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Effects of Quercetin on Adiponectin-Mediated Insulin Sensitivity in Polycystic Ovary Syndrome: A Randomized Placebo-Controlled Double-Blind Clinical Trial

N Rezvan, A Moini, L Janani, K Mohammad, A Saedisomeolia, M Nourbakhsh, S Gorgani-Firuzjaee, M Mazaherioun, M J Hosseinzadeh-Attar
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2017 49(2):115

Bibliography

PubMed
PMID 27824398
Funding
Funding was not specified in the indexed record or the disclosure metadata available for this entry.
Competing interests
A competing-interest declaration was not available in the indexed record or the disclosure metadata used for this entry.

Study snapshot

DesignRandomized double-blind placebo-controlled PCOS trial
ModelHuman intervention research
Sample84 women with PCOS
InterventionQuercetin 1,000 mg/day versus placebo
Duration12 weeks
EndpointsSource-specific outcomes described in the key findings

What the study showed, in plain terms

Published in 2017, this source examined hormones and reproductive health. Design: Randomized double-blind placebo-controlled PCOS trial. Sample/model: 84 women with PCOS. The exposure or intervention was Quercetin 1,000 mg/day versus placebo. Follow-up or treatment period: 12 weeks.

Adiponectin measures increased and HOMA-IR, testosterone and LH decreased relative to placebo.

Short disease-specific study. Companion receptor-expression reporting belongs to the same registered trial, not a separate replication.

Continue with Quercetin Data Center

For topic-level interpretation, read Quercetin Benefits: What Human Studies Actually Show. This is a related guide; the citation panel separately identifies articles that directly cite this paper.

Key findings

  • Adiponectin measures increased and HOMA-IR, testosterone and LH decreased relative to placebo.
  • The recorded outcome domains were Source-specific outcomes described in the key findings.
  • The result applies to the tested exposure: Quercetin 1,000 mg/day versus placebo; 12 weeks.

What this study can and cannot tell us

  • Short disease-specific study. Companion receptor-expression reporting belongs to the same registered trial, not a separate replication.
  • An individual controlled trial must be interpreted alongside its comparator, sample size, endpoint selection and independent replication. It does not validate a different commercial formulation or a general longevity claim.
  • Companion or correction records are linked below. They should not be counted automatically as independent replications; see the individual source notes for the relationship.
  • Source basis: Source check: PubMed abstract and indexed metadata; full methods were not independently confirmed for this entry. Missing method details, funding information or participant denominators are not inferred.

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