Evidence map›Paper›PMID 42582553›Full record

ArticleJournal of diabetes and metabolic disorders2026

Association of a near-MC4R gene variant (rs17782313) with hyperphagia among patients with severe obesity.

Armita Kakavand Hamidi, Mahsa Foroutan, Zeynab Nickhah Klashami, Forough Taheri, Mojgan Asadi, Fatemeh Bandarian, Mahsa Mohammad Amoli

Abstract read
In one paragraph

Article in Journal of diabetes and metabolic disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Armita Kakavand HamidiObesity and Eating Habits Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Mahsa ForoutanDepartment of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Zeynab Nickhah KlashamiMetabolic Disorders Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Forough TaheriEndocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Mojgan AsadiEndocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Fatemeh BandarianMetabolomics and Genomics Research Center, Endocrinology and Metabolism Molecular- Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
Mahsa Mohammad AmoliMetabolic Disorders Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Obesity is a multifaceted issue influenced by genetic, environmental, and psychological factors. Genetic predispositions significantly contribute to the risk of obesity in individuals. A deficiency in the melanocortin-4 receptor ( Methods: Genotypes of the near-MC4R variant rs17782313 were compared between patients with severe obesity and hyperphagia (cases) and patients with severe obesity without hyperphagia (controls). Factors such as body mass index (BMI), family history of obesity before puberty, and age at onset of obesity were also assessed. The genotyping of the Results: Analysis of the variant rs17782313 demonstrated a statistically significant positive association with hyperphagia among patients with obesity (ꭓ Conclusion: These findings underscore the importance of genetic factors in understanding hyperphagic behaviors. The

Indexed as

Genetic variantsHyperphagiaMC4R (Melanocortin-4 Receptor)ObesitySNP (Single Nucleotide Polymorphism)

Identifiers

PMID42582553
PMCPMC13457990

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.