» Articles » PMID: 34469867

The Role of Atorvastatin in Collateral Circulation Formation Induced by Encephaloduroarteriosynangiosis: a Prospective Trial

Overview
Journal Neurosurg Focus
Specialty Neurosurgery
Date 2021 Sep 1
PMID 34469867
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: This prospective study was designed to confirm the role of atorvastatin in collateral circulation formation induced by encephaloduroarteriosynangiosis (EDAS) in patients with moyamoya disease (MMD).

Methods: Patients who were diagnosed with MMD at the Department of Neurosurgery in the Fifth Medical Center of Chinese PLA General Hospital, Beijing, China, between June 2017 and May 2018 were included. Blood samples were obtained from an antecubital vein and were analyzed using flow cytometry. Endothelial progenitor cells (EPCs) were defined as CD34brCD133+CD45dimKDR+. All patients included in the study underwent EDAS. Patients voluntarily chose whether to undergo atorvastatin treatment after EDAS. The correlation between atorvastatin and good postoperative collateral circulation was evaluated.

Results: A total of 106 patients with MMD were included in this study. Fifty-three patients (50%) received atorvastatin treatment. The baseline characteristics did not display statistically significant differences between the atorvastatin-treated and non-atorvastatin groups. Seventy-eight (42.9%) of the 182 hemispheres investigated postoperatively were classified as grade A collateral circulation, 47 (25.8%) as grade B, and 57 (31.3%) as grade C. Multivariate analysis revealed that only atorvastatin was significantly correlated with good collateral circulation after EDAS (p = 0.041).

Conclusions: The results of this prospective clinical trial have indicated that atorvastatin administered at 20 mg daily is safe and effective for the formation of postoperative collateral induced by EDAS.

Citing Articles

Medical Management of Adult Moyamoya Disease: A Review and Relevant Cases With Ischemic Events.

Bang O, Fujimura M J Stroke. 2025; 27(1):1-18.

PMID: 39916450 PMC: 11834343. DOI: 10.5853/jos.2024.04273.


Is medical management useful in Moyamoya disease?.

Muengtaweepongsa S, Panpattanakul V World J Clin Cases. 2024; 12(3):466-473.

PMID: 38322475 PMC: 10841962. DOI: 10.12998/wjcc.v12.i3.466.


To explore the effectiveness of atorvastatin in the postoperative formation of collateral blood vessels after encephaloduroarteriosynangiosis in patients with moyamoya disease: a prospective double-blind randomized controlled study.

Gao G, Wang Q, Hao F, Wang X, Liu S, Wang M Front Neurol. 2023; 14:1169253.

PMID: 37332989 PMC: 10270285. DOI: 10.3389/fneur.2023.1169253.


Physiological and pathophysiological mechanisms of the molecular and cellular biology of angiogenesis and inflammation in moyamoya angiopathy and related vascular diseases.

Dorschel K, Wanebo J Front Neurol. 2023; 14:661611.

PMID: 37273690 PMC: 10236939. DOI: 10.3389/fneur.2023.661611.


Association between statin therapy and the risk of stroke in patients with moyamoya disease: a nationwide cohort study.

Yoo J, Jeon J, Baik M, Kim J Stroke Vasc Neurol. 2022; 8(4):276-283.

PMID: 36549762 PMC: 10512045. DOI: 10.1136/svn-2022-001985.