165
Views
9
CrossRef citations to date
0
Altmetric
Original Article

Growth and nutritional status in children and adolescents with cystic fibrosis

&
Pages 145-153 | Received 02 Nov 2006, Accepted 22 Nov 2007, Published online: 09 Jul 2009

References

  • Bell SC, Shepherd RW. Optimising nutrition in cystic fibrosis. J Cyst Fibros 2002; 1: 47–50
  • Beker L, Russek-Cohen E, Fink R. Stature as a prognostic factor in cystic fibrosis survival. J Am Dietetic Assoc 2001; 101: 438–442
  • Bożkowa K, Siwińska-Gołębiowska H, Rutkowski J, Nowakowska A. Epidemiologia mukowiscydozy u dzieci w Polsce. Pediatria Polska 1971; 46: 677–684
  • Bożkowa K, Cichy W, Jarosz J, Książyk J, Łukasik M, Mazurczak T, Milanowski A, Nowakowska A, Orlik T, Pawlik J, Piotrowski R, Pogorzelski A, Prusak J, Sands D, Skorupa W, Stolarczyk A, Teysseire M, Walkowiak J, Wierzbicka M, Witt M, Żebrak J. Zasady rozpoznawania i leczenia mukowiscydozę. Standardy Medyczne 2002; 2: 29–36
  • Bucuvalas JC, Chernausek SD. Growth hormone and cystic fibrosis: good for more than growth?. J Pediatr 2001; 139: 616–618
  • Byard PJ. The adolescent growth spurt in children with cystic fibrosis. Ann Hum Biol 1994; 21: 229–240
  • Charzewski J, Łaska-Mierzejewska T, Piechaczek H, Łukaszewska I. Age at menarche of Warsaw girls 1986–1997. Phys Educ Sport 1998; 1: 61–67
  • Cole T, Bellizzi MC, Flegal KM, Dietz WH. Establishing a standard definition for child overweight and obesity worldwide: international survey. BMJ 2000; 320: 1240–1243
  • Collins CL, MacDonald-Wicks L, Rowe S, O’Loughlin EV, Henry R. Normal growth in cystic fibrosis associated with a specialized centre. Arch Dis in Child 1999; 81: 241–246
  • Colombo C, Battezzati A. Growth failure in cystic fibrosis: a true need for anabolic agents?. J Pediatr 2004; 146: 303–305
  • Galli-Tsinopoulou A, Moudiou T, Mamopulos A, Karamouzis M, Nousia-Arvanitakis S. Multifollicular ovaries in female adolescents with cystic fibrosis. Fertil Steril 2006; 85: 1484–1487
  • Grabowska J, Łuczak B. Rozwój biologiczny dzieci i młodzieży chorych na mukowiscydozę. Antropologia a medycyna i promocja zdrowia 1996; 1: 142–154
  • Haeusler G, Frisch H, Waldhor T, Gotz M. Perspectives of longitudinal growth in cystic fibrosis from birth to adult age. Eur J Pediatr 1994; 153: 158–163
  • Hubert D. Mucoviscidose. EMC-Medecine 2005; 2: 34–41
  • Johannes H, Nir M, Hobby N, Koch Ch, Schwarz M. Severity of cystic fibrosis in patients homozygous and heterozygous for Δ508 mutations. Lancet 1991; 337: 631–634
  • Johannesson M, Gottlieb C, Hjelte L. Delayed puberty in girls with cystic fibrosis despite good clinical status. Pediatrics 1997; 99: 29–34
  • Johannesson M, Carlson M, Bergsten Brucefors A, Hjelte L. Cystic fibrosis through a female perspective: Psychosocial issues and information concerning puberty and motherhood. Patient Educ Couns 1998; 34: 115–123
  • Kerem E, Corey M, Kerem B, Rommens J, Markiewicz D, Levison H, Tsui L, Durie P. The relation between genotype and phenotype in cystic fibrosis – analysis of the most common mutation (Δ508). N Engl J Med 1990; 323: 1517–1522
  • Kosińska M, Szwed A, Cieślik J, Goździk J, Karbowy K. Assessment of the biological condition and nutritional status of adult patients with cystic fibrosis. Anthropol Rev 2005; 68: 53–64
  • Kurniewicz-Witczakowa R, Mięsowicz I, Niedźwiedzka Z, Kopczyńska-Sikorska J. Kryteria antropologiczne w ocenie prawidłowego rozwoju dziecka oraz w wybranych zespołach klinicznych. Anthropol Rev 1976; 62: 281–289
  • Lai H-Ch, Corey M, Simmons S, Kosorek M, Farrell F. Comparison of growth status of patients with cystic fibrosis between the United States and Canada. Am J Clin Nutr 1999; 69: 531–538
  • Laursen EM, Koch C, Petersen JH, Muller J. Secular changes in anthropometric data in cystic fibrosis patients. Acta Paediatrica 1999; 88: 169–174
  • Łaska-Mierzejewska T, Olszewska E. Antropologiczna ocena zmian rozwarstwienia społecznego populacji wiejskiej w Polsce w okresie 1967–2001. 2003, Badania dziewcząt. AWF w Warszawie
  • Mahaney MC, McCox KS. Developmental delays and pulmonary disease severity in cystic fibrosis. Hum Biol 1986; 58: 445–460
  • Małecka-Tendera E. Postępy endokrynologii wieku rozwojowego w 2003 roku. Medycyna Praktyczna 2004; 2: 82–86
  • Martin R, Saller K. Lehrbuch der Anthropologie 1957–1959, Stuttgart: G. Fischer
  • Martinez SM, Preece MA, Grant DB. Body proportions in precocious puberty. Acta Paediatrica Scandinaviensis 1984; 73: 185–188
  • McKone EF, Emerson SS, Edwards KL, Ajtken ML. Effect of genotype on phenotype and mortality in cystic fibrosis: A retrospective cohort study. Lancet 2003; 361: 1671–1676
  • Mei Z, Grummer-Strawn LM, Pietrobelli A, Goulding A, Goran MI, Dietz WH. Validity of body mass index compared with other body-composition screening indexes for the assessment of body fatness in children and adolescents. Am J Clin Nutr 2002; 75: 978–985
  • Morison S, Dodge JA, Cole TJ, Lewis PA, Coles EC, Geddes D, Russell G, Littlewood J, Scott MT. Height and weight in cystic fibrosis: a cross sectional study. Arch Dis Child 1997; 77: 497–500
  • Nir M, Lanng S, Johansen H, Koch Ch. Long term survival and nutritional data in patients with cystic fibrosis treated in a Danish centre. Thorax 1996; 51: 1023–1027
  • Nowakowska A, Bal J, Obersztyn E, Sands D, Maciejko D, Mazurczak T. Próba zależności pomiędzy fenotypem a genotypem wśród 65 chorych na mukowiscydozę. Pediatria Polska 1995; 70: 633–638
  • Palczewska I, Niedźwiedzka Z. Wskaźniki rozwoju somatycznego dzieci i młodzieży warszawskiej. Medycyna Wieku Rozwojowego 2001; 5: 19–55
  • Penesar S. Could growth retardation in cystic fibrosis be partly due to deficient steroid and thyroid hormonogenesis?. Med Hypotheses 1999; 53: 530–532
  • Pogorzelski A, Piotrowski R, Witt M, Bal J, Żebrak J, Nowakowska A, Milanowski A, Sobczyńska-Tomaszewska A, Rutkiewicz E. Charakterystyka kliniczna polskich chorych na mukowiscydozę z mutacją 2001, 3849+10kbc→T w obrębie genu CFTR. Pediatria Polska 76:573–577
  • Sharma R, Florea V, Bolger A, Doehner W, Florea N, Coats A, Hodson M, Anker S, Henein M. Wasting as an independent predictor of mortality in patients with cystic fibrosis. Thorax 2001; 56: 746–750
  • Shepherd R. Achieving genetic potential for nutrition and growth in cystic fibrosis. J Pediatr 2002; 140: 393–395
  • Sinaasappel M, Stern M, Littelwood J, Wolfe S, Steinkamp G, Heijerman H, Robberecht E, Shepherd R. Achieving genetic potential for nutrition and growth in cystic fibrosis. J Pediatr 2002; 140: 393–395
  • Stallings V, Tomezsko JL, Schall JI, Mascarenhas MR, Stettler N, Scanlin TF, Zemel BS. Adolescent development and energy expenditure in females with cystic fibrosis. Clin Nutr 2005; 24: 737–745
  • Szczepanik M, Krawczyński M, Cichy W, Walkowiak J. Rozwój fizyczny dzieci z mukowiscydozą z województwa wielkopolskiego. Pediatria Praktyczna 2000; 8: 397–410
  • Wales JKH, Herber SM, Taitz LS. Height and body proportions in child abuse. Arch Dis Child 1992; 67: 632–635
  • Walkowiak J. Stan odżywienia i rozwój fizyczny dzieci chorych na mukowiscydozę w świetle podstawowych wskaźników wagowych i wzrostowych. Przegląd Pediatryczny 1998; 28: 208–212
  • Zhang Z, Lai HJ. Comparison of the use of body mass index percentiles and percentage of ideal body weight to screen for malnutrition in children with cystic fibrosis. Am J Clin Nutr 2004; 80: 982–991

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.