The impact of the elimination diet on growth and nutrient intake in children with food protein induced gastrointestinal allergies

Rosan Meyer, Claire De Koker, Robert Dziubak, Heather Godwin, Gloria Dominguez-Ortega, Adriana Chebar Lozinsky, Ana-Kristina Skrapac, Yara Gholmie, Kate Reeve, Neil Shah, Rosan Meyer, Claire De Koker, Robert Dziubak, Heather Godwin, Gloria Dominguez-Ortega, Adriana Chebar Lozinsky, Ana-Kristina Skrapac, Yara Gholmie, Kate Reeve, Neil Shah

Abstract

Background: Non immunoglobulin E (IgE) mediated allergies affecting the gastrointestinal tract require an elimination diet to aid diagnosis. The elimination diet may entail multiple food eliminations that contribute significantly to macro- and micro-nutrient intake which are essential for normal growth and development. Previous studies have indicated growth faltering in children with IgE-mediated allergy, but limited data is available on those with delayed type allergies. We therefore performed a study to establish the impact on growth before and after commencing an elimination diets in children with food protein induced non-IgE mediated gastrointestinal allergies.

Methods: A prospective, observational study was performed at the tertiary gastroenterology department. Children aged 4 weeks-16 years without non-allergic co-morbidities who were required to follow an elimination diet for suspected food protein induced gastrointestinal allergies were included. Growth parameters pre-elimination were taken from clinical notes and post-elimination measurements (weight and height) were taken a minimum of 4 weeks after the elimination diet. A 3-day estimated food diary was recorded a minimum of 4 weeks after initiating the elimination diet, including also any hypoallergenic formulas or over the counter milk alternatives that were consumed.

Results: We recruited 130 children: 89 (68.5 %) boys and a median age of 23.3 months [IQR 9.4-69.2]. Almost all children (94.8 %) in this study eliminated CM from their diet and average contribution of energy in the form of protein was 13.8 % (SD 3.9), 51.2 % (SD 7.5) from carbohydrates and 35 % (SD 7.5) from fat. In our cohort 9 and 2.8 % were stunted and wasted respectively. There was a statistically significant improvement in weight-for-age (Wtage) after the 4 week elimination diet. The elimination diet itself did not improve any of the growth parameters, but achieving energy and protein intake improved Wtage and WtHt respectively, vitamin and/or mineral supplements and hypoallergenic formulas were positively associated with WtHt and Wtage.

Conclusion: With appropriate dietary advice, including optimal energy and protein intake, hypoallergenic formulas and vitamins and mineral supplementation, growth parameters increased from before to after dietary elimination. These factors were positively associated with growth, irrespective of the type of elimination diet and the numbers of foods eliminated.

Keywords: Anthropometric measures; Growth; Malnutrition; Non-IgE mediated allergy; Nutrients.

Figures

Fig. 1
Fig. 1
Combinations of food elimination diets. MS milk and soya, MES milk, egg and soya, MEWS milk, egg, wheat and soya, +random additional foods to the list
Fig. 2
Fig. 2
Percentage of patients with insufficient intake, meeting their requirements or excessive intake

References

    1. Venter C, Pereira B, Grundy J, Clayton CB, Roberts G, Higgins B, Dean T. Incidence of parentally reported and clinically diagnosed food hypersensitivity in the first year of life. J Allergy Clin Immunol. 2006;117:1118–1124. doi: 10.1016/j.jaci.2005.12.1352.
    1. Johansson SG, Bieber T, Dahl R, Friedmann PS, Lanier BQ, Lockey RF, Motala C, Ortega Martell JA, Platts-Mills TA, Ring J, Thien F, Van CP, Williams HC. Revised nomenclature for allergy for global use: report of the Nomenclature Review Committee of the World Allergy Organization, October 2003. J Allergy Clin Immunol. 2004;113:832–836. doi: 10.1016/j.jaci.2003.12.591.
    1. Heine RG. Allergic gastrointestinal motility disorders in infancy and early childhood. Pediatr Allergy Immunol. 2008;19:383–391. doi: 10.1111/j.1399-3038.2008.00785.x.
    1. Venter C, Meyer R. Session 1: allergic disease: the challenges of managing food hypersensitivity. Proc Nutr Soc. 2010;69:11–24. doi: 10.1017/S0029665109991832.
    1. Boyce JA, Assa’ad A, Burks AW, Jones SM, Sampson HA, Wood RA, Plaut M, Cooper SF, Fenton MJ, Arshad SH, Bahna SL, Beck LA, Byrd-Bredbenner C, Camargo CA, Jr, Eichenfield L, Furuta GT, Hanifin JM, Jones C, Kraft M, Levy BD, Lieberman P, Luccioli S, McCall KM, Schneider LC, Simon RA, Simons FE, Teach SJ, Yawn BP, Schwaninger JM. Guidelines for the diagnosis and management of food allergy in the United States: summary of the NIAID-sponsored expert panel report. Nutr Res. 2011;31:61–75. doi: 10.1016/j.nutres.2011.01.001.
    1. Meyer R, Schwarz C, Shah N. A review on the diagnosis and management of food-induced gastrointestinal allergies. Curr Allergy Clin Immunol. 2012;25:1–8.
    1. Heine RG. Gastroesophageal reflux disease, colic and constipation in infants with food allergy. Curr Opin Allergy Clin Immunol. 2006;6:220–225. doi: 10.1097/01.all.0000225164.06016.5d.
    1. Groetch M, Nowak-Wegrzyn A. Practical approach to nutrition and dietary intervention in pediatric food allergy. Pediatr Allergy Immunol. 2013;24:212–221. doi: 10.1111/pai.12035.
    1. Isolauri E, Sutas Y, Salo MK, Isosomppi R, Kaila M. Elimination diet in cow’s milk allergy: risk for impaired growth in young children. J Pediatr. 1998;132:1004–1009. doi: 10.1016/S0022-3476(98)70399-3.
    1. Flammarion S, Santos C, Guimber D, Jouannic L, Thumerelle C, Gottrand F, Deschildre A. Diet and nutritional status of children with food allergies. Pediatr Allergy Immunol. 2011;22:161–165. doi: 10.1111/j.1399-3038.2010.01028.x.
    1. Vieira MC, Morais MB, Spolidoro JV, Toporovski MS, Cardoso AL, Araujo GT, Nudelman V, Fonseca MC. A survey on clinical presentation and nutritional status of infants with suspected cow’ milk allergy. BMC Pediatr. 2010;10:25. doi: 10.1186/1471-2431-10-25.
    1. Chebar LA, Meyer R, De KC, Dziubak R, Godwin H, Reeve K, Dominguez OG, Shah N. Time to symptom improvement using elimination diets in non-IgE mediated gastrointestinal food allergies. Pediatr Allergy Immunol. 2015;26:403–408. doi: 10.1111/pai.12404.
    1. World Health Organization, UNICEF. WHO child growth standards and the identification of severe acute malnutrition in infants and children. Geneva:World Health Organization; 2009. p. 1–12.
    1. Scientific Advisory Commitee on Nutrition . The nutritional wellbeing of the British population. Belfast: TSO; 2008. pp. 1–162.
    1. Marshall TA, Stumbo PJ, Warren JJ, Xie XJ. Inadequate nutrient intakes are common and are associated with low diet variety in rural, community-dwelling elderly. J Nutr. 2001;131:2192–2196.
    1. World Health Organization. Global database on child growth and malnutrition; 2004. . Accessed 3 May 2016
    1. Meyer R, De KC, Dziubak R, Venter C, Dominguez-Ortega G, Cutts R, Yerlett N, Skrapak AK, Fox AT, Shah N. Malnutrition in children with food allergies in the UK. J Hum Nutr Diet. 2013;27:227–235. doi: 10.1111/jhn.12149.
    1. Himes JH. Minimal time intervals for serial measurements of growth with recumbent length of stature of individual children. Acta Paediatr. 1999;88:120–125. doi: 10.1111/j.1651-2227.1999.tb01068.x.
    1. Food Standards Agency. National diet and nutrition survey. Results from years 1, 2, 3 and 4 (combined) of the rolling programme (2008/2009–2011/2012). In: Bates B, Lennox A, Prentice A, Bates C, Page P, Nicholson S, Swan G, editors. London: Public Health England; 2014. p. 1–158.
    1. Lambert J, Agostoni C, Elmadfa I, Hulshof K, Krause E, Livingstone B, Socha P, Pannemans D, Samartin S. Dietary intake and nutritional status of children and adolescents in Europe. Br J Nutr. 2004;92(Suppl. 2):S147–S211. doi: 10.1079/BJN20041160.
    1. Joint WHO/FAO/UNU Expert Consultation. Protein and amino acid requirements in human nutrition. World Health Organization. Geneva:WHO Press; 2007. p. 1–265.
    1. Golden MH. Proposed recommended nutrient densities for moderately malnourished children. Food Nutr Bull. 2009;30:S267–S342. doi: 10.1177/15648265090303S302.
    1. Kabir I, Malek MA, Mazumder RN, Rahman MM, Mahalanabis D. Rapid catch-up growth of children fed a high-protein diet during convalescence from shigellosis. Am J Clin Nutr. 1993;57:441–445.
    1. Kabir I, Butler T, Underwood LE, Rahman MM. Effects of a protein-rich diet during convalescence from shigellosis on catch-up growth, serum proteins, and insulin-like growth factor-I. Pediatr Res. 1992;32:689–692. doi: 10.1203/00006450-199212000-00014.
    1. Meyer R, De KC, Dziubak R, Godwin H, Dominguez-Ortega G, Shah N. Dietary elimination of children with food protein induced gastrointestinal allergy—micronutrient adequacy with and without a hypoallergenic formula? Clin Transl Allergy. 2014;4:31. doi: 10.1186/2045-7022-4-31.
    1. Lanigan JA, Wells JC, Lawson MS, Lucas A. Validation of food diary method for assessment of dietary energy and macronutrient intake in infants and children aged 6–24 months. Eur J Clin Nutr. 2001;55:124–129. doi: 10.1038/sj.ejcn.1601128.

Source: PubMed

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