Autoimmune polyendocrine syndrome epidemiology and demographics

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Epidemiology and Demographics

Incidence

• The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
• In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.

Prevalence

• The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
• In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.
• The prevalence of Autoimmune polyendocrine syndrome is estimated to be 1 in 25,000 inhabitants in Finland, which id the hisghest prevalence.

• In Finland, where the highest number of patient groups with APS type 1 has been reported, the estimated prevalence is about 1 in 25,000 inhabitants.

• APS type I, is a very rare disorder.

Case-fatality rate

• In [year], the incidence of [disease name] is approximately [number range] per 100,000 individuals with a case-fatality rate of [number range]%.
• The case-fatality rate of [disease name] is approximately [number range].

Age

• Autoimmune polyendocrine syndrome (APS) type 1 commonly affects children in the age group of 3-5 or in 13-15 years of age.
• Autoimmune polyendocrine syndrome (APS) type 0 commonly affects adults in the third and fourth decade of life.
• Most cases of autoimmune polyendocrine syndrome (APS) type 1 and type 2 are symptomatic by early thirties.

Race

• There is no racial predilection to [disease name].
• [Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].

Gender

• Females are more commonly affected by autoimmune polyendocrine syndrome than men.

Region

• The majority of autoimmune polyendocrine syndrome cases are reported in Finland and Iran.
• APS type 1 is more commonly seen in Finns, Sardinians, and Iranian Jews. It can be attributed to consanguineous marriages and/or clustering of descendants of common family founders.
• Other less frequent regions include Norway, Germany,northern Italy and northern Britain.

APS TYPE 1 syndrome is rare but has an increased prevalence in certain populations (e.g., inhabitants of Finland and Sardinia and Iranian Jews). APS type 1 frequencies in other ethnic groups include 4 cases per 100,000 in Finland, 7 cases per 100,000 in Sardinians and 11 cases per 100,000 in Iranian Jews.