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Hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications

BACKGROUND: Previous studies reported higher incidences of venous thromboembolism and cardiovascular disease in schizophrenia patients and higher indicators of thrombosis, thrombocyte activation, and platelet dysfunction. OBJECTIVES: To check if first-episode schizophrenia (FES) patients have a hype...

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Autores principales: Zheng, Caiji, Liu, Haiyan, Tu, Weifeng, Lin, Lingyun, Xu, Haiyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540600/
https://www.ncbi.nlm.nih.gov/pubmed/37781686
http://dx.doi.org/10.1177/20451253231200257
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author Zheng, Caiji
Liu, Haiyan
Tu, Weifeng
Lin, Lingyun
Xu, Haiyun
author_facet Zheng, Caiji
Liu, Haiyan
Tu, Weifeng
Lin, Lingyun
Xu, Haiyun
author_sort Zheng, Caiji
collection PubMed
description BACKGROUND: Previous studies reported higher incidences of venous thromboembolism and cardiovascular disease in schizophrenia patients and higher indicators of thrombosis, thrombocyte activation, and platelet dysfunction. OBJECTIVES: To check if first-episode schizophrenia (FES) patients have a hypercoagulable state and determine whether acute and chronic antipsychotics have the same effect on blood coagulation or fibrinolysis-related biomarkers. DESIGN: Case-control study. METHODS: A total of 81 participants were grouped in FES, chronic schizophrenia (CS), and healthy controls (HCs). In addition to demographic data and clinical characteristics, immunological analyses were performed to measure plasma levels of D-dimer, plasminogen activator inhibitor-1 (PAI-1), soluble P selectin (sP-sel), tissue plasminogen activator (tPA), thrombotic precursor protein (TpP), and von Willebrand’s disease factor (vWF). RESULTS: Compared to HC group, FES patients showed higher PAI-1 (28.61 ng/ml versus 15.69 ng/ml), sP-sel (2.78 ng/ml versus 1.18 ng/ml), and TpP (15.61 µg/ml versus 5.59 µg/ml) along with a higher PAI-1/tPA (3.12 versus 2.00). Acute antipsychotic medication reduced higher PAI-1 (28.61 → 21.99), sP-sel (2.78 → 1.87), tPA (9.59 → 5.83), TpP (15.61 → 10.54), and vWF (383.18 → 291.08) in FES patients. However, plasma sP-sel and vWF in CS patients returned to the pre-treatment levels in FES patients, and PAI-1/tPA significantly decreased compared to FES patients. CONCLUSION: These results suggest a hypercoagulable state in FES patients and demonstrate contrast effects of acute and chronic antipsychotics on coagulation or fibrinolysis in schizophrenia patients.
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spelling pubmed-105406002023-09-30 Hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications Zheng, Caiji Liu, Haiyan Tu, Weifeng Lin, Lingyun Xu, Haiyun Ther Adv Psychopharmacol Original Research BACKGROUND: Previous studies reported higher incidences of venous thromboembolism and cardiovascular disease in schizophrenia patients and higher indicators of thrombosis, thrombocyte activation, and platelet dysfunction. OBJECTIVES: To check if first-episode schizophrenia (FES) patients have a hypercoagulable state and determine whether acute and chronic antipsychotics have the same effect on blood coagulation or fibrinolysis-related biomarkers. DESIGN: Case-control study. METHODS: A total of 81 participants were grouped in FES, chronic schizophrenia (CS), and healthy controls (HCs). In addition to demographic data and clinical characteristics, immunological analyses were performed to measure plasma levels of D-dimer, plasminogen activator inhibitor-1 (PAI-1), soluble P selectin (sP-sel), tissue plasminogen activator (tPA), thrombotic precursor protein (TpP), and von Willebrand’s disease factor (vWF). RESULTS: Compared to HC group, FES patients showed higher PAI-1 (28.61 ng/ml versus 15.69 ng/ml), sP-sel (2.78 ng/ml versus 1.18 ng/ml), and TpP (15.61 µg/ml versus 5.59 µg/ml) along with a higher PAI-1/tPA (3.12 versus 2.00). Acute antipsychotic medication reduced higher PAI-1 (28.61 → 21.99), sP-sel (2.78 → 1.87), tPA (9.59 → 5.83), TpP (15.61 → 10.54), and vWF (383.18 → 291.08) in FES patients. However, plasma sP-sel and vWF in CS patients returned to the pre-treatment levels in FES patients, and PAI-1/tPA significantly decreased compared to FES patients. CONCLUSION: These results suggest a hypercoagulable state in FES patients and demonstrate contrast effects of acute and chronic antipsychotics on coagulation or fibrinolysis in schizophrenia patients. SAGE Publications 2023-09-27 /pmc/articles/PMC10540600/ /pubmed/37781686 http://dx.doi.org/10.1177/20451253231200257 Text en © The Author(s), 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Zheng, Caiji
Liu, Haiyan
Tu, Weifeng
Lin, Lingyun
Xu, Haiyun
Hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications
title Hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications
title_full Hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications
title_fullStr Hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications
title_full_unstemmed Hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications
title_short Hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications
title_sort hypercoagulable state in patients with schizophrenia: different effects of acute and chronic antipsychotic medications
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540600/
https://www.ncbi.nlm.nih.gov/pubmed/37781686
http://dx.doi.org/10.1177/20451253231200257
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