Evidence map›Paper›PMID 30061840›Full record

ReviewFrontiers in physiology2018

Nanotherapeutics for Treatment of Pulmonary Arterial Hypertension.

Victor Segura-Ibarra, Suhong Wu, Nida Hassan, Jose A Moran-Guerrero, Mauro Ferrari, Ashrith Guha, Harry Karmouty-Quintana, Elvin Blanco

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  8. Lung transplantation for pulmonary hypertension.Journal of thoracic disease · 2021
    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

8 authors at 6 institutions in 2 countries.

Victor Segura-IbarraDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, United States.
Suhong WuDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, United States.
Nida HassanDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, United States.
Jose A Moran-GuerreroDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, United States.
Mauro FerrariDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, United States.
Ashrith GuhaDepartment of Cardiology, Houston Methodist DeBakey Heart and Vascular Center, Houston Methodist Hospital, Houston, TX, United States.
Harry Karmouty-QuintanaDepartment of Biochemistry and Molecular Biology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, United States.
Elvin BlancoDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX, United States.
Houston Methodist · USThe University of Texas Health Science Center at Houston · USCornell University · USMethodist Hospital · USMethodist Hospital · USTecnológico de Monterrey · MX

Funding

3'UTR Shortening In Pulmonary Vascular DiseaseR01HL138510 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KARMOUTY-QUINTANA, HARRY · 2017 to 2021
$2.3M
NHLBI NIH HHS R01 HL138510
6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is a devastating and fatal chronic lung disease. While current pharmacotherapies have improved patient quality of life, PAH drugs suffer from limitations in the form of short-term pharmacokinetics, instability, and poor organ specificity. Traditionally, nanotechnology-based delivery strategies have proven advantageous at increasing both circulation lifetimes of chemotherapeutics and accumulation in tumors due to enhanced permeability through fenestrated vasculature. Importantly, increased nanoparticle (NP) accumulation in diseased tissues has been observed pre-clinically in pathologies characterized by endothelial dysfunction and remodeled vasculature, including myocardial infarction and heart failure. Recently, this phenomenon has also been observed in preclinical models of PAH, leading to the exploration of NP-based drug delivery as a therapeutic modality in PAH. Herein, we discussed the advantages of NPs for efficacious treatment of PAH, including heightened therapeutic delivery to diseased lungs for increased drug bioavailability, as well as highlighted innovative nanotherapeutic approaches for PAH.

Indexed as

chronic lung diseasedrug deliverynanomedicinenanoparticlespulmonary arterial hypertension

Identifiers

PMID30061840
PMCPMC6055049
OpenAlexW2808807954

What OpenQuestion holds

Textmetadata
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.