Sturge-Weber综合征尿液血管生成因子与神经系统预后的纵向前瞻性研究

Brooke Kimbrell, Kieran D. McKenney, SangEun Yeom, Isabelle Iannotti, Alyssa Day, Kelly Harmon, Alison Sebold, Lindsay Smegal, Katherine Kaplan, Cassie Daisy, Rama Aldakhlallah, Michael Taylor, Anna Pinto, Adrienne Hammill, Marsha A. Moses, Anne Comi
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引用次数: 0

摘要

该研究通过尿液血管生成因子确定了Sturge-Weber综合征(SWS)神经功能预后的生物标志物,并在SWS队列中获取了纵向自然史数据。在研究期间,男性性别与认知功能神经评分的恶化有关。两岁前开始癫痫发作的年龄与神经评分恶化密切相关。患有 SWS 的儿童与认知功能相关的神经生活质量较低。在学龄儿童中,癫痫发作严重程度、男性和较早的发病年龄与较差的生活神经质量有关。与对照组相比,SWS 患儿尿液中的碱性成纤维细胞生长因子升高,而血管内皮生长因子升高则与较好的神经评分有关。这项研究是首个针对 SWS 患者的多中心、前瞻性纵向研究。该研究确定了重要的临床预后因素,如癫痫发作年龄和男性性别,按年龄组划分的症状进展情况,并表明需要进一步研究血管生成机制和潜在的生物标志物。
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Longitudinal prospective study of Sturge–Weber syndrome urine angiogenic factors and neurological outcome

Objective

This study identified biomarkers of neurological outcome in Sturge-Weber syndrome (SWS) via urine angiogenic factors and captured longitudinally derived natural history data within an SWS cohort.

Methods

This longitudinal, prospective, multicentered study of 61 people with SWS aged 0.4–55 years reports port-wine birthmark score, Neuroscore, Neuro-Quality of Life, and urine angiogenic factors over a two-year period.

Results

Cognitive Neuroscore worsened over time for children aged 0–2 years. Male sex was associated with worsening Cognitive Function Neuroscore during the study. Age of seizure onset before 2 years was strongly associated with worse Neuroscore. Children with SWS had low Neuro-Quality of Life related to cognitive function. Seizure severity, male sex, and earlier age of seizure onset were associated with worse Neuro-Quality of Life in school-aged children. Children with SWS have elevated basic fibroblast growth factor in their urine compared with controls, whereas higher vascular endothelial growth factor was associated with better Neuroscore.

Interpretation

This study is the first multicenter, prospective, and longitudinal study of people with SWS. It identifies significant clinical prognostic factors such as age of seizure onset and male sex, informs symptom progression over time by age group, and suggests that further study of angiogenic mechanisms and potential biomarkers are needed.

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