The Expression of Genes Related to Lipid Metabolism and Metabolic Disorders in Children before and after Hematopoietic Stem Cell Transplantation-A Prospective Observational Study.
Wojciech CzogałaMałgorzata CzogałaKinga KwiecińskaMirosław Bik MultanowskiPrzemysław J TomasikPrzemysław HałubiecAgnieszka ŁazarczykKarol MiklusiakSzymon SkoczeńPublished in: Cancers (2021)
Metabolic disorders in children after hematopoietic stem cell transplantation (HSCT) are poorly characterized. However, it is known that dyslipidemia and insulin resistance are particularly common in these patients. We conducted a prospective study of 27 patients treated with HSCT to assess the possibility of predicting these abnormalities. We measured gene expressions using a microarray technique to identify differences in expression of genes associated with lipid metabolism before and after HSCT. In patients treated with HSCT, total cholesterol levels were significantly higher after the procedure compared with the values before HSCT. Microarray analysis revealed statistically significant differences in expressions of three genes, DPP4, PLAG1, and SCD, after applying the Benjamini-Hochberg procedure (pBH < 0.05). In multiple logistic regression, the increase of DPP4 gene expression before HCST (as well as its change between pre- and post-HSCT status) was associated with dyslipidemia. In children treated with HSCT, the burden of lipid disorders in short-term follow-up seems to be lower than before the procedure. The expression pattern of DPP4 is linked with dyslipidemia after the transplantation.
Keyphrases
- hematopoietic stem cell
- poor prognosis
- gene expression
- young adults
- insulin resistance
- genome wide
- end stage renal disease
- minimally invasive
- newly diagnosed
- fatty acid
- genome wide identification
- chronic kidney disease
- bioinformatics analysis
- binding protein
- acute myeloid leukemia
- metabolic syndrome
- adipose tissue
- risk factors
- peritoneal dialysis
- stem cells
- copy number
- high fat diet
- polycystic ovary syndrome
- low density lipoprotein
- transcription factor
- cell therapy
- drug induced
- glycemic control