Preliminary results of pravastatin on non-hemorrhagic vertebral artery dissection: an exploratory randomized and controlled study

Abstract Background There is limited information about the pleiotropic effects of statin on cerebrovascular diseases. The authors aimed to investigate the effect of pravastatin on non-hemorrhagic vertebral artery dissection (VAD) in a clinical setting. Methods An exploratory randomized and controlle...

Full description

Saved in:
Bibliographic Details
Main Authors: Hyun Jin Han, Keun Young Park, Chang Ki Jang, Joonho Chung, Yong Bae Kim, Sung Ho Lee, Kangmin Kim, Hyun-Seung Kang, Jeong Eun Kim, Won-Sang Cho
Format: Article
Language:English
Published: BMC 2025-06-01
Series:BMC Neurology
Subjects:
Online Access:https://doi.org/10.1186/s12883-025-04257-7
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850137984215547904
author Hyun Jin Han
Keun Young Park
Chang Ki Jang
Joonho Chung
Yong Bae Kim
Sung Ho Lee
Kangmin Kim
Hyun-Seung Kang
Jeong Eun Kim
Won-Sang Cho
author_facet Hyun Jin Han
Keun Young Park
Chang Ki Jang
Joonho Chung
Yong Bae Kim
Sung Ho Lee
Kangmin Kim
Hyun-Seung Kang
Jeong Eun Kim
Won-Sang Cho
author_sort Hyun Jin Han
collection DOAJ
description Abstract Background There is limited information about the pleiotropic effects of statin on cerebrovascular diseases. The authors aimed to investigate the effect of pravastatin on non-hemorrhagic vertebral artery dissection (VAD) in a clinical setting. Methods An exploratory randomized and controlled study was designed for the non-hemorrhage VAD (CRIS, KCT00035970). Primary outcomes were 1- and 6-month radiologic changes on vessel wall magnetic resonance imaging (VW-MRI), with secondary outcomes related to the clinical and laboratory parameters, and safety outcomes of the pravastatin use. Results Finally, 23 patients were enrolled, consisting of 12 in the pravastatin group and 11 in the control with similar baseline characteristics except the age (55.0 versus 45.5 years, P = .01). Morphologic changes in the early period (0–1 month) were more improved or resolved in the pravastatin group with a borderline significance (crude odds ratio: 7.500 [95% confidence interval: 0.921-64.047], P = .06). However, age-adjusted analysis showed no difference in morphologic changes between the groups (adjusted odds ratio: 0.853 [95% confidence interval: 0.033-22.020], P = .92). The serum level of high-sensitivity C-reactive protein (hs-CRP) in the pravastatin group showed a descending tendency in the early period (Z-score: -1.843, P = .07), whereas it significantly increased in the control (Z-score: -2.371, P = .02). There were no safety issues at all. Conclusion Pravastatin had a borderline significant effect on the recovery of non-hemorrhage VAD with no additional adverse effects. A further study with a larger scale is expected to make more concrete evidences about the pleiotropic effects of statin on the non-hemorrhagic VAD. Trial registration The present study registered in a clinical research information service approved by World Health Organization (CRIS, KCT00035970, Registered on 7 March 2019; available at: https://cris.nih.go.kr/cris/search/detailSearch.do?seq=25234%26status=5%26seq_group=12949%26search_page=M ).
format Article
id doaj-art-3436706abd8e46f5bbf30eaddf79b4b0
institution OA Journals
issn 1471-2377
language English
publishDate 2025-06-01
publisher BMC
record_format Article
series BMC Neurology
spelling doaj-art-3436706abd8e46f5bbf30eaddf79b4b02025-08-20T02:30:42ZengBMCBMC Neurology1471-23772025-06-012511910.1186/s12883-025-04257-7Preliminary results of pravastatin on non-hemorrhagic vertebral artery dissection: an exploratory randomized and controlled studyHyun Jin Han0Keun Young Park1Chang Ki Jang2Joonho Chung3Yong Bae Kim4Sung Ho Lee5Kangmin Kim6Hyun-Seung Kang7Jeong Eun Kim8Won-Sang Cho9Departments of Neurosurgery, Severance HospitalDepartments of Neurosurgery, Severance HospitalYongin Severance HospitalGangnam Severance HospitalDepartments of Neurosurgery, Severance HospitalDepartment of Neurosurgery, Seoul National University Hospital, Seoul National University College of MedicineDepartment of Neurosurgery, Seoul National University Hospital, Seoul National University College of MedicineDepartment of Neurosurgery, Seoul National University Hospital, Seoul National University College of MedicineDepartment of Neurosurgery, Seoul National University Hospital, Seoul National University College of MedicineDepartment of Neurosurgery, Seoul National University Hospital, Seoul National University College of MedicineAbstract Background There is limited information about the pleiotropic effects of statin on cerebrovascular diseases. The authors aimed to investigate the effect of pravastatin on non-hemorrhagic vertebral artery dissection (VAD) in a clinical setting. Methods An exploratory randomized and controlled study was designed for the non-hemorrhage VAD (CRIS, KCT00035970). Primary outcomes were 1- and 6-month radiologic changes on vessel wall magnetic resonance imaging (VW-MRI), with secondary outcomes related to the clinical and laboratory parameters, and safety outcomes of the pravastatin use. Results Finally, 23 patients were enrolled, consisting of 12 in the pravastatin group and 11 in the control with similar baseline characteristics except the age (55.0 versus 45.5 years, P = .01). Morphologic changes in the early period (0–1 month) were more improved or resolved in the pravastatin group with a borderline significance (crude odds ratio: 7.500 [95% confidence interval: 0.921-64.047], P = .06). However, age-adjusted analysis showed no difference in morphologic changes between the groups (adjusted odds ratio: 0.853 [95% confidence interval: 0.033-22.020], P = .92). The serum level of high-sensitivity C-reactive protein (hs-CRP) in the pravastatin group showed a descending tendency in the early period (Z-score: -1.843, P = .07), whereas it significantly increased in the control (Z-score: -2.371, P = .02). There were no safety issues at all. Conclusion Pravastatin had a borderline significant effect on the recovery of non-hemorrhage VAD with no additional adverse effects. A further study with a larger scale is expected to make more concrete evidences about the pleiotropic effects of statin on the non-hemorrhagic VAD. Trial registration The present study registered in a clinical research information service approved by World Health Organization (CRIS, KCT00035970, Registered on 7 March 2019; available at: https://cris.nih.go.kr/cris/search/detailSearch.do?seq=25234%26status=5%26seq_group=12949%26search_page=M ).https://doi.org/10.1186/s12883-025-04257-7PravastatinPleiotropic effectsVertebral artery dissectionMagnetic resonance imagingPilot study
spellingShingle Hyun Jin Han
Keun Young Park
Chang Ki Jang
Joonho Chung
Yong Bae Kim
Sung Ho Lee
Kangmin Kim
Hyun-Seung Kang
Jeong Eun Kim
Won-Sang Cho
Preliminary results of pravastatin on non-hemorrhagic vertebral artery dissection: an exploratory randomized and controlled study
BMC Neurology
Pravastatin
Pleiotropic effects
Vertebral artery dissection
Magnetic resonance imaging
Pilot study
title Preliminary results of pravastatin on non-hemorrhagic vertebral artery dissection: an exploratory randomized and controlled study
title_full Preliminary results of pravastatin on non-hemorrhagic vertebral artery dissection: an exploratory randomized and controlled study
title_fullStr Preliminary results of pravastatin on non-hemorrhagic vertebral artery dissection: an exploratory randomized and controlled study
title_full_unstemmed Preliminary results of pravastatin on non-hemorrhagic vertebral artery dissection: an exploratory randomized and controlled study
title_short Preliminary results of pravastatin on non-hemorrhagic vertebral artery dissection: an exploratory randomized and controlled study
title_sort preliminary results of pravastatin on non hemorrhagic vertebral artery dissection an exploratory randomized and controlled study
topic Pravastatin
Pleiotropic effects
Vertebral artery dissection
Magnetic resonance imaging
Pilot study
url https://doi.org/10.1186/s12883-025-04257-7
work_keys_str_mv AT hyunjinhan preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT keunyoungpark preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT changkijang preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT joonhochung preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT yongbaekim preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT sungholee preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT kangminkim preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT hyunseungkang preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT jeongeunkim preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy
AT wonsangcho preliminaryresultsofpravastatinonnonhemorrhagicvertebralarterydissectionanexploratoryrandomizedandcontrolledstudy