Background: We introduce a pathogenetic concept which explains the present
known clinical and experimental facts.
Materials and methods: The known clinical risk factors for glaucomatous opt
ic neuropathy as well as the outcomes of the experimental studies were syst
ematically collected.
Results: IOP fluctuations are more damaging than a stable increased IOP, re
duced circulation due to vascular dysregulation is more damaging than reduc
ed circulation due to arteriosclerosis and the glaucomatous damage is clear
ly different from a pure ischemic lesion.
Conclusions: Although IOP can damage mechanically, IOP fluctuation and bloo
d pressure drops may lead to short term ischemia, followed by a reperfusion
damage. A vascular dysregulation interferes with the autoregulation of ocu
lar perfusion and renders the eye more sensitive to IOP increase or blood p
ressure decrease.