Evidence map›Paper›PMID 26390436›Full record

ArticlePloS one2015

Integrative Analysis of Transcriptomic and Epigenomic Data to Reveal Regulation Patterns for BMD Variation.

Ji-Gang Zhang, Li-Jun Tan, Chao Xu, Hao He, Qing Tian, Yu Zhou, Chuan Qiu, Xiang-Ding Chen, Hong-Wen Deng

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
1.5field-weighted citation impact, top 17% 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, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. High Bone Mass Disorders: New Insights From Connecting the Clinic and the Bench.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Review
  7. Review
  8. Epigenetic regulation of bone mass.Best practice & research. Clinical endocrinology & metabolism · 2022
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Perinatal DNA Methylation at CDKN2A Is Associated With Offspring Bone Mass: Findings From the Southampton Women's Survey.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017
    Article
  14. Cytosolic proteome profiling of monocytes for male osteoporosis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2017
    Article
  15. Review
  16. Epigenetic Regulation of Bone Remodeling and Its Impacts in Osteoporosis.International journal of molecular sciences · 2016
    Review
  17. Review
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

9 authors at 2 institutions in 2 countries.

Ji-Gang ZhangCenter of Genomics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America; Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America.
Li-Jun TanLaboratory of Molecular and Statistical Genetics, Hunan Normal University, Changsha, Hunan, 410081, China.
Chao XuCenter of Genomics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America; Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America.
Hao HeCenter of Genomics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America; Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America.
Qing TianCenter of Genomics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America; Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America.
Yu ZhouCenter of Genomics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America; Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America.
Chuan QiuCenter of Genomics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America; Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America.
Xiang-Ding ChenLaboratory of Molecular and Statistical Genetics, Hunan Normal University, Changsha, Hunan, 410081, China.
Hong-Wen DengCenter of Genomics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America; Department of Biostatistics and Bioinformatics, Tulane University, New Orleans, Louisiana, 70112, United States of America; Laboratory of Molecular and Statistical Genetics, Hunan Normal University, Changsha, Hunan, 410081, China.
Tulane University · USHunan Normal University · CN

Funding

Proteome-wide Expression Study of Osteogenic CellsP50AR055081 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2007 to 2012
$5.0M
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
Epigenomewide DNA Methylation Study for Osteoporosis RiskR01AR059781 · NIAMS · TULANE UNIVERSITY OF LOUISIANA · PI DENG, HONG-WEN · 2012 to 2016
$3.1M
Identification of Proteins Important for Male OsteoporosisR01AR057049 · NIAMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2009 to 2013
$2.4M
Genomic search for bone mass QTLsR01AG026564 · NIA · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2007 to 2010
$2.3M
Genome-wide association study of periodontitisRC2DE020756 · NIDCR · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN, GENCO, ROBERT J · 2009 to 2009
$173k
Genetics of Osteoporotic Fractures in ChineseR03TW008221 · FIC · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2009 to 2011
$171k
FIC NIH HHS R03 TW008221FIC NIH HHS R03TW008221NIAMS NIH HHS P50 AR055081NIAMS NIH HHS P50AR055081NIAMS NIH HHS R01 AR050496NIAMS NIH HHS R01AR050496NIAMS NIH HHS R01 AR057049NIAMS NIH HHS R01AR057049NIAMS NIH HHS R01 AR059781NIA NIH HHS R01 AG026564NIA NIH HHS R01AG026564NIDCR NIH HHS RC2 DE020756NIDCR NIH HHS RC2DE020756
6 · The paper itself

Abstract

Integration of multiple profiling data and construction of functional gene networks may provide additional insights into the molecular mechanisms of complex diseases. Osteoporosis is a worldwide public health problem, but the complex gene-gene interactions, post-transcriptional modifications and regulation of functional networks are still unclear. To gain a comprehensive understanding of osteoporosis etiology, transcriptome gene expression microarray, epigenomic miRNA microarray and methylome sequencing were performed simultaneously in 5 high hip BMD (Bone Mineral Density) subjects and 5 low hip BMD subjects. SPIA (Signaling Pathway Impact Analysis) and PCST (Prize Collecting Steiner Tree) algorithm were used to perform pathway-enrichment analysis and construct the interaction networks. Through integrating the transcriptomic and epigenomic data, firstly we identified 3 genes (FAM50A, ZNF473 and TMEM55B) and one miRNA (hsa-mir-4291) which showed the consistent association evidence from both gene expression and methylation data; secondly in network analysis we identified an interaction network module with 12 genes and 11 miRNAs including AKT1, STAT3, STAT5A, FLT3, hsa-mir-141 and hsa-mir-34a which have been associated with BMD in previous studies. This module revealed the crosstalk among miRNAs, mRNAs and DNA methylation and showed four potential regulatory patterns of gene expression to influence the BMD status. In conclusion, the integration of multiple layers of omics can yield in-depth results than analysis of individual omics data respectively. Integrative analysis from transcriptomics and epigenomic data improves our ability to identify causal genetic factors, and more importantly uncover functional regulation pattern of multi-omics for osteoporosis etiology.

Indexed as

AdultBone DensityComputational BiologyEpigenomicsFemaleGene Expression ProfilingGene Regulatory NetworksGenetic VariationHumansMicroRNAsOsteoporosisRNA, MessengerSignal TransductionTranscriptomeYoung AdultMicroRNAsRNA, Messenger

Identifiers

PMID26390436
PMCPMC4577125
OpenAlexW2189136748

What OpenQuestion holds

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LicenceCC BY
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.