Overexpression of miR-199b-5p in Colony Forming Unit-Hill's Colonies Positively Mediates the Inflammatory Response in Subclinical Cardiovascular Disease Model: Metformin Therapy Attenuates Its Expression.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
25 Jul 2024
Historique:
received: 25 06 2024
revised: 20 07 2024
accepted: 21 07 2024
medline: 10 8 2024
pubmed: 10 8 2024
entrez: 10 8 2024
Statut: epublish

Résumé

Well-controlled type 1 diabetes (T1DM) is characterized by inflammation and endothelial dysfunction, thus constituting a suitable model of subclinical cardiovascular disease (CVD). miR-199b-5p overexpression in murine CVD has shown proatherosclerotic effects. We hypothesized that miR-199b-5p would be overexpressed in subclinical CVD yet downregulated following metformin therapy. Inflammatory and vascular markers were measured in 29 individuals with T1DM and 20 matched healthy controls (HCs). miR-199b-5p expression in CFU-Hill's colonies was analyzed from each study group, and correlations with inflammatory/vascular health indices were evaluated. Significant upregulation of miR-199b-5p was observed in T1DM, which was significantly downregulated by metformin. miR-199b-5p correlated positively with vascular endothelial growth factor-D and c-reactive protein (CRP: nonsignificant). ROC analysis determined miR-199b-5p to define subclinical CVD by discriminating between HCs and T1DM individuals. ROC analyses of HbA1c and CRP showed that the upregulation of miR-199b-5p in T1DM individuals defined subclinical CVD at HbA1c > 44.25 mmol and CRP > 4.35 × 10

Identifiants

pubmed: 39125657
pii: ijms25158087
doi: 10.3390/ijms25158087
pii:
doi:

Substances chimiques

MicroRNAs 0
Metformin 9100L32L2N
mirn199 microRNA, human 0
Sirtuin 1 EC 3.5.1.-
C-Reactive Protein 9007-41-4
STAT3 Transcription Factor 0
Hypoglycemic Agents 0
Jagged-1 Protein 0
Biomarkers 0
JAG1 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Diabetes Research and Wellness Foundation
ID : None
Organisme : Diabetes Research Fund at Queen Elizabeth Hospital, UK
ID : None

Auteurs

Sherin Bakhashab (S)

Biochemistry Department, King Abdulaziz University, P.O. Box 80218, Jeddah 21589, Saudi Arabia.
Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Center of Excellence in Genomic Medicine Research, King Abdulaziz University, P.O. Box 80216, Jeddah 21589, Saudi Arabia.

Rosie Barber (R)

Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Biosciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.

Josie O'Neill (J)

Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Biosciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.

Catherine Arden (C)

Biosciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.

Jolanta U Weaver (JU)

Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK.
Department of Diabetes, Queen Elizabeth Hospital, Gateshead, Newcastle upon Tyne NE9 6SH, UK.
Vascular Biology and Medicine Theme, Newcastle University, Newcastle upon Tyne NE1 7RU, UK.

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Classifications MeSH