Please use this identifier to cite or link to this item:
https://doi.org/10.1186/s12916-017-0813-9
Title: | Genetics of vascular dementia - review from the ICVD working group | Authors: | Ikram, M.A Bersano, A Manso-Calderón, R Jia, J.-P Schmidt, H Middleton, L Nacmias, B Siddiqi, S Adams, H.H.H |
Keywords: | Alzheimer disease autosomal dominant disorder autosomal recessive disorder CADASIL CARASIL cerebrovascular accident cerebrovascular disease COL4A1 gene disease association Fabry disease gene gene identification genetics genome-wide association study GLA gene HTRA1 gene human monogenic disorder multiinfarct dementia NOTCH3 gene phenotype retinal vasculopathy with cerebral leukodystrophy Review TREX1 gene dementia diagnostic imaging disease course genetic polymorphism genetics multiinfarct dementia nuclear magnetic resonance imaging apolipoprotein E aryldialkylphosphatase Apolipoproteins E Aryldialkylphosphatase Dementia Dementia, Vascular Disease Progression Humans Magnetic Resonance Imaging Polymorphism, Genetic |
Issue Date: | 2017 | Citation: | Ikram, M.A, Bersano, A, Manso-Calderón, R, Jia, J.-P, Schmidt, H, Middleton, L, Nacmias, B, Siddiqi, S, Adams, H.H.H (2017). Genetics of vascular dementia - review from the ICVD working group. BMC Medicine 15 (1) : 48. ScholarBank@NUS Repository. https://doi.org/10.1186/s12916-017-0813-9 | Rights: | Attribution 4.0 International | Abstract: | Background: Vascular dementia is a common disorder resulting in considerable morbidity and mortality. Determining the extent to which genes play a role in disease susceptibility and their pathophysiological mechanisms could improve our understanding of vascular dementia, leading to a potential translation of this knowledge to clinical practice. Discussion: In this review, we discuss what is currently known about the genetics of vascular dementia. The identification of causal genes remains limited to monogenic forms of the disease, with findings for sporadic vascular dementia being less robust. However, progress in genetic research on associated phenotypes, such as cerebral small vessel disease, Alzheimer's disease, and stroke, have the potential to inform on the genetics of vascular dementia. We conclude by providing an overview of future developments in the field and how such work could impact patients and clinicians. Conclusion: The genetic background of vascular dementia is well established for monogenic disorders, but remains relatively obscure for the sporadic form. More work is needed for providing robust findings that might eventually lead to clinical translation. @ 2017 The Author(s). | Source Title: | BMC Medicine | URI: | https://scholarbank.nus.edu.sg/handle/10635/179519 | ISSN: | 17417015 | DOI: | 10.1186/s12916-017-0813-9 | Rights: | Attribution 4.0 International |
Appears in Collections: | Elements Staff Publications |
Show full item record
Files in This Item:
File | Description | Size | Format | Access Settings | Version | |
---|---|---|---|---|---|---|
10_1186_s12916-017-0813-9.pdf | 980.25 kB | Adobe PDF | OPEN | None | View/Download |
This item is licensed under a Creative Commons License