Literature DB >> 26882172

Supplementation of ursodeoxycholic acid improves fat digestion and absorption in cystic fibrosis patients with mild liver involvement.

Sławomira Drzymała-Czyż1, Katarzyna Jończyk-Potoczna, Aleksandra Lisowska, Marek Stajgis, Jarosław Walkowiak.   

Abstract

BACKGROUND: Ursodeoxycholic acid (UDCA) supplementation is recommended for cystic fibrosis (CF) patients with associated liver disease. However, its effect on fat digestion and absorption is not known.
MATERIALS AND METHODS: In 23 patients with mild liver involvement, a C-mixed triglyceride breath test was performed on UDCA supplementation (with and without pancreatic enzymes - standard and increased dose) and after 1 month of UDCA withdrawal. Cumulative percentage dose recovery [CPDR; median (interquartile range)] has been considered to reflect lipid digestion and absorption.
RESULTS: The enzyme supplementation resulted in a significant CPDR improvement [0% (0-0) vs. 4.6% (0.4-6.0); P<0.00046]. With the increased dose of enzymes in 16 patients with abnormal C-mixed triglyceride breath test results and lipase dose less than 3000 U/g of fat, higher CPDR values [8.6% (5.6-12.7); P<0.000027] were observed. However, a 1-month UDCA withdrawal resulted in a significant reduction in (P<0.000031) fat digestion and absorption [2.9% (0.7-5.8)].
CONCLUSION: UDCA supplementation seems to enhance lipid digestion and absorption in pancreatic insufficient CF patients with mild liver involvement. This finding points toward the potential impact of UDCA supplementation on nutritional status in CF patients with liver disease and underscores the often overlooked role of factors other than pancreatic enzymes on digestion and absorption of fats in CF.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 26882172     DOI: 10.1097/MEG.0000000000000593

Source DB:  PubMed          Journal:  Eur J Gastroenterol Hepatol        ISSN: 0954-691X            Impact factor:   2.566


  5 in total

Review 1.  Cystic fibrosis liver disease: A condition in need of structured transition and continuity of care.

Authors:  Julian Hercun; Fernando Alvarez; Catherine Vincent; Marc Bilodeau
Journal:  Can Liver J       Date:  2019-08-27

Review 2.  Reasonableness of Enriching Cow's Milk with Vitamins and Minerals.

Authors:  Dagmara Woźniak; Wojciech Cichy; Małgorzata Dobrzyńska; Juliusz Przysławski; Sławomira Drzymała-Czyż
Journal:  Foods       Date:  2022-04-08

Review 3.  Pancreatic Enzyme Replacement Therapy in Cystic Fibrosis.

Authors:  Peter N Freswick; Elizabeth K Reid; Maria R Mascarenhas
Journal:  Nutrients       Date:  2022-03-23       Impact factor: 5.717

4.  Fat Malabsorption and Ursodeoxycholic Acid Treatment in Children With Reduced Organic Solute Transporter-α (SLC51A) Expression.

Authors:  Rune Rose Tronstad; Siren Berland; Erling Tjora; Khadija El Jellas; Ingvild Aukrust; Kurt Kristensen; Dag Tveitnes; Anders Molven; Hanns-Ulrich Marschall; Anuradha Rao; Paul A Dawson
Journal:  JPGN Rep       Date:  2022-07-25

5.  Fat-Soluble Vitamins in Standard vs. Liposomal Form Enriched with Vitamin K2 in Cystic Fibrosis: A Randomized Multi-Center Trial.

Authors:  Jan Krzysztof Nowak; Patrycja Krzyżanowska-Jankowska; Sławomira Drzymała-Czyż; Joanna Goździk-Spychalska; Irena Wojsyk-Banaszak; Wojciech Skorupa; Ewa Sapiejka; Anna Miśkiewicz-Chotnicka; Jan Brylak; Barbara Zielińska-Psuja; Aleksandra Lisowska; Jarosław Walkowiak
Journal:  J Clin Med       Date:  2022-01-17       Impact factor: 4.241

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.