Evidence map›Paper›PMID 27628047›Full record

ArticleJournal of bone and mineral metabolism2017

Association between SNPs and haplotypes in the METTL21C gene and peak bone mineral density and body composition in Chinese male nuclear families.

Fei Zhao, Li-Hong Gao, Shan-Shan Li, Zhan-Ying Wei, Wen-Zhen Fu, Jin-Wei He, Yu-Juan Liu, Yun-Qiu Hu, Jing Dong, Zhen-Lin Zhang

Abstract read
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In one paragraph

Article in Journal of bone and mineral metabolism, 2017. 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
1.0field-weighted citation impact, top 21% 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, 9 citations in OpenAlex.

  1. Review
  2. Frontiers in endocrinology · 2021
    Article
  3. Article
  4. Genetics of Bone and Muscle Interactions in Humans.Current osteoporosis reports · 2019
    Review
  5. Article
  6. 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

10 authors at 2 institutions in 1 country.

Fei ZhaoDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China.
Li-Hong GaoDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China.
Shan-Shan LiDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China.
Zhan-Ying WeiDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China.
Wen-Zhen FuDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China.
Jin-Wei HeDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China.
Yu-Juan LiuDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China.
Yun-Qiu HuDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China.
Jing DongDepartment of Endocrinology, Shanxi Medical University Affiliated First Hospital, Taiyuan, 030001, China.
Zhen-Lin ZhangDivision of Osteoporosis and Bone Disease, Metabolic Bone Disease and Genetic Research Unit, Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Six People's Hospital, Shanghai, 200233, China. ZZL2002@medmail.com.cn.
Shanghai Jiao Tong University · CNFirst Hospital of Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The methyltransferase-like 21C gene (METTL21C), which is mainly expressed in muscle, can promote the differentiation of myoblasts to myotubes and reduce glucocorticoid-induced apoptosis of osteocytes. The purpose of this study was to explore the association between single nucleotide polymorphisms of METTL21C and peak bone mineral density (BMD), body mass index, total fat mass (TFM), and total lean mass (TLM) in Chinese young men. Fifteen tagging single nucleotide polymorphisms were genotyped, and haplotype blocks were derived in 400 Chinese male nuclear families. The peak BMD of the lumbar and hip, TFM, and TLM were measured by dual-energy X-ray absorptiometry. The association analyses were performed by a quantitative transmission disequilibrium test. Both TLM and TFM had a significant positive effect on peak BMD, but the positive regulation of TLM was stronger than that of TFM. After 1000 permutations, significant within-family associations were found between rs9585961 and lumbar spine BMD and femoral neck BMD, rs9518810 and femoral neck BMD, and rs599976 and body mass index, TFM, and percentage fat mass (all P < 0.05). The association analyses with haplotypes showed that haplotype AG in block 1 was significantly associated with TFM (P = 0.031) and haplotype CAG in block 2 was significantly associated with lumbar spine BMD (P = 0.020). Our study, for the first time, demonstrates that the polymorphisms and haplotypes of METTL21C contribute to the peak BMD and TFM in Chinese males, which suggests that as a quantitative trait locus with potential pleiotropy it may have an influence on osteoporosis and obesity.

Indexed as

Nuclear FamilyAbsorptiometry, PhotonAsian PeopleBody CompositionBone DensityFemaleGenetic Association StudiesGenotypeHaplotypesHumansLinkage DisequilibriumMaleMethyltransferasesMiddle AgedMultivariate AnalysisPolymorphism, Single NucleotideMethyltransferasesFat massMETTL21CPeak bone mineral densityQuantitative transmission disequilibrium testSingle nucleotide polymorphism

Identifiers

PMID27628047
OpenAlexW2518701735

What OpenQuestion holds

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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.