News

A deficiency in leptin — the hormone that signals the brain when a person has eaten enough — may lead to the development of ANCA-associated vasculitis (AAV), according to a new case study from India. The report, “ANCA-associated Vasculitis in a Case of Congenital Leptin Deficiency,” was published…

Excessive activation of a defense mechanism of neutrophils — key immune cells in ANCA-associated vasculitis (AAV) — is a potential biomarker for active disease, according to researchers. Their study, “Excessive neutrophil extracellular trap formation in ANCA-associated vasculitis is independent of ANCA,” was published in the journal Kidney…

Patients with granulomatosis with polyangiitis whose autoantibodies are against the myeloperoxidase protein (MPO) have increased disease activity at diagnosis but milder kidney manifestations than other vasculitis patients. Based on findings from a retrospective analysis, a research team in China proposes that these patients should be considered a unique subtype of…

Tracheobronchial stenosis, a lung complication characterized by the narrowing of the trachea and bronchi, is common in patients with granulomatosis with polyangiitis (GPA) and is often the first disease symptom, researchers have found. However, despite its frequent occurrence, there are no standardized treatment protocols for this serious complication. More prospective…

Granulomatosis with polyangiitis (GPA) patients often experience eye involvement, suggesting an ophthalmologist is necessary for proper disease management and better outcomes, according to Egyptian researchers. Their study, “Relationship of ocular presentation in granulomatosis with polyangiitis to autoantibodies and disease activity,” was published in the journal Zeitschrift für…

Treatment with immunosuppressants does not improve kidney function, but is associated with reduced risk of vasculitis relapse in a rare subset of patients with ANCA vasculitis (AAV), a new study reports. The research, “Patient Outcomes in Renal-Limited Antineutrophil Cytoplasmic Antibody Vasculitis With Inactive Histology,” was published…