Magnetic resonance imaging showing parietal atrophy of the brain in late-onset Alzheimer’s disease
Authors:
D. Šilhán 1,2; I. Ibrahim 3; J. Tintěra 3; A. Bartoš 1,2
Authors place of work:
Neurologická klinika 3. LF UK a FN Královské Vinohrady, Praha
1; Národní ústav duševního zdraví, Klecany
2; Institut klinické a experimentální medicíny, Praha
3
Published in the journal:
Cesk Slov Neurol N 2019; 82(1): 91-95
Category:
Original Paper
doi:
https://doi.org/10.14735/amcsnn201991
Summary
Aim:
Our intention was to assess whether a scoring of parietal atrophy on MRI of the brain using a simple visual assessment named PAS (Parietal Atrophy Score) could be used in the diagnosis of late-onset Alzheimer‘s disease.
Patients and methods:
The structure of the parietal lobes was evaluated by our visual scale named PAS, which is based on semiquantitative scoring of atrophy of three structures in the parietal region: sulcus cingularis posterior, precuneus and parietal gyri. Parietal atrophy was assessed in 24 patients with late-onset Alzheimer‘s disease in the stage of mild dementia (Mini-Mental State Examination; MMSE 21 ± 3 points) and 26 age-matched individuals with normal scores on the MMSE (29 ± 1 point).
Results:
We did not find any statistically significant difference in the size of any structure of the right and left parietal lobe according to the PAS visual scale between control individuals and patients with Alzheimer‘s disease (p > 0.05 in all cases).
Conclusion:
During late-onset Alzheimer‘s disease there is no significant reduction of parietal cortex until the stage of mild dementia compared to normal aging. Parietal atrophy evaluated according to the PAS visual scale is not an appropriate marker to be used in the diagnosis of late-onset Alzheimer‘s disease in mild stages.
Key words:
Parietal Atrophy Score – parietal atrophy – magnetic resonance imaging – Alzheimer‘s disease – dementia – aging – sulcus cingularis posterior – precuneus – parietal gyri
The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study.
The Editorial Board declares that the manuscript met the ICMJE “uniform requirements” for biomedical papers.
磁共振成像显示晚发性阿尔茨海默氏症患者大脑顶叶萎缩
目的:
我们的目的是评估大脑MRI上的顶叶萎缩评分是否可以用于晚发性阿尔茨海默病的诊断。
患者和方法:
顶叶的结构是通过我们命名为PAS的视觉量表来评估的,它是基于对顶叶区域萎缩的三个结构的半定量评分:后扣带沟、楔前叶和顶叶回。对24例晚发阿尔茨海默氏症轻度痴呆(微精神状态检查;MMSE 21±3分),年龄匹配者26例,MMSE得分正常(29±1分)。
结果:
对照个体与阿尔茨海默病患者的PAS视觉量表比较,未发现左右顶叶结构大小差异有统计学意义(p > 0.05)。
结论:
在晚发性阿尔茨海默病中,直到轻度痴呆阶段,顶叶皮层与正常年龄相比没有明显的减少。根据PAS视觉量表评估的顶叶萎缩并不适合用于轻度迟发性阿尔茨海默病的诊断。
关键词:
顶叶萎缩评分-顶叶萎缩-磁共振成像-阿尔茨海默氏症-痴呆-衰老-颈沟后-楔前叶-顶叶回
Zdroje
1. Bartoš A, Kukal J. Magnetická rezonance mozku u pacientů s Alzheimerovou chorobou. Psychiatrie 2005; 9 (Suppl 3): 39– 42.
2. Harper L, Barkhof F, Scheltens P et al. An algorithmic approach to structural imaging in dementia. J Neurol Neurosurg Psychiatry 2014; 85(6): 692– 698. doi: 10.1136/ jnnp-2013-306285.
3. Scheltens P, Leys D, Barkhof F et al. Atrophy of medial temporal lobes on MRI in probable Alzheimers disease and normal aging: diagnostic-value and neuropsychological correlates. J Neurol Neurosurg Psychiatry 1992; 55(10): 967– 972.
4. Ten Kate M, Barkhof F, Boccardi M et al. Task Force for the Roadmap of Alzheimer’s Biomarkers. Clinical validity of medial temporal atrophy as a biomarker for Alzheimer’s disease in the context of a structured 5-phase development framework. Neurobiol Aging 2017; 52: 167– 182. doi: 10.1016/ j.neurobiolaging.2016.05.024.
5. Bartoš A, Zach P, Diblíková F et al. Vizuální kategorizace mediotemporální atrofie na MR mozku u Alzheimerovy nemoci. Psychiatrie 2007; 11 (Suppl 3): 49– 52.
6. Liu Y, Paajanen T, Zhang Y et al. Analysis of regional MRI volumes and thicknesses as predictors of conversion from mild cognitive impairment to Alzheimer‘s disease. Neurobiol Aging 2010, 31(8): 1375– 1385. doi: 10.1016/ j.neurobiolaging.2010.01.022.
7. Fennema-Notestine C, McEvoy LK, Hagler DJ et al. Structural neuroimaging in the detection and prognosis of pre-clinical and early AD. Behav Neurol 2009; 21(1): 3– 12. doi: 10.3233/ BEN-2009-0230.
8. Jack CR, Shiung MM, Gunter JL et al. Comparison of different MRI brain atrophy rate measures with clinical disease progression in AD. Neurology 2004; 62(4): 591– 600.
9. Vemuri P, Jack CR. Role of structural MRI in Alzheimer’s disease. Alzheimers Res Ther 2010; 2(4): 23. doi: 10.1186/ alzrt47.
10. Pol LA, Hensel A, Flier WM et al. Hippocampal atrophy on MRI in frontotemporal lobar degeneration and Alzheimer‘s disease. J Neurol Neurosurg Psychiatry 2006; 77(4): 439– 442. doi: 10.1136/ jnnp.2005.075341.
11. Harper L, Fumagalli GG, Barkhof F et al. MRI visual rating scales in the diagnosis of dementia: evaluation in 184 post-mortem confirmed cases. Brain 2016; 139(Pt 4): 1211– 1225. doi: 10.1093/ brain/ aww005.
12. Hu WT, Wang Z, Lee VM et al. Distinct cerebral perfusion patterns in FTLD and AD. Neurology 2010, 75(10): 881– 888. doi: 10.1212/ WNL.0b013e3181f11e35.
13. Landau SM, Harvey D, Madison CM et al. Associations between cognitive, functional, and FDG-PET measures of decline in AD and MCI. Neurobiol Aging 2011; 32(7): 1207– 1218. doi: 10.1016/ j.neurobiolaging.2009.07.002.
14. Lehmann M, Koedam EL, Barnes J et al. Posterior cerebral atrophy in the absence of medial temporal lobe atrophy in pathologically-confirmed Alzheimer’s disease. Neurobiol Aging 2012; 33(3): 627.e1– 627.e12. doi: 10.1016/ j.neurobiolaging.2011.04.003.
15. Frisoni GB, Pievani M, Testa C et al. The topography of grey matter involvement in early and late onset Alzheimer‘s disease. Brain 2007; 130(Pt 3): 720– 730. doi: 10.1093/ brain/ awl377.
16. Ishii K, Kawachi T, Sasaki H et al. Voxel-based morphometric comparison between early- and late-onset mild Alzheimer‘s disease and assessment of diagnostic performance of Z score images. Am J Neuroradiol 2005; 26(2): 333– 340.
17. Shiino A, Watanabe T, Kitagawa T et al. Different atrophic patterns in early- and late-onset Alzheimer‘s disease and evaluation of clinical utility of a method of regional z-score analysis using voxel-based morphometry. Dement Geriatr Cogn Disord 2008; 26(2): 175– 186. doi: 10.1159/ 000151241.
18. Šilhán D, Ibrahim I, Tintěra J et al. Parietální atrofický skór na magnetické rezonanci mozku u normálně stárnoucích osob. Cesk Slov Neurol N 2018; 81/ 114(4): 414– 419. doi: 10.14735/ amcsnn2018414.
19. McKhann GM, Knopman DS, Chertkow H et al. The diagnosis of dementia due to Alzheimer‘s disease: recommendations from the National Institute on Aging-Alzheimer‘s Association workgroups on diagnostic guidelines for Alzheimer‘s disease. Alzheimers Dement 2011; 7(3): 263– 269. doi: 10.1016/ j.jalz.2011.03.005.
20. Bartoš A. Netestuj, ale POBAV: písemné záměrné Pojmenování OBrázků A jejich Vybavení jako krátká kognitivní zkouška. Cesk Slov Neurol N 2016; 79/ 112(6), 671– 679.
21. Bartoš A. Test gest (TEGEST) k rychlému vyšetření epizodické paměti u mírné kognitivní poruchy. Cesk Slov Neurol N 2018; 81/ 114(1): 37– 44. doi: 10.14735/ amcsnn201837.
22. Bartoš A, Janoušek M, Petroušová R et al. Tři časy Testu kreslení hodin hodnocené BaJa skórováním u časné Alzheimerovy nemoci. Cesk Slov Neurol N 2016; 79/ 112(4): 406– 412.
23. Bartoš A, Raisová M. Testy a dotazníky pro vyšetřování kognitivních funkcí, nálady a soběstačnosti. Praha: Mladá fronta 2015.
24. Koedam EL, Lehman M, Van der Flier WM et al. Visual assessment of posterior atrophy development of a MRI rating scale. Eur Radiol 2011; 21(12): 2618– 2625. doi: 10.1007/ s00330-011-2205-4.
Štítky
Paediatric neurology Neurosurgery NeurologyČlánok vyšiel v časopise
Czech and Slovak Neurology and Neurosurgery
2019 Číslo 1
- Advances in the Treatment of Myasthenia Gravis on the Horizon
- Memantine Eases Daily Life for Patients and Caregivers
- Spasmolytic Effect of Metamizole
Najčítanejšie v tomto čísle
- Mild traumatic brain injury management – consensus statement of the Czech Neurological Society CMS JEP
- Chronic subdural haematoma
- Oligoclonal IgG and free light chains – comparison between agarose and polyacrylamide isoelectric focusing
- Ketogenic diet – effective treatment of childhood and adolescent epilepsies