Pancreatic enzyme supplementation versus placebo for improvement of gastrointestinal symptoms in non-responsive celiac disease: A cross-over randomized controlled trial

被引:5
作者
Yoosuf, Shakira [1 ,2 ,3 ]
Barrett, Caitlin G. [1 ]
Papamichael, Konstantinos [1 ]
Madoff, Sarah E. [1 ,4 ]
Kurada, Satya [1 ,5 ]
Hansen, Joshua [1 ,2 ,6 ]
Silvester, Jocelyn A. [1 ,2 ,3 ]
Therrien, Amelie [1 ,2 ]
Singh, Prashant [1 ,2 ,7 ]
Dennis, Melinda [1 ,2 ]
Leffler, Daniel A. [1 ,2 ,8 ]
Kelly, Ciaran P. [1 ,2 ]
机构
[1] Beth Israel Deaconess Med Ctr, Celiac Ctr, Dept Med, Div Gastroenterol, Boston, MA 02215 USA
[2] Harvard Med Sch, Celiac Res Program, Boston, MA 02215 USA
[3] Chettinad Hosp & Res Inst, Chennai, India
[4] Maimonides Hosp, Brooklyn, NY USA
[5] Indiana Univ Sch Med, Div Gastroenterol & Hepatol, Indianapolis, IN USA
[6] Boston Childrens Hosp, Div Gastroenterol Hepatol & Nutr, Boston, MA USA
[7] Univ Michigan, Div Gastroenterol, Ann Arbor, MI USA
[8] Takeda Pharmaceut Int Co, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
diarrhea; sprue; malabsorption; exocrine pancreatic insufficiency; proton pump inhibitors; pancreas; dyspepsia; EXOCRINE INSUFFICIENCY; LARAZOTIDE ACETATE; FECAL ELASTASE-1; PREVALENCE; ETIOLOGIES; MANAGEMENT; DIAGNOSIS; DIARRHEA; SPRUE;
D O I
10.3389/fmed.2022.1001879
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Pancreatic Exocrine Insufficiency (PEI) is a possible cause of recurrent/persistent symptoms in celiac disease. Although pancreatic enzyme supplementation may be used to treat non-responsive celiac disease (NRCD) in clinical practice, clinical outcomes are variable and there is limited and low quality evidence to support this practice. The aim of this study was to assess the efficacy of pancreatic enzyme supplements (PES) for improvement of gastrointestinal symptoms in NRCD.Methods: Prospective, randomized, placebo-controlled, double-blind, cross-over trial in adults with NRCD examining Celiac Disease-Gastrointestinal Symptom Rating Scale (CeD-GSRS) scores on PES (pancrelipase co-administered with omeprazole) versus placebo (omeprazole only) during a 10-day treatment period. The study was registered under the clinical trials registry ( number, NCT02475369) on 18 Jun 2015.Results: Twelve participants (nine female) were included in the per-protocol analysis; one participant had low fecal elastase-1. Pancrelipase was not associated with significant change in CeD-GSRS compared to placebo (-0.03 versus -0.26; P = 0.366). There was a significant decrease in mean values of total CeD-GSRS scores (3.58 versus 2.90, P = 0.004), abdominal pain (2.92 versus 2.42, P = 0.009), and diarrhea sub-scores (3.44 versus 2.92, P = 0.037) during the run-in period with omeprazole.Conclusion:In this prospective, cross-over randomized, placebo-controlled study, PES did not improve symptoms in patients with NRCD. It is unclear whether this is a trial effect or related to administration of omeprazole.
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页数:7
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