Evidence map›Paper›PMID 27052207›Full record

ArticleHeart and vessels2017

Ezetimibe enhances and stabilizes anticoagulant effect of warfarin.

Takehiro Hashikata, Minako Yamaoka-Tojo, Ryota Kakizaki, Teruyoshi Nemoto, Kazuhiro Fujiyoshi, Sayaka Namba, Lisa Kitasato, Takuya Hashimoto, Shunsuke Ishii, Ryo Kameda and 3 more

Abstract read
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In one paragraph

Article in Heart and vessels, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Article
  3. 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

13 authors at 1 institution in 1 country.

Takehiro HashikataDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan. t_hashikata@med.kitasato-u.ac.jp.
Minako Yamaoka-TojoDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Ryota KakizakiDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Teruyoshi NemotoDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Kazuhiro FujiyoshiDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Sayaka NambaDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Lisa KitasatoDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Takuya HashimotoDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Shunsuke IshiiDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Ryo KamedaDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Takao ShimohamaDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Taiki TojoDepartment of Rehabilitation, Kitasato University School of Allied Health Sciences, 1-15-1 Kitasato, Minami-ku, Sagamihara, Kanagawa, 252-0373, Japan.
Junya AkoDepartment of Cardiovascular Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Kitasato University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ezetimibe reduces plasma levels of low-density lipoprotein cholesterol by inhibiting Niemann-Pick C1-like protein 1 (NPC1L1). A recent study demonstrated that NPC1L1 plays an important role in absorption of fat-soluble vitamins including vitamin K. We evaluated whether the add-on treatment of ezetimibe affects anticoagulation in patients taking warfarin. Between October 2007 and March 2015, the administration of ezetimibe was started to a total of 101 outpatients who were already on oral anticoagulation with warfarin. We retrospectively analyzed blood lipid levels, prothrombin time international normalized ratio (PT-INR) and time in therapeutic INR range (TTR). Seventy-one patients (70 %) showed increase in PT-INR after ezetimibe treatment (1.96 ± 0.45 to 2.20 ± 0.61, p < 0.001). It was necessary to reduce the warfarin dose in 9 of 101 patients for clinical indication. There was a significant positive correlation between change in PT-INR and statin usage at baseline (p = 0.03). The mean value of changes in PT-INR of patients with taking statin was significantly larger than that of patients without taking statin (0.34 ± 0.54 vs. 0.06 ± 0.36, p = 0.03). There was an increase in the TTR (52 ± 26 to 61 ± 23 %, p < 0.0001) and a decrease in the frequency to change the dose of warfarin after the ezetimibe treatment [45 times of 735 examination days (6 %) to 20 times of 695 examination days (3 %), p = 0.02]. Our data suggest possible drug interaction between warfarin and ezetimibe. Ezetimibe may increase and stabilize the anticoagulant effect of warfarin, especially in patients taking statins.

Indexed as

AgedAnticholesteremic AgentsAnticoagulantsBlood CoagulationCholesterol, LDLDrug Therapy, CombinationDyslipidemiasEzetimibeFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsInternational Normalized RatioJapanLinear ModelsMaleMiddle AgedAnticholesteremic AgentsAnticoagulantsCholesterol, LDLEzetimibeHydroxymethylglutaryl-CoA Reductase InhibitorsWarfarinEzetimibeNiemann–Pick C1-like protein 1Time in therapeutic rangeVitamin KWarfarin

Identifiers

PMID27052207
OpenAlexW2318859417

What OpenQuestion holds

Texttitle and abstract
Read underepoch 390

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 OpenQuestion graph.