Evidence map›Paper›PMID 25848204›Full record

ArticleClinical ophthalmology (Auckland, N.Z.)2015

Measurement of serum and vitreous concentrations of anti-type II collagen antibody in diabetic retinopathy.

Atsuko Nakaizumi, Masanori Fukumoto, Teruyo Kida, Hiroyuki Suzuki, Seita Morishita, Takaki Satou, Hidehiro Oku, Tsunehiko Ikeda, Kimitoshi Nakamura

Open access · goldAbstract read
In one paragraph

Article in Clinical ophthalmology (Auckland, N.Z.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Possible roles of anti-type II collagen antibody and innate immunity in the development and progression of diabetic retinopathy.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2022
    Review
  3. Article
  4. Article
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 2 institutions in 1 country.

Atsuko NakaizumiDepartment of Ophthalmology, Osaka Medical College, Takatsuki City, Osaka, Japan.
Masanori FukumotoDepartment of Ophthalmology, Osaka Medical College, Takatsuki City, Osaka, Japan.
Teruyo KidaDepartment of Ophthalmology, Osaka Medical College, Takatsuki City, Osaka, Japan.
Hiroyuki SuzukiDepartment of Ophthalmology, Osaka Medical College, Takatsuki City, Osaka, Japan.
Seita MorishitaDepartment of Ophthalmology, Osaka Medical College, Takatsuki City, Osaka, Japan.
Takaki SatouDepartment of Ophthalmology, Osaka Medical College, Takatsuki City, Osaka, Japan.
Hidehiro OkuDepartment of Ophthalmology, Osaka Medical College, Takatsuki City, Osaka, Japan.
Tsunehiko IkedaDepartment of Ophthalmology, Osaka Medical College, Takatsuki City, Osaka, Japan.
Kimitoshi NakamuraNakamura Eye Clinic, Nagano, Japan.
Osaka Medical and Pharmaceutical University · JPNakamura Toho Research Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutoimmune mechanisms have been postulated as a cause of diabetic retinopathy (DR), as several autoantibodies have reportedly been detected in the serum of DR patients. In this present study, we measured serum and vitreous levels of anti-type II collagen (anti-II-C) antibodies in DR patients and investigated their association with the mechanism of development of DR. PATIENTS AND

methodsBlood samples were obtained from patients with proliferative DR and from patients with diabetic macular edema who underwent vitrectomy at Osaka Medical College, Takatsuki City, Osaka, Japan. Diabetic patients without DR were also included. The control group consisted of age- and sex-matched patients with noninflammatory eye diseases who underwent eye surgery for retinal detachment or for cataracts. The levels of anti-II-C immunoglobulin (Ig)G antibody in the vitreous and serum were measured using a human/monkey anti-II-C IgG assay kit.

resultsThe serum levels of anti-II-C IgG antibody were significantly higher in the DR patients than in the patients with noninflammatory eye disease (56.8±33.8 units/mL versus 30.5±13.7 units/mL, respectively; P<0.05, Fisher's exact test). These levels were also significantly higher in the diabetic patients without DR than in the patients with noninflammatory eye disease (76.3±49.7 units/mL versus 30.5±13.7 units/mL, respectively; P<0.01, Fisher's exact test). However, anti-II-C IgG antibody levels were unable to be detected in all of the obtained vitreous fluid samples.

conclusionThe development and progression of DR may be related to a mechanism involving intraocular type II collagen, which normally has immunological tolerance as a sequestered antigen. In DR, the disruption of the blood-retinal barrier leads to contact between the intraocular type II collagen and immunocompetent cells, and to subsequent activation of the autoimmune mechanism.

Indexed as

autoimmune mechanismblood–retinal barrierserumvitreous

Identifiers

PMID25848204
PMCPMC4376299
OpenAlexW2090376466

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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.