Serum lactate dehydrogenase activity as a biomarker in children with sickle cell disease

Sandra O'Driscoll1, Susan E Height, Moira C Dick

  • 1Department of Paediatric Haematology, King's College School of Medicine, King's College Hospital, Denmark Hill, London, UK.

Insights

Serum lactate dehydrogenase (LDH) levels are higher in children with sickle cell disease (HbSS) and correlate with cerebral vasculopathy. This finding highlights LDH as a potential marker for stroke risk in these patients.

Area of Science:

  • Hematology
  • Pediatrics
  • Neurology

Background:

  • Sickle cell disease (SCD) encompasses HbSS and HbSC genotypes, each with distinct clinical manifestations.
  • Cerebral vasculopathy is a significant complication in SCD, increasing the risk of stroke.
  • Transcranial Doppler (TCD) scanning is a key tool for assessing cerebral blood flow velocity and identifying vasculopathy.

Purpose of the Study:

  • To investigate serum lactate dehydrogenase (LDH) levels in children with HbSS and HbSC.
  • To determine the relationship between LDH levels and cerebral vasculopathy detected by TCD in pediatric SCD patients.

Main Methods:

  • Retrospective analysis of pediatric patients with HbSS (n=97) and HbSC (n=18) who underwent TCD in 2006.
  • Measurement and comparison of serum LDH levels between HbSS and HbSC groups.
  • Correlation analysis between LDH levels and TCD parameters in HbSS patients.

Main Results:

  • Serum LDH levels were significantly higher in children with HbSS compared to HbSC (581 IU/l vs. 305 IU/l, P < 0.001).
  • In HbSS patients, LDH showed significant correlations with hemoglobin, reticulocytes, aspartate transaminase, and creatinine.
  • LDH levels positively correlated with TCD measurements in the middle and anterior cerebral artery circulations in children with HbSS.

Conclusions:

  • Elevated serum LDH is characteristic of HbSS in children.
  • Serum LDH levels are associated with cerebral vasculopathy in children with HbSS.
  • LDH may serve as a potential biomarker for identifying children with SCD at higher risk for cerebrovascular complications.

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