Evidence map›Paper›PMID 39654371›Full record

ArticleCNS neuroscience & therapeutics2024

Comparing Outcomes of Moyamoya Disease and Moyamoya Syndrome in a Real-World Scenario: A Cohort Study.

Xiao-Peng Wang, Jing-Jie Li, Qian-Nan Wang, Gan Gao, Dan Yu, Qian Zhang, Si-Meng Liu, Min-Jie Wang, Xiang-Yang Bao, Lian Duan

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in CNS neuroscience & therapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Xiao-Peng WangSenior Department of Neurosurgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China.ORCID 0000-0002-5244-2586
Jing-Jie LiSenior Department of Neurosurgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Qian-Nan WangSenior Department of Neurosurgery, The Eighth Medical Center of Chinese PLA General Hospital, Beijing, China.
Gan GaoSenior Department of Neurosurgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Dan YuSenior Department of Neurosurgery, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Qian ZhangSenior Department of Neurosurgery, The Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Si-Meng LiuSenior Department of Neurosurgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Min-Jie WangSenior Department of Neurosurgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Xiang-Yang BaoSenior Department of Neurosurgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China.
Lian DuanSenior Department of Neurosurgery, The First Medical Center of Chinese PLA General Hospital, Beijing, China.ORCID 0000-0001-7210-056X

Funding

National Natural Science Foundation of China 82171280National Natural Science Foundation of China 82201451
6 · The paper itself

Abstract

backgroundMoyamoya disease (MMD) and moyamoya syndrome (MMS) are rare cerebrovascular conditions with unclear distinctions in clinical presentation and prognosis.

aimThis study assessed potential differences between MMD and MMS patients using real-world data on clinical manifestations, surgical outcomes, and stroke risk factors.

methodsThis multicenter, retrospective cohort study examined patients with MMD or MMS treated at three tertiary academic hospitals in China, with a mean follow-up of 11.2 ± 3.1 years. Clinical differences were compared between MMD and MMS, and postoperative cerebrovascular events were compared between patients who underwent surgery and those with conservative management. Primary outcomes were postoperative ischemic and hemorrhagic strokes. Risk factors were evaluated via multivariate Cox regression analysis.

resultsOf the 2565 patients, 2349 had MMD and 216 had MMS. After 1:1 propensity-score matching, no significant differences were observed between these two cohorts. Surgical patients had fewer cerebrovascular events than those who received conservative treatment (HR, 0.487; 95% CI, 0.334-0.711; p < 0.001). Preadmission modified Rankin scale scores > 2 (HR, 3.139; 95% CI, 1.254-7.857; p = 0.015) and periprocedural complications (HR, 8.666; 95% CI, 3.476-21.604; p < 0.001) were independent stroke risk factors in patients with MMD. Periprocedural complications (HR, 31.807; 95% CI, 10.916-92.684; p < 0.001) increased stroke risk in patients with MMS.

conclusionsThis real-world study revealed substantial clinical overlap between MMD and MMS. Both groups derived significant benefits from surgical revascularization, suggesting distinction may not be necessary to guide surgical management decisions. Optimizing preoperative status and preventing periprocedural complications may improve outcomes in these rare cerebrovascular conditions.

trial registrationThis study has been registered in the Chinese Clinical trial registry (registration number: ChiCTR2200064160).

Indexed as

Moyamoya DiseaseAdolescentAdultChinaCohort StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedPostoperative ComplicationsRetrospective StudiesTreatment OutcomeYoung Adultmoyamoya diseasemoyamoya syndromemulticenterpropensity‐score matchingreal‐world studyrevascularization

Identifiers

PMID39654371
PMCPMC11628736

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.