Evidence map›Paper›PMID 20062564›Full record

ArticleMolecular vision2010

An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population.

Fang Lu, Peiquan Zhao, Yinchuan Fan, Shibo Tang, Jianbin Hu, Xiaoqi Liu, Xian Yang, Yiye Chen, Tao Li, Chuntao Lei and 6 more

Open access · greenAbstract read
In one paragraph

Article in Molecular vision, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
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    Review
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  10. Preservation of cone photoreceptors after a rapid yet transient degeneration and remodeling in cone-only Nrl-/- mouse retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    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

16 authors at 1 institution in 1 country.

Fang LuCenter for Human Molecular Biology & Genetics, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, Sichuan, China.
Peiquan Zhao
Yinchuan Fan
Shibo Tang
Jianbin Hu
Xiaoqi Liu
Xian Yang
Yiye Chen
Tao Li
Chuntao Lei
Jiyun Yang
Ying Lin
Shi Ma
Chunyong Li
Yi Shi
Zhenglin Yang
Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeSingle nucleotide polymorphisms (SNPs) in the complement component 1 inhibitor (SERPING1) gene have been shown to be significantly associated with age-related macular degeneration (AMD) in Caucasian populations. A replication study of an association between these SNPs and AMD in a Chinese population is reported in this study.

methodsSix SNPs, including rs2511990, rs1005510, rs11546660, rs2511989, rs2511988, and rs4926 in SERPING1 were genotyped in a Han Chinese subject group using the SNaPshot method of ABI. This subject group was composed of 194 patients with choroidal neovascularization (CNV or wet) AMD, 78 patients with soft drusen, and 285 matched controls. P values of the SNPs were calculated using an additive model. Haplotype frequencies between cases and controls were compared by chi2 analysis. The haplotype analysis was performed using Haploview 4.0.

resultsNone of the six SNPs showed significant association with AMD. None of the major haplotypes were observed to be significantly associated with AMD or choroidal neovascularization AMD (CNV) after a stringent Bonferroni correction.

conclusionsWe demonstrate that SNPs in SERPING1 are not significantly associated with AMD in the mainland Han Chinese population.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAgedAsian PeopleCase-Control StudiesChinaComplement C1 Inactivator ProteinsComplement C1 Inhibitor ProteinEthnicityFemaleHaplotypesHumansMacular DegenerationMalePhenotypePolymorphism, Single NucleotideComplement C1 Inactivator ProteinsComplement C1 Inhibitor ProteinSERPING1 protein, human

Identifiers

PMID20062564
PMCPMC2803124
OpenAlexW2140858486

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.