Differences in the socio-economic distribution of inflammatory bowel disease and microscopic colitis

被引:8
|
作者
Sonnenberg, A. [1 ,2 ]
Turner, K. O. [1 ]
Genta, R. M. [1 ,3 ]
机构
[1] Miraca Life Sci, Irving, TX USA
[2] Oregon Hlth & Sci Univ, Portland, OR 97201 USA
[3] Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA
关键词
Demographic characteristics; environmental epidemiology; socio-economic risk factors; ZIP codes; ESOPHAGEAL EOSINOPHILIA; HELICOBACTER-PYLORI; PREVALENCE;
D O I
10.1111/codi.13378
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim Inflammatory bowel disease (IBD) and microscopic colitis are characterized by different geographical distributions across the USA. In this cross-sectional study we utilized demographic and socio-economic information associated with individual ZIP codes to further delineate the epidemiological characteristics of the two diseases. Method A total of 813 057 patients who underwent colonoscopy between 2008 and 2014 were extracted from an electronic database of histopathology reports. The prevalence of patients with IBD or microscopic colitis was expressed as percentage of the population associated with specific demographic (age, sex, ethnicity) and socio-economic characteristics (population size, housing value, annual income, tertiary education). Results Both diseases were more common among subjects from ZIP codes with predominantly White residents and less common among subjects from ZIP codes with predominantly non-White residents such as Black, Hispanic and Asian. These ethnic variations were more pronounced in microscopic colitis than IBD. Markers of affluence, such as average residential house value and annual income, were positively associated with IBD and negatively with microscopic colitis. The prevalence of both diseases was positively correlated with tertiary education. Conclusion The occurrence of both IBD and microscopic colitis is influenced by environmental risk factors. The differences in the demographic, ethnic and socioeconomic distributions of the two diseases suggest that different sets of risk factors affect the two diseases and that their aetiology is unrelated.
引用
收藏
页码:38 / 44
页数:7
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