Gess Adam, Christiansen Stephen P, Pond David, Peters Charles
Department of Ophthalmology, University of Minnesota, Minneapolis, Minnesota 55455, USA.
J AAPOS. 2008 Jun;12(3):273-6. doi: 10.1016/j.jaapos.2007.11.012. Epub 2008 Mar 24.
X-linked adrenoleukodystrophy (X-ALD) is an inherited disease characterized by cerebral demyelination, adrenal insufficiency, and progressive neurological deterioration. Hematopoietic cell transplantation (HCT) is the only effective treatment. Visual dysfunction is a common component of the disease and may continue to progress in patients after HCT. This study was designed to determine prognostic factors predictive of vision loss after HCT.
A retrospective chart review was performed for all boys who had HCT for cerebral X-ALD at the University of Minnesota between 1991 and 2002. Patients were included if they survived 100 days post-HCT and had pre- and post-HCT ophthalmology evaluation. Complete data were available for 14 patients. Patient characteristics examined included HLA match status, graft-versus-host disease prophylaxis, source of HCT, reason for diagnosis, age at treatment, magnetic resonance imaging (MRI) severity score, pattern of demyelination on MRI, and pretreatment performance intelligence quotient (IQ). Univariate analysis was performed for correlation with posttransplant visual acuity and optic disk pallor.
Factors significantly correlated with loss of visual acuity after HCT included pretransplant MRI severity score >11 (p = 0.03), pretransplant performance IQ <76 (p = 0.02), and the presence of pretransplant parieto-occipital demyelination on MRI (p = 0.03). Additionally, the presence of pretransplant parieto-occipital demyelination on MRI was found to correlate with the development of new optic disk pallor after HCT (p = 0.05).
This study identifies patient characteristics predictive of vision loss after HCT for X-ALD. Decisions about treatment for X-ALD rely heavily upon prognostic information about adverse outcomes following HCT. These findings will aid clinicians counseling patients considering HCT for X-ALD.
X连锁肾上腺脑白质营养不良(X-ALD)是一种遗传性疾病,其特征为脑白质脱髓鞘、肾上腺功能不全和进行性神经功能恶化。造血细胞移植(HCT)是唯一有效的治疗方法。视觉功能障碍是该疾病的常见组成部分,并可能在HCT后患者中继续进展。本研究旨在确定预测HCT后视力丧失的预后因素。
对1991年至2002年在明尼苏达大学因脑型X-ALD接受HCT的所有男孩进行回顾性病历审查。如果患者在HCT后存活100天且有HCT前后的眼科评估,则纳入研究。14例患者有完整数据。检查的患者特征包括HLA匹配状态、移植物抗宿主病预防、HCT来源、诊断原因、治疗时年龄、磁共振成像(MRI)严重程度评分、MRI上的脱髓鞘模式以及预处理时的表现智商(IQ)。对与移植后视力和视盘苍白的相关性进行单因素分析。
与HCT后视力丧失显著相关的因素包括移植前MRI严重程度评分>11(p = 0.03)、移植前表现IQ<76(p = 0.02)以及MRI上存在移植前顶枕叶脱髓鞘(p = 0.03)。此外,发现MRI上存在移植前顶枕叶脱髓鞘与HCT后新的视盘苍白的发展相关(p = 0.05)。
本研究确定了X-ALD患者HCT后视力丧失的预测特征。X-ALD的治疗决策在很大程度上依赖于HCT后不良结局的预后信息。这些发现将有助于临床医生为考虑X-ALD进行HCT的患者提供咨询。