Cargando…

Candidate drugs for preventive treatment of unruptured intracranial aneurysms: A cross-sectional study

BACKGROUND AND PURPOSE: Establishment of drug therapy to prevent rupture of unruptured intracranial aneurysms (IAs) is needed. Previous human and animal studies have gradually clarified candidate drugs for preventive treatment of IA rupture. However, because most of these candidates belong to classe...

Descripción completa

Detalles Bibliográficos
Autores principales: Shimizu, Kampei, Imamura, Hirotoshi, Tani, Shoichi, Adachi, Hidemitsu, Sakai, Chiaki, Ishii, Akira, Kataoka, Hiroharu, Miyamoto, Susumu, Aoki, Tomohiro, Sakai, Nobuyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880482/
https://www.ncbi.nlm.nih.gov/pubmed/33577580
http://dx.doi.org/10.1371/journal.pone.0246865
_version_ 1783650712852365312
author Shimizu, Kampei
Imamura, Hirotoshi
Tani, Shoichi
Adachi, Hidemitsu
Sakai, Chiaki
Ishii, Akira
Kataoka, Hiroharu
Miyamoto, Susumu
Aoki, Tomohiro
Sakai, Nobuyuki
author_facet Shimizu, Kampei
Imamura, Hirotoshi
Tani, Shoichi
Adachi, Hidemitsu
Sakai, Chiaki
Ishii, Akira
Kataoka, Hiroharu
Miyamoto, Susumu
Aoki, Tomohiro
Sakai, Nobuyuki
author_sort Shimizu, Kampei
collection PubMed
description BACKGROUND AND PURPOSE: Establishment of drug therapy to prevent rupture of unruptured intracranial aneurysms (IAs) is needed. Previous human and animal studies have gradually clarified candidate drugs for preventive treatment of IA rupture. However, because most of these candidates belong to classes of drugs frequently co-administered to prevent cardiovascular diseases, epidemiological studies evaluating these drugs simultaneously should be performed. Furthermore, because drugs included in the same class may have different effects in terms of disease prevention, drug-by-drug assessments are important for planning intervention trials. MATERIALS AND METHODS: We performed a cross-sectional study enrolling patients diagnosed with IAs between July 2011 and June 2019 at our institution. Patients were divided into ruptured or unruptured groups. The drugs investigated were selected according to evidence suggested by either human or animal studies. Univariate and multivariate logistic regression analyses were performed to assess the association of drug treatment with rupture status. We also performed drug-by-drug assessments of the association, including dose-response relationships, with rupture status. RESULTS: In total, 310 patients with ruptured and 887 patients with unruptured IAs were included. Multivariate analysis revealed an inverse association of statins (odds ratio (OR), 0.54; 95% confidence interval (CI) 0.38–0.77), calcium channel blockers (OR, 0.41; 95% CI 0.30–0.58), and angiotensin II receptor blockers (ARBs) (OR, 0.67; 95% CI 0.48–0.93) with ruptured IAs. Moreover, inverse dose-response relationships with rupture status were observed for pitavastatin and rosuvastatin among statins, benidipine, cilnidipine, and amlodipine among calcium channel blockers, and valsartan, azilsartan, candesartan, and olmesartan among ARBs. Only non-aspirin non-steroidal anti-inflammatory drugs were positively associated with ruptured IAs (OR, 3.24; 95% CI 1.71–6.13). CONCLUSIONS: The present analysis suggests that several types of statins, calcium channel blockers, and ARBs are candidate drugs for preventive treatment of unruptured IAs.
format Online
Article
Text
id pubmed-7880482
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-78804822021-02-19 Candidate drugs for preventive treatment of unruptured intracranial aneurysms: A cross-sectional study Shimizu, Kampei Imamura, Hirotoshi Tani, Shoichi Adachi, Hidemitsu Sakai, Chiaki Ishii, Akira Kataoka, Hiroharu Miyamoto, Susumu Aoki, Tomohiro Sakai, Nobuyuki PLoS One Research Article BACKGROUND AND PURPOSE: Establishment of drug therapy to prevent rupture of unruptured intracranial aneurysms (IAs) is needed. Previous human and animal studies have gradually clarified candidate drugs for preventive treatment of IA rupture. However, because most of these candidates belong to classes of drugs frequently co-administered to prevent cardiovascular diseases, epidemiological studies evaluating these drugs simultaneously should be performed. Furthermore, because drugs included in the same class may have different effects in terms of disease prevention, drug-by-drug assessments are important for planning intervention trials. MATERIALS AND METHODS: We performed a cross-sectional study enrolling patients diagnosed with IAs between July 2011 and June 2019 at our institution. Patients were divided into ruptured or unruptured groups. The drugs investigated were selected according to evidence suggested by either human or animal studies. Univariate and multivariate logistic regression analyses were performed to assess the association of drug treatment with rupture status. We also performed drug-by-drug assessments of the association, including dose-response relationships, with rupture status. RESULTS: In total, 310 patients with ruptured and 887 patients with unruptured IAs were included. Multivariate analysis revealed an inverse association of statins (odds ratio (OR), 0.54; 95% confidence interval (CI) 0.38–0.77), calcium channel blockers (OR, 0.41; 95% CI 0.30–0.58), and angiotensin II receptor blockers (ARBs) (OR, 0.67; 95% CI 0.48–0.93) with ruptured IAs. Moreover, inverse dose-response relationships with rupture status were observed for pitavastatin and rosuvastatin among statins, benidipine, cilnidipine, and amlodipine among calcium channel blockers, and valsartan, azilsartan, candesartan, and olmesartan among ARBs. Only non-aspirin non-steroidal anti-inflammatory drugs were positively associated with ruptured IAs (OR, 3.24; 95% CI 1.71–6.13). CONCLUSIONS: The present analysis suggests that several types of statins, calcium channel blockers, and ARBs are candidate drugs for preventive treatment of unruptured IAs. Public Library of Science 2021-02-12 /pmc/articles/PMC7880482/ /pubmed/33577580 http://dx.doi.org/10.1371/journal.pone.0246865 Text en © 2021 Shimizu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shimizu, Kampei
Imamura, Hirotoshi
Tani, Shoichi
Adachi, Hidemitsu
Sakai, Chiaki
Ishii, Akira
Kataoka, Hiroharu
Miyamoto, Susumu
Aoki, Tomohiro
Sakai, Nobuyuki
Candidate drugs for preventive treatment of unruptured intracranial aneurysms: A cross-sectional study
title Candidate drugs for preventive treatment of unruptured intracranial aneurysms: A cross-sectional study
title_full Candidate drugs for preventive treatment of unruptured intracranial aneurysms: A cross-sectional study
title_fullStr Candidate drugs for preventive treatment of unruptured intracranial aneurysms: A cross-sectional study
title_full_unstemmed Candidate drugs for preventive treatment of unruptured intracranial aneurysms: A cross-sectional study
title_short Candidate drugs for preventive treatment of unruptured intracranial aneurysms: A cross-sectional study
title_sort candidate drugs for preventive treatment of unruptured intracranial aneurysms: a cross-sectional study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880482/
https://www.ncbi.nlm.nih.gov/pubmed/33577580
http://dx.doi.org/10.1371/journal.pone.0246865
work_keys_str_mv AT shimizukampei candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT imamurahirotoshi candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT tanishoichi candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT adachihidemitsu candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT sakaichiaki candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT ishiiakira candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT kataokahiroharu candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT miyamotosusumu candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT aokitomohiro candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy
AT sakainobuyuki candidatedrugsforpreventivetreatmentofunrupturedintracranialaneurysmsacrosssectionalstudy