Division of Epidemiology and Community Health, University of Minnesota School of Public Health, Minneapolis, MN, USA.
Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
J Alzheimers Dis. 2023;92(1):229-239. doi: 10.3233/JAD-220765.
Reduced kidney function is related to brain atrophy and higher risk of dementia. It is not known whether kidney impairment is associated with higher levels of circulating amyloid-β and brain amyloid-β deposition, which could contribute to elevated risk of dementia.
To investigate whether kidney impairment is associated with higher levels of circulating amyloid-β and brain amyloid-β deposition.
This cross-sectional study was performed within the community-based Atherosclerosis Risk in Communities (ARIC) Study cohort. We used estimated glomerular filtration rate (eGFR) based on serum creatinine and cystatin C levels and urine albumin-to-creatinine ratio (ACR) to assess kidney function. Amyloid positivity was defined as a standardized uptake value ratios > 1.2 measured with florbetapir positron emission tomography (PET) (n = 340). Plasma amyloid-β1 - 40 and amyloid-β1 - 42 were measured using a fluorimetric bead-based immunoassay (n = 2,569).
Independent of demographic and cardiovascular risk factors, a doubling of ACR was associated with 1.10 (95% CI: 1.01,1.20) higher odds of brain amyloid positivity, but not eGFR (odds ratio per 15 ml/min/1.73 m2 lower eGFR: 1.08; 95% CI: 0.95,1.23). A doubling of ACR was associated with a higher level of plasma amyloid-β1 - 40 (standardized difference: 0.12; 95% CI: 0.09,0.14) and higher plasma amyloid-β1 - 42 (0.08; 95% CI: 0.05,0.10). Lower eGFR was associated with higher plasma amyloid-β1 - 40 (0.36; 95% CI: 0.33,0.39) and higher amyloid-β1 - 42 (0.32; 95% CI: 0.29,0.35).
Low clearance of amyloid-β and elevated brain amyloid positivity may link impaired kidney function with elevated risk of dementia. kidney function should be considered in interpreting amyloid biomarker results in clinical and research setting.
肾功能下降与脑萎缩和更高的痴呆风险相关。目前尚不清楚肾脏损伤是否与循环中的淀粉样蛋白-β水平升高和脑内淀粉样蛋白-β沉积相关,而后者可能导致痴呆风险升高。
旨在探究肾脏损伤是否与循环中的淀粉样蛋白-β水平升高和脑内淀粉样蛋白-β沉积相关。
本横断面研究在基于社区的动脉粥样硬化风险研究(ARIC)队列中进行。我们使用基于血清肌酐和胱抑素 C 水平以及尿白蛋白与肌酐比值(ACR)的估算肾小球滤过率(eGFR)来评估肾功能。淀粉样蛋白阳性定义为氟-18 标记的正电子发射断层扫描(PET)示标准化摄取值比(SUVr)>1.2(n=340)。使用荧光微珠免疫分析测定血浆淀粉样蛋白β1-40 和淀粉样蛋白β1-42(n=2569)。
独立于人口统计学和心血管危险因素,ACR 加倍与脑淀粉样蛋白阳性的比值比增加 1.10(95%CI:1.01,1.20)相关,但与 eGFR 无关(每降低 15ml/min/1.73m2 的 eGFR,比值比为 1.08;95%CI:0.95,1.23)。ACR 加倍与血浆淀粉样蛋白β1-40 水平升高(标准化差值:0.12;95%CI:0.09,0.14)和血浆淀粉样蛋白β1-42 水平升高(0.08;95%CI:0.05,0.10)相关。eGFR 降低与血浆淀粉样蛋白β1-40 水平升高(0.36;95%CI:0.33,0.39)和淀粉样蛋白β1-42 水平升高(0.32;95%CI:0.29,0.35)相关。
淀粉样蛋白清除率降低和脑内淀粉样蛋白阳性率升高可能将肾功能受损与痴呆风险升高联系起来。在临床和研究环境中解释淀粉样蛋白生物标志物结果时,应考虑肾脏功能。