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Leukocyte glucose 6 phosphate dehydrogenase (G6PD) as prognostic indicator in children with acute lymphocytic

G S Devi1, M H Prasad, P P Reddy

  • 1Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Begumpet, Hyderabad, India.

Insights

Glucose-6-phosphate dehydrogenase (G6PD) activity is often decreased in acute lymphocytic leukemia (ALL) patients. Leukocyte G6PD levels and karyotype may serve as diagnostic and prognostic indicators for ALL.

Area of Science:

  • Hematology
  • Oncology
  • Biochemistry

Background:

  • Acute lymphocytic leukemia (ALL) is a significant hematologic malignancy.
  • Glucose-6-phosphate dehydrogenase (G6PD) is a crucial enzyme in red blood cell metabolism.
  • The role of G6PD activity in ALL pathogenesis and prognosis requires further elucidation.

Purpose of the Study:

  • To investigate G6PD enzyme activity in patients diagnosed with ALL before initiating therapy.
  • To explore the correlation between leukocyte G6PD levels, myelocyte percentage, and patient karyotype.
  • To assess the potential of G6PD activity as a diagnostic and prognostic biomarker in ALL.

Main Methods:

  • G6PD activity was measured in leukocytes of 37 ALL patients prior to treatment.
  • Statistical analysis was performed to correlate G6PD levels with myelocyte percentage and cytogenetic data (karyotype).
  • Prognostic significance was evaluated based on G6PD activity and karyotype status.

Main Results:

  • Significantly decreased G6PD activity was observed in 78.37% of ALL patients.
  • G6PD variation correlated with the percentage of myelocytes.
  • A strong correlation was found between G6PD activity, karyotype, and patient prognosis: normal G6PD/normal karyotype indicated good prognosis, while abnormal G6PD/abnormal karyotype suggested poor prognosis. Intermediate prognoses were observed in mixed cases.

Conclusions:

  • Leukocyte G6PD activity is frequently diminished in patients with ALL.
  • G6PD levels, in conjunction with karyotype analysis, demonstrate potential as valuable diagnostic and prognostic tools for acute lymphocytic leukemia.
  • Further research is warranted to explore the precise mechanisms underlying G6PD alterations in ALL.

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