Literature DB >> 1458303

Cystic fibrosis: nutrition.

P R Durie1, P B Pencharz.   

Abstract

There has been renewed interest in examining the multiple causes of undernutrition and growth failure in cystic fibrosis. It is now recognized that undernutrition is caused by unfavourable energy balance rather than an inherent component of the disease. Furthermore, there appears to be a direct association between the degree of undernutrition and the severity of pulmonary disease, which in turn affects overall prognosis. Energy imbalance may be caused by three main factors: increased energy loss because of nutrient maldigestion; reduced energy intake due to an improper diet and/or anorexia from respiratory disease, abdominal symptoms or clinical depression and increased energy expenditure with advanced lung disease. Most patients are capable of compensating for these factors; provided energy intake is sufficient, normal growth velocity and nutritional status is maintained. However, in a minority of older patients, when advanced lung disease supervenes, energy expenditure rises resulting in an energy deficit. Undernutrition, with loss of energy stores and lean tissue may in turn contribute to progressive deterioration of lung function. When this occurs, long-term invasive methods of nutritional support can restore energy balance.

Entities:  

Mesh:

Year:  1992        PMID: 1458303     DOI: 10.1093/oxfordjournals.bmb.a072580

Source DB:  PubMed          Journal:  Br Med Bull        ISSN: 0007-1420            Impact factor:   4.291


  9 in total

1.  Normal growth in cystic fibrosis associated with a specialised centre.

Authors:  C E Collins; L MacDonald-Wicks; S Rowe; E V O'Loughlin; R L Henry
Journal:  Arch Dis Child       Date:  1999-09       Impact factor: 3.791

2.  Perceived body image and eating behavior in young adults with cystic fibrosis and their healthy peers.

Authors:  J Abbott; S Conway; C Etherington; J Fitzjohn; L Gee; A Morton; H Musson; A K Webb
Journal:  J Behav Med       Date:  2000-12

3.  Percutaneous endoscopic gastrostomy feeding in patients with cystic fibrosis.

Authors:  S G Williams; F Ashworth; A McAlweenie; S Poole; M E Hodson; D Westaby
Journal:  Gut       Date:  1999-01       Impact factor: 23.059

Review 4.  Early and late outcome of cystic fibrosis screening.

Authors:  M R Green; L T Weaver
Journal:  J R Soc Med       Date:  1994       Impact factor: 5.344

Review 5.  Nutritional management of cystic fibrosis.

Authors:  A MacDonald
Journal:  Arch Dis Child       Date:  1996-01       Impact factor: 3.791

6.  Clinical outcome in relation to care in centres specialising in cystic fibrosis: cross sectional study.

Authors:  R Mahadeva; K Webb; R C Westerbeek; N R Carroll; M E Dodd; D Bilton; D A Lomas
Journal:  BMJ       Date:  1998-06-13

Review 7.  Cystic fibrosis in adults. From researcher to practitioner.

Authors:  G P Marelich; C E Cross
Journal:  West J Med       Date:  1996-04

8.  Elevated incidence of dental caries in a mouse model of cystic fibrosis.

Authors:  Marcelo A Catalán; Kathleen Scott-Anne; Marlise I Klein; Hyun Koo; William H Bowen; James E Melvin
Journal:  PLoS One       Date:  2011-01-31       Impact factor: 3.240

9.  Improvement of nutrient absorption may enhance systemic oxidative stress in cystic fibrosis patients.

Authors:  G V Shmarina; A L Pukhalsky; S N Kokarovtseva; D A Pukhalskaya; E A Kalashnikova; N I Kapranov; N J Kashirskaja
Journal:  Mediators Inflamm       Date:  2001-04       Impact factor: 4.711

  9 in total

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