Evidence map›Paper›PMID 30363648›Full record

ReviewParkinson's disease2018

A Meta-Analysis of

Yuan Zhang, Li Shu, Xun Zhou, Hongxu Pan, Qian Xu, Jifeng Guo, Beisha Tang, Qiying Sun

Abstract readReview
In one paragraph

Review in Parkinson's disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Association of gender and age at onset with glucocerebrosidase associated Parkinson's disease: a systematic review and meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Pooled it
  2. Article
  3. Article
  4. Consensus Guidance for Genetic Counseling in GBA1 Variants: A Focus on Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Glucocerebrosidase mutations and Parkinson disease.Journal of neural transmission (Vienna, Austria : 1996) · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Genetic variations inFrontiers in neurology · 2022
    Review
  20. Review
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

8 authors.

Yuan ZhangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.ORCID 0000-0003-0577-7129
Li ShuDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.ORCID 0000-0003-4609-4666
Xun ZhouDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Hongxu PanDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Qian XuDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Jifeng GuoDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.ORCID 0000-0002-3658-3928
Beisha TangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.ORCID 0000-0003-2120-1576
Qiying SunNational Clinical Research Center for Geriatric Disorders, Changsha, Hunan 410078, China.ORCID 0000-0002-2031-8345

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background

methodMedline, Embase, and Cochrane were used to perform the searching. Strict selection criteria were followed in screening for new published articles or data. Revman 5.3 software was applied to perform the total statistical analysis, and funnel plots in the software were used to assess the publication biases.

resultsA total of 26 articles including 931

conclusionOur results demonstrated that there were unique clinical features in

Identifiers

PMID30363648
PMCPMC6180987

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.