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Genetics Home Reference: your guide to understanding genetic conditions
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HADH

Reviewed April 2010

What is the official name of the HADH gene?

The official name of this gene is “hydroxyacyl-CoA dehydrogenase.”

HADH is the gene's official symbol. The HADH gene is also known by other names, listed below.

What is the normal function of the HADH gene?

The HADH gene provides instructions for making an enzyme called 3-hydroxyacyl-CoA dehydrogenase that is important for converting certain fats to energy. This enzyme is involved in a process called fatty acid oxidation, in which several enzymes work in a step-wise fashion to break down (metabolize) fats and convert them to energy. The role of 3-hydroxyacyl-CoA dehydrogenase is to metabolize groups of fats called medium-chain fatty acids and short-chain fatty acids. These fatty acids are found in foods such as milk and certain oils and are produced when larger fatty acids are metabolized.

3-hydroxyacyl-CoA dehydrogenase functions in mitochondria, the energy-producing centers within cells. This enzyme is especially important for the normal functioning of the heart, liver, kidneys, muscles, and pancreas. The pancreas makes enzymes that help digest food, and it also produces insulin, which controls how much sugar is passed from the blood into cells for conversion to energy.

3-hydroxyacyl-CoA dehydrogenase is essential in the process that converts medium-chain and short-chain fatty acids to ketones, the major source of energy used by the heart and muscles. During prolonged periods without food (fasting) or when energy demands are increased, ketones are also important for the liver and other tissues.

How are changes in the HADH gene related to health conditions?

3-hydroxyacyl-CoA dehydrogenase deficiency - caused by mutations in the HADH gene

At least three mutations in the HADH gene have been found to cause 3-hydroxyacyl-CoA dehydrogenase deficiency. These mutations change single protein building blocks (amino acids) used to make the 3-hydroxyacyl-CoA dehydrogenase enzyme. These changes probably alter the 3-dimensional shape of the enzyme, which impairs its normal function.

With a shortage (deficiency) of functional 3-hydroxyacyl-CoA dehydrogenase, medium-chain and short-chain fatty acids are not metabolized properly. As a result, these fatty acids are not converted to energy, which can lead to signs and symptoms of 3-hydroxyacyl-CoA dehydrogenase deficiency such as lack of energy (lethargy) and low blood sugar (hypoglycemia). Medium-chain and short-chain fatty acids that are not broken down can build up in tissues and damage the liver, heart, and muscles, causing serious complications.

other disorders - caused by mutations in the HADH gene

Mutations in the HADH gene have been reported in a small number of people with familial hyperinsulinism. This disorder is characterized by abnormally high levels of insulin (hyperinsulinism) and unusually low blood sugar (hypoglycemia).

Researchers have identified at least five HADH gene mutations that cause familial hyperinsulinism. These mutations severely reduce 3-hydroxyacyl-CoA dehydrogenase activity, either by impairing the enzyme's function or by decreasing the amount of this enzyme in cells. Researchers believe that inadequate 3-hydroxyacyl-CoA dehydrogenase activity in the pancreas leads to excessive insulin secretion and hypoglycemia in people with familial hyperinsulinism. It is unclear why the HADH gene mutations that cause familial hyperinsulinism seem to affect only the pancreas.

Where is the HADH gene located?

Cytogenetic Location: 4q22-q26

Molecular Location on chromosome 4: base pairs 107,989,713 to 108,035,174

The HADH gene is located on the long (q) arm of chromosome 4 between positions 22 and 26.

The HADH gene is located on the long (q) arm of chromosome 4 between positions 22 and 26.

More precisely, the HADH gene is located from base pair 107,989,713 to base pair 108,035,174 on chromosome 4.

See How do geneticists indicate the location of a gene? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genelocation) in the Handbook.

Where can I find additional information about HADH?

You and your healthcare professional may find the following resources about HADH helpful.

You may also be interested in these resources, which are designed for genetics professionals and researchers.

What other names do people use for the HADH gene or gene products?

  • HAD
  • HADH1
  • HADHSC
  • HCDH_HUMAN
  • HHF4
  • hydroxyacyl-Coenzyme A dehydrogenase
  • L-3-hydroxyacyl-Coenzyme A dehydrogenase
  • L-3-hydroxyacyl-Coenzyme A dehydrogenase, short chain
  • medium and short chain L-3-hydroxyacyl-coenzyme A dehydrogenase
  • MGC8392
  • M/SCHAD
  • SCHAD
  • short chain 3-hydroxyacyl-CoA dehydrogenase

See How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.

What glossary definitions help with understanding HADH?

acids ; CoA ; coenzyme A ; congenital ; deficiency ; dehydrogenase ; enzyme ; familial ; fasting ; fatty acids ; gene ; hyperinsulinism ; hypoglycemia ; insulin ; lethargy ; mitochondria ; oxidation ; pancreas ; protein ; secretion

You may find definitions for these and many other terms in the Genetics Home Reference Glossary (http://www.ghr.nlm.nih.gov/glossary).

References

  • Bennett MJ, Russell LK, Tokunaga C, Narayan SB, Tan L, Seegmiller A, Boriack RL, Strauss AW. Reye-like syndrome resulting from novel missense mutations in mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase. Mol Genet Metab. 2006 Sep-Oct;89(1-2):74-9. Epub 2006 May 24. (http://www.ncbi.nlm.nih.gov/pubmed/16725361?dopt=Abstract)
  • Clayton PT, Eaton S, Aynsley-Green A, Edginton M, Hussain K, Krywawych S, Datta V, Malingre HE, Berger R, van den Berg IE. Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion. J Clin Invest. 2001 Aug;108(3):457-65. (http://www.ncbi.nlm.nih.gov/pubmed/11489939?dopt=Abstract)
  • Hussain K, Clayton PT, Krywawych S, Chatziandreou I, Mills P, Ginbey DW, Geboers AJ, Berger R, van den Berg IE, Eaton S. Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene. J Pediatr. 2005 May;146(5):706-8. (http://www.ncbi.nlm.nih.gov/pubmed/15870679?dopt=Abstract)
  • Kapoor RR, James C, Flanagan SE, Ellard S, Eaton S, Hussain K. 3-Hydroxyacyl-coenzyme A dehydrogenase deficiency and hyperinsulinemic hypoglycemia: characterization of a novel mutation and severe dietary protein sensitivity. J Clin Endocrinol Metab. 2009 Jul;94(7):2221-5. doi: 10.1210/jc.2009-0423. Epub 2009 May 5. (http://www.ncbi.nlm.nih.gov/pubmed/19417036?dopt=Abstract)
  • Molven A, Matre GE, Duran M, Wanders RJ, Rishaug U, Njølstad PR, Jellum E, Søvik O. Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation. Diabetes. 2004 Jan;53(1):221-7. (http://www.ncbi.nlm.nih.gov/pubmed/14693719?dopt=Abstract)
  • NCBI Gene (http://www.ncbi.nlm.nih.gov/gene/3033)
  • OMIM: 3-HYDROXYACYL-CoA DEHYDROGENASE (http://omim.org/entry/601609)
  • Yang SY, He XY, Schulz H. 3-Hydroxyacyl-CoA dehydrogenase and short chain 3-hydroxyacyl-CoA dehydrogenase in human health and disease. FEBS J. 2005 Oct;272(19):4874-83. Review. (http://www.ncbi.nlm.nih.gov/pubmed/16176262?dopt=Abstract)

 

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

 
Reviewed: April 2010
Published: July 28, 2014