Evidence map›Paper›PMID 31832174›Full record

ArticleBone & joint research2019

Evaluation of common variants in the

W Zheng, C Liu, M Lei, Y Han, X Zhou, C Li, S Sun, X Ma

Open access · goldAbstract read
In one paragraph

Article in Bone & joint research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Gut microbiome and osteoporosis: a review.Bone & joint research · 2020
    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 2 institutions in 1 country.

W ZhengDepartment of Orthopaedics, Affiliated Hospital of Hebei University, Baoding, China.
C LiuDepartment of Pharmacology, Department of Medicine, Hebei University, Baoding, China.
M LeiDepartment of Orthopaedics, Affiliated Hospital of Hebei University, Baoding, China.
Y HanDepartment of Orthopaedics, Affiliated Hospital of Hebei University, Baoding, China.
X ZhouDepartment of Orthopaedics, Affiliated Hospital of Hebei University, Baoding, China.
C LiDepartment of Orthopaedics, Affiliated Hospital of Hebei University, Baoding, China.
S SunDepartment of Orthopaedics, Affiliated Hospital of Hebei University, Baoding, China.
X MaDepartment of Orthopaedics, Affiliated Hospital of Hebei University, Baoding, China.
Affiliated Hospital of Hebei University · CNHebei University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objective of this study was to investigate the association of four single-nucleotide polymorphisms (SNPs) of the cannabinoid receptor 2 (

methodsChinese patients with OP were recruited between March 2011 and December 2015 from our hospital. In this study, a total of 1267 post-menopausal female patients (631 OP patients and 636 control patients) were selected. The mean age of all subjects was 69.2 years (sd 15.8). A generalized multifactor dimensionality reduction (GMDR) model and logistic regression model were used to examine the interaction between SNP and obesity on OP. For OP patient-control haplotype analyses, the SHEsis online haplotype analysis software (http://analysis.bio-x.cn/) was employed.

resultsThe logistic regression model revealed that the C allele of rs2501431 and the G allele of rs3003336 were associated with increased OP risk, compared with those with wild genotype. However, no significant correlations were found when analyzing the association of rs4237 and rs2229579 with OP risk. The GMDR analysis suggested that the interaction model composed of two factors, rs3003336 and abdominal obesity (AO), was the best model with statistical significance (p-value from sign test (P

conclusionOur results suggested that the C allele of rs2501431 and the G allele of rs3003336 of the

Indexed as

CNR2HaplotypeInteractionObesityOsteoporosisPolymorphism

Identifiers

PMID31832174
PMCPMC6888734
OpenAlexW2983088160

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.