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新发多发性硬化症患者社会认知缺陷的神经基础。

The neural substrates of social cognition deficits in newly diagnosed multiple sclerosis patients.

机构信息

Neurology Section, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

Kessler Foundation, 120 Eagle'Rock Ave, Suite 100, East Hanover, New Jersey, 07936, USA.

出版信息

Ann Clin Transl Neurol. 2024 Jul;11(7):1798-1808. doi: 10.1002/acn3.52085. Epub 2024 Jun 13.


DOI:10.1002/acn3.52085
PMID:38872257
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11251485/
Abstract

OBJECTIVE: Cognitive and affective symptoms in multiple sclerosis (MS) can be independently impaired and have different pathways of progression. Cognitive alterations have been described since the earliest MS stages; by contrast, the social cognition (SC) domain has never been investigated in the first year from MS diagnosis. We aimed to evaluate SC and unravel its neural bases in newly diagnosed MS patients. METHODS: Seventy MS patients underwent at diagnosis a 3 T-MRI and a neuropsychological/SC assessment (median time between diagnosis and MRI/cognitive evaluation = 0 months). We tested two matched reference samples: 31 relapsing-remitting MS patients with longer course (mean ± SD disease duration = 7.0 ± 4.5 years) and 38 healthy controls (HCs). Cortical thicknesses (CTh) and volumes of brain regions were calculated. RESULTS: Newly diagnosed MS patients performed significantly lower than HCs in facial emotion recognition (global: p < 0.001; happiness: p = 0.041, anger: p = 0.007; fear: p < 0.001; disgust: p = 0.004) and theory of mind (p = 0.005), while no difference was found between newly diagnosed and longer MS patients. Compared to lower performers, higher performers in facial emotion recognition showed greater volume of amygdala (p = 0.032) and caudate (p = 0.036); higher performers in theory of mind showed greater CTh in lingual gyrus (p = 0.006), cuneus (p = 0.024), isthmus cingulate (p = 0.038), greater volumes of putamen (p = 0.016), pallidum (p = 0.029), and amygdala (p = 0.032); patients with higher empathy showed lower cuneus CTh (p = 0.042) and putamen volume (p = 0.007). INTERPRETATIONS: SC deficits are present in MS patients since the time of diagnosis and remain persistent along the disease course. Specific basal, limbic, and occipital areas play a significant role in the pathogenesis of these alterations.

摘要

目的:多发性硬化症(MS)中的认知和情感症状可能会独立受损,并具有不同的进展途径。早在 MS 的早期阶段就已经描述了认知改变;相比之下,在 MS 诊断后的第一年,从未研究过社会认知(SC)领域。我们旨在评估新诊断的 MS 患者的 SC 并揭示其神经基础。

方法:70 名 MS 患者在诊断时接受了 3T-MRI 和神经心理学/ SC 评估(诊断和 MRI/认知评估之间的中位数时间为 0 个月)。我们测试了两个匹配的参考样本:31 名具有较长病程的复发缓解型 MS 患者(平均病程±标准差为 7.0±4.5 年)和 38 名健康对照者(HCs)。计算了皮质厚度(CTh)和脑区的体积。

结果:新诊断的 MS 患者在面部情绪识别(整体:p<0.001;高兴:p=0.041,生气:p=0.007;恐惧:p<0.001;厌恶:p=0.004)和心理理论(p=0.005)方面的表现明显低于 HCs,而新诊断的 MS 患者与病程较长的 MS 患者之间无差异。与表现较低的患者相比,在面部情绪识别中表现较好的患者杏仁核(p=0.032)和尾状核(p=0.036)体积更大;在心理理论方面表现较好的患者舌回(p=0.006)、楔前叶(p=0.024)、扣带回峡部(p=0.038)的 CTh 更大,壳核(p=0.016)、苍白球(p=0.029)和杏仁核(p=0.032)体积更大;同理心较高的患者楔叶 CTh(p=0.042)和壳核体积(p=0.007)较低。

解释:MS 患者在诊断时就存在 SC 缺陷,并且在疾病过程中仍然持续存在。特定的基底神经节、边缘和枕叶区域在这些改变的发病机制中起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/bce1dfc133f0/ACN3-11-1798-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/3a58fc334ec3/ACN3-11-1798-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/e01dcbfb0ea4/ACN3-11-1798-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/29f3d96c2777/ACN3-11-1798-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/21c435d4ecc3/ACN3-11-1798-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/bce1dfc133f0/ACN3-11-1798-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/3a58fc334ec3/ACN3-11-1798-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/e01dcbfb0ea4/ACN3-11-1798-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/29f3d96c2777/ACN3-11-1798-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/21c435d4ecc3/ACN3-11-1798-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f500/11251485/bce1dfc133f0/ACN3-11-1798-g003.jpg

相似文献

[1]
The neural substrates of social cognition deficits in newly diagnosed multiple sclerosis patients.

Ann Clin Transl Neurol. 2024-7

[2]
Social cognition deficits and the role of amygdala in relapsing remitting multiple sclerosis patients without cognitive impairment.

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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J Neurol. 2024-6

[9]
Abnormalcortical thickness in relapsing-remitting multiple sclerosis, correlations with cognition impairment, and effect of modified Bushenyisui decoction on cognitive function of multiple sclerosis.

J Tradit Chin Med. 2021-4

[10]
Cortical Thickness and Serum NfL Explain Cognitive Dysfunction in Newly Diagnosed Patients With Multiple Sclerosis.

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本文引用的文献

[1]
Altered social cognition in early relapsing remitting multiple sclerosis.

Mult Scler Relat Disord. 2023-10

[2]
Functional and structural brain MRI changes associated with cognitive worsening in multiple sclerosis: a 3-year longitudinal study.

J Neurol. 2023-9

[3]
Cortical lesions at diagnosis predict long-term cognitive impairment in multiple sclerosis: A 20-year study.

Eur J Neurol. 2023-5

[4]
Facial emotion impairment in multiple sclerosis is linked to modifying observation strategies of emotional faces.

Mult Scler Relat Disord. 2023-1

[5]
Theory of mind, emotion recognition and emotional reactivity factors in early multiple sclerosis: Results from a South American cohort.

Appl Neuropsychol Adult. 2024

[6]
Resting-state functional brain connectivity for human mentalizing: biobehavioral mechanisms of theory of mind in multiple sclerosis.

Soc Cogn Affect Neurosci. 2022-6-3

[7]
Relapsing-remitting and secondary-progressive multiple sclerosis patients differ in decoding others' emotions by their eyes.

Eur J Neurol. 2022-2

[8]
Regional brain atrophy is related to social cognition impairment in multiple sclerosis.

Arq Neuropsiquiatr. 2021-8

[9]
Theory of mind and its neuroanatomical correlates in people with multiple sclerosis.

Mult Scler Relat Disord. 2021-10

[10]
Social cognition in multiple sclerosis and its subtypes: A meta-analysis.

Mult Scler Relat Disord. 2021-7

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