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Propranolol Therapy in Infantile Hemangioma: It Is Not Just About the Beta.
Lee, James C; Modiri, Omeed; England, Ryan W; Shawber, Carrie J; Wu, June K.
Afiliação
  • Lee JC; From the Departments of Surgery and Obstetrics and Gynecology, NewYork-Presbyterian Hospital/Columbia University Irving Medical Center.
  • Modiri O; From the Departments of Surgery and Obstetrics and Gynecology, NewYork-Presbyterian Hospital/Columbia University Irving Medical Center.
  • England RW; From the Departments of Surgery and Obstetrics and Gynecology, NewYork-Presbyterian Hospital/Columbia University Irving Medical Center.
  • Shawber CJ; From the Departments of Surgery and Obstetrics and Gynecology, NewYork-Presbyterian Hospital/Columbia University Irving Medical Center.
  • Wu JK; From the Departments of Surgery and Obstetrics and Gynecology, NewYork-Presbyterian Hospital/Columbia University Irving Medical Center.
Plast Reconstr Surg ; 147(4): 875-885, 2021 04 01.
Article em En | MEDLINE | ID: mdl-33776033
BACKGROUND: Propranolol, a nonselective ß-adrenergic receptor antagonist, is approved by the U.S. Food and Drug Administration to treat problematic infantile hemangiomas, but a subset of patients experience treatment complications. Parents wary of long-term use and side effects consult plastic surgeons on surgical options or as a second opinion. Understanding the mechanism(s) of action of propranolol will allow plastic surgeons to better inform parents. METHODS: A systemic literature search was performed to query published translational and basic science studies on propranolol effects on infantile hemangiomas and cells derived from these lesions. RESULTS: In experimental studies, propranolol was antiproliferative and cytotoxic against hemangioma endothelial and stem cells and affected infantile hemangioma perivascular cell contractility. Propranolol inhibited migration, network formation, vascular endothelial growth factor A production, and vascular endothelial growth factor receptor 2 activation and down-regulated PI3K/AKT and mitogen-activated protein kinase signaling in hemangioma endothelial cells, but it increased ERK1/2 activity in hemangioma stem cells. At effective clinical doses, measured propranolol plasma concentration is 100 times higher than necessary for complete ß-adrenergic receptor blockade, yet was 10 to 100 times less than required to induce hemangioma stem cell death. CONCLUSIONS: Propranolol targets multiple cell types in infantile hemangiomas by means of ß-adrenergic receptor-dependent and -independent mechanisms. Plasma concentration played a significant role. At clinically relevant doses, incomplete infantile hemangioma suppression may explain the rebound phenomenon and worsening ulceration, and propranolol off target effects may lead to commonly reported adverse effects, such as sleep and gastrointestinal disturbances. Propranolol limitations and complications underscore the importance of surgical treatment options in cases of rebound and severe adverse effects. Surgical intervention remains an important treatment choice when parents are hesitant to use propranolol.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Propranolol / Hemangioma Capilar / Antagonistas Adrenérgicos beta Tipo de estudo: Systematic_reviews Limite: Humans / Infant Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Propranolol / Hemangioma Capilar / Antagonistas Adrenérgicos beta Tipo de estudo: Systematic_reviews Limite: Humans / Infant Idioma: En Ano de publicação: 2021 Tipo de documento: Article