Conway Miriam, Hosking Sarah L
Department of Optometry and Visual Science, City University, London, United Kingdom.
Optom Vis Sci. 2012 Jun;89(6):922-8. doi: 10.1097/OPX.0b013e318257a242.
Sturge-Weber syndrome (SWS) is a condition often associated with facial cutaneous angioma, vascular malformations in the brain, and ocular anomalies such as glaucoma. Reduced cerebral blood flow and ischemia have been well documented. Less is known about ocular blood flow despite the frequent associations between altered hemodynamics and the mechanisms underlying glaucomatous optic neuropathy. The aim of this research was to investigate retrobulbar hemodynamics in patients diagnosed with SWS.
The sample comprised 16 patients diagnosed with SWS and 16 age- and gender-matched normal control subjects. Four patients were diagnosed with both SWS and primary open-angle glaucoma (mean age 34.3 years; SD 26.9 years), three patients with both SWS and closed-angle glaucoma (mean age 23.3 years; SD 18.0 years), and nine patients with SWS and no glaucoma (mean age 17.2 years; SD 9.1 years). Systemic blood pressure and intraocular pressure were measured to determine the mean arterial pressure and ocular perfusion pressure. All patients and subjects underwent ultrasonography of the ophthalmic artery, central retinal artery, and short posterior ciliary arteries.
No significant difference between groups for mean arterial pressure or ocular perfusion pressure (p > 0.05) was recorded. Participants diagnosed with SWS and primary open-angle glaucoma showed significantly reduced end-diastolic velocity (mean 0.036 m/s; SD 0.005 m/s) in their central retinal artery (p = 0.016) when compared against their age-matched normal controls (mean 0.054 m/s; SD 0.010 m/s). Participants diagnosed with SWS and no glaucoma also showed significantly reduced end-diastolic velocity (mean 0.038 m/s; SD 0.015 m/s) in their central retinal artery (p = 0.046) when compared against their age-matched normal controls (mean 0.054 m/s; SD 0.014 m/s).
Retrobulbar hemodynamics appear to be altered in participants diagnosed with SWS irrespective of their diagnosis of glaucoma. Further research is needed to ascertain whether there are any long-term consequences of such changes to ocular physiology.
斯特奇-韦伯综合征(SWS)是一种常与面部皮肤血管瘤、脑部血管畸形以及青光眼等眼部异常相关的病症。脑血流量减少和缺血现象已有充分记录。尽管血流动力学改变与青光眼性视神经病变的潜在机制之间存在频繁关联,但关于眼部血流的了解却较少。本研究的目的是调查被诊断为SWS的患者的球后血流动力学情况。
样本包括16名被诊断为SWS的患者以及16名年龄和性别匹配的正常对照受试者。4名患者同时被诊断为SWS和原发性开角型青光眼(平均年龄34.3岁;标准差26.9岁),3名患者同时被诊断为SWS和闭角型青光眼(平均年龄23.3岁;标准差18.0岁),9名患者患有SWS但无青光眼(平均年龄17.2岁;标准差9.1岁)。测量全身血压和眼压以确定平均动脉压和眼灌注压。所有患者和受试者均接受了眼动脉、视网膜中央动脉和睫状后短动脉的超声检查。
各组之间的平均动脉压或眼灌注压无显著差异(p>0.05)。与年龄匹配的正常对照受试者(平均0.054 m/s;标准差0.010 m/s)相比,被诊断为SWS和原发性开角型青光眼的参与者视网膜中央动脉的舒张末期速度显著降低(平均0.036 m/s;标准差0.005 m/s)(p = 0.016)。与年龄匹配的正常对照受试者(平均0.054 m/s;标准差0.014 m/s)相比,被诊断为SWS但无青光眼的参与者视网膜中央动脉的舒张末期速度也显著降低(平均0.038 m/s;标准差0.015 m/s)(p = 0.046)。
被诊断为SWS的参与者无论是否被诊断为青光眼,其球后血流动力学似乎都发生了改变。需要进一步研究以确定这种眼部生理变化是否有任何长期后果。