Sorrentino Francesco Saverio, Bonifazzi Claudio, Perri Paolo
Department of Surgical Sciences, Unit of Ophthalmology, Ospedale Maggiore, Bologna, Italy.
Department of Biomedical and Surgical Sciences, Section of Human Physiology, University of Ferrara, 44100 Ferrara, Italy.
J Ophthalmol. 2015;2015:405234. doi: 10.1155/2015/405234. Epub 2015 Nov 3.
Retinitis pigmentosa is a clinical and genetic group of inherited retinal disorders characterized by alterations of photoreceptors and retinal pigment epithelium leading to a progressive concentric visual field restriction, which may bring about severe central vision impairment. Haemodynamic studies in patients with retinitis pigmentosa have demonstrated ocular blood flow abnormalities both in retina-choroidal and in retroocular vascular system. Moreover, several investigations have studied the augmentation of endothelin-1 plasma levels systemically in the body and locally in the eye. This might account for vasoconstriction and ischemia, typical in vascular dysregulation syndrome, which can be considered an important factor of reduction of the ocular blood flow in subjects affected by retinitis pigmentosa.
视网膜色素变性是一组临床和遗传的遗传性视网膜疾病,其特征是光感受器和视网膜色素上皮发生改变,导致进行性同心视野受限,这可能会导致严重的中心视力损害。对视网膜色素变性患者的血流动力学研究表明,视网膜脉络膜和眼后血管系统均存在眼部血流异常。此外,多项研究对体内全身和眼部局部内皮素-1血浆水平的升高进行了研究。这可能解释了血管调节异常综合征中典型的血管收缩和缺血,而血管调节异常综合征可被认为是影响视网膜色素变性患者眼部血流减少的一个重要因素。