Background:Conventional magnetic resonance imaging (MRI) is the preferred neuroimaging method in the evaluation ofneuropsychiatric systemic lupus erythematosus (NPSLE).The purpose of this study was to investigate the association between clinical and immunological features with MRI abnormalities in female patients with NPSLE,to screen for the value of conventional MRI in NPSLE.Methods:A total of 59 female NPSLE patients with conventional MRI examinations were enrolled in this retrospective study.All patients were classified into different groups according to MRI abnormalities.Both clinical and immunological features were compared between MRI abnormal and normal groups.One-way analysis of variance was used to compare the systemic lupus erythematosus disease activity index (SLEDAI) score for MRI abnormalities.Multivariate logistic regression analysis investigated the correlation between immunological features,neuropsychiatric manifestations,and MRI abnormalities.Results:Thirty-six NPSLE patients (61％) showed a variety of MRI abnormalities.There were statistically significant differences in SLEDAI scores (P ＜ 0.001),incidence of neurologic disorders (P =0.001),levels of 24-h proteinuria (P =0.001) and immunoglobulin M (P =0.004),and incidence of acute confusional state (P =0.002),cerebrovascular disease (P =0.004),and seizure disorder (P =0.028) between MRI abnormal and normal groups.In the MRI abnormal group,SLEDAI scores for cerebral atrophy (CA),cortex involvement,and restricted diffusion (RD) were much higher than in the MRI normal group (P ＜ 0.001,P =0.002,P =0.038,respectively).Statistically significant positive correlations between seizure disorder and cortex involvement (odds ratio [OR] =14.90;95％ confidence interval [CI],1.50-151.70;P =0.023) and cerebrovascular disease and infratentorial involvement (OR =10.00;95％ CI,1.70-60.00;P =0.012) were found.Conclusions:MRI abnormalities in NPSLE,especially CA,cortex involvement,and RD might be markers of high systemic lupus erythematosus activity.Some MRI abnormalities might correspond to neuropsychiatric manifestations and might be helpful in understanding the pathophysiology of NPSLE.