Evidence map›Paper›PMID 29511375›Full record

ArticleInternational journal of medical sciences2018

Distribution of Cytotoxic T Lymphocyte-Associated Antigen-4 Promoter Polymorphisms in Taiwanese Patients with Type 2 Diabetes Mellitus.

Yung-Luen Shih, Hsu-Feng Lu, Chiao-Wan Hsiao, Kuo-Ting Ho, Pei-Chi Chen, Chien-Ning Huang, Yuanmay Chang, Shang-Jyh Kao, Ming-Yuh Shiau, Yih-Hsin Chang

Open access · goldAbstract read
In one paragraph

Article in International journal of medical sciences, 2018. 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
0.4field-weighted citation impact, top 32% 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, 6 citations in OpenAlex.

  1. Article
  2. Association Between CTLA4 Level and Obesity, Dyslipidemia, and Type 2 Diabetes Mellitus.Medical archives (Sarajevo, Bosnia and Herzegovina) · 2025
    Article
  3. Article
  4. Role of Natural Killer T (NKT) Cells in Type II Diabetes-Induced Vascular Injuries.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
  5. Review
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 4 institutions in 2 countries.

Yung-Luen ShihDepartment of Pathology and Laboratory Medicine, Shin Kong Wu Ho-Su Memorial Hospital, Taipei.
Hsu-Feng LuDepartment of Clinical Pathology, Cheng Hsin General Hospital, Taipei.
Chiao-Wan HsiaoProgram in Molecular Medicine, National Yang-Ming University and Academia Sinica, Taipei.
Kuo-Ting HoDepartment of Biotechnology and Laboratory Science in Medicine, National Yang-Ming University, Taipei.
Pei-Chi ChenDivisions of Endocrinology and Metabolism, Shin Kong Wu Ho-Su Memorial Hospital, Taipei.
Chien-Ning HuangDepartment of Internal Medicine, Chung Shan Medical University Hospital, Taichung.
Yuanmay ChangDepartment of Long Term Care, MacKay Medical College, New Taipei City.
Shang-Jyh KaoPulmonary Division, Shin Kong Wu Ho-Su Memorial Hospital, Taipei.
Ming-Yuh ShiauDepartment of Nursing, College of Nursing, Hungkuang University, Taichung, Taiwan.
Yih-Hsin ChangDepartment of Biotechnology and Laboratory Science in Medicine, National Yang-Ming University, Taipei.
National Yang Ming Chiao Tung University · TWChung Shan Medical University Hospital · TWHungkuang University · TWMemorial Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2DM) is associated with chronic inflammation, suggesting the metabolic abnormalities are originated from or exacerbated by cytokine overproduction. Cytokines and counter-regulatory molecules are crucial in keeping the balance of immune responses and, therefore, are potential candidates involved in T2DM etiology, development and complications. Our previous reports identify several significant associations between the genotypes of cytokine genes and T2DM and/or the clinical lipid parameters, which strongly suggest the participation of immune-regulatory molecules in lipid metabolism. The aim of this study is to determine the distribution of gene encoding cytotoxic T lymphocyte-associated antigen-4 (CTLA-4), a T-cell negative regulator, in T2DM patients and health subjects. Genomic DNA was extracted from 287 Taiwanese T2DM patients and 278 ethnic- and age- matched healthy subjects, and two

Indexed as

Genetic Predisposition to DiseasePromoter Regions, GeneticAdultAgedAsian PeopleCTLA-4 AntigenDiabetes Mellitus, Type 2FemaleGenotypeHumansMaleMiddle AgedPolymorphism, Restriction Fragment LengthT-Lymphocytes, CytotoxicCTLA-4 Antigencytotoxic T lymphocyte-associated antigen-4genetic polymorphismstype 2 diabetes mellitus

Identifiers

PMID29511375
PMCPMC5835710
OpenAlexW2789390062

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.