Evidence map›Paper›PMID 32297643›Full record

Observational studyBioscience reports2020

Association of Gremlin-2 gene polymorphisms with osteoporosis risk in Chinese postmenopausal women.

Yu Feng, Lei Zhu, Yong Gu, Ling-Jun Wang, Bing-Jie Niu, Feng Cai, Liang Chen

Abstract readObservational Study
In one paragraph

Observational study in Bioscience reports, 2020. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Effect ofFrontiers in endocrinology · 2022
    Article
  4. Observational
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.

Yu FengDepartment of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Lei ZhuDepartment of Spine Surgery, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Yong GuDepartment of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Ling-Jun WangDepartment of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Bing-Jie NiuDepartment of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Feng CaiDepartment of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou, China.
Liang ChenDepartment of Orthopaedics, The First Affiliated Hospital of Soochow University, Suzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Gremlin-2 (GREM2) plays crucial roles in modulating bone homeostasis through the bone morphogenetic protein-2 pathway. However, GREM2 gene variants in osteoporosis were less frequent in a Chinese population. Therefore, the present study recruited 310 patients with osteoporosis and 339 healthy postmenopausal women to assess the correlation of GREM2 gene polymorphisms with the risk of osteoporosis. Polymerase chain reaction (PCR) and Sanger sequencing were utilized to genotype samples. The results showed that GREM2 gene rs4454537, not rs11588607, polymorphism was significantly associated with an increased risk of osteoporosis in postmenopausal women. Moreover, stratified analyses indicated a significant association between rs4454537 polymorphisms and body mass index of <25 kg/m2. Additionally, the association between GREM2 rs4454537 polymorphism and clinical characteristics was assessed, which showed that this locus decreased the bone mineral density (BMD) in postmenopausal osteoporotic individuals. Furthermore, individuals with CC genotype appeared to have a higher GREM2 expression compared with those bearing the TT genotype of rs4454537 polymorphism. However, the genotype distribution of rs4454537 polymorphism showed no statistical difference between osteoporotic patients as a function of fracture status. In summary, GREM2 rs4454537 polymorphism decreases BMD and increases osteoporotic risk in postmenopausal women.

Indexed as

Genetic Predisposition to DiseaseAbsorptiometry, PhotonAgedAllelesBone DensityCase-Control StudiesCytokinesFemaleHipHumansIncidenceLumbar VertebraeMiddle AgedOsteoporosis, PostmenopausalOsteoporotic FracturesPolymorphism, Single NucleotideCytokinesGREM2 protein, humanCase–control studyGREM2osteoporosispostmenopausal women

Identifiers

PMID32297643
PMCPMC7182657

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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.