Evidence map›Paper›PMID 26617902›Full record

ArticleInternational journal of clinical and experimental pathology2015

COL8A1 rs13095226 polymorphism shows no association with neovascular age-related macular degeneration or polypoidal choroidal vasculopathy in Chinese subjects.

Yang Yu, Lvzhen Huang, Bin Wang, Chunfang Zhang, Yujing Bai, Xiaoxin Li

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  3. Disease markers · 2019
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  5. Association ofIn vivo (Athens, Greece)
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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

6 authors at 1 institution in 1 country.

Yang YuDepartment of Ophthalmology, Peking University People's Hospital Beijing, China ; Key Laboratory of Vision Loss and Restoration, Ministry of Education Beijing, China ; Beijing Key Laboratory for The Diagnosis and Treatment of Retinal and Choroid Diseases China.
Lvzhen HuangDepartment of Ophthalmology, Peking University People's Hospital Beijing, China ; Key Laboratory of Vision Loss and Restoration, Ministry of Education Beijing, China ; Beijing Key Laboratory for The Diagnosis and Treatment of Retinal and Choroid Diseases China.
Bin WangDepartment of Ophthalmology, Peking University People's Hospital Beijing, China ; Key Laboratory of Vision Loss and Restoration, Ministry of Education Beijing, China ; Beijing Key Laboratory for The Diagnosis and Treatment of Retinal and Choroid Diseases China.
Chunfang ZhangDepartment of Clinical Epidemiology, Peking University People's Hospital Beijing, China.
Yujing BaiDepartment of Ophthalmology, Peking University People's Hospital Beijing, China ; Key Laboratory of Vision Loss and Restoration, Ministry of Education Beijing, China ; Beijing Key Laboratory for The Diagnosis and Treatment of Retinal and Choroid Diseases China.
Xiaoxin LiDepartment of Ophthalmology, Peking University People's Hospital Beijing, China ; Key Laboratory of Vision Loss and Restoration, Ministry of Education Beijing, China ; Beijing Key Laboratory for The Diagnosis and Treatment of Retinal and Choroid Diseases China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAge-related macular degeneration (AMD) is the main cause of visual impairment and legal blindness in older individuals. COL8A1 rs13095226 variants have recently been implicated associated with neovascular age-related macular degeneration (nAMD) and Polypoidal Choroidal Vasculopathy (PCV) in American studies. The aim of this study was to investigate the association between the COL8A1 rs13095226 Polymorphism and neovascular age-related macular degeneration (nAMD) and polypoidal choroidal vasculopathy (PCV) in Chinese people.

methods900 Chinese subjects-300 cases with nAMD, 300 cases with PCV and 300 controls, were enrolled in a cross-sectional observational study. The diagnoses of nAMD and PCV were confirmed by Fundus photography, Fluorescence Fundus Angiography (FFA) and Indocyanine Green Angiography (ICGA). Genomic DNA was extracted from venous blood leukocytes and genotypes of rs13095226 were determined by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Differences in allele distribution between cases and controls were tested by chi-square tests, with age and gender adjusted by logistic regression analysis.

resultThe COL8A1 rs13095226 polymorphism was not statistically significantly different from the nAMD or PCV to the normal controls (P>0.05) in Chinese Population. The association remained insignificant after adjustment for age and gender differences (P>0.05).

conclusionsThis case-control study indicated that the COL8A1 rs13095226 polymorphism is not associated with nAMD or PCV, which suggesting this gene maybe not a susceptibility gene locus for nAMD or PCV in Chinese subjects.

Indexed as

AdultAgedAged, 80 and overAllelesAsian PeopleCase-Control StudiesChoroidCollagen Type VIIICollagen Type XVIIICross-Sectional StudiesFemaleFluorescein AngiographyGenotypeHumansMaleMiddle AgedCOL18A1 protein, humanCollagen Type VIIICollagen Type XVIIICOL8A1geneticsNeovascular age-related macular degenerationpolypoidal choroidal vasculopathy

Identifiers

PMID26617902
PMCPMC4637718
OpenAlexW2186834825

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.