Evidence map›Paper›PMID 25313004›Full record

ReviewCurrent vascular pharmacology2015

Phenomics of Vascular Disease: The Systematic Approach to the Combination Therapy.

Yeshan Han, Li Li, Yaping Zhang, Hong Yuan, Linda Ye, Jianzhong Zhao, Dayue Darrel Duan

Open access · greenAbstract readReview
In one paragraph

Review in Current vascular pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Phenomic Studies on Diseases: Potential and Challenges.Phenomics (Cham, Switzerland) · 2023
    Review
  5. Article
  6. Article
  7. Markers of Endothelial Cells in Normal and Pathological Conditions.Biochemistry (Moscow) Supplement. Series A, Membrane and cell biology · 2020
    Article
  8. Article
  9. Review
  10. Novel Biomarkers and Treatments of Cardiac Diseases.BioMed research international · 2016
    Article
  11. 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

7 authors at 1 institution in 1 country.

Yeshan Han
Li Li
Yaping Zhang
Hong Yuan
Linda Ye
Jianzhong Zhao
Dayue Darrel DuanLaboratory of Cardiovascular Phenomics, Department of Pharmacology, University of Nevada School of Medicine, Center for Molecular Medicine 303F, 1664 N Virginia Street/MS 318, Reno, Nevada 89557-0318, USA. dduan@medicine.nevada.edu.
University of Nevada, Reno · US

Funding

The CLC-3 chloride channels in the heartR01HL113598 · NHLBI · UNIVERSITY OF NEVADA RENO · PI DUAN, DAYUE DARREL · 2013 to 2016
$1.4M
Physiological role of CIC-2 CI channels in heartR01HL063914 · NHLBI · UNIVERSITY OF NEVADA RENO · PI DUAN, DAYUE DARREL · 2002 to 2005
$1.0M
Novel function and mechanism of CFTR in heart failureR21HL106256 · NHLBI · UNIVERSITY OF NEVADA RENO · PI DUAN, DAYUE DARREL · 2011 to 2012
$386k
CSRD VA I01 CX002011NHLBI NIH HHS HL106252NHLBI NIH HHS HL113598NHLBI NIH HHS HL63914NHLBI NIH HHS R01 HL063914NHLBI NIH HHS R01 HL113598NHLBI NIH HHS R21 HL106256
6 · The paper itself

Abstract

Vascular diseases are usually caused by multifactorial pathogeneses involving genetic and environmental factors. Our current understanding of vascular disease is, however, based on the focused genotype/phenotype studies driven by the "one-gene/one-phenotype" hypothesis. Drugs with "pure target" at individual molecules involved in the pathophysiological pathways are the mainstream of current clinical treatments and the basis of combination therapy of vascular diseases. Recently, the combination of genomics, proteomics, and metabolomics has unraveled the etiology and pathophysiology of vascular disease in a big-data fashion and also revealed unmatched relationships between the omic variability and the much narrower definition of various clinical phenotypes of vascular disease in individual patients. Here, we introduce the phenomics strategy that will change the conventional focused phenotype/genotype/genome study to a new systematic phenome/genome/proteome approach to the understanding of pathophysiology and combination therapy of vascular disease. A phenome is the sum total of an organism's phenotypic traits that signify the expression of genome and specific environmental influence. Phenomics is the study of phenome to quantitatively correlate complex traits to variability not only in genome, but also in transcriptome, proteome, metabolome, interactome, and environmental factors by exploring the systems biology that links the genomic and phenomic spaces. The application of phenomics and the phenome-wide associated study (PheWAS) will not only identify a systemically-integrated set of biomarkers for diagnosis and prognosis of vascular disease but also provide novel treatment targets for combination therapy and thus make a revolutionary paradigm shift in the clinical treatment of these devastating diseases.

Indexed as

Medicine, Chinese TraditionalDrug Therapy, CombinationGene-Environment InteractionGenome-Wide Association StudyGenomicsGenotypeHumansMetabolomicsMolecular Targeted TherapyPhenotypePrecision MedicineProteomicsVascular Diseases

Identifiers

PMID25313004
PMCPMC4397150
OpenAlexW2117726260

What OpenQuestion holds

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LicenceCC BY-NC
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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.