دورية أكاديمية

The relationship between VEGF and cerebral vascular territory glucose metabolism is modified by cardiovascular risk in Alzheimer's disease ; Neuroimaging / Optimal neuroimaging measures for early detection

التفاصيل البيبلوغرافية
العنوان: The relationship between VEGF and cerebral vascular territory glucose metabolism is modified by cardiovascular risk in Alzheimer's disease ; Neuroimaging / Optimal neuroimaging measures for early detection
المؤلفون: Tubi, Meral A, Matsiyevskiy, Elizabeth, Hapenney, Matthew N, Riedel, Brandalyn C, Mack, Wendy J, King, Kevin, Thompson, Paul M, Braskie, Meredith N
المصدر: Alzheimer's & Dementia ; volume 16, issue S5 ; ISSN 1552-5260 1552-5279
بيانات النشر: Wiley
سنة النشر: 2020
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: Background Vascular endothelial growth factor (VEGF) regulates angiogenesis, neurogenesis, and glucose transport. Cardiovascular risk factors promote atherosclerosis and disrupt vascular integrity, possibly interfering with VEGF function. Variability in cardiovascular dysfunction severity may explain an inconsistent neuroprotective effect of VEGF across Alzheimer’s disease (AD) studies. Atherosclerosis in the middle and posterior cerebral arteries is associated with AD. We hypothesize that a higher Framingham Risk Score (FRS), a proxy for atherosclerosis severity, will moderate the association between VEGF and glucose metabolism in brain regions supplied by the MCA and PCA. Method In 158 participants (age: 55‐90 years; 39 normal, 80 MCI, 39 AD; 105M/53F) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI), we evaluated whether CSF VEGF levels were associated with bilateral glucose metabolism (FDG‐PET) in gray matter vascular territories supplied by the anterior (ACA), middle (MCA), and posterior cerebral arteries (PCA), each defined by the vascular territory MNI template (Figure‐1, Figure‐2). We evaluated whether FRS modified the regional relationship between VEGF (Figure‐3) and FDG‐PET across all participants and within each diagnostic group. We used a mixed effects linear regression model (covarying for age, sex, education, APOE 4 carrier status, CSF T‐tau, and diagnosis; random effect=site). All p ‐values presented are false discovery rate (FDR) corrected at FDR <5%. Result Higher VEGF was associated with higher FDG‐PET MCA‐SUVR (β=0.170, p =0.043), nominally associated with higher PCA‐SUVR (β=0.129, p =0.078), and not associated with ACA‐SUVR (β=0.092, p =0.244). In all participants, FRS nominally modified the association between VEGF and ACA‐SUVR (VEGF‐FRS interaction β=‐0.040, p =0.066) and MCA‐SUVR (VEGF‐FRS interaction β=‐0.032, p =0.066). In MCI participants alone, FRS significantly modified the association between VEGF and both ACA‐SUVR (VEGF‐FRS interaction β=‐0.078, p =0.014) and ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1002/alz.042308
الإتاحة: https://doi.org/10.1002/alz.042308Test
حقوق: http://onlinelibrary.wiley.com/termsAndConditions#vorTest
رقم الانضمام: edsbas.B243F18D
قاعدة البيانات: BASE