Identification of erythrocyte biomarkers in amyotrophic lateral sclerosis

Catarina Duarte Lima, Susana Pinto, Patrícia Napoleão, Ana Catarina Pronto-Laborinho, Maria Amparo Barros, Teresa Freitas, Mamede De Carvalho, Carlota Saldanha

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)

Abstract

INTRODUCTION: Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease of the motor system. It has been hypothesised that red blood cells (RBCs) may be involved in the disease process by the release of damaging molecules. OBJECTIVE: The aim of this ex vivo study is to compare RBCs biochemical and hemorheological parameters between ALS patients and healthy donors to identify novel biomarkers of the ALS disease. METHODS: We included 82 ALS patients and 40 gender age-matched healthy donors. We performed quantification of erythrocyte aggregation and deformability, nitric oxide (NO) efflux from RBCs, acetylcholinesterase (AChE) enzyme activity and intraerythrocytic concentration of nitrite, nitrate and S-nitrosogluthatione (GSNO). RESULTS: Erythrocyte deformability and AChE activity were increased in patients with ALS in comparison to healthy donors. NO efflux from RBCs and concentration of intraerythrocytic nitrite were lower in ALS patients. In patients, we found that for higher NO range of values the respiratory function is worse and that for higher AChE range of values the RBCs nitrite content increase. CONCLUSION: The results of the present study indicate that NO efflux from RBCs and RBCs AChE should be further explored as potential biomarkers for ALS.

Original languageEnglish
Pages (from-to)423-437
Number of pages15
JournalClinical Hemorheology and Microcirculation
Volume63
Issue number4
DOIs
Publication statusPublished - 2016
Externally publishedYes

Keywords

  • Acetylcholinesterase
  • amyotrophic lateral sclerosis
  • erythrocyte
  • nitric oxide
  • nitrite
  • respiratory function

Fingerprint

Dive into the research topics of 'Identification of erythrocyte biomarkers in amyotrophic lateral sclerosis'. Together they form a unique fingerprint.

Cite this