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Yang, C. Acatalasemia. Encyclopedia. Available online: (accessed on 23 June 2024).
Yang C. Acatalasemia. Encyclopedia. Available at: Accessed June 23, 2024.
Yang, Catherine. "Acatalasemia" Encyclopedia, (accessed June 23, 2024).
Yang, C. (2020, December 23). Acatalasemia. In Encyclopedia.
Yang, Catherine. "Acatalasemia." Encyclopedia. Web. 23 December, 2020.

Acatalasemia is a condition characterized by very low levels of an enzyme called catalase. Many people with acatalasemia never have any health problems related to the condition and are diagnosed because they have affected family members.

genetic conditions

1. Introduction

Some of the first reported individuals with acatalasemia developed open sores (ulcers) inside the mouth that led to the death of soft tissue (gangrene). When mouth ulcers and gangrene occur with acatalasemia, the condition is known as Takahara disease. These complications are rarely seen in more recent cases of acatalasemia, probably because of improvements in oral hygiene.

Studies suggest that people with acatalasemia have an increased risk of developing type 2 diabetes, which is the most common form of diabetes. A higher percentage of people with acatalasemia have type 2 diabetes than in the general population, and the disease tends to develop at an earlier age (in a person's thirties or forties, on average). Researchers speculate that acatalasemia could also be a risk factor for other common, complex diseases; however, only a small number of cases have been studied.

2. Frequency

More than 100 cases of acatalasemia have been reported in the medical literature. Researchers estimate that the condition occurs in about 1 in 12,500 people in Japan, 1 in 20,000 people in Hungary, and 1 in 25,000 people in Switzerland. The prevalence of acatalasemia in other populations is unknown.

3. Causes

Mutations in the CAT gene can cause acatalasemia. This gene provides instructions for making the enzyme catalase, which breaks down hydrogen peroxide molecules into oxygen and water. Hydrogen peroxide is produced through chemical reactions within cells. At low levels, it is involved in several chemical signaling pathways, but at high levels it is toxic to cells. If hydrogen peroxide is not broken down by catalase, additional reactions convert it into compounds called reactive oxygen species that can damage DNA, proteins, and cell membranes.

Mutations in the CAT gene greatly reduce the activity of catalase. A shortage of this enzyme can allow hydrogen peroxide to build up to toxic levels in certain cells. For example, hydrogen peroxide produced by bacteria in the mouth may accumulate in and damage soft tissues, leading to mouth ulcers and gangrene. A buildup of hydrogen peroxide may also damage beta cells of the pancreas, which release a hormone called insulin that helps control blood sugar. Malfunctioning beta cells are thought to underlie the increased risk of type 2 diabetes in people with acatalasemia. It is unclear why some people have no health problems associated with a loss of catalase activity.

Many people with reduced catalase activity do not have an identified mutation in the CAT gene; in these cases, the cause of the condition is unknown. Researchers believe that other genetic and environmental factors can also influence the activity of catalase.

4. Inheritance

Acatalasemia has an autosomal recessive pattern of inheritance, which means both copies of the CAT gene in each cell have mutations. When both copies of the gene are altered, the activity of catalase is reduced to less than 10 percent of normal.

When only one of the two copies of the CAT gene has a mutation, the activity of catalase is reduced by approximately half. This reduction in catalase activity is often called hypocatalasemia. Like acatalasemia, hypocatalasemia usually does not cause any health problems.

5. Other Names for This Condition

  • acatalasia

  • catalase deficiency


  1. Góth L, Eaton JW. Hereditary catalase deficiencies and increased risk ofdiabetes. Lancet. 2000 Nov 25;356(9244):1820-1.
  2. Góth L, Nagy T. Acatalasemia and diabetes mellitus. Arch Biochem Biophys. 2012Sep 15;525(2):195-200. doi: 10.1016/
  3. Góth L, Nagy T. Inherited catalase deficiency: is it benign or a factor invarious age related disorders? Mutat Res. 2013 Oct-Dec;753(2):147-54. doi:10.1016/j.mrrev.2013.08.002.
  4. Góth L, Rass P, Páy A. Catalase enzyme mutations and their association withdiseases. Mol Diagn. 2004;8(3):141-9. Review.
  5. Góth L. A new type of inherited catalase deficiencies: its characterizationand comparison to the Japanese and Swiss type of acatalasemia. Blood Cells MolDis. 2001 Mar-Apr;27(2):512-7.
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