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Akçaağaç Şurubu İdrar Hastalığı ve Beslenme

Yıl 2020, Cilt: 6 Sayı: 3, 317 - 323, 01.01.2020

Öz

Akçaağaç şurubu idrar hastalığı MSUD dallı zincirli amino asitler BCAA olan valin, izolösin ve lösin metabolizmasındaki bozuklukla karakterize bir metabolizma hastalığıdır. İdrar ve plazmada dallı zincirli amino asit artışı gözlenmektedir. İdrarda hastalığın adını aldığı akçaağacı kokusu bulunmaktadır. Otozomal resesif geçişli nadir görülen hastalık, klinik seyir ve tiamine verilen yanıta göre beş tipte incelenmektedir. Hastalığın tıbbi beslenme tedavisi ise akut atak dönem ve uzun süreli diyet uygulaması olmak üzere iki aşamadan oluşmaktadır. Akut dönemde beslenme hedefi vücut sıvıları ve dokularında dallı zincirli amino asitleri ve artık ürünlerini uzaklaştırmaktır. Anne sütüyle beslenen bebeklerde sütün lösin içeriği nedeniyle emzirme sonlandırılabilir. Uzun süreli MSUD beslenme planlamasında ise metabolik kontrolün sağlanması, hastalığın erken tespiti, hastalıkla gelişen nörolojik bozuklukların ve zekâ puanındaki düşüşlerin azaltılması amaçlanmaktadır. Beslenmede dallı zincirli amino asit düzeyini gösteren besin değişim listelerinin kullanılması önerilmektedir. Hastalara dallı zincirli amino asit içermeyen formülalar ile destek sağlanabilir. Bireylerde klinik durumun ve diyetin takibi önemlidir

Kaynakça

  • MacDonald A, Dixon M, White F. Disorders of amino acid metabolism, organic acidaemias and urea cycle defects. Shaw V, Lawson M (eds).Clinical Paediatric Dietetics 3rd ed. Oxford: Blackwell Publishing, 2007; 309-80.
  • Nyhan WL, Barshop BA, Ozand PT. Maple Syrup Urine Disease. In: Arnold H ed. Atlas of Metabolic Disease 2nd ed. Oxford: Oxford University Press, 2005:159-68.
  • Marshal L, Digeoerge A. Maple syrup urine disease in old order Mennonites. Am J Human Genet 1981; 33:139A.
  • Chuang DT, Shih VE. Disorders of branched chain amino acid and keto acid metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D, (eds). Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill, 1995:1239-77.
  • Coskun T. Dallı zincirli amino asitler. In: Coskun T. Amino asit metabolizması ve bozuklukları. Ankara: Alp Ofset Matbaacılık, 2003: 124-35.
  • Neyzi O, Ertuğrul T. Pediyatri, Cilt 1. 4th ed. içinde Demirkol M, ed. Organik asidemiler. İstanbul: Nobel, 2010; 820-3.
  • Fingerhut R, Simon E, Maier EM, et al: Maple syrup urine disease: Newborn screening fails to discriminate between classic and variant forms. Clin Chem 2008; 54(10):1739-41.
  • Chuang DT, Shih VE. Maple syrup urine disease (branched-chain ketoasiduria). In: The Metabolic and Molecular Bases of Inherited Disease. Scriver CR, Beaudet AL, Sly WS, Valle D (eds). New York: McGraw- Hill, 2001: 1971-2005.
  • Morton DH, Strauss KA, Robinson DL et al. Diagnosis and treatment of maple syrup urine disease: A study of 36 patients. Pediatrics 2002; 109:999-1008.
  • Rezvani I, Rosenblatt DS. Valine, leucine, isoleucine, and related organic acidemias. In: Kliegman R; Stanton B; Behrman RE; St Geme JW, Schor NF (eds). Nelson Textbook of Pediatrics. Philadelphia: Elsevier, 2016: 649- 58.
  • Çamur S. 199 Organik Asidemili Hastanın Klinik, Laboratuvar ve Demografik Özelliklerinin Retrospektif olarak Değerlendirilmesi, Uzmanlık Tezi, Hacettepe Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Ankara, 1996.
  • Schadewaldt P, Bodner-Leidecker A, Hammen HW, Wendel U. Significance of Lalloisoleucine in plasma for diagnosis of maple syrup urine disease. Clin Chem 1999; 45:1734-40.
  • Ong LC, Khoo TB, Zulfiqar A, Zarida H, Ruzana A. Computed tomography findings in maple syrup urine disease. Singapore Med J 1998; 39:370-2.
  • Gökmen Özel H. Genetik Metabolik Hastalıklarda Tıbbi Beslenme Tedavisi, Akbulut G. Besin & Beslenme Bakım Süreci. Ankara: Ankara Nobel Tıp Kitapevleri, 2019, 901-2.
  • Mazariegos GV, Morton DH, Sindhi R, Soltys K, Nayyar N, Bond G, et al. Liver transplantation for classical maple syrup urine disease: long-term followup in 37 patients and comparative United Network for Organ Sharing experience. The Journal of Pediatrics 2012; 160(1):116- 21.e1.
  • Strauss KA, Mazariegos GV, Sindhi R, Squires R, Finegold DN, Vockley G, et al. Elective liver transplantation for the treatment of classical maple syrup urine disease. Am J Transplant 2006; 6(3):557-64.
  • MacDonald A. Principles of Dietary Management. In: Hoffmann G, Zschocke J, Nyhan W. (eds). Inherited Metabolic Diseases. Berlin, Heidelberg, Springer, 2017.
  • Handoom B, Megdad E, Al-Qasabi D, Al Mesned M, Hawary R, Al-Nufiee S, Al-Hassnan Z, Alsayed MD, Eldali A. The effects of low protein products availability on growth parameters and metabolic control in selected amino acid metabolism disorders patients. Int J Pediatr Adolesc Med 2018; 5(2):60-8.
  • Özel GH. Diyet tedavisi. İçinde: Çoşkun T, Yurdakök M. Yenidoğanda Kalıtsal Metabolik Hastalıklar. Ankara: Güneş Tıp Kitabevleri, 2014; 348-57.
  • Çoşkun T, Yurdakök M. Yenidoğanda Kalıtsal Metabolik Hastalıklar. Ankara: Güneş Tıp Kitabevleri, 2014; 29-81.
  • Chuang DT, Shih VE. Maple syrup urine disease (branched- chain ketoaciduria). In: Valle D, et al. (eds). The online metabolic and molecular bases of inherited disease. New York, McGraw Hill, 2010.
  • Frazier DM, Allgeier C, Homer C, et al. Nutrition management guideline for maple syrup urine disease: An evidence- and consensus-based approach. Mol Genet Metab 2014; 112(3):210-7.
  • Zubarioglu T. Nutritional Treatment in Maple Syrup Urine Disease: General Information, International Inborn Errors of Metabolism and Nutrition Congress, İstanbul 2019, 45-47. http://metabolizma2019.org/ International_Inborn_Errors%20_of_Metabolism_and_ Nutrition_Congress_1014_April_2019_Istanbul.pdf Erişim: 22.07.19
  • Strauss KA, Wardley B, Robinson D, Hendrickson C, Rider NL, Puffenberger EG, et al. Classical maple syrup urine disease and brain development: Principles of management and formula design. Molecular Genetics and Metabolism 2010; 99(4):333-45.
  • Coskun T. Çocuklarda beslenme durumunun değerlendirilmesi. Çocuklarda enteral ve parenteral beslenme. Ankara: Sinem Ofset, 1997, S:28-38.
  • Lo C. Laboratory assessment of nutritional status. In: Nutrition in Pediatrics. Basic science and clinical application, WA Walker and JB Watkins (eds.). Toronto, BC Decker, 1997, 29-43.
  • Clemmons DR, Seek MM, Underwood LE. Supplemental essential amino acids augment the somatomedin-C/ insulin-like growth factor I response to refeeding after fasting. Metabolism 1985; 34:391-5.

Maple Syrup Urine Disease and Nutrition

Yıl 2020, Cilt: 6 Sayı: 3, 317 - 323, 01.01.2020

Öz

Maple syrup urine disease MSUD is a metabolic disease characterized by a defect in the metabolism of valine, isoleucine, and leucine, which are branched-chain amino acids BCAA . An increase in branched-chain amino acids is observed in the urine and plasma. In the urine, there is a maple smell that the disease takes its name from. This rare autosomal recessive disorder is studied in five types according to the clinical course and response to thiamine. Medical nutrition therapy has two stages. Dietary treatments are applied during the acute attack period and over the long-term. The aim of nutrition in the acute period is to remove branched-chain amino acids and residual products in the body fluids and tissues. Breastfeeding might need to be terminated due to the leucine content of the milk. The aim of long-term MSUD nutrition planning is providing metabolic control, early detection of the disease, and reduction of neurological disorders. Nutrient exchange lists showing the level of branched-chain amino acids within the diet are recommended. Support might be provided with formulas that do not contain branched-chain amino acids. The follow-up of the clinical condition and diet is important in these patients

Kaynakça

  • MacDonald A, Dixon M, White F. Disorders of amino acid metabolism, organic acidaemias and urea cycle defects. Shaw V, Lawson M (eds).Clinical Paediatric Dietetics 3rd ed. Oxford: Blackwell Publishing, 2007; 309-80.
  • Nyhan WL, Barshop BA, Ozand PT. Maple Syrup Urine Disease. In: Arnold H ed. Atlas of Metabolic Disease 2nd ed. Oxford: Oxford University Press, 2005:159-68.
  • Marshal L, Digeoerge A. Maple syrup urine disease in old order Mennonites. Am J Human Genet 1981; 33:139A.
  • Chuang DT, Shih VE. Disorders of branched chain amino acid and keto acid metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D, (eds). Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill, 1995:1239-77.
  • Coskun T. Dallı zincirli amino asitler. In: Coskun T. Amino asit metabolizması ve bozuklukları. Ankara: Alp Ofset Matbaacılık, 2003: 124-35.
  • Neyzi O, Ertuğrul T. Pediyatri, Cilt 1. 4th ed. içinde Demirkol M, ed. Organik asidemiler. İstanbul: Nobel, 2010; 820-3.
  • Fingerhut R, Simon E, Maier EM, et al: Maple syrup urine disease: Newborn screening fails to discriminate between classic and variant forms. Clin Chem 2008; 54(10):1739-41.
  • Chuang DT, Shih VE. Maple syrup urine disease (branched-chain ketoasiduria). In: The Metabolic and Molecular Bases of Inherited Disease. Scriver CR, Beaudet AL, Sly WS, Valle D (eds). New York: McGraw- Hill, 2001: 1971-2005.
  • Morton DH, Strauss KA, Robinson DL et al. Diagnosis and treatment of maple syrup urine disease: A study of 36 patients. Pediatrics 2002; 109:999-1008.
  • Rezvani I, Rosenblatt DS. Valine, leucine, isoleucine, and related organic acidemias. In: Kliegman R; Stanton B; Behrman RE; St Geme JW, Schor NF (eds). Nelson Textbook of Pediatrics. Philadelphia: Elsevier, 2016: 649- 58.
  • Çamur S. 199 Organik Asidemili Hastanın Klinik, Laboratuvar ve Demografik Özelliklerinin Retrospektif olarak Değerlendirilmesi, Uzmanlık Tezi, Hacettepe Üniversitesi Tıp Fakültesi Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Ankara, 1996.
  • Schadewaldt P, Bodner-Leidecker A, Hammen HW, Wendel U. Significance of Lalloisoleucine in plasma for diagnosis of maple syrup urine disease. Clin Chem 1999; 45:1734-40.
  • Ong LC, Khoo TB, Zulfiqar A, Zarida H, Ruzana A. Computed tomography findings in maple syrup urine disease. Singapore Med J 1998; 39:370-2.
  • Gökmen Özel H. Genetik Metabolik Hastalıklarda Tıbbi Beslenme Tedavisi, Akbulut G. Besin & Beslenme Bakım Süreci. Ankara: Ankara Nobel Tıp Kitapevleri, 2019, 901-2.
  • Mazariegos GV, Morton DH, Sindhi R, Soltys K, Nayyar N, Bond G, et al. Liver transplantation for classical maple syrup urine disease: long-term followup in 37 patients and comparative United Network for Organ Sharing experience. The Journal of Pediatrics 2012; 160(1):116- 21.e1.
  • Strauss KA, Mazariegos GV, Sindhi R, Squires R, Finegold DN, Vockley G, et al. Elective liver transplantation for the treatment of classical maple syrup urine disease. Am J Transplant 2006; 6(3):557-64.
  • MacDonald A. Principles of Dietary Management. In: Hoffmann G, Zschocke J, Nyhan W. (eds). Inherited Metabolic Diseases. Berlin, Heidelberg, Springer, 2017.
  • Handoom B, Megdad E, Al-Qasabi D, Al Mesned M, Hawary R, Al-Nufiee S, Al-Hassnan Z, Alsayed MD, Eldali A. The effects of low protein products availability on growth parameters and metabolic control in selected amino acid metabolism disorders patients. Int J Pediatr Adolesc Med 2018; 5(2):60-8.
  • Özel GH. Diyet tedavisi. İçinde: Çoşkun T, Yurdakök M. Yenidoğanda Kalıtsal Metabolik Hastalıklar. Ankara: Güneş Tıp Kitabevleri, 2014; 348-57.
  • Çoşkun T, Yurdakök M. Yenidoğanda Kalıtsal Metabolik Hastalıklar. Ankara: Güneş Tıp Kitabevleri, 2014; 29-81.
  • Chuang DT, Shih VE. Maple syrup urine disease (branched- chain ketoaciduria). In: Valle D, et al. (eds). The online metabolic and molecular bases of inherited disease. New York, McGraw Hill, 2010.
  • Frazier DM, Allgeier C, Homer C, et al. Nutrition management guideline for maple syrup urine disease: An evidence- and consensus-based approach. Mol Genet Metab 2014; 112(3):210-7.
  • Zubarioglu T. Nutritional Treatment in Maple Syrup Urine Disease: General Information, International Inborn Errors of Metabolism and Nutrition Congress, İstanbul 2019, 45-47. http://metabolizma2019.org/ International_Inborn_Errors%20_of_Metabolism_and_ Nutrition_Congress_1014_April_2019_Istanbul.pdf Erişim: 22.07.19
  • Strauss KA, Wardley B, Robinson D, Hendrickson C, Rider NL, Puffenberger EG, et al. Classical maple syrup urine disease and brain development: Principles of management and formula design. Molecular Genetics and Metabolism 2010; 99(4):333-45.
  • Coskun T. Çocuklarda beslenme durumunun değerlendirilmesi. Çocuklarda enteral ve parenteral beslenme. Ankara: Sinem Ofset, 1997, S:28-38.
  • Lo C. Laboratory assessment of nutritional status. In: Nutrition in Pediatrics. Basic science and clinical application, WA Walker and JB Watkins (eds.). Toronto, BC Decker, 1997, 29-43.
  • Clemmons DR, Seek MM, Underwood LE. Supplemental essential amino acids augment the somatomedin-C/ insulin-like growth factor I response to refeeding after fasting. Metabolism 1985; 34:391-5.
Toplam 27 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Derleme
Yazarlar

Zeynep Kaya Bu kişi benim

Hande Öngün Yılmaz Bu kişi benim

Yayımlanma Tarihi 1 Ocak 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 6 Sayı: 3

Kaynak Göster

Vancouver Kaya Z, Öngün Yılmaz H. Akçaağaç Şurubu İdrar Hastalığı ve Beslenme. Akd Tıp D. 2020;6(3):317-23.