TY - JOUR
T1 - Compositional volumetry of non-calcified coronary plaques by multislice computed tomography
T2 - An ex vivo feasibility study
AU - Bruining, Nico
AU - Roelandt, Jos R.T.C.
AU - Verheye, Stefan
AU - Knaapen, Michiel
AU - Onuma, Yoshinobu
AU - Regar, Evelyn
AU - Cademartiri, Filippo
AU - De Winter, Sebastiaan
AU - Van Langenhove, Glenn
AU - Serruys, Patrick W.
AU - Hamers, Ronald
AU - De Feyter, Pim J.
PY - 2009/11
Y1 - 2009/11
N2 - Aims: Non-invasive quantitative compositional analysis of coronary plaque would be a major advantage to study coronary artery disease. This study explores the application to use the Hounsfield units (HU) distribution of coronary plaques imaged by multislice computed tomography-coronary angiography (MSCT-CA). Methods and results: A dedicated computer-assisted method was developed to measure the HU distribution within a coronary plaque by MSCT-CA. To test the feasibility of the method, an ex vivo left anterior descending (LAD) coronary specimen, excised during autopsy, was imaged both by non-enhanced and enhanced MSCT-CA. Quantitative histology was used as a reference. To test the feasibility of the new volumetric analytic method, the MSCT-CA data were compared with volumetric histopathology. The coronary specimen, with a heterogeneously distributed plaque composition without large areas of calcification, was histologically sampled at five different locations, 5 mm apart, where at each location 15 sections were taken at 100 μm intervals, resulting in 75 individual histology sections. Tri-chrome Masson staining was used for histology quantification of three plaque/tissue components: smooth muscle cells (SMC), collagen and calcium. MSCT plaque composition was defined as "lower-HU" or "higher-HU" plaque and "calcium" based on the HU distribution. Comparison of the MSCT defined tissue components against histology showed a good relationship without significant differences. Conclusions: This ex vivo study shows the feasibility of using the Hounsfield unit distribution to perform compositional coronary plaque volumetry by MSCT-CA. The results are encouraging.
AB - Aims: Non-invasive quantitative compositional analysis of coronary plaque would be a major advantage to study coronary artery disease. This study explores the application to use the Hounsfield units (HU) distribution of coronary plaques imaged by multislice computed tomography-coronary angiography (MSCT-CA). Methods and results: A dedicated computer-assisted method was developed to measure the HU distribution within a coronary plaque by MSCT-CA. To test the feasibility of the method, an ex vivo left anterior descending (LAD) coronary specimen, excised during autopsy, was imaged both by non-enhanced and enhanced MSCT-CA. Quantitative histology was used as a reference. To test the feasibility of the new volumetric analytic method, the MSCT-CA data were compared with volumetric histopathology. The coronary specimen, with a heterogeneously distributed plaque composition without large areas of calcification, was histologically sampled at five different locations, 5 mm apart, where at each location 15 sections were taken at 100 μm intervals, resulting in 75 individual histology sections. Tri-chrome Masson staining was used for histology quantification of three plaque/tissue components: smooth muscle cells (SMC), collagen and calcium. MSCT plaque composition was defined as "lower-HU" or "higher-HU" plaque and "calcium" based on the HU distribution. Comparison of the MSCT defined tissue components against histology showed a good relationship without significant differences. Conclusions: This ex vivo study shows the feasibility of using the Hounsfield unit distribution to perform compositional coronary plaque volumetry by MSCT-CA. The results are encouraging.
KW - Coronary artery disease
KW - Histology
KW - Multislice computed tomography
UR - http://www.scopus.com/inward/record.url?scp=77955506317&partnerID=8YFLogxK
U2 - 10.4244/EIJV5I5A91
DO - 10.4244/EIJV5I5A91
M3 - Article
C2 - 20142176
AN - SCOPUS:77955506317
SN - 1774-024X
VL - 5
SP - 558
EP - 564
JO - EuroIntervention
JF - EuroIntervention
IS - 5
ER -