<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(5)</volume><submitter>Las Heras F</submitter><funding>Canadian Institutes of Health Research</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The diagnosis of ankylosing spondylitis is made from a combination of clinical features and the presence of radiographic evidence that may be detected only after many years of inflammatory back pain. It is not uncommon to have a diagnosis confirmed 5 to 10 years after the initial onset of symptoms. Development of a more-sensitive molecular imaging technology to detect structural changes in the joints would lead to earlier diagnosis and quantitative tracking of ankylosis progression. Progressive ankylosis (ank/ank) mice have a loss of function in the Ank gene, which codes for a regulator of PPi transport. In this study, we used these ank/ank mutant mice to assess a noninvasive, quantitative measure of joint ankylosis with near-infrared (NIR) molecular imaging in vivo.&lt;h4>Methods&lt;/h4>Three age groups (8, 12, and 18 weeks) of ank/ank (15 mice) and wild-type littermates (12 +/+ mice) were assessed histologically and radiographically. Before imaging, OsteoSense 750 (bisphosphonate pamidronate) was injected i.v. Whole-body images were analyzed by using the multispectral Maestro imaging system.&lt;h4>Results&lt;/h4>OsteoSense 750 signals in the paw joints were higher in ank/ank mice in all three age groups compared with controls. In the spine, significantly higher OsteoSense 750 signals were detected early, in 8-week-old ank/ank mice compared with controls, although minimal radiographic differences were noted at this time point. The molecular imaging changes in the ank/ank spine (8 weeks) were supported by histologic changes, including calcium apatite crystals at the edge of the vertebral bodies and new syndesmophyte formation.&lt;h4>Conclusions&lt;/h4>Changes in joint pathology of ank/ank mice, as evaluated by histologic and radiographic means, are qualitative, but only semiquantitative. In contrast, molecular imaging provides a quantitative assessment. Ankylosis in ank/ank mice developed simultaneously in distal and axial joints, contrary to the previous notion that it is a centripetal process. NIR imaging might be feasible for early disease diagnosis and for monitoring disease progression in ankylosing spondylitis.</pubmed_abstract><journal>Arthritis research &amp; therapy</journal><pagination>R163</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3308096</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Aberrant axial mineralization precedes spinal ankylosis: a molecular imaging study in ank/ank mice.</pubmed_title><pmcid>PMC3308096</pmcid><pubmed_authors>Las Heras F</pubmed_authors><pubmed_authors>Inman RD</pubmed_authors><pubmed_authors>Pritzker KP</pubmed_authors><pubmed_authors>DaCosta RS</pubmed_authors><pubmed_authors>Tsui HW</pubmed_authors><pubmed_authors>Erwin WM</pubmed_authors><pubmed_authors>Netchev G</pubmed_authors><pubmed_authors>Tsui FW</pubmed_authors><pubmed_authors>Haroon N</pubmed_authors><pubmed_authors>Chiu B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aberrant axial mineralization precedes spinal ankylosis: a molecular imaging study in ank/ank mice.</name><description>&lt;h4>Introduction&lt;/h4>The diagnosis of ankylosing spondylitis is made from a combination of clinical features and the presence of radiographic evidence that may be detected only after many years of inflammatory back pain. It is not uncommon to have a diagnosis confirmed 5 to 10 years after the initial onset of symptoms. Development of a more-sensitive molecular imaging technology to detect structural changes in the joints would lead to earlier diagnosis and quantitative tracking of ankylosis progression. Progressive ankylosis (ank/ank) mice have a loss of function in the Ank gene, which codes for a regulator of PPi transport. In this study, we used these ank/ank mutant mice to assess a noninvasive, quantitative measure of joint ankylosis with near-infrared (NIR) molecular imaging in vivo.&lt;h4>Methods&lt;/h4>Three age groups (8, 12, and 18 weeks) of ank/ank (15 mice) and wild-type littermates (12 +/+ mice) were assessed histologically and radiographically. Before imaging, OsteoSense 750 (bisphosphonate pamidronate) was injected i.v. Whole-body images were analyzed by using the multispectral Maestro imaging system.&lt;h4>Results&lt;/h4>OsteoSense 750 signals in the paw joints were higher in ank/ank mice in all three age groups compared with controls. In the spine, significantly higher OsteoSense 750 signals were detected early, in 8-week-old ank/ank mice compared with controls, although minimal radiographic differences were noted at this time point. The molecular imaging changes in the ank/ank spine (8 weeks) were supported by histologic changes, including calcium apatite crystals at the edge of the vertebral bodies and new syndesmophyte formation.&lt;h4>Conclusions&lt;/h4>Changes in joint pathology of ank/ank mice, as evaluated by histologic and radiographic means, are qualitative, but only semiquantitative. In contrast, molecular imaging provides a quantitative assessment. Ankylosis in ank/ank mice developed simultaneously in distal and axial joints, contrary to the previous notion that it is a centripetal process. NIR imaging might be feasible for early disease diagnosis and for monitoring disease progression in ankylosing spondylitis.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011</publication><modification>2022-02-09T11:37:11.924Z</modification><creation>2019-03-27T00:51:23Z</creation></dates><accession>S-EPMC3308096</accession><cross_references><pubmed>21992149</pubmed><doi>10.1186/ar3482</doi></cross_references></HashMap>