Inflammation assessment in patients with arthritis using a novel in vivo fluorescence optical imaging technology
Background Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In experimental models of arthritis, FOI findings corresponded to histologically proven synovitis. This is the first comparative study of FOI with...
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Published in | Annals of the rheumatic diseases Vol. 71; no. 4; pp. 504 - 510 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and European League Against Rheumatism
01.04.2012
BMJ Publishing Group Elsevier Limited BMJ Group |
Series | Extended report |
Subjects | |
Online Access | Get full text |
ISSN | 0003-4967 1468-2060 1468-2060 |
DOI | 10.1136/annrheumdis-2010-148288 |
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Abstract | Background Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In experimental models of arthritis, FOI findings corresponded to histologically proven synovitis. This is the first comparative study of FOI with other imaging modalities in humans with arthritis. Methods 252 FOI examinations (Xiralite system, mivenion GmbH, Berlin, Germany; ICG bolus of 0.1 mg/kg/body weight, sequence of 360 images, one image per second) were compared with clinical examination (CE), ultrasonography (US) and MRI of patients with arthritis of the hands. Results In an FOI sequence, three phases could be distinguished (P1–P3). With MRI as reference, FOI had a sensitivity of 76% and a specificity of 54%, while the specificity of phase 1 was 94%. FOI had agreement rates up to 88% versus CE, 64% versus greyscale US, 88% versus power Doppler US and 83% versus MRI, depending on the compared phase and parameter. FOI showed a higher rate of positive results compared to CE, US and MRI. In individual patients, FOI correlated significantly (p<0.05) with disease activity (Disease Activity Score 28, r=0.41), US (r=0.40) and RAMRIS (Rheumatoid Arthritis MRI Score) (r=0.56). FOI was normal in 97.8% of joints of controls. Conclusion ICG-enhanced FOI is a new technology offering sensitive imaging detection of inflammatory changes in subjects with arthritis. FOI was more sensitive than CE and had good agreement with CE, US in power Doppler mode and MRI, while showing more positive results than these. An adequate interpretation of an FOI sequence requires a separate evaluation of all phases. For the detection of synovitis and tenosynovitis, FOI appears to be as informative as 1.5 T MRI and US. |
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AbstractList | Background Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In experimental models of arthritis, FOI findings corresponded to histologically proven synovitis. This is the first comparative study of FOI with other imaging modalities in humans with arthritis. Methods 252 FOI examinations (Xiralite system, mivenion GmbH, Berlin, Germany; ICG bolus of 0.1 mg/kg/body weight, sequence of 360 images, one image per second) were compared with clinical examination (CE), ultrasonography (US) and MRI of patients with arthritis of the hands. Results In an FOI sequence, three phases could be distinguished (P1–P3). With MRI as reference, FOI had a sensitivity of 76% and a specificity of 54%, while the specificity of phase 1 was 94%. FOI had agreement rates up to 88% versus CE, 64% versus greyscale US, 88% versus power Doppler US and 83% versus MRI, depending on the compared phase and parameter. FOI showed a higher rate of positive results compared to CE, US and MRI. In individual patients, FOI correlated significantly (p<0.05) with disease activity (Disease Activity Score 28, r=0.41), US (r=0.40) and RAMRIS (Rheumatoid Arthritis MRI Score) (r=0.56). FOI was normal in 97.8% of joints of controls. Conclusion ICG-enhanced FOI is a new technology offering sensitive imaging detection of inflammatory changes in subjects with arthritis. FOI was more sensitive than CE and had good agreement with CE, US in power Doppler mode and MRI, while showing more positive results than these. An adequate interpretation of an FOI sequence requires a separate evaluation of all phases. For the detection of synovitis and tenosynovitis, FOI appears to be as informative as 1.5 T MRI and US. Background Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In experimental models of arthritis, FOI findings corresponded to histologically proven synovitis. This is the first comparative study of FOI with other imaging modalities in humans with arthritis. Methods 252 FOI examinations (Xiralite system, mivenion GmbH, Berlin, Germany; ICG bolus of 0.1 mg/kg/body weight, sequence of 360 images, one image per second) were compared with clinical examination (CE), ultrasonography (US) and MRI of patients with arthritis of the hands. Results In an FOI sequence, three phases could be distinguished (P1â[euro]"P3). With MRI as reference, FOI had a sensitivity of 76% and a specificity of 54%, while the specificity of phase 1 was 94%. FOI had agreement rates up to 88% versus CE, 64% versus greyscale US, 88% versus power Doppler US and 83% versus MRI, depending on the compared phase and parameter. FOI showed a higher rate of positive results compared to CE, US and MRI. In individual patients, FOI correlated significantly (p<0.05) with disease activity (Disease Activity Score 28, r=0.41), US (r=0.40) and RAMRIS (Rheumatoid Arthritis MRI Score) (r=0.56). FOI was normal in 97.8% of joints of controls. Conclusion ICG-enhanced FOI is a new technology offering sensitive imaging detection of inflammatory changes in subjects with arthritis. FOI was more sensitive than CE and had good agreement with CE, US in power Doppler mode and MRI, while showing more positive results than these. An adequate interpretation of an FOI sequence requires a separate evaluation of all phases. For the detection of synovitis and tenosynovitis, FOI appears to be as informative as 1.5 T MRI and US. Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In experimental models of arthritis, FOI findings corresponded to histologically proven synovitis. This is the first comparative study of FOI with other imaging modalities in humans with arthritis. 252 FOI examinations (Xiralite system, mivenion GmbH, Berlin, Germany; ICG bolus of 0.1 mg/kg/body weight, sequence of 360 images, one image per second) were compared with clinical examination (CE), ultrasonography (US) and MRI of patients with arthritis of the hands. In an FOI sequence, three phases could be distinguished (P1-P3). With MRI as reference, FOI had a sensitivity of 76% and a specificity of 54%, while the specificity of phase 1 was 94%. FOI had agreement rates up to 88% versus CE, 64% versus greyscale US, 88% versus power Doppler US and 83% versus MRI, depending on the compared phase and parameter. FOI showed a higher rate of positive results compared to CE, US and MRI. In individual patients, FOI correlated significantly (p<0.05) with disease activity (Disease Activity Score 28, r=0.41), US (r=0.40) and RAMRIS (Rheumatoid Arthritis MRI Score) (r=0.56). FOI was normal in 97.8% of joints of controls. ICG-enhanced FOI is a new technology offering sensitive imaging detection of inflammatory changes in subjects with arthritis. FOI was more sensitive than CE and had good agreement with CE, US in power Doppler mode and MRI, while showing more positive results than these. An adequate interpretation of an FOI sequence requires a separate evaluation of all phases. For the detection of synovitis and tenosynovitis, FOI appears to be as informative as 1.5 T MRI and US. Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In experimental models of arthritis, FOI findings corresponded to histologically proven synovitis. This is the first comparative study of FOI with other imaging modalities in humans with arthritis.BACKGROUNDIndocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In experimental models of arthritis, FOI findings corresponded to histologically proven synovitis. This is the first comparative study of FOI with other imaging modalities in humans with arthritis.252 FOI examinations (Xiralite system, mivenion GmbH, Berlin, Germany; ICG bolus of 0.1 mg/kg/body weight, sequence of 360 images, one image per second) were compared with clinical examination (CE), ultrasonography (US) and MRI of patients with arthritis of the hands.METHODS252 FOI examinations (Xiralite system, mivenion GmbH, Berlin, Germany; ICG bolus of 0.1 mg/kg/body weight, sequence of 360 images, one image per second) were compared with clinical examination (CE), ultrasonography (US) and MRI of patients with arthritis of the hands.In an FOI sequence, three phases could be distinguished (P1-P3). With MRI as reference, FOI had a sensitivity of 76% and a specificity of 54%, while the specificity of phase 1 was 94%. FOI had agreement rates up to 88% versus CE, 64% versus greyscale US, 88% versus power Doppler US and 83% versus MRI, depending on the compared phase and parameter. FOI showed a higher rate of positive results compared to CE, US and MRI. In individual patients, FOI correlated significantly (p<0.05) with disease activity (Disease Activity Score 28, r=0.41), US (r=0.40) and RAMRIS (Rheumatoid Arthritis MRI Score) (r=0.56). FOI was normal in 97.8% of joints of controls.RESULTSIn an FOI sequence, three phases could be distinguished (P1-P3). With MRI as reference, FOI had a sensitivity of 76% and a specificity of 54%, while the specificity of phase 1 was 94%. FOI had agreement rates up to 88% versus CE, 64% versus greyscale US, 88% versus power Doppler US and 83% versus MRI, depending on the compared phase and parameter. FOI showed a higher rate of positive results compared to CE, US and MRI. In individual patients, FOI correlated significantly (p<0.05) with disease activity (Disease Activity Score 28, r=0.41), US (r=0.40) and RAMRIS (Rheumatoid Arthritis MRI Score) (r=0.56). FOI was normal in 97.8% of joints of controls.ICG-enhanced FOI is a new technology offering sensitive imaging detection of inflammatory changes in subjects with arthritis. FOI was more sensitive than CE and had good agreement with CE, US in power Doppler mode and MRI, while showing more positive results than these. An adequate interpretation of an FOI sequence requires a separate evaluation of all phases. For the detection of synovitis and tenosynovitis, FOI appears to be as informative as 1.5 T MRI and US.CONCLUSIONICG-enhanced FOI is a new technology offering sensitive imaging detection of inflammatory changes in subjects with arthritis. FOI was more sensitive than CE and had good agreement with CE, US in power Doppler mode and MRI, while showing more positive results than these. An adequate interpretation of an FOI sequence requires a separate evaluation of all phases. For the detection of synovitis and tenosynovitis, FOI appears to be as informative as 1.5 T MRI and US. |
Author | Schwenke, Carsten Werner, Stephanie G Schirner, Michael Kurtz, Bernward Backhaus, Marina Ohrndorf, Sarah Schott, Peter Langer, Hans-Eckhard Lind-Albrecht, Gudrun Bastian, Hans Bahner, Malte Burmester, Gerd R |
AuthorAffiliation | 2 Department of Rheumatology and Clinical Immunology, Charité-University Medicine Berlin, Berlin, Germany 3 mivenion GmbH, Berlin, Germany 1 RHIO (Rheumatology, Immunology, Osteology) Center Duesseldorf and RHIO Research Institute, Duesseldorf, Germany 5 SCOSSIS Statistical Consulting, Berlin, Germany 4 Department of Radiology, Evangelisches Krankenhaus Duesseldorf, Duesseldorf, Germany |
AuthorAffiliation_xml | – name: 2 Department of Rheumatology and Clinical Immunology, Charité-University Medicine Berlin, Berlin, Germany – name: 3 mivenion GmbH, Berlin, Germany – name: 1 RHIO (Rheumatology, Immunology, Osteology) Center Duesseldorf and RHIO Research Institute, Duesseldorf, Germany – name: 4 Department of Radiology, Evangelisches Krankenhaus Duesseldorf, Duesseldorf, Germany – name: 5 SCOSSIS Statistical Consulting, Berlin, Germany |
Author_xml | – sequence: 1 givenname: Stephanie G surname: Werner fullname: Werner, Stephanie G email: gerd.burmester@charite.de organization: RHIO (Rheumatology, Immunology, Osteology) Center Duesseldorf and RHIO Research Institute, Duesseldorf, Germany – sequence: 2 givenname: Hans-Eckhard surname: Langer fullname: Langer, Hans-Eckhard email: gerd.burmester@charite.de organization: RHIO (Rheumatology, Immunology, Osteology) Center Duesseldorf and RHIO Research Institute, Duesseldorf, Germany – sequence: 3 givenname: Sarah surname: Ohrndorf fullname: Ohrndorf, Sarah email: gerd.burmester@charite.de organization: Department of Rheumatology and Clinical Immunology, Charité-University Medicine Berlin, Berlin, Germany – sequence: 4 givenname: Malte surname: Bahner fullname: Bahner, Malte email: gerd.burmester@charite.de organization: mivenion GmbH, Berlin, Germany – sequence: 5 givenname: Peter surname: Schott fullname: Schott, Peter email: gerd.burmester@charite.de organization: Department of Radiology, Evangelisches Krankenhaus Duesseldorf, Duesseldorf, Germany – sequence: 6 givenname: Carsten surname: Schwenke fullname: Schwenke, Carsten email: gerd.burmester@charite.de organization: SCOSSIS Statistical Consulting, Berlin, Germany – sequence: 7 givenname: Michael surname: Schirner fullname: Schirner, Michael email: gerd.burmester@charite.de organization: mivenion GmbH, Berlin, Germany – sequence: 8 givenname: Hans surname: Bastian fullname: Bastian, Hans email: gerd.burmester@charite.de organization: Department of Rheumatology and Clinical Immunology, Charité-University Medicine Berlin, Berlin, Germany – sequence: 9 givenname: Gudrun surname: Lind-Albrecht fullname: Lind-Albrecht, Gudrun email: gerd.burmester@charite.de organization: RHIO (Rheumatology, Immunology, Osteology) Center Duesseldorf and RHIO Research Institute, Duesseldorf, Germany – sequence: 10 givenname: Bernward surname: Kurtz fullname: Kurtz, Bernward email: gerd.burmester@charite.de organization: Department of Radiology, Evangelisches Krankenhaus Duesseldorf, Duesseldorf, Germany – sequence: 11 givenname: Gerd R surname: Burmester fullname: Burmester, Gerd R email: gerd.burmester@charite.de organization: Department of Rheumatology and Clinical Immunology, Charité-University Medicine Berlin, Berlin, Germany – sequence: 12 givenname: Marina surname: Backhaus fullname: Backhaus, Marina email: gerd.burmester@charite.de organization: Department of Rheumatology and Clinical Immunology, Charité-University Medicine Berlin, Berlin, Germany |
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Copyright | Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2015 INIST-CNRS Copyright: 2012 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2012 |
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Keywords | Human In vivo Technology Diseases of the osteoarticular system Rheumatology Optical imaging Arthritis Inflammation |
Language | English |
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Snippet | Background Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In... Indocyanine green (ICG)-enhanced fluorescence optical imaging (FOI) is an established technology for imaging of inflammation in animal models. In experimental... |
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SubjectTerms | Adult Aged Aged, 80 and over Agreements Arthritis - diagnosis Arthritis - diagnostic imaging Arthritis, Psoriatic - diagnosis Arthritis, Psoriatic - diagnostic imaging Arthritis, Rheumatoid - diagnosis Arthritis, Rheumatoid - diagnostic imaging Biological and medical sciences Case-Control Studies Clinical and Epidemiological Research Coloring Agents Confidence intervals Diagnostic Imaging - methods Disease Diseases of the osteoarticular system Female Fluorescence Hand Joints - diagnostic imaging Hand Joints - pathology Hands Humans Image Interpretation, Computer-Assisted - methods Indocyanine Green Inflammation Integrated software Laboratories Magnetic Resonance Imaging - methods Male Medical sciences Microscopy, Fluorescence - methods Middle Aged Miscellaneous. Osteoarticular involvement in other diseases NMR Nuclear magnetic resonance Patients Sensitivity and Specificity Statistical analysis Studies Synovitis - diagnosis Synovitis - diagnostic imaging Ultrasonic imaging Ultrasonography Young Adult |
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Title | Inflammation assessment in patients with arthritis using a novel in vivo fluorescence optical imaging technology |
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