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阿尔茨海默病的早期检测:¹¹C-PiB PET 在认知障碍不一致的双胞胎中的应用。

Early detection of Alzheimer disease: ¹¹C-PiB PET in twins discordant for cognitive impairment.

机构信息

Turku PET Centre, University of Turku, Turku, Finland.

出版信息

Neurology. 2011 Aug 2;77(5):453-60. doi: 10.1212/WNL.0b013e318225118e. Epub 2011 Jun 22.

DOI:10.1212/WNL.0b013e318225118e
PMID:21700581
Abstract

OBJECTIVE

The aim of this study was to investigate whether cognitively preserved monozygotic or dizygotic cotwins of persons with Alzheimer disease (AD) exhibit increased brain amyloid accumulation.

METHODS

We performed a cross-sectional carbon-11 labeled 2-(4'-methylaminophenyl)-6-hydroxybenzothiazole ((11)C)-Pittsburgh compound B (PiB) PET study on 9 monozygotic and 8 dizygotic twin pairs discordant for cognitive impairment as well as on 9 healthy elderly control subjects. (11)C-PiB uptake was analyzed with Statistical Parametric Mapping and with region of interest analysis with the region-to-cerebellum ratio as a measure of tracer uptake.

RESULTS

Cognitively preserved monozygotic cotwins of cognitively impaired probands had increased cortical (11)C-PiB uptake (117%-121% of control mean) in their temporal and parietal cortices and the posterior cingulate. Cognitively preserved dizygotic subjects did not differ from the controls. Further, the cognitively preserved monozygotic subjects showed similar (11)C-PiB uptake patterns as their cognitively impaired cotwins. The cognitively impaired subjects (monozygotic and dizygotic individuals combined) showed typical Alzheimer-like patterns of (11)C-PiB uptake.

CONCLUSIONS

Genetic factors appear to influence the development of Alzheimer-like β-amyloid plaque pathology. The dissociation between cognitive impairment and brain β-amyloidosis in monozygotic twins implies that there may be important environmental/acquired factors that modulate the relationship between brain amyloidosis and neurodegeneration. AD may be detectable in high-risk individuals in its presymptomatic stage with (11)C-PiB PET, but clinical follow-up will be needed to confirm this.

摘要

目的

本研究旨在探讨认知正常的阿尔茨海默病(AD)患者的同卵或异卵双胞胎是否存在脑内淀粉样蛋白蓄积增加的现象。

方法

我们对 9 对认知障碍不一致的同卵和 8 对异卵双胞胎以及 9 名健康老年对照者进行了横断面 11C 标记 2-(4'-甲基氨基苯基)-6-羟基苯并噻唑(11C)-匹兹堡化合物 B(PiB)PET 研究。采用统计参数映射和感兴趣区分析方法分析 11C-PiB 摄取,以区域与小脑的比值作为示踪剂摄取的衡量标准。

结果

认知正常的同卵双胞胎受检者的颞叶和顶叶皮质以及后扣带回皮质存在皮质(11C)-PiB 摄取增加(比对照组平均值高 117%至 121%)。认知正常的异卵受检者与对照组无差异。此外,认知正常的同卵受检者与认知障碍的同卵受检者表现出相似的(11C)-PiB 摄取模式。认知障碍的受检者(同卵和异卵个体合并)表现出典型的阿尔茨海默样(11C)-PiB 摄取模式。

结论

遗传因素似乎会影响阿尔茨海默样β-淀粉样斑块病理的发展。同卵双胞胎中认知障碍与脑β-淀粉样蛋白沉积分离,提示可能存在重要的环境/获得性因素来调节脑淀粉样蛋白沉积与神经退行性变之间的关系。使用(11C)-PiB PET 可以在无症状阶段检测到 AD 的高危个体,但需要进行临床随访来确认这一点。

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