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Genetics of vascular dementia - review from the ICVD working group

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机构: [1]Department of Epidemiology, Erasmus MC, Rotterdam, The Netherlands. [2]Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands. [3]Department of Neurology, Erasmus MC, Rotterdam, The Netherlands. [4]Cerebrovascular Unit IRCCS Foundation Neurological Institute C. Besta, Milan, Italy. [5]Department of Neurology, University Hospital of Salamanca, Salamanca, Spain. [6]Institute of Biomedical Research of Salamanca (IBSAL), University of Salamanca-CSIC-SACYL, Salamanca, Spain. [7]Department of Neurology, Xuan Wu Hospital, Capital Medical University, Beijing, China. [8]Department of Neurology, Medical University of Graz, Graz, Austria. [9]Neuroepidemiology and Ageing Research Unit, School of Public Health, Imperial College London, London, UK. [10]Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy. [11]IBGE, Islamabad, Pakistan. [12]Department of Epidemiology, Erasmus MC University Medical Center, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
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关键词: Vascular dementia Cerebral small vessel disease Genetics Magnetic resonance imaging

摘要:
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

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出版当年[2016]版:
大类 | 1 区 医学
小类 | 1 区 医学:内科
最新[2023]版:
大类 | 1 区 医学
小类 | 1 区 医学:内科
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出版当年[2015]版:
Q1 MEDICINE, GENERAL & INTERNAL
最新[2023]版:
Q1 MEDICINE, GENERAL & INTERNAL

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第一作者机构: [1]Department of Epidemiology, Erasmus MC, Rotterdam, The Netherlands. [2]Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands. [3]Department of Neurology, Erasmus MC, Rotterdam, The Netherlands. [12]Department of Epidemiology, Erasmus MC University Medical Center, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
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通讯机构: [1]Department of Epidemiology, Erasmus MC, Rotterdam, The Netherlands. [2]Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands. [3]Department of Neurology, Erasmus MC, Rotterdam, The Netherlands. [12]Department of Epidemiology, Erasmus MC University Medical Center, Wytemaweg 80, 3015 CN Rotterdam, The Netherlands.
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