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Nutrition in cystic fibrosis: a historical overview

Published online by Cambridge University Press:  28 February 2007

John A. Dodge
John A. Dodge
Affiliation:
Department of Child Health, The Queen's University of Belfast, Grosvenor Road, Belfast BT12 6BJ, Northern Ireland
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Abstract

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Type
Symposium on ‘Cystic Fibrosis’
Information
Proceedings of the Nutrition Society , Volume 51 , Issue 2 , August 1992 , pp. 225 - 235
Copyright
Copyright © The Nutrition Society 1992

References

Abman, S. H., Accurso, F. J. & Bowman, C. M. (1986). Persistent morbidity and mortality of protein calorie malnutrition in young infants with CF. Journal of Pediatric Gastroenterology and Nutrition 5,393–396.Google ScholarPubMed
Allan, J. D., Mason, A. & Moss, A. D. (1973). Nutritional supplementation in treatment with cystic fibrosis of the pancreas. American Journal of Diseases of Children 126,22–26.Google ScholarPubMed
Andersen, D. H. (1938). Cystic fibrosis of the pancreas and its relation to celiac disease. A clinical and pathologic study. American Journal of Diseases of Children 56,344–349.CrossRefGoogle Scholar
Andersen, D. H. (1939). Cystic fibrosis of the pancreas, vitamin A deficiency and bronchiectasis. Journal of Pediatrics 15,763–771.CrossRefGoogle Scholar
Ater, J. L., Herbst, J. J., Landau, S. A. & O'Brien, R. T. (1983). Relative anemia and iron deficiency in cystic fibrosis. Pediatrics 71, 810–814.CrossRefGoogle ScholarPubMed
Ausiello, D. A. (1990). The regulation of Na+ channels by G proteins and phospholipids. Pediatric Pulmonology, Suppl. 5, 135–136.Google Scholar
Blackfan, K. D. & Wolbach, S. B. (1933). Vitamin A deficiency in infants. A clinical and pathological study. Journal of Pediatrics 3,679–706.CrossRefGoogle Scholar
British Paediatric Association Working Party on Cystic Fibrosis (1988). Cystic fibrosis in the United Kingdom 1977–85: an improving picture. Brirish Medical Journal 297,2599–1602.Google Scholar
Brooks, H. L., Driebe, W. T. & Schemmer, G. G. (1990). Xerophthalmia and cystic fibrosis. Archives of Ophthalmology 108,354–357.CrossRefGoogle ScholarPubMed
Carlstedt-Duke, J., Bronnegard, M. & Strandvik, B. (1986). Pathological regulation of arachidonic acid release in cystic fibrosis: the putative basic defect. Proceedings of the National Academy of Sciences USA 83, 9202–9206.CrossRefGoogle ScholarPubMed
Castillo, R., Landon, C., Eckhardt, K., Moms, V., Levander, Q. A. & Lewiston, N. (1981). Selenium and vitamin E status in cystic fibrosis. Journal of Pediatrics 99,583–585.CrossRefGoogle ScholarPubMed
Corey, M., McLaughlin, F. J., Williams, M. & Levison, H. (1988). A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. Journal of Clinical Epidemiology 41,583–591.CrossRefGoogle ScholarPubMed
Cynamon, H. A., Milov, D. E., Valenstein, E. & Wagner, M. (1988). Effect of vitamin E deficiency on neurologic function in patients with cystic fibrosis. Journal of Pediatrics 113,637–640.CrossRefGoogle ScholarPubMed
di Sant'Agnese, P. A., Darling, R. C., Perera, G. A. & Shea, E. (1953). Abnormal electrolyte composition of sweat in cystic fibrosis of pancreas; clinical significance and relationships to disease. Pediatrics 12,549–563.CrossRefGoogle Scholar
Dodge, J. A., Custance, J. M., Goodchild, M. C., Laing, S. C. & Vaughan, M. (1990). Paradoxical effects of essential fatty acid supplementation on lipid profiles and sweat electrolytes in cystic fibrosis. British Journal of Nutrition 63, 259–271.CrossRefGoogle ScholarPubMed
Dodge, J. A. & Yassa, J. G. (1978). Zinc deficiency syndrome in a British youth with cystic fibrosis. British Medical Journal i, 411.CrossRefGoogle Scholar
Dworkin, B., Newman, L. J., Berezin, S., Rosenthal, W. S., Schwarz, S. M. & Weiss, L. (1987). Low blood selenium levels in patients with cystic fibrosis compared to controls and healthy adults. Journal of Parenteral and Enteral Nutrition 11, 38–41.CrossRefGoogle ScholarPubMed
Eiberg, H., Mohr, J., Schmiegelow, K., Nielsen, L. S. & Williamson, R. (1985). Linkage relationships of paraoxonase (PON) with other markers: indication of PON-cystic fibrosis synteny. Clinical Genetics 28, 265–271.CrossRefGoogle ScholarPubMed
Elias, E., Muller, D. P. R. & Scott, J. (1981). Spinocerebellar disorders in association with cystic fibrosis or chronic cholestasis and virtually undetectable serum concentrations of vitamin E. Lancet ii, 1319–1321.CrossRefGoogle Scholar
Fanconi, G., Uehlinger, E. & Knauer, C. (1936). Das Coeliaksyndrom bei Angelbosener zystisher Pankreas fibromatose und Bronchiektasien. Weiner Medische Wochenschrift 86,753–756.Google Scholar
Faraj, B. A., Caplan, D. B., Camp, V. M., Piker, E. & Kutner, M. (1986). Low levels of pytidoxal 5'-phosphate in patients with cystic fibrosis. Pediatrics 78, 278–282.CrossRefGoogle Scholar
Farber, S. (1945). Some organic digestive disturbances in early life. Journal of Michigan State Medical Society 44,487–594.Google Scholar
Francis, D. E. M. (1981). Diets for children with cystic fibrosis. Cystic Fibrosis News 16,8–10.Google Scholar
Gaskin, K., Gurwitz, D., Durie, P., Corey, M., Levison, H. & Forstner, G. (1982). Improved respiratory prognosis in CF patients with normal fat absorption. Pediatrics 100,857–862.Google ScholarPubMed
Green, C. G., Doershuk, C. F. & Stern, R. C. (1985). Symptomatic hypomagnesemia in cystic fibrosis. Journal of Pediatrics 107,425–428.CrossRefGoogle ScholarPubMed
Guggino, W. B. & Hwang, T. C. (1990). Regulation of chloride channels in normal and CF airways. Pediatric Pulmonology, Suppl. 5, 1319–1321.Google Scholar
Halsted, J. A. & Smith, J. C. (1970). Plasma zinc in health and disease. Lancet i, 322–324.CrossRefGoogle Scholar
Heinrich, H. C., Bender-Gotze, C. & Gabbe, E. E. (1977). Absorption of inorganic iron (59Fe2+) in relation to iron stores in pancreatic exocrine insufficiency due to cystic fibrosis. Klinische Wochenschrift 55, 587.CrossRefGoogle ScholarPubMed
Kerem, B.-S., Rommens, J. M., Buchanan, J. A., Markiewicz, D., Cox, T. K., Chakravarti, A., Buchwald, M. & Tsui, L.-C. (1989). Identification of the Cystic Fibrosis Gene: Genetic Analysis. Science 245, 1073–1080.CrossRefGoogle ScholarPubMed
Kerem, E., Corey, M., Kerem, B.-S., Rornmens, J., Markiewicz, D., Levison, H., Tsui, L.-C. & Durie, P. (1990). The relation between genotype and phenotype in cystic fibrosis - analysis of the most common mutation (delta F508). New England Journal of Medicine 323, 1517–1522.CrossRefGoogle ScholarPubMed
Kraemer, R., Rudeberg, A., Hadorn, B. & Rossi, E. (1978). Relative underweight in cystic fibrosis and its prognostic value. Acta Paediatrica Scandinavica 67,33–37.CrossRefGoogle Scholar
Lloyd-Still, J. D., Bohan, T., Hughes, S. & Wessel, H. V. (1990 a). Acyl carnitine is low in cord blood in cystic fibrosis. Acta Paediatrica Scandinavica 79, 427–430.CrossRefGoogle Scholar
Lloyd-Still, J. D. & Ganther, H. E. (1981). Selenium and glutathione peroxidase levels in cystic fibrosis. Pediatrics 65, 1010.CrossRefGoogle Scholar
Lloyd-Still, J. D., Howars, C. & Wessel, H. (1990 b). Carnitine metabolites in infants with CF: a prospective study. Pediatric Pulmonology, Suppl. 5,226 Abstr.Google Scholar
McIntosh, I., Lorenzo, M. L. & Brock, D. J. H. (1989). Frequency of △F508 mutation on cystic fibrosis chromosomes in UK. Lancet ii, 1404–1405.CrossRefGoogle Scholar
Mischler, E. H., Chesney, P. J., Chesney, R. W. & Mazess, R. B. (1979). Demineralization in cystic fibrosis detected by direct photon absorptiometry. American Journal of Diseases of Children 133, 632–635.CrossRefGoogle ScholarPubMed
Mischler, E. H., Marcus, M. S., Sondel, S. A., Laxova, A., Carey, P., Langhough, R. & Farrell, P. M. (1991). Nutritional assessment of infants with cystic fibrosis diagnosed through screening. Pediatric Pulmonology, Suppl. (In the Press).CrossRefGoogle ScholarPubMed
Navarro, J., Maherzi, A. & Faucaud, P. (1989). Influence of intravenous fatty acid supplementation on nasal transepithelial potential difference in cystic fibrosis patients. Pediatric Pulmonology Suppl. 4, 147–148.Google Scholar
Neve, J., van Geffel, R., Hanocq, M. & Molle, L. (1983). Plasma and erythrocyte zinc, copper and selenium in cystic fibrosis. Acta Paediatrica Scandinavica 72, 437–440.CrossRefGoogle ScholarPubMed
O'Loughlin, E. V., Forbes, kD., Parsons, H., Smith, B., Cooper, D. & Gall, D. G. (1984). Nutritional rehabilitation in malnourished patients with cystic fibrosis: effect on the course of the disease. In Cystic Fibrosis Horizons, p. 97 [D., Lawson, editor]. Chichester: J. Wiley & Sons Ltd.Google Scholar
O'Rawe, A., McIntosh, I., Dodge, J. A., Brock, D. J. H., Redmond, J. A., Ward, R. & MacPherson, A. J. S. (1992). Increased energy expenditure in cystic fibrosis is associated with specific mutations. Clinical Science 82,71–76.CrossRefGoogle ScholarPubMed
Quinton, P. M. & Bijman, J. L. (1983). Higher bioelectric potentials due to decreased chloride absorption in the sweat glands of patients with cystic fibrosis. New England Journal of Medicine 308, 1185–1189.CrossRefGoogle ScholarPubMed
Rayner, R. J., Tyrrell, J. C., Hiller, E. J., Marenah, C., Neugebauer, M. A., Vernon, S. A. & Brimlow, G. (1989). Night blindness and conjunctival xerosis caused by vitamin A deficiency in patients with cystic fibrosis. Archives of Disease in Childhood 64, 1151–1156.CrossRefGoogle ScholarPubMed
Reardon, M. C., Hammond, K. B., Accurso, F. J., Fisher, C. D., McCabe, E. R. B., Cotton, E. K. & Bowman, C. M. (1984). Nutritional deficits exist before 2 months of age in some infants with cystic fibrosis identified by screening test. Journal of Pediatrics 105, 271–274.CrossRefGoogle ScholarPubMed
Reiter, E. O., Brugman, S. M., Pike, J. W., Pitt, M., Dokoh, S., Haussler, M. R., Gerstle, R. S. & Taussig, L. M. (1985). Vitamin D metabolites in adolescents and young adults with cystic fibrosis: Effects of sun and season. Journal of Pediatrics 106,21–26.CrossRefGoogle Scholar
Riordan, J. R., Rommens, J. M., Kerem, B.-S., Alon, N., Rozmahel, R., Grzelczak, Z., Zielenski, J., Lok, S., Plavsic, N., Chou, J.-L., Drumm, M. L., Iannuzzi, M. C., Collins, F. S. & Tsui, L.-C. (1989). Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science 245, 1066–1073.CrossRefGoogle ScholarPubMed
Rommens, J. M., Iannuzzi, M. C., Kerem, B.-S., Drumm, M. L., Melmer, G., Dean, M., Rozmahel, R., Cole, J. L., Kennedy, D., Hidaka, N., Zsiga, M., Buchwald, M., Riordan, J. R., Tsui, L.-C., Collins, F. S. (1989). Identification of the cystic fibrosis gene: chromosome walking and jumping. Science 245,1059–1065.CrossRefGoogle ScholarPubMed
Rucker, R. W. & Harrison, G. M. (1973). Vitamin BIZ deficiency in cystic fibrosis. New England JournaI of Medicine 289,289–329.Google Scholar
Russell, R. M., Dutta, S. K., Oaks, E. V., Rosenberg, I. H. & Giovetti, A. C. (1980). Impairment of folic acid absorption by oral pancreatic extracts. Digestive Diseases and Sciences 25, 369–373.CrossRefGoogle ScholarPubMed
Sitrin, M. D., Lieberman, F., Jensen, W. E., Noronha, A., Milbum, C. & Addington, W. (1987). Vitamin E deficiency and neurologic disease in adults with cystic fibrosis. Annals of Internal Medicine 107, 51–54.CrossRefGoogle ScholarPubMed
Sokol, R. J., Reardon, M. C., Accurso, F. J., Stall, C., Narkewicz, M., Abman, S. H. & Hammond, K. B. (1989). Fat-soluble-vitamin status during the first year of life in infants with cystic fibrosis identified by screening of newborns. American Journal of Clinical Nutrition 50, 1064–1071.CrossRefGoogle ScholarPubMed
Soutter, V. L., Kristidis, P., Gruca, M. A. & Gaskin, K. J. (1986). Chronic undernutntiodgrowth retardation in cystic fibrosis. Clinics in Gastroenterology 15, 137–146.CrossRefGoogle ScholarPubMed
Stead, R. J., Muller, D. P. R., Matthews, S., Hodson, M. E. & Batten, J. C. (1986). Effect of abnormal liver function on vitamin E status and supplementation in adults with cystic fibrosis. Gut 27, 714–718.CrossRefGoogle ScholarPubMed
Stead, R. J., Redington, A. N., Hinks, L., Clayton, B., Hodson, M. & Batten, J. C. (1985). Selenium deficiency and possible increased risk of carcinoma in adults with cystic fibrosis. Lancet ii, 862–863.CrossRefGoogle Scholar
Treem, W. R. & Stanley, C. A. (1989). Massive hepatomegaly, steatosis, and secondary plasma carnitine deficiency in an infant with cystic fibrosis. Pediatrics 83, 993–997.CrossRefGoogle Scholar
Underwood, B. A. & Denning, C. R. (1972). Blood and liver concentrations of vitamins A and E in children with cystic fibrosis. Pediatric Research 6, 26–31.CrossRefGoogle Scholar
van Caillie-Bertrand, M., Bieville, F. D. E., Neijens, H., Kerrebijn, K., Fernandes, J. & Degenhart, H. (1982). Trace metals in cystic fibrosis. Acta Paediatrica Scandinavica 71,203–207.CrossRefGoogle ScholarPubMed
Wallach, J. & Garmaise, B. (1979). In Trace Substances in Enviromental Health, pp. 322–324 [Hemphill, D. D., editor]. Columbia: University of Missouri.Google Scholar
Watson, R. D., Cannon, R. A., Kurland, G. S., Cox, K. L. & Frates, R. C. (1985). Selenium responsive myositis during prolonged home total parenteral nutrition in cystic fibrosis. Journal of Parenteral and Enteral Nutrition 9,58–60.CrossRefGoogle ScholarPubMed
Yassa, J. G., Prosser, R. & Dodge, J. A. (1978). Effects of an artificial diet on growth of patients with cystic fibrosis. Archives of Disease in Childhood 53,777–783.CrossRefGoogle ScholarPubMed