Evidence map›Paper›PMID 29888052›Full record

ArticleAMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science2018

A Network-Biology Informed Computational Drug Repositioning Strategy to Target Disease Risk Trajectories and Comorbidities of Peripheral Artery Disease.

Khader Shameer, Garrett Dow, Benjamin S Glicksberg, Kipp W Johnson, Yi Ze, Max S Tomlinson, Ben Readhead, Joel T Dudley, Iftikhar J Kullo

Open access · greenAbstract read
In one paragraph

Article in AMIA Joint Summits on Translational Science proceedings. AMIA Joint Summits on Translational Science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
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  4. 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

9 authors at 2 institutions in 1 country.

Khader ShameerDepartment of Genetics and Genomics, Icahn Institute of Genomics and Multiscale Biology, Institute of Next Generation Healthcare, Icahn School of Medicine at Mount Sinai, Mount Sinai Health System, New York, NY.
Garrett DowDepartment of Medicinal Chemistry, University of Michigan, Ann Arbor, MI.
Benjamin S GlicksbergDepartment of Genetics and Genomics, Icahn Institute of Genomics and Multiscale Biology, Institute of Next Generation Healthcare, Icahn School of Medicine at Mount Sinai, Mount Sinai Health System, New York, NY.
Kipp W JohnsonDepartment of Genetics and Genomics, Icahn Institute of Genomics and Multiscale Biology, Institute of Next Generation Healthcare, Icahn School of Medicine at Mount Sinai, Mount Sinai Health System, New York, NY.
Yi ZeDepartment of Cardiovascular Diseases, Mayo Clinic, Rochester, MN.
Max S TomlinsonDepartment of Genetics and Genomics, Icahn Institute of Genomics and Multiscale Biology, Institute of Next Generation Healthcare, Icahn School of Medicine at Mount Sinai, Mount Sinai Health System, New York, NY.
Ben ReadheadDepartment of Genetics and Genomics, Icahn Institute of Genomics and Multiscale Biology, Institute of Next Generation Healthcare, Icahn School of Medicine at Mount Sinai, Mount Sinai Health System, New York, NY.
Joel T DudleyDepartment of Genetics and Genomics, Icahn Institute of Genomics and Multiscale Biology, Institute of Next Generation Healthcare, Icahn School of Medicine at Mount Sinai, Mount Sinai Health System, New York, NY.
Iftikhar J KulloPopulation Health Science and Policy, Mount Sinai Health System, New York, NY.
Mayo Clinic in Arizona · USUniversity of Michigan–Ann Arbor · US

Funding

MSHS Translational Science HubUL1TR001433 · NCATS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI WRIGHT, ROSALIND J · 2015 to 2019
$26.6M
NCATS NIH HHS UL1 TR001433
6 · The paper itself

Abstract

Currently, drug discovery approaches focus on the design of therapies that alleviate an index symptom by reengineering the underlying biological mechanism in agonistic or antagonistic fashion. For example, medicines are routinely developed to target an essential gene that drives the disease mechanism. Therapeutic overloading where patients get multiple medications to reduce the primary and secondary side effect burden is standard practice. This single-symptom based approach may not be scalable, as we understand that diseases are more connected than random and molecular interactions drive disease comorbidities. In this work, we present a proof-of-concept drug discovery strategy by combining network biology, disease comorbidity estimates, and computational drug repositioning, by targeting the risk factors and comorbidities of peripheral artery disease, a vascular disease associated with high morbidity and mortality. Individualized risk estimation and recommending disease sequelae based therapies may help to lower the mortality and morbidity of peripheral artery disease.

Identifiers

PMID29888052
PMCPMC5961807
OpenAlexW2982584582

What OpenQuestion holds

Textmetadata
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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.