TY - JOUR
T1 - Translational models for vascular cognitive impairment: A review including larger species
AU - Hainsworth, Atticus H.
AU - Allan, Stuart M.
AU - Boltze, Johannes
AU - Cunningham, Catriona
AU - Farris, Chad
AU - Head, Elizabeth
AU - Ihara, Masafumi
AU - Isaacs, Jeremy D.
AU - Kalaria, Raj N.
AU - Lesnik Oberstein, Saskia A.M.J.
AU - Moss, Mark B.
AU - Nitzsche, Björn
AU - Rosenberg, Gary A.
AU - Rutten, Julie W.
AU - Salkovic-Petrisic, Melita
AU - Troen, Aron M.
PY - 2017/1/25
Y1 - 2017/1/25
N2 - Disease models are useful for prospective studies of pathology, identification of molecular and cellular mechanisms, pre-clinical testing of interventions, and validation of clinical biomarkers. Here, we review animal models relevant to vascular cognitive impairment (VCI). A synopsis of each model was initially presented by expert practitioners. Synopses were refined by the authors, and subsequently by the scientific committee of a recent conference (International Conference on Vascular Dementia 2015). Only peer-reviewed sources were cited. Methods: We included models that mimic VCI-related brain lesions (white matter hypoperfusion injury, focal ischaemia, cerebral amyloid angiopathy) or reproduce VCI risk factors (old age, hypertension, hyperhomocysteinemia, high-salt/high-fat diet) or reproduce genetic causes of VCI (CADASIL-causing Notch3 mutations). Conclusions: We concluded that (1) translational models may reflect a VCI-relevant pathological process, while not fully replicating a human disease spectrum; (2) rodent models of VCI are limited by paucity of white matter; and (3) further translational models, and improved cognitive testing instruments, are required.
AB - Disease models are useful for prospective studies of pathology, identification of molecular and cellular mechanisms, pre-clinical testing of interventions, and validation of clinical biomarkers. Here, we review animal models relevant to vascular cognitive impairment (VCI). A synopsis of each model was initially presented by expert practitioners. Synopses were refined by the authors, and subsequently by the scientific committee of a recent conference (International Conference on Vascular Dementia 2015). Only peer-reviewed sources were cited. Methods: We included models that mimic VCI-related brain lesions (white matter hypoperfusion injury, focal ischaemia, cerebral amyloid angiopathy) or reproduce VCI risk factors (old age, hypertension, hyperhomocysteinemia, high-salt/high-fat diet) or reproduce genetic causes of VCI (CADASIL-causing Notch3 mutations). Conclusions: We concluded that (1) translational models may reflect a VCI-relevant pathological process, while not fully replicating a human disease spectrum; (2) rodent models of VCI are limited by paucity of white matter; and (3) further translational models, and improved cognitive testing instruments, are required.
UR - http://www.scopus.com/inward/record.url?scp=85010817825&partnerID=8YFLogxK
U2 - 10.1186/s12916-017-0793-9
DO - 10.1186/s12916-017-0793-9
M3 - Short survey
C2 - 28118831
AN - SCOPUS:85010817825
SN - 1078-8956
VL - 15
JO - BMC Medicine
JF - BMC Medicine
IS - 1
M1 - 16
ER -