Evidence map›Paper›PMID 22865508›Full record

ArticleDocumenta ophthalmologica. Advances in ophthalmology2012

Inverse pattern of photoreceptor abnormalities in retinitis pigmentosa and cone-rod dystrophy.

Midori Yokochi, Danjie Li, Masayuki Horiguchi, Shoji Kishi

Open access · hybridAbstract read
In one paragraph

Article in Documenta ophthalmologica. Advances in ophthalmology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Clinical and Molecular Aspects of C2orf71/PCARE in Retinal Diseases.International journal of molecular sciences · 2023
    Review
  2. Article
  3. Novel mutations inMolecular vision · 2019
    Article
  4. Article
  5. Article
  6. Tomographic comparison of cone-rod and rod-cone retinal dystrophies.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2014
    Article
  7. 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

4 authors at 2 institutions in 1 country.

Midori YokochiDepartment of Ophthalmology, Gunma University School of Medicine, 3-39-22 Showamachi, Maebashi, 371-8511, Japan. ykcmdr@yahoo.co.jp
Danjie LiDepartment of Ophthalmology, Gunma University School of Medicine, 3-39-22 Showamachi, Maebashi, 371-8511, Japan.
Masayuki HoriguchiDepartment of Ophthalmology, Fujita Health University School of Medicine, Aichi, Japan.
Shoji KishiDepartment of Ophthalmology, Gunma University School of Medicine, 3-39-22 Showamachi, Maebashi, 371-8511, Japan.
Gunma University · JPFujita Health University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo determine the characteristics of the photoreceptor abnormalities in retinitis pigmentosa (RP) and cone-rod dystrophy (CRD).

methodsWe evaluated the photoreceptor abnormalities using spectral-domain optical coherence tomography (SD-OCT) in 28 patients with RP and 17 patients with CRD. The OCT images and full-field electroretinograms were obtained from 21 eyes in normal subjects who were age-matched to patients with RP and CRD and served as controls.

resultsEyes with RP and CRD had markedly decreased rod responses (6.5 and 57.5 % of normal value), maximal responses (9.6 and 51.6 %), cone (16.5 and 25.8 %), and 30-Hz flicker responses (17.8 and 30.1 % of normal value), and their P values were smaller than 0.0003. On comparison of ERG data between RP and CRD, they had statistically significant differences in rod responses (P < 0.0003) and maximal responses (P < 0.0003). However, there were no statistical differences in cone response and a weak difference in 30-Hz flicker responses (P < 0.017). The best-corrected visual acuity was -0.03 ± 0.09 (logMAR, mean ± standard deviation [SD]) in eyes with RP, but 0.57 ± 0.54 in eyes with CRD. SD-OCT showed that eyes with RP had an intact reflective line at the junction between the photoreceptor inner and outer segment (IS/OS) at the fovea, while eyes with CRD had no IS/OS. The extent of the central visual field was correlated with the IS/OS length at the macula in eyes with RP.

conclusionThe distribution patterns of the IS/OS line help to differentiate between RP and CRD.

Indexed as

AdolescentAdultAgedAged, 80 and overChildChild, PreschoolElectroretinographyFemaleHumansMaleMiddle AgedRetinal Cone Photoreceptor CellsRetinal Photoreceptor Cell Inner SegmentRetinal Photoreceptor Cell Outer SegmentRetinal Rod Photoreceptor CellsRetinitis PigmentosaCone–rod dystrophyFull-field electroretinogramGoldmann perimetryOptical coherence tomographyPhotoreceptor inner and outer segment (IS/OS)Retinitis pigmentosa

Identifiers

PMID22865508
PMCPMC3490076
OpenAlexW2022460102

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.