Altered white matter microstructure in lupus patients: a diffusion tensor imaging study

The purpose of this study was to investigate whether white matter microstructure is altered in patients suffering from systemic lupus erythematosus (SLE), and if so, whether such alterations differed between patients with and without neuropsychiatric symptoms. Structural MRI and diffusion tensor ima...

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Veröffentlicht in:Arthritis research & therapy 2018-02, Vol.20 (1), p.21-21, Article 21
Hauptverfasser: Nystedt, Jessika, Nilsson, Markus, Jönsen, Andreas, Nilsson, Petra, Bengtsson, Anders, Lilja, Åsa, Lätt, Jimmy, Mannfolk, Peter, Sundgren, Pia C
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Sprache:eng
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Zusammenfassung:The purpose of this study was to investigate whether white matter microstructure is altered in patients suffering from systemic lupus erythematosus (SLE), and if so, whether such alterations differed between patients with and without neuropsychiatric symptoms. Structural MRI and diffusion tensor imaging (DTI) were performed in 64 female SLE patients (mean age 36.9 years, range 18.2-52.2 years) and 21 healthy controls (mean age 36.7 years, range 23.3-51.2 years) in conjunction with clinical examination, laboratory tests, cognitive evaluation, and self-assessment questionnaires. The patients were subgrouped according to the American College of Rheumatology Neuropsychiatric Systemic Lupus Erythematosus case definitions into non-neuropsychiatric SLE (nonNPSLE) and neuropsychiatric SLE (NPSLE). Comparisons between the SLE group and healthy controls showed that the mean fractional anisotropy (FA) was significantly reduced in the right rostral cingulum (p = 0.038), the mid-sagittal corpus callosum (CC) (p = 0.050), and the forceps minor of the CC (p = 0.015). The mean diffusivity (MD) was significantly increased in the left hippocampal cingulum (p = 0.017). No significant differences in MD or FA values were identified between NPSLE and nonNPSLE patients. Disease duration among all SLE patients correlated significantly with reduced FA in the CC (p 
ISSN:1478-6362
1478-6354
1478-6362
DOI:10.1186/s13075-018-1516-0