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February 11, 2026Scientific Reports0 citationsOpen Access

Genetic variability in thrombopoietin receptor and GATA1 influences response to eltrombopag in dengue-induced thrombocytopenia

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MSMohammad SayemRRRazoan Al RimonSASaruar Alam

Key Points

  • To explore how genetic variants in the thrombopoietin receptor and GATA1 affect eltrombopag response in patients with dengue-induced thrombocytopenia.
  • Patients enrolled in a phase-II trial of eltrombopag were analyzed for genetic variants using Sanger sequencing.
  • Univariate and multivariate logistic regression analyses were conducted to assess associations with drug response.
  • TPOR variant Ch1:43804387T > G linked to slower natural recovery in control group with lower platelet counts.
  • Heterozygous carriers of certain TPOR variants showed improved recovery with eltrombopag treatment.
  • GATA1 variants were associated with faster natural platelet recovery, but no independent predictors for treatment response were identified.

Abstract

Integrating pharmacogenetic studies into clinical trials enhances personalized medicine by identifying genetic variations that influence drug efficacy and safety. Eltrombopag, a thrombopoietin receptor agonist, has shown efficacy in treating thrombocytopenia associated with various conditions, including dengue fever, though variability in patient response remains poorly understood. This study investigates the impact of genetic variants in the thrombopoietin receptor (TPOR) and GATA1 transcription factor on eltrombopag response in dengue-induced thrombocytopenia. Exonic and flanking region variants of TPOR and GATA1 were analyzed by Sanger sequencing in patients enrolled in a phase-II trial of eltrombopag. Univariate and multivariate logistic regression analyses were performed to assess associations between genetic variants and drug response. The TPOR variant Ch1:43804387T > G (S129R) was linked to slower natural recovery in the control group, with significantly lower platelet counts from day 3 onwards (p G and Ch1:43804421 C > A (intronic) showed a compounded disadvantage in natural recovery, which was mitigated by eltrombopag. Patients heterozygous for Ch1:43803796G > A (E36K) exhibited significantly reduced treatment efficacy, with lower platelet counts from day 2 onwards (p A (S129N) was associated with significantly faster natural platelet recovery in the control group (p < 0.05). However, logistic regression analysis did not identify any specific variant as a statistically significant independent predictor of binary treatment response (Responder vs. Non-responder at Day 7). The study suggests TPOR variants as potential biomarkers for predicting eltrombopag response, while GATA1 variants may influence natural recovery dynamics in dengue-induced thrombocytopenia. These findings contribute to patient stratification and optimized therapeutic strategies. Further research combining pharmacogenetic and pharmacokinetic factors is essential for fully understanding eltrombopag response variability and advancing personalized treatment approaches.

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Cite This Study

Sayem et al. (2026) studied this question.

synapsesocial.com/papers/698be001058ab1890a13b9ebhttps://doi.org/10.1038/s41598-026-37871-7
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