Evidence mapPaperPMID 41800110Full record

ArticleDose-response : a publication of International Hormesis Society

The Quercetin Paradox, Evaluation of its Therapeutic Efficacy as a Nutraceutical in Clinical Trials: Evidence and Speculation.

Raquel García Alvarez, Juan Luis Chávez-Pacheco, Nelly Francisca Altamirano-Bustamante, Edelmira Solorio-López, Josefina Gómez-Garduño, Liliana Rivera-Espinosa

Abstract read
In one paragraph

Article in Dose-response : a publication of International Hormesis Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Raquel García AlvarezPharmacology Laboratory, National Institute of Pediatrics, Mexico City, Mexico.ORCID https://orcid.org/0000-0003-3563-134X
Juan Luis Chávez-PachecoPharmacology Laboratory, National Institute of Pediatrics, Mexico City, Mexico.ORCID https://orcid.org/0000-0001-6919-4497
Nelly Francisca Altamirano-BustamanteEndocrinology Service, National Institute of Pediatrics, Mexico City, Mexico.
Edelmira Solorio-LópezPharmacology Laboratory, National Institute of Pediatrics, Mexico City, Mexico.ORCID https://orcid.org/0000-0003-2981-2347
Josefina Gómez-GarduñoPharmacology Laboratory, National Institute of Pediatrics, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-0226-3651
Liliana Rivera-EspinosaPharmacology Laboratory, National Institute of Pediatrics, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-1334-0026

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Quercetin, a dietary flavonoid typically consumed as a glycoside, is available in supplements in its aglycone form. This aglycone form is the most studied in preclinical and clinical research because of its antioxidant, anti-inflammatory, and metabolic properties. Several clinical trials have demonstrated the benefits of quercetin for enzymatic, metabolic and cardiovascular health, approximately 60% of these studies fail to verify the actual concentration administered, generating uncertainty on their findings. Objective: This study aimed to evaluate the concentration, stability, and cost-concentration of commercial quercetin nutraceutical formulations. Methodology: The concentrations of five commercial brands were quantified by high-performance liquid chromatography. Stability was assessed over 6 months at both room temperature and 40°C. Results: Only one brand contained the amount labeled; three contained approximately 80%, and one contained merely 14.8%. This study is the first to evaluate the long and thermal stability of quercetin in nutraceutical products, demonstrating that the active ingredient remains stable for at least 6 months. Brand C was identified as the most suitable option. Conclusion: There was significant variability in the quercetin concentration of commercial supplements. These findings underscore the need for stricter regulatory oversight to ensure the quality, therapeutic efficacy, and safety of nutraceutical products.

Indexed as

clinical trialcostdietarynutraceuticalsquercetinstabilitysupplements

Identifiers

PMID41800110
PMCPMC12966558

What Socratic holds

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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 Socratic graph.