Home > Publications Database > Transferability of European-derived Alzheimer's disease polygenic risk scores across multiancestry populations. > print |
001 | 280053 | ||
005 | 20250824001733.0 | ||
024 | 7 | _ | |a 10.1038/s41588-025-02227-w |2 doi |
024 | 7 | _ | |a pmid:40533518 |2 pmid |
024 | 7 | _ | |a pmc:PMC12283339 |2 pmc |
024 | 7 | _ | |a 1061-4036 |2 ISSN |
024 | 7 | _ | |a 1546-1718 |2 ISSN |
024 | 7 | _ | |a altmetric:178159776 |2 altmetric |
037 | _ | _ | |a DZNE-2025-00890 |
041 | _ | _ | |a English |
082 | _ | _ | |a 570 |
100 | 1 | _ | |a Nicolas, Aude |0 0009-0005-2606-2765 |b 0 |
245 | _ | _ | |a Transferability of European-derived Alzheimer's disease polygenic risk scores across multiancestry populations. |
260 | _ | _ | |a London |c 2025 |b Macmillan Publishers Limited, part of Springer Nature |
336 | 7 | _ | |a article |2 DRIVER |
336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1753363270_5553 |2 PUB:(DE-HGF) |x Letter |
336 | 7 | _ | |a ARTICLE |2 BibTeX |
336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
520 | _ | _ | |a A polygenic score (PGS) for Alzheimer's disease (AD) was derived recently from data on genome-wide significant loci in European ancestry populations. We applied this PGS to populations in 17 European countries and observed a consistent association with the AD risk, age at onset and cerebrospinal fluid levels of AD biomarkers, independently of apolipoprotein E locus (APOE). This PGS was also associated with the AD risk in many other populations of diverse ancestries. A cross-ancestry polygenic risk score improved the association with the AD risk in most of the multiancestry populations tested when the APOE region was included. Finally, we found that the PGS/polygenic risk score captured AD-specific information because the association weakened as the diagnosis was broadened. In conclusion, a simple PGS captures the AD-specific genetic information that is common to populations of different ancestries, although studies of more diverse populations are still needed to better characterize the genetics of AD. |
536 | _ | _ | |a 353 - Clinical and Health Care Research (POF4-353) |0 G:(DE-HGF)POF4-353 |c POF4-353 |f POF IV |x 0 |
588 | _ | _ | |a Dataset connected to CrossRef, PubMed, , Journals: pub.dzne.de |
650 | _ | 7 | |a Apolipoproteins E |2 NLM Chemicals |
650 | _ | 7 | |a Biomarkers |2 NLM Chemicals |
650 | _ | 2 | |a Alzheimer Disease: genetics |2 MeSH |
650 | _ | 2 | |a Alzheimer Disease: epidemiology |2 MeSH |
650 | _ | 2 | |a Alzheimer Disease: cerebrospinal fluid |2 MeSH |
650 | _ | 2 | |a Humans |2 MeSH |
650 | _ | 2 | |a Multifactorial Inheritance: genetics |2 MeSH |
650 | _ | 2 | |a Genetic Predisposition to Disease |2 MeSH |
650 | _ | 2 | |a White People: genetics |2 MeSH |
650 | _ | 2 | |a Genome-Wide Association Study |2 MeSH |
650 | _ | 2 | |a Europe: epidemiology |2 MeSH |
650 | _ | 2 | |a Apolipoproteins E: genetics |2 MeSH |
650 | _ | 2 | |a Female |2 MeSH |
650 | _ | 2 | |a Risk Factors |2 MeSH |
650 | _ | 2 | |a Male |2 MeSH |
650 | _ | 2 | |a Polymorphism, Single Nucleotide |2 MeSH |
650 | _ | 2 | |a Aged |2 MeSH |
650 | _ | 2 | |a Biomarkers: cerebrospinal fluid |2 MeSH |
650 | _ | 2 | |a Genetic Risk Score |2 MeSH |
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