Evidence map›Paper›PMID 29633594›Full record

ArticleCell journal2018

OX40 Gene and Serum Protein Expression Profiles in Patients with Parkinson's Disease.

Azadeh Seyedjoodaki, Fereshteh Alsahebfosoul, Nahid Eskandari, Vahid Shaygannejad, Mansour Salehi, Mohammad Kazemi, Mostafa Manian, Omid Mirmosayyeb, Mohammad Taghi Kardi

Open access · greenAbstract read
In one paragraph

Article in Cell journal, 2018. 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
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0citing papers in PubMed
–field-weighted citation impact, top 71% 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, 0 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

9 authors at 3 institutions in 1 country.

Azadeh SeyedjoodakiDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Fereshteh AlsahebfosoulDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Nahid EskandariDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Vahid ShaygannejadDepartment Neuroscience, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran.
Mansour SalehiDepartment of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran.
Mohammad KazemiDepartment of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran.
Mostafa ManianDepartment of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Omid MirmosayyebDepartment Neuroscience, School of Medicine, Isfahan University of Medical Science, Isfahan, Iran.
Mohammad Taghi KardiDepartment of Biology, Faculty of Science, University of Isfahan, Isfahan, Iran.
Isfahan University of Medical Sciences · IRUniversity of Isfahan · IRIran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesInflammation of the immune system and the central nervous system has been known as an important predisposing factor for Parkinson's disease (PD). Increased expression of OX40 protein (CD134) is a known factor for increased inflammation and initiation of NF-kappa-B signaling pathway in different diseases. We aimed to investigate the expression of OX40 at the transcript and serum protein levels. MATERIALS AND

methodsTwenty individuals with PD and 20 healthy individuals, as controls, were enrolled in this casecontrol study. Expression of OX40 at the transcript level and serum protein levels were measured by quantitative real-time polymerase chain reaction (qRT-PCR) and enzyme-linked immunosorbent assays respectively.

resultsThe mean expression level of OX40 was increased in patients but not at a significant level (P>0.05). Consistently, the mean serum concentration of OX40 showed a mild, but non-significant, increase in the patients (P>0.05).

conclusionsWe conclude that OX40 expression at either the transcript or protein level has no diagnostic utility in asymptomatic PD. This shows the need for clinical, cellular and interventional research to detect new robust biomarkers.

Indexed as

NeurodegenerativeOX40Parkinson’s Disease

Identifiers

PMID29633594
PMCPMC5893288
OpenAlexW3022140778

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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.