350 rub
Journal №1 for 2015 г.
Article in number:
Vitamins and amino acids in cystic fibrosis
Authors:
Anastasiya Dykyy - Research, Trondheim, Norvay
Abstract:
Cystic fibrosis (CF) is a single gene disorder which affects multiple organs. Due to intestinal malabsorption, several micronutrients, such as vitamins, are not adequately absorbed. Low vitamin A, D and E levels and unbalanced amino acid metabolism were found in most studies. This review summarises the available knowledge of vitamin and amino acids deficiencies in CF patients.
Pages: 32-37
References
- Braga S.F. and Almgren M.M. Complementary therapies in cystic fibrosis: nutritional supplements and herbal products // J. Pharm. Pract. 2013. V. 26. № 1. P. 14-17.
- O'Brien C.E., Harden H., and Com G. A survey of nutrition practices for patients with cystic fibrosis // Nutr. Clin. Pract. 2013. V. 28. № 2. P. 237-241.
- Kashirskaya N., Tolstova V., and Kapranov N. Cystic fibrosis - a national priority program in the Russian Federatuin - 2008 // Pediatria. 2008. V. 87. № 4. P. 6-14.
- Saleheen D., Frossard P.M. The cradle of the deltaF508 mutation // J. Ayub. Med. Coll. Abbottabad. 2008. V. 20. № 4. P. 157-160.
- Siwamogsatham O. et al. Relationship Between Fat-Soluble Vitamin Supplementation and Blood Concentrations in Adolescent and Adult Patients With Cystic Fibrosis // Nutrition in Clinical Practice. 2014.
- Dodge J.A. and Turck D. Cystic fibrosis: nutritional consequences and management // Best Pract. Res. Clin. Gastroenterol. 2006. V. 20. № 3. P. 531-546.
- Carr S.B. and McBratney J. The role of vitamins in cystic fibrosis // J.R. Soc. Med. 2000. 93 Suppl 38. P. 14-19.
- Yadav K. et al. Evaluation of micronutrient profile of North Indian children with cystic fibrosis: a case-control study // Pediatr. Res. 2014. V. 75. № 6. P. 762-766.
- Liou T.G. et al. Predictive 5-Year Survivorship Model of Cystic Fibrosis // American Journal of Epidemiology. 2001. V. 153. № 4. P. 345-352.
- Gozdzik J. et al. Relationship between nutritional status and pulmonary function in adult cystic fibrosis patients // J. Physiol. Pharmacol. 2008. V. 59. Suppl 6. P. 253-260.
- Feranchak A.P. et al. Prospective, long-term study of fat-soluble vitamin status in children with cystic fibrosis identified by newborn screen // The Journal of Pediatrics. 1999. V. 135. № 5. P. 601-610.
- Rana M. et al. Fat-soluble vitamin deficiency in children and adolescents with cystic fibrosis // Journal of Clinical Pathology. 2014. V. 67. № 7. P. 605-608.
- Wilson D.C. and Pencharz P.B. Nutrition and cystic fibrosis // Nutrition. 1998. V. 14. № 10. P. 792-795.
- Hollander F.M. et al. Self-reported use of vitamins and other nutritional supplements in adult patients with cystic fibrosis. Is daily practice in concordance with recommendations - // International Journal for Vitamin and Nutrition Research. 2010. V. 80. № 6. P. 408-415.
- Sokol R.J. et al. Fat-soluble-vitamin status during the first year of life in infants with cystic fibrosis identified by screening of newborns // Am. J. Clin. Nutr. 1989. V. 50. № 5. P. 1064-1071.
- Back E.I. et al. Antioxidant deficiency in cystic fibrosis: when is the right time to take action - // Am. J. Clin. Nutr. 2004. V. 80. № 2. P. 374-384.
- Lezo A. et al. Oxidative stress in stable cystic fibrosis patients: do we need higher antioxidant plasma levels - // J. Cyst. Fibros. 2013. V. 12. № 1. P. 35-41.
- Chandra R.K. Increased bacterial binding to respiratory epithelial cells in vitamin A deficiency // Bmj. 1988. V. 297. № 6652. P. 834-835.
- Scott J. et al. Rickets in adult cystic fibrosis with myopathy, pancreatic insufficiency and proximal renal tubular dysfunction // Am. J. Med. 1977. V. 63.№ 3. P. 488-492.
- Ott S.M. and Aitken M.L. Osteoporosis in patients with cystic fibrosis // Clin. Chest. Med. 1998. V. 19. № 3. P. 555-567.
- Harshman S.G., E. Saltzman and Booth S.L. Vitamin K: dietary intake and requirements in different clinical conditions // Curr. Opin. Clin. Nutr. Metab. Care. 2014. V. 17. № 6. P. 531-538.
- Costa M. et al. Diabetes: A major co-morbidity of cystic fibrosis // Diabetes and Metabolism. 2005. V. 31. № 3.P. 221-232.
- Dolan T.F. and Gibson Jr. L.E. Possibility of cystic fibrosis in infants with vitamin K deficiency // J. Pediatr. 1970. V. 77. № 3. P. 515.
- Conway S.P. et al. Vitamin K Status Among Children With Cystic Fibrosis and Its Relationship to Bone Mineral Density and Bone Turnover // Pediatrics. 2005. V. 115. № 5.P. 1325-1331.
- Grievink L. et al. Dietary intake of antioxidant (pro)-vitamins, respiratory symptoms and pulmonary function: the MORGEN study // Thorax. 1998. V. 53. № 3. P. 166-171.
- Winklhofer-Roob B.M. et al. Plasma vitamin C concentrations in patients with cystic fibrosis: evidence of associations with lung inflammation // Am. J. Clin. Nutr. 1997. V. 65. № 6. P. 1858-1866.
- Foucaud P. et al. Selenium and vitamin E in mucoviscidosis // Arch. Fr. Pediatr. 1988. V. 45. № 6. P. 383-386.
- Stead R. et al. Selenium deficiency and possible increased risk of carcinoma in adults with cystic fibrosis // The Lancet. 1985. V. 326. № 8460. P. 862-863.
- Richard M.J. et al. Selenium and oxidant injury in patients with cystic fibrosis // Adv. Exp. Med. Biol. 1990. 264: P. 175-178.
- Oledzka I. et al. Capillary electromigration techniques as tools for assessing the status of vitamins A, C and E in patients with cystic fibrosis // J. Pharm. Biomed. Anal. 2014. C. 102. P. 45-53.
- Wood L.G. et al. Oxidative stress in cystic fibrosis: dietary and metabolic factors // J. Am. Coll. Nutr. 2001. V. 20. 2 Suppl. P. 157-165.
- Jacob R.A. et al. Zinc status and vitamin A transport in cystic fibrosis // American Journal of Clinical. Nutrition. 1978. V. 31. № 4. P. 638-644.
- Solomons N.W. et al. Some biochemical indices of nutrition in treated cystic fibrosis patients // Am. J. Clin. Nutr. 1981. V. 34. № 4. P. 462-474.
- Hanly J.G. et al. Hypovitaminosis D and response to supplementation in older patients with cystic fibrosis // Q.J. Med. 1985. V. 56. № 219. P. 377-385.
- Henderson R.C. and Lester G. Vitamin D levels in children with cystic fibrosis // South. Med. J. 1997. V. 90. № 4. P. 378-383.
- Engelen M.P. et al. Stimulated nitric oxide production and arginine deficiency in children with cystic fibrosis with nutritional failure // J Pediatr, 2013. V. 163. № 2. P. 369-375.
- Grasemann H. et al. Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis // Respir. Res. 2006. № 7. P. 87.
- Grasemann H. et al. L-ornithine derived polyamines in cystic fibrosis airways // PLoS One. 2012. V. 7. № 10. P. e46618.