Sclerostin is expressed in the atherosclerotic plaques of patients who undergoing carotid endarterectomy.


Journal

Diabetes/metabolism research and reviews
ISSN: 1520-7560
Titre abrégé: Diabetes Metab Res Rev
Pays: England
ID NLM: 100883450

Informations de publication

Date de publication:
01 2019
Historique:
received: 01 06 2018
revised: 09 08 2018
accepted: 18 08 2018
pubmed: 26 8 2018
medline: 30 5 2019
entrez: 26 8 2018
Statut: ppublish

Résumé

Sclerostin (SC) is a monomeric glycoprotein expressed by osteocytes that affects bone formation. Recent studies have suggested a potential role for this protein in the pathophysiology of vascular diseases. The aim of the present study was to investigate SC expression in atherosclerotic plaques of patients affected by severe atherosclerotic disease who underwent carotid endarterectomy. We also evaluated possible differences in SC expression between patients with and without type 2 diabetes (T2D). This was a cross-sectional study involving 46 patients aged 55 to 80 years (mean, 71.1 ± 6.7 years, 36 men, 15 patients with T2D) who underwent carotid endarterectomy. Immunohistochemical levels of SC were evaluated in the atherosclerotic plaques by double-staining immunochemistry, and serum SC levels were evaluated by enzyme-linked immunosorbent assay. Sclerostin was present in the atherosclerotic plaques of all subjects investigated and increased significantly in the media compared with the intima (P < 0.0001) as well as in vascular smooth muscle cells (VSMCs) compared with the infiltrating macrophages (P < 0.0001). However, no significant difference in SC expression was observed between patients with and without T2D. No correlation was found between serum and immunohistochemical levels of SC; significantly increased SC serum levels were detected in males compared with females (P = 0.049). We have demonstrated, for the first time, the expression of SC in VSMCs of atherosclerotic plaques, suggesting a potential role for this protein in the development of atherosclerosis. Further studies are needed to understand if the role played by SC is detrimental or protective in the atherosclerotic disease process.

Sections du résumé

BACKGROUND
Sclerostin (SC) is a monomeric glycoprotein expressed by osteocytes that affects bone formation. Recent studies have suggested a potential role for this protein in the pathophysiology of vascular diseases. The aim of the present study was to investigate SC expression in atherosclerotic plaques of patients affected by severe atherosclerotic disease who underwent carotid endarterectomy. We also evaluated possible differences in SC expression between patients with and without type 2 diabetes (T2D).
METHODS
This was a cross-sectional study involving 46 patients aged 55 to 80 years (mean, 71.1 ± 6.7 years, 36 men, 15 patients with T2D) who underwent carotid endarterectomy. Immunohistochemical levels of SC were evaluated in the atherosclerotic plaques by double-staining immunochemistry, and serum SC levels were evaluated by enzyme-linked immunosorbent assay.
RESULTS
Sclerostin was present in the atherosclerotic plaques of all subjects investigated and increased significantly in the media compared with the intima (P < 0.0001) as well as in vascular smooth muscle cells (VSMCs) compared with the infiltrating macrophages (P < 0.0001). However, no significant difference in SC expression was observed between patients with and without T2D. No correlation was found between serum and immunohistochemical levels of SC; significantly increased SC serum levels were detected in males compared with females (P = 0.049).
CONCLUSIONS
We have demonstrated, for the first time, the expression of SC in VSMCs of atherosclerotic plaques, suggesting a potential role for this protein in the development of atherosclerosis. Further studies are needed to understand if the role played by SC is detrimental or protective in the atherosclerotic disease process.

Identifiants

pubmed: 30144272
doi: 10.1002/dmrr.3069
doi:

Substances chimiques

Adaptor Proteins, Signal Transducing 0
Bone Morphogenetic Proteins 0
Genetic Markers 0
SOST protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e3069

Informations de copyright

© 2018 John Wiley & Sons, Ltd.

Auteurs

Gaetano Leto (G)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Luca D'Onofrio (L)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Federica Lucantoni (F)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Simona Zampetti (S)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Giuseppe Campagna (G)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Chiara Foffi (C)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Chiara Moretti (C)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Angela Carlone (A)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Andrea Palermo (A)

Unit of Endocrinology and Diabetes Department of Medicine, Campus Bio-Medico University of Rome, Rome, Italy.

Martina Leopizzi (M)

Department of medical-Surgical Sciences and Biotechnology, Polo Pontino Sapienza University of Rome, Rome, Italy.

Natale Porta (N)

Department of medical-Surgical Sciences and Biotechnology, Polo Pontino Sapienza University of Rome, Rome, Italy.

Marco Massucci (M)

Department of Vascular Surgery, Santa Maria Goretti Hospital, Latina, Italy.

Andrea Lenzi (A)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Giovanni Battista Bertoletti (GB)

Department of Vascular Surgery, Santa Maria Goretti Hospital, Latina, Italy.

Carlo Della Rocca (CD)

Department of medical-Surgical Sciences and Biotechnology, Polo Pontino Sapienza University of Rome, Rome, Italy.

Raffaella Buzzetti (R)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

Articles similaires

Genome, Chloroplast Phylogeny Genetic Markers Base Composition High-Throughput Nucleotide Sequencing

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C

Classifications MeSH