Evidence map›Paper›PMID 28714010›Full record

ArticleMolecular medicine reports2017

PTPRQ as a potential biomarker for idiopathic normal pressure hydrocephalus.

Yuki Nagata, Masahiko Bundo, Saiko Sugiura, Masahiro Kamita, Masaya Ono, Kotaro Hattori, Sumiko Yoshida, Yu-Ichi Goto, Katsuya Urakami, Shumpei Niida

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.5field-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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Review
  4. Cerebrospinal Fluid Biomarkers in iNPH: A Narrative Review.Diagnostics (Basel, Switzerland) · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Review
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

10 authors at 3 institutions in 1 country.

Yuki NagataMedical Genome Center, National Center for Geriatrics and Gerontology, Aichi 474‑8511, Japan.
Masahiko BundoDepartment of Experimental Neuroimaging, National Center for Geriatrics and Gerontology, Obu, Aichi 474‑8511, Japan.
Saiko SugiuraDepartment of Otolaryngology, National Center for Geriatrics and Gerontology, Obu, Aichi 474‑8511, Japan.
Masahiro KamitaDivision of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Chuo‑ku, Tokyo 104‑0045, Japan.
Masaya OnoDivision of Chemotherapy and Clinical Research, National Cancer Center Research Institute, Chuo‑ku, Tokyo 104‑0045, Japan.
Kotaro HattoriMedical Genome Center, National Center of Neurology and Psychiatry, Kodaira, Tokyo 187‑8551, Japan.
Sumiko YoshidaMedical Genome Center, National Center of Neurology and Psychiatry, Kodaira, Tokyo 187‑8551, Japan.
Yu-Ichi GotoMedical Genome Center, National Center of Neurology and Psychiatry, Kodaira, Tokyo 187‑8551, Japan.
Katsuya UrakamiDepartment of Biological Regulation, School of Health Science, Faculty of Medicine, Tottori University, Yonago, Tottori 683‑8503, Japan.
Shumpei NiidaMedical Genome Center, National Center for Geriatrics and Gerontology, Aichi 474‑8511, Japan.
National Center for Geriatrics and Gerontology · JPNational Center of Neurology and Psychiatry · JPTottori University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic normal pressure hydrocephalus (iNPH) is caused by the accumulation of cerebrospinal fluid (CSF) and is characterized by gait disturbance, urinary incontinence, and dementia. iNPH dementia is treatable by shunt operation; however, since the cognitive symptoms of iNPH are often similar to those of other dementias, including Alzheimer's disease (AD), accurate diagnosis of iNPH is difficult. To overcome this problem, the identification of novel diagnostic markers to distinguish iNPH and AD is warranted. Using comparative proteomic analysis of CSF from patients with iNPH and AD, protein tyrosine phosphatase receptor type Q (PTPRQ) was identified as a candidate biomarker protein for discriminating iNPH from AD. ELISA analysis indicated that the PTPRQ concentration in the CSF was significantly higher in patients with iNPH compared with those with AD. In addition, the PTPRQ concentration in the CSF of non‑responders to shunt operation (SNRs) tended to be relatively lower compared with that in the responders. PTPRQ may be a useful biomarker for discriminating between patients with iNPH and AD, and may be a potential companion biomarker to identify SNRs among patients with iNPH. Additional large‑scale analysis may aid in understanding the novel aspects of iNPH.

Indexed as

AgedAnimalsAudiometry, Pure-ToneBiomarkersBrainFemaleHearingHumansHydrocephalus, Normal PressureMaleMiceReceptor-Like Protein Tyrosine Phosphatases, Class 3Reproducibility of ResultsBiomarkersPTPRQ protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 3

Identifiers

PMID28714010
PMCPMC5547938
OpenAlexW2735998560

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.