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帕金森病患者的 ON 时间与总每日 OFF 时间中体验到的 OFF 时间相比,ON 时间的重要性。

Importance of time to ON versus wearing OFF in total daily OFF time experienced by patients with Parkinson's disease.

机构信息

Parkinson's Disease and Movement Disorders Center of Boca Raton, 951 NW 13th St, Bldg. 5-E, Boca Raton, FL, 33486, USA.

Department of Neurology, Thomas Jefferson University, 901 Walnut Street, Suite 400, Philadelphia, PA, 19107, USA.

出版信息

Parkinsonism Relat Disord. 2023 Sep;114:105495. doi: 10.1016/j.parkreldis.2023.105495. Epub 2023 Jul 22.

Abstract

Most patients with Parkinson's disease (PD) receiving levodopa (LD)/DOPA decarboxylase inhibitors develop motor fluctuations with an increasing amount of OFF time, negatively impacting patient quality of life. Herein, we review the evidence supporting the substantial, yet underappreciated contribution of delays in time to ON (including delayed ON and no ON) to total daily OFF time. Most clinical studies use patient diaries that do not capture time to ON and wearing OFF separately as related to LD dosing, and consequently, most OFF time has generally been attributed to wearing OFF. Hence, most treatment regimens focus on reducing wearing OFF by changing LD dosing/formulations and/or using "ON-extenders" (eg, catechol-o-methyltransferase inhibitors, monoamine oxidase-B inhibitors, extended-release amantadine, and adenosine A receptor antagonists). However, the literature describing approved treatments for PD that has focused on delays in time to ON is sparse and suggests this type of OFF may comprise more than twice the amount of total daily OFF time as wearing OFF. Here, we advocate for the importance of measuring and adequately addressing delays in time to ON and build support for the consistent inclusion of the time to ON measurement in future clinical trials.

摘要

大多数接受左旋多巴(LD)/DOPA 脱羧酶抑制剂治疗的帕金森病(PD)患者会出现运动波动,随着“关期”时间的增加,这会对患者的生活质量产生负面影响。在此,我们回顾了支持“开期”延迟(包括延迟开期和无开期)对总“关期”时间有实质性但被低估的贡献的证据。大多数临床研究使用的患者日记不能分别记录与 LD 剂量相关的“开期”时间和“关期”时间,因此,大多数“关期”时间通常归因于“关期”时间。因此,大多数治疗方案都集中在通过改变 LD 剂量/配方和/或使用“开期延长剂”(如儿茶酚-O-甲基转移酶抑制剂、单胺氧化酶-B 抑制剂、延释金刚烷胺和腺嘌呤 A 受体拮抗剂)来减少“关期”时间。然而,描述专注于“开期”延迟的 PD 获批治疗方法的文献很少,这表明这种类型的“关期”可能占总“关期”时间的两倍以上。在这里,我们提倡测量和充分解决“开期”延迟的重要性,并支持在未来的临床试验中始终包括“开期”时间的测量。

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