Open AccessBrain involvement in rheumatoid arthritis: A magnetic resonance spectroscopy study
Author(s) -
Emmer Bart J.,
van der Bijl A. Egon,
Huizinga Tom W. J.,
Breedveld Ferdinand C.,
Steens Stefan C. A.,
Th. Bosma Gerlof P.,
van Buchem Mark A.,
van der Grond Jeroen
Publication year - 2009
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.24932
Subject(s) - rheumatoid arthritis , medicine , choline , creatine , erythrocyte sedimentation rate , inflammation , magnetic resonance imaging , gastroenterology , endocrinology , radiology
Objective Tumor necrosis factor α was recently implicated as an important mediator of communication between the peripheral and cerebral immune systems in an animal model of chronic inflammation. The purpose of this study was to examine by proton magnetic resonance spectroscopy ( 1 H‐MRS) the influence of inflammation on cerebral metabolism in patients with rheumatoid arthritis (RA). Methods Single‐voxel 1 H‐MRS of the centrum semiovale was performed on 35 RA patients (6 men and 29 women; mean ± SD age 51.8 ± 14.6 years) and 28 healthy age‐ and sex‐matched control subjects (9 men and 19 women; mean ± SD age 50.2 ± 10.4 years). None of the study subjects had any neurologic signs or symptoms. Clinical markers of disease activity were correlated with the 1 H‐MRS findings. Results Patients with active RA, as reflected by an elevated erythrocyte sedimentation rate (ESR), had a significantly higher ratio of choline to creatine and a significantly lower ratio of N ‐acetylaspartate to choline than did patients with inactive RA, as reflected by a normal ESR. Moreover, the ratios of choline to creatine and NAA to choline were significantly correlated with the ESR after correction for age, sex, smoking status, handedness, alcohol consumption, medication use, and disease duration. Medication use had no additional effect on these associations. Conclusion Our data show that systemic inflammation in RA is associated with metabolic changes in the brain.