Your browser doesn't support javascript.
loading
Microcalcification and Thoracic Aortopathy: A Window Into Disease Severity.
Fletcher, Alexander J; Nash, Jennifer; Syed, Maaz B J; Macaskill, Mark G; Tavares, Adriana A S; Walker, Niki; Salcudean, Hannah; Leipsic, Jonathon A; Lim, Kelvin H H; Madine, Jillian; Wallace, William; Field, Mark; Newby, David E; Bouchareb, Rihab; Seidman, Michael A; Akhtar, Riaz; Sellers, Stephanie L.
Afiliação
  • 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.
  • Nash J; Department of Child Health, University of Glasgow, School of Medicine and Dentistry, United Kingdom (A.J.F.).
  • 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.
  • Macaskill MG; 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.
  • Tavares AAS; Edinburgh Imaging Facility, Queens Medical Research Institute (M.G.M., A.A.S.T.), University of Edinburgh, United Kingdom.
  • Walker N; Edinburgh Imaging Facility, Queens Medical Research Institute (M.G.M., A.A.S.T.), University of Edinburgh, United Kingdom.
  • Salcudean H; 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.
  • Leipsic JA; Scottish Adult Congenital Cardiology Service, Golden Jubilee National Hospital, Clydebank, Glasgow, United Kingdom (N.W.).
  • Lim KHH; 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.).
  • Madine J; 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.).
  • Wallace W; Department of Cardiothoracic Surgery, Royal Infirmary of Edinburgh, United Kingdom (K.H.H.L.).
  • 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.
  • Newby DE; Liverpool Centre for Cardiovascular Sciences (J.M.), University of Liverpool, United Kingdom.
  • Bouchareb R; Division of Pathology (W.W.), University of Edinburgh, United Kingdom.
  • Seidman MA; Institute of Systems, Molecular and Integrative Biology, Faculty of Health and Life Sciences (J.M., M.F., R.A.), University of Liverpool, United Kingdom.
  • Akhtar R; Department of Cardiothoracic Surgery, Liverpool Heart and Chest Hospital (LCCS), United Kingdom (M.F.).
  • Sellers SL; 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.
Arterioscler Thromb Vasc Biol ; 42(8): 1048-1059, 2022 08.
Article em En | MEDLINE | ID: mdl-35770666
ABSTRACT

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]; P≤0.00010) or moderate histopathologic degeneration (n=30; 3.74 [0.87-11.80]; P<0.042) compared with control samples (n=18; 0.79 [0.36-1.90]). Alkaline phosphatase (n=26; P=0.0019) and OPN (osteopontin; n=26; P=0.0045) staining were increased in tissue with early aortopathy. Increasingly severe histopathologic degeneration was related to reduced microcalcification (n=82; Spearman ρ, -0.51; P<0.0001)-a process closely linked with elastin loss (n=82; Spearman ρ, -0.43; P<0.0001) and lower tissue elastic modulus (n=28; Spearman ρ, 0.43; P=0.026).18F-sodium fluoride autoradiography demonstrated good correlation with histologically quantified microcalcification (n=66; r=0.76; P<0.001) and identified areas of focal weakness in vivo.

CONCLUSIONS:

Medial microcalcification is a marker of aortopathy, although progression to severe aortopathy is associated with loss of both elastin fibers and microcalcification.18F-sodium fluoride positron emission tomography quantifies medial microcalcification and is a feasible noninvasive imaging modality for identifying aortic wall disruption with major translational promise.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Calcinose / Elastina Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Calcinose / Elastina Idioma: En Ano de publicação: 2022 Tipo de documento: Article