Evidence map›Paper›PMID 12392587›Full record

Trial reportBritish journal of clinical pharmacology2002

Direct in vivo evidence of a vascular statin: a single dose of cerivastatin rapidly increases vascular endothelial responsiveness in healthy normocholesterolaemic subjects.

Hisako Omori, Hirotaka Nagashima, Yukio Tsurumi, Atsushi Takagi, Naoko Ishizuka, Nobuhisa Hagiwara, Masatoshi Kawana, Hiroshi Kasanuki

Open access · bronzeAbstract readClinical TrialRandomized Controlled Trial
In one paragraph

Trial report in British journal of clinical pharmacology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

24 citing papers in PubMed, 95 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Review
  8. Article
  9. The role of statins in the prevention of preeclampsia.American journal of obstetrics and gynecology · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Statins as first-line therapy for acute coronary syndrome?Experimental and clinical cardiology · 2012
    Article
  15. Article
  16. The anti-ischemic and anti-anginal properties of statins.Current atherosclerosis reports · 2011
    Review
  17. Farnesyltransferase inhibitor improved survival following endotoxin challenge in mice.Biochemical and biophysical research communications · 2010
    Article
  18. Review
  19. Article
  20. Endothelial dysfunction in diabetes mellitus.Vascular health and risk management · 2007
    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

8 authors at 1 institution in 1 country.

Hisako OmoriDepartment of Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjyuku-ku, Tokyo 162-8666, Japan.
Hirotaka Nagashima
Yukio Tsurumi
Atsushi Takagi
Naoko Ishizuka
Nobuhisa Hagiwara
Masatoshi Kawana
Hiroshi Kasanuki
Tokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsHMG-CoA reductase inhibitors (statins) have been demonstrated to have in vitro vascular effects. The aim of this study was to determine whether statins actually have in vivo vascular effects independent of their cholesterol-lowering effect.

methodsWe investigated the effect of a single dose of cerivastatin on vascular endothelial function by measuring flow-mediated dilatation of the brachial artery on ultrasound in 30 healthy volunteers with normal serum cholesterol concentrations. They were randomized to either placebo group (n = 15) or cerivastatin group (n = 15), and flow-mediated dilatation and endothelium-dependent dilatation were evaluated at before and 1 h, 3 h, 6 h, and 12 h after administration of placebo or cerivastatin.

resultsThere were no differences in total cholesterol, LDL cholesterol, HDL cholesterol, triglycerides, malondialdehyde-LDL, and high-sensitivity C-reactive protein before and after administration of placebo or cerivastatin. Cerivastatin significantly increased flow-mediated dilatation at 3 h (P < 0.001), and this increase rapidly returned to the baseline level 6 h after administration. Endothelium--independent dilatation of brachial artery was not altered.

conclusionsA single dose of cerivastatin increased vascular endothelial responsiveness. Our data suggest that cerivastatin has a direct effect on the blood vessels that is independent of its lipid-lowering effect, and thus can be considered as a vascular statin.

Indexed as

AdultAnalysis of VarianceBlood Flow VelocityBrachial ArteryDouble-Blind MethodHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMalePyridinesVasodilationcerivastatinHydroxymethylglutaryl-CoA Reductase InhibitorsPyridines

Identifiers

PMID12392587
PMCPMC1874448
OpenAlexW1543253499

What OpenQuestion holds

Textmetadata
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.