Evidence map›Paper›PMID 33997039›Full record

ArticleBioMed research international2021

A Bioinformatic Investigation of the Mechanism Underlying Migraine-Induced Erectile Dysfunction.

Ji-Sheng Wang, Sheng Deng, Qi Zhao, Kai-Ge Zhang, Bing-Hao Bao, Jun-Long Feng, Fan-Chao Meng, Heng-Heng Dai, Xiao Li, Hai-Song Li and 1 more

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. 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
0.5field-weighted citation impact, top 40% 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, 3 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

11 authors at 3 institutions in 1 country.

Ji-Sheng WangFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, BJ 100029, China.
Sheng DengFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, BJ 100029, China.
Qi ZhaoFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, BJ 100029, China.
Kai-Ge ZhangFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, BJ 100029, China.
Bing-Hao BaoFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, BJ 100029, China.
Jun-Long FengFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, BJ 100029, China.
Fan-Chao MengFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, BJ 100029, China.
Heng-Heng DaiFirst Clinical Medical College, Beijing University of Chinese Medicine, Beijing, BJ 100029, China.
Xiao LiThe First Affiliated Hospital, Henan University of Chinese Medicine, Zhengzhou 450000, China.
Hai-Song LiAndrology Department, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, BJ 100700, China.ORCID https://orcid.org/0000-0002-6306-2570
Bin WangAndrology Department, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, BJ 100700, China.ORCID https://orcid.org/0000-0002-4774-8476
Beijing University of Chinese Medicine · CNDongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CNFirst Affiliated Hospital of Henan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOver recent years, an increasing body of literature has focused on the relationship between erectile dysfunction (ED) and migraine. However, the specific mechanism is unclear. MATERIALS AND

methodsWe used a bioinformatic database to predict the targets and pathways associated with migraine and ED. Twenty male SD rats were randomly divided into a blank group (Group A,

resultsThere are 117 intersection targets of migraine and ED, involving 188 cell biological processes (BP), 21 cellular components (CC), 31 molecular functions (MF), and 65 signaling pathways. HE staining results show that there were no significant differences between Group A and Group B with regard to any of the parameters. Compared with Group A, the levels of the PI3K, p-AKT, and p-mTOR proteins and PI3K, AKT, and mTOR mRNAs in Group B decreased (

conclusionsThe decline of erectile function in a rat model of migraine was associated with the PI3K/Akt/mTOR signaling pathway.

Indexed as

Erectile DysfunctionMigraine DisordersPenisAnimalsComputational BiologyMalePhosphatidylinositol 3-KinasesProtein Interaction MapsProto-Oncogene Proteins c-aktRatsRats, Sprague-DawleySignal TransductionTOR Serine-Threonine KinasesMTOR protein, humanPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID33997039
PMCPMC8112924
OpenAlexW3157611395

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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.