Cai Huimin, Zhao Tan, Pang Yana, Fu Xiaofeng, Ren Ziye, Quan Shuiyue, Jia Longfei
Innovation Centre for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Centre for Geriatric Diseases, Beijing 100053, China.
Brain. 2025 Feb 3;148(2):480-492. doi: 10.1093/brain/awae230.
Systemic inflammation with alterations in inflammatory markers is involved in ageing and Alzheimer's disease. However, few studies have investigated the longitudinal trajectories of systemic inflammatory markers during ageing and Alzheimer's disease, and specific markers contributing to Alzheimer's disease remain undetermined. In this study, a longitudinal cohort (cohort 1: n = 290; controls, 136; preclinical Alzheimer's disease, 154) and a cross-sectional cohort (cohort 2: n = 351; controls, 62; Alzheimer's disease, 63; vascular dementia, 58; Parkinson's disease dementia, 56; behavioural variant frontotemporal dementia, 57; dementia with Lewy bodies, 55) were included. Plasma levels of inflammatory markers were measured every 2 years during a 10-year follow-up in the longitudinal cohort and once in the cross-sectional cohort. The study demonstrated that the inflammatory markers significantly altered during both ageing and the development of Alzheimer's disease. However, only complement C3, interleukin-1β and interleukin-6 exhibited significant changes in participants with preclinical Alzheimer's disease, and their longitudinal changes were significantly associated with the development of Alzheimer's disease compared to controls over the 10-year follow-up. In the cross-sectional cohort, complement C3 demonstrated specificity to Alzheimer's disease, while interleukin-1β and interleukin-6 were also altered in other dementias. The study provides a new perspective on the involvement of inflammatory markers in the ageing process and the development of Alzheimer's disease, implying that regulating inflammation may have a pivotal role in promoting successful ageing and in the prevention and treatment of Alzheimer's disease.
炎症标志物改变所引发的全身炎症与衰老及阿尔茨海默病相关。然而,很少有研究调查衰老和阿尔茨海默病过程中全身炎症标志物的纵向变化轨迹,且导致阿尔茨海默病的特定标志物仍未确定。在本研究中,纳入了一个纵向队列(队列1:n = 290;对照组136例;临床前阿尔茨海默病患者154例)和一个横断面队列(队列2:n = 351;对照组62例;阿尔茨海默病患者63例;血管性痴呆患者58例;帕金森病痴呆患者56例;行为变异型额颞叶痴呆患者57例;路易体痴呆患者55例)。在纵向队列的10年随访期间,每2年测量一次炎症标志物的血浆水平,在横断面队列中则测量一次。该研究表明,炎症标志物在衰老和阿尔茨海默病发展过程中均有显著改变。然而,只有补体C3、白细胞介素-1β和白细胞介素-6在临床前阿尔茨海默病患者中表现出显著变化,并且在10年随访期间,与对照组相比,它们的纵向变化与阿尔茨海默病的发展显著相关。在横断面队列中,补体C3对阿尔茨海默病具有特异性,而白细胞介素-1β和白细胞介素-6在其他痴呆症中也发生了改变。该研究为炎症标志物参与衰老过程和阿尔茨海默病发展提供了新的视角,意味着调节炎症可能在促进成功衰老以及预防和治疗阿尔茨海默病方面发挥关键作用。