Hostname: page-component-586b7cd67f-dlnhk Total loading time: 0 Render date: 2024-11-26T21:39:47.642Z Has data issue: false hasContentIssue false

Serum phospholipid fatty acid profile and dietary intake in an adult Mediterranean population with cystic fibrosis

Published online by Cambridge University Press:  08 March 2007

Gabriel Olveira*
Affiliation:
Endocrinology and Nutrition Service, 4a planta, Pabellón A, Carlos Haya University Hospital, Avenida Carlos Haya, Malaga 29010, Spain
Antonio Dorado
Affiliation:
Pneumology Service, Carlos Haya University Hospital, Malaga, Spain
Casilda Olveira
Affiliation:
Pneumology Service, Carlos Haya University Hospital, Malaga, Spain
Alicia Padilla
Affiliation:
Pneumology Service, Carlos Haya University Hospital, Malaga, Spain
Gemma Rojo-Martínez
Affiliation:
Endocrinology and Nutrition Service, 4a planta, Pabellón A, Carlos Haya University Hospital, Avenida Carlos Haya, Malaga 29010, Spain
Eva García-Escobar
Affiliation:
Endocrinology and Nutrition Service, 4a planta, Pabellón A, Carlos Haya University Hospital, Avenida Carlos Haya, Malaga 29010, Spain
Inmaculada Gaspar
Affiliation:
Pneumology Service, Carlos Haya University Hospital, Malaga, Spain
Montserrat Gonzalo
Affiliation:
Endocrinology and Nutrition Service, 4a planta, Pabellón A, Carlos Haya University Hospital, Avenida Carlos Haya, Malaga 29010, Spain
Federico Soriguer
Affiliation:
Endocrinology and Nutrition Service, 4a planta, Pabellón A, Carlos Haya University Hospital, Avenida Carlos Haya, Malaga 29010, Spain
*
*Corresponding author: Dr Gabriel Olveira-Fuster, fax +34 952 28 67 04, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

The relative importance of the usual diet in serum phospholipids in subjects with cystic fibrosis (CF) has been poorly studied. To compare the fatty acid profile in serum phospholipids from adult CF subjects with that of healthy subjects, and determine the role of the normal diet in this profile, we studied thirty-seven adult CF subjects with stable pulmonary disease and thirty-seven healthy controls matched for age, sex and nutritional status. A dietary questionnaire was obtained, anthropometric data were recorded, and the fatty acid profile measured by GLC. Compared with the controls, the percentages of myristic, palmitoleic and stearic acids and total MUFA were significantly higher in the CF group, and DHA, linoleic acid, total PUFA and n−6 fatty acids were significantly lower in the CF group. The CF subjects with worse pulmonary function and with pancreatic insufficiency had significantly lower levels of linoleic and n−6 fatty acids. The total energy intake was significantly higher in the CF subjects, although the energy distribution in the CF subjects and the controls was not different for the carbohydrates, lipids and proteins. No differences were detected in fat intake for MUFA (51 (sd 4) v. 52 (sd 4) %) or saturated fatty acids (33·5 (sd 5) v. 31·2 (sd 3·8) %), but the PUFA were slightly lower in the CF subjects (15·4 (sd 4·5) v. 17·4 (sd 4·2) %; P=0·02). The usual dietary intake of fatty acids by adult CF subjects does not appear to explain the difference in the fatty acid profile compared with controls. This suggests an abnormal fatty acid metabolism in CF subjects.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2006

References

Alastrue, A, Rull, M, Camps, I, Ginesta, C, Melus, MR & Salva, JANuevas normas y consejos en la valoración de los parámetros antropométricos en nuestra poblacion: indice adiposo-muscular, indices ponderales y tablas percentiles de los datos antropometricosú tiles en una valoración nutricional (New norms and advice in the valuation of the anthropometric parameters in our population: fat-muscle index, ponderal indices and percentile scores of the anthropometric data used in an evaluation of nutritional status).. Med Clin (Barc) (1988) 91, 223236.Google Scholar
Anthony, H, Bines, J, Phelan, P & Paxton, SRelation between dietary intake and nutritional status in cystic fibrosis. Arch Dis Child (1998) 78, 443447.CrossRefGoogle ScholarPubMed
Arija, V, Salas-Salvadó, J, Fernández-Ballart, J, Serra, L & Aranceta, JNecesidades energéticas. Guías Alimentarias para la Población Española (In Spanish) pp.345351 [Sociedad Española, deNutrición, Comunitaria editor]. Madrid: IM&C SA. (2001)Google Scholar
Beckles, WN, Elliot, TM & Everard, ML n3 Fatty acids (from fish oils) for cystic fibrosis (Cochrane Methodology Review). In The Cochrane Library, issue 4, Chichester, UK: John Wiley & Sons Ltd. (2003)Google Scholar
Benabdeslam, H, Garcia, I, Bellon, G, Gilly, R & Revol, ABiochemical assessment of the nutritional status of cystic fibrosis patients treated with pancreatic enzyme extracts. Am J Clin Nutr (1998) 67, 912918.CrossRefGoogle ScholarPubMed
Bhalla, M, Turcios, N, Aponte, V, Jenkins, M, Leitman, BS, McCauley, DL & Naidich, DPCystic fibrosis: scoring system with thinsection CT. Radiology (1991) 179, 783788.CrossRefGoogle ScholarPubMed
Carlstedt-Duke, J, Bronnegard, M & Strandvik, BPathological regulation of arachidonic acid release in cystic fibrosis: the putative basic defect. Proc Natl Acad Sci USA (1986) 83, 92029206.CrossRefGoogle ScholarPubMed
Christophe, A & Robberecht, EDirected modification instead of normalization of fatty acid patterns in cystic fibrosis: an emerging concept. Curr Opin Clin Nutr Metab Care (2001) 4, 111113.CrossRefGoogle ScholarPubMed
Christophe, A, Robberecht, E, Franckx, H, De Baets, F & van de Pas, MEffect of administration of gamma.linolenic acid on the fatty acid composition of serum phospholipids and cholesteryl esters in patients with cystic fibrosis. Ann Nutr Metab (1994) 38, 4047.CrossRefGoogle ScholarPubMed
Cystic Fibrosis Foundation Clinical practice guidelines for cystic fibrosis. Bethesda, MD: Cystic Fibroais Foundation. (1997)Google Scholar
De Vizia, B, Raia, V, Spano, C, & Pavlidis, C & Pavlidis, CEffect of an 8- month treatment with 3 fatty acids (eicosapentanoic and docosahexaenoic) in patient with cystic fibrosis. J Parenter Enteral Nutr (2003) 27, 5257.CrossRefGoogle ScholarPubMed
Diabetes and Nutrition Study Group of the Spanish Diabetes Association Diabetes Nutrition and Complications Trials trends in nutritional pattern between 1993 and 2000 and targets of diabetes treatment in a sample of Spanish people with diabetes. Diabetes Care (2004) 27, 984987.Google Scholar
Freedman, SD, Blanco, PG, Zaman, MM et al. Association of cystic fibrosis with abnormalities in fatty acid metabolism. N Engl J Med (2004) 350, 560569.CrossRefGoogle ScholarPubMed
Freedman, SD, Katz, MH, Parker, EM, Laposata, M, Urman, MY & Alvarez, JGA membrane lipid imbalance plays a role in the phenotypic expression of cystic fibrosis in cftr -/- mice. Proc Natl Acad Sci USA (1999) 96, 1339514000.CrossRefGoogle Scholar
García-Almeida, JM, González-Romero, E, Olveira, G, Martýnez- Alfaro, B, Esteva, I, Dobarganes, M & Soriguer, FNutritional study of the Bajo Guadalhorce. Clin Nutr (2001) 20, Suppl.3, 72.Google Scholar
Kawchak, DA, Zhao, H, Scanlin, TF, Tomezsko, JL, Cnaan, A & Stallings, VALongitudinal, prospective analysis of dietary intake in children with cystic fibrosis. J Pediatr (1996) 129, 119129.CrossRefGoogle ScholarPubMed
Lai, HC, Kosorok, MR, Laxova, A, Davis, LA, FitzSimmon, SC & Farrell, PMNutritional status of patients with cystic fibrosis with meconium ileus: a comparison with patients without meconium ileus and diagnosed early through neonatal screening. Pediatrics (2000) 105, 5361.CrossRefGoogle ScholarPubMed
Lepage, G, Yesair, DW, Ronco, N, Champagne, J, Bureau, N, Chemtob, S, Berube, D & Roy, CCEffect of an organized lipid matrix on lipid absorption and clinical outcomes in patients with cystic fibrosis. J Pediatr (2002) 141, 178185.CrossRefGoogle ScholarPubMed
Lloyd-Still, JD, Bibus, DM, Powers, CA, Johnson, SB & Holman, RTEssential fatty acid deficiency and predisposition to lung disease in cystic fibrosis. Acta Paediatr (1996) 85, 14261432.CrossRefGoogle ScholarPubMed
Mataix, JTabla de Composición de Alimentos Españoles, 2nd ed. (In Spanish) Granada, Spain: Servicio de Publicaciones de la Universidad de Granada (Granada University Publications Service). (1995)Google Scholar
Mora, I, Orejas, G, Bousoño, C, Cue, R, Ramos, E & Crespo, MValoración del estado nutricional en un grupo de pacientes con fibrosis quística (Nutritional status assessment in a group of cystic fibrosis patients). An Esp Pediatr (1996) 44, 4044.Google Scholar
Moreiras, O, Carbajal, A & Cabrera, MLLa Composición de los Alimentos. (In Spanish) Madrid: Eudema SA. (1992)Google Scholar
Parsons, HG, O'Loughlin, EV, Forbes, D, Cooper, D & Gall, DSupplemental calories improve essential fatty acid deficiency in cystic fibrosis patients. Pediatr Res (1988) 24, 353356.CrossRefGoogle ScholarPubMed
Picarelli, A, Greco, M, Di Giovambattista, F, Ramazzotti, A, Cedrone, C, Corazziari, E & Torsoli, AQuantitative determination of faecal fat, nitrogen and water by means of a spectrophotometric technique: near infrared reflectance analysis (NIRA). Assessment of its accuracy and reproducibility compared with chemical methods. Clin Chim Acta (1995) 234, 147156.CrossRefGoogle ScholarPubMed
Ramsey, BW, Farrel, PM & Pencharz, PNutritional assessment and management in cystic fibrosis: a consensus report. The Consensus Committee. Am J Clin Nutr (1992) 55, 108116.CrossRefGoogle ScholarPubMed
Roca, J, Sanchis, J, Agustí Vidal, A, Segarra, F & Navajas, DSpirometric reference values for a Mediterranean population. Bull Eur Physiopathol Respir (1982) 18, 101102.Google Scholar
Roulet, M, Frascarolo, P, Rappaz, I & Pilet, MEssential fatty acid deficiency in well nourished young cystic fibrosis patients. Eur J Pediatr (1997) 156, 952956.CrossRefGoogle ScholarPubMed
Sanchis, J, Casan, P, Castillo, J, González Mangado, N, Palenciano, L & Roca, JNormativa para la espirometrýa forzada (Norm for the forced spirometer). Arch Bronconeumol (1989) 25, 132142.Google Scholar
Sociedad Espańola de Nutrición Comunitaria Guías Alimentarias para la Población Espańola (In Spanish) Madrid: IM& SA. (2001)Google Scholar
Sockrider, MM, Swank, PR, Seilheimer, DK & Schidlow, DMeasuring clinical status in cystic fibrosis: internal validity and reliability of a modified NIH score. Pediatr Pulmonol (1994) 17, 8696.CrossRefGoogle ScholarPubMed
Soriguer, F, Esteva, I, Rojo-Martínez, G et al. Prevalence of diabetes mellitus type LADA in South Spain. Diabetes Res Clin Pract (2002) 56, 213220.CrossRefGoogle Scholar
Soriguer, F, Rojo-Martinez, G, Dobarganes, MC,et al.. Hypertension is related to the degradation of dietary frying oils. Am J Clin Nutr (2003) 78, 10921097.CrossRefGoogle Scholar
Soriguer, F, Serna, S, Valverde, E, Hernando, J, Martín-Reyes, A, Soriguer, M, Pareja, A, Tinahones, F & Esteva, ILipid, protein and calorie content of different Atlantic and Mediterranean fish, shellfish and mollusc commonly eaten in the south of Spain. Eur J Epidemiol (1997) 13, 451463.CrossRefGoogle ScholarPubMed
Strandvik, B, Gronowitz, E, Enlund, F, Martinsson, T & Wahlstróm, JEssential fatty acid deficiency in relation to genotype in patients with cystic fibrosis. J Pediatr (2001) 139, 650655.CrossRefGoogle ScholarPubMed
Tomezsko, JL, Stallings, VA & Scanlin, TFDietary intake of healthy children with cystic fibrosis compared with normal control children. Pediatrics (1992) 90, 547553.CrossRefGoogle ScholarPubMed
Welsh, M & Smith, AMolecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell (1993) 73, 12511254.CrossRefGoogle ScholarPubMed
Werner, A, Bongers, MEJ, Bijvelds, MJ, de Jonge, HR & Verkade, HJNo indications for altered essential fatty acid metabolism in two murine models for cystic fibrosis. J Lipid Res (2004) 45, 22772286.CrossRefGoogle ScholarPubMed
White, H, Morton, AM, Peckham, DG & Conway, SPDietary intakes in adult patients with cystic fibrosis – do they achieve guidelines?. J Cyst Fibros (2004) 3, 17.CrossRefGoogle ScholarPubMed