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原发性肌张力障碍中无可靠的灰质改变。

No reliable gray matter alterations in idiopathic dystonia.

作者信息

Wang Zhen-Yu, Chen Fei, Sun Hai-Hua, Li Hua-Liang, Hu Jian-Bin, Dai Zhen-Yu, Wang Shu

机构信息

Department of Radiology, Affiliated Hospital 6 of Nantong University, Yancheng Third People's Hospital, Yancheng, China.

Department of Neurology, Affiliated Hospital 6 of Nantong University, Yancheng Third People's Hospital, Yancheng, China.

出版信息

Front Neurol. 2025 Mar 3;16:1510115. doi: 10.3389/fneur.2025.1510115. eCollection 2025.

Abstract

BACKGROUND

The structural brain abnormalities associated with idiopathic dystonia (ID) remain inadequately understood. Previous voxel-based morphometry (VBM) studies examining whole-brain gray matter (GM) volume alterations in patients with ID have reported inconsistent and occasionally contradictory findings.

METHODS

We performed a coordinate-based meta-analysis (CBMA) using the latest seed-based d mapping with permutation of subject images (SDM-PSI) technique to identify consistent GM alterations in patients with ID at the whole-brain level. Additionally, meta-regression analyses were conducted to explore the potential moderating effects of age, gender, and disease duration on GM volume.

RESULTS

The CBMA incorporated 27 VBM studies, comprising 32 datasets with a total of 840 patients with ID and 834 healthy controls. Our analysis did not identify consistent or reliable GM alterations in patients with ID. The robustness of these findings was confirmed through a jackknife sensitivity analysis. Meta-regression analyses revealed that disease duration significantly influenced GM volume in the right insula.

CONCLUSION

Based on the best practice guidelines for CBMA, we utilized the most recent SDM-PSI algorithm to perform a new CBMA that included a larger group of individuals with ID. However, in contrast to previous CBMAs, we did not observe any consistent alterations in GM in ID. The findings suggest that using GM volume assessed by VBM as an imaging marker for ID may not be reliable. This could be attributed to ID being a functional disorder, or the inconsistency in GM alterations may be influenced by demographic and clinical variations, differences in imaging protocols and analysis methods, or small sample sizes. It is imperative to control for subject characteristics, employ standardized VBM methodologies, and enhance sample sizes in future research.

摘要

背景

与特发性肌张力障碍(ID)相关的大脑结构异常仍未得到充分理解。先前基于体素的形态计量学(VBM)研究检查了ID患者全脑灰质(GM)体积变化,报告结果不一致,有时甚至相互矛盾。

方法

我们使用最新的基于种子点的d映射与受试者图像置换(SDM-PSI)技术进行了基于坐标的荟萃分析(CBMA),以确定ID患者在全脑水平上一致的GM变化。此外,进行了荟萃回归分析,以探讨年龄、性别和病程对GM体积的潜在调节作用。

结果

CBMA纳入了27项VBM研究,包括32个数据集,共有840例ID患者和834名健康对照。我们的分析未发现ID患者存在一致或可靠的GM变化。通过留一法敏感性分析证实了这些发现的稳健性。荟萃回归分析显示,病程对右侧岛叶的GM体积有显著影响。

结论

基于CBMA的最佳实践指南,我们利用最新的SDM-PSI算法进行了一项新的CBMA,纳入了更多的ID患者。然而,与之前的CBMA不同,我们在ID中未观察到GM的任何一致变化。研究结果表明,将VBM评估的GM体积用作ID的成像标志物可能不可靠。这可能是因为ID是一种功能性障碍,或者GM变化的不一致可能受到人口统计学和临床差异、成像协议和分析方法的差异或样本量小的影响。在未来的研究中,控制受试者特征、采用标准化的VBM方法并增加样本量势在必行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fa6/11911186/f36bb6299e6a/fneur-16-1510115-g001.jpg

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