TY - JOUR
T1 - The association of glucose metabolism measures and diabetes status with Alzheimer's disease biomarkers of amyloid and tau
T2 - a systematic review and meta-analysis
AU - van Gils, Veerle
AU - Rizzo, Marianna
AU - Côte, Jade
AU - Viechtbauer, Wolfgang
AU - Fanelli, Giuseppe
AU - Salas-Salvadó, Jordi
AU - Wimberley, Theresa
AU - Bulló, Mònica
AU - Fernandez-Aranda, Fernando
AU - Dalsgaard, Søren
AU - Visser, Pieter Jelle
AU - Jansen, Willemijn J
AU - Vos, Stephanie J B
PY - 2024/4
Y1 - 2024/4
N2 - Conflicting evidence exists on the relationship between diabetes mellitus (DM) and Alzheimer's disease (AD) biomarkers. Therefore, we conducted a random-effects meta-analysis to evaluate the correlation of glucose metabolism measures (glycated hemoglobin, fasting blood glucose, insulin resistance indices) and DM status with AD biomarkers of amyloid-β and tau measured by positron emission tomography or cerebrospinal fluid. We selected 37 studies from PubMed and Embase, including 11,694 individuals. More impaired glucose metabolism and DM status were associated with higher tau biomarkers (r=0.11[0.03–0.18], p=0.008; I2=68%), but were not associated with amyloid-β biomarkers (r=-0.06[-0.13–0.01], p=0.08; I
2=81%). Meta-regression revealed that glucose metabolism and DM were specifically associated with tau biomarkers in population settings (p=0.001). Furthermore, more impaired glucose metabolism and DM status were associated with lower amyloid-β biomarkers in memory clinic settings (p=0.004), and in studies with a higher prevalence of dementia (p<0.001) or lower cognitive scores (p=0.04). These findings indicate that DM is associated with biomarkers of tau but not with amyloid-β. This knowledge is valuable for improving dementia and DM diagnostics and treatment.
AB - Conflicting evidence exists on the relationship between diabetes mellitus (DM) and Alzheimer's disease (AD) biomarkers. Therefore, we conducted a random-effects meta-analysis to evaluate the correlation of glucose metabolism measures (glycated hemoglobin, fasting blood glucose, insulin resistance indices) and DM status with AD biomarkers of amyloid-β and tau measured by positron emission tomography or cerebrospinal fluid. We selected 37 studies from PubMed and Embase, including 11,694 individuals. More impaired glucose metabolism and DM status were associated with higher tau biomarkers (r=0.11[0.03–0.18], p=0.008; I2=68%), but were not associated with amyloid-β biomarkers (r=-0.06[-0.13–0.01], p=0.08; I
2=81%). Meta-regression revealed that glucose metabolism and DM were specifically associated with tau biomarkers in population settings (p=0.001). Furthermore, more impaired glucose metabolism and DM status were associated with lower amyloid-β biomarkers in memory clinic settings (p=0.004), and in studies with a higher prevalence of dementia (p<0.001) or lower cognitive scores (p=0.04). These findings indicate that DM is associated with biomarkers of tau but not with amyloid-β. This knowledge is valuable for improving dementia and DM diagnostics and treatment.
KW - Homeostatic Model Assessment for Insulin Resistance (HOMA-IR)
KW - Mini Mental Status Examination (MMSE)
KW - amyloid-beta
KW - cerebrospinal fluid (CSF)
KW - elderly persons
KW - fasting blood glucose (FBG)
KW - glycated haemoglobin (HbA1c)
KW - positron emission tomography (PET)
KW - tau
KW - type 2 DM mellitus (T2DM)
U2 - 10.1016/j.neubiorev.2024.105604
DO - 10.1016/j.neubiorev.2024.105604
M3 - (Systematic) Review article
SN - 0149-7634
VL - 159
JO - Neuroscience and Biobehavioral Reviews
JF - Neuroscience and Biobehavioral Reviews
M1 - 105604
ER -