认知正常老年人血清脑源性神经营养因子与轻度认知损伤的进展

IF 13 1区 医学 Q1 CLINICAL NEUROLOGY Alzheimer's & Dementia Pub Date : 2025-01-09 DOI:10.1002/alz.088177
Kyungtae Kim, Min Soo Byun, Dahyun Yi, Joon Hyung Jung, Bo Kyung Sohn, Gijung Jung, Hyejin Ahn, Jun‐Young Lee, Yun‐Sang Lee, Yu Kyeong Kim, Dong Young Lee
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This study aimed to examine whether higher serum BDNF in cognitively normal (CN) older adults is related to less common progression to MCI and to identify potential moderators of this relationship.MethodA total of 278 CN older adults between 55 and 90 years of age were enrolled. All participants underwent comprehensive clinical assessments, serum BDNF level measurement, and multimodal brain imaging including Pittsburgh compound B (PIB)‐positron emission tomography (PET) at baseline, and followed up for up to 4 years. Serum BDNF levels were divided into two categories by median value of serum BDNF level: < 21448.5 pg/mL (low BDNF), and > 21448.5 pg/mL (high BDNF). Cox model was used to analyze the relationship between baseline BDNF levels and the risk for MCI progression controlling for potential confounders. We also ran sensitivity analyses stratified by sex, age, education, apolipoprotein E ε4 (APOE4) positivity, and amyloid PET positivity.ResultDuring follow‐up, 24 participants developed MCI. Controlling for age, sex, education and APOE4 positivity, low BDNF group had significantly more frequent progression to MCI than high BDNF group (hazard ratio for MCI, 2.98; 95% CI, 1.17‐7.56; p=0.02) and these association persisted even after controlling for amyloid PET positivity and vascular risk factor score as additional covariates (hazard ratio, 2.98; 95% CI, 1.17‐7.55; p=0.02). Sensitivity analyses revealed that the associations were apparent only among women, participants aged younger than 75 years, those without college degrees, and amyloid negative participants (Table).ConclusionHigher serum BDNF levels may protect against future occurrence of MCI in cognitively healthy older adults. 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引用次数: 0

摘要

脑源性神经营养因子(BDNF)与神经元存活、突触可塑性和长期记忆的改善有关。一些人体研究也报告了血液BDNF水平较低与记忆功能较差和痴呆之间的关系。先前的一项纵向研究也表明,较高的血清BDNF水平与总体痴呆和阿尔茨海默病(AD)痴呆的风险较低相关。然而,尚不确定血清BDNF水平降低是否先于轻度认知障碍(MCI)的发作,即痴呆前期。本研究旨在研究认知正常(CN)老年人血清BDNF升高是否与MCI进展较少有关,并确定这种关系的潜在调节因子。方法共纳入278名55 ~ 90岁的中国老年人。所有参与者在基线时接受了全面的临床评估、血清BDNF水平测量和多模态脑成像(包括匹兹堡化合物B (PIB) -正电子发射断层扫描(PET)),并随访长达4年。按血清BDNF水平中位数将血清BDNF水平分为两类:21448.5 pg/mL(低BDNF), >;21448.5 pg/mL(高BDNF)。采用Cox模型分析基线BDNF水平与MCI进展风险之间的关系,控制潜在混杂因素。我们还按性别、年龄、教育程度、载脂蛋白E ε4 (APOE4)阳性和淀粉样蛋白PET阳性进行了敏感性分析。结果随访期间,24例患者发生轻度认知损伤。在控制年龄、性别、教育程度和APOE4阳性的情况下,低BDNF组进展为轻度认知损伤的频率明显高于高BDNF组(轻度认知损伤的风险比为2.98;95% ci, 1.17‐7.56;p=0.02),即使在控制淀粉样蛋白PET阳性和血管危险因素评分作为附加协变量后,这种关联仍然存在(风险比,2.98;95% ci, 1.17‐7.55;p = 0.02)。敏感性分析显示,这种关联仅在女性、年龄小于75岁的参与者、没有大学学位的参与者和淀粉样蛋白阴性的参与者中明显(表)。结论较高的血清BDNF水平可能对认知健康老年人MCI的未来发生有保护作用。这种影响在女性和年轻、受教育程度较低或淀粉样PET阴性的个体中更为突出。
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Serum brain‐derived neurotrophic factor and progression to MCI in cognitively normal older adults
BackgroundBrain derived neurotropic factor (BDNF) has been associated with improved neuronal survival and synaptic plasticity and long‐term memory. Some human studies also reported the relationship between lower blood BDNF levels and poorer memory function and dementia. A prior longitudinal study also demonstrated higher serum BDNF levels were associated with lower risk of overall dementia and Alzheimer’s disease (AD) dementia. However, it remains uncertain whether reduced serum BDNF levels precede the onset of mild cognitive impairment (MCI), which is known as pre‐dementia stage. This study aimed to examine whether higher serum BDNF in cognitively normal (CN) older adults is related to less common progression to MCI and to identify potential moderators of this relationship.MethodA total of 278 CN older adults between 55 and 90 years of age were enrolled. All participants underwent comprehensive clinical assessments, serum BDNF level measurement, and multimodal brain imaging including Pittsburgh compound B (PIB)‐positron emission tomography (PET) at baseline, and followed up for up to 4 years. Serum BDNF levels were divided into two categories by median value of serum BDNF level: < 21448.5 pg/mL (low BDNF), and > 21448.5 pg/mL (high BDNF). Cox model was used to analyze the relationship between baseline BDNF levels and the risk for MCI progression controlling for potential confounders. We also ran sensitivity analyses stratified by sex, age, education, apolipoprotein E ε4 (APOE4) positivity, and amyloid PET positivity.ResultDuring follow‐up, 24 participants developed MCI. Controlling for age, sex, education and APOE4 positivity, low BDNF group had significantly more frequent progression to MCI than high BDNF group (hazard ratio for MCI, 2.98; 95% CI, 1.17‐7.56; p=0.02) and these association persisted even after controlling for amyloid PET positivity and vascular risk factor score as additional covariates (hazard ratio, 2.98; 95% CI, 1.17‐7.55; p=0.02). Sensitivity analyses revealed that the associations were apparent only among women, participants aged younger than 75 years, those without college degrees, and amyloid negative participants (Table).ConclusionHigher serum BDNF levels may protect against future occurrence of MCI in cognitively healthy older adults. Such influence appears more prominent in women and younger, less educated, or amyloid PET negative individuals.
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来源期刊
Alzheimer's & Dementia
Alzheimer's & Dementia 医学-临床神经学
CiteScore
14.50
自引率
5.00%
发文量
299
审稿时长
3 months
期刊介绍: Alzheimer's & Dementia is a peer-reviewed journal that aims to bridge knowledge gaps in dementia research by covering the entire spectrum, from basic science to clinical trials to social and behavioral investigations. It provides a platform for rapid communication of new findings and ideas, optimal translation of research into practical applications, increasing knowledge across diverse disciplines for early detection, diagnosis, and intervention, and identifying promising new research directions. In July 2008, Alzheimer's & Dementia was accepted for indexing by MEDLINE, recognizing its scientific merit and contribution to Alzheimer's research.
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