Source:http://linkedlifedata.com/resource/pubmed/id/17602826
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2007-9-28
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pubmed:abstractText |
Aneurysms remain a significant medical problem and our current understanding of aneurysm formation and developmental stages remains incomplete. Noninvasive 3-D micro-ultrasound (3-D micro-US) imaging technologies designed for noninvasive evaluation of small laboratory animals diminish risks associated with invasive examination and provide in-situ (live) analysis of vascular morphological changes, which enables quantitative measurements of live biological specimens. We demonstrate here that aneurysm morphology can be quantified using 3-D micro-US, and we validate this methodology through comparison of geometric measures with those obtained from 3-D serial histologic records in a mouse model of accelerated aneurysm formation. Aneurysms were induced in Balb/C mice after C57Bl/6 mouse aortic transplant with injections of a pro-inflammatory viral serpin with a mutated reactive site. Aortic transplant segments were imaged 28 days after transplant using 3-D micro-US. Upon sacrifice, the aortas were excised and histology sections (5-microm thick) were digitized, co-registered using mutual information and stacked to form 3-D images. Surfaces of the mouse aorta and aneurysm were manually segmented from the 3-D micro-US and histology images. Comparisons with 3-D histology images demonstrated that 3-D micro-US allowed in-vivo analysis of aneurysm morphology, including total aneurysm area, plaque growth and lumen size. Linear regression of 3-D US-derived aneurysm and plaque volumes vs. 3-D histology-derived volumes resulted in slopes of 1.30 (R(2) = 0.96) and 1.20 (R(2) = 0.98), respectively, demonstrating that 3-D micro-US measurements can be used to track aneurysm growth in a mouse aortic transplant model.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0301-5629
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
33
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1552-60
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pubmed:dateRevised |
2009-12-14
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pubmed:meshHeading |
pubmed-meshheading:17602826-Animals,
pubmed-meshheading:17602826-Aorta, Abdominal,
pubmed-meshheading:17602826-Aortic Aneurysm,
pubmed-meshheading:17602826-Atherosclerosis,
pubmed-meshheading:17602826-Imaging, Three-Dimensional,
pubmed-meshheading:17602826-Membrane Proteins,
pubmed-meshheading:17602826-Mice,
pubmed-meshheading:17602826-Mice, Inbred BALB C,
pubmed-meshheading:17602826-Mice, Inbred C57BL,
pubmed-meshheading:17602826-Mice, Transgenic,
pubmed-meshheading:17602826-Models, Animal,
pubmed-meshheading:17602826-Mutation,
pubmed-meshheading:17602826-Plasminogen Activator Inhibitor 1,
pubmed-meshheading:17602826-Staining and Labeling,
pubmed-meshheading:17602826-Transplantation, Homologous,
pubmed-meshheading:17602826-Ultrasonography, Doppler
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pubmed:year |
2007
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pubmed:articleTitle |
Measurements of aneurysm morphology determined by 3-d micro-ultrasound imaging as potential quantitative biomarkers in a mouse aneurysm model.
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pubmed:affiliation |
Robarts Research Institute, London, Ontario, Canada.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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