Pernille L. Kjeldsen , Peter Parbo , Kim V. Hansen , Joel F.A. Aanerud , Rola Ismail , Peter H. Nissen , Rikke B. Dalby , Malene F. Damholdt , Per Borghammer , David J. Brooks
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All subjects underwent <em>APOE</em> genotyping, <sup>11</sup>C-PiB PET, MRI, and cognitive testing. We explored differences in Aβ load, Aβ lateralisation, and Aβ distribution, as well as associations between Aβ distribution and cognition.</p></div><div><h3>Results</h3><p>The Aβ asymmetry index (AI) differed between groups, with pAD having the highest Aβ AI as compared to both controls and MCI. There was no clear Aβ lateralisation in pAD, but there was a non-significant trend towards Aβ being more left-lateralised in MCI. There were no correlations between the cognitive scores and Aβ AI or Aβ lateralisation in pAD or MCI.</p></div><div><h3>Conclusion</h3><p>The distribution of Aβ is most asymmetrical in pAD, as Aβ first starts accumulating, and it then becomes less asymmetrical in MCI, when Aβ has spread further, suggesting that more pronounced asymmetrical Aβ distribution may be a distinguishing factor in pAD. Longitudinal studies examining the distribution of Aβ across the AD continuum are needed.</p></div>","PeriodicalId":72131,"journal":{"name":"Aging brain","volume":"2 ","pages":"Article 100048"},"PeriodicalIF":1.7000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/56/bf/main.PMC9997142.pdf","citationCount":"0","resultStr":"{\"title\":\"Asymmetric amyloid deposition in preclinical Alzheimer’s disease: A PET study\",\"authors\":\"Pernille L. Kjeldsen , Peter Parbo , Kim V. Hansen , Joel F.A. Aanerud , Rola Ismail , Peter H. Nissen , Rikke B. Dalby , Malene F. Damholdt , Per Borghammer , David J. Brooks\",\"doi\":\"10.1016/j.nbas.2022.100048\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>The typical spatial pattern of amyloid-β (Aβ) in diagnosed Alzheimer’s disease (AD) is that of a symmetrical hemispheric distribution. 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引用次数: 0
摘要
淀粉样蛋白-β (a β)在阿尔茨海默病(AD)诊断中的典型空间分布是对称的半球分布。然而,在阿尔茨海默病的早期,Aβ可能不对称分布。PET上的Aβ分布已经在MCI和AD中进行了研究,但尚未在临床前AD (pAD)中进行直接研究。我们使用11C-Pittsburgh Compound B (PiB) PET检测了Aβ在pAD和MCI患者中的分布。方法本PET研究回顾性纳入79例受试者,包括34例对照组、24例pAD和21例MCI。所有受试者均进行了APOE基因分型、11C-PiB PET、MRI和认知测试。我们探索了Aβ负荷、Aβ侧化和Aβ分布的差异,以及Aβ分布与认知之间的关系。结果Aβ不对称指数(AI)组间存在差异,pAD组的Aβ AI高于对照组和MCI组。pAD中没有明显的a β偏侧化,但MCI中a β偏左的趋势不明显。pAD或MCI患者的认知评分与Aβ AI或Aβ偏侧化无相关性。结论a β在pAD中分布最不对称,首先开始积聚,然后随着a β进一步扩散,在MCI中分布不对称程度降低,提示更明显的a β分布不对称可能是pAD的一个区分因素。需要对AD连续体中Aβ的分布进行纵向研究。
Asymmetric amyloid deposition in preclinical Alzheimer’s disease: A PET study
Introduction
The typical spatial pattern of amyloid-β (Aβ) in diagnosed Alzheimer’s disease (AD) is that of a symmetrical hemispheric distribution. However, Aβ may be asymmetrically distributed in early stages of AD. Aβ distribution on PET has previously been explored in MCI and AD, but it has yet to be directly investigated in preclinical AD (pAD). We examined how Aβ was distributed in individuals with pAD and MCI using 11C-Pittsburgh Compound B (PiB) PET.
Methods
In this PET study, 79 subjects were retrospectively enrolled, including 34 controls, 24 pAD, and 21 MCI. All subjects underwent APOE genotyping, 11C-PiB PET, MRI, and cognitive testing. We explored differences in Aβ load, Aβ lateralisation, and Aβ distribution, as well as associations between Aβ distribution and cognition.
Results
The Aβ asymmetry index (AI) differed between groups, with pAD having the highest Aβ AI as compared to both controls and MCI. There was no clear Aβ lateralisation in pAD, but there was a non-significant trend towards Aβ being more left-lateralised in MCI. There were no correlations between the cognitive scores and Aβ AI or Aβ lateralisation in pAD or MCI.
Conclusion
The distribution of Aβ is most asymmetrical in pAD, as Aβ first starts accumulating, and it then becomes less asymmetrical in MCI, when Aβ has spread further, suggesting that more pronounced asymmetrical Aβ distribution may be a distinguishing factor in pAD. Longitudinal studies examining the distribution of Aβ across the AD continuum are needed.