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Inflammatory biomarker profile in children with cystic fibrosis: preliminary study

Published online by Cambridge University Press:  14 June 2010

N. H. Slobodianik ,
M. S. Feliu ,
P. Perris ,
S. Barbeito ,
I. Strasnoy ,
A. Franchello  and
M. Ferraro
N. H. Slobodianik*
Affiliation:
Department of Nutrition and Food Science, School of Pharmacy and Biochemistry, University of Buenos Aires, Bueno Aires, Argentina
M. S. Feliu
Affiliation:
Department of Nutrition and Food Science, School of Pharmacy and Biochemistry, University of Buenos Aires, Bueno Aires, Argentina
P. Perris
Affiliation:
Department of Nutrition and Food Science, School of Pharmacy and Biochemistry, University of Buenos Aires, Bueno Aires, Argentina
S. Barbeito
Affiliation:
Nutrition Service, Pedro de Elizalde Hospital, Buenos Aires, Argentina
I. Strasnoy
Affiliation:
Nutrition Service, Pedro de Elizalde Hospital, Buenos Aires, Argentina
A. Franchello
Affiliation:
Nutrition Service, Pedro de Elizalde Hospital, Buenos Aires, Argentina
M. Ferraro
Affiliation:
Nutrition Service, Pedro de Elizalde Hospital, Buenos Aires, Argentina
*
*Corresponding author: Dr N. H. Slobodianik, fax +54 11 4 964 8243, email [email protected]
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Abstract

The aim of this preliminary study was to determine specific proteins, related to inflammation process and nutritional status as well as to total antioxidant capacity, in children suffering from cystic fibrosis (CF). The study was performed on 17 nonhospitalized children (12 boys and 5 girls) with CF aged 3 months to 10 years, who were assisted at the Nutrition Service from Pedro de Elizalde Hospital. Transferrin, transthyretin, ceruloplasmin (Cp), haptoglobin, C-reactive protein (CRP) and fibrinogen were measured by single radial immunodiffusion techniques. Total antioxidant capacity (TAC) was determined by a decolorization assay. Statistical analyses were performed by the Student's t test. Transferrin and transthyretin values were lower in CF patients in comparison with data obtained from healthy children (reference group, RG). The decreased transferrin concentration and the tendency towards low plasma transthyretin values suggested an abnormal nutritional status. However, higher Cp and haptoglobin levels were shown in patients than in RG. The fact that 23 and 50% of patients exceeded the desirable values for fibrinogen (<285·0 mg/dl) and CRP (<0·2 mg/dl), respectively, should be highlighted. The TAC (mM; Trolox equivalents) was shown to be lower in the CF group than in RG. The diminished TAC concomitant with an increased plasma Cp concentration would exacerbate the inflammatory status and could explain the depression of the immune system. These preliminary results could explain the need to include biochemical and functional parameters in the early nutritional status evaluation in CF patients in order to use appropriate nutritional and pharmacological therapies and consequently to improve their survival and quality of life.

Keywords

Cystic fibrosisChildrenBiochemical parametersProteinsTotal antioxidant capacity
Type
3rd International Immunonutrition Workshop
Information
Proceedings of the Nutrition Society , Volume 69 , Issue 3 , August 2010 , pp. 354 - 356
Copyright
Copyright © The Authors 2010

Abbreviations:
CF

cystic fibrosis

Cp

ceruloplasmin

TAC

total antioxidant capacity

TTR

transthyretin

Cystic fibrosis (CF) is an inherited disease characterized by an abnormality in the body's salt, water and mucus-making cells. As the movement of salt and water in and out of cells is altered, mucus becomes thickened. This fact can affect many organs and body systems including the following: the respiratory system – sinuses and lungs; the digestive system – pancreas, liver, gallbladder and intestines; the reproductive system – especially in males, where sperm-carrying ducts become clogged; and sweat glands(Reference Rossenstein and Cutting1).

In children with CF, this mucus can also prevent the normal absorption of essential nutrients and fat in the gut, leading to poor digestion, slow growth, impairment of weight gain, greasy bowel movements and increased vulnerability to infections. Diminished secretion of pancreatic enzymes is the main cause of poor growth, fatty diarrhoea and deficiency in fat-soluble vitamins(Reference Nichols, Chmiel and Berger2, Reference Koletzko and Reinhardt3).

Nutrition plays an essential role in the management of CF, particularly in infants with their high energy requirements due to rapid growth. Most infants are already malnourished at the time of clinical diagnosis, due to an energy imbalance with increased losses and unachieved energy requirements(Reference Koletzko and Reinhardt3). This imbalance can be explained by increased energy expenditure, high nutritional requirements and decreased oral intake. During the last few decades, improved treatment measures and nutritional support applied to CF patients have increased their survival and quality of life(Reference Nichols, Chmiel and Berger2, Reference Molina Arias, Prieto Bozano and Sarria Oses4–Reference Pencharz and Durie8). Therefore, the study of the nutritional status of these patients must be included among the main factors involved in the CF evolution, prognosis and survival(Reference Koletzko and Reinhardt3).

Moreover, a vicious cycle of airway obstruction, infection and inflammation continues to cause most of the morbidity and mortality in this pathology(Reference Nichols, Chmiel and Berger2). Numerous links exist between progression of CF lung disease and oxidative stress(Reference Cantin, White and Cross9, Reference Lands, Grey and Grenier10).

Therefore, this preliminary study was aimed to determine specific plasma proteins related to inflammation and nutritional status, and total antioxidant capacity (TAC), in non-hospitalized children suffering from CF.

Material and methods

The study was performed on 17 non-hospitalized children (12 boys and 5 girls) with CF aged 3 months to 10 years, who were assisted at the Nutrition Service from Pedro de Elizalde Hospital. Blood samples were collected from fasting patients. Transferrin, transthyretin (TTR), ceruloplasmin (Cp), haptoglobin, C-reactive protein and fibrinogen were measured by single radial immunodiffusion techniques by using commercially available kits (Diffuplate, Biocientifica, Buenos Aires, Argentina and Binding Site, UK)(Reference Mancini, Carbonara and Heremans11). TAC was determined by a decolorization assay applicable to both lipophilic and hydrophilic antioxidants, including flavonoids, hydroxycinnamates, carotenoids and plasma antioxidants(Reference Miller, Rice-Evans and Davies12, Reference Re, Pellegrini and Proteggente13). Statistical analyses were performed using the Student's t test.

The report was approved by the Ethics Committee from the University of Buenos Aires, and informed consent was obtained from parents before recruiting the patients into the study.

Plasma fractions results were expressed as X with standard deviation and were compared using the Student's t test with published data obtained in our laboratory from healthy children of both sexes and a similar age range (reference group)(Reference Feliu and Slobodianik14, Reference Feliu and Slobodianik15); C-reactive protein and fibrinogen concentrations were compared with the desirable values provided by international bibliography. TAC reference value was obtained in healthy children assessed in the same hospital for periodic control (M. Insani, unpublished results).

Table 1. Studied biochemical parameters and total antioxidant capacity (TAC)

(mean values and standard deviation)

* Significantly different at a level of P<0·01.

Results

When the population tested was divided by age range (3 months–2 years and >2 years), no differences were observed in all the studied biomarkers. That is the reason why we analyzed the population as a whole.

Lower values of the nutritional status-related plasma proteins (transferrin and TTR) were found in CF patients (Table 1) in comparison with data obtained in our laboratory from healthy children of both sexes and a similar age range (reference group) (P<0·01), 50% of children showing TTR values below 20·0 mg/dl, which is related to protein deficiency(Reference Ingengleek and Young16). However, both Cp and haptoglobin levels were found higher in CF patients in relation to the reference group. It should be highlighted that 23 and 50% of patients exceeded the desirable values for fibrinogen (<285·0 mg/dl) and C-reactive protein (<0·2 mg/dl), respectively.

TAC(Reference Miller, Rice-Evans and Davies12, Reference Re, Pellegrini and Proteggente13) was significantly lower in CF patients than in healthy children.

Discussion

Previous findings by our working group in children suffering from CF suggest that the immune system, evaluated through the levels of C3c and C4c fractions and the activity of adenosine deaminase (a T lymphocyte-related enzyme) was altered(Reference Perris, Feliu and Barbeito17). Moreover, the decreased transferrin concentration and the tendency towards low plasma TTR values found in this preliminary report suggested an abnormal nutritional status(Reference Ingengleek and Young16). TTR shows the same behaviour reported in adults suffering from this pathology, but adult patients show higher transferrin levels than children(Reference Emmett, Miller and Crowle18). In acute phase reactions such as infections and chronic inflammation (situations observed in children suffering from CF), transferrin concentration could be reduced. Moreover, TTR synthesis is inhibited by TNFβ; this outcome could explain the concentration levels of this protein fraction found in children suffering from CF(Reference Topfer, Trefz and Zawta19).

In addition, the observed increase in Cp and haptoglobin plasma levels could be related to a concomitant inflammatory status; in fact, the increased synthesis of these acute phase proteins has been shown to be induced by pro-inflammatory cytokines, such as IL-6, IL-1 and TNFα(Reference Topfer, Trefz and Zawta19). The CF group showed higher levels of fibrinogen and C-reactive protein together with lower values of HDL-cholesterol (27·8 (SD 10·3) mg/dl) than in the reference group; this result would confirm an inflammatory status in children at risk of CVD(Reference Myers, Rifai and Tracy20); moreover, the described pro-oxidant activity of Cp could be considered as another independent risk factor for CVD in this population(Reference Fox, Mukhopadhyay and Ehrenwal21). On the other hand, several studies have reported that inflammation is an event occurring prior to infection in patients with CF(Reference Rottner, Freyssinet and Martínez22).

Oxidative stress may play a significant role in the pathophysiology of CF. The lung, the main organ responsible for morbidity and mortality in this disease, is particularly vulnerable to high levels of oxidative stress(Reference Lands, Grey and Grenier10, Reference Cantin, White and Cross23).

The diminished TAC in non-hospitalized children concomitant with an increased plasma Cp concentration would exacerbate the inflammatory status and could explain the depression of the immune system due to the deterioration of the immune cells and/or their function.

Conclusions

Careful nutritional management has an important effect on growth and survival rates in CF (a complex disease that requires clinical care); the abnormalities in the oxidant– antioxidant balance raise several possibilities for therapeutic interventions concomitant with specific nutritional support adjusted to individual needs. Long-term studies are required to examine the effects of nutritional interventions on key clinical outcomes in CF(Reference Cantin, White and Cross23).

These preliminary results performed on low specific half-life plasma fractions related to both inflammation and nutritional status (transferrin 7–10 days, TTR 1–2 days, haptoglobin 2–4 days) could explain the need to include these biochemical and functional parameters in the early evaluation of non-hospitalized CF patients. This inclusion would allow us to analyse the patient's nutritional and inflammatory evolution and to design appropriate nutritional and pharmacological therapies, these actions being able to improve the survival and life quality of these patients.

Acknowledgements

This work was partially supported by the University of Buenos Aires (B074). The authors declare no conflict of interest. N. H. S., M. S. F. and P. P. performed biochemical determinations, analysis and discussion of results. S. B., I. S., A. F. and M. F. selected the patients, obtained the samples and participated in the elaboration of the manuscript.

References

1.Rossenstein, BJ & Cutting, GR (1998) The diagnosis of cystic fibrosis. A consensus statement. J Pediatr 132, 589–595.CrossRefGoogle Scholar
2.Nichols, D, Chmiel, J & Berger, M (2008) Chronic inflammation in the cystic fibrosis lung: alterations in inter- and intracellular signaling. Clin Rev Allergy Immunol 4, 146–162.CrossRefGoogle Scholar
3.Koletzko, S & Reinhardt, D (2001) Nutritional challenges of infants with cystic fibrosis. Early Hum Dev 65, S53–S61.Google Scholar
4.Molina Arias, M, Prieto Bozano, G, Sarria Oses, J et al. . (2001) Cystic fibrosis: nutritional considerations. An Esp Pediatr 54, 575–581.Google Scholar
5.Hankard, R, Munck, A & Navarro, J (2002) Nutrition and growth in cystic fibrosis. Horm Res 58, Suppl. 1, S16–S20.Google Scholar
6.Anton, DT, Moraru, D, Cirdei, E et al. . (2006) Malnutrition and complex nutritional therapy in cystic fibrosis. Rev Med Chir Soc Med Nat Lasi 110, 801–806.Google Scholar
7.Dodge, JA & Turck, D (2006) Cystic fibrosis: nutritional consequences and management. Best Pract Res Clin Gastroenterol 20, 531–546.CrossRefGoogle ScholarPubMed
8.Pencharz, PB & Durie, PR (2000) Pathogenesis of malnutrition in cystic fibrosis and its treatment. Clin Nutr 19, 387–394.CrossRefGoogle ScholarPubMed
9.Cantin, AM, White, TB, Cross, CE et al. . (2007) Antioxidants in cystic fibrosis. Conclusions from the CF antioxidant workshop, Bethesa, Maryland. Free Radic Biol Med 42, 15–31.CrossRefGoogle Scholar
10.Lands, LC, Grey, VL & Grenier, C (2000) Total plasma antioxidant capacity in Cystic fibrosis. Pediatr Pulmonol 29, 81–87.3.0.CO;2-N>CrossRefGoogle ScholarPubMed
11.Mancini, G, Carbonara, AO & Heremans, GF (1965) Immunochemical quantitation of antigen by single radial immunodiffusion. Immunochemistry 2, 235–254.CrossRefGoogle ScholarPubMed
12.Miller, NJ, Rice-Evans, CA, Davies, NJ et al. . (1993) A novel method for measuring antioxidant capacity and its application to monitoring the antioxidant status in premature neonates. Clin Sci 84, 407–412.Google Scholar
13.Re, R, Pellegrini, N, Proteggente, A et al. . (1999) Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Radic Biol Med 26, 1231–1237.Google Scholar
14.Feliu, MS & Slobodianik, NH (1992) Valores de Referencia de fracciones séricas de utilidad en estudios de nutrición,en niños. Acta Bioquím. Latinoam xxvi, 319–327.Google Scholar
15.Feliu, MS & Slobodianik, NH (1992) Valores de Referencia de fracciones séricas específicas en niños. Estudio preliminar. Bioline 6, 6–8.Google Scholar
16.Ingengleek, Y & Young, V (1994) Transthyretin (Prealbumin) in health and disease: nutritional implications. Annu Rev Nutr 14, 495–533.CrossRefGoogle Scholar
17.Perris, P, Feliu, MS, Barbeito, S et al. . (2008) Serum C3c and C4c concentrations and adenosine deaminase activity of children with cystic fibrosis: preliminary study. Proc Nutr Soc 67(OCE), E59.CrossRefGoogle Scholar
18.Emmett, M, Miller, JL & Crowle, AJ (1987) Protein abnormalities in adult respiratory distress syndrome, tuberculosis, and cystic fibrosis sera. Proc Soc Exp Biol Med 184, 74–82.CrossRefGoogle ScholarPubMed
19.Topfer, G, Trefz, B & Zawta, B (2000) Proteins: Questions and Answers for Medical Diagnosis. Germany: Roche Diagnosis GmbH.Google Scholar
20.Myers, G, Rifai, N, Tracy, R et al. . (2004) CDC/AHA Workshop on Markers of Inflammation and Cardiovascular Disease. Circulation 110, 545–549.Google Scholar
21.Fox, PL, Mukhopadhyay, C, Ehrenwal, E et al. . (2000) Ceruloplasmin and cardiovascular disease. Free Radic Biol Med 28, 1735–1744.Google Scholar
22.Rottner, M, Freyssinet, JM & Martínez, MC (2009) Mechanisms of the noxious inflammatory cycle in cystic fibrosis. Respir Res 10, 23–34.CrossRefGoogle ScholarPubMed
23.Cantin, AM, White, TB, Cross, CE et al. . (2007) Antioxidants in cystic fibrosis. Free Radic Biol Med 42, 15–31.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Studied biochemical parameters and total antioxidant capacity (TAC)(mean values and standard deviation)