Overweight and Obesity in Patients With Cystic Fibrosis: A Center-Based Analysis

被引:69
作者
Hanna, Reem M. [1 ]
Weiner, Daniel J. [1 ]
机构
[1] UPMC, Childrens Hosp Pittsburgh, Dept Pediat, Div Pulm Med Allergy & Immunol, Pittsburgh, PA USA
关键词
pancreatic insufficiency; nutritional status; lung function; cystic fibrosis; NUTRITIONAL-STATUS; LUNG-FUNCTION; CLINICAL-PRACTICE; CHILDREN; PREVALENCE; CHILDHOOD; SURVIVAL; COHORT; ADULTS; TRENDS;
D O I
10.1002/ppul.23033
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
ObjectiveCystic fibrosis (CF) has long been associated with malnutrition. However, due to early diagnosis, nutritional supplements, and increased prevalence of obesity in the general population, overweight, and obesity in the CF patient population is becoming a concern. The aim of this study was to determine the prevalence of obesity and overweight in patients with CF seen at our center, to analyze factors associated with nutritional status, to evaluate the relation between nutritional status and lung function, and to document any adverse health outcomes. MethodsThe CF Patient Registry was queried for patients aged 2-18 who were seen at our center between June 2011 and June 2012. Nutritional statuses of patients were classified in accordance with the CF Foundation guidelines. Analysis of variance was utilized to analyze the differences in lung function between the five weight status groups. ResultsOf the 226 patients with CF aged 2-18 years, 129 (57%) had a BMI percentile consistent with a healthy weight status, 16 (7%) were in nutritional failure, 28 (12%) were at risk of nutritional failure, 35 (15%) were overweight, and 18 (8%) were obese. Based on fecal elastase levels, 50% of the overweight patients and 20% of the obese patients were pancreatic insufficient. FEV1 % predicted was lowest in patients with nutritional failure (P=0.005). No significant differences were noted between the other four weight groups. In our obese and overweight population, three patients have impaired glucose tolerance, one has CF-related diabetes (CFRD) with fasting hyperglycemia, three have hypertension, and one has obstructive sleep apnea (OSA). ConclusionsThe prevalence of overweight and obesity in our CF center is noteworthy, and a significant number of the patients were pancreatic insufficient. In our patient population, overweight, and obesity were not associated with further improvement of lung function. Nutritional approaches need to address the adverse outcomes of overweight and obesity. Pediatr Pulmonol. 2015; 50:35-41. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:35 / 41
页数:7
相关论文
共 21 条
[11]   Clinical Care Guidelines for Cystic Fibrosis-Related Diabetes A position statement of the American Diabetes Association and a clinical practice guideline of the Cystic Fibrosis Foundation, endorsed by the Pediatric Endocrine Society [J].
Moran, Antoinette ;
Brunzell, Carol ;
Cohen, Richard C. ;
Katz, Marcia ;
Marshall, Bruce C. ;
Onady, Gary ;
Robinson, Karen A. ;
Sabadosa, Kathryn A. ;
Stecenko, Arlene ;
Slovis, Bonnie .
DIABETES CARE, 2010, 33 (12) :2697-2708
[12]  
Ogden CL, 2012, JAMA-J AM MED ASSOC, V307, P483, DOI [10.1001/jama.2012.39, 10.1001/jama.2012.40]
[13]   Physiology of obesity and effects on lung function [J].
Salome, Cheryl M. ;
King, Gregory G. ;
Berend, Norbert .
JOURNAL OF APPLIED PHYSIOLOGY, 2010, 108 (01) :206-211
[14]  
Sinaasappel M, 2002, J Cyst Fibros, V1, P51, DOI 10.1016/S1569-1993(02)00032-2
[15]   Birth prevalence and survival in cystic fibrosis - A national cohort study in the Netherlands [J].
Slieker, MG ;
Uiterwaal, CSPM ;
Sinaasappel, M ;
Heijerman, HGM ;
van der Laag, J ;
van der Ent, CK .
CHEST, 2005, 128 (04) :2309-2315
[16]   Overweight, ethnicity, and the prevalence of hypertension in school-aged children [J].
Sorof, JM ;
Lai, DJ ;
Turner, J ;
Poffenbarger, T ;
Portman, RJ .
PEDIATRICS, 2004, 113 (03) :475-482
[17]   Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: Results of a systematic review [J].
Stallings, Virginia A. ;
Stark, Lori J. ;
Robinson, Karen A. ;
Feranchak, Andrew P. ;
Quinton, Hebe .
JOURNAL OF THE AMERICAN DIETETIC ASSOCIATION, 2008, 108 (05) :832-839
[18]   Relationship between nutritional status and lung function in cystic fibrosis: cross sectional and longitudinal analyses from the German CF quality assurance (CFQA) project [J].
Steinkamp, G ;
Wiedemann, B .
THORAX, 2002, 57 (07) :596-601
[19]  
Stephenson AL1, 2013, AM J CLIN NUTR, V97, P872, DOI [10.3945/ajcn.112.051409, DOI 10.3945/AJCN.112.051409.]
[20]   Obesity and Metabolic Syndrome and Functional and Structural Brain Impairments in Adolescence [J].
Yau, Po Lai ;
Castro, Mary Grace ;
Tagani, Adrian ;
Tsui, Wai Hon ;
Convit, Antonio .
PEDIATRICS, 2012, 130 (04) :E856-E864