Fasting blood glucose and cerebrospinal fluid Alzheimer’s biomarkers in non-diabetic cognitively normal elders: the CABLE study
Author(s) -
YaNan Ou,
XueNing Shen,
HeYing Hu,
Hao Hu,
Zuo-Teng Wang,
Wei Xu,
Qiang Dong,
Lan Tan,
JinTai Yu
Publication year - 2020
Publication title -
aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 90
ISSN - 1945-4589
DOI - 10.18632/aging.102921
Subject(s) - cerebrospinal fluid , medicine , biomarker , apolipoprotein e , endocrinology , diabetes mellitus , alzheimer's disease , apolipoprotein b , plasma glucose , disease , biology , cholesterol , biochemistry
It is unclear how blood glucose levels mediate the pathology of Alzheimer's disease (AD). This study aimed to investigate whether fasting blood glucose (FBG) levels are associated with cerebrospinal fluid (CSF) biomarkers preferentially affected by AD in non-diabetic cognitively normal elders. A total of 499 non-diabetic cognitively normal elders were from the Chinese Alzheimer's Biomarker and LifestyLE (CABLE) study. We detected the associations of FBG with individual CSF measures using multiple linear regression models controlling for age, sex, educational level, and apolipoprotein E ( APOE) ε4 genotype. Fasting blood glucose level was positively correlated with CSF Aβ 42 level (β = 0.045, p = 0.010), CSF Aβ 42 /Aβ 40 ratio (β = 0.005, p < 0.001), Aβ 42 /P-tau ratio (β = 0.282, p = 0.013), and Aβ 42 /T-tau ratio (β = 0.050, p = 0.040). Interaction analysis indicated that gender affected the correlations of FBG level with CSF Aβ 40 (p < 0.001) and Aβ 42 /Aβ 40 ratio (p < 0.001). This study raises additional questions about the role of blood glucose in the predisposition to AD and supports the possibility of targeting these processes in pre-symptomatic AD trials in non-diabetic elders.
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