Affiliations 

  • 1 Blood Disorder Genetics & Thalassemia, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus
  • 2 Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, MA
  • 3 Muhimbili Sickle Cell Program, Department of Hematology and Blood Transfusion, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania
  • 4 Malaysian Node of the Human Variome Project, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Malaysia
  • 5 Faculty of Life Sciences and Medicine, King's College London, London, United Kingdom
Blood Adv, 2026 Oct 27;10(20):6932-6945.
PMID: 42566761 DOI: 10.1182/bloodadvances.2025018935

Abstract

Genetic 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.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.