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痴呆患者神经精神症状与脑灌注的相关性:一项应用 99mTc-SPECT-HMPAO 和布罗德曼脑区分析的研究。

Correlation of Neuropsychiatric Symptoms in Dementia with Brain Perfusion: A 99mTc-SPECT-HMPAO Study with Brodmann Areas Analysis.

机构信息

Nuclear Medicine Department, University Hospital of Larissa, Thessaly, Greece.

Nuclear Medicine Department, "Alexandra" General Hospital, Athens, Greece.

出版信息

Curr Alzheimer Res. 2021;18(12):970-983. doi: 10.2174/1567205019666211220130505.

Abstract

BACKGROUND

Neuropsychiatric symptoms (NPSs) are common in dementia. Their evaluation is based on Neuropsychiatric Inventory (NPI). Neuroimaging studies have tried to elucidate the underlying neural circuits either in isolated NPSs or in specific forms of dementia.

OBJECTIVE

The objective of this study is to evaluate the correlation of NPS in the NPI with Brodmann areas (BAs) perfusion, for revealing BAs involved in the pathogenesis of NPSs in dementia of various etiologies.

METHODS

We studied 201 patients (82 with Alzheimer's disease, 75 with Frontotemporal dementia, 27 with Corticobasal Syndrome, 17 with Parkinson Disease/Lewy Body Dementia). Exploratory factor analysis was carried out to evaluate underlying groups of BAs, and Principal Component analysis was chosen as extraction method using Varimax rotation. Partial correlation coefficients were computed to explore the association of factors obtained from analysis and NPI items controlling for age, educational yeas, and ACE-R.

RESULTS

We found 6 BAs Factors(F); F1 (BAs 8,9,10,11,24,32,44,45,46,47, bilaterally), F2 (BAs 4,5,6,7,23,31, bilaterally), F3 (BAs 19,21,22,37,39,40, bilaterally), F4 (BAs 20,28,36,38, bilaterally), F5 (BAs 25, bilaterally) and F6 (BAs 17,18, bilaterally). Significant and negative correlation was found between NPI1 (delusions) and F3,F6, NPI2 (hallucinations) and F6, NPI7 (apathy) and F1,F4,F5, NPI3 (agitation) - NPI10 (aberrant motor behavior) - NPI12 (eating disorders) and F1. We did not find any significant correlation for NPI4,5,6,8,9,11 (depression, anxiety, euphoria, disinhibition, irritability, sleep disorders, respectively).

CONCLUSION

Several NPSs share the same BAs among different types of dementia, while the manifestation of the rest may be attributed to different neural networks. These findings may have an impact on patients' treatment.

摘要

背景

神经精神症状(NPS)在痴呆中很常见。它们的评估基于神经精神疾病问卷(NPI)。神经影像学研究试图阐明孤立的 NPS 或特定形式的痴呆症的潜在神经回路。

目的

本研究旨在评估 NPI 中的 NPS 与布罗德曼脑区(BA)灌注之间的相关性,以揭示不同病因痴呆症中 NPS 发病机制所涉及的 BA。

方法

我们研究了 201 名患者(82 名阿尔茨海默病患者、75 名额颞叶痴呆患者、27 名皮质基底节综合征患者、17 名帕金森病/路易体痴呆患者)。进行了探索性因子分析,以评估 BA 的潜在分组,并选择主成分分析作为提取方法,使用 Varimax 旋转。计算偏相关系数以探索从分析中获得的因子与 NPI 项目的关联,控制年龄、教育年限和 ACE-R。

结果

我们发现了 6 个 BA 因子(F1[BA8、9、10、11、24、32、44、45、46、47,双侧]、F2[BA4、5、6、7、23、31,双侧]、F3[BA19、21、22、37、39、40,双侧]、F4[BA20、28、36、38,双侧]、F5[BA25,双侧]和 F6[BA17、18,双侧])。NPI1(妄想)与 F3、F6,NPI2(幻觉)与 F6,NPI7(淡漠)与 F1、F4、F5,NPI3(激越)-NPI10(异常运动行为)-NPI12(饮食障碍)与 F1 之间存在显著且负相关。我们没有发现 NPI4、5、6、8、9、11(抑郁、焦虑、欣快、去抑制、易怒、睡眠障碍)之间存在任何显著相关性。

结论

不同类型痴呆症中存在几种 NPS 共享相同的 BA,而其余的表现可能归因于不同的神经网络。这些发现可能对患者的治疗产生影响。

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