Biomarkers of brain injury in foals with neonatal maladjustment syndrome
TL;DR
Higher BDNF, S100B, and pregnane concentrations were consistent with NMS, and might allow for neurological assessment, and might allow for neurological assessment.
Abstract
Abstract Background Plasma concentrations of brain-derived neurotrophic factor (BDNF), glial-fibrillary-acidic protein (GFAP), and astrocytic protein S100B, might be linked to the pathophysiology of Neonatal Maladjustment Syndrome (NMS). Hypothesis/Objectives To measure serum concentration of BDNF and S100B, plasma concentration of GFAP, and neurosteroids (progesterone and 17α-hydroxyprogesterone) in foals with NMS, foals presented for other diseases, including premature, and healthy foals, and determine their association with outcome. Animals Fourteen healthy foals, 19 NMS foals, 39 foals hospitalized for other diseases < 7 days of age. Methods In this prospective, longitudinal study, concentrations of biomarkers were determined in all foals on admission, at day 1 and 2 of hospitalization. Plasma or serum concentration of biomarkers was measured with ELISA and single-molecule-array technology. Results Forty-eight foals survived, 10 did not survive. Serum BDNF concentration was lower after 24 h of hospitalization in NMS foals (baseline: 3.0, 1.9-4.1 g/mL; day 1: 2.0, 1.2-2.8 pg/mL) (P = .02). Serum S100B was higher in septic foals with NMS (marginal means, 95% CI, 435.3, 290-580 ng/mL) compared to septic foals without NMS (238.9, 164.6-313.2 ng/mL) on admission (P = .01). Pregnane concentrations were higher in NMS foals compared to healthy and sick foals over the first 48 h of hospitalization (P < .05). Conclusions and clinical importance Higher BDNF, S100B, and pregnane concentrations were consistent with NMS, and might allow for neurological assessment.