Background Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency is a disorder of fatty acid ß-oxidation, occurring in at least 1 in 20,000 live births. The enzyme deficiency is medium-chain acyl-CoA dehydrogenase, one of four mitochondrial acyl-CoA dehydrogenases that carry out the initial dehydrogenation step in the ß-oxidation of fatty acids. MCAD deficiency results in an impaired ability to oxidize dietary and endogenous fatty acids of medium-chain length (6 – 12 carbons).
Clinical
MCAD deficiency generally presents between the second month and the second year of life, although onset as early as two days and as late as adulthood has been reported. Clinical presentation is often triggered by a seemingly innocuous illness like otitis media or a viral syndrome. The initiating event is probably prolonged fasting, which increases lipolysis and the need for fatty acid oxidation. Symptoms include vomiting, lethargy, apnea, coma, cardiopulmonary arrest, or sudden unexplained death. Initial symptoms often precede the onset of profound hypoglycemia, and are probably related to high free fatty acid levels. Hypoglycemia occurs from an inability to meet gluconeogenic requirements during fasting despite activation of an alternate pathway of substrate production (protein catabolism). Physical examination of the acutely ill child is remarkable for mild to moderate hepatomegaly, and some patients may also have demonstrable muscle weakness. Without prior indication of metabolic disease, 20–25 percent of patients with this disease will die with their first episode of illness. Cerebral edema, and fatty liver, heart, and kidneys are noted at autopsy, often leading to a misdiagnosis of Reye’s syndrome or Sudden Infant Death Syndrome (SIDS). This disorder accounts for about one percent of SIDS deaths.
Testing
Newborn Screening by tandem mass spectrometry of the heel stick dried blood spot identifies elevated levels of octanoylcarnitine (C8 acylcarnitine), usually accompanied by decanoyl (C10), hexanoyl (C6) and decenoyl (C10:1) carnitine esters. When symptomatic, laboratory examination of blood may reveal hypoglycemia, metabolic acidosis, mild lactic acidosis, hyperammonemia, elevated BUN, and high uric acid levels. Serum transaminases are usually elevated. The urine often shows inappropriately low or absent ketones due to impaired fatty acid oxidation. Low serum and urine carnitines are typically found in the untreated patient. Biochemical testing of blood and urine for carnitine, acylcarnitines, acylglycines, and organic acids is diagnostic for this disorder. A generalized dicarboxylic aciduria is noted, characterized by elevations of suberylglycine and hexanoylglycine. In fibroblasts, the activity of medium chain acyl-CoA dehydrogenase is severely deficient in affected individuals, while heterozygous carriers for the disease usually have intermediate levels of activity, but are otherwise clinically and metabolically unaffected. Detection of mutations in the MCAD gene on chromosome 1 in affected individuals confirms the biochemical results and accurately detects asymptomatic carriers among other family members. A common 985A>G mutation is responsible for up to 85% of cases. DNA analysis of postmortem tissue is possible when plasma and urine samples are not available. Prenatal diagnosis is possible by enzyme assay of amniocyte cultures. DNA analysis in amniocytes or chorionic villi can also be helpful in the diagnosis of an affected fetus in at-risk pregnancies.
Treatment
Fundamental to the medical management of MCAD is the need to avoid fasting, particularly during periods of high metabolic stress, such as illness. Overnight fasts should be managed with nighttime or late evening feedings where appropriate. The addition of food-grade cornstarch mixed in liquid at bedtime has also helped to decrease the frequency of morning hypoglycemia in some patients. High carbohydrate intake should be encouraged during illnesses, with initiation of intravenous glucose supplementation if the child is unsuccessful in keeping down fluids or unable to take adequate oral feedings. The preventive efficacy of a low fat diet versus a normal fat diet is unclear, but high intake of long and medium-chain fatty acids should be avoided. Supplementation with oral L-carnitine has been associated with a reduction in the frequency and severity of episodes. The continued need for carnitine supplementation post-puberty is uncertain, and has not been adequately studied. Because the diagnosis and therapy of MCAD deficiency is complex, the pediatrician is advised to manage the patient in close collaboration with a consulting pediatric metabolic disease specialist. It is recommended that parents travel with a letter of treatment guidelines from the patient’s physician.
Inheritance
This disorder most often follows an autosomal recessive inheritance pattern. With recessive disorders affected patients usually have two copies of a disease gene (or mutation) in order to show symptoms. People with only one copy of the disease gene (called carriers) generally do not show signs or symptoms of the condition but can pass the disease gene to their children. When both parents are carriers of the disease gene for a particular disorder, there is a 25% chance with each pregnancy that they will have a child affected with the disorder. As with all genetic diseases, genetic counseling may be appropriate to help families understand recurrence risks and ensure that they receive proper evaluation and care.
References Coates, P.M., Hale, D.E., Stanley, C.A., et al. Genetic deficiency of medium chain Acyl-CoA dehydrogenase. Studies in cultured skin fibroblasts and peripheral mononuclear leukocytes. Pediatric Research 19:672, 1985. Roe, C.R., Millington, D.S., Maltby, D.A., et al. Recognition of Medium Chain Acyl-CoA Dehydrogenase Deficiency in asymptomatic siblings of children dying of Sudden Infant Death or Reye like syndromes. J Pediatrics 108:13, 1986. Ding, J-H, Roe, C.R., Iafolla, A.K., et al. Diagnosis of Medium Chain Acyl-CoA Dehydrogenase Deficiency in children dying suddenly without explanation by mutation analysis in post-mortem fixed tissue. New England J of Medicine 325:61, 1991. Roe, C.R. and Ding, J-H. Mitochondrial Fatty Acid Oxidation Disorders. In The Metabolic and Molecular Basis of Inherited Disease. 8th Edition, 2001. Scriver, Beaudet, et al. McGraw-Hill. Chapter 101, pg.2297-2326. Nada, M.A., Chace, D.H., Spracher, H., et al. Investigation of beta oxidation intermediates in normal and MCAD-deficient fibroblasts using tandem mass spectrometry. Biochem Molec Med 54:59, 1995. Nada, M.A., Vianey-Saban, C., Roe, C.R., et al. Prenatal diagnosis of mitochondrial fatty acid oxidation defects. Prenatal Diag 16:117, 1996.
Web Sites
SaveBabies.org
Site established and maintained by parents of newborns affected with a rare genetic defect, with information for parents and professionals and links to other informative sites.
National Newborn Screening and Genetics Resource Center
Provides information and resources in the area of newborn screening and genetics to benefit health professionals, the public health community, consumers and government officials.
Disclaimers
The analyses conducted by PerkinElmer Genetics produce results that can be used by qualified physicians in the diagnosis of disorders described herein. Evidence of these conditions will be detected in the vast majority of affected individuals; however, due to genetic variability, age of the patient at the time of specimen collection, quality of the specimen, health status of the patient, and other variables, such conditions may not be detected in all affected patients. PerkinElmer Genetics makes no warranty whatsoever, express or implied, including any warranty as to accuracy, completeness or timeliness, concerning the information contained herein, and you should not assume that such information is complete or the most up-to-date information available. PerkinElmer Genetics shall not be liable for any loss, claim or damages caused in whole or in part by our provision of, or your use of, any of the information contained herein. As a general statement, this information was drawn from published literature and is not drawn from our patient population or screening experience. The information contained herein is not intended to be a substitute for professional medical advice and should not be used for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions.
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