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家族性多发性硬化症中白质的广泛破坏:扩散张量成像和神经突方向离散度与密度成像研究

Widespread Disruptions of White Matter in Familial Multiple Sclerosis: DTI and NODDI Study.

作者信息

Gharaylou Zeinab, Sahraian Mohammad Ali, Hadjighassem Mahmoudreza, Kohanpour Mohsen, Doosti Rozita, Nahardani Shima, Moghadasi Abdorreza Naser

机构信息

Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.

Brain and Spinal Cord Injury Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Front Neurol. 2021 Aug 16;12:678245. doi: 10.3389/fneur.2021.678245. eCollection 2021.

DOI:10.3389/fneur.2021.678245
PMID:34484098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8415561/
Abstract

Diffusion tensor imaging (DTI) is a noninvasive, quantitative MRI technique that measures white matter (WM) integrity. Many brain dimensions are heritable, including white matter integrity measured with DTI. Family studies are valuable to provide insights into the interactive effects of non-environmental factors on multiple sclerosis (MS). To examine the contribution of familial factors to the diffusion signals across WM microstructure, we performed DTI and calculated neurite orientation dispersion plus density imaging (NODDI) diffusion parameters in two patient groups comprising familial and sporadic forms of multiple sclerosis and their unaffected relatives. We divided 111 subjects (49 men and 62 women: age range 19-60) into three groups conforming to their MS history. The familial MS group included 30 participants (patients; = 16, healthy relatives; = 14). The sporadic group included 41 participants (patients; = 10, healthy relatives; = 31). Forty age-matched subjects with no history of MS in their families were defined as the control group. To study white matter integrity, two methods were employed: one for calculating the mean of DTI, FA, and MD parameters on 18 tracts using Tracts Constrained by Underlying Anatomy (TRACULA) and the other for whole brain voxel-based analysis using tract-based spatial statistics (TBSS) on NDI and ODI parameters derived from NODDI and DTI parameters. Voxel-based analysis showed considerable changes in FA, MD, NDI, and ODI in the familial group when compared with the control group, reflecting widespread impairment of white matter in this group. The analysis of 18 tracts with TRACULA revealed increased MD and FA reduction in more tracts (left and right ILF, UNC, and SLFT, forceps major and minor) in familial MS patients vs. the control group. There were no significant differences between the patient groups. We found no consequential changes in healthy relatives of both patient groups in voxel-based and tract analyses. Considering the multifactorial etiology of MS, familial studies are of great importance to clarify the effects of certain predisposing factors on demyelinating brain pathology.

摘要

扩散张量成像(DTI)是一种无创的定量磁共振成像技术,用于测量白质(WM)的完整性。许多脑维度是可遗传的,包括用DTI测量的白质完整性。家族研究对于深入了解非环境因素对多发性硬化症(MS)的交互作用很有价值。为了研究家族因素对整个白质微结构扩散信号的贡献,我们对两组患者进行了DTI检查,并计算了神经突方向离散度加密度成像(NODDI)扩散参数,这两组患者分别为家族性和散发性多发性硬化症患者及其未受影响的亲属。我们将111名受试者(49名男性和62名女性,年龄范围19 - 60岁)根据其MS病史分为三组。家族性MS组包括30名参与者(患者16名,健康亲属14名)。散发性组包括41名参与者(患者10名,健康亲属31名)。40名年龄匹配且家族中无MS病史的受试者被定义为对照组。为了研究白质完整性,采用了两种方法:一种是使用基于解剖结构约束的轨迹(TRACULA)计算18条轨迹上DTI、FA和MD参数的平均值,另一种是对从NODDI和DTI参数导出的NDI和ODI参数,使用基于轨迹的空间统计(TBSS)进行全脑体素分析。基于体素的分析显示,与对照组相比,家族性组的FA、MD、NDI和ODI有显著变化,反映出该组白质广泛受损。用TRACULA对18条轨迹的分析显示,与对照组相比,家族性MS患者更多轨迹(左右下纵束、钩束和上纵束、大脑镰和小脑镰)的MD增加且FA降低。两组患者之间无显著差异。在基于体素和轨迹的分析中,我们发现两组患者的健康亲属均无相应变化。考虑到MS的多因素病因,家族研究对于阐明某些易感因素对脱髓鞘脑病理的影响非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e95f/8415561/51747cfedddc/fneur-12-678245-g0007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e95f/8415561/2e47337c9043/fneur-12-678245-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e95f/8415561/357fada96a24/fneur-12-678245-g0002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e95f/8415561/51747cfedddc/fneur-12-678245-g0007.jpg

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本文引用的文献

1
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2
Common genetic variation influencing human white matter microstructure.常见遗传变异影响人类白质微观结构。
Science. 2021 Jun 18;372(6548). doi: 10.1126/science.abf3736.
3
Gray Matter Matters: A Longitudinal Magnetic Resonance Voxel-Based Morphometry Study of Primary Progressive Multiple Sclerosis.
Automated three-dimensional major white matter bundle segmentation using diffusion magnetic resonance imaging.
基于弥散磁共振成像的全自动三维白质束分割
Anat Sci Int. 2023 Jul;98(3):318-336. doi: 10.1007/s12565-023-00715-9. Epub 2023 Apr 5.
4
Disrupted topological properties of the structural brain network in patients with cerebellar infarction on different sides are associated with cognitive impairment.不同侧小脑梗死患者脑结构网络拓扑属性的破坏与认知障碍有关。
Front Neurol. 2022 Sep 20;13:982630. doi: 10.3389/fneur.2022.982630. eCollection 2022.
5
Effects of 3-month CPAP therapy on brain structure in obstructive sleep apnea: A diffusion tensor imaging study.3个月持续气道正压通气治疗对阻塞性睡眠呼吸暂停患者脑结构的影响:一项扩散张量成像研究
Front Neurol. 2022 Aug 22;13:913193. doi: 10.3389/fneur.2022.913193. eCollection 2022.
灰质至关重要:一项基于体素的原发性进行性多发性硬化纵向磁共振形态学研究
Front Neurol. 2020 Nov 12;11:581537. doi: 10.3389/fneur.2020.581537. eCollection 2020.
4
NODDI in clinical research.临床研究中的神经突方向离散与密度成像(NODDI)
J Neurosci Methods. 2020 Dec 1;346:108908. doi: 10.1016/j.jneumeth.2020.108908. Epub 2020 Aug 16.
5
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6
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7
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Mult Scler Relat Disord. 2019 Jan;27:294-297. doi: 10.1016/j.msard.2018.11.011. Epub 2018 Nov 13.
9
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Neurol Neuroimmunol Neuroinflamm. 2018 Sep 26;5(6):e502. doi: 10.1212/NXI.0000000000000502. eCollection 2018 Nov.
10
NLR-Dependent Regulation of Inflammation in Multiple Sclerosis.多发性硬化症中炎症的 NLR 依赖性调节
Front Immunol. 2018 Jan 18;8:2012. doi: 10.3389/fimmu.2017.02012. eCollection 2017.