Peripheral Microvascular Abnormalities Associated with Open-Angle Glaucoma.
Elise V Taniguchi, Izabela N F Almeida, Carolina P B Gracitelli, Cecília Agapito, Claudio Zett, Letícia Sant'Ana, Cristiane Kayser, Tiago S Prata, Augusto Paranhos
Summary
Significant peripheral microvascular abnormalities were found in patients with OAG compared to controls, suggesting that microvascular changes might play a role in the pathogenesis of the disease.
Abstract
PURPOSE
To investigate peripheral microvascular abnormalities associated with patients with open-angle glaucoma (OAG).
DESIGN
This was a cross-sectional study.
PARTICIPANTS
Patients with OAG and controls.
METHODS
All subjects underwent detailed ophthalmic evaluation, including Humphrey visual field (HVF) tests and swept source OCT. To evaluate peripheral microvascular abnormalities, nailfold capillaroscopy (NFC) and laser Doppler imaging (LDI) were performed. The presence of microhemorrhages, tortuous capillaries, dilated capillaries, avascular areas, and the capillary density, among other characteristics, were recorded using NFC; fingertip blood flow (FBF) was measured using LDI at different time points, before and 1, 10, and 20 minutes after exposure to a cold stimulus. In addition, venous blood samples were collected to measure serum endothelin-1 (ET-1) concentrations as well as serum autoantibodies.
MAIN OUTCOME MEASURES
Presence of microhemorrhages, tortuous capillaries, and dilated capillaries; FBF; ET-1; and autoantibodies.
RESULTS
Sixty-eight subjects (43 patients with OAG and 25 controls) were enrolled in the study. Microhemorrhages were found in the nail bed of 65.1% of the patients with OAG compared with 25.0% of the controls (P = 0.003). There was a significant difference in the mean FBF at the baseline in patients with OAG versus controls (293.6 ± 100.2 vs 388.8 ± 52.0 perfusion units, respectively, P 0.05, for all) showed any difference between the 2 groups.
CONCLUSIONS
Significant peripheral microvascular abnormalities were found in patients with OAG compared to controls, suggesting that microvascular changes might play a role in the pathogenesis of the disease. In addition, part of these peripheral microvascular abnormalities seems to be correlated with both functional and structural glaucomatous damage. FINANCIAL DISCLOSURE(S): The author(s) have no proprietary or commercial interest in any materials discussed in this article.
Keywords
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