Predicted Trait | |
Reported Trait | Alzheimer's disease |
Mapped Trait(s) | Alzheimer disease (MONDO_0004975) |
Score Construction | |
PGS Name | AD-PRS_57 |
Development Method | |
Name | Clumping and Thresholding (C+T) |
Parameters | p < 1e-5, R^2 < 0.001 |
Variants | |
Original Genome Build | GRCh37 |
Number of Variants | 57 |
Effect Weight Type | beta |
PGS Source | |
PGS Catalog Publication (PGP) ID | PGP000196 |
Citation (link to publication) | Najar J et al. Alzheimers Dement (Amst) (2021) |
Ancestry Distribution | |
Source of Variant Associations (GWAS) | European: 100% 63,926 individuals (100%) |
PGS Evaluation | European: 100% 1 Sample Sets |
Study Identifiers | Sample Numbers | Sample Ancestry | Cohort(s) |
---|---|---|---|
GWAS Catalog: GCST007511 Europe PMC: 30820047 |
63,926 individuals | European | ADGC, CHARGE, EADI, GERAD, PERADES |
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 |
---|---|---|---|---|---|---|---|---|
PPM002141 | PSS001052| European Ancestry| 2,052 individuals |
PGP000196 | Najar J et al. Alzheimers Dement (Amst) (2021) |
Reported Trait: Incident dementia | HR: 1.09 [1.01, 1.19] | — | — | Age at blood sampling, birth year, sex, PCs(1-10) | — |
PPM002142 | PSS001052| European Ancestry| 2,052 individuals |
PGP000196 | Najar J et al. Alzheimers Dement (Amst) (2021) |
Reported Trait: Incident dementia in APOE ɛ4 non-carriers | HR: 1.15 [1.05, 1.27] | — | — | Age at blood sampling, birth year, sex, PCs(1-10) | — |
PPM002146 | PSS001052| European Ancestry| 2,052 individuals |
PGP000196 | Najar J et al. Alzheimers Dement (Amst) (2021) |
Reported Trait: Incident dementia in individuals aged 95 or above | HR: 1.15 [1.01, 1.32] | — | — | Age at blood sampling, birth year, sex, 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 |
---|---|---|---|---|---|---|---|---|
PSS001052 | The diagnosis of dementia at each examination was based on Diagnostic and Statistical Manual of Mental Disorders Third Edition‐Revised (DSM‐III‐R) criteria, using information from neuropsychiatric examinations and close informant interviews. Dementia diagnoses for individuals lost to follow‐up were based on information obtained from the Swedish Inpatient Registry until 2012. Age of dementia onset was based on information provided by close informants, the examinations, and the Swedish Inpatient Register. If no information could be obtained from these sources, the age of onset was determined as the mid‐point between the last examination at which dementia criteria were not fulfilled and the first with a dementia diagnosis. Information on deaths during follow‐up was obtained from the Swedish Population Registry until December 31, 2016. Of the 605 dementia cases, 182 were carriers of an APOE ɛ4 allele. | Mean = 7.2 years Sd = 4.7 years |
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European | — | NR | Gothenburg H70 Birth Cohort studies |