Plasma levels of advanced glycation end products are associated with haemolysis-related organ complications in sickle cell patients

Erfan Nur, Dees P. Brandjes, John-John B. Schnog, Hans-Martin Otten, Karin Fijnvandraat, Casper G. Schalkwijk, Bart J. Biemond*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review


Oxidative stress plays an important role in the pathophysiology of sickle cell disease (SCD). Plasma levels of advanced glycation end products (AGEs) are increased under oxidative conditions and are associated with disease severity in diabetes and inflammatory diseases. We investigated whether AGEs are increased in sickle cell patients and whether they are associated with SCD-related complications. Plasma levels of the AGEs pentosidine, N epsilon-(carboxymethyl)lysine (CML) and N epsilon-(carboxyethyl)lysine (CEL) were measured using single-column high performance liquid chromatography with fluorescence detection (pentosidine) and ultra performance liquid chromatography-tandem mass spectrometry (CML and CEL). Plasma levels of pentosidine and CML were increased in HbSS/HbS beta 0-thalassaemia (n = 60) and HbSC/HbS beta+-thalassaemia (n = 42) patients during steady state as compared to healthy HbAA controls (n = 30) without increments during painful crisis. CEL levels were comparable between all groups. Pentosidine and CML levels correlated significantly to haemolytic rate during the clinically asymptomatic state while pentosidine was significantly related to the number of haemolysis-related organ complications. The increased plasma AGE levels in sickle cell patients and their association with haemolysis and haemolysis-related complications suggest AGEs might be implicated in the pathophysiology of the haemolytic phenotype of SCD. Measurement of AGEs might be useful in predicting organ complications in SCD.
Original languageEnglish
Pages (from-to)62-69
JournalBritish Journal of Haematology
Issue number1
Publication statusPublished - Oct 2010


  • sickle cell disease
  • advanced glycation end products
  • oxidative stress
  • haemolysis
  • organ damage

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