Behçet's disease epidemiology and demographics: Difference between revisions
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===Age=== | ===Age=== | ||
*Behçet disease commonly affects young adults 20 to 40 years of age<ref name="pmid105280403">{{cite journal |vauthors=Sakane T, Takeno M, Suzuki N, Inaba G |title=Behçet's disease |journal=N. Engl. J. Med. |volume=341 |issue=17 |pages=1284–91 |date=October 1999 |pmid=10528040 |doi=10.1056/NEJM199910213411707 |url=}}</ref> | *Behçet disease commonly affects young adults 20 to 40 years of age.<ref name="pmid105280403">{{cite journal |vauthors=Sakane T, Takeno M, Suzuki N, Inaba G |title=Behçet's disease |journal=N. Engl. J. Med. |volume=341 |issue=17 |pages=1284–91 |date=October 1999 |pmid=10528040 |doi=10.1056/NEJM199910213411707 |url=}}</ref> | ||
===Race=== | ===Race=== | ||
| Line 24: | Line 24: | ||
===Gender=== | ===Gender=== | ||
*[[Male|Males]] are more commonly affected by Behçet disease than [[Female|females]]. The [[male]] to [[female]] ratio ranges from approximately 11 to 1 to 2 to 1 | *[[Male|Males]] are more commonly affected by Behçet disease than [[Female|females]]. The [[male]] to [[female]] ratio ranges from approximately 11 to 1 to 2 to 1. | ||
===Region=== | ===Region=== | ||
*The majority of Behçet disease cases are reported along the ancient silk road (from eastern Asia to the Mediterranean)<ref name="pmid10528040">{{cite journal |vauthors=Sakane T, Takeno M, Suzuki N, Inaba G |title=Behçet's disease |journal=N. Engl. J. Med. |volume=341 |issue=17 |pages=1284–91 |date=October 1999 |pmid=10528040 |doi=10.1056/NEJM199910213411707 |url=}}</ref> | *The majority of Behçet disease cases are reported along the ancient silk road (from eastern Asia to the Mediterranean).<ref name="pmid10528040">{{cite journal |vauthors=Sakane T, Takeno M, Suzuki N, Inaba G |title=Behçet's disease |journal=N. Engl. J. Med. |volume=341 |issue=17 |pages=1284–91 |date=October 1999 |pmid=10528040 |doi=10.1056/NEJM199910213411707 |url=}}</ref> | ||
*Behçet disease is most common in Turkey | *Behçet disease is most common in Turkey. | ||
===Neurologic disease=== | ===Neurologic disease=== | ||
*Occurs in less than 10 percent of patients with Behçet syndrome in most series<ref name="pmid9591220">{{cite journal| author=Serdaroğlu P| title=Behçet's disease and the nervous system. | journal=J Neurol | year= 1998 | volume= 245 | issue= 4 | pages= 197-205 | pmid=9591220 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9591220 }} </ref><ref name="pmid19444529">{{cite journal| author=Siva A, Saip S| title=The spectrum of nervous system involvement in Behçet's syndrome and its differential diagnosis. | journal=J Neurol | year= 2009 | volume= 256 | issue= 4 | pages= 513-29 | pmid=19444529 | doi=10.1007/s00415-009-0145-6 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19444529 }} </ref><ref name="pmid19161910">{{cite journal| author=Al-Araji A, Kidd DP| title=Neuro-Behçet's disease: epidemiology, clinical characteristics, and management. | journal=Lancet Neurol | year= 2009 | volume= 8 | issue= 2 | pages= 192-204 | pmid=19161910 | doi=10.1016/S1474-4422(09)70015-8 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19161910 }} </ref> | *Occurs in less than 10 percent of patients with Behçet syndrome in most series.<ref name="pmid9591220">{{cite journal| author=Serdaroğlu P| title=Behçet's disease and the nervous system. | journal=J Neurol | year= 1998 | volume= 245 | issue= 4 | pages= 197-205 | pmid=9591220 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9591220 }} </ref><ref name="pmid19444529">{{cite journal| author=Siva A, Saip S| title=The spectrum of nervous system involvement in Behçet's syndrome and its differential diagnosis. | journal=J Neurol | year= 2009 | volume= 256 | issue= 4 | pages= 513-29 | pmid=19444529 | doi=10.1007/s00415-009-0145-6 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19444529 }} </ref><ref name="pmid19161910">{{cite journal| author=Al-Araji A, Kidd DP| title=Neuro-Behçet's disease: epidemiology, clinical characteristics, and management. | journal=Lancet Neurol | year= 2009 | volume= 8 | issue= 2 | pages= 192-204 | pmid=19161910 | doi=10.1016/S1474-4422(09)70015-8 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19161910 }} </ref> | ||
* | *[[Male|Males]] are more commonly affected by neurological Behçet disease than [[Female|females]]. | ||
==References== | ==References== | ||
Revision as of 13:20, 15 May 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hamid Qazi, MD, BSc [2]
Overview
The prevalence of Behçet disease is approximately 0.12 to 7.5 per 100,000 individuals in the United States. Behçet disease commonly affects young adults 20 to 40 years of age. Males are more commonly affected by Behçet disease than females. Behçet disease usually affects individuals of the Turkish, Asian, and Middle Eastern populations. Middle Eastern and Asian individuals are more likely to develop Behçet disease due to the increased incidence of skin pathergy and HLA-B51 antigen. The male to female ratio ranges from approximately 11 to 1 to 2 to 1. The majority of Behçet disease cases are reported along the ancient silk road (from eastern Asia to the Mediterranean).
Epidemiology and Demographics
Prevalence
- The prevalence of Behçet disease is approximately 80 to 370 per 100,000 individuals in Turkey[1][2]
- The prevalence of Behçet disease is approximately 13.5 to 20 per 100,000 individuals in Iran, Japan, Korea, China and Saudi Arabia[1]
- The prevalence of Behçet disease is approximately 7.1 per 100,000 individuals in Paris, France[3]
- The prevalence of Behçet disease is approximately 2.4 per 100,000 individuals in European ancestry[3]
- The prevalence of Behçet disease is approximately 34.6 per 100,000 individuals in North African ancestry[3]
- The prevalence of Behçet disease is approximately 17.5 per 100,000 individuals in Asian ancestry[3]
- The prevalence of Behçet disease is approximately 0.12 to 7.5 per 100,000 individuals in the United States[4]
Age
- Behçet disease commonly affects young adults 20 to 40 years of age.[5]
Race
- Behçet disease usually affects individuals of the Turkish, Asian, and Middle Eastern populations.
- Middle Eastern and Asian individuals are more likely to develop Behçet disease due to the increased incidence of skin pathergy and HLA-B51 antigen
Gender
- Males are more commonly affected by Behçet disease than females. The male to female ratio ranges from approximately 11 to 1 to 2 to 1.
Region
- The majority of Behçet disease cases are reported along the ancient silk road (from eastern Asia to the Mediterranean).[1]
- Behçet disease is most common in Turkey.
Neurologic disease
- Occurs in less than 10 percent of patients with Behçet syndrome in most series.[6][7][8]
- Males are more commonly affected by neurological Behçet disease than females.
References
- ↑ 1.0 1.1 1.2 Sakane T, Takeno M, Suzuki N, Inaba G (October 1999). "Behçet's disease". N. Engl. J. Med. 341 (17): 1284–91. doi:10.1056/NEJM199910213411707. PMID 10528040.
- ↑ Sarica-Kucukoglu R, Akdag-Kose A, KayabalI M, Yazganoglu KD, Disci R, Erzengin D; et al. (2006). "Vascular involvement in Behçet's disease: a retrospective analysis of 2319 cases". Int J Dermatol. 45 (8): 919–21. doi:10.1111/j.1365-4632.2006.02832.x. PMID 16911374.
- ↑ 3.0 3.1 3.2 3.3 Mahr A, Belarbi L, Wechsler B, Jeanneret D, Dhote R, Fain O, Lhote F, Ramanoelina J, Coste J, Guillevin L (December 2008). "Population-based prevalence study of Behçet's disease: differences by ethnic origin and low variation by age at immigration". Arthritis Rheum. 58 (12): 3951–9. doi:10.1002/art.24149. PMID 19035493.
- ↑ Calamia KT, Wilson FC, Icen M, Crowson CS, Gabriel SE, Kremers HM (May 2009). "Epidemiology and clinical characteristics of Behçet's disease in the US: a population-based study". Arthritis Rheum. 61 (5): 600–4. doi:10.1002/art.24423. PMC 3024036. PMID 19405011.
- ↑ Sakane T, Takeno M, Suzuki N, Inaba G (October 1999). "Behçet's disease". N. Engl. J. Med. 341 (17): 1284–91. doi:10.1056/NEJM199910213411707. PMID 10528040.
- ↑ Serdaroğlu P (1998). "Behçet's disease and the nervous system". J Neurol. 245 (4): 197–205. PMID 9591220.
- ↑ Siva A, Saip S (2009). "The spectrum of nervous system involvement in Behçet's syndrome and its differential diagnosis". J Neurol. 256 (4): 513–29. doi:10.1007/s00415-009-0145-6. PMID 19444529.
- ↑ Al-Araji A, Kidd DP (2009). "Neuro-Behçet's disease: epidemiology, clinical characteristics, and management". Lancet Neurol. 8 (2): 192–204. doi:10.1016/S1474-4422(09)70015-8. PMID 19161910.