Adult-onset Still's disease epidemiology and demographics: Difference between revisions
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===Incidence and prevalence=== | ===Incidence and prevalence=== | ||
* There is a dearth of data regarding the incidence and prevalence of adult-onset Still's disease (AOSD). | * There is a dearth of data regarding the incidence and prevalence of adult-onset Still's disease (AOSD). | ||
* | * The disease occurs worldwide and ausually affects young adults (age 16-35 years, with a mean of | ||
* In France, the annual incidence of ASD was estimated to be 0.16 per 100,000 individuals.<ref name="pmid7668903">{{cite journal |vauthors=Magadur-Joly G, Billaud E, Barrier JH, Pennec YL, Masson C, Renou P, Prost A |title=Epidemiology of adult Still's disease: estimate of the incidence by a retrospective study in west France |journal=Ann. Rheum. Dis. |volume=54 |issue=7 |pages=587–90 |date=July 1995 |pmid=7668903 |pmc=1009940 |doi= |url=}}</ref> | * In France, the annual incidence of ASD was estimated to be 0.16 per 100,000 individuals.<ref name="pmid7668903">{{cite journal |vauthors=Magadur-Joly G, Billaud E, Barrier JH, Pennec YL, Masson C, Renou P, Prost A |title=Epidemiology of adult Still's disease: estimate of the incidence by a retrospective study in west France |journal=Ann. Rheum. Dis. |volume=54 |issue=7 |pages=587–90 |date=July 1995 |pmid=7668903 |pmc=1009940 |doi= |url=}}</ref> | ||
* In Japan, the annual incidence of ASD was estimated to be 0.22 per 100,000 individuals.<ref name="pmid9465547">{{cite journal |vauthors=Wakai K, Ohta A, Tamakoshi A, Ohno Y, Kawamura T, Aoki R, Kojima M, Lin Y, Hashimoto S, Inaba Y, Minowa M, Aizawa S, Ichikawa Y, Miyasaka N |title=Estimated prevalence and incidence of adult Still's disease: findings by a nationwide epidemiological survey in Japan |journal=J Epidemiol |volume=7 |issue=4 |pages=221–5 |date=December 1997 |pmid=9465547 |doi= |url=}}</ref> | |||
===Age=== | ===Age=== | ||
Revision as of 16:28, 20 April 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Epidemiology and Demographics
Incidence and prevalence
- There is a dearth of data regarding the incidence and prevalence of adult-onset Still's disease (AOSD).
- The disease occurs worldwide and ausually affects young adults (age 16-35 years, with a mean of
- In France, the annual incidence of ASD was estimated to be 0.16 per 100,000 individuals.[1]
- In Japan, the annual incidence of ASD was estimated to be 0.22 per 100,000 individuals.[2]
Age
- Aging adults affected by adult-onset Still's disease (AOSD) have a higher rate of development of complications related to AOSD and a higher mortality rate compared to younger individuals.[3]
Gender
- Adult-onset Still's disease (AOSD) affects females more than females.[4]
Race
- Adult-onset Still's disease (AOSD) affects Caucasians more than other races.[5]
Geographic distribution
References
- ↑ Magadur-Joly G, Billaud E, Barrier JH, Pennec YL, Masson C, Renou P, Prost A (July 1995). "Epidemiology of adult Still's disease: estimate of the incidence by a retrospective study in west France". Ann. Rheum. Dis. 54 (7): 587–90. PMC 1009940. PMID 7668903.
- ↑ Wakai K, Ohta A, Tamakoshi A, Ohno Y, Kawamura T, Aoki R, Kojima M, Lin Y, Hashimoto S, Inaba Y, Minowa M, Aizawa S, Ichikawa Y, Miyasaka N (December 1997). "Estimated prevalence and incidence of adult Still's disease: findings by a nationwide epidemiological survey in Japan". J Epidemiol. 7 (4): 221–5. PMID 9465547.
- ↑ "Epidemiology of Hospitalized Adult Onset Still's Disease in United States - ACR Meeting Abstracts".
- ↑ "Epidemiology of Hospitalized Adult Onset Still's Disease in United States - ACR Meeting Abstracts".
- ↑ "Epidemiology of Hospitalized Adult Onset Still's Disease in United States - ACR Meeting Abstracts".