Buono Lawrence M, Foroozan Rod, Sergott Robert C, Savino Peter J
Neuro-Ophthalmology Service, Wills Eye Hospital, Thomas Jefferson Medical College, Philadelphia, PA, USA.
Curr Opin Ophthalmol. 2002 Dec;13(6):362-70. doi: 10.1097/00055735-200212000-00004.
Normal tension glaucoma and dominant optic atrophy share many overlapping clinical features, and differentiating between these two diseases is often difficult. The gene responsible for dominant optic atrophy is the OPA1 gene located on chromosome 3. This gene encodes for a protein product that is involved in mitochondrial metabolic function. Recent genetic linkage analysis of patients with normal tension glaucoma has shown an association with polymorphisms of the OPA1 gene. This association suggests that normal tension glaucoma may actually be a hereditary optic neuropathy with a pathophysiology based in mitochondrial dysfunction.
正常眼压性青光眼和显性遗传性视神经萎缩具有许多重叠的临床特征,区分这两种疾病往往很困难。导致显性遗传性视神经萎缩的基因是位于3号染色体上的OPA1基因。该基因编码一种参与线粒体代谢功能的蛋白质产物。最近对正常眼压性青光眼患者的基因连锁分析表明,其与OPA1基因的多态性有关。这种关联表明,正常眼压性青光眼可能实际上是一种基于线粒体功能障碍病理生理学的遗传性视神经病变。