Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Jun 18;16(6):e0250025.
doi: 10.1371/journal.pone.0250025. eCollection 2021.

Takayasu arteritis: Prevalence and clinical presentation in Switzerland

Affiliations

Takayasu arteritis: Prevalence and clinical presentation in Switzerland

Andrea D Gloor et al. PLoS One. .

Abstract

Objective: Takayasu arteritis (TAK) is a rare immune-mediated vasculitis of the aorta and its branches. Aims were to calculate prevalence and incidence in Switzerland, to assess disease activity and performance of MR-Angiography (MRA).

Methods: 31 patients were recorded in a database, 27 were followed prospectively up to 3 years. Prevalence was calculated based on data of the national statistical bureau. Disease activity was defined using the revised EULAR criteria. MRA depicted stenotic changes and aortic wall enhancement.

Results: A disease prevalence of 14.5/1.000.000 inhabitants and an incidence of 0.3/1.000.000 per year was calculated. Aortic wall enhancement was found in 10 patients while in clinical and serological remission. EULAR criteria missed 5 patients with disease activity with isolated elevations of ESR/CRP. Arterial stenosis did not change over time in 5 cases, it improved in 2 and increased in 7. At follow-up 16 patients were treated with tocilizumab, 11/16 in monotherapy, 5 patients were treatment-free, 25/27 stayed in remission.

Conclusion: In addition to prevalence and incidence, our data show that MRA qualifies to detect subclinical disease activity, but, on the other hand, that EULAR criteria may miss disease activity in case of isolated elevation of ESR/CRP.

PubMed Disclaimer

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. TAK patients in Switzerland.
Displayed are Swiss cantons and their populations per km2. The number of patients (in black) are displayed per canton.
Fig 2
Fig 2. Disease activity and medication.
Disease activity (A) and medication of each patient over time (years) (B). 27/31 patients were followed prospectively up to 3 years. DMARDs: Disease-modifying antirheumatic drugs.
Fig 3
Fig 3. Vessel involvement.
Pattern of vessel involvement of 31 TAK patients as determined by imaging and/or clinical findings.

Similar articles

Cited by

References

    1. Kerr GS, Hallahan CW, Giordano J, Leavitt RY, Fauci AS, Rottem M, et al.. Takayasu arteritis. Ann Intern Med. 1994;120(11):919–29. doi: 10.7326/0003-4819-120-11-199406010-00004 - DOI - PubMed
    1. Saritas F, Donmez S, Direskeneli H, Pamuk ON. The epidemiology of Takayasu arteritis: a hospital-based study from northwestern part of Turkey. Rheumatol Int. 2016;36(7):911–6. doi: 10.1007/s00296-016-3445-z - DOI - PubMed
    1. Watts R, Al-Taiar A, Mooney J, Scott D, Macgregor A. The epidemiology of Takayasu arteritis in the UK. Rheumatology (Oxford). 2009;48(8):1008–11. doi: 10.1093/rheumatology/kep153 - DOI - PubMed
    1. Koide K. Takayasu arteritis in Japan. Heart Vessels Suppl. 1992;7:48–54. doi: 10.1007/BF01744544 - DOI - PubMed
    1. Toshihiko N. Current status of large and small vessel vasculitis in Japan. Int J Cardiol. 1996;54 Suppl:S91–8. doi: 10.1016/s0167-5273(96)88777-8 - DOI - PubMed

Publication types

MeSH terms