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Record W4395663592 · doi:10.1101/2024.04.23.24306257

Association of Genetically Predicted Levels of Circulating Blood Lipids with Coronary Artery Disease Incidence

2024· preprint· en· W4395663592 on OpenAlexaff
Hasanga D. Manikpurage, Jasmin Ricard, Ursula Houessou, Jérôme Bourgault, Éloi Gagnon, Émilie Gobeil, Arnaud Girard, Zhonglin Li, Aïda Eslami, Patrick Mathieu, Yohan Bossé, Benoît J. Arsenault, Sébastien Thériault

Bibliographic record

VenuemedRxiv · 2024
Typepreprint
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic Associations and Epidemiology
Canadian institutionsUniversité LavalInstitut universitaire de cardiologie et de pneumologie de Québec
Fundersnot available
KeywordsIncidence (geometry)Coronary artery diseaseDiseaseMedicineInternal medicineCardiologyAssociation (psychology)Psychology

Abstract

fetched live from OpenAlex

Abstract Background Estimating the genetic risk of coronary artery disease (CAD) is now possible by aggregating data from genome-wide association studies (GWAS) into polygenic risk scores (PRS). Combining multiple PRS for specific circulating blood lipids could improve risk prediction. Here, we sought to evaluate the performance of PRS derived from CAD and blood lipids GWAS to predict the incidence of CAD. Methods This study included individuals aged between 40 and 69 recruited in UK Biobank (UKB). We conducted GWAS for blood lipids measured by nuclear magnetic resonance in individuals without lipid-lowering treatments (n=73,915). Summary statistics were used to derive and calculate PRS in the remaining participants (n=318,051). A PRS CAD was also derived using the CARDIoGRAMplusC4D GWAS. Hazard ratios (HR) for CAD (9,017 / 301,576; median follow-up time: 12.6 years) were calculated per standard deviation increase in each PRS. Discrimination capacity and goodness of fit of the models were evaluated. Results Out of 30 PRS, 28 were significantly associated with the incidence of CAD ( P <0.05). The optimal combination of PRS included PRS for CAD, VLDL-C, total cholesterol and triglycerides. Discriminative capacities were significantly increased in the model including PRS CAD and clinical risk factors (CRF) (C-statistic=0.778 [0.773-0.782]) compared to the model with CRF only (C-statistic=0.755 [0.751-0.760]). Although the C-statistic remained similar when independent lipids PRS were added to the model with PRS CAD and CRF (C-statistic=0.778 [0.773-0.783]), the goodness of fit was significantly increased (chi-square test statistic=20.18, P =1.56e-04). Conclusions Although independently associated with CAD incidence, blood lipids PRS provide modest improvement in the predictive performance when added to PRS CAD . Highlights Genome-wide association studies were conducted on 29 selected lipid traits measured by nuclear magnetic resonance spectroscopy in 73,915 participants from UK Biobank who were not taking lipid-lowering treatment. Polygenic risk scores for 27 out of 29 of these traits were associated with the incidence of coronary artery disease (CAD) in 9,017 cases out of 301,576 individuals followed for a median of 12.6 years. When combined to a PRS for coronary artery disease, there was a significant but modest improvement in the discrimination capacity for incident CAD. PRS for certain lipid traits might help to stratify the risk of CAD. Graphical Abstract

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.003
metaresearch head score (Gemma)0.009
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.016

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0030.009
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0030.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.015
GPT teacher head0.254
Teacher spread0.240 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations1
Published2024
Admission routes1
Has abstractyes

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