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- W2969002020 abstract "Propose of review Neuropsychiatric systemic lupus erythematosus (NPSLE) is an emerging frontier in lupus care encompassing a wide spectrum of clinical manifestations. Its pathogenesis remains poorly understood because of the complexity of pathophysiologic mechanisms involved and limited access to tissue. We highlight recent advances in the pathophysiology of neuropsychiatric lupus. Recent findings Disruption of blood–brain barrier (BBB) facilitating entrance of neurotoxic antibodies into the central nervous system (CNS), neuroinflammation and cerebral ischemia are the key mechanisms. Disruption of the BBB may occur not only at the traditional BBB, but also at the blood–cerebrospinal fluid barrier. Certain autoantibodies, such as anti-N-methyl-d-aspartate receptors, antiribosomal P and antiphospholipid antibodies may cause injury in subsets of patients with diffuse neuropsychiatric disease. Activation of microglia via autoantibodies, interferon-a or other immune reactants, may amplify the inflammatory response and promote neuronal damage. New inflammatory pathways, such as TWEAK/Fn14, Bruton's tyrosine kinase, Nogo-a and ACE may represent additional potential targets of therapy. Novel neuroimaging techniques suggest alterations in brain perfusion and metabolism, increased concentration of neurometabolites, indicative of glial activation, vasculopathy and neuronal impairment. Summary NPSLE encompasses a diverse phenotype with distinct pathogenic mechanisms, which could be targeted by novel therapies or repositioning of existing drugs." @default.
- W2969002020 created "2019-08-22" @default.
- W2969002020 creator A5025805658 @default.
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- W2969002020 date "2019-11-01" @default.
- W2969002020 modified "2023-10-18" @default.
- W2969002020 title "Update on the pathogenesis of central nervous system lupus" @default.
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- W2969002020 doi "https://doi.org/10.1097/bor.0000000000000655" @default.
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