Evidence map›Paper›PMID 15621996›Full record

ArticleAnnals of surgery2005

Treatment with simvastatin suppresses the development of experimental abdominal aortic aneurysms in normal and hypercholesterolemic mice.

Eric F Steinmetz, Celine Buckley, Murray L Shames, Terri L Ennis, Sarah J Vanvickle-Chavez, Dongli Mao, Lee A Goeddel, Cherady J Hawkins, Robert W Thompson

Open access · greenAbstract read
In one paragraph

Article in Annals of surgery, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 3 pooled it
9.9field-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

50 citing papers in PubMed, 3 syntheses or guidelines pooled it, 168 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Eric F SteinmetzDepartment of Surgery (Section of Vascular Surgery), Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Celine Buckley
Murray L Shames
Terri L Ennis
Sarah J Vanvickle-Chavez
Dongli Mao
Lee A Goeddel
Cherady J Hawkins
Robert W Thompson
Washington University in St. Louis · US

Funding

MOLECULAR MECHANISMS OF ANEURYSMAL DEGENERATIONR01HL056701 · NHLBI · WASHINGTON UNIVERSITY · PI THOMPSON, ROBERT W. · 2000 to 2009
$3.2M
ANEURYSM RESEARCH CORE COLLABORATIVE R01R01HL064333 · NHLBI · WASHINGTON UNIVERSITY · PI THOMPSON, ROBERT W. · 1999 to 2002
$224k
MOLECULAR MECHANISMS OF ANEURYSMAL DEGENERATIONR29HL056701 · NHLBI · WASHINGTON UNIVERSITY · PI THOMPSON, ROBERT W. · 1996 to 1999
–
NHLBI NIH HHS HL56701NHLBI NIH HHS HL64333NHLBI NIH HHS R01 HL056701NHLBI NIH HHS R29 HL056701
6 · The paper itself

Abstract

objectiveTo determine if treatment with hydroxymethylglutaryl-coenzyme A reductase inhibitors (statins) can influence the development of experimental abdominal aortic aneurysms (AAAs). SUMMARY BACKGROUND DATA: AAAs are associated with atherosclerosis, chronic inflammation, and matrix metalloproteinase (MMP)-mediated connective tissue destruction. Because statins exert antiinflammatory activities independent of their lipid-lowering effects, these agents may help suppress aneurysmal degeneration.

methodsC57Bl/6 wild-type and hypercholesterolemic apoE-deficient mice underwent transient perfusion of the aorta with elastase followed by subcutaneous treatment with either 2 mg/kg simvastatin per day or vehicle. Aortic diameter (AD) was measured before and 14 days after elastase perfusion. The extent of aortic dilatation (DeltaAD) was determined with AAAs defined as DeltaAD >100%.

resultsWild-type mice treated with simvastatin exhibited a 21% reduction in DeltaAD and a 33% reduction in AAAs compared with vehicle-treated controls. Suppression of AAAs in simvastatin-treated mice was associated with preservation of medial elastin and vascular smooth muscle cells, as well as a relative reduction in aortic wall expression of MMP-9 and a relative increase in expression of TIMP-1. In hypercholesterolemic apoE-deficient mice, treatment with simvastatin was associated with a 26% reduction in DeltaAD and a 30% reduction in AAAs. Treatment with simvastatin had no effect on serum cholesterol levels in either normal or hypercholesterolemic mice.

conclusionsTreatment with simvastatin suppresses the development of experimental AAAs in both normal and hypercholesterolemic mice. The mechanisms of this effect are independent of lipid-lowering and include preservation of medial elastin and smooth muscle cells, as well as altered aortic wall expression of MMPs and their inhibitors.

Indexed as

AnimalsAortic Aneurysm, AbdominalElastinHydroxymethylglutaryl-CoA Reductase InhibitorsHypercholesterolemiaMaleMatrix MetalloproteinasesMiceMice, Inbred C57BLModels, AnimalMyocytes, Smooth MuscleSimvastatinTissue Inhibitor of MetalloproteinasesTunica MediaElastinHydroxymethylglutaryl-CoA Reductase InhibitorsMatrix MetalloproteinasesSimvastatinTissue Inhibitor of Metalloproteinases

Identifiers

PMID15621996
PMCPMC1356851
OpenAlexW206738081

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.