Sublingual microvasculature in diabetic patients.


Journal

Microvascular research
ISSN: 1095-9319
Titre abrégé: Microvasc Res
Pays: United States
ID NLM: 0165035

Informations de publication

Date de publication:
05 2020
Historique:
received: 06 07 2019
revised: 24 12 2019
accepted: 24 12 2019
pubmed: 4 1 2020
medline: 21 7 2020
entrez: 4 1 2020
Statut: ppublish

Résumé

Diabetes is associated with micro- and macrovascular complications. The aim of the study was to investigate microvascular parameters (glycocalyx dimensions, perfused and total capillary density) in vivo in patients with type 1 and type 2 diabetes mellitus. In vivo sublingual videomicroscopy using sidestream darkfield - derived imaging was performed in 36 patients with diabetes mellitus (type 1: n = 20, type 2: n = 16) and compared to a control group of 36 healthy volunteers. Patients with HbA1c levels ≥ 8% had a significantly higher perfused boundary region (PBR; signifying the loss of glycocalyx dimensions) compared to patients with HbA1c levels < 8%, which was more pronounced in type 1 diabetes (2.08 μm [1.95-2.16 μm] vs.1.9 μm [1.66-1.94 μm], p = .029). Capillary density did not differ significantly between patients with diabetes and healthy controls. PBR was inversely related to RBC filling percentage and perfused capillary density in diabetic patients (r = -0.754, p < .001 and r = -0.505, p = .002, respectively) as well as in healthy volunteers (r = -0.701, p < .001 and r = -0.150, p = n.s.) signifying the association between glycocalyx dimensions and microvessel perfusion. Renal parameters were associated with microvascular perfusion in patients with type 2 diabetes (correlation between eGFR and perfused capillary density: r = 0. 568, p = .027/RBC filling percentage: r = 0.657, p = .008). In addition, the ratio of perfused/total capillary density correlated with CRP levels in type 2 diabetes (r = 0.682, p = .021). In conclusion, diabetes is associated with loss of glycocalyx density.

Identifiants

pubmed: 31899168
pii: S0026-2862(19)30176-1
doi: 10.1016/j.mvr.2019.103971
pii:
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
hemoglobin A1c protein, human 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

103971

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest. The manuscript is part of the PhD thesis of Dr. Patricia P. Wadowski (Medical University of Vienna, published 2019).

Auteurs

Patricia P Wadowski (PP)

Department of Internal Medicine II, Division of Angiology, Medical University of Vienna, Vienna, Austria.

Alexandra Kautzky-Willer (A)

Department of Medicine III, Division of Endocrinology, Medical University of Vienna, Vienna, Austria.

Thomas Gremmel (T)

Department of Internal Medicine II, Division of Angiology, Medical University of Vienna, Vienna, Austria.

Renate Koppensteiner (R)

Department of Internal Medicine II, Division of Angiology, Medical University of Vienna, Vienna, Austria.

Peter Wolf (P)

Department of Medicine III, Division of Endocrinology, Medical University of Vienna, Vienna, Austria.

Sebastian Ertl (S)

Department of Internal Medicine II, Division of Angiology, Medical University of Vienna, Vienna, Austria; Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.

Constantin Weikert (C)

Department of Internal Medicine II, Division of Angiology, Medical University of Vienna, Vienna, Austria.

Christian Schörgenhofer (C)

Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria.

Bernd Jilma (B)

Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Austria. Electronic address: bernd.jilma@meduniwien.ac.at.

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Classifications MeSH