Publication Information (EuropePMC) | |
Title | Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. |
PubMed ID | 32887874(Europe PMC) |
doi | 10.1038/s41467-020-17558-x |
Publication Date | Sept. 4, 2020 |
Journal | Nat Commun |
Author(s) | Saw J, Yang ML, Trinder M, Tcheandjieu C, Xu C, Starovoytov A, Birt I, Mathis MR, Hunker KL, Schmidt EM, Jackson L, Fendrikova-Mahlay N, Zawistowski M, Brummett CM, Zoellner S, Katz A, Coleman DM, Swan K, O'Donnell CJ, Million Veteran Program, Zhou X, Li JZ, Gornik HL, Assimes TL, Stanley JC, Brunham LR, Ganesh SK. |
Polygenic Score ID & Name | PGS Publication ID (PGP) | Reported Trait | Mapped Trait(s) (Ontology) | Number of Variants |
Ancestry distribution GWAS Dev Eval |
Scoring File (FTP Link) |
---|---|---|---|---|---|---|
PGS004899 (PRS_SCAD) |
PGP000629 | Saw J et al. Nat Commun (2020) |
Spontaneous coronary artery dissection | spontaneous coronary artery dissection | 7 | - |
https://ftp.ebi.ac.uk/pub/databases/spot/pgs/scores/PGS004899/ScoringFiles/PGS004899.txt.gz |
PGS Performance Metric ID (PPM) |
Evaluated Score |
PGS Sample Set ID (PSS) |
Performance Source | Trait |
PGS Effect Sizes (per SD change) |
Classification Metrics | Other Metrics | Covariates Included in the Model |
PGS Performance: Other Relevant Information |
---|---|---|---|---|---|---|---|---|---|
PPM021316 | PGS004899 (PRS_SCAD) |
PSS011682| Ancestry Not Reported| 412 individuals |
PGP000629 | Saw J et al. Nat Commun (2020) |
Reported Trait: Spontaneous coronary artery dissection | OR: 1.82 [1.09, 3.02] β: 0.597 (0.259) |
— | — | Age, sex | — |
PPM021317 | PGS004899 (PRS_SCAD) |
PSS011685| European Ancestry| 373,056 individuals |
PGP000629 | Saw J et al. Nat Commun (2020) |
Reported Trait: Myocardial infarction | HR: 0.91 [0.89, 0.93] β: -0.094 (0.011) |
— | — | Age, sex, genotyping array and batch, PCs (1-4) | — |
PPM021318 | PGS004899 (PRS_SCAD) |
PSS011685| European Ancestry| 373,056 individuals |
PGP000629 | Saw J et al. Nat Commun (2020) |
Reported Trait: Myocardial infarction in males | HR: 0.91 [0.89, 0.93] β: -0.092 (0.013) |
— | — | Age, genotyping array and batch, PCs (1-4) | — |
PPM021319 | PGS004899 (PRS_SCAD) |
PSS011685| European Ancestry| 373,056 individuals |
PGP000629 | Saw J et al. Nat Commun (2020) |
Reported Trait: Myocaridal infarction in females | HR: 0.91 [0.87, 0.95] β: -0.099 (0.022) |
— | — | Age, genotyping array and batch, PCs (1-4) | — |
PPM021320 | PGS004899 (PRS_SCAD) |
PSS011683| European Ancestry| 294,465 individuals |
PGP000629 | Saw J et al. Nat Commun (2020) |
Reported Trait: Coronary artery disease | β: -0.05 (0.004) OR: 0.95 [0.94, 0.96] |
— | — | Age (at the time of event in cases and at the time of last VA visit prior to August 2018 for controls), sex, PCs(1-10) | — |
PPM021321 | PGS004899 (PRS_SCAD) |
PSS011683| European Ancestry| 294,465 individuals |
PGP000629 | Saw J et al. Nat Commun (2020) |
Reported Trait: Coronary artery disease in males | OR: 0.95 [0.94, 0.96] β: -0.05 (0.004) |
— | — | Age (at the time of event in cases and at the time of last VA visit prior to August 2018 for controls), PCs(1-10) | — |
PPM021322 | PGS004899 (PRS_SCAD) |
PSS011684| European Ancestry| 314,434 individuals |
PGP000629 | Saw J et al. Nat Commun (2020) |
Reported Trait: Myocardial infarction | OR: 0.96 [0.95, 0.98] β: -0.04 (0.009) |
— | — | Age (at the time of event in cases and at the time of last VA visit prior to August 2018 for controls), sex, PCs(1-10) | — |
PPM021323 | PGS004899 (PRS_SCAD) |
PSS011684| European Ancestry| 314,434 individuals |
PGP000629 | Saw J et al. Nat Commun (2020) |
Reported Trait: Myocardial infarction in males | OR: 0.96 [0.95, 0.98] β: -0.039 (0.009) |
— | — | Age (at the time of event in cases and at the time of last VA visit prior to August 2018 for controls), PCs(1-10) | — |
PGS Sample Set ID (PSS) |
Phenotype Definitions and Methods | Participant Follow-up Time | Sample Numbers | Age of Study Participants | Sample Ancestry | Additional Ancestry Description | Cohort(s) | Additional Sample/Cohort Information |
---|---|---|---|---|---|---|---|---|
PSS011685 | MI events were defined pre- enrollment by self-reported medical history and post-enrollment by hospital epi- sode statistics using ICD, Version 10 diagnosis codes (I21, I22, I23, or I24). Events were censored on the date of loss to follow-up, death, or if individuals remained event free up to March 31, 2017. | — | [ ,
45.86 % Male samples |
— | European | — | UKB | — |
PSS011682 | All individuals had multifocal FMD. Cases show those with spontaneous coronary artery dissection. | — | [
|
— | Not reported | — | CCGB | Cases from Cleveland Clinic FMD Biorepository |
PSS011683 | An individual was classified as a case if he or she had ≥1 admission to a VA hospital with discharge diagnosis of acute myocardial infarction (AMI) or ≥1 procedure code for revascularization of the coronary arteries or ≥2 ICD codes for CAD (410-414) on ≥2 dates. | — | [
|
— | European | — | MVP | — |
PSS011684 | Cases are individuals with evidence of hospitilisation for myocardial infarction. | — | [
|
— | European | — | MVP | — |