Báo cáo y học: "Long term evaluation of disease progression through the quantitative magnetic resonance imaging of symptomatic knee osteoarthritis patients: correlation with clinical symptoms and radiographic change" pps

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Báo cáo y học: "Long term evaluation of disease progression through the quantitative magnetic resonance imaging of symptomatic knee osteoarthritis patients: correlation with clinical symptoms and radiographic change" pps

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Available online http://arthritis-research.com/content/8/1/R21 Research article Vol No Open Access Long term evaluation of disease progression through the quantitative magnetic resonance imaging of symptomatic knee osteoarthritis patients: correlation with clinical symptoms and radiographic changes Jean-Pierre Raynauld1, Johanne Martel-Pelletier1, Marie-Josée Berthiaume2, Gilles Beaudoin3, Denis Choquette4, Boulos Haraoui4, Hyman Tannenbaum5, Joan M Meyer6, John F Beary6, Gary A Cline6 and Jean-Pierre Pelletier1 1Osteoarthritis Research Unit, University of Montreal Hospital Centre, Notre-Dame Hospital, Department of Medicine, University of Montreal, Montreal, Quebec, Canada of Montreal Hospital Centre, Notre-Dame Hospital, Department of Radiology, University of Montreal, Montreal, Quebec, Canada 3University of Montreal Hospital Centre, Notre-Dame Hospital, Department of Physics and Biomedical Engineering, University of Montreal, Montreal, Quebec, Canada 4University of Montreal Hospital Centre, Notre-Dame Hospital, Department of Medicine, University of Montreal, Montreal, Quebec, Canada 5McGill University Health Centre, Montreal General Hospital, Department of Medicine, McGill University, Montreal, Quebec, Canada 6Procter & Gamble Pharmaceuticals, Mason, Ohio, USA 2University Corresponding author: Jean-Pierre Raynauld, jp.raynauld@videotron.ca Received: Sep 2005 Revisions requested: 14 Oct 2005 Revisions received: 14 Nov 2005 Accepted: 25 Nov 2005 Published: 30 Dec 2005 Arthritis Research & Therapy 2006, 8:R21 (doi:10.1186/ar1875) This article is online at: http://arthritis-research.com/content/8/1/R21 © 2005 Raynauld et al.; licensee BioMed Central Ltd This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited Abstract The objective of this study was to further explore the cartilage volume changes in knee osteoarthritis (OA) over time using quantitative magnetic resonance imaging (qMRI) These were correlated with demographic, clinical, and radiological data to better identify the disease risk features We selected 107 patients from a large trial (n = 1,232) evaluating the effect of a bisphosphonate on OA knees The MRI acquisitions of the knee were done at baseline, 12, and 24 months Cartilage volume from the global, medial, and lateral compartments was quantified The changes were contrasted with clinical data and other MRI anatomical features Knee OA cartilage volume losses were statistically significant compared to baseline values: -3.7 ± 3.0% for global cartilage and -5.5 ± 4.3% for the medial compartment at 12 months, and -5.7 ± 4.4% and -8.3 ± 6.5%, respectively, at 24 months Three different populations were identified according to cartilage volume loss: fast (n = 11; - 13.2%), intermediate (n = 48; -7.2%), and slow (n = 48; -2.3%) progressors The predictors of fast progressors were the presence of severe meniscal extrusion (p = 0.001), severe medial tear (p = 0.005), medial and/or lateral bone edema (p = 0.03), high body mass index (p < 0.05, fast versus slow), weight (p < 0.05, fast versus slow) and age (p < 0.05 fast versus slow) The loss of cartilage volume was also slightly associated with less knee pain No association was found with other Western Ontario McMaster Osteoarthritis Index (WOMAC) scores, joint space width, or urine biomarker levels Meniscal damage and bone edema are closely associated with more cartilage volume loss These data confirm the significant advantage of qMRI for reliably measuring knee structural changes at as early as 12 months, and for identifying risk factors associated with OA progression Introduction Diarthrodial joint damage assessment of the knee joint in particular is crucial for monitoring OA disease progression and for eventually evaluating the therapeutic effect of disease With the aging of the world population, osteoarthritis (OA) is becoming an increasingly common cause of disability [1,2] BMI = body mass index; DMOAD = disease modifying osteoarthritis drug; JSW = joint space width; MRI = magnetic resonance imaging; NSAID = nonsteroidal anti-inflammatory drug; OA = osteoarthritis; qMRI = quantitative MRI; U-CTX-II = urinary C-terminal crosslinking telopeptide of collagen type II; WOMAC = Western Ontario McMaster Osteoarthritis Index Page of 12 (page number not for citation purposes) Arthritis Research & Therapy Vol No Raynauld et al modifying osteoarthritis drugs (DMOADs) on its anatomical structure Improvements in the standardization and interpretation of knee and hip radiographs have produced more accurate measurements of both joint space width (JSW) and the progression of joint space narrowing [3] X-ray data from a recent study [4], however, showed that OA disease progression, especially in the knee joint, is heterogeneous; only 13.2% of the 2,483 knee OA patients followed for 24 months could be characterized as progressors (which might be of clinical significance), as defined by a changed JSW outside of the measurement error (JSW change >0.6 mm) Therefore, the use of JSW changes in knee OA studies is such that a minimum follow-up of at least 24 months and a cohort of several thousands is necessary to establish the effect of pharmacological interventions on OA disease progression Magnetic resonance imaging (MRI) allows for the precise visualization of joint structures such as cartilage, bone, synovium, ligaments, and menisci, as well as their pathological changes Our group [5,6], among others [7-12], have recently developed and validated a system capable of quantifying knee cartilage volume using MRI acquisitions combined with dedicated software Data showed [13] that rapid disease progression might have been predicted at the outset of the study based on certain clinical variables: being female, having a high body mass index (BMI), experiencing a higher level of pain and stiffness, and having reduced joint mobility Fast disease progression was further predicted by concomitant meniscal damage, mainly in the form of tears and meniscal extrusions [14] The simultaneously collected standardized knee radiographs displayed no correlation, however, between the changes in JSW and the concomitant loss of cartilage volume [13] A large clinical trial assessing the effects of a bisphosphonate on knee OA structural changes was recently completed A subset of 110 of these patients underwent MRI in addition to the clinical standardized radiograph and biomarker evaluations, as per the study protocol In this longitudinal study, we assessed this larger cohort of OA patients and identified risk factors for greater disease progression The cartilage volume changes contrasted with the clinical, radiological, and biomarker data We felt it was necessary to confirm our previous results [13,14] and provide new and clinically relevant information from this larger patient cohort recruited through an OA clinical trial and, therefore, corresponding to a more stringent inclusion and exclusion criteria Moreover, the results would also confirm the applicability of MRI cartilage volume quantification to the day-to-day reality of a clinical trial Materials and methods Patient selection A subset of 110 patients was selected from 1,232 patients enrolled in a large clinical trial evaluating the impact of a bisphosphonate on knee OA This specific subset of patients was recruited from the outpatient Rheumatology Clinic at the Page of 12 (page number not for citation purposes) University of Montreal Hospital Centre (CHUM), Notre-Dame Hospital, and from the Rheumatic Disease Centre of Montreal, both in Montreal, Quebec, Canada Both male and female patients were eligible for the study if they were between 40 and 80 years old, fulfilled the American College of Rheumatology criteria for knee OA [15], and had symptomatic disease that required medical treatment in the form of acetaminophen, traditional nonsteroidal anti-inflammatory drugs (NSAIDs), or selective cyclooxygenase-2 inhibitors Eligible patients were required to display radiological evidence of OA of the affected knee on a radiograph obtained within six months of the outset of the study Finally, patients had to have a minimum JSW of the medial compartment of between and mm, at least one osteophyte, and a narrower medial compartment compared to the lateral compartment The measurements were done from a baseline film using the standardized semi-flexed view, which was contrasted with follow-up films No patient had sole lateral compartment disease Patients were excluded if they had chondrocalcinosis or an acute or chronic infection (including tuberculosis); if their OA of the knee was secondary to other conditions, including inflammation, sepsis, metabolic abnormalities, and trauma; or if they displayed any contraindication to the use of MRI Further exclusion factors included patients' history of past or present gastrointestinal ulceration, their receipt of an intraarticular corticoid injection in the study knee within the six months prior to the outset of the study, as well as their classification as radiological grade IV on the Kellgren-Lawrence scale for the study knee or severe (class IV) functional disability In patients in whom both knees were symptomatic, we chose the most symptomatic knee for the investigation Patients were permitted to receive simple analgesics or NSAIDs, the regimens of which could be changed according to the preference of the rheumatologist and the clinical course of the patient Such regimens, as well as any changes to them, were closely monitored and noted Because of its potential to promote OA cartilage degeneration, the use of indomethacin was not permitted [16] A centralized ethics committee approved this study, and each patient gave informed consent Clinical evaluation Patients underwent clinical evaluation at baseline and every months thereafter until 24 months They were first evaluated on the basis of the Western Ontario McMaster Osteoarthritis Index (WOMAC), a tri-dimensional self-administered questionnaire that probes pain (5 items), stiffness (2 items), and physical function (17 items) [17] Its French-Canadian translation has been fully validated and established as reliable [18] In addition, the patients themselves used a visual analog scale to make a global assessment of their condition (patient global assessment: = very good; 100 = very bad) and to rate the pain they were experiencing that day (patient pain score: = no pain; 100 = most severe pain) Finally, the SF-36, a generic quality of life instrument, was administered to the patients at Available online http://arthritis-research.com/content/8/1/R21 each visit [19] A washout of medications was done prior to the clinical evaluation; NSAIDs were discontinued at least 48 hours prior to the investigation and acetaminophen, 24 hours The clinical evaluators were blinded to the results of previous radiological or MRI data Knee X-rays The JSW of the target knees was evaluated at baseline and at 12 and 24 months of follow-up, at the narrowest point in the medial tibio-femoral compartment according to the published protocol [20] This protocol allows for the standardization of radiographs by positioning the knee in a semi-flexed position under fluoroscopic guidance and by fixing a metal sphere to the fibula head to correct the effects of the radiographic magnification The films were digitized using a Lumiscan 200 laser film digitizer (Lumisys Inc., Sunnyvale, CA, USA), prior to which all films were bar-coded to ensure that, on digitization, the computer database would link patient/visit data to the JSW measurement obtained from each radiograph Each of the radiographs measured the minimum JSW in the medial compartment using the automated computerized method of measurement [21] In the rare occurrence that the radiographic quality of the film prevented the implementation of automatic JSW measurement software, manual intervention was required In such cases, manual intervention ensured reliable JSW measurement by aiding the algorithm to trace the articular contour [22] The variation coefficient for JSW measurement for the original reliability study was 1% for repeat radiographs (test/retest) of the knee in the semi-flexed position [20] The reproducibility of the method was also reassessed recently by Buckland-Wright and colleagues [23]; data showed that 45% of the examinations achieved high quality, that is, JSW difference between repeat films

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Mục lục

  • Abstract

  • Introduction

  • Materials and methods

    • Patient selection

    • Clinical evaluation

    • Knee X-rays

    • Knee MRI

    • Meniscal damage and bone edema

    • Biomarkers

    • Statistical analysis

    • Results

      • Patient characteristics

      • Cartilage volume changes over time

      • Characteristics of the slow, intermediate, and fast progressors

      • Comparison of changes in cartilage volume and JSW versus clinical parameters over time

      • Multilinear regression analysis

      • Medial compartment cartilage volume versus joint space width

      • Correlation between meniscal extrusion and JSW at baseline and over time

      • Cartilage volume and JSW versus urinary C-terminal crosslinking telopeptide of collagen type II

      • Discussion

      • Conclusion

      • Competing interests

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