Metallomics and proteomics of the biological fluids in ALS patients: preliminary data

Introduction. Amyotrophic Lateral Sclerosis (ALS) is a rare neurodegenerative disorder characterized by selective degeneration of both upper and lower motor neurons in the brain, brainstem, and spinal cord. This results in paralysis due to muscle weakness and atrophy, leading to death in 3-5 years1. Genetic and environmental factors are involved in the pathogenesis of the disease and metals metabolism have been linked to ALS2. Methods. The study enrolled 7 patients and 5 controls (age matched, living in the same geographical area). For metal quantitation, samples were analyzed by ICP-MS. For proteomic analyses, immobilized pH gradient covered the 4-10 pH range. Image analyses were carried out with Image Master Software. Statistical analyses were carried out with Student’s t-test. Results. Among the 20 metals analyzed, As concentration resulted significantly lower in patients than in controls (p=0.007); Hg also was found in lower concentration in patients, but with a lower statistical significance (p=0.13). Higher concentration of Al in patients was detected (p=0.08). In this study, we were not able to confirm the higher concentrations of Ni and Pb in patients previously described in a smaller cohort3. Our proteomics data show that APOA2 is decreased by 30% in patients with respect to controls. Furthermore, AHSG and SAP showed a significant decrease in patients with a story of more than 10 years of disease. Conclusions. Impaired metal homeostasis, attributable to environmental exposure, could lead to mineral overload. Besides promoting oxidative stress, metals can compete for the binding sites of metal-containing proteins, such as those containing iron-sulfur clusters3. At present, no literature data link APOA2 to ALS, but the fact that its mRNA is processed by TDP43, provides a possible connection with the disease. The proteins differentially expressed belong to the group of Acute Phase Reaction proteins, possibly linking ALS to a chronic inflammation status. Acknowledgements. We thank “Comitato per la Fondazione Giovanni Raffo – Onlus” for support and partial funding of this work. References. 1 Chiò et al. (2013) Global epidemiology of amyotrophiclateral sclerosis: a systematic review of the published literature. Neuroepidemiology 2 Hadzhieva et al. (2014) Review: iron metabolism and the role of iron in neurodegenerative disorders. Neuropathol Appl Neurobiol 3 De Benedetti et al. (2016) Serum metal evaluation in a small cohort of Amyotrophic Lateral Sclerosis patients reveals high levels of thiophylic species. Peptidomics