TY - JOUR
T1 - Reduced retinal vessel response to flicker stimulation but not to exogenous nitric oxide in type 1 diabetes
AU - Pemp, Berthold
AU - Garhofer, Gerhard
AU - Weigert, Günther
AU - Karl, Katharina
AU - Resch, Hemma
AU - Wolzt, Michael
AU - Schmetterer, Leopold
PY - 2009
Y1 - 2009
N2 - PURPOSE. Various studies have shown that retinal vessels in patients with diabetes mellitus have a reduced capacity to adapt to changes in perfusion pressure and to stimulation with flickering light. Structural and functional changes in retinal vessels in diabetes could lead to a general reduction of vasodilator and/or vasoconstrictor capacity. To gain more insight into this topic, we compared the response of retinal vessel diameters to systemic glyceryl trinitrate (GTN) and stimulation with diffuse luminance flicker in patients with diabetes and healthy control subjects. METHODS. Twenty patients with type 1 diabetes mellitus featuring no or mild nonproliferative diabetic retinopathy and 20 healthy, age-matched subjects were included in this study. A vessel analyzer was used for measurement of diameters of retinal arteries and veins. The response of diameters was measured continuously during stimulation with flickering light, as well as immediately after sublingual application of 0.8 mg GTN. RESULTS. The response of retinal vessels to flickering light was significantly reduced in the patients with diabetes (arteries: 2.9% in diabetes versus 7.0% in control subjects, P > 0.002; veins: 4.6% in diabetes versus 6.8% in control subjects, P > 0.020). GTN-induced vasodilatation was not different between the patients with diabetes and the healthy control subjects P ≥ 0.70). CONCLUSIONS. The present study confirmed reduced response of retinal vessels to stimulation with flickering light in diabetes. The response of retinal vessels to a direct NO-donor, however, was maintained. This result indicates that abnormal flickerinduced vasodilatation in diabetes is not a consequence of generally reduced retinal vascular reactivity (ClinicalTrials.gov number, NCT00432029).
AB - PURPOSE. Various studies have shown that retinal vessels in patients with diabetes mellitus have a reduced capacity to adapt to changes in perfusion pressure and to stimulation with flickering light. Structural and functional changes in retinal vessels in diabetes could lead to a general reduction of vasodilator and/or vasoconstrictor capacity. To gain more insight into this topic, we compared the response of retinal vessel diameters to systemic glyceryl trinitrate (GTN) and stimulation with diffuse luminance flicker in patients with diabetes and healthy control subjects. METHODS. Twenty patients with type 1 diabetes mellitus featuring no or mild nonproliferative diabetic retinopathy and 20 healthy, age-matched subjects were included in this study. A vessel analyzer was used for measurement of diameters of retinal arteries and veins. The response of diameters was measured continuously during stimulation with flickering light, as well as immediately after sublingual application of 0.8 mg GTN. RESULTS. The response of retinal vessels to flickering light was significantly reduced in the patients with diabetes (arteries: 2.9% in diabetes versus 7.0% in control subjects, P > 0.002; veins: 4.6% in diabetes versus 6.8% in control subjects, P > 0.020). GTN-induced vasodilatation was not different between the patients with diabetes and the healthy control subjects P ≥ 0.70). CONCLUSIONS. The present study confirmed reduced response of retinal vessels to stimulation with flickering light in diabetes. The response of retinal vessels to a direct NO-donor, however, was maintained. This result indicates that abnormal flickerinduced vasodilatation in diabetes is not a consequence of generally reduced retinal vascular reactivity (ClinicalTrials.gov number, NCT00432029).
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U2 - 10.1167/iovs.08-3260
DO - 10.1167/iovs.08-3260
M3 - Article
C2 - 19369238
AN - SCOPUS:70349249516
SN - 0146-0404
VL - 50
SP - 4029
EP - 4032
JO - Investigative Ophthalmology and Visual Science
JF - Investigative Ophthalmology and Visual Science
IS - 9
ER -