Maturity onset diabetes of the young and fibrin-related thrombosis risk.


Journal

Diabetes & vascular disease research
ISSN: 1752-8984
Titre abrégé: Diab Vasc Dis Res
Pays: England
ID NLM: 101234011

Informations de publication

Date de publication:
Historique:
entrez: 18 12 2020
pubmed: 19 12 2020
medline: 26 1 2021
Statut: ppublish

Résumé

Fibrin network characteristics determine predisposition to cardiovascular disease (CVD). Individuals with type 1 (T1DM) and type 2 diabetes mellitus (T2DM) have higher risk of CVD and display deranged fibrin network structure. Those with maturity onset diabetes of the young (MODY) may also be at increased risk but their fibrin clot properties have not been studied. Plasma clots properties from 13 individuals with HNF1A-MODY, 12 matched-individuals with T2DM and 12 with T1DM were studied using a validated turbidimetric assay and confocal microscopy. Plasma levels of fibrinogen, plasminogen activator inhibitor-1, complement C3 and C-reactive protein were also measured. MODY clot maximum absorbance was 0.37 ± 0.03 AU, similar to T1DM (0.32 ± 0.03 AU; HNF1A-MODY fibrin network alterations are at least as pronounced as in T1DM but less thrombotic than T2DM clots. Differences in fibrin clot characteristics comparing HNF1A-MODY and T2DM may, in part, relate to lower C3 levels.

Sections du résumé

BACKGROUND
Fibrin network characteristics determine predisposition to cardiovascular disease (CVD). Individuals with type 1 (T1DM) and type 2 diabetes mellitus (T2DM) have higher risk of CVD and display deranged fibrin network structure. Those with maturity onset diabetes of the young (MODY) may also be at increased risk but their fibrin clot properties have not been studied.
METHODS
Plasma clots properties from 13 individuals with HNF1A-MODY, 12 matched-individuals with T2DM and 12 with T1DM were studied using a validated turbidimetric assay and confocal microscopy. Plasma levels of fibrinogen, plasminogen activator inhibitor-1, complement C3 and C-reactive protein were also measured.
RESULTS
MODY clot maximum absorbance was 0.37 ± 0.03 AU, similar to T1DM (0.32 ± 0.03 AU;
CONCLUSIONS
HNF1A-MODY fibrin network alterations are at least as pronounced as in T1DM but less thrombotic than T2DM clots. Differences in fibrin clot characteristics comparing HNF1A-MODY and T2DM may, in part, relate to lower C3 levels.

Identifiants

pubmed: 33334146
doi: 10.1177/1479164120963048
pmc: PMC7919224
doi:

Substances chimiques

Biomarkers 0
C3 protein, human 0
Complement C3 0
HNF1A protein, human 0
Hepatocyte Nuclear Factor 1-alpha 0
Plasminogen Activator Inhibitor 1 0
SERPINE1 protein, human 0
Fibrin 9001-31-4
C-Reactive Protein 9007-41-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1479164120963048

Subventions

Organisme : British Heart Foundation
ID : FS/19/45/34443
Pays : United Kingdom

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Auteurs

R C Sagar (RC)

Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, West Yorkshire, UK.

F Phoenix (F)

Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, West Yorkshire, UK.

G Thanabalasingham (G)

Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, UK.

K Naseem (K)

Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, West Yorkshire, UK.

R A Ajjan (RA)

Leeds Institute of Cardiovascular and Metabolic Medicine, Faculty of Medicine and Health, University of Leeds, Leeds, West Yorkshire, UK.

K R Owen (KR)

Oxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, UK.
Oxford NIHR Biomedical Research Centre, Churchill Hospital, Oxford, UK.

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Classifications MeSH