Evidence map›Paper›PMID 27757216›Full record

ArticleHematology reports2016

GBT440 Inhibits Sickling of Sickle Cell Trait Blood Under

Kobina Dufu, Josh Lehrer-Graiwer, Eleanor Ramos, Donna Oksenberg

Open access · goldAbstract read
In one paragraph

Article in Hematology reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.4field-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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Sickle Cell Anemia and Its Phenotypes.Annual review of genomics and human genetics · 2018
    Review
  8. Voxelotor (GBT440) produces interference in measurements of hemoglobin S.Clinica chimica acta; international journal of clinical chemistry · 2018
    Article
  9. Article
  10. 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

4 authors at 1 institution in 1 country.

Kobina DufuGlobal Blood Therapeutics Inc. , San Francisco, CA, USA.
Josh Lehrer-GraiwerGlobal Blood Therapeutics Inc. , San Francisco, CA, USA.
Eleanor RamosGlobal Blood Therapeutics Inc. , San Francisco, CA, USA.
Donna OksenbergGlobal Blood Therapeutics Inc. , San Francisco, CA, USA.
Global Blood Therapeutics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In sickle cell trait (SCT), hemoglobin A (HbA) and S (HbS) are co-expressed in each red blood cell (RBC). While homozygous expression of HbS (HbSS) leads to polymerization and sickling of RBCs resulting in sickle cell disease (SCD) characterized by hemolytic anemia, painful vaso-occlusive episodes and shortened life-span, SCT is considered a benign condition usually with minor or no complications related to sickling. However, physical activities that cause increased tissue oxygen demand, dehydration and/or metabolic acidosis leads to increased HbS polymerization and life-threatening complications including death. We report that GBT440, an agent being developed for the treatment of SCD, increases the affinity of oxygen for Hb and inhibits

Indexed as

exertional sicklinghemoglobin oxygen affinityrhabdomylosissickle cell diseaseSickle cell trait

Identifiers

PMID27757216
PMCPMC5062624
OpenAlexW2524416073

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.