Evidence map›Paper›PMID 32141822›Full record

Trial reportThe Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology2020

The effect of twelve weeks of treatment with ezetimibe on HDV RNA level in patients with chronic hepatitis D.

Zaigham Abbas, Muhammad Saad, Muhammad Asim, Minaam Abbas, Shoukat Ali Samejo

Open access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. [Current status of diagnosis and treatment and progress in drug research and development for hepatitis D].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
    Review
  3. Review
  4. Review
  5. Review
  6. [Study of the inhibitory effect of cell entry inhibitory ezetimibe on hepatitis B virus in vitro].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2021
    Article
  7. Review
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

5 authors at 1 institution in 1 country.

Zaigham AbbasDepartment of Hepato-Gastroenterology, Dr. Ziauddin University Hospital Clifton, Karachi, Pakistan.
Muhammad SaadDepartment of Hepato-Gastroenterology, Dr. Ziauddin University Hospital Clifton, Karachi, Pakistan.
Muhammad AsimDepartment of Hepato-Gastroenterology, Dr. Ziauddin University Hospital Clifton, Karachi, Pakistan.
Minaam AbbasDepartment of Hepato-Gastroenterology, Dr. Ziauddin University Hospital Clifton, Karachi, Pakistan.
Shoukat Ali SamejoDepartment of Hepato-Gastroenterology, Dr. Ziauddin University Hospital Clifton, Karachi, Pakistan.
Ziauddin Hospital · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsSodium taurocholate co-transporting polypeptide (NTCP) is the receptor for the hepatitis B virus (HBV) and hepatitis D virus (HDV) entry into hepatocytes. Ezetimibe is a cholesterol-lowering drug that possesses the pharmacophore features to inhibit NTCP. This study evaluates the efficacy of ezetimibe in patients with chronic HDV infection in a nonrandomized trial. MATERIALS AND

methodsThis proof of concept phase 2 trial evaluated the efficacy and safety of ezetimibe 10 mg daily in (interferon treatment-experienced or interferon ineligible) patients with chronic hepatitis D (CHD). Forty-four patients with CHD were recruited, 38 male and 6 female patients, mean age 35.2±8.7 (range 19-64). Fifteen (34%) patients were on concomitant nucleoside therapy, and cirrhosis was present in 14 subjects. The primary therapeutic endpoint was a decline in HDV RNA at one log or more from the baseline at week 12.

resultsThe mean HDV RNA level was 5.4±1.3 log10 IU/mL. HBeAg was non-reactive in 43 (98%). HBV DNA was undetectable in 28 (64%). One patient stopped treatment at week 4, and one patient did not follow-up. One log or more reduction in the HDV RNA levels was observed in 18/44 (41%) patients. No log reduction occurred in 16 patients, and 8 experienced a log increase. No adverse effects from the concomitant nucleoside analogue use or clinical cirrhosis were observed. The drug exhibited a positive safety profile.

conclusionTreatment of CHD patients with ezetimibe resulted in a one log reduction of viral load in 43% (18/42) of the patients who completed the 12 weeks of therapy.

Indexed as

AdultAntiviral AgentsEzetimibeFemaleHepatitis D, ChronicHepatitis Delta VirusHumansLiver CirrhosisMaleMiddle AgedOrganic Anion Transporters, Sodium-DependentProof of Concept StudyRNA, ViralSymportersTreatment OutcomeViral LoadAntiviral AgentsEzetimibeOrganic Anion Transporters, Sodium-DependentRNA, Viralsodium-bile acid cotransporterSymporters

Identifiers

PMID32141822
PMCPMC7062136
OpenAlexW3009610825

What OpenQuestion holds

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Registered trials

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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.