Lilamand Matthieu, Bouaziz-Amar Elodie, Dumurgier Julien, Cognat Emmanuel, Hourregue Claire, Mouton-Liger François, Sanchez Manuel, Troussière Anne-Cécile, Martinet Matthieu, Hugon Jacques, Paquet Claire
Université Paris Cité, INSERM Unit UMR S-1144, Paris, France.
Department of Geriatrics, Lariboisière-Fernand Widal Hospital GHU AP-HP.Nord, Paris, France.
J Gerontol A Biol Sci Med Sci. 2023 Mar 30;78(4):645-652. doi: 10.1093/gerona/glac234.
Metabolic dysfunction and dysregulation of leptin signaling have been linked to Alzheimer's disease (AD)'s pathophysiology. The objectives of this study were to examine the associations between plasma leptin, cerebrospinal fluid (CSF), beta-amyloid (Aβ), and tau biomarkers (AT[N] status) and with the stage of cognitive impairment.
Cross-sectional analysis of data from cognitively impaired patients from a tertiary memory clinic. Plasma leptin levels were compared according to the stage of cognitive impairment and biomarker profiles, using the AT(N) classification. Linear regression models were performed to examine the relationship between leptin and CSF biomarkers. Results were adjusted for age, gender, body mass index (BMI), and APOE ε4. In a subgroup of A+T+ individuals, we compared the 2-year evolution of Mini-Mental State Examination scores, according to the participants' tertile of plasma leptin levels.
We included 1 036 participants (age 68.7 ± 9.1, females = 54.1%). A+T+ and A+T- patients had significantly lower plasma leptin levels than amyloid negative participants (p < .01). CSF Aβ concentration was significantly associated with lower plasma leptin β = -4.3 (1.5), p = .005 unadjusted; and β = -3.4 (1.6), p = .03 after adjustment for age, female gender, BMI, and APOE ε4. Patients with major neurocognitive disorder due to AD had a difference of leptin of -7.3 ng/mL 95% confidence interval (CI; -11.8; -2.8), p = .0002, compared to individuals with other causes of cognitive impairment. Leptin was not associated with the slope of cognitive decline.
Plasma leptin levels were associated with CSF Aβ and with the diagnosis of AD confirmed by CSF biomarkers, suggesting a molecular interplay between leptin metabolism and brain amyloid deposition.
代谢功能障碍和瘦素信号失调与阿尔茨海默病(AD)的病理生理学有关。本研究的目的是探讨血浆瘦素、脑脊液(CSF)、β-淀粉样蛋白(Aβ)和tau生物标志物(AT[N]状态)之间的关联以及与认知障碍阶段的关系。
对来自三级记忆诊所的认知障碍患者的数据进行横断面分析。根据认知障碍阶段和生物标志物谱,使用AT(N)分类比较血浆瘦素水平。进行线性回归模型以检查瘦素与脑脊液生物标志物之间的关系。结果针对年龄、性别、体重指数(BMI)和APOE ε4进行了调整。在A+T+个体亚组中,我们根据参与者血浆瘦素水平的三分位数比较了简易精神状态检查分数的2年变化情况。
我们纳入了1036名参与者(年龄68.7±9.1岁,女性占54.1%)。A+T+和A+T-患者的血浆瘦素水平显著低于淀粉样蛋白阴性参与者(p<.01)。脑脊液Aβ浓度与较低的血浆瘦素显著相关,未调整时β=-4.3(1.5),p=.005;在调整年龄、女性性别、BMI和APOE ε4后,β=-3.4(1.6),p=.03。与其他认知障碍原因的个体相比,因AD导致的重度神经认知障碍患者的瘦素差异为-7.3 ng/mL,95%置信区间(CI;-11.8;-2.8),p=.0002。瘦素与认知衰退斜率无关。
血浆瘦素水平与脑脊液Aβ以及脑脊液生物标志物确诊的AD诊断相关,提示瘦素代谢与脑淀粉样蛋白沉积之间存在分子相互作用。