# Evaluation of the effect of olive extracts on blood pressure and cardiovascular health markers in adults: Findings from a double-blind, placebo-controlled, randomised trial

**Authors:** Stef Lauwers, Annelies Breynaert, Annelies Verlaet, Erik Fransen, Tijs Bringmans, Lynn Roth, Emmy Tuenter, Johan Bosmans, Nina Hermans

PMC · DOI: 10.1371/journal.pone.0344278 · 2026-03-10

## TL;DR

This study tested olive extract's effect on blood pressure and heart health in adults but found no significant benefit over a placebo.

## Contribution

The study provides new empirical evidence on the cardiovascular effects of a standardized olive extract in a placebo-controlled trial.

## Key findings

- Both olive extract and placebo groups showed similar reductions in systolic blood pressure.
- Olive extract did not significantly lower cholesterol or LDL levels compared to placebo.
- The extract was well-tolerated but did not show a significant hypotensive benefit.

## Abstract

Despite advances in reducing cardiovascular disease (CVD) incidence, CVD mortality has increased, emphasising the need for new preventive strategies. Polyphenol-rich olive extracts have been proposed to lower blood pressure by reducing oxidative stress and enhancing nitric oxide production. This double-blind, placebo-controlled, randomised study aims to examine whether a standardised olive extract can lead to a reduction in blood pressure, lipid levels, and biological markers of oxidative stress after supplementation in the context of primary CVD prevention. In this trial, 56 participants with a systolic blood pressure ≥ 130 mmHg received capsules containing 440 mg olive dry extract (123.5 ± 9.4 mg oleuropein, 25.0 ± 3.8 mg hydroxytyrosol) or placebo on a daily basis over eight weeks. Both groups showed significant reductions in systolic blood pressure with a larger decrease in the intervention group as compared to the control group (intervention: −8.3 ± 2.2 mmHg, control: −7.3 ± 2.2 mmHg). However, this decrease was not found significantly different between the two groups. Moreover, total cholesterol, LDL, and apo B levels decreased in both groups, but with no significant difference between them. These results indicate that the olive extract was well-tolerated, although no significant hypotensive benefit was observed, with effects paralleling typical placebo responses in hypertension trials. Literature reports conflicting results on the hypotensive effect of olive polyphenols, indicating the need for further research with well-designed clinical trials. This trial was registered on Clinicaltrials.gov in April 2021, ID NCT04874961.

## Linked entities

- **Chemicals:** oleuropein (PubChem CID 5281544), hydroxytyrosol (PubChem CID 82755)
- **Diseases:** cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Diseases:** type 2 diabetes (MESH:D003924), nephropathies (MESH:D007674), depression (MESH:D003866), muscle aches (MESH:D063806), impaired glucose tolerance (MESH:D018149), chronic diseases (MESH:D002908), muscle cramps (MESH:D009120), rheumatoid arthritis (MESH:D001172), Hypertension (MESH:D006973), death (MESH:D003643), CKD-EPI (MESH:D012080), CVD (MESH:D002318), arthralgia (MESH:D018771), weight (MESH:D015431), hair loss (MESH:D000505), stroke (MESH:D020521), overweight (MESH:D050177), SBP (MESH:D007022), acute inflammation (MESH:D007249), headache (MESH:D006261), muscle stiffness (MESH:D019042), insomnia (MESH:D007319), muscle weakness (MESH:D018908), diabetes mellitus (MESH:D003920), Chronic Kidney Disease (MESH:D051436)
- **Chemicals:** luteolin-7-O-glucoside (MESH:C066408), Polyphenol (MESH:D059808), GSH (MESH:D005978), BP (MESH:C038809), lipid (MESH:D008055), microcrystalline cellulose (MESH:C109691), OLE (MESH:C002769), alcohol (MESH:D000438), creatinine (MESH:D003404), glucose (MESH:D005947), magnesium (MESH:D008274), flavonoids (MESH:D005419), FFQ (-), olive oil (MESH:D000069463), secoiridoids (MESH:D039823), silicon dioxide (MESH:D012822), FC (MESH:C095424), potassium (MESH:D011188), triptans (MESH:D014363), sodium (MESH:D012964), K3 (MESH:C058433), NADPH (MESH:D009249), Homocysteine (MESH:D006710), phenols (MESH:D010636), fatty acids (MESH:D005227), MDA (MESH:D008315), unsaturated fats (MESH:D005224), talc (MESH:D013627), calcium phosphate (MESH:C020243), ethanol (MESH:D000431), C-peptide (MESH:D002096), Cholesterol (MESH:D002784), NO (MESH:D009569), trans fatty acids (MESH:D044242), blood glucose (MESH:D001786), HT (MESH:C005975), sugar (MESH:D000073893), salt (MESH:D012492), vanillic acid (MESH:D014641), zinc (MESH:D015032), EDTA (MESH:D004492), triglyceride (MESH:D014280), verbascoside (MESH:C058956), rutin (MESH:D012431)
- **Species:** Solanum tuberosum (potatoes, species) [taxon 4113], gut metagenome (species) [taxon 749906], Homo sapiens (human, species) [taxon 9606], Olea europaea (common olive, species) [taxon 4146], Olea (olives, genus) [taxon 4145]
- **Mutations:** Glu298Asp, term of 0

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12974854/full.md

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Source: https://tomesphere.com/paper/PMC12974854