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本文引用的文献

1
Open-label study of the short-term effects of memantine on FDG-PET in frontotemporal dementia.一项关于美金刚对额颞叶痴呆患者 FDG-PET 短期影响的开放性研究。
Neuropsychiatr Dis Treat. 2011;7:415-24. doi: 10.2147/NDT.S22635. Epub 2011 Jul 13.
2
Memantine in behavioral variant frontotemporal dementia: negative results.美金刚在行为变异型额颞叶痴呆中的应用:阴性结果。
J Alzheimers Dis. 2011;23(4):749-59. doi: 10.3233/JAD-2010-101632.
3
Divergent network connectivity changes in behavioural variant frontotemporal dementia and Alzheimer's disease.行为变异型额颞叶痴呆和阿尔茨海默病的网络连接连通性变化不同。
Brain. 2010 May;133(Pt 5):1352-67. doi: 10.1093/brain/awq075. Epub 2010 Apr 21.
4
Effect of memantine treatment on regional cortical metabolism in Alzheimer's disease.盐酸美金刚治疗对阿尔茨海默病患者区域性皮质代谢的影响。
Am J Geriatr Psychiatry. 2010 Jul;18(7):606-14. doi: 10.1097/JGP.0b013e3181ca3a4e.
5
Frontotemporal dementia and pharmacologic interventions.额颞叶痴呆与药物干预。
J Neuropsychiatry Clin Neurosci. 2010 Winter;22(1):19-29. doi: 10.1176/jnp.2010.22.1.19.
6
Test-retest variability of high resolution positron emission tomography (PET) imaging of cortical serotonin (5HT2A) receptors in older, healthy adults.健康老年成年人皮质5-羟色胺(5HT2A)受体的高分辨率正电子发射断层扫描(PET)成像的重测变异性。
BMC Med Imaging. 2009 Jul 6;9:12. doi: 10.1186/1471-2342-9-12.
7
Cholinergic modulation of the cerebral metabolic response to citalopram in Alzheimer's disease.胆碱能对阿尔茨海默病患者大脑对西酞普兰代谢反应的调节作用
Brain. 2009 Feb;132(Pt 2):392-401. doi: 10.1093/brain/awn326. Epub 2009 Jan 19.
8
A 6-month, open-label study of memantine in patients with frontotemporal dementia.一项针对额颞叶痴呆患者的美金刚6个月开放标签研究。
Int J Geriatr Psychiatry. 2008 Jul;23(7):754-9. doi: 10.1002/gps.1973.
9
Decomposition of metabolic brain clusters in the frontal variant of frontotemporal dementia.额颞叶痴呆额叶变异型中代谢性脑簇的分解
Neuroimage. 2006 Apr 15;30(3):871-8. doi: 10.1016/j.neuroimage.2005.10.016. Epub 2005 Dec 15.
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Predominant ventromedial frontopolar metabolic impairment in frontotemporal dementia.额颞叶痴呆中主要的腹内侧额极代谢损害
Neuroimage. 2003 Sep;20(1):435-40. doi: 10.1016/s1053-8119(03)00346-x.

氟脱氧葡萄糖正电子发射断层扫描在语义性痴呆患者接受美金刚治疗 6 个月后的应用:一项开放性先导研究。

Fluorodeoxyglucose positron emission tomography in semantic dementia after 6 months of memantine: an open-label pilot study.

机构信息

Division of Neurology, Baycrest, Toronto, Canada.

出版信息

Int J Geriatr Psychiatry. 2013 Mar;28(3):319-25. doi: 10.1002/gps.3832. Epub 2012 Jun 4.

DOI:10.1002/gps.3832
PMID:22674572
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3467357/
Abstract

OBJECTIVES

To follow up on the increases we reported in normalized metabolic activity in salience network hubs from a 2-month open-label study of memantine in frontotemporal dementia (FTD).

METHODS

We repeated fluorodeoxyglucose positron emission tomography (FDG-PET) after 6 months of drug use and subjected the data to Statistical Parametrical Mapping (SPM) analysis to reveal clusters of significant change from baseline. We also sought correlations between changes in behavioral disturbances on the Frontal Behavioral Inventory (FBI) and the PET signal.

RESULTS

Recruitment of one progressive nonfluent aphasia and one behavioral variant FTD precluded statistical analysis for any FTD subtype other than semantic dementia (SD). The baseline-to-6-month interval showed increased normalized metabolic activity in the left orbitofrontal cortex (p < 0.002) for five participants with SD. The 2-6-month interval revealed a late increase in normalized metabolic activity in the left insula (p < 0.013), right insula (p < 0.009), and left anterior cingulate (p < 0.005). The right anterior cingulate showed both an initial increase and a delayed further increase (2-6 months, p < 0.016). FBI scores worsened by 43.3%. One participant with SD opted not to continue memantine beyond 2 months yet showed similar FDG-PET increases.

CONCLUSIONS

Increases in normalized cortical metabolic activity in salience network hubs were sustained in SD over a 6-month period. Because one participant without medication also showed these changes, further investigation is recommended through a double-blind, placebo-controlled study with FDG-PET as an outcome measure.

摘要

目的

跟进我们在额颞叶痴呆(FTD)的美金刚 2 个月开放标签研究中报告的突显网络枢纽正常代谢活性增加。

方法

我们在使用药物 6 个月后重复进行氟脱氧葡萄糖正电子发射断层扫描(FDG-PET),并对数据进行统计参数映射(SPM)分析,以揭示从基线开始的显著变化簇。我们还寻求了额叶行为量表(FBI)上行为障碍变化与 PET 信号之间的相关性。

结果

一名进行性非流利性失语症和一名行为变异型额颞叶痴呆患者的招募排除了除语义性痴呆(SD)以外的任何 FTD 亚型的统计分析。基线至 6 个月的间隔显示,5 名 SD 患者的左侧眶额皮质的正常代谢活性增加(p < 0.002)。2-6 个月的间隔显示左侧岛叶(p < 0.013)、右侧岛叶(p < 0.009)和左侧前扣带回(p < 0.005)的正常代谢活性晚期增加。右侧前扣带回显示出初始增加和延迟进一步增加(2-6 个月,p < 0.016)。FBI 评分恶化了 43.3%。一名 SD 患者选择在 2 个月后不再继续使用美金刚,但仍显示出类似的 FDG-PET 增加。

结论

在 6 个月的时间内,突显网络枢纽的正常皮质代谢活性增加在 SD 中持续存在。由于一名未用药的参与者也表现出这些变化,因此建议通过双盲、安慰剂对照研究,以 FDG-PET 作为结果测量进一步进行调查。