Evidence map›Paper›PMID 30837870›Full record

ArticleFrontiers in pharmacology2019

Beta2-Adrenergic Receptor Polymorphisms and Haplotypes Associate With Chronic Pain in Sickle Cell Disease.

Ellie H Jhun, Nilanjana Sadhu, Xiaoyu Hu, Yingwei Yao, Ying He, Diana J Wilkie, Robert E Molokie, Zaijie Jim Wang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. PhenylethanolaminePharmacogenomics · 2020
    Article
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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 2 institutions in 1 country.

Ellie H JhunDepartment of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, United States.
Nilanjana SadhuDepartment of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, United States.
Xiaoyu HuDepartment of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, United States.
Yingwei YaoDepartment of Biobehavioral Health Science, College of Nursing, University of Illinois at Chicago, Chicago, IL, United States.
Ying HeDepartment of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, United States.
Diana J WilkieDepartment of Biobehavioral Health Science, College of Nursing, University of Illinois at Chicago, Chicago, IL, United States.
Robert E MolokieDepartment of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, United States.
Zaijie Jim WangDepartment of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL, United States.
University of Illinois Chicago · USUniversity of Florida · US

Funding

Molecular mechanism and targeting of chronic pain in sickle cell diseaseR35HL140031 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WANG, ZAIJIE JIM · 2018 to 2024
$4.6M
Multidisciplinary Oral Science TrainingT32DE018381 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI COOPER, LYNDON F · 2008 to 2019
$3.6M
HL-Phenotypic Characterization of Chronic Pain in Adults with Sickle Cell DiseaseR01HL124945 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MOLOKIE, ROBERT E, WANG, ZAIJIE JIM · 2014 to 2017
$3.2M
Computerized PAINRelievelt for Adult Sickle Cell DiseaseR01HL078536 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WILKIE, DIANA J · 2006 to 2009
$3.1M
NHLBI NIH HHS R01 HL078536NHLBI NIH HHS R01 HL124945NHLBI NIH HHS R35 HL140031NIDCR NIH HHS T32 DE018381
6 · The paper itself

Abstract

Pain in sickle cell disease (SCD) is severe, variable, and inadequately comprehended. The β2-adrenergic receptor (

Indexed as

beta2-adrenergic receptorchronic painhaplotypesickle cell diseasesingle nucleotide polymorphism

Identifiers

PMID30837870
PMCPMC6390066
OpenAlexW2914469072

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.