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      Brain Magnetic Resonance Imaging in Newly Diagnosed Systemic Lupus Erythematosus

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          Abstract

          Objective

          We wished to determine the prevalence of cerebral atrophy and focal lesions in a cohort of patients with newly diagnosed systemic lupus erythematosus (SLE) and the association of these brain abnormalities with clinical characteristics.

          Methods

          A total of 97 patients with SLE, within 9 months of diagnosis, with 4 or more American College of Rheumatology classification criteria, were enrolled. Brain magnetic resonance imaging was performed.

          Results

          The patients were 97% female, mean age 38.1 (SD 12.2) years, education 15.1 (2.8) years; 59 Caucasian, 11 African American, 19 Hispanic, 5 Asian, and 3 other ethnicity. Cerebral atrophy was prevalent in 18% (95% CI 11%–27%): mild in 12%, moderate in 5%. Focal lesions were prevalent in 8% (95% CI 4%–16%): mild in 2%, moderate in 5%, severe in 1%. Patients with cerebral atrophy were more likely to have anxiety disorder (p = 0.04). Patients with focal lesions were more likely to be African American (p = 0.045) and had higher Safety of Estrogens in Lupus Erythematosus National Assessment SLEDAI scores (p = 0.02) and anti-dsDNA (p = 0.05).

          Conclusion

          In this population with newly diagnosed SLE, brain abnormalities were prevalent in 25% of patients. These findings suggest that the brain may be affected extremely early in the course of SLE, even before the clinical diagnosis of SLE is made. Followup of these patients is planned, to determine the reversibility or progression of these abnormalities and their association with and potential predictive value for subsequent neuropsychiatric SLE manifestations.

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          Author and article information

          Journal
          7501984
          5243
          J Rheumatol
          J. Rheumatol.
          The Journal of rheumatology
          0315-162X
          18 January 2017
          15 September 2008
          December 2008
          30 January 2017
          : 35
          : 12
          : 2348-2354
          Affiliations
          Johns Hopkins University, Baltimore, Maryland; Cedars-Sinai Medical Center/David Geffen School of Medicine at UCLA, Los Angeles, California; South Texas Veterans Health Care System, San Antonio, Texas; and University of Texas Health Science Center at San Antonio, San Antonio, Texas, USA
          Author notes
          Address reprint requests to Dr. M. Petri, Johns Hopkins University, 1830 East Monument Street, Suite 7500, Baltimore, MD 21205. mpetri@ 123456jhmi.edu

          M. Petri, MD, MPH, Professor; M. Naqibuddin, MBBS, MPH, Johns Hopkins University; K.A. Carson, ScM, Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; D.J. Wallace, MD; M.H. Weisman, MD, Cedars-Sinai Medical Center/David Geffen School of Medicine at UCLA; S.L. Holliday, PhD, ABPP, Chief, Psychology Service, South Texas Veterans Health Care System, San Antonio, TX; M. Sampedro, Johns Hopkins University; S. Narayana, PhD, Research Imaging Center and Department of Radiology, UT Health Science Center, San Antonio, TX; P.T. Fox, MD, Research Imaging Center, UT Health Science Center, South Texas Veterans Health Care System; C. Franklin, BS, Research Imaging Center, UT Health Science Center; P. Padilla, BS; R.L. Brey, MD, Department of Neurology, UT Health Science Center.

          Article
          PMC5278777 PMC5278777 5278777 nihpa843255
          10.3899/jrheum.071010
          5278777
          18793003
          ee39d9b5-0746-4cd1-a4a7-694d1cfddcb1
          History
          Categories
          Article

          MAGNETIC RESONANCE IMAGING,SYSTEMIC LUPUS ERYTHEMATOSUS,CEREBRAL ATROPHY

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