Cerebral Blood Flow Predicts Conversion of Mild Cognitive Impairment into Alzheimer's Disease and Cognitive Decline: An Arterial Spin Labeling Follow-up Study

被引:31
作者
Duan, Wenna [1 ]
Zhou, Grace D. [1 ]
Balachandrasekaran, Arvind [2 ]
Bhumkar, Ashish B. [1 ]
Boraste, Paresh B. [1 ]
Becker, James T. [3 ]
Kuller, Lewis H. [4 ]
Lopez, Oscar L. [5 ]
Gach, H. Michael [6 ]
Dai, Weiying [1 ]
机构
[1] SUNY Binghamton, Comp Sci, Binghamton, NY 13902 USA
[2] Harvard Med Sch, Boston Childrens Hosp, Boston, MA 02115 USA
[3] Univ Pittsburgh, Psychiat Psychol & Neurol, Pittsburgh, PA USA
[4] Univ Pittsburgh, Dept Epidemiol, Pittsburgh, PA 15261 USA
[5] Univ Pittsburgh, Neurol & Psychiat, Pittsburgh, PA USA
[6] Washington Univ, Radiat Oncol Radiol & Biomed Engn, St Louis, MO 63110 USA
关键词
Alzheimer's disease; arterial spin labeling; cerebral blood flow; longitudinal study; mild cognitive impairment; prediction; POSITRON-EMISSION-TOMOGRAPHY; CARDIOVASCULAR HEALTH; AMYLOID DEPOSITION; GLUCOSE-METABOLISM; CSF BIOMARKERS; PERFUSION MRI; FDG-PET; MCI; DEMENTIA; MEMORY;
D O I
10.3233/JAD-210199
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: This is the first longitudinal study to assess regional cerebral blood flow (rCBF) changes during the progression from normal control (NC) through mild cognitive impairment (MCI) and Alzheimer's disease (AD). Objective: We aim to determine if perfusion MRI biomarkers, derived from our prior cross-sectional study, can predict the onset and cognitive decline of AD. Methods: Perfusion MRIs using arterial spin labeling (ASL) were acquired in 15 stable-NC, 14 NC-to-MCI, 16 stable-MCI, and 18 MCI/AD-to-AD participants from the Cardiovascular Health Study (CHS) cognition study. Group comparisons, predictions of AD conversion and time to conversion, and Modified Mini-Mental State Examination (3MSE) from rCBF were performed. Results: Compared to the stable-NC group: 1) the stable-MCI group exhibited rCBF decreases in the right temporoparietal (p = 0.00010) and right inferior frontal and insula (p = 0.0094) regions; and 2) the MCI/AD-to-AD group exhibited rCBF decreases in the bilateral temporoparietal regions (p = 0.00062 and 0.0035). Compared to the NC-to-MCI group, the stableMCI group exhibited a rCBF decrease in the right hippocampus region (p = 0.0053). The baseline rCBF values in the posterior cingulate cortex (PCC) (p = 0.0043), bilateral superior medial frontal regions (BSMF) (p = 0.012), and left inferior frontal (p = 0.010) regions predicted the 3MSE scores for all the participants at follow-up. The baseline rCBF in the PCC and BSMF regions predicted the conversion and time to conversion from MCI to AD (p < 0.05; not significant after multiple corrections). Conclusion: We demonstrated the feasibility of ASL in detecting rCBF changes in the typical AD-affected regions and the predictive value of baseline rCBF on AD conversion and cognitive decline.
引用
收藏
页码:293 / 305
页数:13
相关论文
共 82 条
  • [61] MEMORY AND REGIONAL CEREBRAL BLOOD-FLOW IN MILDLY SYMPTOMATIC ALZHEIMERS-DISEASE
    REED, BR
    JAGUST, WJ
    SEAB, JP
    OBER, BA
    [J]. NEUROLOGY, 1989, 39 (11) : 1537 - 1539
  • [62] Preclinical evidence of Alzheimer's disease in persons homozygous for the epsilon 4 allele for apolipoprotein E
    Reiman, EM
    Caselli, RJ
    Yun, LS
    Chen, KW
    Bandy, D
    Minoshima, S
    Thibodeau, SN
    Osborne, D
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (12) : 752 - 758
  • [63] Metabolic correlates of clinical heterogeneity in questionable Alzheimer's disease
    Salmon, Eric
    Lekeu, Francoise
    Garraux, Gaetan
    Guillaume, Benedicte
    Magis, Delphine
    Luxen, A.
    Moonen, G.
    Collette, F.
    [J]. NEUROBIOLOGY OF AGING, 2008, 29 (12) : 1823 - 1829
  • [64] High-precision plasma β-amyloid 42/40 predicts current and future brain amyloidosis
    Schindler, Suzanne E.
    Bollinger, James G.
    Ovod, Vitaliy
    Mawuenyega, Kwasi G.
    Li, Yan
    Gordon, Brian A.
    Holtzman, David M.
    Morris, John C.
    Benzinger, Tammie L. S.
    Xiong, Chengjie
    Fagan, Anne M.
    Bateman, Randall J.
    [J]. NEUROLOGY, 2019, 93 (17) : E1647 - E1659
  • [65] Alzheimer's disease: Genes, proteins, and therapy
    Selkoe, DJ
    [J]. PHYSIOLOGICAL REVIEWS, 2001, 81 (02) : 741 - 766
  • [66] Cerebral metabolic and cognitive decline in persons at genetic risk for Alzheimer's disease
    Small, GW
    Ercoli, LM
    Silverman, DHS
    Huang, SC
    Komo, S
    Bookheimer, SY
    Lavretsky, H
    Miller, K
    Siddarth, P
    Rasgon, NL
    Mazziotta, JC
    Saxena, S
    Wu, HM
    Mega, MS
    Cummings, JL
    Saunders, AM
    Pericak-Vance, MA
    Roses, AD
    Barrio, JR
    Phelps, ME
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) : 6037 - 6042
  • [67] A longitudinal characterization of perfusion in the aging brain and associations with cognition and neural structure
    Staffaroni, Adam M.
    Cobigo, Yann
    Elahi, Fanny M.
    Casaletto, Kaitlin B.
    Walters, Samantha M.
    Wolf, Amy
    Lindbergh, Cutter A.
    Rosen, Howard J.
    Kramer, Joel H.
    [J]. HUMAN BRAIN MAPPING, 2019, 40 (12) : 3522 - 3533
  • [68] Longitudinal stability of CSF tau levels in Alzheimer patients
    Sunderland, T
    Wolozin, B
    Galasko, D
    Levy, J
    Dukoff, R
    Bahro, M
    Lasser, R
    Motter, R
    Lehtimäki, T
    Seubert, P
    [J]. BIOLOGICAL PSYCHIATRY, 1999, 46 (06) : 750 - 755
  • [69] TENG EL, 1987, J CLIN PSYCHIAT, V48, P314
  • [70] A Novel Grading Biomarker for the Prediction of Conversion From Mild Cognitive Impairment to Alzheimer's Disease
    Tong, Tong
    Gao, Qinquan
    Guerrero, Ricardo
    Ledig, Christian
    Chen, Liang
    Rueckert, Daniel
    [J]. IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2017, 64 (01) : 155 - 165