Capillary pressure may predict preclinical changes in the eye
dc.contributor.author | Gooding, KM | |
dc.contributor.author | Tooke, JE | |
dc.contributor.author | von Lany, H | |
dc.contributor.author | Mitra, M | |
dc.contributor.author | Ling, R | |
dc.contributor.author | Ball, CI | |
dc.contributor.author | Mawson, D | |
dc.contributor.author | Skinner, K | |
dc.contributor.author | Shore, AC | |
dc.date.accessioned | 2019-02-19T13:09:43Z | |
dc.date.issued | 2010-06-06 | |
dc.description.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. | en_GB |
dc.description.sponsorship | Diabetes UK | en_GB |
dc.description.sponsorship | National Institute for Health Research (NIHR) | en_GB |
dc.identifier.citation | Vol. 53 (9), pp. 2029 - 2035 | en_GB |
dc.identifier.doi | 10.1007/s00125-010-1805-x | |
dc.identifier.uri | http://hdl.handle.net/10871/35983 | |
dc.language.iso | en | en_GB |
dc.publisher | Springer Verlag | en_GB |
dc.relation.url | http://www.ncbi.nlm.nih.gov/pubmed/20526763 | en_GB |
dc.rights | © The Author(s) 2010. open access. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. | en_GB |
dc.subject | Adult | en_GB |
dc.subject | Aged | en_GB |
dc.subject | Diabetic Retinopathy | en_GB |
dc.subject | Female | en_GB |
dc.subject | Fovea Centralis | en_GB |
dc.subject | Humans | en_GB |
dc.subject | Macula Lutea | en_GB |
dc.subject | Macular Edema | en_GB |
dc.subject | Male | en_GB |
dc.subject | Middle Aged | en_GB |
dc.subject | Obesity | en_GB |
dc.subject | Tomography, Optical Coherence | en_GB |
dc.subject | Capillary pressure | en_GB |
dc.subject | Fluid filtration | en_GB |
dc.subject | Fovea thickness | en_GB |
dc.subject | Macular oedema | en_GB |
dc.title | Capillary pressure may predict preclinical changes in the eye | en_GB |
dc.type | Article | en_GB |
dc.date.available | 2019-02-19T13:09:43Z | |
dc.identifier.issn | 0012-186X | |
exeter.place-of-publication | Germany | |
dc.description | This is the final version. Available on open access from Springer Verlag via the DOI in this record | en_GB |
dc.identifier.journal | Diabetologia | en_GB |
dc.rights.uri | https://creativecommons.org/licenses/by-nc/3.0/ | en_GB |
dcterms.dateAccepted | 2010-04-30 | |
rioxxterms.version | VoR | en_GB |
rioxxterms.licenseref.startdate | 2010-04-30 | |
rioxxterms.type | Journal Article/Review | en_GB |
refterms.dateFCD | 2019-02-19T13:06:12Z | |
refterms.versionFCD | VoR | |
refterms.dateFOA | 2019-02-19T13:09:46Z |
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Except where otherwise noted, this item's licence is described as © The Author(s) 2010. open access. This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.