Evidence map›Paper›PMID 23349225›Full record

SynthesisJournal of medical genetics2013

Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture.

Joo-Yeon Hwang, Seung Hun Lee, Min Jin Go, Beom-Jun Kim, Ikuyo Kou, Shiro Ikegawa, Yan Guo, Hong-Wen Deng, Soumya Raychaudhuri, Young Jin Kim and 22 more

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in Journal of medical genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Global impact of micronutrients in modern human evolution.American journal of human genetics · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Using GWAS to identify novel therapeutic targets for osteoporosis.Translational research : the journal of laboratory and clinical medicine · 2017
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
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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

32 authors at 11 institutions in 5 countries.

Joo-Yeon HwangCenter for Genome Science, National Institute of Health, Chungcheongbuk-do, Republic of Korea.
Seung Hun Lee
Min Jin Go
Beom-Jun Kim
Ikuyo Kou
Shiro Ikegawa
Yan Guo
Hong-Wen Deng
Soumya Raychaudhuri
Young Jin Kim
Ji Hee Oh
Youngdoe Kim
Sanghoon Moon
Dong-Joon Kim
Heejo Koo
My-Jung Cha
Min Hye Lee
Ji Young Yun
Hye-Sook Yoo
Young-Ah Kang
Eun-Hee Cho
Sang-Wook Kim
Ki Won Oh
Moo Il Kang
Ho Young Son
Shin-Yoon Kim
Ghi Su Kim
Bok-Ghee Han
Yoon Shin Cho
Myeong-Chan Cho
Jong-Young Lee
Jung-Min Koh
Korea National Institute of Health · KRKangwon National University · KRCatholic University of Korea · KRKyungpook National University Hospital · KRXi'an Jiaotong University · CNAsan Medical Center · KRHallym University · KRHarvard University · USNational Institutes of Health · USSungkyunkwan University · KRUniversity of Ulsan · KR

Funding

ROBUST AND POWERFUL TEST OF CANDIDATE GENES TO BONE MASSR01AR050496 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2004 to 2013
$3.8M
Identification of Proteins Important for Male OsteoporosisR01AR057049 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2009 to 2013
$2.4M
NIAMS NIH HHS R01 AR050496NIAMS NIH HHS R01 AR057049
6 · The paper itself

Abstract

backgroundOsteoporotic fracture (OF) as a clinical endpoint is a major complication of osteoporosis. To screen for OF susceptibility genes, we performed a genome-wide association study and carried out de novo replication analysis of an East Asian population.

methodsAssociation was tested using a logistic regression analysis. A meta-analysis was performed on the combined results using effect size and standard errors estimated for each study.

resultsIn a combined meta-analysis of a discovery cohort (288 cases and 1139 controls), three hospital based sets in replication stage I (462 cases and 1745 controls), and an independent ethnic group in replication stage II (369 cases and 560 for controls), we identified a new locus associated with OF (rs784288 in the MECOM gene) that showed genome-wide significance (p=3.59×10(-8); OR 1.39). RNA interference revealed that a MECOM knockdown suppresses osteoclastogenesis.

conclusionsOur findings provide new insights into the genetic architecture underlying OF in East Asians.

Indexed as

AgedCase-Control StudiesDNA-Binding ProteinsGene Expression RegulationGene Knockdown TechniquesGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansMDS1 and EVI1 Complex Locus ProteinMiddle AgedOsteogenesisOsteoporosisOsteoporotic FracturesPolymorphism, Single NucleotideProto-OncogenesDNA-Binding ProteinsMDS1 and EVI1 Complex Locus ProteinMECOM protein, humanTranscription Factors

Identifiers

PMID23349225
PMCPMC4169276
OpenAlexW2103758702

What OpenQuestion holds

Textmetadata
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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.