixed

Study Type

Systematic review and meta-analysis

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in effects of supplementation with vegetable sources of alpha-linolenic acid (ala) on inflammatory markers and lipid profile in individuals with chronic

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

bidity and mortality in chronic kidney disease (CKD). Alpha-linolenic acid (ALA), an essential fatty acid mainly found in vegetable sources, has been associated with anti-inflammatory effects and improving lipid profile. This systematic review and meta-analysis investigate the effects of supplementation with vegetable sources of ALA on inflammatory marker and lipid profile in individuals with CKD.

How They Measured It

See study for outcome measures

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3

To investigate the effects of ALA (Alpha-Linolenic Acid) in association of polyunsaturated fatty acid intake on inflammatory gene expression and multiple sclerosis: a systematic review and meta-analysis.

2022 1353 participants 144 weeks ALA (Alpha-Linolenic Acid) (dose not specified)
Review/Other Mixed

Study Type

Systematic review and meta-analysis

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in association of polyunsaturated fatty acid intake on inflammatory gene expression and multiple sclerosis: a systematic review and meta-analysis.

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

1353 participants

Duration

144 weeks

Results

(p > 0.05). In this meta-analysis of cohort studies, blood omega-3 FA concentrations were inversely related to inflammatory gene expression (IGE) and EDSS score, which indicates that they may hold great potential markers for the diagnosis, prognosis, and management of MS. However, further clinical trials are required to confirm the potential effects of the omega-3 FAs on MS disease management.

How They Measured It

See study for outcome measures

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4

To investigate the effects of ALA (Alpha-Linolenic Acid) in can omega-3 fatty acids serve as a preventive strategy for age-related macular degeneration? a systematic review and meta-analysis.

2026 ? participants Duration not specified ALA (Alpha-Linolenic Acid) (dose not specified)
Review/Other Mixed

Study Type

Systematic review and meta-analysis

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in can omega-3 fatty acids serve as a preventive strategy for age-related macular degeneration? a systematic review and meta-analysis.

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

anti-VEGF) therapies are available for neovascular AMD (nAMD), effective preventive strategies remain limited. Long-chain omega-3 polyunsaturated fatty acids (ω-3 PUFAs), particularly eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), have biological plausibility for retinal protection through structural roles in photoreceptor membranes and anti-inflammatory lipid mediator pathways.

How They Measured It

See study for outcome measures

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5

To investigate the effects of ALA (Alpha-Linolenic Acid) in the effect of plant-derived low-ratio linoleic acid/α-linolenic acid on markers of glucose controls: a systematic review and meta-analysis.

2023 ? participants Duration not specified ALA (Alpha-Linolenic Acid) (dose not specified)
Review/Other Mixed

Study Type

Systematic review and meta-analysis

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in the effect of plant-derived low-ratio linoleic acid/α-linolenic acid on markers of glucose controls: a systematic review and meta-analysis.

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

rding to the Begg and Egger tests. Furthermore, the conducted sensitivity analyses indicated stability, as the effects of the low-ratio LA/ALA diet on various glycemic and related metrics remained unchanged even after removing individual studies. Overall, based on the available studies, it can be concluded that the low-ratio LA/ALA diet has limited impact on blood glucose-related biomarker levels.

How They Measured It

See study for outcome measures

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Clinical trials

1

To investigate the effects of ALA (Alpha-Linolenic Acid) in the effects of α-linolenic acid intake on skin and blood vessel health and subjective fatigue in middle-aged japanese females: a randomized, double-bl

2025 ? participants Duration not specified ALA (Alpha-Linolenic Acid) (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in the effects of α-linolenic acid intake on skin and blood vessel health and subjective fatigue in middle-aged japanese females: a randomized, double-bl

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

α-Linolenic acid (ALA) has antioxidant and anti-inflammatory effects. Previous studies have shown its effects on skin, blood vessels, and subjective fatigue; however, most were conducted in populations with low n-3 fatty acid intake.

How They Measured It

See study for outcome measures

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2

To investigate the effects of ALA (Alpha-Linolenic Acid) in red blood cell polyunsaturated fatty acids and mortality following breast cancer.

2024 ? participants Duration not specified ALA (Alpha-Linolenic Acid) (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in red blood cell polyunsaturated fatty acids and mortality following breast cancer.

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

Intake of polyunsaturated fatty acids (PUFA) may affect mortality following breast cancer; however, epidemiological studies have relied on the self-reported assessment of PUFA intake. Herein, we examined the associations between red blood cell (RBC) PUFAs and mortality.

How They Measured It

See study for outcome measures

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3

To investigate the effects of ALA (Alpha-Linolenic Acid) in the effects of concurrent alpha-linolenic acid, l-carnitine supplementation on clinical symptoms, mental health, and quality of life in women with mig

2025 ? participants Duration not specified ALA (Alpha-Linolenic Acid) (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in the effects of concurrent alpha-linolenic acid, l-carnitine supplementation on clinical symptoms, mental health, and quality of life in women with mig

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

Migraine, as a widespread neurological condition, substantially impacts quality of life, particularly among women. Therefore, this study aimed to explore the potential effects of alpha-linolenic acid (ALA) and L-carnitine co-supplementation on migraine symptoms, mental health, and life quality in women with migraine.

How They Measured It

See study for outcome measures

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4

To investigate the effects of ALA (Alpha-Linolenic Acid) in dietary n-3 alpha-linolenic and n-6 linoleic acids modestly lower serum lipoprotein(a) concentration but differentially influence other atherogenic li

2024 ? participants Duration not specified 174550 g
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in dietary n-3 alpha-linolenic and n-6 linoleic acids modestly lower serum lipoprotein(a) concentration but differentially influence other atherogenic li

Dose

174550 g

Participants

Participants not specified

Duration

Duration not specified

Results

5 %. Linoleic acid may increase Lp(a) concentration through its endogenous conversion to arachidonic acid, a process regulated by the fatty acid desaturase (FADS) gene cluster. We aimed to compare the Lp(a) and other lipoprotein trait-modulating effects of dietary alpha-linolenic (ALA) and linoleic acids (LA). Additionally, we examined whether FADS1 rs174550 genotype modifies Lp(a) responses.

How They Measured It

See study for outcome measures

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5

To investigate the effects of ALA (Alpha-Linolenic Acid) in nut consumption, linoleic and α-linolenic acid intakes, and genetics: how fatty acid desaturase 1 impacts plasma fatty acids and type 2 diabetes risk

2025 ? participants Duration not specified 1 g
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in nut consumption, linoleic and α-linolenic acid intakes, and genetics: how fatty acid desaturase 1 impacts plasma fatty acids and type 2 diabetes risk

Dose

1 g

Participants

Participants not specified

Duration

Duration not specified

Results

diabetes. However, genetic variants in the fatty acid desaturase 1 gene (FADS1) may influence individual responses to plant-based fats. We explored whether FADS1 variants influence the relationships of LA and α-linolenic acid (ALA) intakes and nut consumption with plasma phospholipid fatty acid profiles and type 2 diabetes risk in a large-scale cohort study and a randomized controlled trial.

How They Measured It

See study for outcome measures

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6

To investigate the effects of ALA (Alpha-Linolenic Acid) in changes in polyunsaturated fatty acids during treatment of malnourished children may be insufficient to reach required essential fatty acid levels - a

2023 ? participants Duration not specified ALA (Alpha-Linolenic Acid) (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in changes in polyunsaturated fatty acids during treatment of malnourished children may be insufficient to reach required essential fatty acid levels - a

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

Severe acute malnutrition (SAM) is a global concern. Studies on the impact of ready-to-use therapeutic foods (RUTFs) on polyunsaturated fatty acids (PUFA) are almost non-existent. The aim was to investigate the change in whole-blood PUFA and nutrition and health markers among Cambodian children with SAM after treatment with RUTFs.

How They Measured It

See study for outcome measures

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7

To investigate the effects of ALA (Alpha-Linolenic Acid) in effects of varied omega-3 fatty acid supplementation on postpartum mental health and the association between prenatal erythrocyte omega-3 fatty acid l

2023 ? participants 12 weeks 2.0 g/day
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in effects of varied omega-3 fatty acid supplementation on postpartum mental health and the association between prenatal erythrocyte omega-3 fatty acid l

Dose

2.0 g/day

Participants

Participants not specified

Duration

12 weeks

Results

ved from the MIBS results. In the case-control study of the historical control, high levels of α-linolenic acid in maternal erythrocytes were associated with an EPDS score of <9 (odds ratio of 0.23, 95% confidence interval: 0.06, 0.84, p = 0.018 for trend). The results of this study suggest that consumption of α-linolenic acid during pregnancy may stabilize postpartum mental health.

How They Measured It

See study for outcome measures

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8

To investigate the effects of ALA (Alpha-Linolenic Acid) in fatty acid correlations with homa-ir and homa-% β are differentially dictated by their serum free and total pools and flaxseed oil supplementation.

2023 ? participants Duration not specified ALA (Alpha-Linolenic Acid) (dose not specified)
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in fatty acid correlations with homa-ir and homa-% β are differentially dictated by their serum free and total pools and flaxseed oil supplementation.

Dose

ALA (Alpha-Linolenic Acid) (dose not specified)

Participants

Participants not specified

Duration

Duration not specified

Results

The SIFFA and SITFA pools have different relationships with HOMA-IR and HOMA-% β for each of pre- and post-intervention. It is concluded that the data support both the primary and the secondary hypotheses indicating that they are correct.

How They Measured It

See study for outcome measures

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9

To investigate the effects of ALA (Alpha-Linolenic Acid) in evaluation of influencing factors on metabolism of land-based n-3 poly unsaturated fatty acids-the koala study.

2023 134 participants 12 weeks 16 g
Human Study RCT Double-Blind Placebo Mixed

Study Type

Randomized, double-blind, placebo-controlled

Purpose

To investigate the effects of ALA (Alpha-Linolenic Acid) in evaluation of influencing factors on metabolism of land-based n-3 poly unsaturated fatty acids-the koala study.

Dose

16 g

Participants

134 participants

Duration

12 weeks

Results

( p < 0.01). The conversion into EPA was higher in men than in women (69 vs. 39%, p = 0.043) and in subjects with low EPA status compared to participants with high EPA status (79 vs. 29%, p < 0.001). A high LA status attenuates the conversion rate. In line with the literature, no clear effects on blood lipids and parameters of glucose metabolism were found in relation to ALA supplementation.

How They Measured It

See study for outcome measures

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Frequently Asked Questions

Common questions about ALA (Alpha-Linolenic Acid) research

What does the research say about ALA (Alpha-Linolenic Acid)?

There are currently 22 peer-reviewed studies on ALA (Alpha-Linolenic Acid) (Alpha-linolenic acid (C18:3 n-3)), involving 102,806 total participants. Research covers Cardiovascular Risk Reduction, Systematic reviews, Clinical trials. The overall evidence strength is rated as Strong.

How strong is the evidence for ALA (Alpha-Linolenic Acid)?

The evidence is currently rated as "Strong Evidence". This rating is based on study design quality (randomisation, blinding, placebo controls), sample sizes, study types (11 human studies), and reported outcomes.

What health goals has ALA (Alpha-Linolenic Acid) been studied for?

ALA (Alpha-Linolenic Acid) has been researched for: Cardiovascular Risk Reduction, Systematic reviews, Clinical trials. Each area has its own body of evidence which you can explore in the study breakdowns above.

Are the studies on ALA (Alpha-Linolenic Acid) based on human trials?

Yes, 11 out of 22 studies are human trials. Human trials carry more weight in our evidence scoring system.