Evidence map›Paper›PMID 27668119›Full record

ArticleParkinson's disease2016

Analysis of LRRK2, SNCA, and ITGA8 Gene Variants with Sporadic Parkinson's Disease Susceptibility in Chinese Han Population.

Jie Fang, Kehui Yi, Mingwei Guo, Xingkai An, Hongli Qu, Qing Lin, Min Bi, Qilin Ma

Open access · goldAbstract read
In one paragraph

Article in Parkinson's disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 23% of its field
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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Decrease inInternational journal of molecular sciences · 2021
    Article
  2. Article
  3. A Comprehensive Analysis of the Association BetweenFrontiers in molecular neuroscience · 2018
    Article
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 at 3 institutions in 1 country.

Jie FangDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Kehui YiThe First Clinical Medical College of Fujian Medical University, Fuzhou, China.ORCID 0000-0002-0030-8393
Mingwei GuoDepartment of Neurology, The First Affiliated Hospital of Gannan Medical University, Ganzhou, China.ORCID 0000-0002-5480-8596
Xingkai AnDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.ORCID 0000-0003-1842-6387
Hongli QuDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.ORCID 0000-0003-0201-4310
Qing LinDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.ORCID 0000-0002-9726-8913
Min BiDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China.ORCID 0000-0001-8768-6137
Qilin MaDepartment of Neurology, The First Affiliated Hospital of Xiamen University, Xiamen, China; The First Clinical Medical College of Fujian Medical University, Fuzhou, China.ORCID 0000-0002-1387-2647
First Affiliated Hospital of Xiamen University · CNFujian Medical University · CNFirst Affiliated Hospital of Gannan Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background. Parkinson's disease (PD) is an age-related neurodegenerative disease affected by multiple genetic and environmental factors. We performed a case-control study on candidate gene to scrutinize whether genetic variants in LRRK2, SNCA, and ITGA8 genes could be associated with sporadic PD in Chinese Han population. Methods. Five single-nucleotide polymorphisms (SNPs) of LRRK2 (rs1491942), SNCA (rs2301134, rs2301135, and rs356221), and ITGA8 (rs7077361) were selected and genotyped among 583 unrelated PD patients and 558 healthy controls. Results. Rs1491942 of LRRK2 gene had a significantly higher genotype frequency (P = 3.543E - 09) and allelic G/C frequencies (P = 2.601E - 10) in PD patients than controls. Rs2301135 of SNCA gene also showed an obvious difference in genotype frequency (P = 4.394E - 07) and allelic G/C frequencies (P = 9.116E - 13) between PD patients and controls. SNPs rs2301134 and rs356221 of SNCA gene and rs7077361 of ITGA8 gene lacked the significant association with the susceptibility of PD in Chinese Han population. Conclusions. Our study firstly expresses that rs1491942 of LRRK2 and rs2301135 of SNCA gene are substantially associated with sporadic Parkinson's disease in Chinese Han population.

Identifiers

PMID27668119
PMCPMC5030423
OpenAlexW2517810069

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Registered trials

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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.