Effects of higher serum lipid levels on the risk of parkinson’s disease: A systematic review and meta-analysis
Frontiers in Neurology, ISSN: 1664-2295, Vol: 11, Page: 597
2020
- 16Citations
- 21Captures
- 1Mentions
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Metrics Details
- Citations16
- Citation Indexes16
- 16
- Captures21
- Readers21
- 21
- Mentions1
- News Mentions1
- News1
Most Recent News
Effects of Higher Serum Lipid Levels on the Risk of Parkinson's Disease: A Systematic Review and Meta-Analysis.
Front Neurol. 2020;11:597. Epub 2020 Jun 26 Authors: Jiang Z, Xu X, Gu X, Ou R, Luo X, Shang H, Song W PubMed: 32670190 Submit Comment
Review Description
Background: The causal relationship between serum lipid levels and the risk of Parkinson’s disease (PD) remains largely uncertain. We summarized the existing controversial evidence on this topic. Methods: We searched the electronic databases for observational studies from January 1988 to March 2020. We applied random-effects models to calculate pooled relative risk (RR) with their 95% confidence intervals (CI). Random-effects dose-response meta-analyses were further conducted to explore the dose-risk relationship. Results: Twelve cohort studies and three case-control studies were included in this meta-analysis. Higher levels of serum low-density lipoprotein cholesterol (LDL-C) were inversely associated with the subsequent risk of PD (RR 0.73, 95% CI 0.57–0.93), whereas, there were no associations between serum levels of total cholesterol (TC) (RR 0.91, 95% CI 0.73–1.13), high-density lipoprotein cholesterol (HDL-C) (RR 0.97, 95% CI 0.73–1.27), or triglycerides (TG) (RR 0.85, 95% CI 0.55–1.29) and the risk of PD. Further dose-response meta-analysis revealed that every 38.6 mg/dL (1mmol/L) increase in serum LDL-C correlates with a 7% decreased risk of PD. Conclusions: Our paper supports the protective effect of higher serum LDL-C on the subsequent risk of PD. More prospective cohort studies are warranted to confirm the conclusion, and further fundamental researches are needed to elucidate the underlying biological mechanisms.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85088242504&origin=inward; http://dx.doi.org/10.3389/fneur.2020.00597; http://www.ncbi.nlm.nih.gov/pubmed/32670190; https://www.frontiersin.org/article/10.3389/fneur.2020.00597/full; https://www.frontiersin.org/articles/10.3389/fneur.2020.00597/supplementary-material/10.3389/fneur.2020.00597.s002; http://dx.doi.org/10.3389/fneur.2020.00597.s002; https://www.frontiersin.org/articles/10.3389/fneur.2020.00597/supplementary-material/10.3389/fneur.2020.00597.s001; http://dx.doi.org/10.3389/fneur.2020.00597.s001; https://dx.doi.org/10.3389/fneur.2020.00597.s001; https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2020.00597/full; https://dx.doi.org/10.3389/fneur.2020.00597; https://dx.doi.org/10.3389/fneur.2020.00597.s002
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