Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Rheumawire Feb 9, 2004 Progression continues even during RA remission Amsterdam, the Netherlands - Clinical remission is seen as the key to preventing joint destruction in rheumatoid arthritis (RA), but a new study by Dutch researchers shows that, in a significant number of patients, even documented clinical remission is not a reliable indicator of disease quiescence [1]. Clinically significant joint damage progression occurred in 15% of RA patients in persistent remission examined radiologically by Drs Esmeralda TH Molenaar, andre E Voskuyl (University Medical Center, Amsterdam), and colleagues over a 2-year period. The study is reported in the January issue of Arthritis & Rheumatism, and the investigators say their work " suggests the need for markers that predict progression during periods of low disease activity and for drugs that prevent damage that is independent of disease activity. " The study included 187 RA patients in clinical remission who were followed up clinically and radiologically for 2 years. Remission was defined using a modification of American College of Rheumatology criteria (omitting fatigue, which had not been uniformly included in the regular patient assessments). Joint damage was assayed by the Sharp/van der Heijde method. Patients were required to have been in remission for 6 months before study entry and were allowed to take disease-modifying antirheumatic drugs (DMARDs) and nonsteroidal anti-inflammatory drugs (NSAIDs). Patients taking glucocorticoids were excluded. Patients were assessed every 3 months for exacerbation, which was defined as no longer meeting the criteria for clinical remission or as having a DMARD therapy change by the treating rheumatologists because of worsening of arthritis activity. Remission persisted throughout the study period in 52% of patients who met the ACR criteria for remission at baseline and in 42% of those who had Disease Activity Scale (DAS) of <1.6 at entry, but median radiologic score for the total group increased from 21 at baseline to 25 after 2 years (p<0.001). As might be expected, clinically significant radiologic progression (change in the Sharp/van der Heijde score of >5) was more common in patients who had exacerbations than in those in remission (23% vs 7%, p=0.001), but Voskuyl tells rheumawire that radiologic progression, as shown by development of an erosion in a previously unaffected joint, was observed in about 15% of the patients who remained in clinical remission. " These findings suggest that joint destruction may (in part) occur independently of the presence of synovitis, " Voskuyl says. " Radiologic progression can occur during a state of persistent remission as defined by our remission criteria but also as defined by the ACR and DAS criteria. " Voskuyl advises monitoring patients in remission every 3 months and intervening quickly. " Even low disease activity must be treated vigorously to retard progression of joint damage or development of new erosions. This is because progressive joint damage is related to functional performance, " he says. This evidence that synovitis and joint destruction occur somewhat independently adds to previous work showing that levels of bone markers are increased in RA patients even during remissions and that a reduction of such bone markers is associated with a reduction in long-term joint damage, regardless of the levels of clinically apparent disease activity. Voskuyl suggests that this means that the definition of remission should be changed to include structurally as well as clinically inactive disease. " It remains to be determined which parameter is most useful. Bone or cartilage markers or joint destruction as determined by imaging (ie, x-ray of hands and feet) may be helpful and should be investigated in the future, " Voskuyl says. " Urinary type 2 collagen C-telopeptide also may be useful for monitoring bone change and is currently being investigated. " In an editorial that accompanies the article, Dr R Kirwan (Bristol Royal Infirmary, UK) says that it " offers further evidence that the link between inflammation and erosions is not clear-cut " and that possibly several pathologic processes are " proceeding in parallel in the rheumatoid joint. " Kirwan also warns that, in view of this possibility, researchers testing new therapies should resist " the assumption that the control of inflammation, even by direct attack on the cells thought responsible, will result in suppression of erosions. " Janis Sources 1. Molenaar ET, Voskuyl AE, Dinant HJ, et al. Progression of radiologic damage in patients with rheumatoid arthritis in clinical remission. Arthritis Rheum 2004 Jan; 50(1):36-42. 2. Kirwan JR. The synovium in rheumatoid arthritis: evidence for (at least) two pathologies. Arthritis Rheum 2004 Jan; 50(1):1-4. I'll tell you where to go! Mayo Clinic in Rochester http://www.mayoclinic.org/rochester s Hopkins Medicine http://www.hopkinsmedicine.org Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2004 Report Share Posted July 29, 2004 , That is very interesting. I had x-rays done of hand and feet around the time I was diagnosed. Do you know how often should new x-rays be done? I am writing this down as a topic to discuss at my next rheumy visit. Do you have a link to this study? Jennie > Rheumawire > Feb 9, 2004 > > > Progression continues even during RA remission > > > Amsterdam, the Netherlands - Clinical remission is seen as the key to > preventing joint destruction in rheumatoid arthritis (RA), but a new > study by Dutch researchers shows that, in a significant number of > patients, even documented clinical remission is not a reliable indicator > of disease quiescence [1]. Clinically significant joint damage > progression occurred in 15% of RA patients in persistent remission > examined radiologically by Drs Esmeralda TH Molenaar, andre E > Voskuyl (University Medical Center, Amsterdam), and colleagues over a > 2-year period. The study is reported in the January issue of Arthritis & > Rheumatism, and the investigators say their work " suggests the need for > markers that predict progression during periods of low disease activity > and for drugs that prevent damage that is independent of disease > activity. " > > The study included 187 RA patients in clinical remission who were > followed up clinically and radiologically for 2 years. Remission was > defined using a modification of American College of Rheumatology > criteria (omitting fatigue, which had not been uniformly included in the > regular patient assessments). Joint damage was assayed by the Sharp/van > der Heijde method. Patients were required to have been in remission for > 6 months before study entry and were allowed to take disease- modifying > antirheumatic drugs (DMARDs) and nonsteroidal anti-inflammatory drugs > (NSAIDs). Patients taking glucocorticoids were excluded. > > Patients were assessed every 3 months for exacerbation, which was > defined as no longer meeting the criteria for clinical remission or as > having a DMARD therapy change by the treating rheumatologists because of > worsening of arthritis activity. > > Remission persisted throughout the study period in 52% of patients who > met the ACR criteria for remission at baseline and in 42% of those who > had Disease Activity Scale (DAS) of <1.6 at entry, but median radiologic > score for the total group increased from 21 at baseline to 25 after 2 > years (p<0.001). As might be expected, clinically significant radiologic > progression (change in the Sharp/van der Heijde score of >5) was more > common in patients who had exacerbations than in those in remission (23% > vs 7%, p=0.001), but Voskuyl tells rheumawire that radiologic > progression, as shown by development of an erosion in a previously > unaffected joint, was observed in about 15% of the patients who remained > in clinical remission. > > " These findings suggest that joint destruction may (in part) occur > independently of the presence of synovitis, " Voskuyl says. " Radiologic > progression can occur during a state of persistent remission as defined > by our remission criteria but also as defined by the ACR and DAS > criteria. " > > Voskuyl advises monitoring patients in remission every 3 months and > intervening quickly. " Even low disease activity must be treated > vigorously to retard progression of joint damage or development of new > erosions. This is because progressive joint damage is related to > functional performance, " he says. > > This evidence that synovitis and joint destruction occur somewhat > independently adds to previous work showing that levels of bone markers > are increased in RA patients even during remissions and that a reduction > of such bone markers is associated with a reduction in long-term joint > damage, regardless of the levels of clinically apparent disease > activity. > > Voskuyl suggests that this means that the definition of remission should > be changed to include structurally as well as clinically inactive > disease. " It remains to be determined which parameter is most useful. > Bone or cartilage markers or joint destruction as determined by imaging > (ie, x-ray of hands and feet) may be helpful and should be investigated > in the future, " Voskuyl says. " Urinary type 2 collagen C-telopeptide > also may be useful for monitoring bone change and is currently being > investigated. " > > In an editorial that accompanies the article, Dr R Kirwan (Bristol > Royal Infirmary, UK) says that it " offers further evidence that the link > between inflammation and erosions is not clear-cut " and that possibly > several pathologic processes are " proceeding in parallel in the > rheumatoid joint. " > > Kirwan also warns that, in view of this possibility, researchers testing > new therapies should resist " the assumption that the control of > inflammation, even by direct attack on the cells thought responsible, > will result in suppression of erosions. " > > Janis > > Sources > > 1. Molenaar ET, Voskuyl AE, Dinant HJ, et al. Progression of radiologic > damage in patients with rheumatoid arthritis in clinical remission. > Arthritis Rheum 2004 Jan; 50(1):36-42. > > 2. Kirwan JR. The synovium in rheumatoid arthritis: evidence for (at > least) two pathologies. Arthritis Rheum 2004 Jan; 50(1):1-4. > > > > > > I'll tell you where to go! > > Mayo Clinic in Rochester > http://www.mayoclinic.org/rochester > > s Hopkins Medicine > http://www.hopkinsmedicine.org Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2004 Report Share Posted July 29, 2004 Jennie, the best I can do is give you the link to the abstract. To view the full text requires a subscription, and I don't have one to that journal. Perhaps your rheumatologist does. Arthritis & Rheumatism Volume 50, Issue 1 , Pages 36 - 42 " Progression of radiologic damage in patients with rheumatoid arthritis in clinical remission " : http://www3.interscience.wiley.com/cgi-bin/abstract/106600984/ABSTRACT How often X-rays are done is highly dependent on the individual rheumatologist and the disease characteristics of the patient in question. I'll tell you where to go! Mayo Clinic in Rochester http://www.mayoclinic.org/rochester s Hopkins Medicine http://www.hopkinsmedicine.org [ ] Re: Progression continues even during RA remission > , > > That is very interesting. I had x-rays done of hand and feet around > the time I was diagnosed. Do you know how often should new x-rays be > done? I am writing this down as a topic to discuss at my next rheumy > visit. Do you have a link to this study? > > Jennie > > > > Rheumawire > > Feb 9, 2004 > > > > > > Progression continues even during RA remission > > > > > > Amsterdam, the Netherlands - Clinical remission is seen as the key > to > > preventing joint destruction in rheumatoid arthritis (RA), but a new > > study by Dutch researchers shows that, in a significant number of > > patients, even documented clinical remission is not a reliable > indicator > > of disease quiescence [1]. Clinically significant joint damage > > progression occurred in 15% of RA patients in persistent remission > > examined radiologically by Drs Esmeralda TH Molenaar, andre E > > Voskuyl (University Medical Center, Amsterdam), and colleagues over > a > > 2-year period. The study is reported in the January issue of > Arthritis & > > Rheumatism, and the investigators say their work " suggests the need > for > > markers that predict progression during periods of low disease > activity > > and for drugs that prevent damage that is independent of disease > > activity. " > > > > The study included 187 RA patients in clinical remission who were > > followed up clinically and radiologically for 2 years. Remission was > > defined using a modification of American College of Rheumatology > > criteria (omitting fatigue, which had not been uniformly included > in the > > regular patient assessments). Joint damage was assayed by the > Sharp/van > > der Heijde method. Patients were required to have been in remission > for > > 6 months before study entry and were allowed to take disease- > modifying > > antirheumatic drugs (DMARDs) and nonsteroidal anti-inflammatory > drugs > > (NSAIDs). Patients taking glucocorticoids were excluded. > > > > Patients were assessed every 3 months for exacerbation, which was > > defined as no longer meeting the criteria for clinical remission or > as > > having a DMARD therapy change by the treating rheumatologists > because of > > worsening of arthritis activity. > > > > Remission persisted throughout the study period in 52% of patients > who > > met the ACR criteria for remission at baseline and in 42% of those > who > > had Disease Activity Scale (DAS) of <1.6 at entry, but median > radiologic > > score for the total group increased from 21 at baseline to 25 after > 2 > > years (p<0.001). As might be expected, clinically significant > radiologic > > progression (change in the Sharp/van der Heijde score of >5) was > more > > common in patients who had exacerbations than in those in remission > (23% > > vs 7%, p=0.001), but Voskuyl tells rheumawire that radiologic > > progression, as shown by development of an erosion in a previously > > unaffected joint, was observed in about 15% of the patients who > remained > > in clinical remission. > > > > " These findings suggest that joint destruction may (in part) occur > > independently of the presence of synovitis, " Voskuyl > says. " Radiologic > > progression can occur during a state of persistent remission as > defined > > by our remission criteria but also as defined by the ACR and DAS > > criteria. " > > > > Voskuyl advises monitoring patients in remission every 3 months and > > intervening quickly. " Even low disease activity must be treated > > vigorously to retard progression of joint damage or development of > new > > erosions. This is because progressive joint damage is related to > > functional performance, " he says. > > > > This evidence that synovitis and joint destruction occur somewhat > > independently adds to previous work showing that levels of bone > markers > > are increased in RA patients even during remissions and that a > reduction > > of such bone markers is associated with a reduction in long-term > joint > > damage, regardless of the levels of clinically apparent disease > > activity. > > > > Voskuyl suggests that this means that the definition of remission > should > > be changed to include structurally as well as clinically inactive > > disease. " It remains to be determined which parameter is most > useful. > > Bone or cartilage markers or joint destruction as determined by > imaging > > (ie, x-ray of hands and feet) may be helpful and should be > investigated > > in the future, " Voskuyl says. " Urinary type 2 collagen C-telopeptide > > also may be useful for monitoring bone change and is currently being > > investigated. " > > > > In an editorial that accompanies the article, Dr R Kirwan > (Bristol > > Royal Infirmary, UK) says that it " offers further evidence that the > link > > between inflammation and erosions is not clear-cut " and that > possibly > > several pathologic processes are " proceeding in parallel in the > > rheumatoid joint. " > > > > Kirwan also warns that, in view of this possibility, researchers > testing > > new therapies should resist " the assumption that the control of > > inflammation, even by direct attack on the cells thought > responsible, > > will result in suppression of erosions. " > > > > Janis > > > > Sources > > > > 1. Molenaar ET, Voskuyl AE, Dinant HJ, et al. Progression of > radiologic > > damage in patients with rheumatoid arthritis in clinical remission. > > Arthritis Rheum 2004 Jan; 50(1):36-42. > > > > 2. Kirwan JR. The synovium in rheumatoid arthritis: evidence for (at > > least) two pathologies. Arthritis Rheum 2004 Jan; 50(1):1-4. Quote Link to comment Share on other sites More sharing options...
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