Blood plasma and bone marrow interstitial fluid metabolomics of sickle cell disease patients with osteonecrosis: An exploratory study to dissect biochemical alterations.

Clin Chim Acta

Metabolomics Research Group, Departamento de Química Orgânica, Instituto de Química, Universidade Federal da Bahia, Salvador, Brazil. Electronic address:

Published: January 2023

AI Article Synopsis

  • Sickle cell disease (SCD) often leads to vaso-occlusive crises, which can result in severe organ damage including osteonecrosis (ON), affecting up to 50% of SCD patients.
  • A study used NMR-based untargeted metabolomics to analyze blood plasma and bone marrow interstitial fluid from SCD patients with osteonecrosis, identifying metabolic changes linked to different disease stages.
  • Citrate may serve as a potential biomarker to distinguish SCD patients with and without osteonecrosis, while metabolites like acetate, creatinine, and glucose were associated with various disease stages; however, the study's findings are limited by small sample sizes and lack of validation.

Article Abstract

Individuals with sickle cell disease (SCD) often experience numerous vaso-occlusive crisis events throughout their lives, which can progress to severe damage of several organs, including avascular necrosis, also known as osteonecrosis (ON). Osteonecrosis is one of the most devastating musculoskeletal clinical manifestations of sickle cell disease, afflicting up to 50% of the SCD patients. Herein, a NMR-based untargeted metabolomics approach was used to assess the metabolome alterations of blood plasma and bone marrow interstitial fluid (BMIF) samples of SCD patients with osteonecrosis. Furthermore, biochemical signatures associated with different osteonecrosis stages were assessed by analysing the metabolome of blood plasma and bone marrow interstitial fluid samples of SCD patients with different stages of the disease based on the Fiat and Arlet classification (FAC). Multivariate statistical analysis allowed a clear discrimination between the studied groups and it provided important insights into the different osteonecrosis stages. Citrate was pointed out as a possible biomarker to differentiate SCD patients with and without osteonecrosis. Acetate, creatinine, histidine, tyrosine, glucose, and NI5 seems to be key metabolites associated to different stages of the disease. Although this is a pioneer exploratory study, we acknowledge that fact that it is limited by the group sizes and absence of a validation cohort. Nevertheless, multivariate statistical analyses indicated that the metabolome of blood plasma and BMIF samples encompasses a complex metabolic regulation system for osteonecrosis.

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http://dx.doi.org/10.1016/j.cca.2022.11.026DOI Listing

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