[18F]-D3FSP β-amyloid PET imaging in older adults and alzheimer's disease.

IF 8.6 1区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Anqi Li, Ruiyue Zhao, Mingkai Zhang, Pan Sun, Yue Cai, Lin Zhu, Hank Kung, Ying Han, Xinlu Wang, Tengfei Guo
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引用次数: 0

Abstract

Purpose: [18F]-D3FSP is a new β-amyloid (Aβ) PET imaging tracer designed to decrease nonspecific signals in the brain by reducing the formation of the N-demethylated product. However, its optimal reference region for calculating the standardized uptake value ratio (SUVR) and its relation to the well-established biomarkers of Alzheimer's disease (AD) are still unclear.

Methods: We recruited 203 participants from the Greater Bay Area Healthy Aging Brain Study (GHABS) to undergo [18F]-D3FSP Aβ PET imaging. We analyzed plasma Aβ42/Aβ40, p-Tau181, glial fibrillary acidic protein (GFAP), and neurofilament light (NfL) using the Simoa platform. We compared the standardized uptake value (SUV) of five reference regions (cerebellum, cerebellum cortex, brainstem/PONs, white matter, composite of the four regions above) and AD typical cortical region (COMPOSITE) SUVR among different clinical groups. The association of D3FSP SUVR with plasma biomarkers, imaging biomarkers, and cognition was also investigated.

Results: Brainstem/PONs SUV showed the lowest fluctuation across diagnostic groups, and COMPOSITE D3FSP SUVR had an enormous effect distinguishing cognitively impaired (CI) individuals from cognitively unimpaired (CU) individuals. COMPOSITE SUVR (Referred to brainstem/PONs) was positively correlated with p-Tau181 (p < 0.001), GFAP (p < 0.001), NfL (p = 0.014) in plasma and temporal-metaROI tau deposition (p < 0.001), and negatively related to plasma Aβ42/Aβ40 (p < 0.001), temporal-metaROI cortical thickness (p < 0.01), residual hippocampal volume (p < 0.001) and cognition (p < 0.001). The voxel-wise analysis replicated these findings.

Conclusion: This study suggests brainstem/PONs as an optimal reference region for calculating D3FSP SUVR to quantify cortical Aβ plaques in the brain. [18F]-D3FSP could distinguish CI from CU and strongly correlates with well-established plasma biomarkers, tau PET, neurodegeneration, and cognitive decline. However, future head-to-head comparisons of [18F]-D3FSP PET images with other validated Aβ PET tracers or postmortem results are crucial.

Abstract Image

老年人和阿尔茨海默病的[18F]-D3FSP β 淀粉样蛋白 PET 成像。
目的:[18F]-D3FSP是一种新型β-淀粉样蛋白(Aβ)PET成像示踪剂,旨在通过减少N-去甲基化产物的形成来降低脑内的非特异性信号。然而,其用于计算标准化摄取值比(SUVR)的最佳参考区域及其与阿尔茨海默病(AD)公认生物标志物的关系仍不清楚:我们从大湾区健康老龄化脑研究(GHABS)中招募了203名参与者进行[18F]-D3FSP Aβ PET成像。我们使用 Simoa 平台分析了血浆 Aβ42/Aβ40、p-Tau181、神经纤维酸性蛋白 (GFAP) 和神经丝光 (NfL)。我们比较了不同临床群体中五个参考区域(小脑、小脑皮质、脑干/PONs、白质、上述四个区域的复合区域)的标准化摄取值(SUV)和 AD 典型皮质区域(COMPOSITE)的 SUVR。此外,还研究了D3FSP SUVR与血浆生物标志物、影像生物标志物和认知能力的关系:结果:脑干/PONs SUV 在各诊断组中的波动最小,COMPOSITE D3FSP SUVR 在区分认知障碍(CI)患者和认知功能未受损(CU)患者方面效果显著。COMPOSITE SUVR(指脑干/PONs)与 p-Tau181(p 42/Aβ40(p)呈正相关:本研究表明,脑干/PONs 是计算 D3FSP SUVR 以量化大脑皮质 Aβ 斑块的最佳参考区域。[18F]-D3FSP可区分CI和CU,并与已确定的血浆生物标志物、tau PET、神经变性和认知功能下降密切相关。不过,未来将[18F]-D3FSP PET图像与其他经过验证的Aβ PET示踪剂或尸检结果进行头对头比较至关重要。
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来源期刊
CiteScore
15.60
自引率
9.90%
发文量
392
审稿时长
3 months
期刊介绍: The European Journal of Nuclear Medicine and Molecular Imaging serves as a platform for the exchange of clinical and scientific information within nuclear medicine and related professions. It welcomes international submissions from professionals involved in the functional, metabolic, and molecular investigation of diseases. The journal's coverage spans physics, dosimetry, radiation biology, radiochemistry, and pharmacy, providing high-quality peer review by experts in the field. Known for highly cited and downloaded articles, it ensures global visibility for research work and is part of the EJNMMI journal family.
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