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Oral Quercetin Supplementation Enhances Adiponectin Receptor Transcript Expression in Polycystic Ovary Syndrome Patients: A Randomized Placebo-Controlled Double-Blind Clinical Trial

Neda Rezvan, Ashraf Moini, Sattar Gorgani-Firuzjaee, Mohammad Javad Hosseinzadeh-Attar
Cell journal 2018 19(4):627

Bibliography

PubMed
PMID 29105398
PubMed Central
PMC5672102
Funding
Funding was not specified in the indexed record or the disclosure metadata available for this entry.
Competing interests
Reported disclosure: The authors declare no conflict of interest in this study.

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 2018, 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-receptor transcripts and an AMPK measure increased relative to placebo.

Molecular endpoints from a registered PCOS program. They do not independently establish improved fertility or long-term metabolic outcomes.

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-receptor transcripts and an AMPK measure increased 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

  • Molecular endpoints from a registered PCOS program. They do not independently establish improved fertility or long-term metabolic outcomes.
  • 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: accessible full text and indexed metadata. Missing method details, funding information or participant denominators are not inferred.

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