Evidence map›Paper›PMID 21904924›Full record

ArticleRheumatology international2012

Confirmation of C4 gene copy number variation and the association with systemic lupus erythematosus in Chinese Han population.

Yongmei Lv, Sumin He, Zheng Zhang, Yang Li, Dayan Hu, Kunju Zhu, Hui Cheng, Fusheng Zhou, Gang Chen, Xiaodong Zheng and 7 more

Abstract readValidation Study
PubMed Publisher
In one paragraph

Article in Rheumatology international, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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  7. Medical Records-Based Genetic Studies of the Complement System.Journal of the American Society of Nephrology : JASN · 2021
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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

17 authors at 2 institutions in 1 country.

Yongmei LvInstitute of Dermatology and Department of Dermatology at No. 1 Hospital, Anhui Medical University, 81 Meishan Road, Hefei, Anhui, People's Republic of China.
Sumin He
Zheng Zhang
Yang Li
Dayan Hu
Kunju Zhu
Hui Cheng
Fusheng Zhou
Gang Chen
Xiaodong Zheng
Pan Li
Yunqing Ren
Xianyong Yin
Yong Cui
Liangdan Sun
Sen Yang
Xuejun Zhang
Anhui Medical University · CNMinistry of Education of the People's Republic of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The distribution of complement component 4 (C4) gene copy number (GCN) has been validated in European populations. Meanwhile, C4 gene has been identified as a susceptibility gene for systemic lupus erythematosus (SLE). However, the association and the possible phenotype significance remain to be determined intensely in the Chinese population. This study was designed to validate the distribution of C4 GCNs in Chinese Han and the correlation between C4 GCNs and SLE using quantitative real-time polymerase chain reaction in 924 SLE patients and 1,007 controls. The results presented distribution of C4 GCNs in healthy populations and also showed that lower C4 GCN was a risk factor for SLE and higher C4 GCN was a protective factor against the disease susceptibility, which was similar to the report in the Caucasian population. Furthermore, we found the association between C4A GCN and disease subphenotypes of arthritis with SLE. We conclude that the association of C4 GCN with SLE was replicated in Chinese Han population, which highlighted the importance of C4 in SLE pathogenesis of diverse populations.

Indexed as

DNA Copy Number VariationsGene DosageAdultAsian PeopleCase-Control StudiesChinaComplement C4FemaleGene FrequencyGenetic Predisposition to DiseaseHumansLupus Erythematosus, SystemicMaleMiddle AgedOdds RatioPhenotypeComplement C4

Identifiers

PMID21904924
OpenAlexW1972866977

What OpenQuestion holds

Textmetadata
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.