Lipid and hemolysis parameters predicting acute chest syndrome in adulthood with sickle cell disease

Guillaume Feugray1,2, Maximilien Grall3, Cécile Dumesnil4

  • 1Department of General Biochemistry, Normandie Univ, UNIROUEN, INSERM U1096 EnVI, CHU Rouen, Rouen, F-76000, France. guillaume.feugray@chu-rouen.fr.

PubMed

Insights

Biomarkers like total bilirubin and C-reactive protein may predict acute chest syndrome (ACS) in sickle cell disease (SCD) patients. Lower levels of non-HDL-C and small dense LDL cholesterol (sdLDL-C) were associated with a decreased risk of developing ACS.

Area of Science:

  • Hematology
  • Cardiovascular Medicine
  • Genetics

Background:

  • Sickle cell disease (SCD) is a common monogenic disorder impacting around 100,000 individuals in the U.S.
  • Acute chest syndrome (ACS) is a severe, life-threatening complication of SCD.
  • Predicting ACS is crucial for timely intervention and improved patient outcomes.

Purpose of the Study:

  • To evaluate hemolysis and lipid profiles in SCD patients.
  • To identify biomarkers that predict the development of ACS within one year.

Main Methods:

  • Analysis of standard lipid panels (triglycerides, total cholesterol, HDL-C, LDL-C) to calculate non-HDL-C, large buoyant LDL-C, and small dense LDL-C (sdLDL-C) using the Sampson equation.
  • Assessment of hemolysis and hematologic parameters.
  • Logistic regression analysis to determine associations between biomarkers and ACS occurrence in 91 SCD patients.

Main Results:

  • Total bilirubin and C-reactive protein levels were associated with an increased risk of ACS.
  • Non-HDL-C and sdLDL-C levels were associated with a decreased risk of ACS.
  • Thirty-seven patients had a history of ACS, and 6 developed ACS during the study period.

Conclusions:

  • Easily accessible biomarkers measured during steady-state SCD can help predict future ACS development.
  • Further validation studies are necessary to confirm these predictive findings and ensure reproducibility.

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