A Prospective, Cross Sectional Study of PNH Clone in MDS Patients Using High Sensitivity Flowcytometry: A Single

Faran Naim1, Amrita Saraf2, Jasmita Dass2

  • 1Department of Clinical Hematology, Sir Ganga Ram Hospital, New Delhi, India.

Insights

Subclinical paroxysmal nocturnal hemoglobinuria (PNH) clones are found in 30% of myelodysplastic syndrome (MDS) patients in India. Lactate dehydrogenase (LDH) levels can help predict PNH clone presence in MDS.

Area of Science:

  • Hematology
  • Oncology
  • Clinical Diagnostics

Background:

  • Subclinical paroxysmal nocturnal hemoglobinuria (PNH) clones can be present in patients with bone marrow failure syndromes, including aplastic anemia and myelodysplastic syndrome (MDS).
  • The presence of a PNH clone in MDS may have significant prognostic and therapeutic implications.
  • While literature suggests 1-10% of MDS cases harbor a PNH clone, data from India is limited.

Purpose of the Study:

  • To investigate the prevalence of PNH clones in adult MDS patients at presentation in India.
  • To evaluate the correlation between PNH clone size and lactate dehydrogenase (LDH) levels.
  • To determine a potential LDH cut-off for predicting PNH positivity in MDS patients, aiding test prescription in resource-limited settings.

Main Methods:

  • A high-sensitivity PNH assay using a single tube with FLAER, CD157, CD64, CD15, and CD45 antibodies was employed.
  • The study included 30 adult patients diagnosed with MDS at presentation.
  • A PNH clone size greater than 0.01% was considered significant.

Main Results:

  • A PNH clone was detected in 30% of the studied MDS patients.
  • A moderately positive correlation (r=0.735, p=0.001) was observed between PNH clone size and LDH values.
  • An LDH cut-off of 247 IU/L was identified as a potential predictor of a PNH clone (>1%) with moderate sensitivity and specificity.

Conclusions:

  • High-sensitivity PNH assays are effective in detecting even small PNH clones in MDS patients.
  • LDH levels show a significant correlation with PNH clone size in MDS.
  • Establishing an LDH cut-off can assist in judiciously selecting MDS patients for PNH testing, particularly in resource-constrained environments.

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