Evidence map›Paper›PMID 26764266›Full record

ArticleExperimental biology and medicine (Maywood, N.J.)2017

BDKRB2 +9/-9 bp polymorphisms influence BDKRB2 expression levels and NO production in knee osteoarthritis.

Shuo Chen, Lei Zhang, Ruonan Xu, Yunfan Ti, Yunlong Zhao, Liwu Zhou, Jianning Zhao

Open access · greenAbstract read
In one paragraph

Article in Experimental biology and medicine (Maywood, N.J.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 24% 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, 30 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Shuo Chen1 Department of Orthopedics, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Lei Zhang1 Department of Orthopedics, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Ruonan Xu2 Offices of Health Care, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Yunfan Ti1 Department of Orthopedics, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Yunlong Zhao3 Department of Orthopedics, School of Clinical Medicine, Nanjing University, Nanjing 210000, China The first two authors contributed equally to this work.
Liwu Zhou1 Department of Orthopedics, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Jianning Zhao1 Department of Orthopedics, Jinling Hospital, Nanjing University School of Medicine, Nanjing 210002, China.
Nanjing University · CNNanjing General Hospital of Nanjing Military Command · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bradykinin B2 receptor (BDKRB2) plays a key role in the inflammation process of osteoarthritis. Nitric oxide has also long been considered to be a catabolic factor that contributes to inflammatory response and the osteoarthritis disease pathology. Several studies have reported that the BDKRB2 +9/-9 bp polymorphisms are associated with transcription of the receptor. However, the roles of BDKRB2 polymorphisms in inflammation in osteoarthritis remain unclear. This study enrolled 156 subjects with primary knee osteoarthritis and 58 healthy volunteers. BDKRB2 polymorphisms were genotyped, and the mRNA and protein levels of BDKRB2 in synovial tissues from osteoarthritis patients were measured by quantitative real-time polymerase chain reaction and western blot analysis, respectively. Nitric oxide production in serum from patients with osteoarthritis was measured using a nitric oxide assay kit. We found that the mean BDKRB2 mRNA levels were significantly higher in Kallgren-Lawrence grade-4 osteoarthritis patients than patients with lower grade osteoarthritis. The +9/-9 bp polymorphisms significantly affected the BDKRB2 mRNA and protein expression levels in synovial tissues from osteoarthritis subjects. Osteoarthritis patients with +9/-9 and -9/-9 genotypes had higher BDKRB2 expression levels in synovial tissue and nitric oxide production in serum. Moreover, positive correlation was found between the BDKRB2 levels in synovial tissue and nitric oxide production. Compared with health controls, significant increases of nitric oxide production in osteoarthritis were detected which were associated with increasing severity of osteoarthritis. Multiple linear regression analysis (adjusted for gender and age) showed serum nitric oxide level was positively associated with BDKRB2 polymorphism and Kallgren-Lawrence grade and was inversely associated with obesity. Our findings showed that the BDKRB2 +9/-9 bp polymorphisms affected the gene expression and nitric oxide production, which were associated with radiographic severity of osteoarthritis, suggesting that the BDKRB2 +9/ -9 bp polymorphisms may act as a genetic modulator of osteoarthritis, and play an essential role in inflammatory process in osteoarthritis.

Indexed as

FemaleHumansInflammationMaleMiddle AgedNitric OxideOsteoarthritis, KneePolymorphism, GeneticReal-Time Polymerase Chain ReactionReceptor, Bradykinin B2RNA, MessengerSynovial MembraneNitric OxideReceptor, Bradykinin B2RNA, MessengerBradykinin B2 Receptor (BDKRB2)gene polymorphismsinflammationosteoarthritis (OA)

Identifiers

PMID26764266
PMCPMC5298537
OpenAlexW2303893945

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Registered trials

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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.