TY - JOUR
T1 - Exploring the Biological and Mechanical Properties of Abdominal Aortic Aneurysms Using USPIO MRI and Peak Tissue Stress
T2 - A Combined Clinical and Finite Element Study
AU - Conlisk, Noel
AU - Forsythe, Rachael O.
AU - Hollis, Lyam
AU - Doyle, Barry J.
AU - McBride, Olivia M.B.
AU - Robson, Jennifer M.J.
AU - Wang, Chengjia
AU - Gray, Calum D.
AU - Semple, Scott I.K.
AU - MacGillivray, Tom
AU - van Beek, Edwin J.R.
AU - Newby, David E.
AU - Hoskins, Peter R.
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Inflammation detected through the uptake of ultrasmall superparamagnetic particles of iron oxide (USPIO) on magnetic resonance imaging (MRI) and finite element (FE) modelling of tissue stress both hold potential in the assessment of abdominal aortic aneurysm (AAA) rupture risk. This study aimed to examine the spatial relationship between these two biomarkers. Patients (n = 50) > 40 years with AAA maximum diameters > = 40 mm underwent USPIO-enhanced MRI and computed tomography angiogram (CTA). USPIO uptake was compared with wall stress predictions from CTA-based patient-specific FE models of each aneurysm. Elevated stress was commonly observed in areas vulnerable to rupture (e.g. posterior wall and shoulder). Only 16% of aneurysms exhibited co-localisation of elevated stress and mural USPIO enhancement. Globally, no correlation was observed between stress and other measures of USPIO uptake (i.e. mean or peak). It is suggested that cellular inflammation and stress may represent different but complimentary aspects of AAA disease progression.
AB - Inflammation detected through the uptake of ultrasmall superparamagnetic particles of iron oxide (USPIO) on magnetic resonance imaging (MRI) and finite element (FE) modelling of tissue stress both hold potential in the assessment of abdominal aortic aneurysm (AAA) rupture risk. This study aimed to examine the spatial relationship between these two biomarkers. Patients (n = 50) > 40 years with AAA maximum diameters > = 40 mm underwent USPIO-enhanced MRI and computed tomography angiogram (CTA). USPIO uptake was compared with wall stress predictions from CTA-based patient-specific FE models of each aneurysm. Elevated stress was commonly observed in areas vulnerable to rupture (e.g. posterior wall and shoulder). Only 16% of aneurysms exhibited co-localisation of elevated stress and mural USPIO enhancement. Globally, no correlation was observed between stress and other measures of USPIO uptake (i.e. mean or peak). It is suggested that cellular inflammation and stress may represent different but complimentary aspects of AAA disease progression.
KW - Abdominal aortic aneurysms
KW - Finite element analysis
KW - MRI
KW - Patient-specific modelling
KW - USPIO uptake
UR - http://www.scopus.com/inward/record.url?scp=85028558531&partnerID=8YFLogxK
U2 - 10.1007/s12265-017-9766-9
DO - 10.1007/s12265-017-9766-9
M3 - Article
C2 - 28808955
AN - SCOPUS:85028558531
SN - 1937-5387
VL - 10
SP - 489
EP - 498
JO - Journal of Cardiovascular Translational Research
JF - Journal of Cardiovascular Translational Research
IS - 5-6
ER -