Acquired coenzyme Q10 deficiency in children with recurrent food intolerance and allergies

Mitochondrion

Volumn 11, Issue 1, 2011, Pages 127-135

  Miles, Michael V ^a   Putnam, Philip E ^a   Miles, Lili ^a   Tang, Peter H ^a   DeGrauw, Antonius J ^a   Wong, Brenda L ^a   Horn, Paul S ^a,b   Foote, Heather L ^a   Rothenberg, Marc E ^a  

^a UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF CINCINNATI   (United States)

Author keywords

Allergy; Coenzyme Q10; Electron transport chain; Food intolerance; Mitochondria; Muscle pathology; Respiratory chain; Ubiquinone

Indexed keywords

CORTICOSTEROID; PROTON PUMP INHIBITOR; UBIDECARENONE;

ADOLESCENT; ARTICLE; BODY HEIGHT; BODY MASS; BODY WEIGHT; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; DISEASE DURATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME BLOOD LEVEL; ENZYME DEFICIENCY; FEMALE; FOOD ALLERGY; GASTROINTESTINAL DISEASE; HUMAN; HUMAN TISSUE; MALE; MITOCHONDRIAL RESPIRATION; MUSCLE BIOPSY; MUSCLE DISEASE; NEUROLOGIC DISEASE; NUTRITIONAL INTOLERANCE; NUTRITIONAL STATUS; PRIORITY JOURNAL; RESPIRATORY CHAIN;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; ELECTRON TRANSPORT; EOSINOPHILIA; FEMALE; FOOD HYPERSENSITIVITY; GASTROINTESTINAL DISEASES; HUMANS; MALE; MITOCHONDRIA; MITOCHONDRIAL DISEASES; QUADRICEPS MUSCLE; UBIQUINONE;

EID: 78650034161     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mito.2010.08.010     Document Type: Article

References (50)

1. Aeby A., Sznajer Y., Cavé H., Rebuffat E., Van Coster R., Rigal O., Van Bogaert P. Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency. J. Inherit. Metab. Dis. 2007, 30:827.
2. Aguilera-Aguirre L., Bacsi A., Saavedra-Molina A., Kurosky A., Sur S., Boldogh I. Mitochondrial dysfunction increases allergic airway inflammation. J. Immunol. 2009, 183:5379-5387.
3. Artuch R., Vilaseca M.A., Moreno J., Lambruschini N., Cambra F.J., Campistol J. Decreased serum ubiquinone-10 concentrations in phenylketonuria. Am. J. Clin. Nutr. 1999, 70(5):892-895.
4. Bernier F.P., Boneh A., Dennett X., Chow C.W., Cleary M.A., Thorburn D.R. Diagnostic criteria for respiratory chain disorders in adults and children. Neurology 2002, 59:1406-1411.
5. Cooper J.M., Korlipara L.V., Hart P.E., Bradley J.L., Schapira A.H. Coenzyme Q10 and vitamin E deficiency in Friedreich's ataxia: predictor of efficacy of vitamin E and coenzyme Q10 therapy. Eur. J. Neurol. 2008, 15(12):1371-1379.
6. Cordero M.D., De Miguel M., Moreno Fernandez A.M., Carmona Lopez I.M., Garrido Maraver J., Cotan D., Gomez Izquierdo L., Bonal P., Campa F., Bullon P., Navas P., Sanchez Alcazar J.A. Mitochondrial dysfunction and mitophagy activation in blood mononuclear cells of fibromyalgia patients: implication in the pathogenesis of the disease. Arthritis Res. Ther. 2010, 12:R17.
7. Depeint F., Bruce W.R., Shangari N., Mehta R., O'Brien P.J. Mitochondrial function and toxicity: role of the B vitamin family on mitochondrial energy metabolism. Chem. Biol. Interact. 2006, 163:94-112.
8. Duncan A.J., Heales S.J., Mills K., Eaton S., Land J.M., Hargreaves I.P. Determination of coenzyme Q10 status in blood mononuclear cells, skeletal muscle, and plasma by HPLC with di-propoxy-coenzyme Q10 as an internal standard. Clin. Chem. 2005, 51:2380-2382.
9. Ferguson D.D., Foxx-Orenstein A.E. Eosinophilic esophagitis: an update. Dis. Esophagus 2007, 20:2-8.
10. Furuta G.T., Forbes D., Boey C., Dupont C., Putnam P., Roy S., Sabrá A., Salvatierra A., Yamashiro Y., Husby S. Eosinophilic gastrointestinal diseases (EGIDs). J. Pediatr. Gastroenterol. Nutr. 2008, 47:234-238.
11. Gazdík F., Gvozdjáková A., Nádvorníková R., Repická L., Jahnová E., Kucharská J., Piják M.R., Gazdíková K. Decreased levels of coenzyme Q(10) in patients with bronchial asthma. Allergy 2002, 57:811-814.
12. Gellerich F.N., Mayr J.A., Reuter S., Sperl W., Zierz S. The problems of inter-lab variation in methods for mitochondrial disease diagnosis: enzymatic measurement of respiratory chain complexes. Mitochondrion 2004, 4:427-439.
13. Gempel K., Topaloglu H., Talim B., Schneiderat P., Schoser B.G., Hans V.H., Pálmafy B., Kale G., Tokatli A., Quinzii C., Hirano M., Naini A., DiMauro S., Prokisch H., Lochmüller H., Horvath R. The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene. Brain 2007, 130:2037-2044.
14. Haas R.H., Parikh S., Falk M.J., Saneto R.P., Wolf N.I., Darin N., Cohen B.H. Mitochondrial disease: a practical approach for primary care physicians. Pediatrics 2007, 120:1326-1333.
15. Haas R.H., Parikh S., Falk M.J., Saneto R.P., Wolf N.I., Darin N., Wong L.J., Cohen B.H., Naviaux R.K. The in-depth evaluation of suspected mitochondrial disease: The Mitochondrial Medicine Society's Committee on Diagnosis. Mol. Genet. Metab. 2008, 94:16-37.
16. Hargreaves I.P. Coenzyme Q10 in phenylketonuria and mevalonic aciduria. Mitochondrion 2007, 7 Suppl.:75-80.
17. Hershey A.D., Powers S.W., Vockell A.L., Lecates S.L., Ellinor P.L., Segers A., Burdine D., Manning P., Kabbouche M.A. Coenzyme Q10 deficiency and response to supplementation in pediatric and adolescent migraine. Headache 2007, 47(1):73-80.
18. Hui J., Kirby D.M., Thorburn D.R., Boneh A. Decreased activities of mitochondrial respiratory chain complexes in non-mitochondrial respiratory chain diseases. Dev. Med. Child Neurol. 2006, 48:132-136.
19. Jongpiputvanich S., Sueblinvong T., Norapucsunton T. Mitochondrial respiratory chain dysfunction in various neuromuscular diseases. J. Clin. Neurosci. 2005, 12:426-428.
20. Kamei M., Fujita T., Kanbe T., Sasaki K., Oshiba K., Otani S., Matsui-Yuasa I., Morisawa S. The distribution and content of ubiquinone in foods. Int. J. Vitam. Nutr. Res. 1986, 56:57-63.
21. Laguna T.A., Sontag M.K., Osberg I., Wagener J.S., Accurso F.J., Sokol R.J. Decreased total serum coenzyme Q10 concentrations: a longitudinal study in children with cystic fibrosis. J. Pediatr. 2008, 153:402-407.
22. Lee J.S., Hwang J.S., Ryu K.H., Lee E.H., Kim S.H. Mitochondrial respiratory complex I deficiency simulating spinal muscular atrophy. Pediatr. Neurol. 2007, 36:45-47.
23. Liacouras C.A. Eosinophilic esophagitis. Gastroenterol. Clin. North Am. 2008, 37:989-998. xi.
24. Mabalirajan U., Dinda A.K., Kumar S., Roshan R., Gupta P., Sharma S.K., Ghosh B. Mitochondrial structural changes and dysfunction are associated with experimental allergic asthma. J. Immunol. 2008, 181:3540-3548.
25. Matsuoka T., Maeda H., Goto Y., Nonaka I. Muscle coenzyme Q10 in mitochondrial encephalomyopathies. Neuromuscul. Disord. 1991, 1:443-447.
26. McFarland R., Taylor R.W., Turnbull D.M. Mitochondrial disease - its impact, etiology, and pathology. Curr. Top. Dev. Biol. 2007, 77:113-155.
27. Miles L., Miles M.V., Tang P.H., Horn P.S., Wong B.L., DeGrauw T.J., Morehart P.J., Bove K.E. Muscle coenzyme Q: a potential test for mitochondrial activity and redox status. Pediatr. Neurol. 2005, 32:318-324.
28. Miles L., Wong B.L., Dinopoulos A., Morehart P.J., Hofmann I.A., Bove K.E. Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods. Hum. Pathol. 2006, 37:173-184.
29. Miles M.V., Miles L., Tang P.H., Horn P.S., Steele P.E., DeGrauw A.J., Wong B.L., Bove K.E. Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain deficiencies. Mitochondrion 2008, 8:170-180.
30. Molyneux S.L., Florkowski C.M., George P.M., Pilbrow A.P., Frampton C.M., Lever M., Richards A.M. Coenzyme Q10: an independent predictor of mortality in chronic heart failure. J. Am. Coll. Cardiol. 2008, 52:1435-1441.
31. Moslemi A.R., Darin N. Molecular genetic and clinical aspects of mitochondrial disorders in childhood. Mitochondrion 2007, 7:241-252.
32. Oglesbee D., Freedenberg D., Kramer K.A., Anderson B.D., Hahn S.H. Normal muscle respiratory chain enzymes can complicate mitochondrial disease diagnosis. Pediatr. Neurol. 2006, 35:289-292.
33. Okamoto T., Fukui K., Nakamoto M., Kishi T., Kanamori N., Kataoka K., Nishii S., Kishi H., Hiraoka E., Okada A. Serum levels of coenzyme Q10 and lipids in patients during total parenteral nutrition. J. Nutr. Sci. Vitaminol. 1986, 32(1):1-12.
34. Putnam P.E., Rothenberg M.E. Eosinophilic esophagitis: concepts, controversies, and evidence. Curr. Gastroenterol. Rep. 2009, 11:220-225.
35. Quinzii C.M., Kattah A.G., Naini A., Akman H.O., Mootha V.K., DiMauro S., Hirano M. Coenzyme Q deficiency and cerebellar ataxia associated with an aprataxin mutation. Neurology 2005, 64:539-541.
36. Quinzii C.M., DiMauro S., Hirano M. Human coenzyme Q(10) deficiency. Neurochem. Res. 2007, 32:723-727.
37. Quinzii C.M., López L.C., Von-Moltke J., Naini A., Krishna S., Schuelke M., Salviati L., Navas P., DiMauro S., Hirano M. Respiratory chain dysfunction and oxidative stress correlate with severity of primary CoQ10 deficiency. Faseb J. 2008, 22:1874-1885.
38. Rodríguez-Hernández A., Cordero M.D., Salviati L., Artuch R., Pineda M., Briones P., Gómez Izquierdo L., Cotán D., Navas P., Sánchez-Alcázar J.A. Coenzyme Q deficiency triggers mitochondria degradation by mitophagy. Autophagy 2009, 5:19-32.
39. Rötig A., Mollet J., Rio M., Munnich A. Infantile and pediatric quinone deficiency diseases. Mitochondrion 2007, 7(Suppl 1):S112-S121.
40. Sacconi S., Trevisson E., Salviati L., Aymé S., Rigal O., Redondo A.G., Mancuso M., Siciliano G., Tonin P., Angelini C., Auré K., Lombès A., Desnuelle C. Coenzyme Q10 is frequently reduced in muscle of patients with mitochondrial myopathy. Neuromuscul. Disord. 2010, 20:44-48.
41. Sant'Anna A.M., Rolland S., Fournet J.C., Yazbeck S., Drouin E. Eosinophilic esophagitis in children: symptoms, histology and pH probe results. J. Pediatr. Gastroenterol. Nutr. 2004, 39:373-377.
42. Spergel J.M., Brown-Whitehorn T.F., Beausoleil J.L., Franciosi J., Shuker M., Verma R., Liacouras C.A. 14years of eosinophilic esophagitis: clinical features and prognosis. J. Pediatr. Gastroenterol. Nutr. 2009, 48:30-36.
43. Tang P.H., Miles M.V., DeGrauw A., Hershey A., Pesce A. HPLC analysis of reduced and oxidized coenzyme Q(10) in human plasma. Clin. Chem. 2001, 47:256-265.
44. Tang P.H., Miles M.V., Miles L., Quinlan J., Wong B., Wenisch A., Bove K. Measurement of reduced and oxidized coenzyme Q9 and coenzyme Q10 levels in mouse tissues by HPLC with coulometric detection. Clin. Chim. Acta 2004, 341:173-184.
45. Taylor R.W., Schaefer A.M., Barron M.J., McFarland R., Turnbull D.M. The diagnosis of mitochondrial muscle disease. Neuromuscul. Disord. 2004, 14:237-245.
46. Thorburn D.R., Chow C.W., Kirby D.M. Respiratory chain enzyme analysis in muscle and liver. Mitochondrion 2004, 4:363-375.
47. Uusimaa J., Remes A.M., Rantala H., Vainionpää L., Herva R., Vuopala K., Nuutinen M., Majamaa K., Hassinen I.E. Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders. Pediatrics 2000, 105:598-603.
48. Vallance H. Biochemical approach to the investigation of pediatric mitochondrial disease. Pediatr. Dev. Pathol. 2004, 7:633-636.
49. Weber C., Bysted A., Hølmer G. Coenzyme Q10 in the diet-daily intake and relative bioavailability. Mol. Aspects Med. 1997, 18(Suppl):S251-S254.
50. Zeviani M., Di Donato S. Mitochondrial disorders. Brain 2004, 127:2153-2172.