淀粉样蛋白和心脏代谢风险因素对神经退行性疾病血浆神经丝蛋白轻链预后能力的影响

IF 7.9 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's Research & Therapy Pub Date : 2024-09-12 DOI:10.1186/s13195-024-01564-y
Keun You Kim, Eosu Kim, Jun-Young Lee
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引用次数: 0

摘要

血浆神经丝蛋白轻链(NfL)是神经变性(包括阿尔茨海默病)的血液生物标志物。然而,它的作用可能会受到老年人常见疾病的影响,包括淀粉样蛋白-β(Aβ)沉积以及高血压、糖尿病(DM)、肾功能受损和肥胖等心脏代谢风险因素。这项纵向观察研究利用阿尔茨海默病神经影像学倡议队列调查了这些情况如何影响血浆NfL的预后能力。非痴呆参与者(认知功能未受损或轻度认知功能受损)接受了重复评估,包括阿尔茨海默病评估量表-认知子量表(ADAS-Cog)评分、海马体积和白质高密度(WMH)体积,评估间隔为 6 个月或 12 个月。研究人员采用线性混合效应模型来检验血浆NfL与Aβ(通过氟贝他匹正电子发射断层扫描评估)、高血压、糖尿病、肾功能受损或肥胖等各种相关变量之间的相互作用。在平均 62.5 个月的随访期间,对平均年龄为 72.1 岁(n = 720,48.8% 为女性)的基线参与者进行了观察。随着时间的推移,基线时较高的血浆NfL水平与ADAS-Cog评分和WMH体积的急剧增加以及海马体积的急剧减少相关(所有P值均小于0.001)。值得注意的是,基线时的 Aβ 能显著增强血浆 NfL 与 ADAS-Cog 评分(p 值 0.005)和海马体积(p 值 0.004)纵向变化之间的关联。关于ADAS-Cog评分和WMH体积,Aβ对认知功能未受损者的影响比对轻度认知功能受损者的影响更为显著。高血压明显增强了血浆NfL与ADAS-Cog评分、海马体积和WMH体积纵向变化之间的关联(所有P值均小于0.001)。糖尿病会影响血浆NfL与ADAS-Cog评分变化之间的关系(p值<0.001),但不会影响海马体积和WMH体积。肾功能受损不会明显改变血浆NfL与任何结果变量的纵向变化之间的关系。肥胖仅增强了血浆NfL与海马体积变化之间的关联(p值为0.026)。这项研究表明,血浆 NfL 的预后能力可能会在患有 Aβ 或高血压的个体中放大。这一发现强调了在基于 NfL 的非痴呆老年人神经变性预后模型中考虑这些因素的重要性。
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Impact of amyloid and cardiometabolic risk factors on prognostic capacity of plasma neurofilament light chain for neurodegeneration
Plasma neurofilament light chain (NfL) is a blood biomarker of neurodegeneration, including Alzheimer’s disease. However, its usefulness may be influenced by common conditions in older adults, including amyloid-β (Aβ) deposition and cardiometabolic risk factors like hypertension, diabetes mellitus (DM), impaired kidney function, and obesity. This longitudinal observational study using the Alzheimer’s Disease Neuroimaging Initiative cohort investigated how these conditions influence the prognostic capacity of plasma NfL. Non-demented participants (cognitively unimpaired or mild cognitive impairment) underwent repeated assessments including the Alzheimer’s Disease Assessment Scale-Cognitive subscale (ADAS-Cog) scores, hippocampal volumes, and white matter hyperintensity (WMH) volumes at 6- or 12-month intervals. Linear mixed-effect models were employed to examine the interaction between plasma NfL and various variables of interest, such as Aβ (evaluated using Florbetapir positron emission tomography), hypertension, DM, impaired kidney function, or obesity. Over a mean follow-up period of 62.5 months, participants with a mean age of 72.1 years (n = 720, 48.8% female) at baseline were observed. Higher plasma NfL levels at baseline were associated with steeper increases in ADAS-Cog scores and WMH volumes, and steeper decreases in hippocampal volumes over time (all p-values < 0.001). Notably, Aβ at baseline significantly enhanced the association between plasma NfL and longitudinal changes in ADAS-Cog scores (p-value 0.005) and hippocampal volumes (p-value 0.004). Regarding ADAS-Cog score and WMH volume, the impact of Aβ was more prominent in cognitively unimpaired than in mild cognitive impairment. Hypertension significantly heightened the association between plasma NfL and longitudinal changes in ADAS-Cog scores, hippocampal volumes, and WMH volumes (all p-values < 0.001). DM influenced the association between plasma NfL and changes in ADAS-Cog scores (p-value < 0.001) without affecting hippocampal and WMH volumes. Impaired kidney function did not significantly alter the association between plasma NfL and longitudinal changes in any outcome variables. Obesity heightened the association between plasma NfL and changes in hippocampal volumes only (p-value 0.026). This study suggests that the prognostic capacity of plasma NfL may be amplified in individuals with Aβ or hypertension. This finding emphasizes the importance of considering these factors in the NfL-based prognostic model for neurodegeneration in non-demented older adults.
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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
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