TY - JOUR
T1 - Plasma Oxidized Albumin in Acute Ischemic Stroke Is Associated With Better Outcomes.
AU - Rael, Leonard T
AU - Leonard, Jan
AU - Salottolo, Kristin
AU - Bar-Or, Raphael
AU - Bartt, Russell E
AU - Wagner, Jeffrey C
AU - Bar-Or, David
N1 - Rael LT, Leonard J, Salottolo K, Bar-Or R, Bartt RE, Wagner JC, Bar-Or D. Plasma Oxidized Albumin in Acute Ischemic Stroke Is Associated With Better Outcomes. Front Neurol. 2019;10:709. doi: 10.3389/fneur.2019.00709. eCollection 2019. PubMed PMID: 31312177; PubMed Central PMCID: PMC6614430.
PY - 2019/7/2
Y1 - 2019/7/2
N2 - Introduction: Plasma oxidized human serum albumin (OxHSA) is evidence of an active antioxidant mechanism as measured by oxidized species of HSA. CXCL-10 is a pro-inflammatory chemokine associated with ischemic conditions. Accordingly, we examined the relationship of admission OxHSA and CXCL-10 with discharge mRS in acute ischemic stroke (AIS). Methods: Plasma samples and clinical data were collected prospectively at a Comprehensive Stroke Center. Admission biomarkers of oxidative stress, CXCL-10 and %OxHSA, were measured. We examined if CXCL-10 or %OxHSA correlated with age, admission NIHSS score, and discharge mRS score using Spearman's Rank correlation. Logistic regression was performed to identify independent predictors of a favorable discharge mRS (≤2). Results: In 106 consecutive AIS patients, the median age was 73 (IQR 61-84), 47% were male, and the median admission NIHSS score was 11 (IQR 5-19). %OxHSA and CXCL-10 were significantly correlated ( r = 0.23, p = 0.02). Both biomarkers were significantly correlated with age: %OxHSA ( r = 0.44, p < 0.001) and CXCL-10 ( r = 0.32, p = 0.001). Neither biomarker was correlated with admission NIHSS. There was a borderline significant correlation with discharge mRS and %OxHSA ( r = -0.17, p = 0.08), where higher %OxHSA correlated with lower discharge mRS scores. For every 1% increase in %OxHSA, the odds of a favorable discharge mRS increased 11%. The odds of a favorable discharge mRS decreased 18% for every 1-point increase in the initial NIHSS. Conclusions: OxHSA, the result of an oxidative environment and evidence of the strong antioxidant buffering capacity of HSA, correlated with CXCL-10 and discharge mRS, implying that strong antioxidant activity of albumin may confer better outcomes.
AB - Introduction: Plasma oxidized human serum albumin (OxHSA) is evidence of an active antioxidant mechanism as measured by oxidized species of HSA. CXCL-10 is a pro-inflammatory chemokine associated with ischemic conditions. Accordingly, we examined the relationship of admission OxHSA and CXCL-10 with discharge mRS in acute ischemic stroke (AIS). Methods: Plasma samples and clinical data were collected prospectively at a Comprehensive Stroke Center. Admission biomarkers of oxidative stress, CXCL-10 and %OxHSA, were measured. We examined if CXCL-10 or %OxHSA correlated with age, admission NIHSS score, and discharge mRS score using Spearman's Rank correlation. Logistic regression was performed to identify independent predictors of a favorable discharge mRS (≤2). Results: In 106 consecutive AIS patients, the median age was 73 (IQR 61-84), 47% were male, and the median admission NIHSS score was 11 (IQR 5-19). %OxHSA and CXCL-10 were significantly correlated ( r = 0.23, p = 0.02). Both biomarkers were significantly correlated with age: %OxHSA ( r = 0.44, p < 0.001) and CXCL-10 ( r = 0.32, p = 0.001). Neither biomarker was correlated with admission NIHSS. There was a borderline significant correlation with discharge mRS and %OxHSA ( r = -0.17, p = 0.08), where higher %OxHSA correlated with lower discharge mRS scores. For every 1% increase in %OxHSA, the odds of a favorable discharge mRS increased 11%. The odds of a favorable discharge mRS decreased 18% for every 1-point increase in the initial NIHSS. Conclusions: OxHSA, the result of an oxidative environment and evidence of the strong antioxidant buffering capacity of HSA, correlated with CXCL-10 and discharge mRS, implying that strong antioxidant activity of albumin may confer better outcomes.
KW - albumin
KW - inflammation
KW - ischemic stroke
KW - oxidative stress
KW - proteomics
UR - https://scholarlycommons.hcahealthcare.com/neurology/4
UR - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614430/
M3 - Article
JO - Neurology
JF - Neurology
ER -