Presenilin-1 (PSEN1) Mutations: Clinical Phenotypes beyond Alzheimer's Disease
DC Field | Value | Language |
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dc.contributor.author | Yang, Youngsoon | - |
dc.contributor.author | Bagyinszky, Eva | - |
dc.contributor.author | An, Seong Soo A. | - |
dc.date.accessioned | 2023-06-11T02:40:55Z | - |
dc.date.available | 2023-06-11T02:40:55Z | - |
dc.date.created | 2023-05-30 | - |
dc.date.issued | 2023-05 | - |
dc.identifier.issn | 1661-6596 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/88052 | - |
dc.description.abstract | Presenilin 1 (PSEN1) is a part of the gamma secretase complex with several interacting substrates, including amyloid precursor protein (APP), Notch, adhesion proteins and beta catenin. PSEN1 has been extensively studied in neurodegeneration, and more than 300 PSEN1 mutations have been discovered to date. In addition to the classical early onset Alzheimer's disease (EOAD) phenotypes, PSEN1 mutations were discovered in several atypical AD or non-AD phenotypes, such as frontotemporal dementia (FTD), Parkinson's disease (PD), dementia with Lewy bodies (DLB) or spastic paraparesis (SP). For example, Leu113Pro, Leu226Phe, Met233Leu and an Arg352 duplication were discovered in patients with FTD, while Pro436Gln, Arg278Gln and Pro284Leu mutations were also reported in patients with motor dysfunctions. Interestingly, PSEN1 mutations may also impact non-neurodegenerative phenotypes, including PSEN1 Pro242fs, which could cause acne inversa, while Asp333Gly was reported in a family with dilated cardiomyopathy. The phenotypic diversity suggests that PSEN1 may be responsible for atypical disease phenotypes or types of disease other than AD. Taken together, neurodegenerative diseases such as AD, PD, DLB and FTD may share several common hallmarks (cognitive and motor impairment, associated with abnormal protein aggregates). These findings suggested that PSEN1 may interact with risk modifiers, which may result in alternative disease phenotypes such as DLB or FTD phenotypes, or through less-dominant amyloid pathways. Next-generation sequencing and/or biomarker analysis may be essential in clearly differentiating the possible disease phenotypes and pathways associated with non-AD phenotypes. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | MDPI | - |
dc.relation.isPartOf | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - |
dc.title | Presenilin-1 (PSEN1) Mutations: Clinical Phenotypes beyond Alzheimer's Disease | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.description.journalClass | 1 | - |
dc.identifier.wosid | 000986982300001 | - |
dc.identifier.doi | 10.3390/ijms24098417 | - |
dc.identifier.bibliographicCitation | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.24, no.9 | - |
dc.description.isOpenAccess | Y | - |
dc.identifier.scopusid | 2-s2.0-85159288520 | - |
dc.citation.title | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - |
dc.citation.volume | 24 | - |
dc.citation.number | 9 | - |
dc.contributor.affiliatedAuthor | Bagyinszky, Eva | - |
dc.contributor.affiliatedAuthor | An, Seong Soo A. | - |
dc.type.docType | Review | - |
dc.subject.keywordAuthor | presenilin-1 | - |
dc.subject.keywordAuthor | Alzheimer&apos | - |
dc.subject.keywordAuthor | s disease | - |
dc.subject.keywordAuthor | frontotemporal dementia | - |
dc.subject.keywordAuthor | motor diseases | - |
dc.subject.keywordAuthor | dementia with Lewy bodies | - |
dc.subject.keywordAuthor | acne inversa | - |
dc.subject.keywordAuthor | dilated cardiomyopathy | - |
dc.subject.keywordAuthor | risk modifier | - |
dc.subject.keywordPlus | LEWY BODY PATHOLOGY | - |
dc.subject.keywordPlus | FRONTOTEMPORAL DEMENTIA | - |
dc.subject.keywordPlus | TAU PHOSPHORYLATION | - |
dc.subject.keywordPlus | GENE-MUTATIONS | - |
dc.subject.keywordPlus | PICKS-DISEASE | - |
dc.subject.keywordPlus | WILD-TYPE | - |
dc.subject.keywordPlus | ONSET | - |
dc.subject.keywordPlus | BODIES | - |
dc.subject.keywordPlus | GENERATION | - |
dc.subject.keywordPlus | EXPRESSION | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
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