Evidence map›Paper›PMID 42566761›Full record

ReviewBlood advances2026

Modifying quality and equity of care: emerging roles of genetic disease modifiers in β-hemoglobinopathies.

Panayiota L Papasavva, Atinuke M Dosunmu-Ogunbi, Oni O Morohuntodun, Petros Kountouris, Julie Makani, Bin Alwi Zilfalil, Baba P D Inusa, Natasha M Archer, Carsten W Lederer, International Hemoglobinopathy Research Network

Abstract readReview
In one paragraph

Review in Blood advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Panayiota L PapasavvaBlood Disorder Genetics & Thalassemia, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.ORCID 0000-0003-4410-3119
Atinuke M Dosunmu-OgunbiDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA.
Oni O MorohuntodunDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA.
Petros KountourisBlood Disorder Genetics & Thalassemia, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.ORCID 0000-0003-2681-4355
Julie MakaniMuhimbili Sickle Cell Program, Department of Hematology and Blood Transfusion, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.ORCID 0000-0002-4801-6250
Bin Alwi ZilfalilMalaysian Node of the Human Variome Project, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Malaysia.
Baba P D InusaFaculty of Life Sciences and Medicine, King's College London, London, United Kingdom.ORCID 0000-0003-2643-765X
Natasha M ArcherDana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA.
Carsten W LedererBlood Disorder Genetics & Thalassemia, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.ORCID 0000-0003-3920-9584
International Hemoglobinopathy Research Network

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractGenetic disease modifiers (GDMs) strongly affect disease and therapy outcomes, rendering their characterization essential for prognosis, treatment decisions, and therapy development. A paradigm for the importance of GDMs are β-hemoglobinopathies, for which a growing pipeline of emerging curative and disease-modifying therapies are based on the manipulation of GDMs. However, beyond their role as therapeutic targets, GDMs are also gaining clinical importance in the choice and planning of disease-modifying therapies, the selection and customization of curative therapies, and the equitable provision and global reach of therapies across ethnic groups and geo-economic divides. Here, we define roles of GDMs in all 4 of these fields, highlight their potential to promote choice, effectiveness, affordability, and equitable provision of treatment, and emphasize the importance of capacity building through multiethnic GDM-related research. We conclude that consideration of GDMs at all stages of development and care will be critical to addressing the needs of affected communities.

Indexed as

Health EquityHemoglobinopathiesQuality of Health CareHumans

Identifiers

PMID42566761
PMCPMC13682361

What OpenQuestion holds

Textmetadata
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.