TY - JOUR
T1 - Cognitive Impairment and Dementia After Stroke
T2 - Design and Rationale for the DISCOVERY Study
AU - Rost, Natalia S.
AU - Meschia, James F.
AU - Gottesman, Rebecca
AU - Wruck, Lisa
AU - Helmer, Karl
AU - Greenberg, Steven M.
N1 - Funding Information:
DISCOVERY (Determinants of Incident Stroke Cognitive Outcomes and Vascular Effects on Recovery) is jointly supported by the National Institute of Neurological Disorders and Stroke (NINDS) and National Investigation Agency (NIA; U19NS115388).
Funding Information:
DISCOVERY (Determinants of Incident Stroke Cognitive Outcomes and Vascular Effects on Recovery) is jointly supported by the National Institute of Neurological Disorders and Stroke (NINDS) and National Investigation Agency (NIA; U19NS115388). Dr Rost is in part supported by National Institute of Neurological Disorders and Stroke (NINDS)/National Institute on Aging (NIA) U19NS115388, NINDS R01NS082285, NINDS R01NS086905, and she serves as Associate Editor of Stroke. Dr Meschia is in part supported by the NINDS/NIA U19NS115388, NINDS U01NS080168, and he serves as Section Editor for Genetics, Genomics, and Precision Medicine of Stroke. Dr Gottesman is in part supported by NINDS/NIA U19NS115388, National Heart, Lung, and Blood Institute (NHLBI) U01HL096812, NIA R01AG040282, K24AG052573, RF1AG050745, and she served as past Associate Editor of Neurology. Dr Wruck is in part supported by NINDS/NIA U19NS115388. Dr Helmer is in part supported by NINDS/NIA U19NS115388. Dr Greenberg is in part supported by NINDS/NIA U19NS115388, NINDS U24NS107154, U24NS100591, R01NS096730, and NIA R01AG026484.
Funding Information:
Dr Rost is in part supported by National Institute of Neurological Disorders and Stroke (NINDS)/National Institute on Aging (NIA) U19NS115388, NINDS R01NS082285, NINDS R01NS086905, and she serves as Associate Editor of Stroke. Dr Meschia is in part supported by the NINDS/NIA U19NS115388, NINDS U01NS080168, and he serves as Section Editor for Genetics, Genomics, and Precision Medicine of Stroke. Dr Gottesman is in part supported by NINDS/NIA U19NS115388, National Heart, Lung, and Blood Institute (NHLBI) U01HL096812, NIA R01AG040282, K24AG052573, RF1AG050745, and she served as past Associate Editor of Neurology. Dr Wruck is in part supported by NINDS/NIA U19NS115388. Dr Helmer is in part supported by NINDS/NIA U19NS115388. Dr Greenberg is in part supported by NINDS/NIA U19NS115388, NINDS U24NS107154, U24NS100591, R01NS096730, and NIA R01AG026484.
Publisher Copyright:
© 2021 Lippincott Williams and Wilkins. All rights reserved.
PY - 2021/8/1
Y1 - 2021/8/1
N2 - Stroke is a leading cause of the adult disability epidemic in the United States, with a major contribution from poststroke cognitive impairment and dementia (PSCID), the rates of which are disproportionally high among the health disparity populations. Despite the PSCID's overwhelming impact on public health, a knowledge gap exists with regard to the complex interaction between the acute stroke event and highly prevalent preexisting brain pathology related to cerebrovascular and Alzheimer disease or related dementia. Understanding the factors that modulate PSCID risk in relation to index stroke event is critically important for developing personalized prognostication of PSCID, targeted interventions to prevent it, and for informing future clinical trial design. The DISCOVERY study (Determinants of Incident Stroke Cognitive Outcomes and Vascular Effects on Recovery), a collaborative network of thirty clinical performance clinical sites with access to acute stroke populations and the expertise and capacity for systematic assessment of PSCID will address this critical challenge. DISCOVERY is a prospective, multicenter, observational, nested-cohort study of 8000 nondemented ischemic and hemorrhagic stroke patients enrolled at the time of index stroke and followed for a minimum of 2 years, with serial cognitive evaluations and assessments of functional outcome, with subsets undergoing research magnetic resonance imaging and positron emission tomography and comprehensive genetic/genomic and fluid biomarker testing. The overall scientific objective of this study is to elucidate mechanisms of brain resilience and susceptibility to PSCID in diverse US populations based on complex interplay between life-course exposure to multiple vascular risk factors, preexisting burden of microvascular and neurodegenerative pathology, the effect of strategic acute stroke lesions, and the mediating effect of genomic and epigenomic variation.
AB - Stroke is a leading cause of the adult disability epidemic in the United States, with a major contribution from poststroke cognitive impairment and dementia (PSCID), the rates of which are disproportionally high among the health disparity populations. Despite the PSCID's overwhelming impact on public health, a knowledge gap exists with regard to the complex interaction between the acute stroke event and highly prevalent preexisting brain pathology related to cerebrovascular and Alzheimer disease or related dementia. Understanding the factors that modulate PSCID risk in relation to index stroke event is critically important for developing personalized prognostication of PSCID, targeted interventions to prevent it, and for informing future clinical trial design. The DISCOVERY study (Determinants of Incident Stroke Cognitive Outcomes and Vascular Effects on Recovery), a collaborative network of thirty clinical performance clinical sites with access to acute stroke populations and the expertise and capacity for systematic assessment of PSCID will address this critical challenge. DISCOVERY is a prospective, multicenter, observational, nested-cohort study of 8000 nondemented ischemic and hemorrhagic stroke patients enrolled at the time of index stroke and followed for a minimum of 2 years, with serial cognitive evaluations and assessments of functional outcome, with subsets undergoing research magnetic resonance imaging and positron emission tomography and comprehensive genetic/genomic and fluid biomarker testing. The overall scientific objective of this study is to elucidate mechanisms of brain resilience and susceptibility to PSCID in diverse US populations based on complex interplay between life-course exposure to multiple vascular risk factors, preexisting burden of microvascular and neurodegenerative pathology, the effect of strategic acute stroke lesions, and the mediating effect of genomic and epigenomic variation.
KW - Alzheimer disease
KW - biomarker
KW - cognition
KW - dementia
KW - risk factor
UR - http://www.scopus.com/inward/record.url?scp=85111437389&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85111437389&partnerID=8YFLogxK
U2 - 10.1161/STROKEAHA.120.031611
DO - 10.1161/STROKEAHA.120.031611
M3 - Review article
C2 - 34039035
AN - SCOPUS:85111437389
SN - 0039-2499
VL - 52
SP - E499-E516
JO - Stroke
JF - Stroke
IS - 8
ER -