Literature DB >> 8082362

Body composition analysis by dual-energy x-ray absorptiometry in adults with cystic fibrosis.

T Rochat1, D O Slosman, C Pichard, D C Belli.   

Abstract

Assessment of nutritional status is important in cystic fibrosis (CF). We performed body composition analysis by dual-energy x-ray absorptiometry (DXA) in 12 adults with CF, 7 of them with malnutrition as defined by percentage of ideal body weight (IBW) lower than 90. The DXA allowed for determination of bone body mass (BBM), lean body mass (LBM), and fat body mass (FBM). A deficit in BBM and LBM was found to be present in all seven patients with malnutrition when compared with a group of young normal adults. By contrast, deficit in FBM was inconstant. Deficits in bone and lean were associated with each other. They did not depend on the severity of steatorrhea, but were highly correlated to ventilatory impairment. In conclusion, DXA provides new and potentially useful information on the nutritional status of these patients. In addition, it confirms the close association of malnutrition and lung disease in CF.

Entities:  

Mesh:

Year:  1994        PMID: 8082362     DOI: 10.1378/chest.106.3.800

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  8 in total

1.  Correlates of prepubertal bone mineral density in cystic fibrosis.

Authors:  R H Haslam; D J Borovnicar; D B Stroud; B J Strauss; J E Bines
Journal:  Arch Dis Child       Date:  2001-08       Impact factor: 3.791

2.  Bone mineral content in cystic fibrosis patients: correlation with fat-free mass.

Authors:  F Salamoni; M Roulet; F Gudinchet; M Pilet; D Thiébaud; P Burckhardt
Journal:  Arch Dis Child       Date:  1996-04       Impact factor: 3.791

3.  Normal bone mineral density in cystic fibrosis.

Authors:  D S Hardin; R Arumugam; D K Seilheimer; A LeBlanc; K J Ellis
Journal:  Arch Dis Child       Date:  2001-04       Impact factor: 3.791

4.  Vitamin d deficiency in cystic fibrosis.

Authors:  William B Hall; Amy A Sparks; Robert M Aris
Journal:  Int J Endocrinol       Date:  2010-01-28       Impact factor: 3.257

5.  Adaptation of commensal proliferating Escherichia coli to the intestinal tract of young children with cystic fibrosis.

Authors:  Susana Matamouros; Hillary S Hayden; Kyle R Hager; Mitchell J Brittnacher; Kristina Lachance; Eli J Weiss; Christopher E Pope; Anne-Flore Imhaus; Colin P McNally; Elhanan Borenstein; Lucas R Hoffman; Samuel I Miller
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-29       Impact factor: 11.205

6.  Body composition and pulmonary function in cystic fibrosis.

Authors:  Saba Sheikh; Babette S Zemel; Virginia A Stallings; Ronald C Rubenstein; Andrea Kelly
Journal:  Front Pediatr       Date:  2014-04-15       Impact factor: 3.418

7.  The long term efficacy of gastrostomy feeding in children with cystic fibrosis on anthropometric markers of nutritonal status and pulmonary function.

Authors:  Helen Truby; Patricia Cowlishaw; Catherine O'Neil; Claire Wainwright
Journal:  Open Respir Med J       Date:  2009-09-04

8.  Measures of body habitus are associated with lung function in adults with cystic fibrosis: a population-based study.

Authors:  Doug L Forrester; Alan J Knox; Alan R Smyth; Andrew W Fogarty
Journal:  J Cyst Fibros       Date:  2012-09-05       Impact factor: 5.482

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.