Vitamins and amino acids in cystic fibrosis

Анастасия Дикий - Тронхейм; Норвегия

Vitamins and amino acids in cystic fibrosis

research article Pages: 32-37

Keywords: cystic fibrosis micronutrients vitamins amino acids imbalance metabolic disorders

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.

How to cite

Анастасия Дикий - Тронхейм, Норвегия Витамины и аминокислоты при муковисцидозе // Вопросы биологической, медицинской и фармацевтической химии. 2015. № 1. С. 32–37.

References

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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.

[1] 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.

[2] 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.

[3] 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.

[4] Saleheen D., Frossard P.M. The cradle of the deltaF508 mutation // J. Ayub. Med. Coll. Abbottabad. 2008. V. 20. № 4. P. 157-160.

[5] 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.

[6] Dodge J.A. and Turck D. Cystic fibrosis: nutritional consequences and management // Best Pract. Res. Clin. Gastroenterol. 2006. V. 20. № 3. P. 531-546.

[7] Carr S.B. and McBratney J. The role of vitamins in cystic fibrosis // J.R. Soc. Med. 2000. 93 Suppl 38. P. 14-19.

[8] 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.

[9] Liou T.G. et al. Predictive 5-Year Survivorship Model of Cystic Fibrosis // American Journal of Epidemiology. 2001. V. 153. № 4. P. 345-352.

[10] 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.

[11] 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.

[12] 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.

[13] Wilson D.C. and Pencharz P.B. Nutrition and cystic fibrosis // Nutrition. 1998. V. 14. № 10. P. 792-795.

[14] 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.

[15] 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.

[16] 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.

[17] 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.

[18] Chandra R.K. Increased bacterial binding to respiratory epithelial cells in vitamin A deficiency // Bmj. 1988. V. 297. № 6652. P. 834-835.

[19] 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.

[20] Ott S.M. and Aitken M.L. Osteoporosis in patients with cystic fibrosis // Clin. Chest. Med. 1998. V. 19. № 3. P. 555-567.

[21] 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.

[22] Costa M. et al. Diabetes: A major co-morbidity of cystic fibrosis // Diabetes and Metabolism. 2005. V. 31. № 3.P. 221-232.

[23] 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.

[24] 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.

[25] 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.

[26] 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.

[27] Foucaud P. et al. Selenium and vitamin E in mucoviscidosis // Arch. Fr. Pediatr. 1988. V. 45. № 6. P. 383-386.

[28] 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.

[29] Richard M.J. et al. Selenium and oxidant injury in patients with cystic fibrosis // Adv. Exp. Med. Biol. 1990. 264: P. 175-178.

[30] 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.

[31] 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.

[32] 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.

[33] 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.

[34] 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.

[35] Henderson R.C. and Lester G. Vitamin D levels in children with cystic fibrosis // South. Med. J. 1997. V. 90. № 4. P. 378-383.

[36] 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.

[37] Grasemann H. et al. Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis // Respir. Res. 2006. № 7. P. 87.

[38] Grasemann H. et al. L-ornithine derived polyamines in cystic fibrosis airways // PLoS One. 2012. V. 7. № 10. P. e46618.

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