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[Rinsho Byori 50 : 571`575, 2002]
Lactate Dehydrogenase M Subunit Deficiency Lactate Dehydrogenase(LDH) M subunit deficiency was first discovered by
urinary discoloration and discrepancy in laboratory data. The response
to ischemic forearm work is characteristic(absence of an increased venous
lactate concentration after ischemic work and a marked increase in venous
pyruvate are found). The increase of pyruvate concentration is specific
to LDH-M subunit deficiency. Glycolysis was markedly retarded in the patient's
muscle in the glyceraldehyde 3-phosphate dehydrogenase(GAPDH) step, possibly
due to the impaired reoxidation of NADH produced by GAPDH activity. Then
the excessive NADH is reoxidized by a -glycerophosphate and glycerol. Therefore,
ATP production is significantly impaired and muscle tissue is damaged.
Molecular analysis revealed a detection of 20 base-pairs in exon 6 in LDH-M
subunit deficiency. This mutation results in a frame-shift translation
and premature termination. |