Evidence map›Paper›PMID 36218131›Full record

ArticleJournal of applied biomedicine2022

Genetic variation in the ADIPOQ gene and serum adiponectin increase the risk of bladder cancer.

Lina Elsalem, Mahmoud A Alfaqih, Samir Al Bashir, Omar Halalsheh, Haneen A Basheer, Khawla Mhedat, Yousef Khader, Klaus Pors

Open access · goldAbstract read
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In one paragraph

Article in Journal of applied biomedicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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  4. 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

8 authors at 3 institutions in 2 countries.

Lina ElsalemJordan University of Science and Technology, Faculty of Medicine, Department of Pharmacology, Irbid, Jordan.
Mahmoud A AlfaqihJordan University of Science and Technology, Faculty of Medicine, Department of Physiology and Biochemistry, Irbid, Jordan.
Samir Al BashirJordan University of Science and Technology, Faculty of Medicine, Department of Pathology and Microbiology, Irbid, Jordan.
Omar HalalshehJordan University of Science and Technology, Faculty of Medicine, Department of General Surgery and Urology, Irbid, Jordan.
Haneen A BasheerZarqa University, Faculty of Pharmacy, Zarqa, Jordan.
Khawla MhedatJordan University of Science and Technology, Faculty of Medicine, Department of Physiology and Biochemistry, Irbid, Jordan.
Yousef KhaderJordan University of Science and Technology, Faculty of Medicine, Department of Public Health and Community Medicine, Irbid, Jordan.
Klaus PorsUniversity of Bradford, Faculty of Life Sciences, The School of Pharmacy and Medical Sciences, Institute of Cancer Therapeutics, West Yorkshire, United Kingdom.
Jordan University of Science and Technology · JOUniversity of Bradford · GBZarqa University · JO

Funding

Deanship of Research of Jordan University of Science and Technology 20200263
6 · The paper itself

Abstract

Bladder cancer (BC) is the 10th most common cancer worldwide. Genetic studies estimated 30% heritability in BC risk. Adiponectin is an adipocytokine that has important roles in the regulation of energy metabolism. Recent evidence suggests dysregulation of adiponectin levels in BC tissues. Serum level of adiponectin is influenced by single nucleotide polymorphisms (SNPs) in the ADIPOQ gene. However, limited evidence is available regarding the association between adiponectin serum levels or SNPs in ADIPOQ and BC risk. This study aimed to assess whether adiponectin serum levels or SNPs in ADIPOQ may modify BC risk. In this case-control study, 114 BC patients were recruited along with 114 controls. Study subjects were genotyped for variations in ADIPOQ SNPs, namely rs17300539, rs266729, rs2241766, and rs1501299. Adiponectin levels were measured from the serum of study subjects. Our analysis showed that the G allele and the GG genotype of rs1501299 were significantly more frequent in BC patients compared to those in the control group (p-value < 0.05). Moreover, two ADIPOQ haplotypes containing the above G allele were associated with increased BC risk (p-value < 0.05). Multivariate analysis showed that increased serum adiponectin, smoking or age were all significant predictors of BC (p-value < 0.05). The data supports use of serum adiponectin and the G allele of rs1501299 SNP in ADIPOQ as potential biomarkers and/or targets in BC. To further validate findings in this study, larger populations of various ethnicities and/or genetic backgrounds are required. More investigations on the functional role of adiponectin in BC will also provide better understanding of potential targeting adiponectin for BC treatment.

Indexed as

AdiponectinUrinary Bladder NeoplasmsCase-Control StudiesGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideAdiponectinADIPOQ protein, humanAdiponectinADIPOQBladder cancerrs1501299Single nucleotide

Identifiers

PMID36218131
OpenAlexW4289550207

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.