Proceedings of the Nutrition Society (1992), 51:225-235 Cambridge University Press

Copyright © The Nutrition Society 1992

doi:10.1079/PNS19920033

Symposium on ‘Cystic Fibrosis’

Nutrition in cystic fibrosis: a historical overview

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [Google Scholar]

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. [OpenURL Query Data]  [Google Scholar]

Andersen, D. H. (1939). Cystic fibrosis of the pancreas, vitamin A deficiency and bronchiectasis. Journal of Pediatrics 15,763–771. [OpenURL Query Data]  [CrossRef]  [Google 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. [OpenURL Query Data]  [PubMed]  [Google Scholar]

Ausiello, D. A. (1990). The regulation of Na⁺ channels by G proteins and phospholipids. Pediatric Pulmonology, Suppl. 5, 135–136. [OpenURL Query Data]  [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. [OpenURL Query Data]  [CrossRef]  [Google 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. [OpenURL Query Data]  [Google Scholar]

Brooks, H. L., Driebe, W. T. & Schemmer, G. G. (1990). Xerophthalmia and cystic fibrosis. Archives of Ophthalmology 108,354–357. [OpenURL Query Data]  [PubMed]  [Google Scholar]

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. [OpenURL Query Data]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [Google 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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

Dodge, J. A. & Yassa, J. G. (1978). Zinc deficiency syndrome in a British youth with cystic fibrosis. British Medical Journal i, 411. [OpenURL Query Data]  [CrossRef]  [Google 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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [CrossRef]  [Google Scholar]

Fanconi, G., Uehlinger, E. & Knauer, C. (1936). Das Coeliaksyndrom bei Angelbosener zystisher Pankreas fibromatose und Bronchiektasien. Weiner Medische Wochenschrift 86,753–756. [OpenURL Query Data]  [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. [OpenURL Query Data]  [PubMed]  [Google Scholar]

Farber, S. (1945). Some organic digestive disturbances in early life. Journal of Michigan State Medical Society 44,487–594. [OpenURL Query Data]  [Google Scholar]

Francis, D. E. M. (1981). Diets for children with cystic fibrosis. Cystic Fibrosis News 16,8–10. [OpenURL Query Data]  [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. [OpenURL Query Data]  [CrossRef]  [Google Scholar]

Green, C. G., Doershuk, C. F. & Stern, R. C. (1985). Symptomatic hypomagnesemia in cystic fibrosis. Journal of Pediatrics 107,425–428. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

Guggino, W. B. & Hwang, T. C. (1990). Regulation of chloride channels in normal and CF airways. Pediatric Pulmonology, Suppl. 5, 1319–1321. [OpenURL Query Data]  [Google Scholar]

Halsted, J. A. & Smith, J. C. (1970). Plasma zinc in health and disease. Lancet i, 322–324. [OpenURL Query Data]  [CrossRef]  [Google 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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

Kraemer, R., Rudeberg, A., Hadorn, B. & Rossi, E. (1978). Relative underweight in cystic fibrosis and its prognostic value. Acta Paediatrica Scandinavica 67,33–37. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

Lloyd-Still, J. D., Bohan, T., Hughes, S. & Wessel, H. V. (1990a). Acyl carnitine is low in cord blood in cystic fibrosis. Acta Paediatrica Scandinavica 79, 427–430. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

Lloyd-Still, J. D. & Ganther, H. E. (1981). Selenium and glutathione peroxidase levels in cystic fibrosis. Pediatrics 65, 1010. [OpenURL Query Data]  [Google Scholar]

Lloyd-Still, J. D., Howars, C. & Wessel, H. (1990b). Carnitine metabolites in infants with CF: a prospective study. Pediatric Pulmonology, Suppl. 5,226 Abstr. [OpenURL Query Data]  [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. [OpenURL Query Data]  [CrossRef]  [Google 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. [OpenURL Query Data]  [PubMed]  [Google Scholar]

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). [OpenURL Query Data]  [Google Scholar]

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. [OpenURL Query Data]  [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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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.

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. [OpenURL Query Data]  [PubMed]  [Google Scholar]

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. [OpenURL Query Data]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google 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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

Rucker, R. W. & Harrison, G. M. (1973). Vitamin BIZ deficiency in cystic fibrosis. New England JournaI of Medicine 289,289–329. [OpenURL Query Data]  [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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [Google Scholar]

Soutter, V. L., Kristidis, P., Gruca, M. A. & Gaskin, K. J. (1986). Chronic undernutntiodgrowth retardation in cystic fibrosis. Clinics in Gastroenterology 15, 137–146. [OpenURL Query Data]  [PubMed]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [Google Scholar]

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. [OpenURL Query Data]  [CrossRef]  [Google 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. [OpenURL Query Data]  [PubMed]  [Google 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. [OpenURL Query Data]  [PubMed]  [Google 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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

Wallach, J. & Garmaise, B. (1979). In Trace Substances in Enviromental Health, pp. 322–324 [Hemphill, D. D., editor]. Columbia: University of Missouri.

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]

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. [OpenURL Query Data]  [PubMed]  [CrossRef]  [Google Scholar]