Micro-CT vs. Whole Body Multirow Detector CT for Analysing Bone Regeneration in an Animal Model.
Compared with multirow detector CT (MDCT), specimen (ex vivo) micro-CT (μCT) has a significantly higher (~ 30 x) spatial resolution and is considered the gold standard for assessing bone above the cellular level. However, it is expensive and time-consuming, and when applied in vivo, the radiation do...
Main Authors: | , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2016-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC5120815?pdf=render |
id |
doaj-1dc8e5ae8a5d40a98903671da2d3cce6 |
---|---|
record_format |
Article |
spelling |
doaj-1dc8e5ae8a5d40a98903671da2d3cce62020-11-25T01:01:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-011111e016654010.1371/journal.pone.0166540Micro-CT vs. Whole Body Multirow Detector CT for Analysing Bone Regeneration in an Animal Model.Oliver BissingerJan S KirschkeFlorian Andreas ProbstMartin StauberKlaus-Dietrich WolffBernhard HallerCarolin GötzChristian PlankAndreas KolkCompared with multirow detector CT (MDCT), specimen (ex vivo) micro-CT (μCT) has a significantly higher (~ 30 x) spatial resolution and is considered the gold standard for assessing bone above the cellular level. However, it is expensive and time-consuming, and when applied in vivo, the radiation dose accumulates considerably. The aim of this study was to examine whether the lower resolution of the widely used MDCT is sufficient to qualitatively and quantitatively evaluate bone regeneration in rats.Forty critical-size defects (5mm) were placed in the mandibular angle of rats and covered with coated bioactive titanium implants to promote bone healing. Five time points were selected (7, 14, 28, 56 and 112 days). μCT and MDCT were used to evaluate the defect region to determine the bone volume (BV), tissue mineral density (TMD) and bone mineral content (BMC).MDCT constantly achieved higher BV values than μCT (10.73±7.84 mm3 vs. 6.62±4.96 mm3, p<0.0001) and consistently lower TMD values (547.68±163.83 mm3 vs. 876.18±121.21 mm3, p<0.0001). No relevant difference was obtained for BMC (6.48±5.71 mm3 vs. 6.15±5.21 mm3, p = 0.40). BV and BMC showed very strong correlations between both methods, whereas TMD was only moderately correlated (r = 0.87, r = 0.90, r = 0.68, p < 0.0001).Due to partial volume effects, MDCT overestimated BV and underestimated TMD but accurately determined BMC, even in small volumes, compared with μCT. Therefore, if bone quantity is a sufficient end point, a considerable number of animals and costs can be saved, and compared with in vivo μCT, the required dose of radiation can be reduced.http://europepmc.org/articles/PMC5120815?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Oliver Bissinger Jan S Kirschke Florian Andreas Probst Martin Stauber Klaus-Dietrich Wolff Bernhard Haller Carolin Götz Christian Plank Andreas Kolk |
spellingShingle |
Oliver Bissinger Jan S Kirschke Florian Andreas Probst Martin Stauber Klaus-Dietrich Wolff Bernhard Haller Carolin Götz Christian Plank Andreas Kolk Micro-CT vs. Whole Body Multirow Detector CT for Analysing Bone Regeneration in an Animal Model. PLoS ONE |
author_facet |
Oliver Bissinger Jan S Kirschke Florian Andreas Probst Martin Stauber Klaus-Dietrich Wolff Bernhard Haller Carolin Götz Christian Plank Andreas Kolk |
author_sort |
Oliver Bissinger |
title |
Micro-CT vs. Whole Body Multirow Detector CT for Analysing Bone Regeneration in an Animal Model. |
title_short |
Micro-CT vs. Whole Body Multirow Detector CT for Analysing Bone Regeneration in an Animal Model. |
title_full |
Micro-CT vs. Whole Body Multirow Detector CT for Analysing Bone Regeneration in an Animal Model. |
title_fullStr |
Micro-CT vs. Whole Body Multirow Detector CT for Analysing Bone Regeneration in an Animal Model. |
title_full_unstemmed |
Micro-CT vs. Whole Body Multirow Detector CT for Analysing Bone Regeneration in an Animal Model. |
title_sort |
micro-ct vs. whole body multirow detector ct for analysing bone regeneration in an animal model. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2016-01-01 |
description |
Compared with multirow detector CT (MDCT), specimen (ex vivo) micro-CT (μCT) has a significantly higher (~ 30 x) spatial resolution and is considered the gold standard for assessing bone above the cellular level. However, it is expensive and time-consuming, and when applied in vivo, the radiation dose accumulates considerably. The aim of this study was to examine whether the lower resolution of the widely used MDCT is sufficient to qualitatively and quantitatively evaluate bone regeneration in rats.Forty critical-size defects (5mm) were placed in the mandibular angle of rats and covered with coated bioactive titanium implants to promote bone healing. Five time points were selected (7, 14, 28, 56 and 112 days). μCT and MDCT were used to evaluate the defect region to determine the bone volume (BV), tissue mineral density (TMD) and bone mineral content (BMC).MDCT constantly achieved higher BV values than μCT (10.73±7.84 mm3 vs. 6.62±4.96 mm3, p<0.0001) and consistently lower TMD values (547.68±163.83 mm3 vs. 876.18±121.21 mm3, p<0.0001). No relevant difference was obtained for BMC (6.48±5.71 mm3 vs. 6.15±5.21 mm3, p = 0.40). BV and BMC showed very strong correlations between both methods, whereas TMD was only moderately correlated (r = 0.87, r = 0.90, r = 0.68, p < 0.0001).Due to partial volume effects, MDCT overestimated BV and underestimated TMD but accurately determined BMC, even in small volumes, compared with μCT. Therefore, if bone quantity is a sufficient end point, a considerable number of animals and costs can be saved, and compared with in vivo μCT, the required dose of radiation can be reduced. |
url |
http://europepmc.org/articles/PMC5120815?pdf=render |
work_keys_str_mv |
AT oliverbissinger microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel AT janskirschke microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel AT florianandreasprobst microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel AT martinstauber microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel AT klausdietrichwolff microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel AT bernhardhaller microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel AT carolingotz microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel AT christianplank microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel AT andreaskolk microctvswholebodymultirowdetectorctforanalysingboneregenerationinananimalmodel |
_version_ |
1725207110525911040 |