Evidence map›Paper›PMID 28758129›Full record

SynthesisJournal of diabetes research2017

The Association of Haptoglobin Gene Variants and Retinopathy in Type 2 Diabetic Patients: A Meta-Analysis.

Huiqun Wu, Huan Wu, Lili Shi, Xinlu Yuan, Ying Yin, Mingjie Yuan, Yushan Zhou, Qianwen Hu, Kui Jiang, Jiancheng Dong

Open access · goldAbstract readMeta-AnalysisReview
In one paragraph

Synthesis in Journal of diabetes research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
0.8field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. 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

10 authors at 2 institutions in 2 countries.

Huiqun WuDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.ORCID 0000-0001-5837-6199
Huan WuDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.ORCID 0000-0001-7810-7121
Lili ShiDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.
Xinlu YuanDepartment of Endocrinology, Affiliated Hospital of Nantong University, Nantong 226001, China.
Ying YinDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.ORCID 0000-0001-6553-1644
Mingjie YuanDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.ORCID 0000-0001-7146-6498
Yushan ZhouDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.ORCID 0000-0002-2370-4196
Qianwen HuDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.
Kui JiangDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.ORCID 0000-0002-0327-7385
Jiancheng DongDepartment of Medical Informatics, Medical School of Nantong University, Nantong 226001, China.
Nantong University · CNUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AIMS/

introductionTo collectively evaluate the association between haptoglobin (Hp) gene variants and diabetic retinopathy (DR) in patients with type 2 diabetes mellitus (T2DM).

methodsA comprehensive literature review was performed for eligible studies. After inclusion and exclusion selection as well as quality assessment, those studies meeting quality standards were included. In this study, diabetic patients with retinopathy were selected as the case group and those ones without DR were treated as the control group. The recessive model, allele model, additive model, heterozygote model, and homozygote model were utilized to investigate the association of three Hp gene variants and DR. Subgroup analysis on different severity of DR including nonproliferative diabetic retinopathy (NPDR) and proliferative diabetic retinopathy (PDR) was also conducted.

resultsSix trials from different regions were finally included. A total of 1145 subjects containing 564 T2DM patients with retinopathy were included. The recessive model, allele model, additive model, and homozygote model results showed that Hp gene variants were not associated with DR, NPDR, and PDR. However, the heterozygote model indicated the association of Hp gene variants with DR.

conclusionsNo association was found between the Hp gene variants and PDR and NPDR. More studies are required to verify these findings.

Indexed as

Genetic VariationAdultAgedChi-Square DistributionDiabetes Mellitus, Type 2Diabetic RetinopathyFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHaptoglobinsHeterozygoteHomozygoteHumansMaleMiddle AgedHaptoglobinsHP protein, human

Identifiers

PMID28758129
PMCPMC5512055
OpenAlexW2731020942

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.