Mackenzie Kimberly D, Ortega Mario, Kessler Yoel, Campos Verena Ramirez, Krasenbaum Lynda J, Carr Karen, Ning Xiaoping, Stratton Jennifer
Teva Pharmaceuticals, Redwood City, CA, United States.
Teva Branded Pharmaceutical Products R&D, Inc., West Chester, PA, United States.
Front Physiol. 2022 Nov 29;13:1067274. doi: 10.3389/fphys.2022.1067274. eCollection 2022.
Calcitonin gene-related peptide (CGRP) pathway-targeted treatments have been shown to be efficacious in the prevention of episodic and chronic migraine. Currently approved therapies include monoclonal antibodies (mAbs) that target CGRP (eptinezumab, fremanezumab, and galcanezumab) and the CGRP receptor (erenumab), and small molecule CGRP receptor antagonists (atogepant and rimegepant). While CGRP pathway-targeted treatments are generally well-tolerated, in a review article by Holzer and Holzer-Petsche published in the January 2022 issue of the authors discussed the role of the CGRP pathway in gastrointestinal physiology, with a specific focus on constipation associated with the use of CGRP pathway-targeted treatments. The authors state that real-world surveys have shown constipation to be a "major adverse event" reported in "more than 50% of patients treated with erenumab, fremanezumab or galcanezumab." As described in the current commentary, the limited data from the cited references in the review article by Holzer and Holzer-Petsche do not support that statement.
降钙素基因相关肽(CGRP)通路靶向治疗已被证明在预防发作性和慢性偏头痛方面有效。目前获批的疗法包括靶向CGRP的单克隆抗体(mAbs)(依普奈珠单抗、夫雷奈珠单抗和加卡奈珠单抗)以及CGRP受体(erenumab),还有小分子CGRP受体拮抗剂(阿托格潘和瑞美吉泮)。虽然CGRP通路靶向治疗通常耐受性良好,但在霍尔泽(Holzer)和霍尔泽 - 佩切(Holzer-Petsche)于2022年1月发表的一篇综述文章中,作者讨论了CGRP通路在胃肠生理学中的作用,特别关注了与使用CGRP通路靶向治疗相关的便秘问题。作者称,现实世界的调查显示便秘是“接受erenumab、夫雷奈珠单抗或加卡奈珠单抗治疗的患者中超过50%报告的‘主要不良事件’”。正如当前评论中所描述的,霍尔泽和霍尔泽 - 佩切综述文章中引用参考文献的有限数据并不支持这一说法。