Capillary pressure may predict preclinical changes in the eye.

Diabetologia

Diabetes and Vascular Medicine, Institute of Biomedical and Clinical Science, Peninsula Medical School, Exeter, UK.

Published: September 2010

AI Article Synopsis

  • The study explores the link between microvascular dysfunction and macular thickness in non-diabetic individuals, finding that capillary pressure is significantly related to fovea thickness measured by optical coherence tomography (OCT).
  • Fovea thickness was found to be within normal limits, but surprisingly, it did not correlate with other microvascular factors like filtration capacity or endothelial function.
  • The results suggest that capillary pressure plays a crucial role in fluid movement across blood vessel walls, indicating potential targets for preventative strategies in managing conditions like diabetic retinopathy.

Article Abstract

Aims/hypothesis: Microvascular dysfunction is associated with end-organ damage. Macular oedema is an important component of diabetic retinopathy. Macular thickness can be accurately quantified by optical coherence tomography (OCT), enabling accurate assessment of the macular prior to clinically apparent abnormalities. We investigated whether macular (fovea) thickness in non-diabetic individuals is related to the microvascular variables controlling fluid filtration across a blood vessel wall, in particular capillary pressure and the microvascular filtration capacity (Kf).

Methods: We recruited 50 non-diabetic individuals (25 men, 25 women; age range: 26-78 years; BMI range: 20-46 kg/m(2)). Fovea thickness was assessed by OCT. Microvascular assessments included: finger nailfold capillary pressure; Kf; microvascular structural assessments, i.e. skin vasodilatory capacity, minimum vascular resistance (MVR) and microvascular distensibility; and endothelial function.

Results: At 214.6 (19.9) microm (mean [SD]), fovea thickness was within normal range. Capillary pressure, adjusted for BMI, was associated with fovea thickness (standardised beta 0.573, p = 0.006, linear regression). Fovea thickness was not associated with Kf, microvascular structural assessments or endothelial function. Capillary pressure was still associated with fovea thickness when adjusted for microvascular variables (Kf, vasodilatory capacity, MVR, microvascular distensibility or endothelial function), or for risk factors for diabetes (systemic blood pressure, insulin sensitivity, inflammation, glycaemic status and lipids) and age.

Conclusions/interpretation: Capillary pressure, a key determinant of movement of fluid across a blood vessel wall, is associated with fovea thickness in non-diabetic individuals. This suggests that with regard to potential preventative or therapeutic targets, attention should be directed at the mechanisms determining retinal microvascular pressure.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2910883PMC
http://dx.doi.org/10.1007/s00125-010-1805-xDOI Listing

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