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  3. Epidemiology and Preventive Medicine / 流行病學與預防醫學研究所
  4. Association of stroke with the receptor-binding profiles of antipsychotics - A case-crossover study
 
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Association of stroke with the receptor-binding profiles of antipsychotics - A case-crossover study

Journal
Biological Psychiatry
Journal Volume
73
Journal Issue
5
Pages
414-421
Date Issued
2013
Author(s)
CHI-SHIN WU  
Wang S.-C.
SUSAN SHUR-FEN GAU  orcid-logo
Tsai H.-J.
Cheng Y.-C.
DOI
10.1016/j.biopsych.2012.07.006
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84873716475&doi=10.1016%2fj.biopsych.2012.07.006&partnerID=40&md5=9d17aa62cf5bcc7f4757dbdbfa1af4d1
https://scholars.lib.ntu.edu.tw/handle/123456789/520505
Abstract
Background: Previous research suggests a link between antipsychotic use and stroke, but the relationships between receptor-binding profiles of antipsychotics and the risk of cerebrovascular events are unclear. Methods: A total of 14,584 patients with incident stroke were enrolled in the National Health Insurance Research Database in Taiwan from 1998 to 2007. We conducted a case-crossover study to compare the rates of antipsychotic use. The effects of receptor-binding profiles of antipsychotics on stroke risk were estimated, while the moderating effects of age, sex, presence of dementia, and duration of antipsychotic treatment were evaluated by stratified analyses. Results: The adjusted odds ratio of stroke risk with antipsychotics exposure was 1.60 (95% confidence interval, 1.51-1.69) using a 14-day time window. The use of antipsychotics with a high binding affinity of M1 muscarinic and α2 adrenergic receptors was associated with a greater risk of stroke than the use of other types of antipsychotics. An increased risk of stroke with antipsychotic use was noted in the patients who were older and/or who suffered from dementia. Moreover, our results showed that stroke risk with antipsychotic use was in a dose-related relationship. Conclusions: Our findings suggest an association between stroke risk and high M1 muscarinic and α2 adrenergic affinity. The clinical implication is to start antipsychotics treatment at low dosages and to closely monitor the side effects in the initial treatment, particularly for individuals with older age and the presence of dementia. ? 2013 Society of Biological Psychiatry.
SDGs

[SDGs]SDG3

Other Subjects
alpha 2 adrenergic receptor; amisulpride; aripiprazole; chlorpromazine; chlorprothixene; clopenthixol; clotiapine; clozapine; flupentixol; fluphenazine; haloperidol; levomepromazine; loxapine; melitracen; moperone; muscarinic M1 receptor; neuroleptic agent; olanzapine; perphenazine; pimozide; prochlorperazine; quetiapine; risperidone; sulpiride; thioridazine; tiotixene; trifluoperazine; ziprasidone; zotepine; adult; aged; article; binding affinity; brain hemorrhage; brain ischemia; cerebrovascular accident; crossover procedure; dementia; drug exposure; drug receptor binding; drug use; female; human; incidence; major clinical study; male; priority journal; risk assessment; Taiwan; treatment duration; Aged; Aged, 80 and over; Antipsychotic Agents; Brain Ischemia; Cross-Over Studies; Databases, Factual; Dementia; Female; Humans; Incidence; Male; Middle Aged; Odds Ratio; Risk; Stroke; Taiwan
Type
journal article

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