Abstract

The pathogenetic role of anticardiolipin antibodies (aCLs) in patients with neuropsychiatric systemic lupus erythematosus (NPSLE) without cerebral infarcts remains elusive. Magnetization transfer imaging (MTI) has proved to be a sensitive tool for detecting diffuse microscopic brain damage in NPSLE patients. In this study we examined the correlation between grey and white matter magnetization transfer ratio (MTR) parameters and the presence of IgM and IgG aCLs and lupus anticoagulant in 18 patients with systemic lupus erythematosus and a history of NPSLE but without cerebral infarcts on conventional magnetic resonance imaging. Lower grey matter mean MTR (P < 0.05), white matter mean MTR (P < 0.05), white matter peak location (P < 0.05) and grey matter peak location (trend toward statistical significance) were observed in IgM aCL-positive patients than in IgM aCL-negative patients. No significant differences were found in MTR histogram parameters with respect to IgG aCL and lupus anticoagulant status, nor with respect to anti-dsDNA or anti-ENA (extractable nuclear antigen) status. This is the first report of an association between the presence of aCLs and cerebral damage in grey and white matter in NPSLE. Our findings suggest that aCLs are associated with diffuse brain involvement in NPSLE patients.

Highlights

  • Central nervous system (CNS) involvement causes neuropsychiatric manifestations in up to 75% of patients with systemic lupus erythematosus (SLE) [1]

  • Our findings suggest that aCLs are associated with diffuse brain involvement in neuropsychiatric systemic lupus erythematosus (NPSLE) patients

  • Using magnetization transfer imaging (MTI) – a quantitative magnetic resonance imaging (MRI) technique that is sensitive to macroscopic and microscopic brain tissue changes [5] – global brain involvement has been detected in patients with neuropsychiatric systemic lupus erythematosus (NPSLE) without explanatory abnormalities on conventional MRI [6,7,8]

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Summary

Introduction

Central nervous system (CNS) involvement causes neuropsychiatric manifestations in up to 75% of patients with systemic lupus erythematosus (SLE) [1]. Using magnetization transfer imaging (MTI) – a quantitative MRI technique that is sensitive to macroscopic and microscopic brain tissue changes [5] – global brain involvement has been detected in patients with neuropsychiatric systemic lupus erythematosus (NPSLE) without explanatory abnormalities on conventional MRI [6,7,8]. ACL = anticardiolipin antibody; ACR = American College of Rheumatology; CNS = central nervous system; ELISA = enzyme-linked immunosorbent assay; ENA = extractable nuclear antigen; Lac = lupus anticoagulant; MRI = magnetic resonance imaging; MTI = magnetization transfer imaging; MTR = magnetization transfer ratio; NPSLE = neuropsychiatric systemic lupus erythematosus; SLE = systemic lupus erythematosus;

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