Evidence map›Paper›PMID 30271161›Full record

Trial reportVascular health and risk management2018

Effects of sarpogrelate, eicosapentaenoic acid and pitavastatin on arterioslcerosis obliterans-related biomarkers in patients with type 2 diabetes (SAREPITASO study).

Shosaku Nomura, Takehito Taniura, Akira Shouzu, Seitaro Omoto, Masahiko Suzuki, Yoshinori Okuda, Tomoki Ito

Open access · goldAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Vascular health and risk management, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. EXCLI journal · 2019
    Review
  8. Review
  9. Risk of Atherosclerosis Due to HMGB1-dependent Platelet-derived Microparticles in Patients with Type 2 Diabetes Mellitus.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Article
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

7 authors at 1 institution in 1 country.

Shosaku NomuraFirst Department of Internal Medicine, Kansai Medical University, Hirakata, nomurash@hirakata.kmu.ac.jp.
Takehito TaniuraDivision of Internal Medicine, Daiwa Hospital, Suita.
Akira ShouzuDivision of Internal Medicine, Saiseikai Izuo Hospital, Osaka.
Seitaro OmotoDivision of Internal Medicine, Korigaoka Yukeikai Hospital, Hirakata.
Masahiko SuzukiDivision of Internal Medicine, Katano Hospital, Katano.
Yoshinori OkudaDivision of Internal Medicine, Meisei Memorial Hospital, Osaka, Japan.
Tomoki ItoFirst Department of Internal Medicine, Kansai Medical University, Hirakata, nomurash@hirakata.kmu.ac.jp.
Kansai Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim was to evaluate the significance of arteriosclerosis obliterans-related biomarkers in patients with type 2 diabetes mellitus (T2DM), and to compare the effects of sarpogrelate, eicosapentaenoic acid (EPA) and pitavastatin on these markers. PATIENTS AND

methodsSeventy-two arteriosclerosis obliterans patients with T2DM were classified into two groups, pitavastatin with either sarpogrelate (PS) or EPA (PE). We observed no differences in all biomarkers between the PS and PE groups before treatments.

resultsThe levels of body mass index, hemoglobin A1c, soluble E-selectin, soluble vascular cell adhesion molecule 1, plasminogen activator inhibitor-1 and platelet-derived microparticle in the PE group decreased significantly after treatment. The ankle branchial pressure index and adiponectin levels significantly increased in the PE group after treatment compared with the PS group.

conclusionThese results suggest that combination therapy using pitavastatin and EPA possesses an antiatherosclerotic effect and may be beneficial for prevention of vascular complications in patients with T2DM.

Indexed as

AdiponectinAgedAged, 80 and overAnkle Brachial IndexArteriosclerosis ObliteransBiomarkersDiabetes Mellitus, Type 2Diabetic AngiopathiesDrug Therapy, CombinationEicosapentaenoic AcidFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsJapanLinear ModelsMaleAdiponectinADIPOQ protein, humanBiomarkersEicosapentaenoic AcidHydroxymethylglutaryl-CoA Reductase InhibitorspitavastatinPlatelet Aggregation InhibitorsQuinolinessarpogrelateSuccinatesadiponectineicosapentaenoic acidEPAPDMPpitavastatinplatelet-derived microparticlesarpogrelateT2DM

Identifiers

PMID30271161
PMCPMC6151091
OpenAlexW2889651756

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY-NC
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.