Evidence map›Paper›PMID 27022133›Full record

ReviewExperimental biology and medicine (Maywood, N.J.)2016

Minireview: Multiomic candidate biomarkers for clinical manifestations of sickle cell severity: Early steps to precision medicine.

Steven R Goodman, Betty S Pace, Kirk C Hansen, Angelo D'alessandro, Yang Xia, Ovidiu Daescu, Stephen J Glatt

Abstract readReview
In one paragraph

Review in Experimental biology and medicine (Maywood, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Sickle cell disease severity: an introduction.Experimental biology and medicine (Maywood, N.J.) · 2016
    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.

Steven R GoodmanDepartment of Pediatrics and Department of Physiology, The University of Tennessee Health Science Center, Memphis, TN 38163, USA sgoodma5@uthsc.edu.
Betty S PaceDepartment of Pediatrics, Augusta University, Augusta, GA 30912, USA.
Kirk C HansenBiochemistry and Molecular Genetics, University of Colorado Denver, Aurora, CO 80202, USA.
Angelo D'alessandroBiochemistry and Molecular Genetics, University of Colorado Denver, Aurora, CO 80202, USA.
Yang XiaBiochemistry and Molecular Biology Department, University of Texas at Houston, TX 77030, USA.
Ovidiu DaescuUniversity of Texas at Dallas, Richardson, TX 75080, USA.
Stephen J GlattDepartment of Psychiatry and Behavioral Sciences, SUNY Upstate Medical University, Syracuse, NY 13210, USA.

Funding

Trangenic Mouse Breeding CoreP01HL114457 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BLACKBURN, MICHAEL R · 2013 to 2017
$10.0M
Metabolites, Sickle Cell Disease, and Novel TherapeuticsR01HL113574 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIA, YANG · 2013 to 2016
$1.5M
NHLBI NIH HHS P01 HL114457NHLBI NIH HHS R01 HL113574
6 · The paper itself

Abstract

In this review, we provide a description of those candidate biomarkers which have been demonstrated by multiple-omics approaches to vary in correlation with specific clinical manifestations of sickle cell severity. We believe that future clinical analyses of severity phenotype will require a multiomic analysis, or an omics stack approach, which includes integrated interactomics. It will also require the analysis of big data sets. These candidate biomarkers, whether they are individual or panels of functionally linked markers, will require future validation in large prospective and retrospective clinical studies. Once validated, the hope is that informative biomarkers will be used for the identification of individuals most likely to experience severe complications, and thereby be applied for the design of patient-specific therapeutic approaches and response to treatment. This would be the beginning of precision medicine for sickle cell disease.

Indexed as

Anemia, Sickle CellBiomarkersFetal HemoglobinGene Expression ProfilingGenetic MarkersHumansMetabolomicsMicroRNAsPrecision MedicineProteomicsSeverity of Illness IndexBiomarkersFetal HemoglobinGenetic MarkersMicroRNAsGenomicsinteractomicsmetabolomicsprecision medicineproteomicssickle cell disease

Identifiers

PMID27022133
PMCPMC4950385

What OpenQuestion holds

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Registered trials

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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.