Evidence map›Paper›PMID 32807123›Full record

ArticleBMC medical genetics2020

Association of MC4R (rs17782313) with diabetes and cardiovascular disease in Korean men and women.

Jae Woong Sull, Gitae Kim, Sun Ha Jee

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2020. 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
1.7field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Melanocortin 4 receptor mutation in obesity.World journal of experimental medicine · 2024
    Review
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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

3 authors at 2 institutions in 1 country.

Jae Woong SullDepartment of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam, Korea.
Gitae KimDepartment of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam, Korea.
Sun Ha JeeDepartment of Epidemiology and Health Promotion, Institute for Health Promotion, Graduate School of Public Health, Yonsei University, Seoul, Korea. jsunha@yuhs.ac.ORCID 0000-0001-9519-3068
Eulji University · KRYonsei University · KR

Funding

Eulji University 2018Ministry of Education 2018R1D1A1B07050834
6 · The paper itself

Abstract

backgroundDiabetes is mostly assessed by the fasting glucose level. Several studies reported that serum fasting glucose levels and cardiovascular disease are associated with MC4R.

methodsA total of 4294 subjects participated in this study. There were 1810 subjects with cardiovascular disease among the 4294 subjects. We used multivariate linear regression models and multiple logistic regression analysis.

resultsIndividuals with the TC/CC genotype had a 1.29-fold higher risk of diabetes than did those with the TT genotype when adjusting for age, sex, and BMI (OR, 1.29; 95% CI, 1.04-1.60). For healthy subjects, the association was significant in women (OR, 1.99; 95% CI, 1.01-3.93). Men with the TC/CC genotype had a 1.21-fold higher risk of cardiovascular disease than did those with the TT genotype when adjusting for age, sex, and BMI (OR, 1.21; 95% CI, 1.04-1.41). The relationship between MC4R and cardiovascular disease was stronger in lean men (OR, 1.40; 95% CI, 1.12-1.74, p = 0.0028) than in overweight men.

conclusionsThis study suggests that the rs17782313 SNP in MC4R is related to diabetes and the SNP is also associated with cardiovascular disease in lean men.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseBlood GlucoseCardiovascular DiseasesDiabetes Mellitus, Type 2FemaleHumansLinear ModelsMaleMiddle AgedOdds RatioPolymorphism, Single NucleotideReceptor, Melanocortin, Type 4Republic of KoreaBlood GlucoseMC4R protein, humanReceptor, Melanocortin, Type 4Fasting glucoseMC4RPolymorphisms

Identifiers

PMID32807123
PMCPMC7433161
OpenAlexW3049167032

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.