| Literature DB >> 32814349 |
Roland Jäger1, Heinz Gisslinger2, Elisabeth Fuchs3, Edith Bogner3, Jelena D Milosevic Feenstra4, Jakob Weinzierl1, Fiorella Schischlik3, Bettina Gisslinger2, Martin Schalling2, Michael Zörer5, Kurt Krejcy5, Christoph Klade5, Robert Kralovics1,3.
Abstract
Interferon-α (IFN-α)-based treatments can induce hematologic and molecular responses (HRs and MRs, respectively) in polycythemia vera (PV); however, patients do not respond equally. Germline genetic factors have been implicated in differential drug responses. We addressed the effect of common germline polymorphisms on HR and MR after treatment of PV in the PROUD-PV and CONTINUATION-PV studies in a total of 122 patients who received ropeginterferon alfa-2b. Genome-wide association studies using longitudinal data on HR and MR over a 36-month follow-up did not reveal any associations at the level of genome-wide statistical significance. Furthermore, we performed targeted association analyses at the interferon lambda 4 (IFNL4) locus, well known for its role in hepatitis C viral clearance and recently reported to influence HR during treatment of myeloproliferative neoplasms. We did not observe any association of IFNL4 polymorphisms with HR in our study cohort; however, we demonstrated a statistically significant effect of the functionally causative IFNL4 diplotype (haplotype pair, including the protein-coding variants rs368234815/rs117648444) on MR (P = 3.91 × 10-4; odds ratio, 10.80; 95% confidence interval, 2.39-69.97) as reflected in differential JAK2V617F mutational burden changes according to IFNL4 diplotype status. Stratification of patients with PV based on IFNL4 functionality may allow for optimizing patient management during IFN-α-based therapy.Entities:
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Year: 2021 PMID: 32814349 PMCID: PMC7980276 DOI: 10.1182/blood.2020005792
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113