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原发性进行性失语症与阿尔茨海默病生物标志物的临床特征。

Clinical Characteristic in Primary Progressive Aphasia in Relation to Alzheimer's Disease Biomarkers.

机构信息

Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Neuroscience Center, Samsung Medical Center, Seoul, Korea.

出版信息

J Alzheimers Dis. 2021;84(2):633-645. doi: 10.3233/JAD-210392.

Abstract

BACKGROUND

Primary progressive aphasia (PPA) is associated with amyloid-β (Aβ) pathology. However, clinical feature of PPA based on Aβ positivity remains unclear.

OBJECTIVE

We aimed to assess the prevalence of Aβ positivity in patients with PPA and compare the clinical characteristics of patients with Aβ-positive (A+) and Aβ-negative (A-) PPA. Further, we applied Aβ and tau classification system (AT system) in patients with PPA for whom additional information of in vivo tau biomarker was available.

METHODS

We recruited 110 patients with PPA (41 semantic [svPPA], 27 non-fluent [nfvPPA], 32 logopenic [lvPPA], and 10 unclassified [ucPPA]) who underwent Aβ-PET imaging at multi centers. The extent of language impairment and cortical atrophy were compared between the A+ and A-PPA subgroups using general linear models.

RESULTS

The prevalence of Aβ positivity was highest in patients with lvPPA (81.3%), followed by ucPPA (60.0%), nfvPPA (18.5%), and svPPA (9.8%). The A+ PPA subgroup manifested cortical atrophy mainly in the left superior temporal/inferior parietal regions and had lower repetition scores compared to the A-PPA subgroup. Further, we observed that more than 90% (13/14) of the patients with A+ PPA had tau deposition.

CONCLUSION

Our findings will help clinicians understand the patterns of language impairment and cortical atrophy in patients with PPA based on Aβ deposition. Considering that most of the A+ PPA patents are tau positive, understanding the influence of Alzheimer's disease biomarkers on PPA might provide an opportunity for these patients to participate in clinical trials aimed for treating atypical Alzheimer's disease.

摘要

背景

原发性进行性失语症(PPA)与淀粉样蛋白-β(Aβ)病理学有关。然而,基于 Aβ 阳性的 PPA 的临床特征仍不清楚。

目的

我们旨在评估 PPA 患者中 Aβ 阳性的患病率,并比较 Aβ 阳性(A+)和 Aβ 阴性(A-)PPA 患者的临床特征。此外,我们在 PPA 患者中应用了 Aβ 和 tau 分类系统(AT 系统),这些患者有额外的体内 tau 生物标志物信息。

方法

我们在多中心招募了 110 名 PPA 患者(41 名语义性 PPA [svPPA]、27 名非流利性 PPA [nfvPPA]、32 名失读症性 PPA [lvPPA]和 10 名未分类性 PPA [ucPPA]),他们接受了 Aβ-PET 成像检查。使用一般线性模型比较 A+和 A-PPA 亚组之间语言损伤和皮质萎缩的程度。

结果

lvPPA 患者的 Aβ 阳性率最高(81.3%),其次是 ucPPA(60.0%)、nfvPPA(18.5%)和 svPPA(9.8%)。A+PPA 亚组表现为左颞上/下顶叶皮质萎缩,与 A-PPA 亚组相比,重复得分较低。此外,我们观察到超过 90%(13/14)的 A+PPA 患者有 tau 沉积。

结论

我们的发现将帮助临床医生了解基于 Aβ 沉积的 PPA 患者的语言损伤和皮质萎缩模式。鉴于大多数 A+PPA 患者为 tau 阳性,了解阿尔茨海默病生物标志物对 PPA 的影响可能为这些患者提供机会,使他们能够参加针对治疗非典型阿尔茨海默病的临床试验。

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