Other
Musculoskeletal Imaging
April 2004

Rheumatoid Arthritis of the Hand and Wrist: Comparison of Three Imaging Techniques

Abstract

OBJECTIVE. The purpose of this study was to compare the relative results from conventional high-field-strength 1.5-T MRI, 0.2-T low-field-strength dedicated extremity MRI, and radiography to detect and grade bone erosions, joint-space narrowing, and synovitis in the hands and wrists of patients with rheumatoid arthritis.
SUBJECTS AND METHODS. Eighteen patients with rheumatoid arthritis underwent conventional high-field-strength MRI, low-field-strength dedicated extremity MRI, and conventional radiography of both hands and wrists. Two independent reviewers searched for the presence and extent of bone erosions, joint-space narrowing, and synovitis. Bone erosions (E scores) and joint-space narrowing (J scores) were evaluated at 14 and 13 sites, respectively, on conventional high-field-strength MRI, low-field-strength dedicated extremity MRI, and radiography, using the Sharp-Genant scoring system. Synovitis (S scores) were evaluated at 13 sites on conventional high-field-strength MRI and low-field-strength dedicated extremity MRI.
RESULTS. For the detection of bone erosions, we found no significant difference (p = 0.71) between conventional high-field-strength MRI (mean ± SD E score, 27.5 ± 9.8) and low-field-strength dedicated extremity MRI (28.8 ± 10.0), but a significant difference (p < 0.001) appeared between MRI and radiography (13.1 ± 8.3). J scores derived from MRI (conventional high-field-strength MRI, 15.2 ± 8.3; low-field-strength dedicated extremity MRI, 14.5 ± 10.4) were higher than those derived from radiography (12.7 ± 9.6), although the difference was not significant (p = 0.70). Conventional high-field-strength MRI (S score, 35.1 ± 8.6) and low-field-strength dedicated extremity MRI (30.8 ± 10.2) were equivalent (p = 0.14) for the evaluation of synovitis. The interobserver agreement for MRI scores was good to excellent (intraclass correlation coefficients, 0.83–0.94).
CONCLUSION. Conventional high-field-strength MRI and low-field-strength dedicated extremity MRI showed similar results in terms of cross-sectional grading of bone erosions, joint-space narrowing, and synovitis in the hands and wrists of patients with rheumatoid arthritis.

Introduction

Rheumatoid arthritis is a systemic inflammatory disorder with an estimated prevalence of 1% [1]. Most patients exhibit a chronic fluctuating course of disease that, if left untreated, can result in progressive joint destruction, deformity, and irreversible long-term disability. The diagnosis of rheumatoid arthritis is based primarily on the 1987 revised criteria of the American College of Rheumatology (formerly, the American Rheumatism Association) [2], including clinical, biologic, and radiologic findings. The joints of the hands are among the first to be affected in rheumatoid arthritis, and they are of particular interest in the assessment of patients with suspected early rheumatoid arthritis [3]. MRI has been shown to be more sensitive than radiography at detecting bone erosions in the hands and wrists of patients with rheumatoid arthritis [4, 5]. In addition, MRI can provide visualization of edema, hyperemia, and joint effusion, as well as visualization of synovial pannus with the use of IV gadolinium injection [48]. Previous MRI studies of small joints with arthritis have been performed mostly on whole-body high-field-strength systems (> 1 T), and few data are available on low-field-strength dedicated extremity MRI for the evaluation of rheumatoid arthritis of the hand and wrist [911]. Dedicated extremity MRI is easier to site than whole-body MRI, offers lower cost and greater patient comfort, and eliminates the problem of claustrophobia and potential biohazards associated with metal in the patient by putting the limb of interest in the magnet bore; it may thus be more feasible than conventional high-field-strength MRI for the evaluation of patients with arthritis of the small joints. To the best of our knowledge, only one study has compared conventional high-field-strength MRI with low-field-strength dedicated extremity MRI in hand arthritis [9], and it showed the same performances for both techniques in terms of erosion detection and evaluation of synovial hypertrophy.
The purpose of our study was to compare results from conventional high-field-strength 1.5-T MRI, low-field-strength dedicated extremity 0.2-T MRI, and radiography to detect and grade bone erosions, joint-space narrowing, and synovitis in the hands and wrists of patients with rheumatoid arthritis.

Subjects and Methods

Patients

Eighteen patients (13 women, five men) with a mean age of 55.5 years (range, 37–77 years) and a proven diagnosis of rheumatoid arthritis as defined by the American College of Rheumatology 1987 revised criteria [2] were consecutively enrolled in this study. All patients were referred from the Rheumatology Clinic at the University of California, San Francisco. Patients with rheumatoid arthritis of less than 6 months duration and those in whom the arthritis began before the age of 16 were excluded. At the time of the study, the mean duration of the disease was 8 years (range, 1–11 years), and all patients were undergoing therapy, including nonsteroidal antiinflammatory drugs (n = 13), methotrexate (n = 11), steroids (n = 9), and hydroxychloroquine (Plaquenil sulfate, Winthrop) (n = 8). The study protocol was ratified by our institutional board review, and all patients signed informed consent forms before participating.

Imaging Procedures

All patients underwent high-field-strength 1.5-T conventional MRI (Signa, General Electric Medical Systems), low-field-strength 0.2-T dedicated extremity MRI (Artoscan, Esaote Biomedica), and radiography of both hands and wrists on the same day.
Radiography.—Posteroanterior images of both hands were obtained using a conventional technique (single-emulsion, single-screen, high-resolution system). The exposure aimed to achieve optimal visualization of the trabeculae and joints: small focal spot, 40 inches (102 cm); focus–field distance, 50–55 kV; 100 mA at 300 msec.
Conventional high-field-strength MRI and low-field-strength dedicated extremity MRI.—Conventional high-field-strength MRI and low-field-strength dedicated extremity MRI were performed on four areas: right and left wrists and right and left fingers. No IV contrast material was used.
On conventional high-field-strength MRI, the following sequences were obtained using a commercial circumferential wrist coil with a 3-inch internal diameter: coronal T1-weighted spin-echo (TR/TE, 600/9; matrix, 512 × 192; field of view, 12 × 12 cm; number of acquisitions, 2; slice thickness, 3 mm; acquisition time, 3 min 30 sec) on both sides, and coronal 3D T2* fast gradient-echo sequences in steady state with frequency-selective fat saturation (29.4/6.3; matrix, 512 × 192; flip angle, 20°; field of view, 12 × 12 cm; number of acquisitions, 2; slice thickness, 1.5 mm; acquisition time, 6 min) on the dominant hand. The choice of the MRI sequences and parameters was aimed at achieving a balance among anatomic coverage, contrast-to-noise ratio, spatial resolution (using the fast gradient-echo sequence), patient tolerance, and technical simplicity.
On low-field-strength dedicated extremity MRI, the following sequences were obtained: coronal T1 isotropic 3D gradient-recalled echo sequences (30/12; matrix, 192 × 160; flip angle, 60°; field of view, 15 × 12 cm; number of acquisitions, 2; slice thickness, 3 mm; acquisition time, 5 min 30 sec) on both sides, and coronal short time inversion recovery sequences (1,000/16; inversion time, 80 msec; matrix, 192 × 136; field of view, 18 × 12 cm; number of acquisitions, 3; slice thickness, 3.5 mm; acquisition time, 6 min 6 sec) on the dominant hand.
The total acquisition time (not including the set-up time) was 26 min for conventional high-field-strength MRI and 34 min for low-field-strength dedicated extremity MRI.

Image Evaluation

Seventy-two MRI examinations and 36 radiographs were evaluated in consensus by two trained observers on three separate occasions. Results from conventional high-field-strength MRI, low-field-strength dedicated extremity MRI, and radiography were evaluated separately—first independently and then in consensus.
The following parameters were assessed: bone erosions and joint-space narrowing on MRI and radiography; synovial hypertrophy and joint effusion together on MRI.
The Genant-modified Sharp radiographic scoring method [12, 13] was used for radiography and adapted for MRI (Table 1). This scoring method was initially developed for radiography and has been successfully used in clinical trials.
TABLE 1 Different Scores Used at Conventional High-Field-Strength MRI, Low-Field-Strength Dedicated Extremity MRI, and Conventional Radiography to Evaluate Erosions, Joint-Space Narrowing, and Synovitis
ScoreScaleNo. of SitesMaximum Score Per Patient
E0-3.51498
J0-413104
S
0-3
13
78
Note.—E, J, and S scores are erosion, joint-space narrowing, and synovitis scores, respectively, evaluated at conventional high-field-strength MRI, low-field-strength dedicated extremity MRI, and conventional radiography.
Radiographic evaluation.—Bone erosions and joint-space narrowing were scored on each radiograph on a paper form using the previously validated method [13] according to the grading system described in the next section. Independent scores for erosions and joint-space narrowing were obtained for each hand and wrist. The intraobserver and interobserver reproducibility of this method was reported previously [13].
Erosion score (E score).—Bone erosions were evaluated at 14 sites in each hand and wrist (including the proximal interphalangeal joints and the metacarpophalangeal joints, the first carpometacarpal joint, the scaphoid bone, and the distal parts of the ulna and the radius), using an 8-point scale from 0 to 3.5 based on the number and size of erosions and the area of bone involved: 0 (normal, no erosions), 0.5 (subtle change, subtle loss of cortical continuity or equivocal findings of bone erosion), 1.0 (mild, definite but small erosions of one or both articular bones, usually at the bare areas, typically involving < 25% of the combined articular surface area), 1.5 (mild to moderate, small to medium erosions usually involving < 25% of the articular surface of one or both articular bones), 2.0 (moderate, medium to large erosions involving as much as 50% of the articular surface of one or both articular bones), 2.5 (moderate to severe, erosion of 50–75% of the articular surfaces), 3.0 (severe, erosion of > 75% but not all articular surfaces), and 3.5 (severe worse, erosion of the entire articular surface).
Joint-space narrowing score (J score).—Joint-space narrowing was evaluated at 13 sites in each hand and wrist. Sites included the proximal interphalangeal joints and the metacarpophalangeal joints, the carpometacarpal joints three to five as a single unit, the pericapitate space (scaphoid–capitate and lunate–capitate combined), and the radiocarpal joint. We used a 5-point scale from 0 to 4: 0 (normal joint space), 1 (mild, narrowing of the joint space width), 2 (moderate, narrowing of the joint space width), 3 (severe, nearly complete loss of the joint space), and 4 (osseous ankylosis or dislocation).
MR image evaluation.—The MR images were evaluated on a workstation using modified version 1.6 software (MRVision). Erosions were defined as focal, sharply marginated defects that replaced normal fatty marrow and cortical and trabecular bone and were continuous with the bone surface. Bone erosions were distinguished from marrow edema principally on the basis of margin sharpness. Erosions were considered to have sharp, well-defined margins, and edema had ill-defined margins. Erosions and joint-space narrowing were scored independently according to the same grading scheme used for the radiographs. Independent scores for erosions and joint-space narrowing were obtained for each hand and wrist.
Synovial hypertrophy score (S score).—Synovial hypertrophy and joint effusion were defined as the presence of interarticular thickened synovium with or without fluid that appeared hypointense on T1- or hyperintense on T2-weighted images (dominant hand) and as hypointense on T1-weighted images (nondominant hand) and were evaluated together as a single measure of synovitis on a 4-point scale from 0 to 3 at 13 sites (the proximal interphalangeal joints and the metacarpophalangeal joints, the first carpometacarpal joint, all wrist joints as a single unit, and the distal radioulnar joint) according to the following scoring system: 0 (none), 1 (mild, > one third maximal potential joint distention), 2 (moderate, ≥ two thirds maximal potential joint distention), 3 (severe, > two thirds maximal potential joint distention).

Statistical Evaluation

The total E scores and J scores obtained from conventional high-field-strength MRI, low-field-strength dedicated extremity MRI, and radiography; and S scores from conventional high-field-strength MRI and low-field-strength dedicated extremity MRI were obtained for each patient by consensus evaluation and compared using the Wilcoxon's signed rank test and the analysis of variance test (two-sample rank sum test) where appropriate. A p value less than 0.05 was considered significant. The interobserver agreement on MRI was evaluated using the intraclass correlation coefficients computed from the independent evaluation results.

Results

The reviewers successfully evaluated the images from all patients, and no joints were believed to be uninterpretable on conventional high-field-strength MRI or low-field-strength dedicated extremity MRI. The interobserver agreement on MRI was good to excellent (intraclass correlation 0.83 for E scores, 0.85 for J scores, and 0.94 for S scores).

Bone Erosions

Bone erosions were generally more conspicuous and well delineated on MR images than on radiographs. The E scores derived from low-field-strength dedicated extremity MRI and high-field-strength MRI were not statistically different (Table 2 and Figs. 1A, 1B, 1C, 1D and 2A, 2B, 2C, 2D). MRI showed more erosions than radiography, with mean E scores more than twice as high on MRI as on radiography.
TABLE 2 Erosion (E), Joint-Space Narrowing (J), and Synovitis (S) Scores Obtained on Conventional High-Field-Strength MRI, Low-Field-Strength Dedicated Extremity MRI, and Radiography
ScoreConventional High-Field-Strength MRILow-Field-Strength Dedicated Extremity MRIRadiographyp
MeanSDMeanSDMeanSD
E27.59.828.810.013.18.3<0.001a
J15.28.314.510.412.79.60.70b
S
35.1
8.6
30.8
10.2


0.14c
Note.—SD = standard deviation, dash (—) indicates that data were not collected.
a
Analysis of variance test for overall comparison and Wilcoxon's signed rank test for the two-by-two comparison of conventional high-field-strength MRI versus low-field-strength dedicated extremity MRI (p=0.71), conventional high-field-strength MRI versus radiography (p<0.001), and low-field-strength dedicated extremity MRI versus radiography (p<0.001).
b
Analysis of variance test. Results not significant.
c
Wilcoxon's signed rank test. Results not significant.
Fig. 1A. 42-year-old woman with rheumatoid arthritis. Posteroanterior radiograph reveals multiple erosions of carpal bones (arrows).
Fig. 1B. 42-year-old woman with rheumatoid arthritis. Unenhanced coronal T1-weighted spin-echo conventional high-field-strength MR image reveals multiple erosions of carpal bones (arrows). Triquetral erosion (arrowhead) is not visible on radiograph because of pisiform superposition.
Fig. 1C. 42-year-old woman with rheumatoid arthritis. Unenhanced coronal T1-weighted gradient-recalled echo low-field-strength dedicated extremity MR image reveals multiple erosions of carpal bones (arrows), seen on two adjacent slices because of different slice location (not shown).
Fig. 1D. 42-year-old woman with rheumatoid arthritis. Adjacent unenhanced coronal T1-weighted gradient-recalled echo low-field-strength dedicated extremity MR image reveals triquetral erosion (arrow) not visible on radiography because of pisiform superposition.
Fig. 2A. 71-year-old woman with rheumatoid arthritis. Unenhanced coronal T1-weighted spin-echo conventional high-field-strength MR image shows multiple erosions and synovitis of left second to fifth metacarpophalangeal joints (arrows).
Fig. 2B. 71-year-old woman with rheumatoid arthritis. Unenhanced coronal T2*-weighted fast gradient-echo conventional high-field-strength MR image in steady state with fat saturation shows multiple erosions and synovitis of left second to fourth metacarpophalangeal joints (arrows).
Fig. 2C. 71-year-old woman with rheumatoid arthritis. Unenhanced coronal T1-weighted gradient-recalled echo low-field-strength dedicated extremity MR image shows multiple erosions and synovitis of left second to fifth metacarpophalangeal joints (arrows).
Fig. 2D. 71-year-old woman with rheumatoid arthritis. Unenhanced coronal T1-weighted gradient-recalled echo low-field-strength dedicated extremity MR image shows multiple erosions and synovitis of left second to fourth metacarpophalangeal joints (arrows).

Joint-Space Narrowing

The J scores derived from conventional high-field-strength MRI and low-field-strength dedicated extremity MRI were not statistically different (Table 2 and Fig. 3A, 3B, 3C, 3D). Joint-space narrowing was rated as more moderate on radiography than it was on MRI, but the difference was not statistically significant.
Fig. 3A. 52-year-old man with rheumatoid arthritis. Posteroanterior radiograph reveals severe joint-space narrowing of carpus and radiocarpal joints, with grade 4 joint ankylosis (arrows) between capitate, scaphoid, lunate, and triquetrum bones.
Fig. 3B. 52-year-old man with rheumatoid arthritis. Unenhanced coronal T1-weighted spin-echo conventional high-field-strength MR image reveals severe joint-space narrowing of carpus and radiocarpal joints, with grade 4 joint ankylosis (arrow) between capitate, scaphoid, lunate, and triquetrum bones.
Fig. 3C. 52-year-old man with rheumatoid arthritis. Unenhanced coronal T2*-weighted fast gradient-echo conventional high-field-strength MR image in steady state with fat saturation reveals severe joint-space narrowing of carpus and radiocarpal joints, with grade 4 joint ankylosis (arrow) between capitate, scaphoid, lunate, and triquetrum bones.
Fig. 3D. 52-year-old man with rheumatoid arthritis. Unenhanced coronal T1-weighted gradient-recalled echo low-field-strength dedicated extremity MR image also reveals severe joint-space narrowing of carpus and radiocarpal joints, with grade 4 joint ankylosis (arrows) between capitate, scaphoid, lunate, and triquetrum bones.

Synovitis

The S scores derived from conventional high-field-strength MRI and low-field-strength dedicated extremity MRI were equivalent (Table 2 and Figs. 2A, 2B, 2C, 2D and 4A, 4B, 4C, 4D).
Fig. 4A. 42-year-old woman with rheumatoid arthritis. Unenhanced coronal T1-weighted spin-echo conventional high-field-strength MR image reveals synovitis (arrows) at ulnar side of wrist and first carpometacarpal joint in low signal.
Fig. 4B. 42-year-old woman with rheumatoid arthritis. Unenhanced coronal T2*-weighted fast gradient-echo conventional high-field-strength MR image in steady state with fat saturation reveals synovitis (arrows) at ulnar side of wrist and first carpometacarpal joint in high signal.
Fig. 4C. 42-year-old woman with rheumatoid arthritis. Unenhanced coronal T1-weighted gradient-recalled echo low-field-strength dedicated extremity MR image reveals synovitis (arrows) at ulnar side of wrist and first carpometacarpal joint in low signal.
Fig. 4D. 42-year-old woman with rheumatoid arthritis. Unenhanced coronal T2-weighted short time inversion recovery low-field-strength dedicated extremity MR image reveals synovitis (arrows) at ulnar side of wrist and first carpometacarpal joint in high signal.

Discussion

Several clinical trials in rheumatoid arthritis have shown the efficacy of aggressive early treatment of patients with active disease [1416]. Imaging techniques have proven useful for assessing the response to therapy and can potentially be used to select the patient population at risk that will benefit most from early aggressive therapy [5, 17]. Radiography of the hand and wrist is the traditional method used for the diagnosis, staging, and follow-up of patients with rheumatoid arthritis, and for the assessment of treatment efficacy in individual patients. Radiography is also the central tool for the evaluation of disease progression and for outcome measurement in rheumatoid arthritis clinical trials; several scoring systems based on radiography have been developed for that purpose [13, 1820] and have been reported to show good interobserver agreement [13, 19]. However, radiography is known to be insensitive to early erosions, and several previous cross-sectional and longitudinal studies have reported that MRI is more sensitive for detecting bone erosions in rheumatoid arthritis of the hand and wrist [4, 5, 11, 21, 22]. In addition, radiography is not a sensitive technique for the detection of synovitis. MRI offers distinct advantages over radiography: In addition to its multiplanar capability, it can image the soft tissues, including the synovial pannus; synovial fluid; and tendons, as well as bone and cartilage. The quantification of synovial volume can potentially be used to monitor the response to therapy and to predict which patients are more likely to develop erosions in 1 year [23]. Moreover, MRI can give power to drug trials by lowering the length of the studies and the number of patients.
The major drawbacks of MRI are its high cost and limited availability. Dedicated low-field-strength MRI devices using less than 1 T offer advantages over high-field-strength systems: lower cost, easier siting, better patient comfort, and reduced patient risk [24]. A few previous studies have compared the usefulness of low-field-strength dedicated extremity MRI versus conventional high-field-strength MRI and have shown equivalent performances for the evaluation of shoulder lesions [25] or lower performances for the ankle and foot [26]. However, low-field-strength dedicated extremity MRI has the drawbacks of lower signal-to-noise ratio [2729], limited anatomic coverage, and longer acquisition time compared with conventional high-field-strength MRI.
In rheumatoid arthritis, most of the previous MRI studies were carried out using high-field-strength systems [4, 5, 7, 8, 3032]. A few studies have used low-field-strength systems [911, 33] and have reported better results than those from radiography. However, only one study has directly compared conventional high-field-strength MRI with low-field-strength dedicated extremity MRI in patients with various forms of arthritis, including rheumatoid arthritis, and it showed no difference in the measurement of synovial membrane volume after gadolinium injection or in the evaluation of bone erosions and bone edema in hand arthritis [9]. That study also found that 64% of patients said that low-field-strength dedicated extremity MRI was more comfortable than conventional high-field-strength MRI when they responded to a questionnaire with a 4-point scale evaluating the discomfort from each MRI technique. Our study showed that low-field-strength dedicated extremity MRI and conventional high-field-strength MRI performed equally well for cross-sectional grading of bone erosions, joint-space narrowing, and synovitis in rheumatoid arthritis. Both MRI techniques detected approximately twice as many erosions as radiography did. They were more sensitive than radiography for the evaluation of joint-space narrowing, although no significant difference appeared, possibly as a result of the small sample size.

Evaluation of Bone Erosions in Rheumatoid Arthritis

A direct link between synovitis and bone damage is still controversial, but strong evidence exists that early bone changes, such as bone edema, rarely occur in the absence of synovitis. Several authors have suggested a MRI-tracked three-step sequence of changes from synovitis to bone edema and then to erosions [7, 34]. Patients with a pronounced carpal synovitis at baseline were more at risk than others to develop erosions at 1 year [23, 35] or 2 years [36]. Direct pathologic confirmation that the erosions seen on MRI represent the same structural lesions that are depicted on radiographs has yet to be reported, but considerable indirect evidence supports this contention. Several studies [5, 7, 37] have reported a higher prevalence of marrow edema in rheumatoid arthritis and have presented evidence to suggest that edema and inflammation in the bone marrow may precede the development of actual bone erosions. However, the patients in those studies had early active disease (< 6 months) and showed substantial progression of erosive damage, and our study examined patients with chronic rheumatoid arthritis on stable therapy.
Further evidence that the bone erosions depicted on MR images are the same lesions that are seen on radiography comes from the study of Foley-Nolan et al. [21], which showed that all erosions detected on radiography were also visible on MRI and that the distribution of the lesions depicted by the two techniques correlated anatomically. In a longitudinal study of patients undergoing active therapy, Ostergaard et al. [6] reported that erosions visible on radiography after 1 year could be seen on MRI at least 6 months earlier and that the lag time between the appearance of erosions on MRI and their emergence on radiography was typically more than 1 year. McQueen et al. [5] also reported that erosions were visible on MRI 6–12 months before they appeared on radiography.

Evaluation of Joint-Space Narrowing in Rheumatoid Arthritis

Our study is the first, to our knowledge, to compare the evaluation of cartilage damage and subsequent joint-space narrowing between MRI and radiography. We found that MRI was more sensitive than radiography, although not significantly so, possibly because of the sample size. We found good interobserver agreement for the evaluation of joint-space narrowing. However, a low to moderate interobserver agreement for the evaluation has been reported recently [38], and the difficulty of differentiating cartilage from synovitis and joint fluid on MRI in small joints must be emphasized.

Evaluation of Synovitis in Rheumatoid Arthritis

In our study, synovitis was visible on both T1-weighted spin-echo and T2* fast gradient-echo sequences (conventional high-field-strength MRI) and on coronal T1-weighted 3D gradient-recalled echo and short time inversion recovery sequences (low-field-strength dedicated extremity MRI) as fluid signal distending the joint cavity. Synovial tissue could not be reliably differentiated from synovial fluid with the sequences used in this study. Discriminating these two components of the synovial cavity typically requires the use of IV contrast material or special sequences such as magnetization transfer [39]. The injection of gadolinium would have increased the complexity, cost, and duration of the examination. Moreover, diffusion of the contrast agent from the synovium into the adjacent joint fluid is known to occur rapidly in small joints and would obscure the synovium. Accordingly, it was decided not to attempt to discriminate between the synovium and synovial fluid, particularly because both were essentially features of the same process of synovitis.

Limitations

Several limitations of our study should be mentioned. First, only a small number of patients were evaluated, which limits the power of the statistical results. However, a fair number of MRI examinations (n = 72) were evaluated. Second, we did not use contrast injection for the evaluation of synovitis, to limit the cost and duration of the examination. Third, we used different T2-weighted sequences for conventional high-field-strength MRI and low-field-strength dedicated extremity MRI. We used a T2* fast gradient-echo in steady-state sequence for conventional high-field-strength MRI to obtain high-resolution images, and a STIR sequence for low-field-strength dedicated extremity MRI, because of the field strength limitation. However, the comparison was based on an overall evaluation including both T1- and T2-weighted images. Fourth, we did not evaluate bone marrow edema because most of our patients had chronic rheumatoid arthritis and were undergoing stable therapy.

Summary

Based on our results, despite its lower image quality and longer acquisition time, low-field-strength MRI compares favorably with high-field-strength MRI in the detection and grading of bone erosions, joint-space narrowing, and synovitis in the hands and wrists of patients with rheumatoid arthritis.

Footnotes

Address correspondence to B. Taouli.
Supported in part by Hoffman-LaRoche.

References

1.
Gabriel SE, Crowson CS, O'Fallon WM. The epidemiology of rheumatoid arthritis in Rochester, Minnesota, 1955–1985. Arthritis Rheum 1999; 42:415 –420
2.
Arnett FC, Edworthy SM, Bloch DA, et al. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum 1988; 31:315 –324
3.
Scott DL, Coulton BL, Popert AJ. Long term progression of joint damage in rheumatoid arthritis. Ann Rheum Dis 1986; 45:373 –378
4.
Klarlund M, Ostergaard M, Jensen KE, Madsen JL, Skjodt H, Lorenzen I. Magnetic resonance imaging, radiography, and scintigraphy of the finger joints: one year follow up of patients with early arthritis—the TIRA group. Ann Rheum Dis 2000; 59:521 –528
5.
McQueen FM, Stewart N, Crabbe J, et al. Magnetic resonance imaging of the wrist in early rheumatoid arthritis reveals a high prevalence of erosions at four months after symptom onset. Ann Rheum Dis 1998; 57:350 –356
6.
Ostergaard M, Hansen M, Stoltenberg M, et al. Magnetic resonance imaging-determined synovial membrane volume as a marker of disease activity and a predictor of progressive joint destruction in the wrists of patients with rheumatoid arthritis. Arthritis Rheum 1999; 42:918 –929
7.
McGonagle D, Conaghan PG, O'Connor P, et al. The relationship between synovitis and bone changes in early untreated rheumatoid arthritis: a controlled magnetic resonance imaging study. Arthritis Rheum 1999; 42:1706 –1711
8.
Sugimoto H, Takeda A, Hyodoh K. Early-stage rheumatoid arthritis: prospective study of the effectiveness of MR imaging for diagnosis. Radiology 2000; 216:569 –575
9.
Savnik A, Malmskov H, Thomsen HS, et al. MRI of the arthritic small joints: comparison of extremity MRI (0.2 T) vs high field MRI (1.5 T). Eur Radiol 2001; 11:1030 –1038
10.
Lindegaard H, Vallo J, Horslev-Petersen K, Junker P, Ostergaard M. Low field dedicated magnetic resonance imaging in untreated rheumatoid arthritis of recent onset. Ann Rheum Dis 2001; 60:770 –776
11.
Backhaus M, Kamradt T, Sandrock D, et al. Arthritis of the finger joints: a comprehensive approach comparing conventional radiography, scintigraphy, ultrasound, and contrast-enhanced magnetic resonance imaging. Arthritis Rheum 1999; 42:1232 –1245
12.
Genant HK. Methods of assessing radiographic change in rheumatoid arthritis. Am J Med 1983; 75:35 –47
13.
Genant HK, Jiang Y, Peterfy C, Lu Y, Redei J, Countryman PJ. Assessment of rheumatoid arthritis using a modified scoring method on digitized and original radiographs. Arthritis Rheum 1998; 41:1583 –1590
14.
van der Heide A, Jacobs JW, Bijlsma JW, et al. The effectiveness of early treatment with “second-line” antirheumatic drugs: a randomized, controlled trial. Ann Intern Med 1996; 124:699 –707
15.
Emery P. Early rheumatoid arthritis: therapeutic strategies. Scand J Rheumatol 1994; 100[suppl]:3 –7
16.
Lipsky PE, van der Heijde DM, St Clair EW, et al. Infliximab and methotrexate in the treatment of rheumatoid arthritis: anti-tumor necrosis factor trial in rheumatoid arthritis with concomitant therapy study group. N Engl J Med 2000; 343:1594 –1602
17.
Sugimoto H, Takeda A, Masuyama J, Furuse M. Early-stage rheumatoid arthritis: diagnostic accuracy of MR imaging. Radiology 1996; 198:185 –192
18.
Larsen A, Dale K, Eek M. Radiographic evaluation of rheumatoid arthritis and related conditions by standard reference films. Acta Radiol Diagn (Stockh) 1977; 18:481 –491
19.
Sharp JT, Bluhm GB, Brook A, et al. Reproducibility of multiple-observer scoring of radiologic abnormalities in the hands and wrists of patients with rheumatoid arthritis. Arthritis Rheum 1985; 28:16 –24
20.
Sharp JT, Young DY, Bluhm GB, et al. How many joints in the hands and wrists should be included in a score of radiologic abnormalities used to assess rheumatoid arthritis? Arthritis Rheum 1985; 28:1326 –1335
21.
Foley-Nolan D, Stack JP, Ryan M, et al. Magnetic resonance imaging in the assessment of rheumatoid arthritis: a comparison with plain film radiographs. Br J Rheumatol 1991; 30:101 –106
22.
Rominger MB, Bernreuter WK, Kenney PJ, Morgan SL, Blackburn WD, Alarcon GS. MR imaging of the hands in early rheumatoid arthritis: preliminary results. RadioGraphics 1993; 13:37 –46
23.
Savnik A, Malmskov H, Thomsen HS, et al. MRI of the wrist and finger joints in inflammatory joint diseases at 1-year interval: MRI features to predict bone erosions. Eur Radiol 2002; 12:1203 –1210
24.
Peterfy CG, Roberts T, Genant HK. Dedicated extremity MR imaging: an emerging technology. Magn Reson Imaging Clin N Am 1998; 6:849 –870
25.
Loew R, Kreitner KF, Runkel M, Zoellner J, Thelen M. MR arthrography of the shoulder: comparison of low field (0.2 T) vs high field (1.5 T) imaging. Eur Radiol 2000; 10:989 –996
26.
Verhoek G, Zanetti M, Duewell S, Zollinger H, Hodler J. MRI of the foot and ankle: diagnostic performance and patient acceptance of a dedicated low field MR scanner. J Magn Reson Imaging 1998; 8:711 –716
27.
Posin JP, Arakawa M, Crooks LE, et al. Hydrogen MR imaging of the head at 0.35 T and 0.7 T: effects of magnetic field strength. Radiology 1985; 157:679 –683
28.
Crooks LE, Arakawa M, Hoenninger J, McCarten B, Watts J, Kaufman L. Magnetic resonance imaging: effects of magnetic field strength. Radiology 1984; 151:127 –133
29.
Hoult DI, Chen CN, Sank VJ. The field dependence of NMR imaging. II. Arguments concerning an optimal field strength. Magn Reson Med 1986; 3:730 –746
30.
McQueen FM, Stewart N, Crabbe J, et al. Magnetic resonance imaging of the wrist in early rheumatoid arthritis reveals progression of erosions despite clinical improvement. Ann Rheum Dis 1999; 58:156 –163
31.
Ostergaard M, Gideon P, Sorensen K, et al. Scoring of synovial membrane hypertrophy and bone erosions by MR imaging in clinically active and inactive rheumatoid arthritis of the wrist. Scand J Rheumatol 1995; 24:212 –218
32.
Sugimoto H, Takeda A, Kano S. Assessment of disease activity in rheumatoid arthritis using magnetic resonance imaging: quantification of pannus volume in the hands. Br J Rheumatol 1998; 37:854 –861
33.
Backhaus M, Burmester GR, Sandrock D, et al. Prospective two year follow up study comparing novel and conventional imaging procedures in patients with arthritic finger joints. Ann Rheum Dis 2002; 61:895 –904
34.
Lee DM, Weinblatt ME. Rheumatoid arthritis. Lancet 2001; 358:903 –911
35.
Huang J, Stewart N, Crabbe J, et al. A 1-year follow-up study of dynamic magnetic resonance imaging in early rheumatoid arthritis reveals synovitis to be increased in shared epitope-positive patients and predictive of erosions at 1 year. Rheumatology (Oxford) 2000; 39:407 –416
36.
McQueen FM, Benton N, Crabbe J, et al. What is the fate of erosions in early rheumatoid arthritis? tracking individual lesions using x rays and magnetic resonance imaging over the first two years of disease. Ann Rheum Dis 2001; 60:859 –868
37.
Lee J, Lee SK, Suh JS, Yoon M, Song JH, Lee CH. Magnetic resonance imaging of the wrist in defining remission of rheumatoid arthritis. J Rheumatol 1997; 24:1303 –1308
38.
Conaghan P, Edmonds J, Emery P, et al. Magnetic resonance imaging in rheumatoid arthritis: summary of OMERACT activities, current status, and plans. J Rheumatol 2001; 28:1158 –1162
39.
Gasson J, Gandy SJ, Hutton CW, Jacoby RK, Summers IR, Vennart W. Magnetic resonance imaging of rheumatoid arthritis in metacarpophalangeal joints. Skeletal Radiol 2000; 29:324 –334

Information & Authors

Information

Published In

American Journal of Roentgenology
Pages: 937 - 943
PubMed: 15039167

History

Submitted: June 18, 2003
Accepted: October 6, 2003
First published: November 23, 2012

Authors

Affiliations

Bachir Taouli
Department of Radiology, University of California, San Francisco, 505 Parnassus Ave., Box 0628, San Francisco, CA 94143-0628.
Department of Radiology, NYU Medical Center, 560 First Ave., TCH-HW202, New York, NY 10016-6497.
Souhil Zaim
Department of Radiology, University of California, San Francisco, 505 Parnassus Ave., Box 0628, San Francisco, CA 94143-0628.
Charles G. Peterfy
Department of Radiology, University of California, San Francisco, 505 Parnassus Ave., Box 0628, San Francisco, CA 94143-0628.
John A. Lynch
Department of Radiology, University of California, San Francisco, 505 Parnassus Ave., Box 0628, San Francisco, CA 94143-0628.
Alexander Stork
Department of Radiology, University of California, San Francisco, 505 Parnassus Ave., Box 0628, San Francisco, CA 94143-0628.
Ali Guermazi
Department of Radiology, University of California, San Francisco, 505 Parnassus Ave., Box 0628, San Francisco, CA 94143-0628.
Bo Fan
Department of Radiology, University of California, San Francisco, 505 Parnassus Ave., Box 0628, San Francisco, CA 94143-0628.
Kenneth H. Fye
Division of Rheumatology, University of California, San Francisco, 400 Parnassus Ave., ACC 587, Box 0326, San Francisco, CA 94143-0326.
Harry K. Genant
Department of Radiology, University of California, San Francisco, 505 Parnassus Ave., Box 0628, San Francisco, CA 94143-0628.

Metrics & Citations

Metrics

Citations

Export Citations

To download the citation to this article, select your reference manager software.

Articles citing this article

View Options

View options

PDF

View PDF

PDF Download

Download PDF

Media

Figures

Other

Tables

Share

Share

Copy the content Link

Share on social media