Anti-inflammatory effect of biologic therapy in patients with psoriatic disease: A prospective cohort FDG PET study
The aim of the study was to evaluate the changes in central vascular inflammation measured by FDG PET and myocardial blood flow reserve (MFR) determined by 82Rb PET following therapy with biologic agents for 6 months in patients with psoriatic arthritis (PsA) and/or cutaneous psoriasis (PsO) (group...
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Published in | Journal of nuclear cardiology Vol. 30; no. 4; pp. 1642 - 1652 |
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Main Authors | , , , , , , , , , , |
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Abstract | The aim of the study was to evaluate the changes in central vascular inflammation measured by FDG PET and myocardial blood flow reserve (MFR) determined by 82Rb PET following therapy with biologic agents for 6 months in patients with psoriatic arthritis (PsA) and/or cutaneous psoriasis (PsO) (group 1) and compare with PsO subjects receiving non-biologic therapy (group 2) and controls (group 3).
Target-to-background ratio (TBR) by FDG PET in the most diseased segment of the ascending aorta (TBRmax) was measured to assess vascular inflammation. 82Rb PET studies were used to assess changes in left ventricular MFR. A total of 34 participants were enrolled in the study (11 in group 1, 13 in group 2, and 10 controls). A significant drop in the thoracic aorta uptake was observed in the biologic-treated group (ΔTBRmax: − .46 ± .55) compared to the PsO group treated with non-biologic therapy (ΔTBRmax: .23 ± .67). Those showing response to biologic agents maintained MFR compared to who showed no response.
In a cohort of psoriasis patients treated with biologics, FDG uptake in the thoracic aorta decreased over the study period. Patients who demonstrated a significant anti-inflammatory response on FDG PET imaging maintained their MFR compared to non-responders. |
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AbstractList | The aim of the study was to evaluate the changes in central vascular inflammation measured by FDG PET and myocardial blood flow reserve (MFR) determined by
Rb PET following therapy with biologic agents for 6 months in patients with psoriatic arthritis (PsA) and/or cutaneous psoriasis (PsO) (group 1) and compare with PsO subjects receiving non-biologic therapy (group 2) and controls (group 3).
Target-to-background ratio (TBR) by FDG PET in the most diseased segment of the ascending aorta (TBR
) was measured to assess vascular inflammation.
Rb PET studies were used to assess changes in left ventricular MFR. A total of 34 participants were enrolled in the study (11 in group 1, 13 in group 2, and 10 controls). A significant drop in the thoracic aorta uptake was observed in the biologic-treated group (ΔTBR
: - .46 ± .55) compared to the PsO group treated with non-biologic therapy (ΔTBR
: .23 ± .67). Those showing response to biologic agents maintained MFR compared to who showed no response.
In a cohort of psoriasis patients treated with biologics, FDG uptake in the thoracic aorta decreased over the study period. Patients who demonstrated a significant anti-inflammatory response on FDG PET imaging maintained their MFR compared to non-responders. The aim of the study was to evaluate the changes in central vascular inflammation measured by FDG PET and myocardial blood flow reserve (MFR) determined by 82Rb PET following therapy with biologic agents for 6 months in patients with psoriatic arthritis (PsA) and/or cutaneous psoriasis (PsO) (group 1) and compare with PsO subjects receiving non-biologic therapy (group 2) and controls (group 3). Target-to-background ratio (TBR) by FDG PET in the most diseased segment of the ascending aorta (TBRmax) was measured to assess vascular inflammation. 82Rb PET studies were used to assess changes in left ventricular MFR. A total of 34 participants were enrolled in the study (11 in group 1, 13 in group 2, and 10 controls). A significant drop in the thoracic aorta uptake was observed in the biologic-treated group (ΔTBRmax: − .46 ± .55) compared to the PsO group treated with non-biologic therapy (ΔTBRmax: .23 ± .67). Those showing response to biologic agents maintained MFR compared to who showed no response. In a cohort of psoriasis patients treated with biologics, FDG uptake in the thoracic aorta decreased over the study period. Patients who demonstrated a significant anti-inflammatory response on FDG PET imaging maintained their MFR compared to non-responders. Aim The aim of the study was to evaluate the changes in central vascular inflammation measured by FDG PET and myocardial blood flow reserve (MFR) determined by 82 Rb PET following therapy with biologic agents for 6 months in patients with psoriatic arthritis (PsA) and/or cutaneous psoriasis (PsO) (group 1) and compare with PsO subjects receiving non-biologic therapy (group 2) and controls (group 3). Methods and Results Target-to-background ratio (TBR) by FDG PET in the most diseased segment of the ascending aorta (TBR max ) was measured to assess vascular inflammation. 82 Rb PET studies were used to assess changes in left ventricular MFR. A total of 34 participants were enrolled in the study (11 in group 1, 13 in group 2, and 10 controls). A significant drop in the thoracic aorta uptake was observed in the biologic-treated group (ΔTBR max : − .46 ± .55) compared to the PsO group treated with non-biologic therapy (ΔTBR max : .23 ± .67). Those showing response to biologic agents maintained MFR compared to who showed no response. Conclusion In a cohort of psoriasis patients treated with biologics, FDG uptake in the thoracic aorta decreased over the study period. Patients who demonstrated a significant anti-inflammatory response on FDG PET imaging maintained their MFR compared to non-responders. AimThe aim of the study was to evaluate the changes in central vascular inflammation measured by FDG PET and myocardial blood flow reserve (MFR) determined by 82Rb PET following therapy with biologic agents for 6 months in patients with psoriatic arthritis (PsA) and/or cutaneous psoriasis (PsO) (group 1) and compare with PsO subjects receiving non-biologic therapy (group 2) and controls (group 3).Methods and ResultsTarget-to-background ratio (TBR) by FDG PET in the most diseased segment of the ascending aorta (TBRmax) was measured to assess vascular inflammation. 82Rb PET studies were used to assess changes in left ventricular MFR. A total of 34 participants were enrolled in the study (11 in group 1, 13 in group 2, and 10 controls). A significant drop in the thoracic aorta uptake was observed in the biologic-treated group (ΔTBRmax: − .46 ± .55) compared to the PsO group treated with non-biologic therapy (ΔTBRmax: .23 ± .67). Those showing response to biologic agents maintained MFR compared to who showed no response.ConclusionIn a cohort of psoriasis patients treated with biologics, FDG uptake in the thoracic aorta decreased over the study period. Patients who demonstrated a significant anti-inflammatory response on FDG PET imaging maintained their MFR compared to non-responders. The aim of the study was to evaluate the changes in central vascular inflammation measured by FDG PET and myocardial blood flow reserve (MFR) determined by 82Rb PET following therapy with biologic agents for 6 months in patients with psoriatic arthritis (PsA) and/or cutaneous psoriasis (PsO) (group 1) and compare with PsO subjects receiving non-biologic therapy (group 2) and controls (group 3).AIMThe aim of the study was to evaluate the changes in central vascular inflammation measured by FDG PET and myocardial blood flow reserve (MFR) determined by 82Rb PET following therapy with biologic agents for 6 months in patients with psoriatic arthritis (PsA) and/or cutaneous psoriasis (PsO) (group 1) and compare with PsO subjects receiving non-biologic therapy (group 2) and controls (group 3).Target-to-background ratio (TBR) by FDG PET in the most diseased segment of the ascending aorta (TBRmax) was measured to assess vascular inflammation. 82Rb PET studies were used to assess changes in left ventricular MFR. A total of 34 participants were enrolled in the study (11 in group 1, 13 in group 2, and 10 controls). A significant drop in the thoracic aorta uptake was observed in the biologic-treated group (ΔTBRmax: - .46 ± .55) compared to the PsO group treated with non-biologic therapy (ΔTBRmax: .23 ± .67). Those showing response to biologic agents maintained MFR compared to who showed no response.METHODS AND RESULTSTarget-to-background ratio (TBR) by FDG PET in the most diseased segment of the ascending aorta (TBRmax) was measured to assess vascular inflammation. 82Rb PET studies were used to assess changes in left ventricular MFR. A total of 34 participants were enrolled in the study (11 in group 1, 13 in group 2, and 10 controls). A significant drop in the thoracic aorta uptake was observed in the biologic-treated group (ΔTBRmax: - .46 ± .55) compared to the PsO group treated with non-biologic therapy (ΔTBRmax: .23 ± .67). Those showing response to biologic agents maintained MFR compared to who showed no response.In a cohort of psoriasis patients treated with biologics, FDG uptake in the thoracic aorta decreased over the study period. Patients who demonstrated a significant anti-inflammatory response on FDG PET imaging maintained their MFR compared to non-responders.CONCLUSIONIn a cohort of psoriasis patients treated with biologics, FDG uptake in the thoracic aorta decreased over the study period. Patients who demonstrated a significant anti-inflammatory response on FDG PET imaging maintained their MFR compared to non-responders. |
Author | Beanlands, Rob S. Fehlmann, Christophe A. Dwivedi, Girish Glassman, Steven J. Karsh, Jacob Zeng, Wanzhen Ward, Natalie C. Wells, George A. Wang, Jerry Boczar, Kevin E. deKemp, Robert A. |
Author_xml | – sequence: 1 givenname: Kevin E. surname: Boczar fullname: Boczar, Kevin E. organization: University of Ottawa Heart Institute, Ottawa, ON, Canada – sequence: 2 givenname: Rob S. surname: Beanlands fullname: Beanlands, Rob S. organization: University of Ottawa Heart Institute, Ottawa, ON, Canada – sequence: 3 givenname: Steven J. surname: Glassman fullname: Glassman, Steven J. organization: Division of Dermatology, The Ottawa Hospital, Ottawa, ON, Canada – sequence: 4 givenname: Jerry surname: Wang fullname: Wang, Jerry organization: University of Ottawa Heart Institute, Ottawa, ON, Canada – sequence: 5 givenname: Wanzhen surname: Zeng fullname: Zeng, Wanzhen organization: University of Ottawa Heart Institute, Ottawa, ON, Canada – sequence: 6 givenname: Robert A. surname: deKemp fullname: deKemp, Robert A. organization: University of Ottawa Heart Institute, Ottawa, ON, Canada – sequence: 7 givenname: Natalie C. surname: Ward fullname: Ward, Natalie C. organization: School of Medicine, University of Western Australia, Perth, WA, Australia – sequence: 8 givenname: Christophe A. surname: Fehlmann fullname: Fehlmann, Christophe A. organization: School of Epidemiology and Public Health, University of Ottawa, Ottawa, ON, Canada – sequence: 9 givenname: George A. surname: Wells fullname: Wells, George A. organization: University of Ottawa Heart Institute, Ottawa, ON, Canada – sequence: 10 givenname: Jacob surname: Karsh fullname: Karsh, Jacob organization: Division of Rheumatology, The Ottawa Hospital, Ottawa, ON, Canada – sequence: 11 givenname: Girish surname: Dwivedi fullname: Dwivedi, Girish email: girish.dwivedi@perkins.uwa.edu.au organization: University of Ottawa Heart Institute, Ottawa, ON, Canada |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36754934$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s12350_023_03250_2 crossref_primary_10_1080_1744666X_2023_2249235 crossref_primary_10_1007_s40336_024_00630_7 crossref_primary_10_1093_rheumatology_keae450 crossref_primary_10_1152_ajpheart_00744_2023 crossref_primary_10_1136_bmjopen_2023_074463 |
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Keywords | cardiovascular disease PET imaging inflammation Psoriatic arthritis |
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4 Gelfand, Neimann, Shin, Wang, Margolis, Troxel (CR28) 2006; 296 Goff, Karimkhani, Boyers, Weinstock, Lott, Hay, Coffeng, Norton, Naldi, Dunnick, Armstrong, Dellavalle (CR27) 2015; 172 Tawakol, Fayad, Mogg, Alon, Klimas, Dansky, Subramanian, Abdelbaky, Rudd, Farkouh, Nunes, Beals, Shankar (CR16) 2013; 62 Baliwag, Barnes, Johnston (CR7) 2015; 73 Tarkin, Joshi, Rudd (CR38) 2014; 11 Yeung, Takeshita, Mehta, Kimmel, Ogdie, Margolis, Shin, Attor, Troxel, Gelfand (CR3) 2013; 149 Mehta, Shin, Joshi, Dey, Armstrong, Duffin, Fuxench, Harrington, Hubbard, Kalb, Menter, Rader, Reilly, Simpson, Takeshita, Torigian, Werner, Troxel, Tyring, Vanderbeek, Van Voorhees, Playford, Ahlman, Alavi, Gelfand (CR35) 2018; 11 Gelfand, Troxel, Lewis, Kurd, Shin, Wang, Margolis, Strom (CR4) 2007; 143 Mehta, Azfar, Shin, Neimann, Troxel, Gelfand (CR29) 2010; 31 Li, Rosenkrans, Wang, Cai (CR37) 2020; 12 Harrington, Dey, Yunus, Joshi, Mehta (CR31) 2017; 312 Piaserico, Osto, Famoso, Montisci, De Michieli, Zanetti, Iliceto, Tona (CR9) 2019; 289 Joshi, Vesey, Williams, Shah, Calvert, Craighead, Yeoh, Wallace, Salter, Fletcher, van Beek, Flapan, Uren, Behan, Cruden, Mills, Fox, Rudd, Dweck, Newby (CR39) 2014; 383 Kim, Lee, Pak, Han, Kim, Kim, Ko, Kim, Kim (CR33) 2019; 80 Cocker, Spence, Hammond, deKemp, Lum, Wells (CR12) 2018; 271 Khraishi, MacDonald, Rampakakis, Vaillancourt, Sampalis (CR23) 2011; 30 Tawakol (10.1007/s12350-023-03204-8_bib11) 2006; 48 Rudd (10.1007/s12350-023-03204-8_bib10) 2002; 105 Anagnostopoulos (10.1007/s12350-023-03204-8_bib22) 2008; 35 Li (10.1007/s12350-023-03204-8_bib37) 2020; 12 McHugh (10.1007/s12350-023-03204-8_bib5) 2003; 42 Piaserico (10.1007/s12350-023-03204-8_bib9) 2019; 289 Fox (10.1007/s12350-023-03204-8_bib40) 2009; 50 Kim (10.1007/s12350-023-03204-8_bib33) 2019; 80 Bengel (10.1007/s12350-023-03204-8_bib36) 2016; 9 Tarkin (10.1007/s12350-023-03204-8_bib38) 2014; 11 Mizoguchi (10.1007/s12350-023-03204-8_bib17) 2011; 4 Mehta (10.1007/s12350-023-03204-8_bib29) 2010; 31 deKemp (10.1007/s12350-023-03204-8_bib19) 2016; 6 Baliwag (10.1007/s12350-023-03204-8_bib7) 2015; 73 Germino (10.1007/s12350-023-03204-8_bib20) 2016; 6 Harrington (10.1007/s12350-023-03204-8_bib31) 2017; 312 Cocker (10.1007/s12350-023-03204-8_bib12) 2018; 271 Wu (10.1007/s12350-023-03204-8_bib41) 2013; 3 Sankowski (10.1007/s12350-023-03204-8_bib1) 2013; 78 Tawakol (10.1007/s12350-023-03204-8_bib16) 2013; 62 Dey (10.1007/s12350-023-03204-8_bib34) 2017; 2 Daghem (10.1007/s12350-023-03204-8_bib6) 2018; 11 Figueroa (10.1007/s12350-023-03204-8_bib13) 2013; 6 Peluso (10.1007/s12350-023-03204-8_bib2) 2018; 13 Joshi (10.1007/s12350-023-03204-8_bib39) 2014; 383 Yeung (10.1007/s12350-023-03204-8_bib3) 2013; 149 Chih (10.1007/s12350-023-03204-8_bib26) 2018; 71 Joseph (10.1007/s12350-023-03204-8_bib42) 2016; 37 Maki-Petaja (10.1007/s12350-023-03204-8_bib32) 2012; 126 Gelfand (10.1007/s12350-023-03204-8_bib4) 2007; 143 Marnane (10.1007/s12350-023-03204-8_bib15) 2012; 71 Puzenat (10.1007/s12350-023-03204-8_bib24) 2010; 24 Goff (10.1007/s12350-023-03204-8_bib27) 2015; 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SubjectTerms | Anti-Inflammatory Agents - therapeutic use Arthritis, Psoriatic - diagnostic imaging Arthritis, Psoriatic - drug therapy Biological Factors - therapeutic use Cardiology cardiovascular disease Coronary vessels Fluorodeoxyglucose F18 - therapeutic use Humans Imaging inflammation Inflammation - diagnostic imaging Medicine Medicine & Public Health Nuclear Medicine Original Original Article PET imaging Positron-Emission Tomography Prospective Studies Psoriasis Psoriasis - diagnostic imaging Psoriasis - drug therapy Psoriatic arthritis Radiology |
Title | Anti-inflammatory effect of biologic therapy in patients with psoriatic disease: A prospective cohort FDG PET study |
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