SynthesisPloS one2016

Statin Use and the Risk of Parkinson's Disease: An Updated Meta-Analysis.

Shuang Bai, Yi Song, Xin Huang, Lidan Peng, Jie Jia, Yu Liu, Hong Lu

Full text readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in PloS one, 2016. The graph read 6 numbers from its abstract, feeding 1 cell of the map, but none could be read as for or against, so it casts no vote. It also reports 3 associations that do not count as treatment evidence, such as RR 0.81 (0.71 to 0.92) for pharmacokinetics & dosing. Cited by 30 papers, 4 of them syntheses that pooled it.

6numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 4 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.

Read, but not usablea number the graph found but could not read as for or against

Pharmacokinetics & dosingan association or prognostic statement, not a treatment comparison · dyslipidemiafeeds one cell of the map
RR 0.810.71 to 0.92
Statin use was associated with a lower risk of PD, with a summary RR of 0.81 (95% CI 0.71-0.92).
Pharmacokinetics & dosingdirection of benefit for this outcome is not defined · against placebo · dyslipidemiafeeds one cell of the map
RR 0.810.71 to 0.92
We combined the 11 studies with a random-effects model, obtaining a summary RR of 0.81 (95% CI 0.71-0.92); that is, there was a 19% reduction in the risk of developing PD for statin users as compared with non-users.
Pharmacokinetics & dosingan association or prognostic statement, not a treatment comparison · against placebo · dyslipidemiafeeds one cell of the map
RR 0.770.62 to 0.97
Statin use was found to be associated with a decreased risk of PD in both case-control studies (RR 0.77, 95% CI 0.62-0.97) and cohort studies (RR 0.82, 95% CI 0.68-0.99).
Pharmacokinetics & dosingan association or prognostic statement, not a treatment comparison · dyslipidemiafeeds one cell of the map
RR 0.710.59 to 0.87
The subgroup of high-quality studies showed an inverse association (RR 0.71, 95% CI 0.59-0.87) between statin and risk of PD, but this association was non-significant in the medium-quality group (RR 0.83, 95% CI 0.78-1.11) (Table 2).
Pharmacokinetics & dosingan association or prognostic statement, not a treatment comparison · dyslipidemiafeeds one cell of the map
RR 0.830.66 to 1.05
Among the individual statins, atorvastatin, lovastatin, simvastatin, and rosuvastatin showed a non-significant inverse association with the risk of PD (RR 0.83, 95% CI 0.66-1.05; RR 0.61, 95% CI 0.16-2.35; RR 0.68, 95% CI 0.45-1.01; and RR 0.88, 95% CI 0.52-1.48, respectively), while pravastatin non-significantly increased the risk of PD (RR 1.35, 95% CI 0.58-3.10).
Pharmacokinetics & dosingcomparator not stated · dyslipidemiafeeds one cell of the map
RR 0.770.56 to 1.07
Long-term statin use decreased the risk of PD almost significantly (RR 0.77, 95% CI 0.56-1.07).

clause the extractor read what became the number

2 · Its place on the map

Where it lands on the map

Rows are treatments, columns are outcomes. The coloured squares are the cells this paper feeds, coloured by the vote it casts there. Click one to jump to what this paper adds to it.

supports the treatmentfavours the comparatorno clear differenceread, but no usable result
3 · What it changes

What it adds to each cell

For every cell the paper feeds: the belief in the claim with and without this paper, and this paper's estimate drawn against every other readable study in the cell. The ringed dot is this paper.

Statins×pharmacokinetics & dosing

No readable resultOpen on the map →What to test next →

2 readable studies in this cell: 0 favour the treatment, 2 find no difference, 0 favour the comparator.

Belief with this paper
0.00contested · 0 families support, 1 contradict · against placebo
Without itNot a counted family in this claim, so removing it changes nothing.
← favours the treatmentfavours the comparator →
1 · no effect
NCT00943124220 enrolled · 2007
Least-Squares Mean Ratio 0.970.93 to 1.00

This paper's own estimate is on a different scale from the rest of the cell, so it is not drawn here.

4 · 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.

5 · Its place in the literature

Who cites it

30 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Trial
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Altered Cholesterol Homeostasis in Huntington's Disease.Frontiers in aging neuroscience · 2022
    Review
  15. A Possible Role for HMG-CoA Reductase Inhibitors and Its Association withInternational journal of molecular sciences · 2021
    Review
  16. Observational
  17. Review
  18. Review
  19. Statins in Neuro-ophthalmology.Neuro-ophthalmology (Aeolus Press) · 2021
    Review
  20. Article
6 · The record

Corrections and comments

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

7 · Who and what money

Authors and funding

7 authors.

Shuang BaiDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Yi SongDepartment of Ultrasound, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Xin HuangDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Lidan PengDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Jie JiaDepartment of Orthopedics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Yu LiuDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Hong LuDepartment of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

Funding

No grant is acknowledged in the PubMed record.

8 · The paper itself

Abstract

The marked sentences are the ones the graph read a number from.

introductionIn response to the ongoing debate over the relationship between the use of statins and the risk of Parkinson's disease (PD), we performed a systematic review and meta-analysis of observational studies to examine their association.

methodsWe conducted a review of the literature using electronic databases supplemented by a manual search to identify potentially relevant case-control or cohort studies. Summary relative risk (RRs) and 95% confidence intervals (CIs) were calculated using a random-effects model. Sensitivity and subgroup analyses were also conducted.

resultsEleven studies (five case-control and six cohort) with a total of 3,513,209 participants and 21,011 PD cases were included. Statin use was associated with a lower risk of PD, with a summary RR of 0.81 (95% CI 0.71-0.92). Sensitivity analysis demonstrated the robustness of results. Subgroup analyses showed that neither study design nor study region significantly influenced the effect estimates. However, subgroup studies adjusted for age or sex had a greater inverse association than did unadjusted analyses (age-adjusted RR 0.75, 95% CI 0.60-0.95; age-unadjusted RR 0.86, 95% CI 0.75-0.99 and sex-adjusted RR 0.76, 95% CI 0.59-0.98; sex-unadjusted RR 0.85, 95% CI 0.79-0.92).

conclusionsResults of this systematic review suggest that statin use is associated with a reduced PD risk. However, randomized controlled trials and more observational studies should be performed before strong conclusions are drawn.

Indexed as

Case-Control StudiesCohort StudiesDatabases, FactualHumansHydroxymethylglutaryl-CoA Reductase InhibitorsHyperlipidemiasParkinson DiseaseRiskHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID27019096
PMCPMC4809483

What OpenQuestion holds

Textfull text, public
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.