Search

Your search keyword '"Ellingsen T"' showing total 505 results
Start Over Author "Ellingsen T"
505 results on '"Ellingsen T"'

4. Risk profiles for rheumatoid arthritis-associated interstitial lung disease in a cohort of patients with five-year follow-up.

Author

Hyldgaard, C, Blegvad, J, Sofiudóttir, BK, Andersen, FD, Isaksen, C, Urbonaviciene, G, Brix, L, Kragstrup, TW, Løgstrup, BB, and Ellingsen, T

Abstract

Objectives: Early identification of interstitial lung disease (ILD) among patients with rheumatoid arthritis (RA) is a challenge for clinicians. The aim of this study was to evaluate screening algorithms for ILD by comparing the proportion of patients assigned a high-risk profile by three recently proposed models. Method: We used the four-factor risk score, categorizing patients into high and low risk; the ILD screening criteria, categorizing patients into high, intermediate, and low risk; and the risk score for detection of subclinical RA-ILD, with four different risk categories, on patients with RA followed for 5 years after the RA diagnosis with pulmonary function tests, dyspnoea score, and pulmonary imaging. Results: The four-factor risk score identified 22% of the cohort (25/115) as eligible for further ILD investigations, while the ILD screening criteria identified 37% as high risk (43/115) and 34% as intermediate risk (39/115). The risk score for detection of subclinical RA-ILD identified 44% of the cohort as being at increased risk, with 7% in the highest risk group. The agreement between high-risk groups in the two clinical ILD screening models was moderate (kappa 0.43). Three patients in the cohort had clinical or subclinical ILD, and they were identified as high risk in the two clinical models. Conclusion: The three algorithms identified approximately one-third of the cohort as being at increased risk of ILD. Further development and validation of these algorithms are needed to reduce false positives and balance the potential benefit of earlier ILD diagnosis and healthcare resources used for respiratory assessment. [ABSTRACT FROM AUTHOR]

Published
2024
Full Text
View/download PDF

6. POS0423 PLASMA METABOLOMIC PROFILES OF PATIENTS WITH ACTIVE PERIPHERAL PSORIATIC ARTHRITIS CAN DIFFERENTIATE TREATMENT RESPONDERS FROM FAILURES: EXPLORATORY FINDINGS FROM THE FLORA TRIAL

Author

Skov Kragsnaes, M., primary, Miguens Blanco, J., additional, Mullish, B., additional, Contreras-Serrano, J. I., additional, Horn, H. C., additional, Munk, H., additional, Pedersen, J. K., additional, Nilsson, A. C., additional, Kristiansen, K., additional, Kjeldsen, J., additional, Marchesi, J., additional, and Ellingsen, T., additional

Published
2023
Full Text
View/download PDF

10. Plasma levels of multiple cardiovascular- and inflammation-related proteins analysed for associations with disease activity and anti-cyclic citrullinated peptide status in active early rheumatoid arthritis

Author

Mašić, D., Stengaard-Pedersen, K., Løgstrup, B. Bridal, Hørslev-Petersen, K., Hetland, M. L., Junker, P., Østergaard, M., Nielsen, C. H., Kruhøffer, M., Bøgebjerg, M. E., Röttger, R., Christensen, R., Ellingsen, T., Mašić, D., Stengaard-Pedersen, K., Løgstrup, B. Bridal, Hørslev-Petersen, K., Hetland, M. L., Junker, P., Østergaard, M., Nielsen, C. H., Kruhøffer, M., Bøgebjerg, M. E., Röttger, R., Christensen, R., and Ellingsen, T.

Abstract

Objective To compare plasma levels of 92 cardiovascular- and inflammation-related proteins (CIRPs) and to analyse for associations with anti-cyclic citrullinated peptide (anti-CCP) status and disease activity in early and treatment-naive rheumatoid arthritis (RA). Methods Olink CVD-III-panel was used to measure 92 CIRP plasma levels in 180 early, treatment-naive, and highly inflamed RA patients from the OPERA trial. CIRP plasma levels as well as correlation between CIRP plasma levels and RA disease activity were compared between anti-CCP groups. CIRP level-based hierarchical cluster analysis was performed in each anti-CCP group separately. Results The study included 117 anti-CCP-positive and 63 anti-CCP-negative RA patients. Among the 92 CIRPs measured, the levels of chitotriosidase-1 (CHIT1) and tyrosine-protein-phosphatase non-receptor-type substrate-1 (SHPS-1) were increased and those of metalloproteinase inhibitor-4 (TIMP-4) decreased in the anti-CCP-negative group compared to anti-CCP-positive group. The strongest associations with RA disease activity were found for interleukin-2 receptor-subunit-alpha (IL2-RA) and E-selectin levels in the anti-CCP-negative group and for C-C-motif chemokine-16 levels (CCL16) in the anti-CCP-positive group. None of the differences passed the Hochberg sequential multiplicity test, however, the CIPRs were interacting and thus the prerequisites of the Hochberg procedure were not fulfilled. CIRP level-based cluster analysis identified two patient clusters in both anti-CCP groups. Demographic and clinical characteristics were similar in the two clusters for each anti-CCP group. Conclusion In active and early RA, the findings regarding CHIT1, SHPS-1 TIMP-4, IL2-RA, E-selectin, and CCL16 differed between the two anti-CCP groups. In addition, we identified two patient clusters that were independent of the anti-CCP status.

Published
2023

11. Prevalence of survey-based criteria for fibromyalgia and impact on hospital burden: a 7 year follow-up study from an outpatient clinic.

Author

Lage-Hansen, PR, Chrysidis, S, Amris, K, Fredslund-Andersen, S, Christensen, R, and Ellingsen, T

Subjects
FIBROMYALGIA, MEDICAL personnel, HEALTH facilities, HOSPITAL utilization, HOSPITALS, MEDICAL specialties & specialists
Abstract

To evaluate the prevalence of survey-based criteria for fibromyalgia (FM) among newly referred patients in a rheumatic outpatient clinic, and to compare the use of secondary healthcare services between survey-based FM and non-FM cases. Newly referred patients to an outpatient clinic were screened for the fulfilment of the 2011 FM survey criteria during a 6 month period in 2013 in this observational cohort study. Demographic data were obtained at baseline. Patients' medical files were evaluated and comparisons between groups were made regarding the use of hospital healthcare facilities during the 7 year observation period. Out of 300 invited patients, 248 (83%) completed the questionnaire; 90 patients (36%) fulfilled survey-based criteria for FM at enrolment. FM cases were primarily women (80% vs 54% of non-FM cases), and received more medications (median 4 vs 3 drugs) and public economic support (62% vs 20%). At the 7 year follow-up, crude analyses showed that FM cases had a higher number of hospital courses (median 10 vs 8) and had undergone more invasive procedures (78% vs 60%). Neurologists (42% vs 28%), gastroenterologists (30% vs 13%), endocrinologists (40% vs 21%), pain specialists (13% vs 3%), psychiatrists (20% vs 7%), and abdominal surgeons (43% vs 30%) were consulted more often by FM than by non-FM cases. Fulfilment of FM survey criteria among newly referred patients to a rheumatic outpatient clinic is frequent. Our study findings show that FM continues to present a challenge for healthcare professionals as well as for patients. ● Fulfilment of FM survey criteria among newly referred patients to a rheumatic outpatient clinic is frequent. ● The burden on the secondary healthcare system for these patients is significant. ● This study suggests the need for increased awareness about the diagnosis of FM among certain medical and surgical specialties. [ABSTRACT FROM AUTHOR]

Published
2023
Full Text
View/download PDF

13. Hand bone loss in early rheumatoid arthritis during a methotrexate-based treat-to-target strategy with or without adalimumab—a substudy of the optimized treatment algorithm in early RA (OPERA) trial

Author

Ørnbjerg, L. M., Østergaard, M., Jensen, T., Hørslev-Petersen, K., Stengaard-Pedersen, K., Junker, P., Ellingsen, T., Ahlquist, P., Lindegaard, H., Linauskas, A., Schlemmer, A., Dam, M. Y., Hansen, I., Lottenburger, T., Ammitzbøll, C. G., Jørgensen, A., Krintel, S. B., Raun, J., Hetland, M. L., Slot, Ole, Nielsen, Lars Kjær, Skjødt, Henrik, Majgaard, Ole, Lorenzen, Tove, Horn, Hans Christian, Kowalski, Marcin, Johansen, Inger Lauge, Pedersen, Peter Mosborg, Manilo, Natalia, Bliddal, Henning, and OPERA Study Group

Published
2017
Full Text
View/download PDF

15. Galectin‐3 is Persistently Increased in Early Rheumatoid Arthritis (RA) and Associates with Anti‐CCP Seropositivity and MRI Bone Lesions, While Early Fibrosis Markers Correlate with Disease Activity

Author

Issa, S. F., Christensen, A. F., Lindegaard, H. M., Hetland, M. L., Hørslev‐Petersen, K., Stengaard‐Pedersen, K., Ejbjerg, B. J., Lottenburger, T., Ellingsen, T., Pedersen, J. K., Junker, K., Svendsen, A., Tarp, U., Østergaard, M., and Junker, P.

Published
2017
Full Text
View/download PDF

16. Prediction of treatment response to adalimumab: a double-blind placebo-controlled study of circulating microRNA in patients with early rheumatoid arthritis

Author

Krintel, S B, Dehlendorff, C, Hetland, M L, Hørslev-Petersen, K, Andersen, K K, Junker, P, Pødenphant, J, Ellingsen, T, Ahlquist, P, Lindegaard, H M, Linauskas, A, Schlemmer, A, Dam, M Y, Hansen, I, Horn, H C, Jørgensen, A, Raun, J, Ammitzbøll, C G, Østergaard, M, Stengaard-Pedersen, K, and Johansen, J S

Published
2016
Full Text
View/download PDF

17. Effect of initiating biologics compared to intensifying conventional DMARDs on clinical and MRI outcomes in established rheumatoid arthritis patients in clinical remission:Secondary analyses of the IMAGINE-RA trial

Author

Møller-Bisgaard, S., Hørslev-Petersen, K., Ejbjerg, B., Hetland, M. L., Christensen, R., Ørnbjerg, L. M., Glinatsi, D., Møller, J. M., Boesen, M., Stengaard-Pedersen, K., Madsen, O. R., Jensen, B., Villadsen, J. A., Hauge, E. M., Bennett, P., Hendricks, O., Asmussen, K., Kowalski, M., Lindegaard, H., Bliddal, H., Krogh, N. S., Ellingsen, T., Nielsen, A. H., Larsen, L., Jurik, A. G., Thomsen, H. S., Østergaard, M., Møller-Bisgaard, S., Hørslev-Petersen, K., Ejbjerg, B., Hetland, M. L., Christensen, R., Ørnbjerg, L. M., Glinatsi, D., Møller, J. M., Boesen, M., Stengaard-Pedersen, K., Madsen, O. R., Jensen, B., Villadsen, J. A., Hauge, E. M., Bennett, P., Hendricks, O., Asmussen, K., Kowalski, M., Lindegaard, H., Bliddal, H., Krogh, N. S., Ellingsen, T., Nielsen, A. H., Larsen, L., Jurik, A. G., Thomsen, H. S., and Østergaard, M.

Abstract

Objectives: To compare the effect of treat-to-target-based escalations in conventional synthetic disease-modifying antirheumatic drugs (csDMARDs) and biologics on clinical disease activity and magnetic resonance imaging (MRI) inflammation in a rheumatoid arthritis (RA) cohort in clinical remission. Method: One-hundred patients with established RA, Disease Activity Score based on 28-joint count–C-reactive protein (DAS28-CRP) < 3.2, and no swollen joints (hereafter referred to as ‘in clinical remission’) who received csDMARDs underwent clinical evaluation and MRI of the wrist and second to fifth metacarpophalangeal joints every 4 months. They followed a 2 year MRI treatment strategy targeting DAS28-CRP ≤ 3.2, no swollen joints, and absence of MRI osteitis, with predefined algorithmic treatment escalation: first: increase in csDMARDs; second: adding a biologic; third: switch biologic. MRI osteitis and Health Assessment Questionnaire (HAQ) (co-primary outcomes) and MRI combined inflammation and Simplified Disease Activity Index (SDAI) (key secondary outcomes) were assessed 4 months after treatment change and expressed as estimates of group differences. Statistical analyses were based on the intention-to-treat population analysed using repeated-measures mixed models. Escalation to first biologic compared to csDMARD escalation more effectively reduced MRI osteitis (difference between least squares means 1.8, 95% confidence interval 1.0–2.6), HAQ score (0.08, 0.03–0.1), MRI combined inflammation (2.5, 0.9–4.1), and SDAI scores (2.7, 1.9–3.5). Treat-to-target-based treatment escalations to biologics compared to escalation in csDMARDs more effectively improved MRI inflammation, physical function, and clinical disease activity in patients with established RA in clinical remission. Treatment escalation in RA patients in clinical remission reduces clinical and MRI-assessed disease activity. Trial registration: Clinicaltrials.gov identifier: NCT01656278.

Published
2022

20. POS0644 IMPACT OF FIBRE AND RED/PROCESSED MEAT INTAKE ON TREATMENT OUTCOMES AMONG PATIENTS WITH CHRONIC INFLAMMATORY DISEASES INITIATING BIOLOGICAL THERAPY: A PROSPECTIVE COHORT STUDY

Author

Overgaard, S. H., primary, Sorensen, S., additional, Munk, H. L., additional, Nexøe, A. B., additional, Glerup, H., additional, Henriksen, R. H., additional, Guldmann, T., additional, Pedersen, N., additional, Saboori, S., additional, Hvid, L., additional, Dahlerup, J. F., additional, Hvas, C. L., additional, Jawhara, M., additional, Andersen, K. W., additional, Kristian Pedersen, A., additional, Nielsen, O. H., additional, Bergenheim, F. H., additional, Brodersen, J. B., additional, Heitmann, B. L., additional, Halldorsson, T. I., additional, Holmskov, U., additional, Bygum, A., additional, Christensen, R., additional, Kjeldsen, J., additional, Ellingsen, T., additional, and Andersen, V., additional

Published
2022
Full Text
View/download PDF

26. Effect of initiating biologics compared to intensifying conventional DMARDs on clinical and MRI outcomes in established rheumatoid arthritis patients in clinical remission: Secondary analyses of the IMAGINE-RA trial

Author

Møller-Bisgaard, S, primary, Hørslev-Petersen, K, additional, Ejbjerg, B, additional, Hetland, ML, additional, Christensen, R, additional, Ørnbjerg, LM, additional, Glinatsi, D, additional, Møller, JM, additional, Boesen, M, additional, Stengaard-Pedersen, K, additional, Madsen, OR, additional, Jensen, B, additional, Villadsen, JA, additional, Hauge, EM, additional, Bennett, P, additional, Hendricks, O, additional, Asmussen, K, additional, Kowalski, M, additional, Lindegaard, H, additional, Bliddal, H, additional, Krogh, NS, additional, Ellingsen, T, additional, Nielsen, AH, additional, Larsen, L, additional, Jurik, AG, additional, Thomsen, HS, additional, and Østergaard, M, additional

Published
2021
Full Text
View/download PDF

28. Efficacy and safety of faecal microbiota tranplantation for active peripheral psoriatic arthritis:A randomised sham-controlled trial

Author

Kragsnaes, M. Skov, Kjeldsen, J., Horn, H. C., Munk, H. L., Pedersen, J. K., Just, S. A., Ahlquist, P., Pedersen, F. Moeller, De Wit, M., Moller, S., Andersen, V., Kristiansen, K., Holt, H. M., Holm, D. Kinggaard, Christensen, R., and Ellingsen, T.

Abstract

Background: Although causality remains to be established, targeting dysbiosis of the intestinal microbiota by faecal microbiota transplantation (FMT) has been proposed as a novel therapeutic option for treatment of extra-intestinal inflammatory diseases.1Objectives: In this proof-of-concept study, we evaluated efficacy and safety of FMT in psoriatic arthritis (PsA).2Methods: In this double-blind, parallel-group, sham-controlled, superiority trial, we randomly allocated (1:1) adults with active peripheral PsA (≥3 swollen joints) despite ongoing treatment with methotrexate to one gastroscopic-guided FMT or sham transplantation into the duodenum. The transplants (50 g faeces) came from one of four healthy, thoroughly screened, anonymous stool donors.3 The primary efficacy endpoint was the proportion of participants experiencing treatment failure (i.e., needing treatment intensification) through 26 weeks. The first key secondary endpoint was change in Health Assessment Questionnaire Disability Index (HAQ-DI) score from baseline to week 26. Safety was monitored throughout the trial. Trial registration number: NCT03058900, ClinicalTrials.gov.Results: Of 97 screened, 31 (32%) underwent randomisation (15 allocated to FMT), all received the assigned intervention, and 30 (97%) completed the 26-week clinical evaluation (Table 1). Treatment failure occurred more frequently in the FMT group than in the sham group (9 [60%] vs 3 [19%]; risk ratio, 3.20; 95% CI, 1.06 to 9.62; P=0.018). During the entire 26 weeks of observation, the rate of the treatment failures was significantly higher in the FMT than in the sham group, see figure 1. Improvement in HAQ-DI score differed between groups (0.07 vs 0.30) by 0.23 points (95% CI, 0.02 to 0.44; P=0.031) in favour of sham. No serious adverse events were observed.Conclusion: In this first interventional randomised controlled trial of FMT in immune-mediated arthritis, FMT was inferior to sham in treating active peripheral PsA. FMT did not appear to result in serious adverse events.

Published
2021

30. Periarticular and generalised bone loss in patients with early rheumatoid arthritis: influence of alendronate and intra-articular glucocorticoid treatment. Post hoc analyses from the CIMESTRA trial

Author

Jensen, T W, Hansen, M S, Hørslev-Petersen, K, Hyldstrup, L, Abrahamsen, B, Langdahl, B, Zerahn, B, Pødenphant, J, Stengaard-Petersen, K, Junker, P, Østergaard, M, Lottenburger, T, Ellingsen, T, Andersen, L S, Hansen, I, Skjødt, H, Pedersen, J K, Lauridsen, U B, Svendsen, A J, Tarp, U, Lindegaard, H, Jurik, Anne Grethe, Vestergaard, Aage, and Hetland, M L

Published
2014
Full Text
View/download PDF

31. OP0010 EFFICACY AND SAFETY OF FAECAL MICROBIOTA TRANSPLANTATION FOR ACTIVE PERIPHERAL PSORIATIC ARTHRITIS: A RANDOMISED SHAM-CONTROLLED TRIAL

Author

Skov Kragsnaes, M., primary, Kjeldsen, J., additional, Horn, H. C., additional, Munk, H. L., additional, Pedersen, J. K., additional, Just, S. A., additional, Ahlquist, P., additional, Moeller Pedersen, F., additional, De Wit, M., additional, Möller, S., additional, Andersen, V., additional, Kristiansen, K., additional, Holt, H. M., additional, Kinggaard Holm, D., additional, Christensen, R., additional, and Ellingsen, T., additional

Published
2021
Full Text
View/download PDF

32. AB0924-PARE EXPERIENCES AND PERCEPTIONS OF PATIENTS WITH PSORIATIC ARTHRITIS PARTICIPATING IN A TRIAL OF FAECAL MICROBIOTA TRANSPLANTATION: A NESTED QUALITATIVE STUDY

Author

Skov Kragsnaes, M., primary, Theodor Sødergren, S., additional, Kjeldsen, J., additional, Horn, H. C., additional, Munk, H. L., additional, Pedersen, J. K., additional, Schufri Klinkby, C., additional, De Wit, M., additional, Gram Ahlmark, N., additional, Tjørnhøj-Thomsen, T., additional, and Ellingsen, T., additional

Published
2021
Full Text
View/download PDF

34. PREDICTORS OF ACHIEVING STRINGENT REMISSION IN PATIENTS WITH ESTABLISHED RHEUMATOID ARTHRITIS IN CLINICAL REMISSION FOLLOWING A TREAT-TO-TARGET STRATEGY:Predictors of achieving stringent remission in patients with established rheumatoid arthritis in clinical remission following a treat-to-target strategy

Author

Møller-Bisgaard, Signe, Georgiadis, S., Hørslev-Petersen, Kim, Ejbjerg, Bo Jannik, Hetland, Merete Lund, Ornbjerg, Lykke, Glinatski, Daniel, Møller, J. Møllenbach, Boesen, M., Stengaard-Pedersen, Kristian, Madsen, Ole Rintek, Jensen, B., Villadsen, J., Hauge, Ellen Margrethe, Bennett, Philip, Hendricks, Oliver, Asmussen, K., Kowalski, M., Lindegaard, H.M., Bliddal, Henning, Steen Krogh, N., Ellingsen, T., Nielsen, A., Balding, L., Jurik, Anne Grethe, Thomsen, H., and Østergaard, M

Published
2020

36. Vitamin D Trajectories in Early Diagnosed, Aggressively Treated Rheumatoid Arthritis Patients:A 10 Year Longitudinal Cohort Study Based on The Danish Cimestra Trial

Author

Herly, M., Stengaard-Pedersen, K., Vestergaard, P., Christensen, R., Möller, S., Ǿstergaard, M., Junker, P., Hetland, M. L., Hørslev-Petersen, K., and Ellingsen, T.

Abstract

Background: Low vitamin D levels are common in Rheumatoid Arthritis (RA)1, and possibly associated with disease course,2 but data on vitamin D levels during long-term disease course has not been reported previously.Objectives: To describe vitamin D trajectories from time of diagnosis through 10 years follow-up in early diagnosed RA patients.Methods: The CIMESTRA trial included 160 newly diagnosed RA-patients, treated aiming at remission with methotrexate and intraarticular steroid, further randomized to ciclosporine or placebo. Vitamin D supplementation was recommended according to national guidelines. Vitamin Dtotal was measured at diagnosis, and year 1, 5 and 10 using LC-MS/MS. 1,25(OH)2D was measured at diagnosis and year 1 using RIA. Linear mixed effects models were used to study vitamin D levels serially. We had fixed effects for time, and patients modelled as a random effect. We tested the hypothesis that percentage of patients achieving Dtotal >= 50 nmol/l during follow-up was 908-CRP during the disease-course were adjusted for age, sex, symptom-duration prior to diagnosis and season of diagnosis.Results: Median Dtotal at baseline was 53 nmol/l (IQR 36-567.8). Dtotal increased significantly during follow-up, independently of level at diagnosis (plt;0.001). Individuals achieving Dtotal>=50nmol/l during follow-up was 80-87 but not as high as 90 and 5, plt;0.002. DAS28-CRP during disease-course was inversely associated with Dtotal trajectories only in crude (β-coefficient (β) -0.0034, 95-0.007; -0.0002) p=0.039) and partially adjusted analyses (β -0.003, 95-0.007; -0.002) p=0.04). Estimate was left insignificant in fully adjusted analyses (β -0.003, 95-0.0006; 0.0001) p=0.06). 1,25(OH)2D levels did not change significantly during follow-up (p=1.00).Conclusion: Dtotal increased significantly during follow-up, but fewer than 900 nmol/l at year 1 and 5. Disease activity during follow-up was associated with Dtotal trajectories only in partially adjusted analyses, while adjustment for possible confounders left estimates insignificant. Results suggest vitamin D supplementation to be recommended in all RA patients.References: Reference List[1]Herly M, Stengaard-Pedersen K, Vestergaard P, et al. The D-vitamin metabolite 1,25(OH)2 D in serum is associated with disease activity and Anti-Citrullinated Protein Antibodies in active and treatment naive, early Rheumatoid Arthritis Patients. Scand J Immunol 2018;88(3):e12704. doi: 10.1111/sji.12704[2]Mouterde G, Gamon E, Rincheval N, et al. Association between Vitamin D deficiency and disease activity, disability and radiographic progression in early rheumatoid arthritis. The ESPOIR cohort. J Rheumatol 2019 doi: 10.3899/jrheum.190795Disclosure of Interests: Mette Herly Grant/research support from: Pfizer Denmark - textquotedblleftUnrestricted Granttextquotedblright for PhD projectDanish Rheumatism Association, Research Grant, Speakers bureau: Speaker for Danish Rheumatism Association, Kristian Stengaard-Pedersen: None declared, Peter Vestergaard: None declared, Robin Christensen: None declared, Sören Möller: None declared, Mikkel Ǿstergaard Grant/research support from: AbbVie, Bristol-Myers Squibb, Celgene, Merck, and Novartis, Consultant of: AbbVie, Bristol-Myers Squibb, Boehringer Ingelheim, Celgene, Eli Lilly, Hospira, Janssen, Merck, Novartis, Novo Nordisk, Orion, Pfizer, Regeneron, Roche, Sandoz, Sanofi, and UCB, Speakers bureau: AbbVie, Bristol-Myers Squibb, Boehringer Ingelheim, Celgene, Eli Lilly, Hospira, Janssen, Merck, Novartis, Novo Nordisk, Orion, Pfizer, Regeneron, Roche, Sandoz, Sanofi, and UCB, Peter Junker: None declared, Merete L. Hetland Grant/research support from: BMS, MSD, AbbVie, Roche, Novartis, Biogen and Pfizer, Consultant of: Eli Lilly, Speakers bureau: Orion Pharma, Biogen, Pfizer, CellTrion, Merck and Samsung Bioepis, Kim Hørslev-Petersen Grant/research support from: Pfizer (Travel expences), Torkell Ellingsen: None declared

Published
2020

42. FRI0019 MRI INFLAMMATION, DISEASE ACTIVITY AND FUNCTIONAL IMPAIRMENT ARE MORE EFFECTIVELY REDUCED BY ESCALATION TO BIOLOGICS COMPARED TO CSDMARD-ESCALATION IN RHEUMATOID ARTHRITIS PATIENTS IN CLINICAL REMISSION FOLLOWING A TREAT-TO-TARGET STRATEGY: SECONDARY ANALYSES OF THE IMAGINE-RA TRIAL

Author

Møller-Bisgaard, S., primary, Hørslev-Petersen, K., additional, Ejbjerg, B., additional, Hetland, M. L., additional, Christensen, R., additional, Ørnbjerg, L., additional, Glinatsi, D., additional, Møllenbach Møller, J., additional, Boesen, M., additional, Stengaard-Pedersen, K., additional, Rintek Madsen, O., additional, Jensen, B., additional, Villadsen, J., additional, Hauge, E. M., additional, Bennett, P., additional, Hendricks, O., additional, Asmussen, K., additional, Kowalski, M., additional, Lindegaard, H. M., additional, Bliddal, H., additional, Steen Krogh, N., additional, Ellingsen, T., additional, Nielsen, A., additional, Jurik, A. G., additional, Balding, L., additional, Thomsen, H., additional, and Ǿstergaard, M., additional

Published
2020
Full Text
View/download PDF

43. OP0018 A MULTICENTER RANDOMIZED STUDY IN EARLY RHEUMATOID ARTHRITIS TO COMPARE ACTIVE CONVENTIONAL THERAPY VERSUS THREE BIOLOGICAL TREATMENTS: 24 WEEK EFFICACY RESULTS OF THE NORD-STAR TRIAL

Author

Hetland, M. L., primary, Haavardsholm, E. A., additional, Rudin, A., additional, Nordström, D., additional, Nurmohamed, M., additional, Gudbjornsson, B., additional, Lampa, J., additional, Hørslev-Petersen, K., additional, Uhlig, T., additional, Gröndal, G., additional, Ǿstergaard, M., additional, Heiberg, M., additional, Twisk, J., additional, Krabbe, S., additional, Lend, K., additional, Olsen, I., additional, Lindqvist, J., additional, Ekwall, A. K. H., additional, Grøn, K. L., additional, Kapetanovic, M. C., additional, Faustini, F., additional, Tuompo, R., additional, Lorenzen, T., additional, Cagnotto, G., additional, Baecklund, E., additional, Hendricks, O., additional, Vedder, D., additional, Sokka-Isler, T., additional, Husmark, T., additional, Ljosa, M. K. A., additional, Brodin, E., additional, Ellingsen, T., additional, Soderbergh, A., additional, Rizk, M., additional, Reckner, Å., additional, Larsson, P., additional, Uhrenholt, L., additional, Just, S. A., additional, Stevens, D., additional, Laurberg, T. B., additional, Bakland, G., additional, and Van Vollenhoven, R., additional

Published
2020
Full Text
View/download PDF

44. AB0194 VITAMIN D TRAJECTORIES IN EARLY DIAGNOSED, AGGRESSIVELY TREATED RHEUMATOID ARTHRITIS PATIENTS: A 10 YEAR LONGITUDINAL COHORT STUDY BASED ON THE DANISH CIMESTRA TRIAL

Author

Herly, M., primary, Stengaard-Pedersen, K., additional, Vestergaard, P., additional, Christensen, R., additional, Möller, S., additional, Ǿstergaard, M., additional, Junker, P., additional, Hetland, M. L., additional, Hørslev-Petersen, K., additional, and Ellingsen, T., additional

Published
2020
Full Text
View/download PDF

45. THU0614-HPR ASSESSING THE EFFECT OF INTERVENTIONS FOR AXIAL SPONDYLOARTHRITIS ACCORDING TO THE ENDORSED ASAS/OMERACT CORE OUTCOME SET: A META-RESEARCH STUDY OF TRIALS INCLUDED IN COCHRANE REVIEWS

Author

Asmussen Andreasen, R., primary, Kristensen, L. E., additional, Baraliakos, X., additional, Strand, V., additional, Mease, P. J., additional, De Wit, M., additional, Ellingsen, T., additional, Jensen Hansen, I. M., additional, Kirkham, J., additional, Wells, G., additional, Tugwell, P., additional, Maxwell, L., additional, Boers, M., additional, Egstrup, K., additional, and Christensen, R., additional

Published
2020
Full Text
View/download PDF

46. AB0209 PREDICTORS OF ACHIEVING STRINGENT REMISSION IN PATIENTS WITH ESTABLISHED RHEUMATOID ARTHRITIS IN CLINICAL REMISSION FOLLOWING A TREAT-TO-TARGET STRATEGY

Author

Møller-Bisgaard, S., primary, Georgiadis, S., additional, Hørslev-Petersen, K., additional, Ejbjerg, B., additional, Hetland, M. L., additional, Ørnbjerg, L., additional, Glinatsi, D., additional, Møllenbach Møller, J., additional, Boesen, M., additional, Stengaard-Pedersen, K., additional, Rintek Madsen, O., additional, Jensen, B., additional, Villadsen, J., additional, Hauge, E. M., additional, Bennett, P., additional, Hendricks, O., additional, Asmussen, K., additional, Kowalski, M., additional, Lindegaard, H. M., additional, Bliddal, H., additional, Steen Krogh, N., additional, Ellingsen, T., additional, Nielsen, A., additional, Balding, L., additional, Jurik, A. G., additional, Thomsen, H., additional, and Ǿstergaard, M., additional

Published
2020
Full Text
View/download PDF

47. FRI0069 EFFECTS OF ADALIMUMAB ADDED TO TREAT-TO-TARGET STRATEGY WITH METHOTREXATE AND INTRA-ARTICULAR TRIAMCINOLONE ON LIPIDS IN EARLY- AND TREATMENT NAÏVE RHEUMATOID PATIENTS: SECONDARY ANALYSES FROM THE MULTICENTER DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED OPERA TRIAL

Author

Masic, D., primary, Stengaard-Pedersen, K., additional, Løgstrup, B. B., additional, Hørslev-Petersen, K., additional, Hetland, M. L., additional, Junker, P., additional, Ǿstergaard, M., additional, Ammitzbøl, C., additional, Möller, S., additional, Christensen, R., additional, and Ellingsen, T., additional

Published
2020
Full Text
View/download PDF

48. MRI bone oedema is the strongest predictor of subsequent radiographic progression in early rheumatoid arthritis. Results from a 2-year randomised controlled trial (CIMESTRA)

Author

Hetland, M L, Ejbjerg, B, Hørslev-Petersen, K, Jacobsen, S, Vestergaard, A, Jurik, A G, Stengaard-Pedersen, K, Junker, P, Lottenburger, T, Hansen, I, Andersen, L S, Tarp, U, Skjødt, H, Pedersen, J K, Majgaard, O, Svendsen, A J, Ellingsen, T, Lindegaard, H, Christensen, A F, Vallø, J, Torfing, T, Narvestad, E, Thomsen, H S, and Østergaard, M

Published
2009
Full Text
View/download PDF

49. Aggressive combination therapy with intra-articular glucocorticoid injections and conventional disease-modifying anti-rheumatic drugs in early rheumatoid arthritis: second-year clinical and radiographic results from the CIMESTRA study

Author

Hetland, M L, Stengaard-Pedersen, K, Junker, P, Lottenburger, T, Hansen, I, Andersen, L S, Tarp, U, Svendsen, A, Pedersen, J K, Skjødt, H, Lauridsen, U B, Ellingsen, T, Hansen, G V O, Lindegaard, H, Vestergaard, A, Jurik, A G, Østergaard, M, and Hørslev-Petersen, K

Published
2008
Full Text
View/download PDF

50. MAGNETIC RESONANCE IMAGING TENOSYNOVITIS AND OSTEITIS ARE INDEPENDENT PREDICTORS OF RADIOGRAPHIC AND MRI DAMAGE PROGRESSION IN RHEUMATOID ARTHRITIS PATIENTS IN CLINICAL REMISSION

Author

Signe Kaas Møller-Bisgaard, Hørslev-Petersen, K., Ejbjerg, B., Merete Lund Hetland, Lykke Midtbøll Ørnbjerg, Daniel Glinatsi, Jakob M Møller, Mikael Boesen, Stengaard-Pedersen, K., Madsen, O., Bente Jensen, Villadsen, J., Hauge, E. M., Philip Bennett, Hendricks, O., Asmussen, K., Kowalski, M., Lindegaard, H. M., Henning Bliddal, Krogh, N. S., Ellingsen, T., Nielsen, A., Lone Larsen, Jurik, A. G., Thomsen, Henrik S., and Mikkel Østergaard

Published
2019

Catalog

Books, media, physical & digital resources
See catalog results