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February 28, 2026Kompass Autoimmun0 citations

Takayasu-Arteriitis: Gerade bei jungen Patientinnen aufmerksam für Gefäßveränderungen sein

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SASabine Adler

Key Points

  • The research aims to evaluate the damage and clinical characteristics associated with Takayasu's arteritis.
  • Conducted a multicentre, prospective, observational study
  • Enrolled patients with Takayasu's arteritis
  • Used the Vasculitis Damage Index and the Large-Vessel Vasculitis Index of Damage for assessment every 6 months
  • 89% of patients showed damage according to VDI
  • New damage occurred in 42% of patients during follow-up
  • History of relapse linked to new damage, with older age correlating to new damage in recent diagnoses

Abstract

Objectives: To evaluate damage and clinical characteristics associated with damage in Takayasu’s arteritis (TAK). Methods: Patients with TAK enrolled in a multicentre, prospective, observational study underwent standardized damage assessment every 6 months using the Vasculitis Damage Index (VDI) and the Large-Vessel Vasculitis Index of Damage (LVVID). Results: The study included 236 patients with TAK: 92% female, 81% Caucasian; median (25th, 75th percentile) disease duration = 2.6 (0.12, 6.9) years. Eighty-four percent had follow-up: median (25th, 75th) duration 4.1 (1.9, 7.5) years. Items of damage were present in 89% on VDI, 87% on LVVID, in the peripheral vascular (76% VDI, 74% LVVID) and cardiac (40% VDI, 45% LVVID) systems. During follow-up, 42% patients had new damage, including major vessel stenosis/arterial occlusion (8%), limb claudication (6%), hypertension (7%), aortic aneurysm (4%) and bypass surgery (4%). Disease-specific damage accounted for >90% of new items. Older age, relapse and longer duration of follow-up were associated with new damage items; a higher proportion of patients without new damage were on MTX (P <0.05). Among 48 patients diagnosed with TAK within 180 days of enrolment, new damage occurred in 31% on VDI and 52% on LVVID. History of relapse was associated with new damage in the entire cohort while in patients with a recent diagnosis, older age at diagnosis was associated with new damage.

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Cite This Study

Sabine Adler (2026) studied this question.

synapsesocial.com/papers/69a286370a974eb0d3c010dehttps://doi.org/10.1159/000550363
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