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Catalytic function of LDH

Lactate dehydrogenase (LDH) is an enzyme (EC 1.1.1.27 (http://www.expasy.org/cgi-bin/nicezyme.pl?1.1.1.27)) present in a wide variety of organisms, including plants and animals. It catalyses the interconversion of pyruvate and lactate with concomitant interconversion of NADH and NAD+. As it can also catalyze the oxidation of hydroxybutyrate, it is occasionally called Hydroxybutyrate Dehydrogenase (HBD).

Contents

Enzyme isoforms

Every LDH molecule consists of four subunits, where each subunit is either H each M (based on their electrophoretic properties.) There are, therefore, five LDH isotypes:

Usually LDH-2 is the predominant form in the serum. An LDH-1 level higher than the LDH-2 level (a "flipped pattern"), suggests myocardial infarction (damage to heart tissues releases heart LDH, which is rich in LDH-1, into the bloodstream). The use of this pheonomenon to diagnose infarction has been largely superseded by the use of Troponin I or T measurement.


Genetics in Humans

The H and M subunits are encoded by two different genes:

  • The M subunit is encoded by LDHA, located on chromosome 11p15.4 (OMIM 150000 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150000))
  • The H subunit is encoded by LDHB, located on chromosome 12p12.2-p12.1 (OMIM 150100 (http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150100))

Mutations of the M subunit have been linked to the rare disease exertional myoglobinuria (see OMIM article), and mutations of the H subunit have been described but do not appear to lead to disease.


Medical use

Hemolysis

In medicine, LDH is often used as a marker of tissue breakdown. As LDH is abundant in red blood cells, it can function as a marker for hemolysis. A blood sample that has been handled incorrectly can show false-positively high levels of LDH due to erythrocyte damage.


Tissue turnover

Other uses are assessment of tissue breakdown in general; this is possible when there are no other indicators of hemolysis. It is used to follow-up cancer patients, as cancer cells have a high rate of turnover, with destroyed cells leading to an elevated LDH activity.


Exudates and transudates

Measuring LDH in pleural effusion (or pericardial fluid) can help in the distinction between exudates (actively secreted fluid, e.g. due to inflammation) or transudates (passively secreted fluid, due to a high hydrostatic pressure or a low oncotic pressure). LDH is elevated (>200 U/l) in an exsudate and low in a transudate. In empyema, the LDH levels generally will exceed 1000 U/l.


Meningitis and encephalitis

The enzyme is also found in cerebrospinal fluid where high levels of lactate dehydrogenase in cerebrospinal fluid are often associated with bacterial meningitis. High levels of the enzyme can also be found in cases of viral meningitis, generally indicating the presence of encephalitis and poor prognosis.


  Results from FactBites:
 
Lactate dehydrogenase - Wikipedia, the free encyclopedia (446 words)
Lactate dehydrogenase (LDH) is an enzyme (EC 1.1.1.27) present in a wide variety of organisms, including plants and animals.
In medicine, LDH is often used as a marker of tissue breakdown.
LDH is elevated (>200 U/l) in an exsudate and low in a transudate.
LDH: The Test (687 words)
Currently, the main use for LDH is as a general indicator of the existence and severity of acute or chronic tissue damage and, sometimes, as a monitor of progressive conditions.
LDH levels may also occasionally be ordered to monitor damage caused by muscle trauma or injury and to help identify hemolytic anemia (anemia caused by the breakage of red blood cells – either because they are unusually fragile or because something is mechanically breaking them (like an artificial heart valve)).
LDH and LDH isoenzymes may still be occasionally ordered along with CK and CK-MB when a patient has symptoms of a heart attack, but this is increasingly rare.
  More results at FactBites »


 
 

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