The influence of body composition on respiratory muscle, lung function and diaphragm thickness in adults with cystic fibrosis

Journal of Cystic Fibrosis

Volumn 6, Issue 6, 2007, Pages 384-390

  Enright, Stephanie ^a   Chatham, Ken ^b   Ionescu, Alina A ^d   Unnithan, Viswanath B ^c   Shale, Dennis J ^d  

^a CARDIFF UNIVERSITY   (United Kingdom)

^b LLANDOUGH HOSPITAL   (United Kingdom)

^c LIVERPOOL HOPE UNIVERSITY   (United Kingdom)

^d UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

Body composition; Cystic fibrosis; Diaphragm thickness

Indexed keywords

ACTION POTENTIAL; ADULT; ARTICLE; BODY COMPOSITION; BODY WEIGHT; BREATHING MUSCLE; CLINICAL ARTICLE; CONTROLLED STUDY; CYSTIC FIBROSIS; DIAPHRAGM; DUAL ENERGY X RAY ABSORPTIOMETRY; ECHOGRAPHY; FEMALE; FORCED EXPIRATORY VOLUME; FUNCTIONAL RESIDUAL CAPACITY; HUMAN; INSPIRATORY CAPACITY; LUNG FUNCTION; LUNG FUNCTION TEST; LUNG VOLUME; MALE; MUSCLE STRENGTH; PHYSICAL ACTIVITY; TOTAL LUNG CAPACITY; WORK CAPACITY;

ADIPOSE TISSUE; ADOLESCENT; ADULT; BODY COMPOSITION; CYSTIC FIBROSIS; FEMALE; HUMANS; MALE; RESPIRATION; RESPIRATORY FUNCTION TESTS; RESPIRATORY MUSCLES;

EID: 35748963836     PISSN: 15691993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jcf.2007.02.006     Document Type: Article

References (49)

1. Kalivianakis M., Minich D.M., Bijleveld C., et al. Fat malabsorption in cystic fibrosis patients receiving enzyme replacement therapy is due to impaired intestinal uptake of long-chain fatty acids. Am J Clin Nutr 69 (1999) 127-134
2. Hallberg K., Grzegorczyk A., Larson G., and Strandvik B. Intentilal permeability in cystic fibrosis in relation to genotype. J Pediatr Gastroenterol Nutr 25 3 (1997) 290-295
3. Shoff S., Ahn H.Y., Davis L., Lai H., and Winconsin Neonatal Screening Group. Temporal associations among energy intake, plasma linoleic acid, and growth improvement in response to treatment initiation after diagnosis in cystic fibrosis. Pediatrics 117 2 (2006) 391-400
4. Dorlöchter L., Røksund O., Helgheim V., Rosendahl, and Fluge G. Resting energy expenditure and lung disease in cystic fibrosis. J Cyst Fibros 1 (2002) 131-136
5. Marin V.B., Velandia S., Hunter B., et al. Energy expenditure, nutritional status, and body composition in children with cystic fibrosis. Nutrition 20 (2004) 181-186
6. Ionescu A.A., Nixon L.S., Evans W.D., Stone M.D., Lewis-Jenkins V., Chatham K., et al. Bone density, body composition, and inflammatory status in cystic fibrosis. Am J Respir Crit Care Med 162 (2000) 789-794
7. Hart N., Tounian A., Clement A., Boule M., Polkey, and Lofanso F. Nutritional status is an important predictor of diaphragm strength in young patients with cystic fibrosis. Am J Clin Nutr 80 (2004) 1201-1206
8. Ionescu A.A., Nixon L.S., Luzio S., Lewis-Jenkins V., Evans W.D., Stone M.D., et al. Pulmonary function, body composition, and protein metabolism in adults with cystic fibrosis. Am J Respir Crit Care Med 165 (2001) 495-500
9. Nixon P.A., Orenstein D.M., and Kelsey S.F. Habitual physical activity in children and adolescents with cystic fibrosis. Med Sci Sports Exerc 33 1 (2001) 30-35
10. Sharma R., Florea V.G., Bolger A.P., Doehner W., Florea N.D., Coates A.J., et al. Wasting as an independent predictor of mortality in patients with cystic fibrosis. Thorax 56 (2001) 746-750
11. Pinet C., Cassart M., Scillia P., Lamotte M., Knoop C., Casimer G., et al. Function and bulk of respiratory and limb muscles in patients with cystic fibrosis. Am J Respir Crit Care Med 168 (2003) 989-994
12. Pinet C., Scillia P., Cassart M., Lamotte M., Knoop C., Melot C., et al. Preferential reduction of quadriceps over respiratory muscle strength and bulk after lung transplantation for cystic fibrosis. Thorax 59 (2004) 783-789
13. Lands L.C., Heigenhauser G.J., and Jones N.L. Respiratory and peripheral muscle function in cystic fibrosis. Am Rev Respir Dis 147 (1993) 865-869
14. Aldritch T.K., and Spiro P. Maximal inspiratory pressure: does reproducibility indicate full effort?. Thorax 50 1 (1995) 40-43
15. Wahner H.W., and Fogelman I. The evaluation of osteoporosis: dual X-ray absorptiometry in clinical practice (1993), Martin Duunitz, London
16. Van Etten L.M., Verstappen F.T., and Westerterp K.R. Effect of body build on weight-training-induced adaptations in body composition and muscle strength. Med Sci Sports Exerc 26 (1994) 515-521
17. Schutz Y., Kyle U.U., and Pichard C. Fat-free mass index percentiles in Caucasians aged 18-98 years. Int J Obes Relat Metab Disord 26 (2002) 953-960
18. Healy M.J. Measuring measurement errors. Stat Med 8 (1989) 893-906
19. De Bruin P.F., Ueki J., Bush A., Khan Y., Watson A., and Pride N.B. Diaphragm thickness and inspiratory strength in patients with Duchenne muscular dystrophy. Thorax 52 (1997) 472-475
20. Ueki J., DeBruin P.F., and Pride N.B. In vivo assessment of diaphragm contraction by ultrasound in normal subjects. Thorax 50 (1995) 1157-1161
21. Kraemer R., and Stoller F. Helium wash-in time as a critica; factor in the determination of functional residual capacity in children. Respiration 52 (1987) 263-271
22. Nixon L.S., Yung B., Bell S.C., Elborn J.S., and Shale D.J. Circulating immunoreactive interleukin-6 in cystic fibrosis. Am J Respir Crit Care Med 157 (1998) 1764-1769
23. Wilson P.W., Paffenbarger R.S.J., Morris J.N., and Havlik R. Assessment methods for physical activity and physical fitness in population studies: report of an NHLBI workshop. Am Heart J 111 (1986) 1177-1192
24. Enright S., Unnithan V.B., and Davies D. Reproducibility of inspiratory work capacity in cystic fibrosis patients. Respir Physiol Neurobiol 25: 150 1 (2006) 35-43
25. Mayos M., Giner J., Cason P., and Sanchis J. Measurement of maximal static respiratory pressure at the mouth with different aor leaks. Chest 100 (1991) 364-366
26. Ionescu A.A., Chatham K., Davies C.A., Nixon L.S., Enright S.J., and Shale D.J. Inspiratory muscle function and body composition in cystic fibrosis. Am J Respir Crit Care Med 158 (1998) 1271-1276
27. McCool F.D., Benditt J.O., Conomos P., Anderson L., Sherman C.B., and Hoppin Jr. F.G. Variability of diaphragm structure among healthy individuals. Am J Respir Crit Care Med 155 (1997) 1323-1328
28. Kelsen S., Ference M., and Kapoor S. Effects of prolonged undernutrition on structure and function of the diaphragm. J Appl Physiol 58 4 (1985) 1354-1359
29. Arora N.S., and Rochester D.F. Effect of body weight and muscularity on human diaphragm muscle mass, thickness and area. J Appl Physiol 52 (1982) 64-70
30. Dureuil B., and Matuszak Y. Alteration in nutritional status and diaphragm muscle function. Reprod Nutr Dev 38 2 (1998) 175-180
31. Enright S.J., Unnithan V.B., Heward C., Withnall L., and Davies D.H. Effect of high-intensity inspiratory muscle training on lung volumes, diaphragm thickness, and exercise capacity in subjects who are healthy. Phys Ther 86 3 (2006) 345-354
32. Enright S., Chatham K., Ionescu A.A., Unnithan V.B., and Shale D.J. Inspiratory muscle training improves lung function and exercise capacity in adults with cystic fibrosis. Chest 126 (2004) 406-411
33. DePalo V.A., Parker A.L., Al-Bilbeisi F., and McCool F.D. Respiratory muscle strength training with non respiratory maneuvers. J Appl Physiol 96 (2003) 731-734
34. Al-Bilbersi F., and McCool F.D. Diaphragm recruitment during non respiratory activities. Am J Respir Crit Care Med 162 (1999) 456-459
35. Faulkner J.A. In: Roussos C., and Macklem P.T. (Eds). Structural and functional adaptations of skeletal muscle. The Thorax Part B (1985), Marcel Dekker, New York 1326-1351
36. Bellemaire F., and Grassino A. Effect of pressure and timing of contraction on human diaphragm fatigue. J Appl Physiol 53 (1982) 1190-1195
37. Roussos C., and Macklem P.T. The respiratory muscles. N Engl J Med 307 (1982) 786-797
38. Jimanez-Fuentes M.A., Gea J., Aguar M.C., Minguella J., Lloreta J., Felez M., et al. Capillary density and respiratory function in the external intercostal muscle. Arch Bronconeumol 35 10 (1999) 471-476
39. Meir A., Redington A., Brophy C., Hodson M., and Green M. Respiratory muscle function in cystic fibrosis. Thorax 45 (1990) 750-752
40. Hayot M., Guillaumont S., Ramonatxo M., Voisin M., and Prefaut C. Determinants of the tension-time index of inspiratory muscles in children with cystic fibrosis. Pediatr Pulmonol 23 5 (1997) 336-343
41. Decramer M., Jiang T.X., and Demedts M. Effects of acute hyperinflation on chest wall mechanics in dogs. J Appl Physiol 63 4 (1997) 1493-1498
42. Decremer M. Hyperinflation and respiratory muscle interaction. Eur Respir J 10 4 (1997) 934-941
43. Hebestreit H., Hebestreit A., Trusen A., and Hughson R.L. Oxygen uptake kinetics are slowed in cystic fibrosis. Med Sci Sports Exerc 37 1 (2005) 10-17
44. Ionescu A.A., Evans W.D., Pettit R.J., Nixon L.S., Stone M.D., and Shale D.J. Hidden depletion of fat-free mass and bone mineral density in adults with cystic fibrosis. Chest 124 (2003) 2220-2228
45. Bolton C.E., Ionescu A.A., Evans W.D., Pettit, and Shale D.J. Altered tissue distribution in adults with cystic fibrosis. Thorax 58 (2003) 885-889
46. Cohn D., Benditt J.O., Eveloff S., and McCool F.D. Diaphragm thickening during inspiration. J Appl Physiol 83 1 (1997) 291-296
47. Misuri G., Colagrande S., Gorini M., Ianddell I., Mancuni M., Duranti R., et al. In vivo ultrasound assessment of respiratory function of abdominal muscles in normal subjects. Eur Respir J 10 (1997) 2861-2867
48. Burns C.B., and Scheinhorn D.J. Evaluation of a single-breath helium dilution total lung capacity in obstructive lung disease. Am Rev Respir Dis 130 4 (1984) 580-583
49. Andersson L.G., Ringqvist I., and Walker A. Total lung capacity measured by body plethysmography and by helium dilution method. A comparative study in different patient groups. Clin Physiol 8 2 (1998) 113-119