The week's pick
Random Articles
Reseach Article
Metabolic Nutri-Expert System: A Comprehensive Tool for Achieving Metabolic Control of Inborn Errors of Amino Acid Metabolism
| International Journal of Computer Applications |
| Foundation of Computer Science (FCS), NY, USA |
| Volume 182 - Number 10 |
| Year of Publication: 2018 |
| Authors: Zohreh Mazloom, Seyedeh Maryam Abdollahzadeh, Vahid Ashktorab, Baran Hashemi, Mojtaba Zandieh, Hossein Moravej, Zohreh Karamizadeh |
10.5120/ijca2018917711
|
Zohreh Mazloom, Seyedeh Maryam Abdollahzadeh, Vahid Ashktorab, Baran Hashemi, Mojtaba Zandieh, Hossein Moravej, Zohreh Karamizadeh . Metabolic Nutri-Expert System: A Comprehensive Tool for Achieving Metabolic Control of Inborn Errors of Amino Acid Metabolism. International Journal of Computer Applications. 182, 10 ( Aug 2018), 1-5. DOI=10.5120/ijca2018917711
Abstract
The main aim of this study was to develop a comprehensive nutritional planning expert system for inborn errors of amino acid metabolism (IEAAM). Metabolic Nutri-Expert System, integrated in the electronic nutritional history record, was designed to accelerate either dietitian or patient/parent knowledge acquisition and education about the particular disease and propose culturally appropriate low protein diet to improve metabolic control or maintain the present health status. The Genetic Metabolic Dietitians International (GMDI) nutritional guideline was used to estimate the recommended nutritional values in the proposed system. The recommended daily Intakes (RDIs) for patients ingesting amino acid mixture, the U.S. Department of agriculture (UDSA) nutrient list, and both Iranian and modern low protein recipes were applied to perform diet planning. The proposed system also allows the user to modify the diet as he/she likes, and to propose his/her own low protein cookery recipes as well. This comprehensive computer system, through the multidisciplinary viewpoint, aimed to at least partially replace some of the regular traditional metabolic dietitian visits and optimize the patient's metabolic control and adherence outcomes.
References
- El-Hattab, A.W., Inborn errors of metabolism. Clinics in perinatology, 2015. 42(2): p. 413-439.
- Hadj-Taieb, S., et al., Aminoacidopathies and organic acidurias in Tunisia: a retrospective survey over 23 years. La Tunisie Medicale, 2012. 90(3): p. 258-261.
- Ho, G., et al., Metabolic Diet App Suite for inborn errors of amino acid metabolism. Molecular genetics and metabolism, 2016. 117(3): p. 322-327.
- Raghuveer, T.S., U. Garg, and W.D. Graf, Inborn errors of metabolism in infancy and early childhood: an update. Am fam physician, 2006. 73(11): p. 1981-90.
- Ramaswamy, M., et al., A Rare Case of Malonic Aciduria Diagnosed by Newborn Screening in Qatar. International Journal of Neonatal Screening, 2017. 3(1): p. 5.
- Campa, K.M., M.A. Lloyd-Puryearb, and K.L. Huntingtonc, Nutritional Treatment for Inborn Errors of Metabolism: Indications, Regulations, and Availability of Medical Foods and Dietary Supplements Using Phenylketonuria as an Example. Mol Genet Metab, 2012. 107(1-2): p. 3-9.
- Bernstein, L.E., F. Rohr, and J.R. Helm, Nutrition Management of Inherited Metabolic Diseases. 2015: Springer.
- García, d.D.L., M. Cuervo, and J. Martinez, Software for performing a global phenotypic and genotypic nutritional assessment. Nutricion hospitalaria, 2013. 28(5): p. 1622-1632.
- Wysocki, T. and L. Gavin, Paternal involvement in the management of pediatric chronic diseases: Associations with adherence, quality of life, and health status. Journal of Pediatric Psychology, 2005. 31(5): p. 501-511.
- Abi-Wardé, M.-T., et al., Long-term metabolic follow-up and clinical outcome of 35 patients with maple syrup urine disease. Journal of inherited metabolic disease, 2017. 40(6): p. 783-792.
- Sweeney, A.L., R.M. Roberts, and J.M. Fletcher, Dietary protein counting as an alternative way of maintaining metabolic control in phenylketonuria, in JIMD Reports-Case and Research Reports, 2011/3. 2011, Springer. p. 131-139.
- ten Hoedt, A.E., et al., " MY PKU": increasing self-management in patients with phenylketonuria. A randomized controlled trial. Orphanet journal of rare diseases, 2011. 6(1): p. 48.
- Wendel, U. and U. Langenbeck, Towards self-monitoring and self-treatment in phenylketonuria—a way to better diet compliance. European journal of pediatrics, 1996. 155(1): p. S105-S107.
- Park, Y., H.S. Jeong, and N. Joo, A study on multi-cultural family wives adapting to Korean cuisine and dietary patterns. Nutrition research and practice, 2010. 4(5): p. 405-413.
- Dhananjayan, R., S. Rajeswari, and S. Swaminathan, Inborn metabolic disorders–An update. International Journal of Bioassays, 2015. 4(3): p. 3719-3728.
Index Terms
Keywords