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尸检中银染颗粒与临床特征的相关性。

Correlation of clinical features with argyrophilic grains at autopsy.

机构信息

The Cleo Roberts Center for Clinical Research, Sun Health Research Institute, 10515 West Santa Fe Drive, Sun City, AZ 85351, USA.

出版信息

Alzheimer Dis Assoc Disord. 2009 Jul-Sep;23(3):229-33. doi: 10.1097/WAD.0b013e318199d833.

DOI:10.1097/WAD.0b013e318199d833
PMID:19812464
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2760041/
Abstract

Argyrophilic grains (AGs) are a pathologic feature found in association with neurodegenerative disease. Some have suggested that these features may occur as a distinctive condition. We reviewed 80 subjects from our tissue bank with pathologically confirmed AGs and identified their clinical features. We compared these subjects' features to the features of subjects with matched clinical diagnoses but without AGs. Subjects with AGs represented 21.7% of the entire autopsy sample from 1999 to 2005 (80 out of 367). Of Alzheimer disease (AD) subjects, 43 out of 233 had AGs (18.4% of AD subjects); 11 out of 42 Parkinson disease with dementia subjects had AGs (26.1% of Parkinson disease with dementia subjects); 2 out of 9 dementia with Lewy bodies subjects had AGs (22.2% of dementia with Lewy bodies subjects); 4 out of 15 mild cognitive impairment subjects had AGs (26.7% of mild cognitive impairment subjects); and 20 out of 68 cognitively normal subjects had AGs (29.4% of cognitively normal). Subjects with AGs tended to be older but only significantly so in AD. Many comorbid non-neurologic health conditions were seen in cases of AGs without any single predilection emerging. AGs occur in approximately 22% of the entire autopsy cohort and are likely associated with advanced age. No distinctive antemortem clinical features were over represented in the AG cases. AGs can occur with or without neurodegenerative conditions and can occur in the absence of significant cognitive decline. AGs are not clearly associated with any single comorbid health condition.

摘要

嗜银颗粒(AGs)是与神经退行性疾病相关的一种病理特征。有人认为这些特征可能是一种独特的疾病。我们回顾了 80 名来自我们组织库的病例,这些病例的组织病理学检查均证实存在 AGs,并确定了其临床特征。我们将这些病例的特征与具有匹配临床诊断但无 AGs 的病例的特征进行了比较。在 1999 年至 2005 年期间,我们的尸检样本中共有 367 例,其中 80 例(21.7%)存在 AGs。在阿尔茨海默病(AD)患者中,233 例患者中有 43 例(18.4%)存在 AGs;42 例帕金森病伴痴呆患者中有 11 例(26.1%)存在 AGs;9 例路易体痴呆患者中有 2 例(22.2%)存在 AGs;15 例轻度认知障碍患者中有 4 例(26.7%)存在 AGs;68 例认知正常患者中有 20 例(29.4%)存在 AGs。存在 AGs 的病例往往年龄较大,但在 AD 患者中差异有统计学意义。在 AGs 病例中观察到许多合并的非神经科健康状况,但没有任何单一的倾向。AGs 发生在大约 22%的尸检队列中,可能与年龄较大有关。在 AG 病例中,没有明显的特征性的生前临床特征被过度代表。AGs 可发生在有或没有神经退行性疾病的情况下,也可发生在没有明显认知能力下降的情况下。AGs 与任何单一的合并健康状况均无明确关联。

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