Evidence map›Paper›PMID 26621580›Full record

ArticlePhytotherapy research : PTR2016

A Phase I Dose Escalation Study Demonstrates Quercetin Safety and Explores Potential for Bioflavonoid Antivirals in Patients with Chronic Hepatitis C.

Nu T Lu, Catherine M Crespi, Natalie M Liu, James Q Vu, Yasaman Ahmadieh, Sheng Wu, Sherry Lin, Amy McClune, Francisco Durazo, Sammy Saab and 4 more

Registry-linked trialOpen access · greenAbstract readClinical Trial, Phase I
In one paragraph

Article in Phytotherapy research : PTR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07487623 (Evaluation of the Hepatoprotective Effects of a Nutritional Supplement Containing Resveratrol, Quercetin, Taurine, Inulin, and Whey Protein on Biochemical, Molecular, and Clinical Markers in Patients With Liver Disease Secondary to Chronic Hepatitis C Virus Infection), which is not on this map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.4field-weighted citation impact, top 11% 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.

NCT07487623 narecruitingnot on this mapstarted 2025, after this paper: background citation

Evaluation of the Hepatoprotective Effects of a Nutritional Supplement Containing Resveratrol, Quercetin, Taurine, Inulin, and Whey Protein on Biochemical, Molecular, and Clinical Markers in Patients With Liver Disease Secondary to Chronic Hepatitis C Virus Infection (RESQUETI Study).

TypeinterventionalSponsorUniversity of GuadalajaraRan2025 to 2026Enrolled26ConditionsLiver Disease Chronic, HEPATITIS C VIRUS CHRONIC INFECTIONArmsresveratrol, quercetin, taurine, whey protein, and inulin, whey protein
3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 100 citations in OpenAlex.

  1. Trial
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  9. Biomaterials research · 2025
    Article
  10. Multidimensional mechanisms of quercetin in diabetic kidney disease.Frontiers in cell and developmental biology · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
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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

14 authors at 5 institutions in 1 country.

Nu T LuDepartment of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, USA.
Catherine M CrespiFielding School of Public Health, Department of Biostatistics, University of California Los Angeles, Los Angeles, USA.
Natalie M LiuDepartment of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, USA.
James Q VuDepartment of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, USA.
Yasaman AhmadiehCollege of Osteopathic Medicine, Touro University, Vallejo, USA.
Sheng WuFielding School of Public Health, Department of Biostatistics, University of California Los Angeles, Los Angeles, USA.
Sherry LinNeuromodulation Division, Boston Scientific Inc., Valencia, USA.
Amy McCluneDepartment of Hepatobiliary Surgery, Kaiser Permanente Sunset, Los Angeles, USA.
Francisco DurazoPfleger Liver Institute, University of California Los Angeles, Los Angeles, USA.
Sammy SaabPfleger Liver Institute, University of California Los Angeles, Los Angeles, USA.
Steven HanPfleger Liver Institute, University of California Los Angeles, Los Angeles, USA.
David C NeimanHuman Performance Laboratory, Appalachian State University- North Carolina Research Campus, Kannapolis, USA.
Simon BeavenPfleger Liver Institute, University of California Los Angeles, Los Angeles, USA.
Samuel W FrenchDepartment of Pathology and Laboratory Medicine, University of California Los Angeles, Los Angeles, USA.
University of California, Los Angeles · USAppalachian State University · USBoston Scientific (United States) · USKaiser Permanente · USTouro University California · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
GASTROENTEROLOGYT32DK007180 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JENSEN, DENNIS MICHAEL · 1986 to 2025
$10.0M
Heat Shock Protein Synthesis Inhibitor Treatment of Hepatitis C Viral InfectionR01DK090794 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FRENCH, SAMUEL WHEELER · 2011 to 2015
$1.7M
NCI NIH HHS CA16042NCI NIH HHS P30 CA016042NIDDK NIH HHS P30 DK041301NIDDK NIH HHS R01 DK090794NIDDK NIH HHS R01DK090794NIDDK NIH HHS T32 DK007180
6 · The paper itself

Abstract

The hepatitis C virus (HCV) infects more than 180 million people worldwide, with long-term consequences including liver failure and hepatocellular carcinoma. Quercetin bioflavonoids can decrease HCV production in tissue culture, in part through inhibition of heat shock proteins. If quercetin demonstrates safety and antiviral activity in patients, then it could be developed into an inexpensive HCV treatment for third world countries or other affected populations that lack financial means to cover the cost of mainstream antivirals. A phase 1 dose escalation study was performed to evaluate the safety of quercetin in 30 untreated patients with chronic HCV infection and to preliminarily characterize quercetin's potential in suppressing viral load and/or liver injury. Quercetin displayed safety in all trial participants. Additionally, 8 patients showed a "clinically meaningful" 0.41-log viral load decrease. There was a positive correlation (r = 0.41, p = 0.03) indicating a tendency for HCV decrease in patients with a lower ratio of plasma quercetin relative to dose. No significant changes in aspartate transaminase and alanine transaminase were detected. In conclusion, quercetin exhibited safety (up to 5 g daily) and there was a potential for antiviral activity in some hepatitis C patients.

Indexed as

AdultAgedAlanine TransaminaseAntiviral AgentsAspartate AminotransferasesDose-Response Relationship, DrugFemaleHepacivirusHepatitis C, ChronicHumansMaleMiddle AgedQuercetinViral LoadAlanine TransaminaseAntiviral AgentsAspartate AminotransferasesQuercetinbioflavonoidsdose escalationhepatitis Cphase Iphytomedicinequercetin

Identifiers

PMID26621580
PMCPMC5590840
OpenAlexW2182048109

What OpenQuestion holds

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Registered trials

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.