Evidence map›Paper›PMID 39425566›Full record

ArticleEuropean journal of neurology2024

Glymphatic system dysfunction and risk of clinical milestones in patients with Parkinson disease.

Cheng Zhou, Xianchen Jiang, Xiaojun Guan, Tao Guo, Jingjing Wu, Haoting Wu, Chenqing Wu, Jingwen Chen, Jiaqi Wen, Sijia Tan and 8 more

Abstract read
In one paragraph

Article in European journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 3 pooled it
–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

26 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Cheng ZhouDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xianchen JiangDepartment of Chronic Noncommunicable Disease, Quzhou Center for Disease Control and Prevention, Quzhou, China.
Xiaojun GuanDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID 0000-0003-2313-4477
Tao GuoDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jingjing WuDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Haoting WuDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Chenqing WuDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jingwen ChenDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jiaqi WenDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Sijia TanDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xiaojie DuanmuDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Jianmei QinDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Weijin YuanDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Qianshi ZhengDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Peiyu HuangDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Baorong ZhangDepartment of Neurology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID 0000-0003-3562-2056
Xiaojun XuDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID 0000-0002-0127-2812
Minming ZhangDepartment of Radiology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID 0000-0003-0145-7558

Funding

National Natural Science Foundation of China 82001767National Natural Science Foundation of China 82071997National Natural Science Foundation of China 82171888National Natural Science Foundation of China 82202089National Natural Science Foundation of China 82202091National Natural Science Foundation of China 82271935National Natural Science Foundation of China 82302132National Natural Science Foundation of China 82302136National Natural Science Foundation of China 82371906National Natural Science Foundation of China 91630314the 13th Five-year Plan for National Key Research and Development Program of China 2016YFC1306600the China Postdoctoral Science Foundation 2023M733085the Natural Science Foundation of Zhejiang Province LQ21H180008the Natural Science Foundation of Zhejiang Province LY22H180002the Natural Science Foundation of Zhejiang Province Z24H180002
6 · The paper itself

Abstract

background and purposeGlymphatic dysfunction may play a significant role in the development of neurodegenerative diseases. We aimed to evaluate the association between glymphatic dysfunction and the risk of malignant event/clinical milestones in Parkinson disease (PD).

methodsThis study included 236 patients from August 2014 to December 2020. Diffusion tensor imaging analysis along the perivascular space (DTI-ALPS) index was calculated as an approximate measure of glymphatic function. The primary outcomes were four clinical milestones including recurrent falls, wheelchair dependence, dementia, and placement in residential or nursing home care. The associations of DTI-ALPS with the risk of clinical milestones were examined using multivariate Cox proportional hazards regression models. Then, logistic regression was repeated using clinical variables and DTI-ALPS index individually and in combination of the two to explore the ability to distinguish patients who reached clinical milestones within a 5-year period.

resultsA total of 175 PD patients with baseline DTI-ALPS index and follow-up clinical assessments were included. A lower DTI-ALPS was independently associated with increased risk of recurrent falls, wheelchair dependence, and dementia. Additionally, in 103 patients monitored over 5 years, a logistic regression model combining clinical variables and DTI-ALPS index showed better performance for predicting wheelchair dependence within 5 years than a model using clinical variables or DTI-ALPS index alone.

conclusionsGlymphatic dysfunction, as measured by the DTI-ALPS index, was associated with increased risk of clinical milestones in patients with PD. This finding implies that therapy targeting the glymphatic system may serve as a viable strategy for slowing down the progression of PD.

Indexed as

Glymphatic SystemParkinson DiseaseAgedAged, 80 and overDiffusion Tensor ImagingDisease ProgressionFemaleHumansMaleMiddle Ageddementiafallsglymphatic systemmagnetic resonance imagingParkinson disease

Identifiers

PMID39425566
PMCPMC11554988

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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.