advertisement
A growing number of mostly small-scale studies are part of an emerging clinical spectrum, in which pseudoexfoliation (PEX) syndrome appears to be associated with cardiovascular and cerebrovascular diseases. These include aneurysms of the abdominal aorta, asymptomatic myocardial dysfunction, transient ischemic attacks, Alzheimer's disease and a history of angina pectoris, arterial hypertension, myocardial infarction, or stroke.1-5 Akarsu and Ünal (924) add to these studies by showing that PEX syndrome is associated with alterations in cerebral hemodynamics. Using transcranial color doppler technology, they measured a significantly lower blood flow velocity and significantly higher resisitivity and pulsatility indices in the middle cerebral artery of 19 patients with PEX glaucoma compared with a healthy age- and sex-matched control group. Adjusted systolic and diastolic blood pressures in both groups and discontinuation of anti-glaucoma medications in the study group suggest a disease-specific association.
Observations indicate a systemic vascular dysfunction in PEX patientsIt may, however, be argued that the functional alterations result from increased IOP in these patients. Yet, another recent study retrospectively investigating 1150 patients with either PEX glaucoma or primary open-angle glaucoma (POAG) found a significantly higher frequency of chronic cerebral disorders (senile dementia, cerebral ischemia) and acute cerebrovascular events (thromboses, embolies, hemorrhages) in the PEX group compared with the POAG group.6 And finally, significantly reduced cerebral blood flow velocities have recently been reported in both PEX patients with and without glaucoma.7 These observations indicate a systemic vascular dysfunction in PEX patients, independent of the presence of glaucoma, which may be either causative or a consequence of the disease. Nevertheless, prospective, randomized multicenter studies are necessary to definitely link PEX syndrome with an increased risk for cardiovascular and cerebrovascular disease.