Department of Biomedical, Surgical and Dental Sciences, University of Milan, Milan, Italy.
Department of Neuroradiology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
J Alzheimers Dis. 2023;93(3):1125-1134. doi: 10.3233/JAD-230095.
Brain iron homeostasis is disrupted in neurodegeneration and areas of iron overload partially overlap with regions of amyloid and tau burden in Alzheimer's disease (AD). Previous studies demonstrated alterations in brain iron accumulation in AD using quantitative susceptibility mapping (QSM).
Here, we investigate brain alterations of QSM values in AD and non-AD patients as compared to healthy controls (HC) in the superior temporal sulcus and its banks (BANKSSTS), one of the top AD-affected regions.
Thirty-four patients who underwent brain MRI including a multi-echo gradient-echo sequence were subdivided into AD (n = 19) and non-AD (n = 15) groups according to their clinical profile, CSF (Aβ42/40) and/or amyloid-PET status. Ten HC were also included. QSM values were extracted from left and right BANKSSTS and compared among groups. Correlation and binomial regression analyses between QSM values and CSF-AD biomarkers were conducted.
QSM in left BANKSSTS was significantly different among groups (p = 0.003, H = 11.40), being higher in AD. QSM values in left BANKSSTS were correlated with Aβ42 (rho -0.55, p = 0.005), Aβ42/40 (rho -0.66, p < 0.001), pTau (rho 0.63, p < 0.001), tTau (rho 0.56, p = 0.005), tTau/Aβ42 (rho 0.68, p < 0.001) and pTau/Aβ42 (rho 0.71, p < 0.001). No correlations between QSM values and amyloid-PET SUVR in the left BANKSSTS were found. QSM values in left BANKSSTS showed good accuracy in discriminating AD (AUC = 0.80, CI95 % [0.66-0.93]). Higher QSM values were independent predictors of Aβ42 (B = 0.63, p = 0.032), Aβ42/40 (B = 0.81, p = 0.028), pTau (B = 0.96, p = 0.046), tTau (B = 0.55, p = 0.027), and tTau/Aβ42 (B = 1.13, p = 0.042) positivity.
Our preliminary data support the potential role of increased QSM values in the left BANKSSTS as an auxiliary imaging biomarker in AD diagnosis.
神经退行性变中脑铁稳态被破坏,铁过载的区域与阿尔茨海默病(AD)中淀粉样蛋白和 tau 负担的区域部分重叠。先前的研究使用定量磁化率映射(QSM)证明了 AD 中脑铁积累的改变。
本研究旨在探讨 AD 和非 AD 患者与健康对照组(HC)相比,在颞上沟及其bank(BANKSSTS)中 QSM 值的脑改变,颞上沟是 AD 影响最严重的区域之一。
34 名接受包括多回波梯度回波序列在内的脑部 MRI 的患者根据其临床特征、脑脊液(Aβ42/40)和/或淀粉样蛋白-PET 状态分为 AD(n = 19)和非 AD(n = 15)组。还纳入了 10 名 HC。从左侧和右侧 BANKSSTS 提取 QSM 值,并在组间进行比较。进行了 QSM 值与 CSF-AD 生物标志物之间的相关性和二项式回归分析。
左 BANKSSTS 中的 QSM 在组间存在显著差异(p = 0.003,H = 11.40),AD 患者的 QSM 值更高。左 BANKSSTS 中的 QSM 值与 Aβ42(rho -0.55,p = 0.005)、Aβ42/40(rho -0.66,p < 0.001)、pTau(rho 0.63,p < 0.001)、tTau(rho 0.56,p = 0.005)、tTau/Aβ42(rho 0.68,p < 0.001)和 pTau/Aβ42(rho 0.71,p < 0.001)呈负相关。左 BANKSSTS 中的 QSM 值与淀粉样蛋白-PET SUVR 之间未发现相关性。左 BANKSSTS 中的 QSM 值在区分 AD 方面具有良好的准确性(AUC = 0.80,CI95%[0.66-0.93])。较高的 QSM 值是 Aβ42(B = 0.63,p = 0.032)、Aβ42/40(B = 0.81,p = 0.028)、pTau(B = 0.96,p = 0.046)、tTau(B = 0.55,p = 0.027)和 tTau/Aβ42(B = 1.13,p = 0.042)阳性的独立预测因子。
我们的初步数据支持左 BANKSSTS 中 QSM 值增加作为 AD 诊断辅助影像学生物标志物的潜在作用。