The coexistence of inflammatory bowel disease (IBD) and bullous pemphigoid (BP) has been reported. No large-scale study to date has explored the relationship between these diseases. This populationbased case-control study examined the association between IBD and BP by using a nationwide database. A total of 5,263 BP patients and 21,052 age-and gender-, hospital visit number-matched controls were identified in the National Health Insurance Research Database of Taiwan (1997-2013). Demographic characteristics and comorbidities including IBD were compared. Logistic regression was conducted to examine the predicting factors for BP. The mean age at diagnosis was 74.88 years and 54.3% of subjects were male. BP patients tended to have more cardiovascular risk factors, autoimmune and neurologic comorbidities, and hematologic cancers than matched controls. There were 20 cases of IBD (0.38%), mostly ulcerative colitis (N = 17, 0.32%) among BP patients, compared to 33 IBD cases (0.16%) among controls (p < 0.001). Ulcerative colitis was found to be significantly associated with BP [adjusted odds ratio (OR) 3.60, 95% confidence interval (CI) 1.91-6.77, p < 0.001] on multivariate analysis. Treatment for IBD was not associated with BP development. Information about diet, lifestyle, alcohol consumption, and smoking habit was not available. We concluded that UC is independently associated with BP. Bullous pemphigoid (BP) is the most common autoimmune bullous disease. It mainly affects the elderly and is characterized by recurrent bullous lesions on trunk and limbs, with high morbidity and mortality. It is associated with autoantibodies against BPAG1 (also called BP 230/dystonin) and BPAG2 (BP180/type XVII collagen). The binding of autoantibodies to their targets activates inflammatory cascades that result in disruption of skin basement membrane integrity and subsequent subepidermal bullae formation 1. The incidence is estimated to be 2.4-23 cases per million people in the general population but rises exponentially to 190-312 cases per million in the over 80 population 2. A large body of evidence has suggested a strong association between BP and neurodegenerative diseases including dementia, cerebrovascular events, epilepsy, multiple sclerosis, and Parkinson's disease 2-6. The molecular link between BP and neurodegenerative disorders has been hypothesized to be based on cross-reactivity with shared autoantibodies of BP 230 and BP180 expressed in neuronal and epithelial tissues 4. Cardiovascular comorbidities have also been observed 3,6,7. The potential mechanisms involve inhibited fibrinolysis and coagulation activation in BP patients and shared expression of BP230 in cardiac muscle and skin 8. Advanced age at onset and frequent medical attention given to BP patients might also contribute to higher detection rates for comorbidities 4 .