Evidence map›Paper›PMID 28181067›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2017

Lack of association between MAOA-uVNTR variants and excessive daytime sleepiness.

Filiz Ozen, Zeynep Yegin, Figen Yavlal, Zuhal Aydan Saglam, Haydar Koc, Ismet Berber

Abstract read
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2017. 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
0.6field-weighted citation impact, top 32% 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, 4 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

6 authors at 4 institutions in 1 country.

Filiz OzenDepartment of Medical Genetics, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Turkey.
Zeynep YeginMedical Laboratory Techniques Program, Vocational School of Health Services, Sinop University, Sinop, Turkey. zyegin@sinop.edu.tr.
Figen YavlalDepartment of Neurology, Faculty of Medicine, Bahcesehir University, Istanbul, Turkey.
Zuhal Aydan SaglamDepartment of Family Medicine, Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Turkey.
Haydar KocDepartment of Statistics, Faculty of Science, Cankiri Karatekin University, Cankiri, Turkey.
Ismet BerberDepartment of Biology, Faculty of Science and Arts, Sinop University, Sinop, Turkey.
Istanbul Medeniyet University · TRSinop University · TRBahçeşehir University · TRÇankırı Karatekin University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sleep disorders are highly prevalent in the population and have dramatic health, social, and economic impacts. However, their treatments may remain symptomatic due to ignorance of molecular factors which may provide fundamental insights into the neurological bases of sleep. Excessive daytime sleepiness (EDS) is a common complaint encountered in neurological practice with significant effects both on individuals and on society. We aimed to investigate the role of monoamine oxidase A (MAOA) as a candidate gene in EDS. Epworth sleepiness scale (ESS) was applied to 221 subjects who were also genotyped for MAOA upstream variable number of tandem repeats (MAOA-uVNTR). Patient group displayed higher ESS values (mean 12.67) when compared with the control group (mean 6.38). However, MAOA-uVNTR genotypes did not show a significant association with ESS scores neither on women nor on men. Finally, these data suggest further replications in different populations. Moreover, the investigation of some other genes together with MAOA and/or some possible regulatory molecular mechanisms may offer a more comprehensive approach in the role of genetic factors contributing to EDS.

Indexed as

AdultDisorders of Excessive SomnolenceFemaleGenetic Association StudiesGenotypeHumansMaleMiddle AgedMinisatellite RepeatsMonoamine OxidasePsychiatric Status Rating ScalesMonoamine Oxidasemonoamine oxidase A, humanExcessive daytime sleepinessMAOA-uVNTRMonoamine oxidase ANeurogeneticsSleepVariable number tandem repeat

Identifiers

PMID28181067
OpenAlexW2586773808

What OpenQuestion holds

Textmetadata
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.