Microcalcification and Thoracic Aortopathy: A Window Into Disease Severity.

aneurysm, dissecting aorta, thoracic aortic aneurysm calcinosis elastin sodium fluoride vascular calcification

Journal

Arteriosclerosis, thrombosis, and vascular biology
ISSN: 1524-4636
Titre abrégé: Arterioscler Thromb Vasc Biol
Pays: United States
ID NLM: 9505803

Informations de publication

Date de publication:
08 2022
Historique:
pubmed: 1 7 2022
medline: 30 7 2022
entrez: 30 6 2022
Statut: ppublish

Résumé

Patients with thoracic aortopathy are at increased risk of catastrophic aortic dissection, carrying with it substantial mortality and morbidity. Although granular medial calcinosis (medial microcalcification) has been associated with thoracic aortopathy, its relationship to disease severity has yet to be established. One hundred one thoracic aortic specimens were collected from 57 patients with thoracic aortopathy and 18 control subjects. Standardized histopathologic scores, immunohistochemistry, and nanoindentation (tissue elastic modulus) were compared with the extent of microcalcification on von Kossa histology and 18F-sodium fluoride autoradiography. Microcalcification content was higher in thoracic aortopathy samples with mild (n=28; 6.17 [2.71-10.39]; Medial microcalcification is a marker of aortopathy, although progression to severe aortopathy is associated with loss of both elastin fibers and microcalcification.

Sections du résumé

BACKGROUND
Patients with thoracic aortopathy are at increased risk of catastrophic aortic dissection, carrying with it substantial mortality and morbidity. Although granular medial calcinosis (medial microcalcification) has been associated with thoracic aortopathy, its relationship to disease severity has yet to be established.
METHODS
One hundred one thoracic aortic specimens were collected from 57 patients with thoracic aortopathy and 18 control subjects. Standardized histopathologic scores, immunohistochemistry, and nanoindentation (tissue elastic modulus) were compared with the extent of microcalcification on von Kossa histology and 18F-sodium fluoride autoradiography.
RESULTS
Microcalcification content was higher in thoracic aortopathy samples with mild (n=28; 6.17 [2.71-10.39];
CONCLUSIONS
Medial microcalcification is a marker of aortopathy, although progression to severe aortopathy is associated with loss of both elastin fibers and microcalcification.

Identifiants

pubmed: 35770666
doi: 10.1161/ATVBAHA.122.317111
pmc: PMC9311465
doi:

Substances chimiques

Sodium Fluoride 8ZYQ1474W7
Elastin 9007-58-3

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1048-1059

Subventions

Organisme : British Heart Foundation
ID : RG/16/10/32375
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 221295/Z/20/Z
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/19/34/34354
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/18/31/33676
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/12/61/29877
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CH/09/002
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CH/09/002/26360
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/18/5/34216
Pays : United Kingdom
Organisme : Wellcome Trust
ID : WT103782AIA
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/16/107/32681
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/19/15/34155
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/17/83/33370
Pays : United Kingdom

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Auteurs

Alexander J Fletcher (AJ)

British Heart Foundation Centre for Cardiovascular Science (A.J.F., J.N., M.B.J.S., N.W., D.E.N.), University of Edinburgh, United Kingdom.
Department of Child Health, University of Glasgow, School of Medicine and Dentistry, United Kingdom (A.J.F.).

Jennifer Nash (J)

British Heart Foundation Centre for Cardiovascular Science (A.J.F., J.N., M.B.J.S., N.W., D.E.N.), University of Edinburgh, United Kingdom.

Maaz B J Syed (MBJ)

British Heart Foundation Centre for Cardiovascular Science (A.J.F., J.N., M.B.J.S., N.W., D.E.N.), University of Edinburgh, United Kingdom.

Mark G Macaskill (MG)

Edinburgh Imaging Facility, Queens Medical Research Institute (M.G.M., A.A.S.T.), University of Edinburgh, United Kingdom.

Adriana A S Tavares (AAS)

Edinburgh Imaging Facility, Queens Medical Research Institute (M.G.M., A.A.S.T.), University of Edinburgh, United Kingdom.

Niki Walker (N)

British Heart Foundation Centre for Cardiovascular Science (A.J.F., J.N., M.B.J.S., N.W., D.E.N.), University of Edinburgh, United Kingdom.
Scottish Adult Congenital Cardiology Service, Golden Jubilee National Hospital, Clydebank, Glasgow, United Kingdom (N.W.).

Hannah Salcudean (H)

Department of Radiology, Division of Cardiology, Cardiovascular Translational Lab at the Centre for Heart Lung Innovation, St. Paul's Hospital and University of British Columbia, Vancouver, Canada (H.S., J.A.L., S.L.S.).

Jonathon A Leipsic (JA)

Department of Radiology, Division of Cardiology, Cardiovascular Translational Lab at the Centre for Heart Lung Innovation, St. Paul's Hospital and University of British Columbia, Vancouver, Canada (H.S., J.A.L., S.L.S.).

Kelvin H H Lim (KHH)

Department of Cardiothoracic Surgery, Royal Infirmary of Edinburgh, United Kingdom (K.H.H.L.).

Jillian Madine (J)

Institute of Systems, Molecular and Integrative Biology, Faculty of Health and Life Sciences (J.M., M.F., R.A.), University of Liverpool, United Kingdom.
Liverpool Centre for Cardiovascular Sciences (J.M.), University of Liverpool, United Kingdom.

William Wallace (W)

Division of Pathology (W.W.), University of Edinburgh, United Kingdom.

Mark Field (M)

Institute of Systems, Molecular and Integrative Biology, Faculty of Health and Life Sciences (J.M., M.F., R.A.), University of Liverpool, United Kingdom.
Department of Cardiothoracic Surgery, Liverpool Heart and Chest Hospital (LCCS), United Kingdom (M.F.).

David E Newby (DE)

British Heart Foundation Centre for Cardiovascular Science (A.J.F., J.N., M.B.J.S., N.W., D.E.N.), University of Edinburgh, United Kingdom.

Rihab Bouchareb (R)

Department of Medicine, Cardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, NY (R.B.).

Michael A Seidman (MA)

Department of Laboratory Medicine and Pathobiology, Toronto General Hospital, Canada (M.A.S.).

Riaz Akhtar (R)

Institute of Systems, Molecular and Integrative Biology, Faculty of Health and Life Sciences (J.M., M.F., R.A.), University of Liverpool, United Kingdom.
Department of Mechanical, Materials and Aerospace Engineering, School of Engineering, University of Liverpool, United Kingdom (R.A.).

Stephanie L Sellers (SL)

Department of Radiology, Division of Cardiology, Cardiovascular Translational Lab at the Centre for Heart Lung Innovation, St. Paul's Hospital and University of British Columbia, Vancouver, Canada (H.S., J.A.L., S.L.S.).

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