Evaluation of food intake in patients with mucopolysaccharidosis

Background Mucopolysaccharidosis (MPS) are inborn errors of metabolism (IEM) recognized by deficient enzymes enrolled in glycosaminoglycans catabolism. The resulting accumulation of glycosaminoglycans leads to clinical progressive and generalized manifestations. Considering the severity of MPS and t...

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Veröffentlicht in:Nutrire : revista de Sociedade Brasileira de Alimentação e Nutrição = journal of the Brazilian Society of Food and Nutrition 2018-12, Vol.43 (1), Article 9
Hauptverfasser: Monteiro, Vaneisse Cristina Lima, Araújo de Oliveira Silva, José, Oliveira, Renata Bernardes, Frangipani, Beatriz Jurkiewicz, Dearo, Patrícia Rossetti, Previdelli, Ágatha Nogueira, Martins, Ana Maria, de Cássia Aquino, Rita, D’Almeida, Vânia
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Sprache:eng
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Zusammenfassung:Background Mucopolysaccharidosis (MPS) are inborn errors of metabolism (IEM) recognized by deficient enzymes enrolled in glycosaminoglycans catabolism. The resulting accumulation of glycosaminoglycans leads to clinical progressive and generalized manifestations. Considering the severity of MPS and the relevance of establishing dietetic strategies to these patients, the present study was tailored to evaluate the food intake in patients with MPS types I, II, and VI. Methods Food intake in patients with MPS I, II, and VI was assessed. A descriptive cross-sectional study was conducted. Energetic demand based on estimated necessity of energy equations and reported food intake was analyzed. Total energetic value and nutrients (vitamins B1, B2, C, calcium, iron, and phosphate) were analyzed in accordance with the standardized interval for macronutrient distribution and the method of apparent adequacy for nutrient intake. Results Food intake of 17 patients (6- to 30-year-olds) was considered adequate regarding macronutrients. Children and adolescents failed in presenting this parameter. Macronutrients were satisfactory in both groups. Children and adolescents displayed increased intake of iron and vitamins B1 ( p  
ISSN:2316-7874
1519-8928
2316-7874
DOI:10.1186/s41110-018-0066-1