Evidence map›Paper›PMID 41585861›Full record

ArticleInternational journal of cardiology. Cardiovascular risk and prevention2026

Risk for coronary artery disease among individuals with normal low-density lipoprotein cholesterol (LDL-C) levels.

Zhuqing Shi, Ashley J Mulford, Jun Wei, Huy Tran, Annabelle Ashworth, S Lilly Zheng, Brian T Helfand, David Duggan, Henry M Dunnenberger, Peter J Hulick and 4 more

Abstract read
In one paragraph

Article in International journal of cardiology. Cardiovascular risk and prevention, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Zhuqing ShiProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, 60201, USA.
Ashley J MulfordGenomic Health Initiative, Endeavor Health, Evanston, IL, 60201, USA.
Jun WeiProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, 60201, USA.
Huy TranProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, 60201, USA.
Annabelle AshworthProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, 60201, USA.
S Lilly ZhengProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, 60201, USA.
Brian T HelfandDepartment of Surgery, Endeavor Health, Evanston, IL, 60201, USA.
David DugganTranslational Genomics Research Institute, TGen - an Affiliate of City of Hope, Phoenix, AZ,USA.
Henry M DunnenbergerNeaman Center for Personalized Medicine, Endeavor 1001 University Place, Health, Evanston, IL,60201, USA.
Peter J HulickNeaman Center for Personalized Medicine, Endeavor 1001 University Place, Health, Evanston, IL,60201, USA.
David J DavidsonCardiovascular Institute, Endeavor Health, 1001 University Place, Evanston, IL, 60201, USA.
Arman QamarCardiovascular Institute, Endeavor Health, 1001 University Place, Evanston, IL, 60201, USA.
Alan R SandersGenomic Health Initiative, Endeavor Health, Evanston, IL, 60201, USA.
Jianfeng XuProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, 60201, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Low-density lipoprotein cholesterol (LDL-C) levels <100 mg/dL are generally considered normal. We tested the controversial hypothesis that a subset of individuals with 'normal' LDL-C levels may have a non-negligible risk of coronary artery disease (CAD) due to inherited factors, including monogenic variants and polygenic risk scores (PGS). Methods: A retrospective analysis of a prospective cohort from the Genomic Health Initiative at Endeavor Health, including 7880 participants without a prior diagnosis of CAD and not on statins at recruitment. Participants were stratified by baseline LDL-C levels and followed for incident CAD. The association of CAD risk with carrier status for pathogenic/likely pathogenic (P/LP) variants in Results: Among participants, 31.2 % had LDL-C <100 mg/dL (normal), 39.5 % had LDL-C 100-129 mg/dL, and 29.3 % had LDL-C ≥130 mg/dL. Over a median follow-up of 8 years, CAD was diagnosed in 5.3 %, 6.9 %, and 7.6 % of participants in these LDL-C groups, respectively. Among those with normal LDL-C, CAD incidence rose to 9.5 % in individuals with high genetic risk (P/LP variants and/or high PGS). Genetic risk was significantly associated with CAD in multivariable models ( Conclusion: Individuals with 'normal' LDL-C levels can have substantial CAD risk if they carry high genetic risk. These findings underscore the importance of incorporating genetic information into CAD risk assessment, even among those with traditionally normal lipid profiles.

Indexed as

APOBCoronary artery disease (CAD)LDLRLow-density lipoprotein cholesterol (LDL-C)monogenicPCSK9Polygenic score (PGS)

Identifiers

PMID41585861
PMCPMC12828546

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Registered trials

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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.