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    Lactate dehydrogenase (LDH) is an enzyme () 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).


        Lactate dehydrogenase
            Enzyme isoforms
            Genetics in Humans
                Hemolysis
                Tissue turnover
                Exudates and transudates
                Meningitis and encephalitis
                HIV and elevated LDH

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    Enzyme isoforms
      LDH-1 (4H) - in the heart
      LDH-3 (2H2M) - in the lungs
      LDH-4 (1H3M) - in the kidneys

    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 The use of this pheonomenon to diagnose infarction has been largely superseded by the use of Troponin I or T measurement.

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    Genetics in Humans
    The M and H subunits are encoded by two different genes:
      The M subunit is encoded by LDHA, located on chromosome 11p15.4 ()
      The H subunit is encoded by LDHB, located on chromosome 12p12.2-p12.1 ()
      A third isoform, LDHC or LDHX, is expressed only in the testis (); its gene is likely a duplicate of LDHA and is also located on the eleventh chromosome (11p15.5-p15.3)

    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.

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    Hemolysis
    In medicine, LDH is often used as a marker of tissue breakdown. As LDH is abundant in red blood cells and 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.
    It can also be used as a marker of myocardial infarction. Following a myocardial infarction, levels of LDH peak at 3-4 days and remain elevated for up to 10 days. In this way, elevated levels of LDH can be useful for determining if a patient has had a myocardial infarction if they come to doctors several days after an episode of chest pain.

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    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 (especially lymphoma) patients, as cancer cells have a high rate of turnover, with destroyed cells leading to an elevated LDH activity.

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    Exudates and transudates
    Measuring LDH in fluid aspirated from a pleural effusion (or pericardial effusion) 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 exudate and low in a transudate. In empyema, the LDH levels generally will exceed 1000 U/l.

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    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.

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    HIV and elevated LDH
    LDH is often measured in HIV patients as a non-specific marker for Pneumocystis jiroveci (formerly Pneumocystis carinii) pneumonia (PCP). Elevated LDH in the setting of upper respiratory symptoms in an HIV patient suggests, but is not diagnostic for, PCP.




     
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    This article is licensed under the GNU Free Documentation License [copyleft]. It uses material from the Wikipedia article "Lactate dehydrogenase". link