Literature DB >> 26465792

Choline Supplementation With a Structured Lipid in Children With Cystic Fibrosis: A Randomized Placebo-Controlled Trial.

Joan I Schall1, Maria R Mascarenhas, Asim Maqbool, Kelly A Dougherty, Okan Elci, Dah-Jyuu Wang, Talissa A Altes, Kevin A Hommel, Walter Shaw, Jeff Moore, Virginia A Stallings.   

Abstract

BACKGROUND: Choline depletion is seen in cystic fibrosis (CF) and pancreatic insufficiency in spite of enzyme treatment and may result in liver, fatty acid, and muscle abnormalities. This study evaluated the efficacy and safety of an easily absorbed choline-rich structured lipid (LYM-X-SORB™ [LXS]) to improve choline status.
METHODS: Children with CF and pancreatic insufficiency were randomized to LXS or placebo in a 12-month double blind trial. Dietary choline intake, plasma cholines, plasma and fecal phospholipids, coefficient of fat absorption, pulmonary function, growth status, body composition, and safety measures were assessed. Magnetic resonance spectroscopy for calf muscle choline and liver fat were assessed in a subgroup and compared with a healthy comparison group matched for age, sex, and body size.
RESULTS: A total of 110 subjects were enrolled (age 10.4 ± 3.0 years). Baseline dietary choline, 88% recommended, increased 3-fold in the LXS group. Plasma choline, betaine, and dimethylglycine increased in the LXS but not placebo (P = 0.007). Plasma lysophosphatidylcholine and phosphatidylcholine increased, and fecal phosphatidylcholine/phosphatidylethanolamine ratio decreased (P ≤ 0.05) in LXS only, accompanied by a 6% coefficient of fat absorption increase (P = 0.001). Children with CF had higher liver fat than healthy children and depleted calf muscle choline at baseline. Muscle choline concentration increased in LXS and was associated with improvement in plasma choline status. No relevant changes in safety measures were evident.
CONCLUSIONS: LXS had improved choline intake, plasma choline status, and muscle choline stores compared with placebo group. The choline-rich supplement was safe, accepted by participants, and improved choline status in children with CF.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 26465792      PMCID: PMC4805439          DOI: 10.1097/MPG.0000000000001004

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  43 in total

1.  Spirometric reference values from a sample of the general U.S. population.

Authors:  J L Hankinson; J R Odencrantz; K B Fedan
Journal:  Am J Respir Crit Care Med       Date:  1999-01       Impact factor: 21.405

2.  Fecal elastase: pancreatic status verification and influence on nutritional status in children with cystic fibrosis.

Authors:  Jacqueline R Cohen; Joan I Schall; Richard F Ittenbach; Babette S Zemel; Virginia A Stallings
Journal:  J Pediatr Gastroenterol Nutr       Date:  2005-04       Impact factor: 2.839

3.  Hepatic lipid accumulation in healthy subjects: a comparative study using spectral fat-selective MRI and volume-localized 1H-MR spectroscopy.

Authors:  Jürgen Machann; Claus Thamer; Birgit Schnoedt; Norbert Stefan; Hans-Ulrich Haring; Claus D Claussen; Andreas Fritsche; Fritz Schick
Journal:  Magn Reson Med       Date:  2006-04       Impact factor: 4.668

4.  Plasma phosphatidylcholine alterations in cystic fibrosis patients: impaired metabolism and correlation with lung function and inflammation.

Authors:  Judith Grothe; Joachim Riethmüller; Sandra M Tschürtz; Marco Raith; Chris J Pynn; Dieter Stoll; Wolfgang Bernhard
Journal:  Cell Physiol Biochem       Date:  2015-03-12

5.  The impact of choline availability on muscle lipid metabolism.

Authors:  Vera Michel; Ratnesh Kumar Singh; Marica Bakovic
Journal:  Food Funct       Date:  2010-12-07       Impact factor: 5.396

6.  Phosphatidylcholine and lysophosphatidylcholine excretion is increased in children with cystic fibrosis and is associated with plasma homocysteine, S-adenosylhomocysteine, and S-adenosylmethionine.

Authors:  Alice H Chen; Sheila M Innis; A George F Davidson; S Jill James
Journal:  Am J Clin Nutr       Date:  2005-03       Impact factor: 7.045

7.  An extremely simple method for extraction of lysophospholipids and phospholipids from blood samples.

Authors:  Zhenwen Zhao; Yan Xu
Journal:  J Lipid Res       Date:  2009-09-25       Impact factor: 5.922

Review 8.  Cystic fibrosis and nutrition: linking phospholipids and essential fatty acids with thiol metabolism.

Authors:  Sheila M Innis; A George F Davidson
Journal:  Annu Rev Nutr       Date:  2008       Impact factor: 11.848

9.  Assessment of phospholipid malabsorption by quantification of fecal phospholipid.

Authors:  Alice Chen; Sheila Innis
Journal:  J Pediatr Gastroenterol Nutr       Date:  2004-07       Impact factor: 2.839

Review 10.  Liver disease in cystic fibrosis.

Authors:  Carla Colombo
Journal:  Curr Opin Pulm Med       Date:  2007-11       Impact factor: 3.155

View more
  8 in total

1.  Effect of Oral Lipid Matrix Supplement on Fat Absorption in Cystic Fibrosis: A Randomized Placebo-Controlled Trial.

Authors:  Virginia A Stallings; Joan I Schall; Asim Maqbool; Maria R Mascarenhas; Belal N Alshaikh; Kelly A Dougherty; Kevin Hommel; Jamie Ryan; Okan U Elci; Walter A Shaw
Journal:  J Pediatr Gastroenterol Nutr       Date:  2016-12       Impact factor: 2.839

2.  Choline supplementation alters some amino acid concentrations with no change in homocysteine in children with cystic fibrosis and pancreatic insufficiency.

Authors:  Belal Alshaikh; Joan I Schall; Asim Maqbool; Maria Mascarenhas; Michael J Bennett; Virginia A Stallings
Journal:  Nutr Res       Date:  2015-12-29       Impact factor: 3.315

3.  Choline.

Authors:  Steven H Zeisel; Kevin C Klatt; Marie A Caudill
Journal:  Adv Nutr       Date:  2018-01-01       Impact factor: 8.701

4.  Pancreatic Function in Chronic Pancreatitis: A Cohort Study Comparing 3 Methods of Detecting Fat Malabsorption and the Impact of Short-term Pancreatic Enzyme Replacement Therapy.

Authors:  Jefferson N Brownell; Joan I Schall; Virginia A Stallings
Journal:  Pancreas       Date:  2019-09       Impact factor: 3.327

5.  Prospective associations of maternal choline status with offspring body composition in the first 5 years of life in two large mother-offspring cohorts: the Southampton Women's Survey cohort and the Growing Up in Singapore Towards healthy Outcomes cohort.

Authors:  Linde van Lee; Sarah R Crozier; Izzuddin M Aris; Mya T Tint; Suresh Anand Sadananthan; Navin Michael; Phaik Ling Quah; Sian M Robinson; Hazel M Inskip; Nicholas C Harvey; Mary Barker; Cyrus Cooper; Sendhil S Velan; Yung Seng Lee; Marielle V Fortier; Fabian Yap; Peter D Gluckman; Kok Hian Tan; Lynette P Shek; Yap-Seng Chong; Keith M Godfrey; Mary F F Chong
Journal:  Int J Epidemiol       Date:  2019-04-01       Impact factor: 7.196

6.  Bone accrual and structural changes over one year in youth with cystic fibrosis.

Authors:  Rosara M Bass; Babette S Zemel; Virginia A Stallings; Mary B Leonard; Jaime Tsao; Andrea Kelly
Journal:  J Clin Transl Endocrinol       Date:  2022-03-25

Review 7.  Choline in cystic fibrosis: relations to pancreas insufficiency, enterohepatic cycle, PEMT and intestinal microbiota.

Authors:  Wolfgang Bernhard
Journal:  Eur J Nutr       Date:  2020-08-14       Impact factor: 5.614

8.  Lumacaftor/ivacaftor therapy is associated with reduced hepatic steatosis in cystic fibrosis patients.

Authors:  Katherine Kutney; Shannon B Donnola; Chris A Flask; Rose Gubitosi-Klug; MaryAnn O'Riordan; Kimberly McBennett; Thomas J Sferra; Beth Kaminski
Journal:  World J Hepatol       Date:  2019-12-27
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.