Trial reportThe Journal of nutrition2026
Acute Effects of a High-Fat Meal Enriched with Pomegranate Seed Oil on Postprandial Lipemia and Endothelial Function in Postmenopausal Women: a Randomized Controlled Crossover Trial.
Trial report in The Journal of nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06042673 (Impact of Pomegranate Seed Oil on Postprandial Cardiovascular Disease Risk Markers in Postmenopausal Women.), which is not on this map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Impact of Pomegranate Seed Oil on Postprandial Cardiovascular Disease Risk Markers in Postmenopausal Women.
Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPostprandial elevation of triacylglycerol (TAG) is associated with endothelial dysfunction and represents an important independent cardiovascular disease (CVD) risk factor in women. Although daily intakes of pomegranate seed oil (PSO, 80% conjugated α-linolenic acids) reduce fasting lipids, little is known about the acute effects on postprandial CVD risk markers.
objectivesThis study compared the impact of a PSO-rich meal with those of a control meal on postprandial TAG (primary outcome measure), lipids, glucose, insulin, microvascular function, and cell adhesion molecule responses in postmenopausal women.
methodsIn a single-blind, randomized controlled postprandial crossover study, 16 postmenopausal women aged ≤65 y were assigned to consume either a PSO-rich or a control meal on 2 separate occasions, 4 to 6 wk apart. A high-fat mixed meal (50 g fat) was provided at breakfast (0 min), and blood samples collected until 480 min postprandially to assess CVD risk markers. Specific time points were selected for blood pressure (BP) (0, 120, 240, 360 and 480 min) and microvascular reactivity (0, 180, 300, and 420 min). Postprandial data were analyzed using linear mixed models.
resultsCompared with the control meal, the PSO-rich meal significantly reduced the postprandial TAG response but glucose, insulin, apolipoprotein B, and non-esterified fatty acid responses were similar. The AUC and incremental AUC (iAUC) for the postprandial acetylcholine (endothelium-dependent vasodilation) induced reactivity response were greater (P ≤ 0.04), and systolic BP lower after the PSO-rich meal than the control meal. Additionally, the iAUC for the pulse wave velocity and AUC/iAUC for the soluble intercellular adhesion molecule-1 responses were lower, whereas plasma nitrite concentrations were higher after the PSO-rich than control meal (P ≤ 0.037).
conclusionsA PSO-rich meal significantly reduced the postprandial TAG response and enhanced endothelial function compared with a control meal, suggesting a potential cardioprotective effect in postmenopausal women. This study was registered at clinicaltrials.gov as NCT06042673 (https://clinicaltrials.gov/study/NCT06042673).
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