动脉瘤性和血管造影阴性蛛网膜下腔出血的白质异常:弥散峰度成像研究

IF 3.4 2区 医学 Q2 NEUROIMAGING Neuroimage-Clinical Pub Date : 2024-01-01 DOI:10.1016/j.nicl.2024.103662
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引用次数: 0

摘要

目的动脉瘤性蛛网膜下腔出血(aSAH)和血管造影阴性蛛网膜下腔出血(anSAH)会导致颅内压突然升高,从而产生剪切力,造成白质束损伤。本研究旨在通过弥散峰度成像(DKI)研究蛛网膜下腔出血和无蛛网膜下腔出血后的全脑白质异常,并探讨这些异常是否与认知功能受损有关。方法34名蛛网膜下腔出血患者、24名无蛛网膜下腔出血患者和17名健康对照组(HC)在发病后5个月接受了DKI MRI扫描和神经心理学评估(测量言语记忆、精神运动速度、执行控制和社会认知)。使用基于道的空间统计方法检查了 DKI 测量(分数各向异性、平均扩散率、轴向扩散率 [AD]、径向扩散率和平均峰度)的差异。结果所有 DKI 测量结果在 aSAH 和 HC 患者之间均存在显著差异,但在 anSAH 和 HC 患者之间未发现显著差异。尽管两组SAH患者在所有DKI参数上都没有明显差异,但效应大小表明,anSAH组可能与HC组更为相似。与 HC 相比,两组 SAH 患者均存在认知障碍。在 aSAH 组中,这些损伤与白质异常之间没有发现明显的关联,但在 anSAH 患者中,较低的精神运动速度评分与较高的 AD 值相关(r = -0.41,p = 0.04)。然而,SAH 组之间没有明显差异,DKI 指标与认知指标之间也没有相关性,只有 anSAH 组的一项精神运动速度测试除外。总之,这项研究表明,虽然anSAH可能不像aSAH那么严重,但它仍然不是一种良性疾病。为了更准确地了解白质损伤,尤其是其发病率,有必要对更多的无SAH患者进行进一步研究。
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White matter abnormalities in aneurysmal and angiographically negative subarachnoid hemorrhage: A diffusion kurtosis imaging study

Objective

Aneurysmal subarachnoid hemorrhage (aSAH) and angiographically negative subarachnoid hemorrhage (anSAH) cause an abrupt rise in intracranial pressure, resulting in shearing forces, causing damage to the white matter tracts. This study aims to investigate whole-brain white matter abnormalities with diffusion kurtosis imaging (DKI) after both aSAH and anSAH and explores whether these abnormalities are associated with impaired cognitive functioning.

Methods

Five months post-ictus, 34 patients with aSAH, 24 patients with anSAH and 17 healthy controls (HC) underwent DKI MRI scanning and neuropsychological assessment (measuring verbal memory, psychomotor speed, executive control, and social cognition). Differences in DKI measures (fractional anisotropy, mean diffusivity, axial diffusivity [AD], radial diffusivity, and mean kurtosis) were examined using tract-based spatial statistics. Significant voxel masks were then correlated with neuropsychological scores.

Results

All DKI measures differed significantly between patients with aSAH and HC, but no significant differences were found between patients with anSAH and HC. Although the two SAH groups did not differ significantly on all DKI parameters, effect sizes indicated that the anSAH group might be more similar to HC. Cognitive impairments were found for both SAH groups relative to HC. No significant associations were found between these impairments and white matter abnormalities in the aSAH group, but lower psychomotor speed scores were associated with higher AD values (r = -0.41, p = 0.04) in patients with anSAH.

Conclusions

Patients with aSAH showed significant white matter diffusion abnormalities, while the anSAH group, despite cognitive deficits, did not. However, there were no significant differences between the SAH groups, and no correlations between DKI metrics and cognitive measures, except for one test on psychomotor speed in the anSAH group. Overall, this study suggests that while anSAH may not be as severe as aSAH, it is still not a benign condition. Further research with larger anSAH cohorts is necessary to gain a more precise understanding of white matter injuries, particularly regarding their prevalence.

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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.
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