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后皮质萎缩和遗忘型阿尔茨海默病中转运体蛋白增加的不同模式。

Distinct patterns of increased translocator protein in posterior cortical atrophy and amnestic Alzheimer's disease.

作者信息

Kreisl William C, Lyoo Chul Hyoung, Liow Jeih-San, Snow Joseph, Page Emily, Jenko Kimberly J, Morse Cheryl L, Zoghbi Sami S, Pike Victor W, Turner R Scott, Innis Robert B

机构信息

Molecular Imaging Branch, National Institute of Mental Health, Bethesda, MD, USA.

Molecular Imaging Branch, National Institute of Mental Health, Bethesda, MD, USA.

出版信息

Neurobiol Aging. 2017 Mar;51:132-140. doi: 10.1016/j.neurobiolaging.2016.12.006. Epub 2016 Dec 16.

Abstract

We sought to determine whether patients with posterior cortical atrophy (PCA) demonstrate a pattern of binding to translocator protein 18 kDa, a marker of microglial activation, that is distinct from that in patients with amnestic presentation of Alzheimer's disease (AD). Eleven PCA patients, 11 amnestic AD patients, and 15 age-matched controls underwent positron emission tomography with C-PBR28 to measure translocator protein 18 kDa. PCA patients showed greater C-PBR28 binding than controls in occipital, posterior parietal, and temporal regions. In contrast, amnestic AD patients showed greater C-PBR28 binding in inferior and medial temporal cortex. Increased C-PBR28 binding overlapped with reduced cortical volume for both PCA and amnestic AD patients, and with areas of reduced glucose metabolism in PCA patients. While both patient groups showed diffuse amyloid binding, PCA patients showed greater binding than amnestic AD patients in bilateral occipital cortex. These results suggest that microglial activation is closely associated with neurodegeneration across different subtypes of AD.

摘要

我们试图确定后皮质萎缩(PCA)患者是否表现出与18 kDa转运体蛋白(一种小胶质细胞激活标志物)的结合模式,该模式不同于遗忘型阿尔茨海默病(AD)患者。11名PCA患者、11名遗忘型AD患者和15名年龄匹配的对照者接受了用C-PBR28进行的正电子发射断层扫描,以测量18 kDa转运体蛋白。PCA患者在枕叶、顶叶后部和颞叶区域的C-PBR28结合比对照者更强。相比之下,遗忘型AD患者在颞叶下部和内侧皮质的C-PBR28结合更强。PCA患者和遗忘型AD患者的C-PBR28结合增加与皮质体积减少重叠,且与PCA患者葡萄糖代谢降低的区域重叠。虽然两组患者均表现出弥漫性淀粉样蛋白结合,但PCA患者在双侧枕叶皮质的结合比遗忘型AD患者更强。这些结果表明,小胶质细胞激活与AD不同亚型的神经退行性变密切相关。

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