Evidence map›Paper›PMID 36097105›Full record

ArticleMolecular biology reports2022

Asian-specific 3'UTR variant in CDKN2B associated with risk of pituitary adenoma.

Byeong Ju Youn, Hyun Sub Cheong, Suhg Namgoong, Lyoung Hyo Kim, In Ki Baek, Jeong-Hyun Kim, Seon-Jin Yoon, Eui Hyun Kim, Se Hoon Kim, Jong Hee Chang and 2 more

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Article in Molecular biology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

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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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

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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

12 authors at 4 institutions in 1 country.

Byeong Ju YounDepartment of Life Science, Sogang University, 04107, Seoul, Republic of Korea.
Hyun Sub CheongDepartment of Genetic Epidemiology, SNP Genetics Inc, Seoul, Republic of Korea.
Suhg NamgoongDepartment of Genetic Epidemiology, SNP Genetics Inc, Seoul, Republic of Korea.
Lyoung Hyo KimDepartment of Genetic Epidemiology, SNP Genetics Inc, Seoul, Republic of Korea.
In Ki BaekDepartment of Life Science, Sogang University, 04107, Seoul, Republic of Korea.
Jeong-Hyun KimAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Seon-Jin YoonDepartment of Neurosurgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Eui Hyun KimDepartment of Neurosurgery, Yonsei University College of Medicine, Seoul, Republic of Korea. EUIHYUNKIM@yuhs.ac.
Se Hoon KimDepartment of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jong Hee ChangDepartment of Neurosurgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Sun Ho KimDepartment of Neurosurgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Hyoung Doo ShinDepartment of Life Science, Sogang University, 04107, Seoul, Republic of Korea. hdshin@sogang.ac.kr.ORCID http://orcid.org/0000-0003-1732-7838
Yonsei University · KRSNP Genetics (South Korea) · KRSogang University · KRUlsan College · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious genomewide association studies (GWASs), single nucleotide polymorphisms (SNPs) on cyclin-dependent kinase inhibitor 2 A (CDKN2A), cyclin-dependent kinase inhibitor 2B (CDKN2B), and cyclin-dependent kinase inhibitor 2B antisense RNA1 (CDKN2B-AS1) were reported as risk loci for glioma, a subgroup of the brain tumor. To further characterize this association with the risk of brain tumors in a Korean population, we performed a fine-mapping association study of CDKN2A, CDKN2B, and CDKN2B-AS1. METHODS AND

resultsA total of 17 SNPs were selected and genotyped in 1,439 subjects which were comprised of 959 patients (pituitary adenoma 335; glioma 324; meningioma 300) and 480 population controls (PCs). We discovered that a 3'untranslated region (3'UTR) variant, rs181031884 of CDKN2B (Asian-specific variant), had significant association with the risk of pituitary adenoma (PA) (Odds ratio = 0.58, P = 0.00003). Also, rs181031884 appeared as an independent causal variant among the significant variants in CDKN2A and CDKN2B, and showed dose-dependent effects on PA.

conclusionsAlthough further studies are needed to verify the impact of this variant on PA susceptibility, our results may help to understand CDKN2B polymorphism and the risk of PA.

Indexed as

GliomaPituitary NeoplasmsRNA, Long Noncoding3' Untranslated RegionsCyclin-Dependent Kinase Inhibitor p15Cyclin-Dependent Kinase Inhibitor p16Genetic Predisposition to DiseaseHumansPolymorphism, Single Nucleotide3' Untranslated RegionsCyclin-Dependent Kinase Inhibitor p15Cyclin-Dependent Kinase Inhibitor p16RNA, Long NoncodingCyclin-dependent kinase inhibitor 2B (CDKN2B)Korean populationPituitary adenoma (PA)Single nucleotide polymorphism (SNP)

Identifiers

PMID36097105
OpenAlexW4295423274

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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.