Evidence map›Paper›PMID 21611200›Full record

ArticlePloS one2011

Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction.

Mineo Kondo, Rikako Sanuki, Shinji Ueno, Yuji Nishizawa, Naozumi Hashimoto, Hiroshi Ohguro, Shuichi Yamamoto, Shigeki Machida, Hiroko Terasaki, Grazyna Adamus and 1 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 28% 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

50 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  6. American journal of ophthalmology case reports · 2024
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  15. A case of melanoma-associated retinopathy with autoantibodies against TRPM1.Documenta ophthalmologica. Advances in ophthalmology · 2020
    Article
  16. Review
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  18. Two cases of unilateral cone-rod dysfunction with negative electroretinograms.Documenta ophthalmologica. Advances in ophthalmology · 2019
    Article
  19. Article
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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 6 institutions in 2 countries.

Mineo KondoDepartment of Ophthalmology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan. kondomi@med.nagoya-u.ac.jp
Rikako Sanuki
Shinji Ueno
Yuji Nishizawa
Naozumi Hashimoto
Hiroshi Ohguro
Shuichi Yamamoto
Shigeki Machida
Hiroko Terasaki
Grazyna Adamus
Takahisa Furukawa
Nagoya University · JPOregon Health & Science University · USSapporo Medical University · JPChiba University · JPChubu University · JPIwate Medical University · JP

Funding

Proteomics CoreP30EY010572 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TED S ACOTT · 1995 to 2026
$19.4M
NEI NIH HHS P30 EY010572PHS HHS E13053
6 · The paper itself

Abstract

backgroundParaneoplastic retinopathy (PR), including cancer-associated retinopathy (CAR) and melanoma-associated retinopathy (MAR), is a progressive retinal disease caused by antibodies generated against neoplasms not associated with the eye. While several autoantibodies against retinal antigens have been identified, there has been no known autoantibody reacting specifically against bipolar cell antigens in the sera of patients with PR. We previously reported that the transient receptor potential cation channel, subfamily M, member 1 (TRPM1) is specifically expressed in retinal ON bipolar cells and functions as a component of ON bipolar cell transduction channels. In addition, this and other groups have reported that human TRPM1 mutations are associated with the complete form of congenital stationary night blindness. The purpose of the current study is to investigate whether there are autoantibodies against TRPM1 in the sera of PR patients exhibiting ON bipolar cell dysfunction. METHODOLOGY/PRINCIPAL

findingsWe performed Western blot analysis to identify an autoantibody against TRPM1 in the serum of a patient with lung CAR. The electroretinograms of this patient showed a severely reduced ON response with normal OFF response, indicating that the defect is in the signal transmission between photoreceptors and ON bipolar cells. We also investigated the sera of 26 patients with MAR for autoantibodies against TRPM1 because MAR patients are known to exhibit retinal ON bipolar cell dysfunction. Two of the patients were found to have autoantibodies against TRPM1 in their sera. CONCLUSION/SIGNIFICANCE: Our study reveals TRPM1 to be one of the autoantigens targeted by autoantibodies in at least some patients with CAR or MAR associated with retinal ON bipolar cell dysfunction.

Indexed as

AgedAutoantibodiesBlotting, WesternElectroretinographyHumansMaleMelanomaParaneoplastic SyndromesRetinal Bipolar CellsRetinal DiseasesTRPM Cation ChannelsAutoantibodiesTRPM1 protein, humanTRPM Cation Channels

Identifiers

PMID21611200
PMCPMC3096646
OpenAlexW1506130534

What OpenQuestion holds

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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.