Evidence map›Paper›PMID 27362442›Full record

Trial reportJournal of medicinal food2016

Clinical Safety of a High Dose of Phycocyanin-Enriched Aqueous Extract from Arthrospira (Spirulina) platensis: Results from a Randomized, Double-Blind, Placebo-Controlled Study with a Focus on Anticoagulant Activity and Platelet Activation.

Gitte S Jensen, Cassandra Drapeau, Miki Lenninger, Kathleen F Benson

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of medicinal food, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 5 pooled it
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 5 syntheses or guidelines pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. The Role ofNutrients · 2025
    Pooled it
  3. Pooled it
  4. Effect ofNutrients · 2021
    Pooled it
  5. Pooled it
  6. Trial
  7. Safety evaluation of blue galdieria extract as a food additive.EFSA journal. European Food Safety Authority · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. C-Phycocyanin andNutrients · 2022
    Article
  14. Article
  15. The Potential ofNutrients · 2022
    Review
  16. Article
  17. Dietary supplements and bleeding.Proceedings (Baylor University. Medical Center) · 2022
    Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Gitte S Jensen1 NIS Labs , Klamath Falls, Oregon, USA .
Cassandra Drapeau2 Cerule LLC , Klamath Falls, Oregon, USA .
Miki Lenninger1 NIS Labs , Klamath Falls, Oregon, USA .
Kathleen F Benson1 NIS Labs , Klamath Falls, Oregon, USA .
Klamath Community College · USOregon Institute of Technology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The goal for this study was to evaluate safety regarding anticoagulant activity and platelet activation during daily consumption of an aqueous cyanophyta extract (ACE), containing a high dose of phycocyanin. Using a randomized, double-blind, placebo-controlled study design, 24 men and women were enrolled after informed consent, and consumed either ACE (2.3 g/day) or placebo daily for 2 weeks. The ACE dose was equivalent to ∼1 g phycocyanin per day, chosen based on the highest dose Generally Recognized as Safe (GRAS) by the U.S. Food and Drug Administration. Consuming ACE did not alter markers for platelet activation (P-selectin expression) or serum P-selectin levels. No changes were seen for activated partial thromboplastin time, thrombin clotting time, or fibrinogen activity. Serum levels of aspartate transaminase (AST) showed a significant reduction after 2 weeks of ACE consumption (P < .001), in contrast to placebo where no changes were seen; the difference in AST levels between the two groups was significant at 2 weeks (P < .02). Reduced levels of alanine transaminase (ALT) were also seen in the group consuming ACE (P < .08). Previous studies showed reduction of chronic pain when consuming 1 g ACE per day. The higher dose of 2.3 g/day in this study was associated with significant reduction of chronic pain at rest and when physically active (P < .05). Consumption of ACE showed safety regarding markers pertaining to anticoagulant activity and platelet activation status, in conjunction with rapid and robust relief of chronic pain. Reduction in AST and ALT suggested improvement in liver function and metabolism.

Indexed as

AdultAlanine TransaminaseAnticoagulantsAspartate AminotransferasesChronic PainDouble-Blind MethodFemaleFibrinogenHumansMaleMiddle AgedPartial Thromboplastin TimePhycocyaninPlacebosPlatelet ActivationP-SelectinAlanine TransaminaseAnticoagulantsAspartate AminotransferasesFibrinogenPhycocyaninPlacebosP-Selectinanticoagulant activityblood pressurechronic painliver enzymesplateletP-selectin

Identifiers

PMID27362442
PMCPMC4948198
OpenAlexW2465519026

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.