Thalamic atrophy and dysconnectivity are associated with cognitive impairment in a multi-center, clinical routine, real-word study of people with relapsing-remitting multiple sclerosis

IF 3.4 2区 医学 Q2 NEUROIMAGING Neuroimage-Clinical Pub Date : 2024-01-01 DOI:10.1016/j.nicl.2024.103609
Robert Zivadinov , Niels Bergsland , Dejan Jakimovski , Bianca Weinstock-Guttman , Lorena Lorefice , Menno M. Schoonheim , Sarah A. Morrow , Mary Ann Picone , Gabriel Pardo , Myassar Zarif , Mark Gudesblatt , Jacqueline A. Nicholas , Andrew Smith , Samuel Hunter , Stephen Newman , Mahmoud A. AbdelRazek , Ina Hoti , Jon Riolo , Diego Silva , Tom A. Fuchs , Ralph HB. Benedict
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Abstract

Background

Prior research has established a link between thalamic pathology and cognitive impairment (CI) in people with multiple sclerosis (pwMS). However, the translation of these findings to pwMS in everyday clinical settings has been insufficient.

Objective

To assess which global and/or thalamic imaging biomarkers can be used to identify pwMS at risk for CI and cognitive worsening (CW) in a real-world setting.

Methods

This was an international, multi-center (11 centers), longitudinal, retrospective, real-word study of people with relapsing-remitting MS (pwRRMS). Brain MRI exams acquired at baseline and follow-up were collected. Cognitive status was evaluated using the Symbol Digit Modalities Test (SDMT). Thalamic volume (TV) measurement was performed on T2-FLAIR, as well as on T1-WI, when available. Thalamic dysconnectivity, T2-lesion volume (T2-LV), and volumes of gray matter (GM), whole brain (WB) and lateral ventricles (LVV) were also assessed.

Results

332 pwMS were followed for an average of 2.8 years. At baseline, T2-LV, LVV, TV and thalamic dysconnectivity on T2-FLAIR (p < 0.016), and WB, GM and TV volumes on T1-WI (p < 0.039) were significantly worse in 90 (27.1 %) CI vs. 242 (62.9 %) non-CI pwRRMS. Greater SDMT decline over the follow-up was associated with lower baseline TV on T2-FLAIR (standardized β = 0.203, p = 0.002) and greater thalamic dysconnectivity (standardized β = -0.14, p = 0.028) in a linear regression model.

Conclusions

PwRRMS with thalamic atrophy and worse thalamic dysconnectivity present more frequently with CI and experience greater CW over mid-term follow-up in a real-world setting.

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在一项针对复发缓解型多发性硬化症患者的多中心临床常规实词研究中,丘脑萎缩和连接障碍与认知障碍有关
背景先前的研究已确定丘脑病理学与多发性硬化症患者(pwMS)认知障碍(CI)之间存在联系。方法 这是一项针对复发缓解型多发性硬化症患者(pwRRMS)的国际性、多中心(11 个中心)、纵向、回顾性、实证研究。研究收集了基线和随访时获得的脑磁共振成像检查结果。认知状况通过符号数字模型测试(SDMT)进行评估。丘脑体积(TV)测量采用T2-FLAIR和T1-WI(如有)。此外,还评估了丘脑连接障碍、T2-病变体积(T2-LV)以及灰质(GM)、全脑(WB)和侧脑室(LVV)的体积。基线时,90 名(27.1%)CI pwRRMS 与 242 名(62.9%)非 CI pwRRMS 相比,T2-FLAIR 上的 T2-LV、LVV、TV 和丘脑连接障碍(p < 0.016)以及 T1-WI 上的 WB、GM 和 TV 容积(p < 0.039)均显著恶化。在线性回归模型中,随访期间SDMT下降幅度较大与T2-FLAIR上基线TV较低(标准化β = 0.203,p = 0.002)和丘脑连接障碍较大(标准化β = -0.14,p = 0.028)相关。
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来源期刊
Neuroimage-Clinical
Neuroimage-Clinical NEUROIMAGING-
CiteScore
7.50
自引率
4.80%
发文量
368
审稿时长
52 days
期刊介绍: NeuroImage: Clinical, a journal of diseases, disorders and syndromes involving the Nervous System, provides a vehicle for communicating important advances in the study of abnormal structure-function relationships of the human nervous system based on imaging. The focus of NeuroImage: Clinical is on defining changes to the brain associated with primary neurologic and psychiatric diseases and disorders of the nervous system as well as behavioral syndromes and developmental conditions. The main criterion for judging papers is the extent of scientific advancement in the understanding of the pathophysiologic mechanisms of diseases and disorders, in identification of functional models that link clinical signs and symptoms with brain function and in the creation of image based tools applicable to a broad range of clinical needs including diagnosis, monitoring and tracking of illness, predicting therapeutic response and development of new treatments. Papers dealing with structure and function in animal models will also be considered if they reveal mechanisms that can be readily translated to human conditions.
期刊最新文献
Corrigendum to "Quantitative susceptibility mapping in multiple sclerosis: A systematic review and meta-analysis" [Neuroimage: Clin. 42 (2024) 103598]. Corrigendum to "Association between clinical features and decreased degree centrality and variability in dynamic functional connectivity in the obsessive-compulsive disorder" [Neuroimage: Clinical 44 (2024) 1-9/103665]. Corrigendum to "Impact of adult-onset multiple sclerosis on MRI-based intracranial volume: A study in clinically discordant monozygotic twins" [NeuroImage Clin. 42 (2024) 103597]. Neurometabolic alterations in children and adolescents with functional neurological disorder Preoperative plasticity in the functional naming network of patients with left insular gliomas
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