Hispanic Ethnicity and Steatohepatitis are associated with increased risk of peptic ulcer disease in the cystic fibrosis population: a national database study

Author:

Mahmoud Maya1,Nwankwo Eugene1,Zhang Zidong2,Matiwala Neel2,Tripathi Rohan2,Mohamed Islam3,Barrios Christopher1,Syn Wing-Kin1,Hachem Christine1

Affiliation:

1. Saint Louis University Hospital

2. Saint Louis University

3. University of Missouri–Kansas City

Abstract

Abstract Background Although cystic fibrosis (CF) is widely considered a lung disease, the prevalence of CF-specific gastrointestinal symptoms and diseases has continued to rise. Peptic ulcer disease (PUD) has not been well-studied among people with CF (PwCF) and may be a common cause of abdominal symptoms. In PwCF, impaired bicarbonate secretion and unbuffered gastric acid production have been attributed to the development of ulcers, although ulcers remain uncommon. The objective of this study was to evaluate the prevalence of PUD in PwCF and assess for possible contributing factors. Methods This study utilized the National Inpatient Sample (NIS) database. All patients 18 years or older with CF were identified from 2014 to 2019. Relevant patient characteristics and procedures were identified using ICD-9 and ICD-10 codes. Linear trend, bivariate analyses, and multiple regression analysis were performed. The outcomes of interest were peptic ulcer disease, pancreatic insufficiency, and nonalcoholic steatohepatitis or NASH. All analyses accounted for complex sampling scheme of the NIS. Results The total prevalence of PwCF in the National Inpatient Sample (NIS) database was 0.08%, and the number was stable year to year from 2014 to 2019. Hispanic patients were more likely to be diagnosed with PUD than other white (aOR 1.802 [1.311,2.476]). Multiple regression analysis indicated that PUD in PwCF was strongly associated with a diagnosis of NASH (aOR 2.421[1.197, 4.898]). PUD patients were less likely to have pancreatic insufficiency compared to the non-PUD group (aOR 0.583 [0.455, 0.745]). All outcomes were adjusted for the use of proton pump inhibitors, H2 blockers, and NSAIDs. Conclusion Although cystic fibrosis has been historically known as a disease of childhood, advancements in therapy have led to prolonged life expectancy and higher prevalence for cystic fibrosis-related digestive diseases. This study revealed a low prevalence of PUD in PwCF. Hispanics and those with NASH are more likely to develop peptic ulcers. To validate these findings, additional multi-center prospective studies are warranted.

Publisher

Research Square Platform LLC

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