Evidence map›Paper›PMID 28740224›Full record

ArticleScientific reports2017

Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease.

Chin-Hsien Lin, K Ray Chaudhuri, Jun-Yu Fan, Chia-I Ko, Alexandra Rizos, Chia-Wen Chang, Han-I Lin, Yih-Ru Wu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

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  11. Inhibition of catechol-Journal of enzyme inhibition and medicinal chemistry · 2021
    Article
  12. Analytical methodologies for sensing catechol-Journal of pharmaceutical analysis · 2021
    Review
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  19. An overview of pain in Parkinson's disease.Clinical parkinsonism & related disorders · 2020
    Article
  20. The Association Analysis ofFrontiers in genetics · 2020
    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 6 institutions in 2 countries.

Chin-Hsien LinDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.
K Ray ChaudhuriMaurice Wohl Clinical Neuroscience Institute and NIHR Biomedical Research Centre, Institute of Psychiatry, Psychology and Neuroscience, King's College Hospital, London, UK.
Jun-Yu FanDepartment of Nursing, Chang Gung University of Science and Technology, Taoyuan, Taiwan.
Chia-I KoDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.
Alexandra RizosNational Parkinson Foundation Centre of Excellence, King's College Hospital, London, London, UK.
Chia-Wen ChangDepartment of Neurology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Linkou, Taiwan.
Han-I LinDepartment of Neurology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan.
Yih-Ru WuDepartment of Neurology, Chang Gung Memorial Hospital, Chang Gung University College of Medicine, Linkou, Taiwan. yihruwu@cgmh.org.tw.
National Taiwan University Hospital · TWChang Gung University · TWChang Gung University of Science and Technology · TWKing's College Hospital · GBKing's College Hospital NHS Foundation Trust · GBLinkou Chang Gung Memorial Hospital · TW

Funding

Parkinson's UK K-1210
6 · The paper itself

Abstract

Pain is a distressing symptom of Parkinson disease (PD). We aim to determine whether the genetic variants of chronic pain-related genes contribute to pain in PD patients. We included 418 PD patients and evaluated pain severity on King's PD pain scale. We genotyped rs6267, rs6269, rs4633, rs4818 and rs4680 of COMT, rs6746030 of SCN9A, and rs1799971 of OPRM1. In total, 193 participants (46.2%) experienced pain. Compared to pain-free PD patients, PD patients with pain had an earlier age of onset, longer disease duration, and higher depression and motor severity (P < 0.01). The frequencies of COMT rs4680 "A" allele were higher in PD patients with pain than those without pain (46.1% vs. 31.1%, P < 0.01). Pain severity was significantly associated with disease duration (P = 0.02), and COMT rs6267 T allele (P < 0.01). We stratified PD by status of depression and the association between COMT rs6267 "GT" genotype and pain severity remained significant (P < 0.01). Furthermore, pain severity was significantly higher in participants having COMT rs4680 "GG" and "GA" genpotypes than those having "AA" genotype (P = 0.04). We concluded that depression and COMT rs4680 "GG" and "GA" genotypes and COMT rs6267 "GT" genotype contribute to pain in PD patients.

Indexed as

Polymorphism, Single NucleotideAgedAge of OnsetCatechol O-MethyltransferaseChronic PainDepressionFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansMaleMiddle AgedNAV1.7 Voltage-Gated Sodium ChannelPain MeasurementParkinson DiseaseReceptors, Opioid, muCatechol O-MethyltransferaseCOMT protein, humanNAV1.7 Voltage-Gated Sodium ChannelOPRM1 protein, humanReceptors, Opioid, muSCN9A protein, human

Identifiers

PMID28740224
PMCPMC5524945
OpenAlexW2737895852

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.