Predicted Trait | |
Reported Trait | Coronary artery disease |
Mapped Trait(s) | coronary artery disease (EFO_0001645) |
Score Construction | |
PGS Name | CAD_GRS_204 |
Development Method | |
Name | Genome-wide significant variants |
Parameters | Variants with a genome-wide significant associations with CAD in GWAS and exome-wide association studies published as of December 2017 |
Variants | |
Original Genome Build | hg19 |
Number of Variants | 204 |
Effect Weight Type | NR |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000043 |
Citation (link to publication) | Morieri ML et al. Diabetes Care (2018) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | |
PGS Evaluation | European: 100% 2 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST005194 Europe PMC: 29212778 |
296,525 individuals | NR | UKB |
GWAS Catalog: GCST004787 Europe PMC: 28714975 |
63,731 individuals | European, NR | NR |
GWAS Catalog: GCST007990 Europe PMC: 28714974 |
120,286 individuals | European | NR |
Europe PMC: 23202125 |
[
|
European, South Asian | 34 cohorts
|
Europe PMC: 28530674 |
[
|
European, South Asian, East Asian, African American or Afro-Caribbean | NR |
Europe PMC: 28584231 |
[ ,
50.81 % Male samples |
European | UKB |
Europe PMC: 26934567 |
[
|
European | NR |
Europe PMC: 28209224 |
[
|
European | NR |
GWAS Catalog: GCST000999 Europe PMC: 21378988 |
15,682 individuals | European | NR |
GWAS Catalog: GCST003116 Europe PMC: 26343387 |
3,139 individuals | African American or Afro-Caribbean | 41 cohorts
|
GWAS Catalog: GCST003116 Europe PMC: 26343387 |
4,095 individuals | Hispanic or Latin American | 41 cohorts
|
GWAS Catalog: GCST003116 Europe PMC: 26343387 |
25,557 individuals | South Asian | 41 cohorts
|
GWAS Catalog: GCST003116 Europe PMC: 26343387 |
141,217 individuals | European | 41 cohorts
|
GWAS Catalog: GCST000999 Europe PMC: 21378988 |
14,790 individuals | South Asian (India, Pakistan) |
NR |
GWAS Catalog: GCST003116 Europe PMC: 26343387 |
2,268 individuals | Greater Middle Eastern (Middle Eastern, North African or Persian) | 40 cohorts
|
GWAS Catalog: GCST003116 Europe PMC: 26343387 |
11,323 individuals | East Asian | 41 cohorts
|
PGS Performance Metric ID (PPM) |
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 |
---|---|---|---|---|---|---|---|---|
PPM000147 | PSS000092| European Ancestry| 5,360 individuals |
PGP000043 | Morieri ML et al. Diabetes Care (2018) |
Reported Trait: Major coronary events (MCE) events among Type 2 Diabetes patients | HR: 1.27 [1.18, 1.37] | — | — | age, sex, ACCORD study covariates (randomized treament assignement, clinical network, genotyping platform, PCs of genetic ancestry) | — |
PPM000148 | PSS000093| European Ancestry| 1,931 individuals |
PGP000043 | Morieri ML et al. Diabetes Care (2018) |
Reported Trait: Major coronary events (MCE) events among Type 2 Diabetes patients | HR: 1.35 [1.16, 1.58] | — | — | age, sex, ORIGIN study covariates (randomized treament assignement, PCs of genetic ancestry) | — |
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 |
---|---|---|---|---|---|---|---|---|
PSS000092 | Incident Major coronary events (MCE) are defined as: fatal or nonfatal coronary artery disease (CAD) events, nonfatal myocardial infarction, or unstable angina | Median = 4.7 years | [ ,
64.8 % Male samples |
Mean = 62.8 years | European | Self reported white | ACCORD | Type 2 Diabetes patients |
PSS000093 | Incident Major coronary events (MCE) are defined as: fatal or nonfatal coronary artery disease (CAD) events, nonfatal myocardial infarction, or unstable angina | Median = 6.2 years | [
|
— | European | Self reported white | ORIGIN | Participants are from the Outcome Reduction With Initial Glargine Intervention (ORIGIN) trial and were enrolled based on having some combination of impaired fasting glucose, impaired glucose tolerance or type 2 diabetes, and high cardiovascular risk |