Evidence map›Paper›PMID 32399675›Full record

ArticleJournal of bone and mineral metabolism2020

Association between LGR4 polymorphisms and peak bone mineral density and body composition.

Wei-Jia Yu, Zeng Zhang, Wen-Zhen Fu, Jin-Wei He, Chun Wang, Zhen-Lin Zhang

Abstract read
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In one paragraph

Article in Journal of bone and mineral metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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  5. Obesity and lipid metabolism in the development of osteoporosis (Review).International journal of molecular medicine · 2024
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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

6 authors at 1 institution in 1 country.

Wei-Jia YuMetabolic Bone Disease and Genetic Research Unit, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated the Sixth People's Hospital, 600 Yi-Shan Rd, Shanghai, 200233, People's Republic of China.
Zeng ZhangDepartment of Orthopedic Surgery, Shanghai Jiao Tong University Affiliated the Sixth People's Hospital, Shanghai, China.
Wen-Zhen FuMetabolic Bone Disease and Genetic Research Unit, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated the Sixth People's Hospital, 600 Yi-Shan Rd, Shanghai, 200233, People's Republic of China.
Jin-Wei HeMetabolic Bone Disease and Genetic Research Unit, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated the Sixth People's Hospital, 600 Yi-Shan Rd, Shanghai, 200233, People's Republic of China.
Chun WangMetabolic Bone Disease and Genetic Research Unit, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated the Sixth People's Hospital, 600 Yi-Shan Rd, Shanghai, 200233, People's Republic of China. chunwang66@hotmail.com.
Zhen-Lin ZhangMetabolic Bone Disease and Genetic Research Unit, Department of Osteoporosis and Bone Diseases, Shanghai Jiao Tong University Affiliated the Sixth People's Hospital, 600 Yi-Shan Rd, Shanghai, 200233, People's Republic of China. zhangzl@sjtu.edu.cn.ORCID http://orcid.org/0000-0002-7093-4584
Shanghai Jiao Tong University · CN

Funding

National Natural Science Foundation of China 81770872the Drug Innovation Program of the National Science and Technology Project 2011ZX09307-001-02the National Program for Support of Top-notch Young Professionals, the Shanghai Health 2013ZYJB1001the Shanghai Hospital Development Center SHDC12013115the Shanghai Jiao Tong Medical/Engineering Foundation YG2014MS18the Shanghai Municipal Education Commission-Gaofeng Clinical Medicine Grant Support 20152527
6 · The paper itself

Abstract

introductionLeucine-rich repeat-containing G protein-coupled receptor 4 (LGR4) could affect differentiation of osteoblasts and bone mass through potentiating Wnt/β-catenin signaling. LGR4 is also relevant to glycolipid metabolism. The present study aims to explore the relationship between genetic variations in LGR4 gene and peak bone mineral density (peak BMD) and body composition phenotypes in Chinese nuclear families. MATERIALS AND

methods22 single-nucleotide polymorphisms (SNPs) were selected and five blocks were constructed in LGR4. Body composition (lean mass and fat mass) and peak BMD were measured by dual-energy X-ray absorptiometry (DXA). Quantitative transmission disequilibrium test (QTDT) analysis was used to explore the relationship between LGR4 genotypes and the mentioned phenotypes.

resultsFor QTDT analysis after 1000 permutations, significant within-family associations were observed between rs11029986 and total fat mass (TFM) and percentage of TFM (PFM) (P = 0.014 and 0.011, respectively), rs12787344, rs4128868, rs4923445, and rs7936621 and body mass index (BMI) (P = 0.008, 0.003, 0.046, and 0.003, respectively), rs11029986 and total hip BMD (P = 0.026), and rs12796247, rs2219783, and lumbar spine BMD (P = 0.013 and 0.027, respectively). Haplotypes GCGT and AAGC (both in block 3) were observed in significant within-family association with BMI (P = 0.003 and 0.002, respectively).

conclusionIt is the first family-based association analysis to explore and demonstrate significant associations between LGR4 genotypes and variations of peak BMD and body composition in young Chinese men. The results are consistent with the findings that recent studies revealed, and confirm the critical relationship between LGR4 gene and both BMD and body composition.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAbsorptiometry, PhotonAdiposityAsian PeopleBody CompositionBone DensityFemaleHaplotypesHumansLinkage DisequilibriumMaleMiddle AgedPolymorphism, Single NucleotideReceptors, G-Protein-CoupledLGR4 protein, humanReceptors, G-Protein-CoupledFat massLean massLGR4Peak bone mineral densityQuantitative transmission disequilibrium test

Identifiers

PMID32399675
OpenAlexW3024161286

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.