Natural history of aortoarteritis (Takayasu's disease)

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Abstract

The natural history of aortoarteritis was studied in 88 patients (54 women and 34 men). The average age was 24.0 ± 8.8 years at onset of symptoms and 28.3 ± 9.9 years at diagnosis. The follow-up period was 83.6 ± 74.4 months from onset and 33.2 ± 37.0 months from diagnosis. Ten patients (11.4%) died during follow-up (0.016 deaths/patient year), and 22 patients (25%) suffered major nonfatal events (0.042 events/patient year). The cumulative survival at 5 and 10 years after the onset was 91.0 ± 3.3% and 84.0 ± 5.6% (mean ± SEM), respectively. The event-free survival rates at the same intervals after onset were 74.9 ± 5.0% and 64.0 ± 7.4%, respectively. The overall survival and event-free survival at 10 years after diagnosis was 80.3 ± 6.5% and 61.6 ± 7.5%, respectively. Patients with no complications or a mild single complication at diagnosis had a higher event-free survival rate than those with severe single complication or multiple complications at 5 years - 97.0 ± 2.9% and 59.7 ± 7.3%, respectively (p < 0.001). Severe hypertension (p < 0.01), severe functional disability (p < 0.01), and evidence of cardiac involvement (p < 0.05) were good predictors of either death or major event on follow-up. These data are useful in making an objective assessment of the prognosis and in planning elective interventions.

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Subramanyan, R., Joy, J., & Balakrishnan, K. G. (1989). Natural history of aortoarteritis (Takayasu’s disease). Circulation, 80(3), 429–437. https://doi.org/10.1161/01.CIR.80.3.429

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