Systemic lupus erythematosus (SLE) is an autoimmune disease and multisystem. About 15-20% of SLE patients develop the disease in childhood and adolescence. The involvement of the central nervous system (CNS) is frequent. However, often it is observed a dissociation between clinical and neuroimaging findings. Some biomarkers associated with neuronal injury have been associated with neuropsychiatric SLE, but their roles in the pathogenesis and its validity and clinical applicability has not been studied in patients cSLE. Objective: To determine the prevalence of neuropsychiatric (NP) manifestations in SLE analyze the prevalence of structural changes and white matter lesions on magnetic resonance imaging (MRI), in addition to determining whether S100B and NF-H may be associated with structural changes and white matter lesion in JSLE patients and controls. Methods: Clinical, laboratory and medication use were assessed. Disease activity was assessed by SLEDAI (SLE Disease Activity Index) and the cumulative damage was analyzed by SDI (Lupus International Collaborating Clinics / American College of Rheumatology Damage Index). Mood disorders were determined through the Depression inventory (BDI) and anxiety (BAI) and Beck's cognitive disturbances were assessed by the Wechsler intelligence test according to age. The NP manifestations were analyzed by reviewing medical records. Neuropsychiatric symptoms were considered present early in the illness when they occurred in the first six months of disease and evolution, as occurred after this period. Patients and controls underwent MRI. The dosage of the markers was performed by ELISA (Enzyme Linked Immuno Sorbent Assay. Results: 71 patients were included in the retrospective study and 51 patients were included in cross-sectional study.