Takayasu's arteritis epidemiology and demographics: Difference between revisions
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* The prevalence of Takayasu arteritis is estimated to be ranges from 4.7 to 33 per million among European people.<ref name="pmid28756072" /> | * The prevalence of Takayasu arteritis is estimated to be ranges from 4.7 to 33 per million among European people.<ref name="pmid28756072" /> | ||
=== | ===Mortality rate=== | ||
===Age=== | ===Age=== | ||
* Most patients with Takayasu arteritis are aged 4-63 years, with the mean age of onset being approximately 30 years. | |||
* Fewer than 15% of cases present in individuals older than 40 years. | |||
===Race=== | ===Race=== | ||
Revision as of 14:05, 22 March 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Farnaz Khalighinejad, MD [2]
Overview
Epidemiology and Demographics
Incidence
- The incidence of Takayasu arteritis is approximately 0.26 per 100,000 individuals worldwide.[1]
- The incidence rates of Takayasu arteritis is approximately 0.15 per 100,000 individuals among European people.[2]
Prevalence
- The prevalence of Takayasu arteritis is estimated to be 2.6-6.4 persons per million population.[3]
- The prevalence of Takayasu arteritis is estimated to be ranges from 4.7 to 33 per million among European people.[2]
Mortality rate
Age
- Most patients with Takayasu arteritis are aged 4-63 years, with the mean age of onset being approximately 30 years.
- Fewer than 15% of cases present in individuals older than 40 years.
Race
- Takayasu arteritis is observed more frequently in patients of Asian or Indian descent. [4]
- Japanese patients with Takayasu arteritis have a higher incidence of aortic arch involvement
- In contrast, series from India report higher incidences of abdominal involvement
Gender
- Female are more commonly affected by Takayasu arteritis than male.[4]
- Females are about 8–9 times more likely to be affected by Takayasu's arteritis than males.
Region
- Takayasu arteritis is rare disease.[5]
- The majority of Takayasu arteritis cases are reported in Japan, South East Asia, India, and Mexico.[6]
References
- ↑ Hall S, Barr W, Lie JT, Stanson AW, Kazmier FJ, Hunder GG (March 1985). "Takayasu arteritis. A study of 32 North American patients". Medicine (Baltimore). 64 (2): 89–99. PMID 2858047.
- ↑ 2.0 2.1 Onen F, Akkoc N (2017). "Epidemiology of Takayasu arteritis". Presse Med. 46 (7-8 Pt 2): e197–e203. doi:10.1016/j.lpm.2017.05.034. PMID 28756072.
- ↑ Hall S, Barr W, Lie JT, Stanson AW, Kazmier FJ, Hunder GG (March 1985). "Takayasu arteritis. A study of 32 North American patients". Medicine (Baltimore). 64 (2): 89–99. PMID 2858047.
- ↑ 4.0 4.1 Numano F, Kobayashi Y (March 1999). "Takayasu arteritis--beyond pulselessness". Intern. Med. 38 (3): 226–32. PMID 10337931.
- ↑ Johnston SL, Lock RJ, Gompels MM (July 2002). "Takayasu arteritis: a review". J. Clin. Pathol. 55 (7): 481–6. PMC 1769710. PMID 12101189.
- ↑ Numano F, Okawara M, Inomata H, Kobayashi Y (September 2000). "Takayasu's arteritis". Lancet. 356 (9234): 1023–5. doi:10.1016/S0140-6736(00)02701-X. PMID 11041416.