Evidence map›Paper›PMID 24385677›Full record

ArticleDisease markers2013

Positive association between GCKR rs780093 polymorphism and coronary heart disease in the aged Han Chinese.

Jiangfang Lian, Jian Guo, Zhikui Chen, Qingjun Jiang, Huadan Ye, Xiaoyan Huang, Xi Yang, Yanna Ba, Jianqing Zhou, Shiwei Duan

Abstract read
In one paragraph

Article in Disease markers, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Cornea Arcus and Dyslipidemia in Unrelated Adults With Monoallelic Germline Variants in theClinical medicine insights. Endocrinology and diabetes · 2026
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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

10 authors.

Jiangfang LianNingbo Medical Center, Lihuili Hospital, Ningbo University, Ningbo, Zhejiang 315041, China.
Jian GuoNingbo Medical Center, Lihuili Hospital, Ningbo University, Ningbo, Zhejiang 315041, China ; Zhejiang Provincial Key Laboratory of Pathophysiology, Ningbo University, Ningbo, Zhejiang 315211, China.
Zhikui ChenNingbo Medical Center, Lihuili Hospital, Ningbo University, Ningbo, Zhejiang 315041, China.
Qingjun JiangNingbo Medical Center, Lihuili Hospital, Ningbo University, Ningbo, Zhejiang 315041, China.
Huadan YeZhejiang Provincial Key Laboratory of Pathophysiology, Ningbo University, Ningbo, Zhejiang 315211, China.
Xiaoyan HuangZhejiang Provincial Key Laboratory of Pathophysiology, Ningbo University, Ningbo, Zhejiang 315211, China.
Xi YangNingbo Medical Center, Lihuili Hospital, Ningbo University, Ningbo, Zhejiang 315041, China.
Yanna BaNingbo Medical Center, Lihuili Hospital, Ningbo University, Ningbo, Zhejiang 315041, China ; Zhejiang Provincial Key Laboratory of Pathophysiology, Ningbo University, Ningbo, Zhejiang 315211, China.
Jianqing ZhouNingbo Medical Center, Lihuili Hospital, Ningbo University, Ningbo, Zhejiang 315041, China.
Shiwei DuanZhejiang Provincial Key Laboratory of Pathophysiology, Ningbo University, Ningbo, Zhejiang 315211, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePrevious studies have confirmed that GCKR rs780093 polymorphism is associated with triglyceride (TG), a known risk factor of coronary heart disease (CHD). The goal of our study is to explore the association of GCKR rs780093 polymorphism with CHD in Han Chinese population. METHODS AND

resultsA total of 568 CHD cases and 494 non-CHD controls were enrolled in the current case-control study. Genotyping was done using melting temperature shift (Tm-shift) approach. Our results also showed that GCKR rs780093 polymorphism was significantly associated with TG level (P = 0.0016). Although there was no significant association between cases and controls (P > 0.05), a breakdown analysis by age yielded a significant association of GCKR rs780093 polymorphism with CHD in individuals aged 65 and older (genotype: χ(2) = 6.86; df = 2; P = 0.03; allele: χ(2) = 4.11; df = 1; P = 0.04).

conclusionOur findings confirmed the contribution of GCKR rs780093 polymorphism to TG metabolism and demonstrated GCKR rs780093 as a risk factor of CHD in individuals aged 65 and older.

Indexed as

Polymorphism, Single NucleotideAdaptor Proteins, Signal TransducingAgedCase-Control StudiesChinaCoronary Artery DiseaseFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHumansMaleMiddle AgedRisk FactorsSequence Analysis, DNATransition TemperatureAdaptor Proteins, Signal TransducingGCKR protein, humanTriglycerides

Identifiers

PMID24385677
PMCPMC3871702

What OpenQuestion holds

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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.