Journal of Cystic Fibrosis
Volume 9, Issue 2 , Pages 135-142 , March 2010

Incorporating genetic potential when evaluating stature in children with cystic fibrosis

  • Zhumin Zhang

      Affiliations

    • Department of Nutritional Sciences, University of Wisconsin, Madison, Wisconsin, United States
  • ,
  • Suzanne M. Shoff

      Affiliations

    • Department of Nutritional Sciences, University of Wisconsin, Madison, Wisconsin, United States
  • ,
  • HuiChuan J. Lai

      Affiliations

    • Department of Nutritional Sciences, University of Wisconsin, Madison, Wisconsin, United States
    • Department of Pediatrics, University of Wisconsin, Madison, Wisconsin, United States
    • Department of Biostatistics and Medical Informatics, University of Wisconsin, Madison, Wisconsin, United States
    • Corresponding Author InformationCorresponding author. Department of Nutritional Sciences, 1415 Linden Drive, Madison, WI 53706, United States. Tel.: +1 608 262 9972; fax: +1 608 262 5860.

Received 3 July 2009 ,Revised 11 January 2010 ,Accepted 13 January 2010.

References 

  1. Foundation Cystic Fibrosis. National Cystic Fibrosis Patients Registry Annual Data Report, 2004. Bethesda, MD; 2005;
  2. Arrigo T, DeLuca F, Sferlazzas C, et al. Young adults with cystic fibrosis are shorter than healthy peers because their parents are also short. Eur J Pediatr. 2005;164:781–782
  3. Lai HJ. Classification of nutritional status in cystic fibrosis. Curr Opin Pulm Med. 2006;12:422–427
  4. Tanner JM, Goldstei H, Whitehou Rh. Standards for childrens height at ages 2–9years allowing for height of parents. Arch Dis Child. 1970;45:755–762
  5. Wingerd J, Solomon IL, Schoen EJ. Parent-specific height standards for preadolescent children of 3 racial groups, with methods for rapid determination. Pediatrics. 1973;52:555–560
  6. Roche AF, Himes JH, Thissen D. Parent-specific adjustments for assessment of recumbent length and stature. Monogr Paediatr. 1981;13:
  7. Falkner F, Tanner JM. In: second edition. Human growth. 3:New York: Plenum Press; 1986;p. 104–107
  8. Himes JH, Roche AF, Thissen D, Moore WM. Parent-specific adjustments for evaluation of recumbent length and stature of children. Pediatrics. 1985;75:304–313
  9. Sorva R, Tolppanen EM, Lankinen S, Perheentupa J. Growth evaluation: parent and child specific height standards. Arch Dis Child. 1989;64:5
  10. Borowitz D, Baker RD, Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr. 2002;35:246–259
  11. Kuczmarski RJ, Ogden CL, Guo SS, et al. 2000 CDC Growth Charts for the United States: methods and development. Vital Health Stat Ser. 2002;11:1–190
  12. Roche AF. Growth, maturation, and body composition: the Fels Longitudinal Study 1929–1991. Cambridge, United Kingdom: Cambridge university Press; 1992;
  13. FitzSimmons SC. The changing epidemiology of cystic fibrosis. J Pediatr. 1993;122:1–9
  14. Wang X, Dockery DW, Wypij D, Fay ME, Ferris BG. Pulmonary function between 6 and 18years of age. Pediatr Pulmonol. 1993;15:75–88
  15. Fleiss JL. Statistical methods for rates and proportions. New York: John Wiley and Sons; 1981;
  16. Landis JR, Koch GG. The measurement of observer agreement for categorical data. Biometrics. 1977;33:159–174
  17. Merrill RM, Richardson. Validity of self-reported height, weight, and body mass index: findings from the National Health and Nutrition Examination Survey, 2001–2006. Prev Chronic Dis 2009;6(4). http://www.cdc.gov/pcd/issues/2009/oct/08_0229.htm.
  18. Lai H, Shoff S. Classification of malnutrition in cystic fibrosis: implications on evaluating and benchmarking clinical practices. Am J Clin Nutr. 2008;88:161–166
  19. Schechter MS, Margolis P. Improving subspecialty healthcare: lessons from cystic fibrosis. J Pediatr. 2005;147:295–301
  20. Acton JD, Kotagal U. Improvements in healthcare: how can we change outcome?. J Pediatr. 2005;147:279–281
  21. Stallings VA, Stark LJ, Robinson KA, Feranchak AP, Quinton H. Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review. J Am Diet Assoc. 2008;108:832–839
  22. U.S. Census Bureau. Population estimates Program. Race and Hispanic origin in 2005. http://www.census.gov/population/pop-profile/dynamic/RACEHO.pdf.
  23. Himes JH, Roche AF, Thissen D. Parent-specific adjustments for assessment of recumbent length and stature. Monogr Paediatr. 1981;13:1–81

PII: S1569-1993(10)00007-X

doi: 10.1016/j.jcf.2010.01.003

Journal of Cystic Fibrosis
Volume 9, Issue 2 , Pages 135-142 , March 2010