Increased prevalence of clonal hematopoiesis in children with sickle cell disease

Recent studies have reached opposing conclusions about whether clonal hematopoiesis (CH) is increased or decreased in patients with sickle cell disease (SCD). Given that CH is typically age-related, its presence in children with SCD could offer unique insights into early-life mutagenesis and disease-related stressors. We tested the primary and secondary hypotheses that children with SCD would have a higher prevalence of CH than age-, sex-, and race-matched children without SCD and that children with hydroxyurea would have a higher CH prevalence than children not treated with hydroxyurea. To address this, we conducted a cross-sectional study in 2 independent cohorts of children aged 0 to 18 years with SCD (N = 1025 and N = 1293, respectively) and a 2957-person matched comparison group. Using a highly sensitive, error-corrected sequencing assay capable of detecting CH at a variant allele frequency of ≥0.5%, we found that children with SCD have a significantly higher prevalence of CH than the comparison group (odds ratio [OR], 4.2; P = 7.4 × 10-13). In addition, CH was not associated with exposure to hydroxyurea therapy (OR, 0.76; P = .44).

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Publication Details

Journal
Blood
Published
2025-12-08
DOI
https://doi.org/10.1182/blood.2025030898
Citations
1
Primary Topic
Hemoglobinopathies and Related Disorders
Type
article
Field-Weighted Citation Impact
1.63
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article

Increased prevalence of clonal hematopoiesis in children with sickle cell disease

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1 citations
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Hemoglobinopathies and Related Disorders
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article

Increased prevalence of clonal hematopoiesis in children with sickle cell disease

Jessica Ulloa, Alexander G. Bick, Victor R. Gordeuk, Caitlyn Vlasschaert, Kristin Wuichet, Santosh L. Saraf, Christopher J. Shore, Yash Pershad, Michael R. DeBaun, Mitchell J. Weiss, Mark Rodeghier, Binal N. Shah, Sara R. Rashkin, Yu Yao, Clifford M. Takemoto
article en
1 citations

Abstract

Recent studies have reached opposing conclusions about whether clonal hematopoiesis (CH) is increased or decreased in patients with sickle cell disease (SCD). Given that CH is typically age-related, its presence in children with SCD could offer unique insights into early-life mutagenesis and disease-related stressors. We tested the primary and secondary hypotheses that children with SCD would have a higher prevalence of CH than age-, sex-, and race-matched children without SCD and that children with hydroxyurea would have a higher CH prevalence than children not treated with hydroxyurea. To address this, we conducted a cross-sectional study in 2 independent cohorts of children aged 0 to 18 years with SCD (N = 1025 and N = 1293, respectively) and a 2957-person matched comparison group. Using a highly sensitive, error-corrected sequencing assay capable of detecting CH at a variant allele frequency of ≥0.5%, we found that children with SCD have a significantly higher prevalence of CH than the comparison group (odds ratio [OR], 4.2; P = 7.4 × 10-13). In addition, CH was not associated with exposure to hydroxyurea therapy (OR, 0.76; P = .44).

BloodVol. 147(13)
Meharry Medical College (US), St. Jude Children's Research Hospital (US), Vanderbilt University (US), Queen's University (CA), University of Illinois Chicago (US), University of Chicago (US), FIT Consulting (Italy) (IT), BH Consulting (Ireland) (IE), Vanderbilt Health (US), Vanderbilt University Medical Center (US)
Openalex Percentile: Top 11%
Hemoglobinopathies and Related Disorders
1.63
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