Evidence map›Paper›PMID 26564225›Full record

ArticleOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2016

Association of osteoporosis with genetic variants of circadian genes in Chinese geriatrics.

Y Li, J Zhou, Y Wu, T Lu, M Yuan, Y Cui, Y Zhou, G Yang, Y Hong

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Article in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.3field-weighted citation impact, top 45% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Novel SNP Combination for Predictive Osteoporotic Diagnosis.International journal of molecular sciences · 2025
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  5. Genetics and pathogenesis of scoliosis.North American Spine Society journal · 2024
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Y LiCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China.
J ZhouCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China.
Y WuCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China.
T LuCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China.
M YuanCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China.
Y CuiCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China.
Y ZhouCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China.
G YangCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China. yanggong@fudan.edu.cn.
Y HongCentral laboratory, The Fifth People's Hospital of Shanghai, Fudan University, Shanghai, 200240, China. hongyangcm@163.com.
Fudan University · CNFudan University Shanghai Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledThis study was designed to investigate the association of circadian gene single nucleotide polymorphisms (SNPs) with the risk of osteoporosis. We found that the rs3781638 GG genotype was positively associated with osteoporosis prevalence in females, whereas the rs2292910 AC genotype was negatively associated with osteoporosis prevalence in a geriatric cohort.

introductionStudies have shown that disruption of endogenous circadian rhythms may increase the risk of developing type II diabetes and obesity, which are reportedly associated with osteoporosis (OP). Thus, abnormalities of circadian genes may indirectly induce OP. Here, we investigated the association of OP with 14 SNPs located in seven circadian genes.

methodsThe research subjects, geriatric residents of Shanghai Minhang, China, diagnosed with OP (N = 171) or osteopenia (N = 226) or without specific diseases (N = 200), were genotyped for 14 genetic variants of circadian genes by competitive allele-specific polymerase chain reaction. The prevalence of polymorphisms among the subject groups and the association between the SNPs and osteoporosis were investigated.

resultsAmong the 14 genotyped SNPs, we found an association between the CRY2 gene rs2292910 SNP and osteoporosis (r = -0.082, p = 0.045) in the geriatric cohort. We found a decreased risk between cryptochrome 2 rs2292910 and OP (A/C odds ratio = 0.647, p = 0.044) but an increased risk between MTNR1B rs3781638 and OP (G/G odds ratio = 2.058, p = 0.044).

conclusionFor the first time, we show that Cry 2 rs2292910 and MTNR1B rs3781638 are associated with osteoporosis in a Chinese geriatric cohort. Therefore, targeting the abnormalities of the CRY2 and MTNR1B genes may be a potential strategy to treat and/or to prevent osteoporosis.

Indexed as

Polymorphism, Single NucleotideAbsorptiometry, PhotonAgedAsian PeopleBody Mass IndexBone DensityCircadian ClocksCircadian Rhythm Signaling Peptides and ProteinsCryptochromesFemaleGenetic Association StudiesGenetic Predisposition to DiseaseGenotypeHumansLinkage DisequilibriumMaleCircadian Rhythm Signaling Peptides and ProteinsCRY2 protein, humanCryptochromesMTNR1B protein, humanReceptor, Melatonin, MT2Cryptochrome 2GeriatricsMTNR1BOsteoporosisSNP

Identifiers

PMID26564225
OpenAlexW2141169336

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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.