Objective. To compare the efficacy of combination therapy with disease-modi
fying antirheumatic drugs (DMARDs) versus single therapy with DMARDs in the
prevention of early cervical spine changes in patients with rheumatoid art
hritis (RA).
Methods. One hundred ninety-five patients with recent-onset RA (mean diseas
e duration 8 months) were randomly assigned to receive a combination of DMA
RDs (sulfasalazine, methotrexate, hydroxychloroquine, and prednisolone) or
a single DMARD with or without prednisolone, After 2 years of followup, cer
vical spine radiographs were taken of 176 of these patients (85 in the comb
ination-therapy group and 91 in the single-therapy group). These radiograph
s were evaluated, and the findings were correlated with the therapy strateg
ies as well as with peripheral joint destruction and clinical and laborator
y variables describing the disease activity.
Results. Anterior atlantoaxial subluxation (aAAS), atlantoaxial impaction (
AAI; i.e., vertical subluxation), and subaxial subluxation (SAS) were found
in only 6 (3.4%), 2 (1.1%), and 5 (2.8%) of the patients, respectively. In
terestingly, none of the patients in the combination-therapy group had aAAS
or AAI, The incidences of aAAS and AAI in the single-therapy group were 6.
6% and 2.2%, respectively. SAS was present in 2 patients (2.2%) in the sing
le-therapy group and in 3 patients (3.5%) in the combination-therapy group.
The difference in the incidence of aAAS between the treatment groups was s
tatistically significant (P = 0.029). None of the patients with cervical sp
ine changes achieved remission of RE during the study.
Conclusion. In the present study, the incidence of cervical spine subluxati
ons in patients treated with single-drug therapy was in accord with finding
s of previous studies. However, none of the patients in the combination-the
rapy group had aAAS or AAI, These findings suggest that early, aggressive c
ombination-DMARD therapy with sulfasalazine, methotrexate, hydroxychloroqui
ne, and prednisolone can prevent or retard the development of rheumatoid at
lantoaxial disorders.