Evidence map›Paper›PMID 25977831›Full record

ArticleParkinson's disease2015

Association Analysis of COQ2 Variant in Dementia and Essential Tremor.

Yin Xia Chao, Ebonne Yu Lin Ng, Huihua Li, Kandiah Nagaendran, Yuen Yih, Mei Sian Chong, Kumar M Prakash, Louis Tan, Wing Lok Au, Yi Zhao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Parkinson's disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

14 authors at 4 institutions in 1 country.

Yin Xia ChaoDepartment of Neurology, Singapore General Hospital, Singapore 169608 ; National Neuroscience Institute, Singapore 308433.ORCID 0000-0003-1185-3511
Ebonne Yu Lin NgDepartment of Neurology, Singapore General Hospital, Singapore 169608 ; National Neuroscience Institute, Singapore 308433.
Huihua LiDuke-NUS Graduate Medical School, Singapore 169857.
Kandiah NagaendranNational Neuroscience Institute, Singapore 308433.
Yuen YihHealth Assessment Centre, Singapore General Hospital, Singapore 169608 ; Health Services Research, Singapore General Hospital, Singapore 169608.
Mei Sian ChongInstitute of Geriatrics and Active Ageing, Tan Tock Seng Hospital, Singapore 308433.ORCID 0000-0001-9324-5901
Kumar M PrakashDepartment of Neurology, Singapore General Hospital, Singapore 169608 ; National Neuroscience Institute, Singapore 308433.
Louis TanNational Neuroscience Institute, Singapore 308433.
Wing Lok AuNational Neuroscience Institute, Singapore 308433.
Yi ZhaoDepartment of Clinical Research, Singapore General Hospital, Singapore 169608.ORCID 0000-0002-3839-6499
Zhi Dong ZhouDepartment of Neurology, Singapore General Hospital, Singapore 169608 ; National Neuroscience Institute, Singapore 308433.ORCID 0000-0001-8480-9939
Murni TioDepartment of Neurology, Singapore General Hospital, Singapore 169608 ; National Neuroscience Institute, Singapore 308433.
Ratnagopal PavanniDepartment of Neurology, Singapore General Hospital, Singapore 169608 ; National Neuroscience Institute, Singapore 308433.
Eng King TanDepartment of Neurology, Singapore General Hospital, Singapore 169608 ; National Neuroscience Institute, Singapore 308433 ; Duke-NUS Graduate Medical School, Singapore 169857 ; Department of Clinical Research, Singapore General Hospital, Singapore 169608.
National Neuroscience Institute · SGSingapore General Hospital · SGDuke-NUS Medical School · SGTan Tock Seng Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective. COQ2 mutations have been reported in Japanese multiple system atrophy (MSA) patients. We examined the role of COQ2 in patients with dementia and essential tremor (ET), two common neurodegenerative conditions. Materials & Methods. A total of 2064 subjects, including 560 patients with dementia, 466 patients with ET, and 1038 healthy controls, were included. Genotyping for the COQ2 V393A (T>C) was carried out. Odds ratio (OR) adjusted by age and gender, together with 95% confidence interval (CI), was reported by means of logistic regression. Results. The frequency of the polymorphic variant V393A heterozygous (T/C) was 2.7% in dementia, 1.1% in ET, and 2.5% in controls (OR = 0.70, 95% confidence interval is 0.29-1.72 for dementia, and OR = 0.47, 95% confidence interval is 0.17-1.31, p = 0.1217 for ET). There was no significant association between V393A variant with dementia and ET. Conclusion. There was no significant association between V393A variant with dementia and ET. COQ2 gene is unlikely to play a significant role in patients with dementia or ET in our population.

Identifiers

PMID25977831
PMCPMC4421028
OpenAlexW2168593006

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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.