Evidence map›Paper›PMID 39072039›Full record

ArticlemedRxiv : the preprint server for health sciences2024

Effect of disclosing a polygenic risk score for coronary heart disease on adverse cardiovascular events: 10-year follow-up of the MI-GENES randomized clinical trial.

Mohammadreza Naderian, Marwan E Hamed, Ali A Vaseem, Kristjan Norland, Ozan Dikilitas, Azin Teymourzadeh, Kent R Bailey, Iftikhar J Kullo

Registry-linked trialAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01936675 (Myocardial Infarction Genes), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.

NCT01936675 nacompletednot on this map

Myocardial Infarction Genes (MI-GENES) Study - Using Genomic Data to Refine Risk Assessment for Heart Attack

TypeinterventionalSponsorMayo ClinicRan2013 to 2014Enrolled216ConditionsCoronary Artery Disease, Myocardial Infarction, Genomic Risk CommunicationArmsGenetic Risk Score
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Mohammadreza NaderianDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Marwan E HamedDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Ali A VaseemDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Kristjan NorlandDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Ozan DikilitasDepartment of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Azin TeymourzadehDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Kent R BaileyDepartment of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota.
Iftikhar J KulloDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.

Funding

Genomic Basis of Susceptibility to COVID-19 Infection and its ComplicationsU01HG006379 · NHGRI · MAYO CLINIC ROCHESTER · PI Richard R. Sharp · 2011 to 2026
$16.5M
NHGRI NIH HHS U01 HG006379
6 · The paper itself

Abstract

Background: The MI-GENES clinical trial (NCT01936675), in which participants at intermediate risk of coronary heart disease (CHD) were randomized to receive a Framingham risk score (FRS Objectives: In a post hoc 10-year follow-up analysis of the MI-GENES trial, we investigated whether disclosure of a PRS for CHD was associated with a reduction in adverse cardiovascular events. Methods: Participants were followed from randomization beginning in October 2013 until September 2023 to ascertain adverse cardiovascular events, testing for CHD, and changes in risk factors, by blinded review of electronic health records. The primary outcome was the time from randomization to the occurrence of the first major adverse cardiovascular event (MACE), defined as cardiovascular death, non-fatal myocardial infarction, coronary revascularization, and non-fatal stroke. Statistical analyses were conducted using Cox proportional hazards regression and linear mixed-effects models. Results: We followed all 203 participants who completed the MI-GENES trial, 100 in FRS Conclusions: The disclosure of an IRS that included a PRS to individuals at intermediate risk for CHD was associated with a lower incidence of MACE after a decade of follow-up, likely due to a higher rate of initiation and longer duration of statin therapy, leading to lower LDL-C levels.

Indexed as

Coronary Artery DiseaseGenetic Risk ScoreHydroxymethylglutaryl-CoA Reductase InhibitorsPrimary PreventionRisk AssessmentStatin

Identifiers

PMID39072039
PMCPMC11275655

What OpenQuestion holds

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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.