Biological status of adult patients with cystic fibrosis

Journal of Physiology and Pharmacology

Volumn 59, Issue SUPPL. 6, 2008, Pages 341-348

  Kosinska, M ^a,c   Szwed, A ^a   Cieslik, J ^a   Gozdzik, J ^b   Cofta, S ^b  

^a ADAM MICKIEWICZ UNIVERSITY   (Poland)

^b POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

^c NONE   (Poland)

Author keywords

Cole index; Developmental retardation; Mutation; Nutrition

Indexed keywords

ADULT; ARTICLE; CONTROL GROUP; CONTROLLED STUDY; CYSTIC FIBROSIS; FEMALE; GROWTH RETARDATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MALNUTRITION; MUTATION; NUTRITIONAL STATUS; POPULATION; WEIGHT REDUCTION; ADOLESCENT; ANTHROPOMETRY; BODY MASS; DISEASE COURSE; PATHOPHYSIOLOGY; PHYSIOLOGY; REGRESSION ANALYSIS;

ADOLESCENT; ADULT; ANTHROPOMETRY; BODY MASS INDEX; CYSTIC FIBROSIS; DISEASE PROGRESSION; FEMALE; HUMANS; MALE; MALNUTRITION; NUTRITIONAL STATUS; REGRESSION ANALYSIS; YOUNG ADULT;

EID: 64549117795     PISSN: 08675910     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (26)

1. Kerem E, Corey M, Kerem B et al. The relation between genotype and phenotype in cystic fibrosis - analysis of the most common mutation (AF508). New Engl J Med 1990; 323: 1517-1522.
2. Strandvik B. Nutritional management of cystic fibrosis. Annales Nestle 1991, 49: 38-46.
3. Corey M, McLaughlin FJ, Williams M, Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol 1988; 41: 583-591.
4. Lai HC, Corey M, Fitzsimmons SC, Kosorok MR, Farrel PM. Comparison of growth status of patients with cystic fibrosis between the United States and Canada. Amer J Clin Nutr 1999; 69:531-538.
5. Rosenfeld M, Davis R, Fitzsimmons S, Pepe M, Ramsey B. Gender gap in cystic fibrosis mortality. Am J Epidemiol 1997; 145: 794-803.
6. Hayllar KM, Williams SG, Wise AE et al. A prognostic model for the prediction of survival in cystic fibrosis. Thorax 1997; 52: 313-317.
7. Corey M, Farewell V. Determinants of mortality from cystic fibrosis in Canada 1970-1989. Am J Epidemiol 1995; 143: 1007-1017.
8. Byard P. Early childhood growth in patients with cystic fibrosis. Ann Hum Biol 1990; 17: 483-499.
9. Landon C, Rosenfeld RG. Short stature and pubertal delay in male adolescents with cystic fibrosis. Am J Dis Child 1984; 138: 388-391.
10. Muller AE, Thamm B, Lietz T, Handrick W, Walter S. Cystic fibrosis: a cause of reduced birth weight? Eur J Pediatr 1999; 158: 264.
11. Kosinska M, Szwed A, Cieslik J, Gozdzik J, Karbowy K. Assessment of the biological condition and nutritional status of adult patients with cystic fibrosis. Anthropol Rev 2005; 68: 53-64.
12. Martin R, Saller K. Lehrbuch der Anthropologie. G. Fischer Verlag, 1957-59, Stuttgart.
13. Cieslik J, Kaczmarek M, Kaliszewska-Drozdowska MD. Dziecko Poznanskie '90. Bogucki Publishing House, Poznan, 1994 (in Polish).
14. Grabowska J, Luczak B. Biological development of children and youths suffering from mucoviscidosis. In Anthropology, Medicine, and Heath Promotion. A Malinowski (ed), Lodz, 1996, pp. 142-154 (in Polish).
15. Ryzko J. Assessment of nutrition status in children. Przeglqd Pediatryczny 1997; 27: 27-30 (in Polish).
16. Mearns MB. Growth and Development. In Cystic Fibrosis. M Hodson, AP Norman, JC Batten (eds), London, Bailliere Tindall, 1983, pp. 183-196.
17. Shepherd R, Holt TL, Thomas BJ, Kay L et al. Nutritional rehabilitation in cystic fibrosis: controlled studies of effects on nutritional growth retardation, body protein turnover, and course of pulmonary disease. J Pediatr 1986; 109: 788-794.
18. Sing CF, Risser DR, Howatt WF, Ericson RP. Phenotypic heterogeneity in cystic fibrosis. Am J Genet 1982; 13: 179-195.
19. Mahaney MC, McCoy KS. Developmental delays and pulmonary disease severity in cystic fibrosis. Hum Biol 1986; 58: 445-460.
20. Corey M, McLaughlin FJ, Williams M, Levison H. A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol 1982; 41: 583-591.
21. Barkhouse LB, Fahey J, Gillespie CT, Cole DE. Quantitating the effect of cystic fibrosis on linear growth by mathematic modelling of longitudinal growth curves. Growth Dev Aging 1989;53: 185-190.
22. Borbel P, Doctter G. Effect of continuous dietary advice on nutrient intake and nutrition status, 21 European Cystic Fibrosis Conference, June 1997, Davos, Switzerland; Abstracts 170.
23. Nowakowska A, Bal J, Obersztyn E, Sands D, Maciejko D, Mazurczak T. An attempt to assess the relationship between phenotype and genotype among 65 patients with mucoviscidosis. Ped Pol 1995; 8: 633-638 (in Polish).
24. Bentur L, Kalnins D, Levison D, Corey M, Durie PR. Dietary intakes of young children with cystic fibrosis: is there a difference? J Pediatr Gastroenterol Nutr 1996; 22: 254-258.
25. Richardson I, Nyulasi I, Cameron K, Ball M, Wilson J. Nutritional status of an adult cystic fibrosis population. Nutrition 2000; 16: 255-259.
26. Kostuch M, Wojcierowski J. Mucoviscidosis. Klinika Pediatryczna 1995; 4: 69-73.