TY - JOUR
T1 - Capillary function progressively deteriorates in prodromal Alzheimer’s disease
T2 - A longitudinal MRI perfusion study
AU - Madsen, Lasse S.
AU - Nielsen, Rune B.
AU - Parbo, Peter
AU - Ismail, Rola
AU - Mikkelsen, Irene K.
AU - Gottrup, Hanne
AU - Østergaard, Leif
AU - Brooks, David J.
AU - Eskildsen, Simon F.
PY - 2022
Y1 - 2022
N2 - Cardiovascular risk factors are associated with the development of Alzheimer’s disease (AD), and increasing evidence suggests that cerebral microvascular dysfunction plays a vital role in the disease progression. Using magnetic resonance imaging, we investigated the two-year changes of the cerebral microvascular blood flow in 11 mild cognitively impaired (MCI) patients with prodromal AD compared to 12 MCI patients without evidence of AD and 10 cognitively intact age-matched controls. The pAD-MCI patients displayed widespread deterioration in microvascular cerebral perfusion associated with capillary dysfunction. No such changes were observed in the other two groups, suggesting that the dysfunction in capillary perfusion is linked to the AD pathophysiology. The observed capillary dysfunction may limit local oxygenation in AD leading to downstream β-amyloid aggregation, tau hyperphosphorylation, neuroinflammation and neuronal dysfunction. The findings are in agreement with the capillary dysfunction hypothesis of AD, suggesting that increasing heterogeneity of capillary blood flow is a primary pathological event in AD.
AB - Cardiovascular risk factors are associated with the development of Alzheimer’s disease (AD), and increasing evidence suggests that cerebral microvascular dysfunction plays a vital role in the disease progression. Using magnetic resonance imaging, we investigated the two-year changes of the cerebral microvascular blood flow in 11 mild cognitively impaired (MCI) patients with prodromal AD compared to 12 MCI patients without evidence of AD and 10 cognitively intact age-matched controls. The pAD-MCI patients displayed widespread deterioration in microvascular cerebral perfusion associated with capillary dysfunction. No such changes were observed in the other two groups, suggesting that the dysfunction in capillary perfusion is linked to the AD pathophysiology. The observed capillary dysfunction may limit local oxygenation in AD leading to downstream β-amyloid aggregation, tau hyperphosphorylation, neuroinflammation and neuronal dysfunction. The findings are in agreement with the capillary dysfunction hypothesis of AD, suggesting that increasing heterogeneity of capillary blood flow is a primary pathological event in AD.
UR - http://dx.doi.org/10.1016/j.nbas.2022.100035
U2 - 10.1016/j.nbas.2022.100035
DO - 10.1016/j.nbas.2022.100035
M3 - Journal article
C2 - 36908896
SN - 2589-9589
VL - 2
JO - Aging Brain
JF - Aging Brain
M1 - 100035
ER -