Evidence map›Paper›PMID 24211787›Full record

ArticleEuropean journal of pharmacology2014

Mechanism-driven phase I translational study of trifluoperazine in adults with sickle cell disease.

Robert E Molokie, Diana J Wilkie, Harriett Wittert, Marie L Suarez, Yingwei Yao, Zhongsheng Zhao, Ying He, Zaijie J Wang

Abstract readClinical Trial, Phase I
In one paragraph

Article in European journal of pharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Precision, integrative medicine for pain management in sickle cell disease.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Review
  5. Review
  6. Pain in sickle cell disease: current and potential translational therapies.Translational research : the journal of laboratory and clinical medicine · 2021
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. The AVPR1A Gene and Its Single Nucleotide Polymorphism rs10877969: A Literature Review of Associations with Health Conditions and Pain.Pain management nursing : official journal of the American Society of Pain Management Nurses · 2018
    Review
  12. Targeting pain at its source in sickle cell disease.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Review
  13. CaMKIIα Mediates the Effect of IL-17 To Promote Ongoing Spontaneous and Evoked Pain in Multiple Sclerosis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  14. Targeting novel mechanisms of pain in sickle cell disease.Hematology. American Society of Hematology. Education Program · 2017
    Review
  15. Pain-measurement tools in sickle cell disease: where are we now?Hematology. American Society of Hematology. Education Program · 2017
    Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Updated Mechanisms of Sickle Cell Disease-Associated Chronic pain.Translational perioperative and pain medicine · 2015
    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

8 authors at 2 institutions in 1 country.

Robert E MolokieUniversity of Illinois at Chicago, College of Medicine, Division of Hematology/Oncology, Chicago, IL, USA; Jesse Brown Veteran's Administration Medical Center, Chicago, IL, USA; University of Illinois at Chicago College of Pharmacy Department of Biopharmaceutical Sciences, Chicago, IL, USA; Comprehensive Sickle Cell Center, University of Illinois Hospital and Health Sciences System, Chicago, IL, USA. Electronic address: remoloki@uic.edu.
Diana J WilkieUniversity of Illinois at Chicago College of Nursing Department of Biobehavioral Health Science, Chicago, IL, USA; Comprehensive Sickle Cell Center, University of Illinois Hospital and Health Sciences System, Chicago, IL, USA.
Harriett WittertUniversity of Illinois at Chicago College of Nursing Department of Biobehavioral Health Science, Chicago, IL, USA.
Marie L SuarezUniversity of Illinois at Chicago College of Nursing Department of Biobehavioral Health Science, Chicago, IL, USA.
Yingwei YaoUniversity of Illinois at Chicago College of Nursing Department of Biobehavioral Health Science, Chicago, IL, USA.
Zhongsheng ZhaoUniversity of Illinois at Chicago College of Nursing Department of Biobehavioral Health Science, Chicago, IL, USA.
Ying HeUniversity of Illinois at Chicago College of Pharmacy Department of Biopharmaceutical Sciences, Chicago, IL, USA.
Zaijie J WangUniversity of Illinois at Chicago College of Pharmacy Department of Biopharmaceutical Sciences, Chicago, IL, USA; Comprehensive Sickle Cell Center, University of Illinois Hospital and Health Sciences System, Chicago, IL, USA.
University of Illinois Chicago · USUniversity of Illinois Hospital & Health Sciences System · US

Funding

Protein kinase mechanisms for chronic pain in sickle cell diseaseR01HL098141 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WANG, ZAIJIE JIM · 2009 to 2017
$2.6M
NHLBI NIH HHS 1R01 HL098141NHLBI NIH HHS R01 HL098141
6 · The paper itself

Abstract

Recent evidence of neuropathic pain among adults with sickle cell disease (SCD) reveals a need for adjuvant analgesic treatments for these patients. Ca(2+)/calmodulin protein kinase IIα (CaMKIIα) has a known role in neuropathic pain and trifluoperazine is a potent CaMKIIα inhibitor. The study aim was to determine trifluoperazine's acute effects, primarily on adverse effects and secondarily on pain intensity reduction, in adults with SCD. In a phase I, open-label study of 6 doses of trifluoperazine (0.5, 1, 2, 5, 7.5, 10mg), we obtained 7-hourly and 24-h repeated measures of adverse effects, pain intensity, and supplemental opioid analgesics in 18 adults with SCD (18 hemoglobin SS disease, 15 women, average age 35.8±8.9 years, ranged 23-53) each of whom received a single dose. Data were analyzed with descriptive statistics. Subjects reported moderate to severe sedative effects at 7.5 and 10mg doses, respectively. Eight subjects reported 50% reduction in chronic pain without severe sedation or supplemental opioid analgesics; one of these subjects had dystonia 24.5h after the 10mg dose. The analgesic effect lasted for at least 24h in 3 subjects. Sedation resolved with caffeine and dystonia resolved with diphenhydramine. Adults with SCD experienced minimal adverse effects at doses under 10mg. In this molecular mechanism-driven translational study, trifluoperazine shows promise as an analgesic drug that is worthy of further testing in a randomized controlled study of adults with SCD starting at a dose of 1mg in repeated doses to determine long-term adverse and analgesic effects.

Indexed as

AdultAnalgesicsAnemia, Sickle CellCalcium-Calmodulin-Dependent Protein Kinase Type 2FemaleHumansMaleMiddle AgedNeuralgiaTrifluoperazineYoung AdultAnalgesicsCalcium-Calmodulin-Dependent Protein Kinase Type 2TrifluoperazineNeuropathic painPhase 1 studySafetySickle cell diseaseTrifluoperazine

Identifiers

PMID24211787
PMCPMC3959657
OpenAlexW2020958756

What OpenQuestion holds

Textmetadata
LicenceTDM
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.