Interaction between flicker-induced vasodilatation and pressure autoregulation in early retinopathy of Type 2 diabetes
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- Bek, T., Hajari, J. & Jeppesen, P. Graefes Arch Clin Exp Ophthalmol (2008) 246: 763. doi:10.1007/s00417-008-0766-y
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Diabetic retinopathy is accompanied with changes in the autoregulation of retinal blood flow secondary to changes in the systemic blood pressure and the retinal metabolism. In the present study we tested the working hypothesis that there is an interaction between these mechanisms that might be relevant for understanding and treating flow disturbances in diabetic retinopathy.
Group 1: twenty normal persons.
Group 2: fourteen patients with type 2 diabetes mellitus and no diabetic retinopathy.
Group 3: twenty type 2 diabetic patients with minimal diabetic retinopathy and a diabetes duration similar to that of the patients in group 2.
The increased blood pressure induced by isometric exercise induced a non-significant vasoconstriction in the normal persons and in the diabetic patients without retinopathy (p = 0.10 and p = 0.84 respectively), and a non-significant vasodilatation in the diabetic patients with mild retinopathy (p = 0.10).
The flicker stimulus elicited a significant vasodilatation of retinal arterioles that decreased significantly from the normal persons to the diabetic patients without and with retinopathy (linear regression, p < 0.01). The flicker-induced vasodilatation was not significantly affected by a simultaneous increase in the arterial blood pressure in normal persons (p = 0.85). Conversely, in the diabetic patients the reduced diameter response during flicker was counteracted by a simultaneous increase in the blood pressure, to a level not differing significantly from the response of normal persons (p = 0.75).
Intervention studies aimed at modifying perfusion in retinal disease should consider the interaction between different mechanisms for autoregulating retinal blood flow. New treatment modalities for retinal vascular disease might need to target several mechanisms of tone control in retinal arterioles simultaneously.