Serum lactate dehydrogenase-3 isoenzyme in chronic granulocytic leukemia

R M Buchsbaum1, F J Liu, J M Trujillo

  • 1Division of Laboratory Medicine, University of Texas M. D. Anderson Cancer Center, Houston 77030.

Insights

Serum lactate dehydrogenase-3 (LD-3) levels are highly indicative of chronic granulocytic leukemia (CGL) activity. Elevated LD-3, assessed by absolute and relative values, shows potential as a sensitive biomarker for CGL detection.

Area of Science:

  • Biochemistry
  • Hematology
  • Oncology

Background:

  • Chronic granulocytic leukemia (CGL) is a myeloproliferative neoplasm.
  • Lactate dehydrogenase (LD) is an enzyme with multiple isoenzymes.
  • LD isoenzyme patterns, particularly LD-3, have been investigated as potential biomarkers in various cancers.

Purpose of the Study:

  • To evaluate the diagnostic utility of serum lactate dehydrogenase-3 (LD-3) activity in patients with chronic granulocytic leukemia (CGL).
  • To assess the correlation between LD-3 levels and CGL disease status (active, partial remission, complete remission).
  • To determine the optimal criteria for measuring LD-3 to maximize clinical sensitivity.

Main Methods:

  • Serum samples from patients with active CGL, partial remission, and complete remission were analyzed.
  • Electrophoresis was used to determine LD isoenzyme patterns.
  • Three criteria for LD-3 elevation were defined: criterion-1 (ratio and absolute value), criterion-2 (ratio only), and criterion-3 (absolute value only, with isomorphic elevation).

Main Results:

  • Abnormal LD-3 activity was observed in 92% of active CGL patients, 40% in partial remission, and 13% in complete remission.
  • Criterion-3 (absolute LD-3 elevation with isomorphic isoenzyme elevation) increased sensitivity for active CGL from 82% to 92%.
  • Mean serum LD-3 and total LD activity differed significantly between disease states but not within active CGL subgroups.

Conclusions:

  • Evaluating serum LD-3 in both absolute and relative terms enhances its clinical sensitivity for CGL.
  • LD-3 shows promise as a useful biomarker for monitoring CGL.
  • Further investigation into unexplained LD-5 elevations in remission patients may be warranted.

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