Evidence map›Paper›PMID 41115240›Full record

ArticleBlood advances2026

Short- and long-term effects of transfusion in β-thalassemia: a longitudinal study of transfusion efficiency factors.

Konstantina Theocharaki, Ioanna Barla, Sophia Delicou, Alkmini T Anastasiadi, Vassilis L Tzounakas, Stella Rouvela, Georgia Tzafa, Elli-Anna Stylianaki, Efthymia-Ioanna Koufogeorgou, Theodore Gousdovas and 14 more

Abstract read
In one paragraph

Article in Blood advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

24 authors.

Konstantina TheocharakiDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0009-0005-5820-3999
Ioanna BarlaDepartment of Chemistry, School of Science, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0003-1352-7816
Sophia DelicouThalassemia and Sickle Cell Unit, Expertise Center of Hemoglobinopathies and Their Complications, Hippokration General Hospital, Athens, Greece.
Alkmini T AnastasiadiDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0009-0007-3165-7493
Vassilis L TzounakasDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0009-0002-3697-001X
Stella RouvelaDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.
Georgia TzafaDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.
Elli-Anna StylianakiLaboratory of Molecular Virology, Hellenic Pasteur Institute, Athens, Greece.ORCID 0009-0002-9177-6260
Efthymia-Ioanna KoufogeorgouLaboratory of Molecular Virology, Hellenic Pasteur Institute, Athens, Greece.
Theodore GousdovasHematology Laboratory-Blood Bank, Aretaieio Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Efthymia PavlouBlood Bank and Hemophilia Unit, Hippokration General Hospital of Athens, Athens, Greece.ORCID 0000-0002-5855-0895
Ioannis V KostopoulosDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0003-1152-6959
Nikolaos SimantirisDepartment of Environment, Faculty of Environment, Ionian University, Zakynthos, Greece.
Niki VassilakiLaboratory of Molecular Virology, Hellenic Pasteur Institute, Athens, Greece.ORCID 0000-0001-7992-3438
Maria MorakiThalassemia and Sickle Cell Unit, Expertise Center of Hemoglobinopathies and Their Complications, Hippokration General Hospital, Athens, Greece.
Konstantinos StamoulisHellenic National Blood Transfusion Centre, Acharnes, Greece.
Ersi VoskaridouCentre of Excellence in Rare Haematological (Haemoglobinopathies) and Rare Metabolic (Gaucher Disease) Diseases, Laiko General Hospital, Athens, Greece.
Efrosyni NomikouBlood Bank and Hemophilia Unit, Hippokration General Hospital of Athens, Athens, Greece.
Ourania TsitsilonisDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.
Nikolaos ThomaidisDepartment of Chemistry, School of Science, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0002-4624-4735
Evangelos GikasDepartment of Chemistry, School of Science, National and Kapodistrian University of Athens, Athens, Greece.
Marianna PolitouHematology Laboratory-Blood Bank, Aretaieio Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Veroniki KomninakaCentre of Excellence in Rare Haematological (Haemoglobinopathies) and Rare Metabolic (Gaucher Disease) Diseases, Laiko General Hospital, Athens, Greece.
Marianna H AntonelouDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Athens, Greece.ORCID 0000-0003-3787-3596

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractThe complex interplay between donor and recipient factors likely influences transfusion outcomes in transfusion-dependent thalassemia (TDT). We investigated physiological responses to transfusion shortly after it and 1 week later, focusing on hemoglobin (Hb) increment (ΔHb) and its determinants, using longitudinal data from 36 patients with TDT and 58 red blood cell (RBC) units. Immediate anemia correction after transfusion was associated with decreases in platelets and nucleated RBCs, increases in ADAMTS13 antigen and plasma amino acid levels, and temporary rises in hemolysis and phthalates. One week after transfusion, at the peak of erythroid suppression, plasma antioxidants and mechanical hemolysis decreased, whereas proteasome activity at the RBC membrane increased. Leukocyte levels declined, markers of thrombotic risk and endothelium dysfunction improved, and hepcidin as well as plasma glutamine and deoxyadenosine, increased. In addition to female sex and anemia, ΔHb was influenced by recipient baseline monocyte levels, hypercoagulability, and plasma metabolites, such as methionine, adenosine, acyl-carnitines, and bile acids. Donor RBC unit factors, including residual platelet levels, RBC proteasome activity, arginine metabolism, and catecholamine content also had significant correlations. Notably, the baseline neutrophil-to-lymphocyte ratio strongly affected ΔHb soon after transfusion, after adjusting for confounders. At the 1-week mark, ΔHb correlated with storability markers, such as oxidative hemolysis and phthalates, which, to our knowledge, is a first-ever described connection. Importantly, the percentage of phosphatidylserine-exposing donor RBCs and the uric acid-dependent antioxidant capacity of the RBC units significantly influenced ΔHb at the 1-week time point. These findings enhance our understanding of transfusion dynamics, paving the way for more personalized and effective care strategies in TDT management.

Indexed as

beta-ThalassemiaBlood TransfusionAdolescentAdultChildFemaleHemoglobinsHemolysisHumansLongitudinal StudiesMaleMiddle AgedTreatment OutcomeYoung AdultHemoglobins

Identifiers

PMID41115240
PMCPMC12805312

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.