Literature DB >> 28829533

Vitamin K supplementation for cystic fibrosis.

Vanitha A Jagannath1, Vidhu Thaker, Anne B Chang, Amy I Price.   

Abstract

BACKGROUND: Cystic fibrosis is a genetic disorder which can lead to multiorgan dysfunction. Malabsorption of fat and fat-soluble vitamins (A, D, E, K) may occur and can cause subclinical deficiencies of some of these vitamins. Vitamin K is known to play an important role in both blood coagulation and bone formation. Supplementation with vitamin K appears to be one way of addressing the deficiency, but there is very limited agreement on the appropriate dose and frequency of use of these supplements. This is an updated version of the review.
OBJECTIVES: To assess the effects of vitamin K supplementation in people with cystic fibrosis and to determine the optimal dose and route of administration of vitamin K for both routine and therapeutic use. SEARCH
METHODS: We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group's Trials Register comprising references identified from comprehensive electronic database searches and handsearches of relevant journals and abstract books of conference proceedings.Most recent search: 30 January 2017. SELECTION CRITERIA: Randomised and quasi-randomised controlled trials of all preparations of vitamin K used as a supplement compared to either no supplementation (or placebo) at any dose or route and for any duration, in children or adults diagnosed with cystic fibrosis (by sweat test or genetic testing). DATA COLLECTION AND ANALYSIS: Two authors independently screened papers, extracted trial details and assessed their risk of bias. MAIN
RESULTS: Two trials (total of 32 participants) each lasting one month were included in the review and were assessed as having a moderate risk of bias. One was a dose-ranging parallel group trial in children (aged 8 to 18 years); and the other (with an older cohort) had a cross-over design comparing supplements to no treatment, but no separate data were reported for the first intervention period. Neither of the trials addressed any of the primary outcomes (coagulation, bone formation and quality of life). Both trials reported the restoration of serum vitamin K and undercarboxylated osteocalcin levels to the normal range after one month of daily supplementation with 1 mg of vitamin K. AUTHORS'
CONCLUSIONS: Evidence from randomised controlled trials on the benefits of routine vitamin K supplementation for people with CF is currently weak and limited to two small trials of short duration. However, no harm was found and until further evidence is available, the present recommendations should be adhered to.

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Year:  2017        PMID: 28829533      PMCID: PMC6483550          DOI: 10.1002/14651858.CD008482.pub5

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  40 in total

Review 1.  Vitamin K supplementation for cystic fibrosis.

Authors:  Vanitha A Jagannath; Zbys Fedorowicz; Vidhu Thaker; Anne B Chang
Journal:  Cochrane Database Syst Rev       Date:  2015-01-18

2.  The effect of vitamin K supplementation on biochemical markers of bone formation in children and adolescents with cystic fibrosis.

Authors:  Polyxeni Nicolaidou; Ilias Stavrinadis; Ioanna Loukou; Anna Papadopoulou; Helen Georgouli; Konstantinos Douros; Kostas N Priftis; Dimitrios Gourgiotis; Yiannis G Matsinos; Stavros Doudounakis
Journal:  Eur J Pediatr       Date:  2006-04-19       Impact factor: 3.183

Review 3.  [Vitamin D, K and bone mineral density].

Authors:  Toshio Okano
Journal:  Clin Calcium       Date:  2005-09

Review 4.  The metabolic functions and mechanism of action of vitamin K.

Authors:  L Uotila
Journal:  Scand J Clin Lab Invest Suppl       Date:  1990

5.  Translation and linguistic validation of a disease-specific quality of life measure for cystic fibrosis.

Authors:  A L Quittner; S Sweeny; M Watrous; P Munzenberger; K Bearss; A Gibson Nitza; L A Fisher; B Henry
Journal:  J Pediatr Psychol       Date:  2000-09

Review 6.  Cystic fibrosis: current trends in respiratory care.

Authors:  Jeffrey S Wagener; Aree A Headley
Journal:  Respir Care       Date:  2003-03       Impact factor: 2.258

Review 7.  Cystic fibrosis since 1938.

Authors:  Pamela B Davis
Journal:  Am J Respir Crit Care Med       Date:  2005-08-26       Impact factor: 21.405

8.  Suboptimal vitamin K status despite supplementation in children and young adults with cystic fibrosis.

Authors:  Kelly A Dougherty; Joan I Schall; Virginia A Stallings
Journal:  Am J Clin Nutr       Date:  2010-06-16       Impact factor: 7.045

9.  Determination of phylloquinone (vitamin K1) in plasma and serum by HPLC with fluorescence detection.

Authors:  Laura Y Wang; Chris J Bates; Liya Yan; Dominic J Harrington; Martin J Shearer; Ann Prentice
Journal:  Clin Chim Acta       Date:  2004-09       Impact factor: 3.786

10.  Assessment of vitamin K deficiency in CF--how much sophistication is useful?

Authors:  Katharina Mosler; Rüdiger von Kries; Cees Vermeer; Jörg Saupe; Thomas Schmitz; Antje Schuster
Journal:  J Cyst Fibros       Date:  2003-06       Impact factor: 5.482

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  4 in total

1.  Vitamin K supplementation for cystic fibrosis.

Authors:  Vanitha A Jagannath; Vidhu Thaker; Anne B Chang; Amy I Price
Journal:  Cochrane Database Syst Rev       Date:  2020-06-04

2.  Vitamin A and beta (β)-carotene supplementation for cystic fibrosis.

Authors:  Jorrit Jv de Vries; Anne B Chang; Catherine M Bonifant; Elizabeth Shevill; Julie M Marchant
Journal:  Cochrane Database Syst Rev       Date:  2018-08-09

3.  Brazilian Guidelines for Nutrition in Cystic Fibrosis.

Authors:  Lenycia de Cassya Lopes Neri; Miriam Isabel Souza Dos Santos Simon; Valéria Laguna Salomão Ambrósio; Eliana Barbosa; Monique Ferreira Garcia; Juliana Ferreira Mauri; Renata Rodrigues Guirau; Mirella Aparecida Neves; Carolina de Azevedo Pedrosa Cunha; Marcelo Coelho Nogueira; Anna Carolina Di Creddo Alves; Jocemara Gurmini; Maria de Fatima Servidoni; Matias Epifanio; Rodrigo Athanazio
Journal:  Einstein (Sao Paulo)       Date:  2022-04-01

4.  Treatment of cystic fibrosis related bone disease.

Authors:  Jagdeesh Ullal; Katherine Kutney; Kristen M Williams; David R Weber
Journal:  J Clin Transl Endocrinol       Date:  2021-12-21
  4 in total

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