Cortical thickness and cognitive impairment in patients with amyotrophic lateral sclerosis

  • Shan YE ,
  • Ping-ping JIN ,
  • Nan ZHANG ,
  • Hai-bo WU ,
  • Lin SHI ,
  • Qiang ZHAO ,
  • Kun YANG ,
  • Hui-shu YUAN ,
  • Dong-sheng FAN
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  • 1. Department of Neurology, Peking University Third Hospital, Beijing 100191, China
    2. Beijing Municipal Key Laboratory of Biomarker and Translational Research in Neurodegenerative Diseases, Beijing 100191, China
    3. Department of Radiology, Peking University Third Hospital, Beijing 100191, China
    4. Department of Imaging and Interventional Radiology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong Special Administrative Region 000852, China
    5. BrainNow Research Institute, Shenzhen 518000, Guangdong, China

Received date: 2020-03-21

  Online published: 2022-12-19

Supported by

the National Natural Science Foundation of China(82001350);the Peking University Third Hospital Key Clinical Projects(BYSY2018048);the Peking University Third Hospital Cohort Construction Project(BYSYDL2019002)

Abstract

Objective: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease with high morbidity and mortality. There are about 5%-15% of ALS patients combining with frontotemporal lobe degeneration (FTLD) at the same time and 50% of patients combing with cognitive function changes. The analysis of cortical thickness based on MRI is an important imaging method to evaluate brain structure. The aim of the study was to explore the changes of brain structure in ALS patients by cortical thickness analysis, and to explore the correlation between the brain structure and cognitive function. Methods: In the study, 18 ALS patients treated in Department of Neurology, Peking University Third Hospital and 18 normal controls (age, gender and education level matched) were included. 3D magnetization prepared rapid gradient echo imaging (MPRAGE) sequence MRI was performed and the cortical thickness was analyzed. At the same time, all the ALS patients took neuropsychology assessments, including: mini-mental state examination (MMSE), verbal fluency test (VFT), Stroop color word test (SCWT), prospective memory (PM), emotional picture perception and recognition, and faux pas story test. Results: After cognitive assessment, two ALS patients had cognitive impairment. One was in accordance with ALS-frontotemporal dementia (FTD) diagnosis and the other one was in accordance with ALS cognitive impairment (ALSci) diagnosis. In all the 18 ALS patients and 18 normal controls, the cortical thickness of the left medial orbitofrontal lobe and the medial temporal lobe were significantly reduced (P < 0.05) in ALS group by the vertex-wise comparison. Cortical thickness of the left entorhinal cortex, the left inferior temporal gyrus, the left medial orbitofrontal lobe and the left insular lobe was significantly reduced (P < 0.05) by the region-wise comparison. However, when only concluded the 16 ALS non-cognitive impairment patients, there was no significant difference between the two groups (P>0.05). There were correlations between the scores of prospective memory, emotional picture perception and recognition, faux pas story test and the cortical thickness of their corresponding regions (P < 0.05). Conclusion: The cortical thickness of ALS patients are correlated with neuropsychological scores which may reflect the changes of cortical structure corresponding to the cognitive assessment, and may provide help for the early diagnosis of cognitive changes in ALS patients.

Cite this article

Shan YE , Ping-ping JIN , Nan ZHANG , Hai-bo WU , Lin SHI , Qiang ZHAO , Kun YANG , Hui-shu YUAN , Dong-sheng FAN . Cortical thickness and cognitive impairment in patients with amyotrophic lateral sclerosis[J]. Journal of Peking University(Health Sciences), 2022 , 54(6) : 1158 -1162 . DOI: 10.19723/j.issn.1671-167X.2022.06.016

References

1 Strong M , Abrahams S , Goldstein L , et al. Amyotrophic lateral sclerosis-frontotemporal spectrum disorder (ALS-FTSD): Revised diagnostic criteria[J]. Amyotroph Lateral Scler Frontotemporal Degener, 2017, 18 (3/4): 153- 174.
2 Hanstock C , Sun K , Choi C , et al. Spectroscopic markers of neurodegeneration in the mesial prefrontal cortex predict survival in ALS[J]. Amyotroph Lateral Scler Frontotemporal Degener, 2020, 21 (3/4): 246- 251.
3 Trojsi F , Nardo F , Siciliano M , et al. Frontotemporal degeneration in amyotrophic lateral sclerosis (ALS): A longitudinal MRI one-year study[J]. CNS Spectr, 2021, 26 (3): 258- 267.
4 Hu T , Hou Y , Wei Q , et al. Patterns of brain regional functional coherence in cognitive impaired ALS[J]. Int J Neurosci, 2020, 130 (8): 751- 758.
5 Brooks BR , Miller RG , Swash M , et al. El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis[J]. Amyotroph Lateral Scler Other Motor Neuron Disord, 2000, 1 (5): 293- 299.
6 Desikan RS , Segonne F , Fischl B , et al. An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest[J]. Neuroimage, 2006, 31 (3): 968- 980.
7 Chiara C , Alessandra D , Stefano FC , et al. Multimodal MRI quantification of the common neurostructural bases within the FTD-ALS continuum[J]. Neurobiol Aging, 2018, 62, 95- 104.
8 Verstraete E , Veldink JH , Hendrikse J , et al. Structural MRI reveals cortical thinning in amyotrophic lateral sclerosis[J]. J Neurol Neurosurg Psychiatry, 2011, 83 (4): 383- 388.
9 Bergmann M . Motor neuron disease/amyotrophic lateral sclerosis: Lessons from ubiquitin[J]. Pathol Res Pract, 1993, 189 (8): 902- 912.
10 Shen D , Hou B , Cui B , et al. Comparing brain structural and perfusion MRI changes across ALS-FTD continuum[J]. Clin Neurophysiol, 2018, 129, e162.
11 Labar KS , Cabeza R . Cognitive neuroscience of emotional memory[J]. Nat Rev Neurosci, 2006, 7 (1): 54- 64.
12 Dolcos F , Labar KS , Cabeza R . Dissociable effects of arousal and valence on prefrontal activity indexing emotional evaluation and subsequent memory: An event-related fMRI study[J]. Neuro-image, 2004, 23 (1): 64- 74.
13 Lule D , Diekmann V , Anders S , et al. Brain responses to emotional stimuli in patients with amyotrophic lateral sclerosis (ALS)[J]. J Neurol, 2007, 254 (4): 519- 527.
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