Abstract
We present a comprehensive global analysis of genetic variants associated with autosomal-dominant Alzheimer's disease (ADAD). A total of 550 variants in the APP, PSEN1 and PSEN2 genes were identified, of which 279 were classified as pathogenic or likely pathogenic based on American College of Medical Genetics and Genomics and the Association for Molecular Pathology criteria, utilizing data from the Dominantly Inherited Alzheimer Network (DIAN), literature and public databases. Symptomatic age at onset (AAO) data were estimated for 227 of these variants, allowing detailed characterization of their frequency, pathogenicity and AAO. Importantly, 226 variants met eligibility criteria for inclusion in disease-modifying clinical trials. Furthermore, we demonstrated the predictive value of mean variant AAO and parental AAO in predicting symptomatic AAO, validated against converters who became symptomatic during follow-up in the DIAN Observational Study. This dataset provides critical insights into the global landscape of ADAD and reveals the genetic and AAO heterogeneity of ADAD variants while refining variant trial eligibility criteria.
| Original language | English |
|---|---|
| Pages (from-to) | 2429-2440 |
| Number of pages | 12 |
| Journal | Brain |
| Volume | 148 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 2025 Jul 1 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2025 Oxford University Press. All rights reserved.
Keywords
- amyloid precursor protein
- pathogenicity
- presenilin-1
- presenilin-2
- prevalence
ASJC Scopus subject areas
- Clinical Neurology
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