Incorporating genetic potential when evaluating stature in children with cystic fibrosis

Journal of Cystic Fibrosis

Volumn 9, Issue 2, 2010, Pages 135-142

  Zhang, Zhumin ^a   Shoff, Suzanne M ^a   Lai, HuiChuan J ^a,b  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

Cystic fibrosis; Height; Lung function; Parent child relationship; Short stature

Indexed keywords

ANTHROPOMETRIC PARAMETERS; ARTICLE; BODY HEIGHT; CHILD; CHILD DEVELOPMENT; CHILD PARENT RELATION; CLINICAL EVALUATION; CONTROLLED STUDY; CYSTIC FIBROSIS; CYSTIC FIBROSIS FOUNDATION TARGET HEIGHT METHOD; DISEASE CLASSIFICATION; FEMALE; HIMES ADJUSTED HEIGHT METHOD; HUMAN; INTERMETHOD COMPARISON; LUNG FUNCTION; MAJOR CLINICAL STUDY; MALE; MATURATION; PREVALENCE; PUBERTY; SCHOOL CHILD; SHORT STATURE; TALL STATURE;

ADOLESCENT; BODY HEIGHT; CHILD; CHILD, PRESCHOOL; CYSTIC FIBROSIS; FEMALE; GROWTH DISORDERS; HUMANS; LUNG; MALE; PARENTS; PREVALENCE; REGISTRIES;

EID: 76749144531     PISSN: 15691993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcf.2010.01.003     Document Type: Article

References (23)

1. Foundation C.F. National Cystic Fibrosis Patients Registry Annual Data Report, 2004 (2005), Bethesda, MD
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 164 (2005) 781-782
3. Lai H.J. Classification of nutritional status in cystic fibrosis. Curr Opin Pulm Med 12 (2006) 422-427
4. Tanner J.M., Goldstei H., and Whitehou Rh. Standards for childrens height at ages 2-9 years allowing for height of parents. Arch Dis Child 45 (1970) 755-762
5. Wingerd J., Solomon I.L., and Schoen E.J. Parent-specific height standards for preadolescent children of 3 racial groups, with methods for rapid determination. Pediatrics 52 (1973) 555-560
6. Roche A.F., Himes J.H., and Thissen D. Parent-specific adjustments for assessment of recumbent length and stature. Monogr Paediatr 13 (1981)
7. Falkner F., and Tanner J.M. Human growth. second edition 3 (1986), Plenum Press, New York 104-107
8. Himes J.H., Roche A.F., Thissen D., and Moore W.M. Parent-specific adjustments for evaluation of recumbent length and stature of children. Pediatrics 75 (1985) 304-313
9. Sorva R., Tolppanen E.M., Lankinen S., and Perheentupa J. Growth evaluation: parent and child specific height standards. Arch Dis Child 64 (1989) 5
10. Borowitz D., Baker R.D., and Stallings V. Consensus report on nutrition for pediatric patients with cystic fibrosis. J Pediatr Gastroenterol Nutr 35 (2002) 246-259
11. Kuczmarski R.J., Ogden C.L., Guo S.S., et al. 2000 CDC Growth Charts for the United States: methods and development. Vital Health Stat Ser 11 (2002) 1-190
12. Roche A.F. Growth, maturation, and body composition: the Fels Longitudinal Study 1929-1991 (1992), Cambridge university Press, Cambridge, United Kingdom
13. FitzSimmons S.C. The changing epidemiology of cystic fibrosis. J Pediatr 122 (1993) 1-9
14. Wang X., Dockery D.W., Wypij D., Fay M.E., and Ferris Jr. B.G. Pulmonary function between 6 and 18 years of age. Pediatr Pulmonol 15 (1993) 75-88
15. Fleiss J.L. Statistical methods for rates and proportions (1981), John Wiley and Sons, New York
16. Landis J.R., and Koch G.G. The measurement of observer agreement for categorical data. Biometrics 33 (1977) 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., and Shoff S. Classification of malnutrition in cystic fibrosis: implications on evaluating and benchmarking clinical practices. Am J Clin Nutr 88 (2008) 161-166
19. Schechter M.S., and Margolis P. Improving subspecialty healthcare: lessons from cystic fibrosis. J Pediatr 147 (2005) 295-301
20. Acton J.D., and Kotagal U. Improvements in healthcare: how can we change outcome?. J Pediatr 147 (2005) 279-281
21. Stallings V.A., Stark L.J., Robinson K.A., Feranchak A.P., and 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 108 (2008) 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 J.H., Roche A.F., and Thissen D. Parent-specific adjustments for assessment of recumbent length and stature. Monogr Paediatr 13 (1981) 1-81