2019
DOI: 10.1161/strokeaha.118.020379
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Genetics of Vascular Cognitive Impairment

Abstract: Vascular dementia (VAD) is the second most common cause of dementia after Alzheimer's and accounts at least 20% of dementia cases. Lesser degrees of cognitive decline due to cerebrovascular disease are even more common, and the umbrella term Vascular Cognitive Impairment (VCI) has been introduced to cover all degrees of cognitive impairment due to cerebrovascular disease, from mild impairment through to dementia.(1)

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Cited by 29 publications
(35 citation statements)
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“…Other unmodifiable risk factors include female sex, although the relationship with VaD is less clear with recent data suggesting no association at least post-stroke (33). Genetic factors may also play a role, but apart from rare disorders such as CADASIL, few specific risk genes are known (39). Apolipoprotein E4 is a strong risk factor for AD especially in women, but the relationship with VaD and PSD is less clear and requires further study (39).…”
Section: Epidemiologymentioning
confidence: 99%
See 1 more Smart Citation
“…Other unmodifiable risk factors include female sex, although the relationship with VaD is less clear with recent data suggesting no association at least post-stroke (33). Genetic factors may also play a role, but apart from rare disorders such as CADASIL, few specific risk genes are known (39). Apolipoprotein E4 is a strong risk factor for AD especially in women, but the relationship with VaD and PSD is less clear and requires further study (39).…”
Section: Epidemiologymentioning
confidence: 99%
“…Genetic factors may also play a role, but apart from rare disorders such as CADASIL, few specific risk genes are known (39). Apolipoprotein E4 is a strong risk factor for AD especially in women, but the relationship with VaD and PSD is less clear and requires further study (39).…”
Section: Epidemiologymentioning
confidence: 99%
“…80 Similar conditions include CARASIL, autosomal dominant HTRA1related cerebral SVD, COL4A1/2, FOXC1/PITX2, Fabry disease, and TREX-related disease. 79,81 In addition to single-gene disorders, other genetic factors, including the ε4 allele of the APOE genotype, may play a role in post-stroke cognitive impairment, which likely reflects a connection between AD and VaD. 82…”
Section: Laboratory Biomarkersmentioning
confidence: 99%
“…The most strongly associated genetic factors of post-stroke cognitive impairment include those genes that cause inherited SVDs. 79 An example of this group of diseases is CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy), caused by a mutation in NOTCH3 gene that encodes a transmembrane receptor involved in remodeling of vascular smooth muscle and angiogenesis, resulting in significant SVD, migraine, strokes, and cognitive impairment. 80 Similar conditions include CARASIL, autosomal dominant HTRA1related cerebral SVD, COL4A1/2, FOXC1/PITX2, Fabry disease, and TREX-related disease.…”
Section: Laboratory Biomarkersmentioning
confidence: 99%
“…могут вызвать СКН; в рамках болезни мелких церебральных артерий выделяют патологические (вследствие артериальной гипертензии -АГ, сахарного диабета, амилоидной ангиопатии и др.) и генетические формы [10,11].…”
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