Guest guest Posted January 16, 2008 Report Share Posted January 16, 2008 Rheumatology Advance Access originally published online on November 24, 2007 Functional MRI in NPSLE patients reveals increased parietal and frontal brain activation during a working memory task compared with controls B. M. Fitzgibbon1, S. L. Fairhall1, I. J. Kirk1, M. Kalev-Zylinska2, K. Pui4, N. Dalbeth2, S. Keelan2, E. 3, M. During2 and F. M. McQueen2 Departments of 1Psychology, 2Molecular Medicine and Pathology, 3Biostatistics, University of Auckland and 4Rheumatology, Auckland District Health Board, Auckland, New Zealand. Abstract Objectives. Anatomical MRI brain scans may not reflect neurological dysfunction in patients with NPSLE. We used blood-oxygen-level-dependent functional MRI (BOLD-fMRI) to investigate working memory function in NPSLE patients. Methods. Twenty-seven females took part: nine NPSLE patients (mean age 40 yrs; SLEDAI 10.9); nine RA patients and nine healthy controls. Subjects were tested using the n-back paradigm for working memory, where patients indicate when a stimulus matches one presented n trials previously. Functional scans used 3 mm slices x 30, repetition time 2570 ms, echo time 50 ms. Echo planar images were superimposed onto T1w anatomical images (Siemens 1.5 T). Data analysis used Brain Voyager QX Version 1.7. Results. During the memory task, there was activation in areas serving working memory, executive function and attention in all groups. Nine regions of interest were selected for activation during working memory (N-back task vs fixation, P 0.005). In six out of nine regions, there was greater activation in the NPSLE group. This reached significance in three regions: the posterior inferior parietal lobules of both hemispheres [brodmann area (BA) 7] separately and combined (P = 0.014, 0.016 and 0.004, respectively), and the supplementary motor area (mid-line frontal lobe)(BA32/6; P = 0.032). Conclusions. NPSLE patients showed greater frontoparietal activation than the other groups during the memory task, suggesting a greater need to recruit extra cortical pathways, possibly to supplement impaired function of standard pathways. http://rheumatology.oxfordjournals.org/cgi/content/abstract/47/1/50 Not an MD Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.