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JACC CardioOncology, 2022-06, Vol.4 (2), p.166-182
2022
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Autor(en) / Beteiligte
Titel
Cardiovascular Disease in Myeloproliferative Neoplasms: State-of-the-Art Review
Ist Teil von
  • JACC CardioOncology, 2022-06, Vol.4 (2), p.166-182
Ort / Verlag
Elsevier
Erscheinungsjahr
2022
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Myeloproliferative neoplasms are associated with increased risk for thrombotic complications. These conditions most commonly involve somatic mutations in genes that lead to constitutive activation of the Janus-associated kinase signaling pathway (eg, Janus kinase 2, calreticulin, myeloproliferative leukemia protein). Acquired gain-of-function mutations in these genes, particularly Janus kinase 2, can cause a spectrum of disorders, ranging from clonal hematopoiesis of indeterminate potential, a recently recognized age-related promoter of cardiovascular disease, to frank hematologic malignancy. Beyond thrombosis, patients with myeloproliferative neoplasms can develop other cardiovascular conditions, including heart failure and pulmonary hypertension. The authors review the pathophysiologic mechanisms of cardiovascular complications of myeloproliferative neoplasms, which involve inflammation, prothrombotic and profibrotic factors (including transforming growth factor–beta and lysyl oxidase), and abnormal function of circulating clones of mutated leukocytes and platelets from affected individuals. Anti-inflammatory therapies may provide cardiovascular benefit in patients with myeloproliferative neoplasms, a hypothesis that requires rigorous evaluation in clinical trials. • MPNs entail increased thrombotic and cardiovascular risks. • Among them: atherothrombosis, heart failure, and pulmonary hypertension. • Genes mutated in MPNs include some seen in CHIP, also raising cardiovascular risk. • Inflammation likely contributes to increased cardiovascular risk in MPN. • Anti-inflammatory therapy in selected MPN patients warrants testing.
Sprache
Englisch
Identifikatoren
eISSN: 2666-0873
DOI: 10.1016/j.jaccao.2022.04.002
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9270630

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