小儿多发性硬化症视功能、视网膜厚度与MRI脑容量的关系。

IF 7.5 1区 医学 Q1 CLINICAL NEUROLOGY
Anna Sosa, Kimberly A O'Neill, Ruben Jauregui, Ugo Nwigwe, Thibo Billiet, Rachel Kenney, Lauren B Krupp, Steven L Galetta, Laura J Balcer, Scott N Grossman
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引用次数: 0

摘要

背景和目的:虽然光学相干断层扫描(OCT) pRNFL和神经节细胞内丛状层厚度的减少已被证明与成人发病的MS (AOMS)队列中的脑萎缩有关,但在儿科发病的MS (POMS)中,OCT和脑MRI测量之间的关系尚不明确。我们的目的是在POMS患者队列中检查OCT测量与体积MRI的相关性,以确定OCT测量是否反映该患者群体的中枢神经退行性变,正如在AOMS队列中看到的那样。方法:这是一项横断面研究,回顾性确定在一个具有POMS和神经眼科专业知识的单一中心评估的POMS患者。作为常规临床护理的一部分,POMS患者由POMS专家进行评估,并进行脑体积MRI,包括全脑(WB)、分区域和灰质(GM)体积分析。POMS患者通常接受神经眼科评估,包括高对比视力、色觉测试和oct。采用广义估计方程(GEE)模型,考虑患者内部、眼间相关性(包括每个患者的两只眼睛)、MS病程和疾病改善治疗效果,确定视觉通路结构和功能与体积MRI测量之间的关系。结果:61例POMS患者(122只眼)中,体积MRI扫描时的平均年龄为19.2岁(SD = 3.7,范围10-27)岁,中位病程为2.8年(范围0-14)年。较低(较差)的pRNFL厚度(平均87.4[17.2]µm)与WB (p < 0.001, GEE模型)、总GM (p = 0.025)和丘脑(p = 0.038)的体积百分位数降低相关。pRNFL变薄也与更大的病变(p = 0.006)和黑洞(p = 0.028)体积相关。色觉和高对比度视力降低与海马体积降低相关(p = 0.012和p = 0.015)。讨论:我们的研究结果表明,视觉通路结构的变化与总体脑容量和GM体积的减少以及更大的病变和黑洞负担有关。总的来说,我们的结果强调了视觉评估在POMS中的重要性,并表明OCT反映了该队列中整体中枢神经退行性变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Relation of Visual Function, Retinal Thickness by Optical Coherence Tomography, and MRI Brain Volume in Pediatric-Onset Multiple Sclerosis.

Relation of Visual Function, Retinal Thickness by Optical Coherence Tomography, and MRI Brain Volume in Pediatric-Onset Multiple Sclerosis.

Relation of Visual Function, Retinal Thickness by Optical Coherence Tomography, and MRI Brain Volume in Pediatric-Onset Multiple Sclerosis.

Relation of Visual Function, Retinal Thickness by Optical Coherence Tomography, and MRI Brain Volume in Pediatric-Onset Multiple Sclerosis.

Background and objectives: While reductions in optical coherence tomography (OCT) pRNFL and ganglion cell-inner plexiform layer thicknesses have been shown to be associated with brain atrophy in adult-onset MS (AOMS) cohorts, the relationship between OCT and brain MRI measures is less established in pediatric-onset MS (POMS). Our aim was to examine the associations of OCT measures with volumetric MRI in a cohort of patients with POMS to determine whether OCT measures reflect CNS neurodegeneration in this patient population, as is seen in AOMS cohorts.

Methods: This was a cross-sectional study with retrospective ascertainment of patients with POMS evaluated at a single center with expertise in POMS and neuro-ophthalmology. As part of routine clinical care, patients with POMS are evaluated by a POMS expert and undergo volumetric brain MRI, including whole-brain (WB), subregional, and gray matter (GM) volume analyses. Patients with POMS are routinely referred to neuro-ophthalmology for evaluation that includes high-contrast visual acuity, color vision testing, and OCT. Generalized estimating equation (GEE) models, accounting for within-patient, intereye correlations (both eyes of each patient were included), MS disease duration, and disease-modifying therapy efficacy, were used to determine the relationship between visual pathway structure and function and volumetric MRI measures.

Results: Among 61 patients (122 eyes) with POMS, the mean age at the time of the volumetric MRI scan was 19.2 (SD = 3.7, range 10-27) years, with a median disease duration of 2.8 (range 0-14) years. Lower (worse) pRNFL thicknesses (mean 87.4 [17.2] µm) were associated with reduced volume percentiles of WB (p < 0.001, GEE models), total GM (p = 0.025), and thalamus (p = 0.038). pRNFL thinning was also associated with greater lesion (p = 0.006) and black hole (p = 0.028) volumes. Reduced color vision and decreased high-contrast visual acuity were associated with lower hippocampal volumes (p = 0.012 and p = 0.015, respectively).

Discussion: Our results demonstrate that changes in visual pathway structures are associated with reductions in overall brain volume and GM volumes, as well as greater lesion and black hole burden. Collectively, our results emphasize the importance of visual assessment in POMS and suggest that OCT reflects overall CNS neurodegeneration in this cohort.

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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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