The effect of the tumour necrosis factor-alpha-inhibitor etanercept on microglial activation patients with mild cognitive impairment—a PET study

A. Gerhard, Richard Sharples, Tsepo Goerttler, K. McDonald, E. Visi, R. Hinz, F. Turkheimer, Isabel Lewzey, K. Herholz, A. Jacobs, C. Holmes
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Abstract

Aim: Microglial activation is increasingly recognised as a factor in the progression of Alzheimer’s disease (AD) and may be modified by systemic inflammatory signals including serum tumour necrosis factor (TNF)-α. The aim was to investigate whether blockade of peripheral TNF-α with peripheral inhibitors such as etanercept reduces microglial activation in prodromal AD. Methods: A one-year, multi-centre, phase 2, double-blind randomised placebo-controlled trial (RPCT) was performed, to assess the effect of weekly 50 mg s.c. etanercept in amyloid positive mild cognitive impaired participants on the change in microglial activation as measured by [11C](R)-PK11195 positron emission tomography (PET). Secondary objectives were to ascertain the change in cortical amyloid load on PET and the change in the Montreal Cognitive Assessment (MoCA). Results: Forty-four subjects consented to the study. Twenty-eight subjects failed screening including six subjects who were amyloid negative on visual read of the AmyvidTM PET scans. Thirteen of sixteen subjects with mild cognitive impairment (MCI) due to AD completed the baseline [11C](R)-PK11195 PET scan and were randomised to either placebo or etanercept. Three patients who consented were not able to complete screening due to early termination of the study following delays in study commencement. [11C](R)-PK11195 binding potential (BP) at baseline showed an almost global increase in MCI patients as compared to age-matched controls. Compliance to medication was high over the twelve-month trial period with etanercept being well tolerated. The study did not achieve statistical power to show a significant effect of etanercept over 52 weeks in the limited number of patients with MCI on microglial activation as measured by [11C](R)-PK11195 PET. Overall uptake of florbetapir in the follow up (FU) scans remained stable. The study was not powered to show statistical differences in psychometric ratings between groups. Conclusions: This study did not show evidence that treatment with etanercept over one year would modulate microglial activation in amyloid positive MCI patients (EudraCT identifier: 2015-002145-63, https://www.clinicaltrialsregister.eu; International Standard Randomised Controlled Trial Number identifier: ISRCTN12472821, https://www.isrctn.com).
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肿瘤坏死因子- α抑制剂依那西普对轻度认知障碍患者小胶质细胞激活的影响——PET研究
目的:小胶质细胞激活越来越被认为是阿尔茨海默病(AD)进展的一个因素,并且可能受到包括血清肿瘤坏死因子(TNF)-α在内的全身炎症信号的修饰。目的是研究用依那西普等外周抑制剂阻断外周TNF-α是否会降低AD前驱小胶质细胞的激活。方法:通过一项为期一年的多中心二期双盲随机安慰剂对照试验(RPCT),评估淀粉样蛋白阳性轻度认知障碍参与者每周服用50 mg s.c.依那西普对[11C](R)-PK11195正电子发射断层扫描(PET)测量的小胶质细胞激活变化的影响。次要目的是确定PET的皮质淀粉样蛋白负荷变化和蒙特利尔认知评估(MoCA)的变化。结果:44名受试者同意本研究。28名受试者未通过筛选,其中6名受试者在AmyvidTM PET扫描的视觉阅读中呈淀粉样蛋白阴性。16名因AD导致轻度认知障碍(MCI)的受试者中有13名完成了基线[11C](R)-PK11195 PET扫描,并随机分配到安慰剂组或依那西普组。三名同意的患者由于研究开始延迟而导致研究提前终止而无法完成筛查。[11C](R)-PK11195结合电位(BP)在基线时显示MCI患者与年龄匹配的对照组相比几乎全面增加。在12个月的试验期间,药物依从性很高,依那西普耐受性良好。通过[11C](R)-PK11195 PET测量,该研究没有达到统计学上的有效性,表明在有限数量的MCI患者中,依那西普在52周内对小胶质细胞激活有显著影响。在随访(FU)扫描中,florbetapir的总体摄取保持稳定。这项研究并没有显示各组之间心理测量评分的统计差异。结论:本研究没有证据表明依那西普治疗一年以上会调节淀粉样蛋白阳性MCI患者的小胶质细胞激活(研究编号:2015-002145-63,https://www.clinicaltrialsregister.eu;国际标准随机对照试验编号标识符:ISRCTN12472821, https://www.isrctn.com)。
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