Morphometric Definition of Alzheimer's Disease Stages by Means of The Tomography Dementia Rating Scale (TDR)

I. Maksimovich
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引用次数: 2

Abstract

Background: The research is dedicated to developing an objective method for determining dementia severity in patients with different AD stages. The method is based on morphometric analysis of specific atrophic changes in temporal lobes detected during cerebral CT and MRI and it allows differentiating these particular changes from those common for other cerebral neurodegenerative diseases. Materials and Methods: 1105 patients aged 28 years to 81 years (mean age 75) were examined: 786 men (71.13%), 319 women (28.61%), 93 had different AD stages-test group, 1012 had another neurodegenerative diseasescontrol group. Results: The scale of dementia stages during AD, Tomography Dementia Rating Scale (TDR), was developed, allowing to determine dementia severity with objective, morphometrically grounded data of atrophic changes in temporal lobes obtained during CT and MRI: 1. Preclinical AD stage-TDR-0: results from atrophic changes in temporal lobes with 4% to 8% tissue mass decrease and cognitive functions decline equal to 26 to 28 MMSE points. 2. Early AD stage-TDR-1: mild dementia resulting from atrophic changes in temporal lobes with 9% to 18% tissue mass decrease, corresponds to CDR-1, is accompanied by cognitive functions decline equal to 20 to 25 MMSE points. 3. Middle AD stage-TDR-2: moderate dementia resulting from atrophic changes in temporal lobes with 19% to 32% tissue mass decrease, corresponds to CDR-2, cognitive functions decline is equal to 12 to 19 MMSE points. 4. Late AD stage-TDR-3: severe dementia resulting from atrophic changes in temporal lobes with 33% to 62% tissue mass decrease, corresponds to CDR-3, cognitive functions decline is equal to MMSE 7 to 11 points. 5. Control group patients did not have any similar changes. Conclusion: The proposed objective, morphometrically validated TDR scale allows to identify preclinical and clinical AD stages; it is easy to use and is complementary to the clinical dementia rating scale. Besides, this scale makes it possible to differentiate AD from other neurodegenerative diseases.
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基于ct痴呆评定量表(TDR)的阿尔茨海默病分期形态学定义
背景:本研究致力于开发一种客观的方法来确定不同AD阶段患者的痴呆严重程度。该方法是基于对大脑CT和MRI检测到的颞叶特定萎缩变化的形态计量学分析,它可以将这些特殊变化与其他脑神经退行性疾病的常见变化区分开来。材料与方法:共检查1105例患者,年龄28 ~ 81岁,平均年龄75岁,其中男性786例(71.13%),女性319例(28.61%),不同AD分期试验组93例,其他神经退行性疾病对照组1012例。结果:开发了阿尔茨海默氏症痴呆分期量表,即断层扫描痴呆评定量表(TDR),允许通过CT和MRI获得的颞叶萎缩变化的客观、形态计量学基础数据来确定痴呆的严重程度。临床前AD阶段- tdr -0:颞叶萎缩改变,组织质量减少4% - 8%,认知功能下降,相当于26 - 28 MMSE点。2. 早期AD - tdr -1:颞叶萎缩性改变引起的轻度痴呆,组织质量减少9% ~ 18%,对应CDR-1,伴有认知功能下降,相当于20 ~ 25 MMSE点。3.AD中期- tdr -2:颞叶萎缩性改变导致的中度痴呆,组织质量下降19% - 32%,对应CDR-2,认知功能下降等于12 - 19 MMSE点。4. AD晚期- tdr -3:颞叶萎缩改变导致的重度痴呆,组织质量下降33% ~ 62%,对应CDR-3,认知功能下降等于MMSE 7 ~ 11分。5. 对照组患者没有类似的变化。结论:提出的客观、形态计量学验证的TDR量表可以识别临床前和临床AD分期;它易于使用,是临床痴呆评定量表的补充。此外,该量表可以将AD与其他神经退行性疾病区分开来。
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