BACKGROUND:Autoantibodies to ApolipoproteinA-1 (anti-ApoA-1 IgG) were shown to predict major adverse cardiovascular events and promote atherogenesis. However, their potential relationship with clinical disability and ischemic lesion volume after acute ischemic stroke (AIS) remains unexplored. MATERIALS AND METHODS: We included n=76 patients admitted for AIS and we investigated whether baseline serum anti-ApoA-1 IgG levels could predict i) AIS-induced clinical disability (assessed by the modified Rankin Scale [mRS]), and ii) AIS-related ischemic lesion volume (assessed by Computed Tomography [CT]). We also evaluated the possible pro-apoptotic and pro-necrotic effects of anti-ApoA-1 IgG on human astrocytoma cell line (U251) using flow cytometry. RESULTS: High levels of anti-ApoA-1 IgG were retrieved in 15.8% (12/76) of patients. Increased baseline levels of anti-ApoA-1 IgG were independently correlated with worse mRS (β=0.364; p=0.002; adjusted odds ratio [OR]: 1.05 [95% CI 1.01-1.09]; p=0.017) and CT-assessed ischemic lesion volume (β=0.333; p<0.001; adjusted OR: 1.06 [95% CI 1.01-1.12]; p=0.048) at 3 months. No difference in baseline clinical, biochemical and radiological characteristics was observed between patients with high versus low levels of anti-ApoA-1 IgG. Incubating human astrocytoma cells with anti-ApoA-1 IgG dose-dependently induced necrosis and apoptosis of U251 cells in vitro. CONCLUSION: anti-ApoA-1 IgG serum levels at AIS onset are associated with poorer clinical recovery and worse brain lesion volume 3 months after AIS. These observations could be partly explained by the deleterious effect of anti-ApoA-1 IgG on human brain cell survival in vitro and may have clinical implication in the prediction of poor outcome in AIS.

Anti-ApoA-1 IgG serum levels predict worse poststroke outcomes

CARBONE, FEDERICO;MONTECUCCO, FABRIZIO;DALLEGRI, FRANCO;
2016

Abstract

BACKGROUND:Autoantibodies to ApolipoproteinA-1 (anti-ApoA-1 IgG) were shown to predict major adverse cardiovascular events and promote atherogenesis. However, their potential relationship with clinical disability and ischemic lesion volume after acute ischemic stroke (AIS) remains unexplored. MATERIALS AND METHODS: We included n=76 patients admitted for AIS and we investigated whether baseline serum anti-ApoA-1 IgG levels could predict i) AIS-induced clinical disability (assessed by the modified Rankin Scale [mRS]), and ii) AIS-related ischemic lesion volume (assessed by Computed Tomography [CT]). We also evaluated the possible pro-apoptotic and pro-necrotic effects of anti-ApoA-1 IgG on human astrocytoma cell line (U251) using flow cytometry. RESULTS: High levels of anti-ApoA-1 IgG were retrieved in 15.8% (12/76) of patients. Increased baseline levels of anti-ApoA-1 IgG were independently correlated with worse mRS (β=0.364; p=0.002; adjusted odds ratio [OR]: 1.05 [95% CI 1.01-1.09]; p=0.017) and CT-assessed ischemic lesion volume (β=0.333; p<0.001; adjusted OR: 1.06 [95% CI 1.01-1.12]; p=0.048) at 3 months. No difference in baseline clinical, biochemical and radiological characteristics was observed between patients with high versus low levels of anti-ApoA-1 IgG. Incubating human astrocytoma cells with anti-ApoA-1 IgG dose-dependently induced necrosis and apoptosis of U251 cells in vitro. CONCLUSION: anti-ApoA-1 IgG serum levels at AIS onset are associated with poorer clinical recovery and worse brain lesion volume 3 months after AIS. These observations could be partly explained by the deleterious effect of anti-ApoA-1 IgG on human brain cell survival in vitro and may have clinical implication in the prediction of poor outcome in AIS.
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11567/843286
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