MRI Bone Oedema is the Strongest Predictor of Subsequent Radiographic Progression in Early RA. Results from a 2 Year Randomized Controlled Trial (CIMESTRA)

Title:

MRI Bone Oedema is the Strongest Predictor of Subsequent Radiographic Progression in Early RA. Results from a 2 Year Randomized Controlled Trial (CIMESTRA)

Category:

17. RA: clinical aspects

Author(s):

Merete Lund Hetland, Bo Ejbjerg, Mikkel Østergaard, Søren Jacobsen, Aage Vestergaard, Anne Grethe Jurik, Kristian Stengaard-Pedersen, Peter Junker, Tine Lottenburger, Ib Hansen, Lis Smedegaard Andersen, Ulrik Tarp, Henrik Skjødt, Jens Kristian Pedersen, Ole Majgaard, Anders J. Svendsen, Torkell Ellingsen, Gert Hansen, Hanne Lindegaard, Jørgen Vallø, Trine Torfing, Henrik S. Thomsen, Kim Hørslev-Petersen. University Hospitals, Copenhagen, South-Denmark and Århus, Denmark

PURPOSE
To identify predictors of radiographic progression in a 2-year randomized, clinical study (RCT) of patients with early (<6 months' duration), active rheumatoid arthritis (RA).
METHODS
In 89 patients, participating in a double-blind, placebo-controlled RCT (the CIMESTRA study (1)), baseline clinical/biochemical disease activity measures (incl. DAS28), magnetic resonance imaging (MRI) of the non-dominant wrist and metacarpophalangeal (MCP)-joints (scored according to the OMERACT RAMRIS), conventional x-rays of hands, wrists and forefeet (Sharp/van der Heijde method), serum anti-cyclic citrullinated peptide antibodies (anti-CCP), and serum IgM RFwere available. Patients were treated aggressively with methotrexate, intra-articular betamethasone and cyclosporine/placebo-cyclosporine, aiming at clinical remission.
A multiple regression analysis with stepwise backward selection was performed with delta Total Sharp/vdHeijde Score (TSS) from 0 to 2 years as the dependent variable. Possible predictive baseline variables were tested: DAS28, TSS, MRI bone oedema score, MRI synovitis score, MRI erosion score, anti-CCP, IgM RF, age, gender, treatment arm, and cumulated betamethasone dose from 0-3 months.
RESULTS
At baseline, the median DAS28 was 5.6 (range 2.4-8.0), 65% were IgM RF positive, 61% were anti-CCP positive, and 56% had radiographic erosions. At 2 years, DAS28 was 2.0 (0.5-5.7), 56% were in DAS-remission, and 26% had progressed radiographically.
The only independent predictor of delta TSS was the MRI bone oedema score (p<0.00001), while the other variables did not reach statistical significance (table). Bone oedema explained 41% of the variation in the progression of radiographic score (Pearson's r=0.64).

Multiple regression analysis before and after stepwise backward selection

All explanatory variables in model

Coefficient

Confidence interval

P value

DAS28

-0.60

-1.48-0.28

0.19

TSS

0.026

-0.15-0.21

0.78

MRI bone oedema score

0.63

0.37-0.89

<0.00001

MRI synovitis score

0.17

-0.10-0.45

0.22

MRI erosion score

0.30

-0.28-0.87

0.32

Anti-CCP

1.93

-1.12-4.99

0.22

IgM RF

-0.38

-3.60-2.85

0,82

Age

0.02

-0.83-0.86

0.69

Gender

-0.75

-3.15-1.65

0.54

Treatment arm

-0.84

-2.80-1.12

0.40

Cumulated steroid

<0.01

-0.37-0.39

0.96

Only significant variables in model

 

 

 

MRI bone odema score

0.75

0.56-0.97

<0.00001


CONCLUSIONS
In early RA patients treated aggressively in a RCT with DMARDs and intraarticular corticosteroids aiming at remission, the OMERACT MRI bone oedema score of MCP and wrist joints at baseline was a strong independent predictor of radiographic progression in hands, wrists or feet during the subsequent 2 years. MRI synovitis score, MRI erosion score, DAS28, anti-CCP and IgM RF were not independent risk factors for radiographic progression.

Disclosures:

M.L. Hetland, None; B. Ejbjerg, None; M. Østergaard, None; S. Jacobsen, None; A. Vestergaard, None; A. Jurik, None; K. Stengaard-Pedersen, None; P. Junker, None; T. Lottenburger, None; I. Hansen, None; L.S. Andersen, None; U. Tarp, None; H. Skjødt, None; J.K. Pedersen, None; O. Majgaard, None; A.J. Svendsen, None; T. Ellingsen, None; G. Hansen, None; H. Lindegaard, None; J. Vallø, None; T. Torfing, None; H.S. Thomsen, None; K. Hørslev-Petersen, None.