Evidence map›Paper›PMID 24505535›Full record

ReviewInternational journal of hematology-oncology and stem cell research2013

Evaluation of Novel Fetal Hemoglobin Inducer Drugs in Treatment of β-Hemoglobinopathy Disorders.

Ali Dehghani Fard, Seyed Ahmad Hosseini, Mohammad Shahjahani, Fatemeh Salari, Kaveh Jaseb

3 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in International journal of hematology-oncology and stem cell research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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.

NCT03651102 phase2 / phase3completednot on this mapstarted 2018, after this paper: background citation

Efficacy and Safety of Low Dose Thalidomide in Transfusion Dependent Thalassemia Patients of Pakistan

TypeinterventionalSponsorBlood Diseases ClinicRan2018 to 2022Enrolled654ConditionsThalassemiaArmsThalidomide and Hydroxyurea
NCT06098014 phase1completednot on this mapstarted 2023, after this paper: background citation

Safety & Efficacy of Thalidomide in Children With Transfusion Dependent Thalassemia: a Quasi Randomized Control Trial in a Tertiary Care Hospital in Bangladesh

TypeinterventionalSponsorBangabandhu Sheikh Mujib Medical University, Dhaka, BangladeshRan2023 to 2024Enrolled60ConditionsTransfusion-dependent ThalassemiaArmsThalidomide Capsules, Placebo
NCT06299670 phase4completednot on this mapstarted 2023, after this paper: background citation

Efficacy of Combination of Hdroxyurea and Thalidomide Over Either Hydroxyurea or Thalidomide Alone in the Treatment of Transfusion Dependent Thalassemia in Children: A Quasi-Randomised Clinical Trial

TypeinterventionalSponsorBangabandhu Sheikh Mujib Medical University, Dhaka, BangladeshRan2023 to 2026Enrolled90ConditionsTransfusion-dependent ThalassemiaArmsThalidomide, Hydroxy Urea, Combinations
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Safety and Efficacy of Thalidomide and Hydroxyurea Combination in Beta Thalassemia Patients.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Promising Response to Thalidomide in Symptomatic β-Thalassemia.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2020
    Article
  14. Potential role of LSD1 inhibitors in the treatment of sickle cell disease: a review of preclinical animal model data.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Review
  15. Inflammation in sickle cell disease.Clinical hemorheology and microcirculation · 2018
    Article
  16. Review
  17. Article
  18. Article
  19. Chromatin looping as a target for altering erythroid gene expression.Annals of the New York Academy of Sciences · 2016
    Review
  20. Review
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

5 authors at 2 institutions in 1 country.

Ali Dehghani FardSarem Cell Research Center-SCRC, Sarem Women's Hospital, Tehran, Iran.
Seyed Ahmad HosseiniDepartment of nutrition, Allied Health Sciences School, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Mohammad ShahjahaniDepartment of Hematology and Blood Banking, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Fatemeh SalariThalassemia and Hemoglobinopathy Research Center, Jundishapur University of Medical Sciences, Ahvaz, Iran.
Kaveh JasebThalassemia and Hemoglobinopathy Research Center, Jundishapur University of Medical Sciences, Ahvaz, Iran.
Ahvaz Jundishapur University of Medical Sciences · IRTarbiat Modares University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe use of fetal hemoglobin (HbF) inducer drugs is considered as a novel approach in treatment of β-hemoglobinopathies, especially β- thalassemia and sickle cell disease. HbF inducers including hydroxyurea, histone deacetylase (HDAC) inhibitor agents such as sodium butyrate, azacitidine, decitabine and new immunomodulator drugs like pomalidomide, lenalidomide and thalidomide can reduce α-globin chain production in erythroid progenitors and improve α: β chain imbalance, the most crucial complication of β-thalassemia. MATERIALS AND

methodsIn this article, we reviewed more than 40 articles published from 1979 to 2012 in the field of fetal hemoglobin augmentation.

resultsRecent studies suggest the synergistic effect of drug combinations in efficient induction of fetal hemoglobin and gene over-expression.

conclusionIt seems that drugs which act with different molecular and epigenetic mechanisms have proper synergistic effects in fetal hemoglobin induction and gene over-expression.

Indexed as

Fetal hemoglobinHistone deacetylaseβ-Hemoglobinopathies

Identifiers

PMID24505535
PMCPMC3913144
OpenAlexW112397445

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.