Combining serum and urine biomarkers in the early diagnosis of mild cognitive impairment that evolves into Alzheimer’s disease in patients with the apolipoprotein E ε4 genotype

Biomarkers ◽  
2014 ◽  
Vol 20 (1) ◽  
pp. 84-88 ◽  
Author(s):  
Chao Wang ◽  
Yongjian Cui ◽  
Jingci Yang ◽  
Jinrong Zhang ◽  
Dongcai Yuan ◽  
...  
Author(s):  
Eva Carro ◽  
Fernando Bartolomé ◽  
Félix Bermejo‐Pareja ◽  
Alberto Villarejo‐Galende ◽  
José Antonio Molina ◽  
...  

2021 ◽  
Vol 84 (6) ◽  
pp. 472-480
Author(s):  
Yulin Luo ◽  
Li Tan ◽  
Joseph Therriault ◽  
Hua Zhang ◽  
Ying Gao ◽  
...  

<b><i>Background:</i></b> Apolipoprotein E (<i>APOE</i>) ε4 is highly associated with mild cognitive impairment (MCI). However, the specific influence of <i>APOE</i> ε4 status on tau pathology and cognitive decline in early MCI (EMCI) and late MCI (LMCI) is poorly understood. Our goal was to evaluate the association of <i>APOE</i> ε4 with cerebrospinal fluid (CSF) tau levels and cognition in EMCI and LMCI patients in the Alzheimer’s Disease Neuroimaging Initiative database, and whether this association was mediated by amyloid-β (Aβ). <b><i>Methods:</i></b> Participants were 269 cognitively normal (CN), 262 EMCI, and 344 LMCI patients. They underwent CSF Aβ42 and tau detection, <i>APOE</i> ε4 genotyping, Mini-Mental State Examination, (MMSE), and Alzheimer’s disease assessment scale (ADAS)-cog assessments. Linear regressions were used to examine the relation of <i>APOE</i> ε4 and CSF tau levels and cognitive scores in persons with and without Aβ deposition (Aβ+ and Aβ−). <b><i>Results:</i></b> The prevalence of <i>APOE</i> ε4 is higher in EMCI and LMCI than in CN (<i>p</i> &#x3c; 0.001 for both), and in LMCI than in EMCI (<i>p</i> = 0.001). <i>APOE</i> ε4 allele was significantly higher in Aβ+ subjects than in Aβ− subjects (<i>p</i> &#x3c; 0.001). Subjects who had a lower CSF Aβ42 level and were <i>APOE</i> ε4-positive experienced higher levels of CSF tau and cognitive scores in EMCI and/or LMCI. <b><i>Conclusions:</i></b> An <i>APOE</i> ε4 allele is associated with increased CSF tau and worse cognition in both EMCI and LMCI, and this association may be mediated by Aβ. We conclude that <i>APOE</i> ε4 may be an important mediator of tau pathology and cognition in the early stages of AD.


Neurocase ◽  
2005 ◽  
Vol 11 (1) ◽  
pp. 3-7 ◽  
Author(s):  
Neelum T. Aggarwal ◽  
Robert S. Wilson ◽  
Todd L. beck ◽  
Julia L. bienias ◽  
Elizabeth Berry-Kravis ◽  
...  

2020 ◽  
Author(s):  
Peter Lee ◽  
Hang-Rai Kim ◽  
Yong Jeong

Abstract There have been several MR imaging biomarkers of Alzheimer’s disease (AD) for early diagnosis. Cortical mean diffusivity (MD) is one of them for the study of the cortical microstructural change in AD. However, several factors may overshadow the feasibility of MD as AD biomarker. Thus, current study investigated feasible gray matter microstructure biomarker with higher sensitivity for early AD detection. With the aim of facilitating the early detection of AD, the Alzheimer’s Disease Neuroimaging Initiative (ADNI) proposed two stages based on the memory performance: early mild cognitive impairment (EMCI) and late mild cognitive impairment (LMCI). We propose single shell DTI measure, ‘ radiality ’, for early AD biomarker. It is a dot product between cortical surface normal vector and primary diffusion direction, which presumably reflects the fiber orientation within the cortical column. Here, we gathered images from ADNI phase 2 & 3; 78 cognitive normal, 51 EMCI, 34 LMCI, and 39 AD patients. Then, we evaluated cortical thickness (CTh), MD, amount of amyloid and tau accumulations using PET, which are conventional AD biomarkers. Radiality was projected on gray matter surface to compare and validate the changes along other neuroimage biomarkers. Results showed decreased radiality primarily in entorhinal, insula, frontal and temporal cortex as disease progress onward. Especially, radiality could delineate the difference between cognitive normal and EMCI group while other biomarkers could not. We looked into the relationship between the radiality and other biomarkers to validate its pathological evidence in AD. Overall, radiality showed high association with conventional biomarkers. Additional ROI analysis exhibit dynamics of AD related changes as stages onward. In conclusion, radiality in cortical gray matter showed AD specific changes and relevance with other conventional AD biomarkers with higher sensitivity. Besides, it could show group differences in early AD changes from EMCI which show advantage for early diagnosis than using conventional biomarkers. We provide the evidence of structure changes with cognitive impairment and suggest radiality as a sensitive biomarker for early diagnose and progress monitor AD.


Sign in / Sign up

Export Citation Format

Share Document