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
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