Evidence map›Paper›PMID 15635109›Full record

Trial reportThe New England journal of medicine2005

C-reactive protein levels and outcomes after statin therapy.

Paul M Ridker, Christopher P Cannon, David Morrow, Nader Rifai, Lynda M Rose, Carolyn H McCabe, Marc A Pfeffer, Eugene Braunwald, Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis in Myocardial Infarction 22 (PROVE IT-TIMI 22) Investigators

4 registry-linked trialsOpen access · bronzeAbstract readClinical TrialMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in The New England journal of medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 638 papers, 13 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
638citing papers in PubMed, 13 pooled it
251.9field-weighted citation impact, top 1% 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.

NCT01082588 phase4completednot on this mapstarted 2010, after this paper: background citation

Phase 4 Study of the Effects of Pravastatin on Cholesterol Levels, Inflammation and Cognition in Schizophrenia

TypeinterventionalSponsorMassachusetts General HospitalRan2010 to 2012Enrolled60ConditionsSchizophrenia, Schizoaffective Disorders, Schizophreniform DisordersArmsPravastatin, Placebo
NCT02988115 phase3completednot on this mapstarted 2016, after this paper: background citation

A Randomized, Double-Blind, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Bempedoic Acid (ETC-1002) 180 mg Compared to Placebo Added to Background Lipid-Modifying Therapy in Patients With Elevated LDL-C Who Are Statin Intolerant

TypeinterventionalSponsorEsperion Therapeutics, Inc.Ran2016 to 2018Enrolled345ConditionsHypercholesterolemia, Atherosclerotic Cardiovascular Disease, Statin Adverse ReactionArmsbempedoic acid, placebo
NCT05062239 narecruitingnot on this mapstarted 2022, after this paper: background citation

Post-Operative Atrial Fibrillation After Surgical Aortic Valve Replacement and the Influence of Statins - Randomized Controlled Trial

TypeinterventionalSponsorLars Peter RiberRan2022 to 2027Enrolled100ConditionsPostoperative Atrial FibrillationArmsDiscontinuance of treatment with statins 7 to 14 days prior to surgery until 30 days postoperative, No-intervention.
NCT05076019 narecruitingnot on this mapstarted 2022, after this paper: background citation

Statin Therapy With Atorvastatin in Surgical Aortic Valve Replacement - a Randomized Controlled Trial

TypeinterventionalSponsorOdense University HospitalRan2022 to 2027Enrolled266ConditionsPostoperative Atrial FibrillationArmsAtorvastatin 80mg, Placebo
3 · Its place in the literature

Who cites it

638 citing papers in PubMed, 13 syntheses or guidelines pooled it, 2,285 citations in OpenAlex.

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  15. Impact of preprocedural biological markers on 10-year mortality in the SYNTAXES trial.EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology · 2022
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578 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Paul M RidkerCenter for Cardiovascular Disease Prevention, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02215, USA. pridker@partners.org
Christopher P Cannon
David Morrow
Nader Rifai
Lynda M Rose
Carolyn H McCabe
Marc A Pfeffer
Eugene Braunwald
Pravastatin or Atorvastatin Evaluation and Infection Therapy-Thrombolysis in Myocardial Infarction 22 (PROVE IT-TIMI 22) Investigators
Brigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStatins lower the levels of low-density lipoprotein (LDL) cholesterol and C-reactive protein (CRP). Whether this latter property affects clinical outcomes is unknown.

methodsWe evaluated relationships between the LDL cholesterol and CRP levels achieved after treatment with 80 mg of atorvastatin or 40 mg of pravastatin per day and the risk of recurrent myocardial infarction or death from coronary causes among 3745 patients with acute coronary syndromes.

resultsPatients in whom statin therapy resulted in LDL cholesterol levels of less than 70 mg per deciliter (1.8 mmol per liter) had lower event rates than those with higher levels (2.7 vs. 4.0 events per 100 person-years, P=0.008). However, a virtually identical difference was observed between those who had CRP levels of less than 2 mg per liter after statin therapy and those who had higher levels (2.8 vs. 3.9 events per 100 person-years, P=0.006), an effect present at all levels of LDL cholesterol achieved. For patients with post-treatment LDL cholesterol levels of more than 70 mg per deciliter, the rates of recurrent events were 4.6 per 100 person-years among those with CRP levels of more than 2 mg per liter and 3.2 events per 100 person-years among those with CRP levels of less than 2 mg per liter; the respective rates among those with LDL cholesterol levels of less than 70 mg per deciliter were 3.1 and 2.4 events per 100 person-years (P<0.001). Although atorvastatin was more likely than pravastatin to result in low levels of LDL cholesterol and CRP, meeting these targets was more important in determining the outcomes than was the specific choice of therapy. Patients who had LDL cholesterol levels of less than 70 mg per deciliter and CRP levels of less than 1 mg per liter after statin therapy had the lowest rate of recurrent events (1.9 per 100 person-years).

conclusionsPatients who have low CRP levels after statin therapy have better clinical outcomes than those with higher CRP levels, regardless of the resultant level of LDL cholesterol. Strategies to lower cardiovascular risk with statins should include monitoring CRP as well as cholesterol.

Indexed as

Anticholesteremic AgentsAtorvastatinBiomarkersCholesterol, LDLCoronary DiseaseC-Reactive ProteinFemaleFluoroquinolonesGatifloxacinHeptanoic AcidsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsIncidenceMaleMiddle AgedMyocardial InfarctionAnticholesteremic AgentsAtorvastatinBiomarkersCholesterol, LDLC-Reactive ProteinFluoroquinolonesGatifloxacinHeptanoic AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsPravastatinPyrroles

Identifiers

PMID15635109
OpenAlexW2118154631

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.