Malsin Elizabeth S, Coleman John M, Wolfe Lisa F, Lam Anna P
Northwestern University Feinberg School of Medicine, Division of Pulmonary and Critical Care Medicine, 240 East Huron Street, McGaw Pavilion, Suite M-349 Chicago, Illinois 60611, USA.
Northwestern University Feinberg School of Medicine, Division of Pulmonary and Critical Care Medicine, 676 North St. Clair, Arkes Pavilion Suite 1400 Chicago, IL 60611, USA.
Respir Med Case Rep. 2019 Feb 16;26:304-306. doi: 10.1016/j.rmcr.2019.02.012. eCollection 2019.
Mirabegron, a β3 adrenergic receptor agonist, is FDA approved for treatment of overactive bladder. Approved in 2012 in the US, there have been no reports of any effects of mirabegron on pulmonary function.
We report the case of a 65 year old male with a history of Parkinson's disease, OSA, and aspiration pneumonia presenting with subacute worsening dyspnea and found to have worsening restrictive ventilatory defect with a pattern consistent with neuromuscular weakness. After recalling that initiation of mirabegron correlated with onset of his worsening symptoms, the patient decided to perform a trial period off the drug. He subsequently reported prompt improvement in his respiratory symptoms, which was confirmed objectively by pulmonary function tests. In this case, mirabegron was temporally associated with subacute worsening of the patient's pulmonary restrictive physiology, with subsequent resolution after discontinuation of the medication.
The mechanism of this adverse effect is unknown, but we speculate that this effect may be potentially mediated by the effect of β3 adrenergic receptor agonism on skeletal muscle, in this case in a patient with pre-existing neuromuscular disease. Careful assessment of patients who develop shortness of breath while on mirabegron should include an assessment for restrictive lung disease secondary neuromuscular dysfunction. Additional study is needed of the effects of β3 agonism on skeletal muscle.
米拉贝隆是一种β3肾上腺素能受体激动剂,已获美国食品药品监督管理局(FDA)批准用于治疗膀胱过度活动症。该药于2012年在美国获批,此前尚无关于米拉贝隆对肺功能有任何影响的报道。
我们报告了一例65岁男性患者,有帕金森病、阻塞性睡眠呼吸暂停(OSA)和吸入性肺炎病史,出现亚急性呼吸困难加重,经检查发现存在进行性加重的限制性通气功能障碍,其模式与神经肌肉无力相符。在回忆起米拉贝隆的起始使用与他症状加重的发作相关后,患者决定进行停药试验期。他随后报告呼吸症状迅速改善,这通过肺功能测试得到客观证实。在该病例中,米拉贝隆在时间上与患者肺部限制性生理功能的亚急性恶化相关,停药后症状随后缓解。
这种不良反应的机制尚不清楚,但我们推测这种效应可能潜在地由β3肾上腺素能受体激动对骨骼肌的作用介导,在本病例中是一名患有既往神经肌肉疾病的患者。对服用米拉贝隆时出现气短的患者进行仔细评估应包括对继发于神经肌肉功能障碍的限制性肺病的评估。需要对β3激动剂对骨骼肌的影响进行更多研究。