Weng Shuo-Chun, Shu Kuo-Hsiung, Tang Yih-Jing, Sheu Wayne Huey-Herng, Tarng Der-Cherng, Wu Ming-Ju, Chen Yi-Ming, Chuang Ya-Wen
Center of Geriatrics and Gerontology, Taichung Veterans General Hospital, Taiwan.
Intern Med. 2012;51(1):29-35. doi: 10.2169/internalmedicine.51.5975. Epub 2012 Jan 1.
A strong positive correlation between estimated glomerular filtration rate (eGFR) multiplied by follow-up time and memory function has been demonstrated previously. The purpose of this study was to investigate the factors affecting progression of cognitive dysfunction in the elderly with different levels of kidney function.
In April 2002, a prospective study on progression of cognitive function was conducted on 356 elderly people. All participants received a comprehensive geriatric assessment, serum biochemical test, homeostasis model assessment (HOMA), and a genetic polymorphism study, including polymorphism of apolipoprotein E (APOE), Cystatin, C-reactive protein (CRP) and tumor necrosis factor (TNF). Lean body mass-adjusted eGFR was used to evaluate severity of chronic kidney disease (CKD), and a clinical dementia rating scale was used to assess cognitive dysfunction. Patients were stratified according to eGFR (≥49 mL/min and <49 mL/min).
Using multivariate logistic regression models, older age (OR=1.27, 95% CI=1.00-1.61) was associated with a high risk for progression of cognitive function in patients with a relatively low eGFR. In patients with lower eGFR, higher mini-mental state examination (MMSE) scores (OR=0.23, 95% CI=0.10-0.54) were correlated with a low risk for progression of cognition, while in patients with higher eGFR, higher MMSE scores (OR=0.39, 95% CI=0.23-0.65) were less correlated with cognitive dysfunction. However, elevated serum plasminogen activator inhibitor-1 (PA1-1) was associated with a high risk for cognitive dysfunction (OR=1.06, 95% CI=1.01-1.11) in patients with a better eGFR.
Age, MMSE score and serum PAI-1 were found to be factors that predicted cognitive dysfunction at different functional levels of CKD.
先前已证明估算肾小球滤过率(eGFR)乘以随访时间与记忆功能之间存在强正相关。本研究的目的是调查影响不同肾功能水平老年人认知功能障碍进展的因素。
2002年4月,对356名老年人进行了认知功能进展的前瞻性研究。所有参与者均接受了全面的老年评估、血清生化检查、稳态模型评估(HOMA)以及基因多态性研究,包括载脂蛋白E(APOE)、胱抑素、C反应蛋白(CRP)和肿瘤坏死因子(TNF)的多态性。采用瘦体重校正的eGFR评估慢性肾脏病(CKD)的严重程度,并用临床痴呆评定量表评估认知功能障碍。患者根据eGFR(≥49 mL/分钟和<49 mL/分钟)进行分层。
使用多因素逻辑回归模型,年龄较大(OR=1.27,95%CI=1.00-1.61)与eGFR相对较低的患者认知功能进展的高风险相关。在eGFR较低的患者中,较高的简易精神状态检查表(MMSE)评分(OR=0.23,95%CI=0.10-0.54)与认知进展的低风险相关,而在eGFR较高的患者中,较高的MMSE评分(OR=0.39,95%CI=0.23-0.65)与认知功能障碍的相关性较小。然而,血清纤溶酶原激活物抑制剂-1(PAI-1)升高与eGFR较好的患者发生认知功能障碍的高风险相关(OR=1.06,95%CI=1.01-1.11)。
年龄、MMSE评分和血清PAI-1是预测CKD不同功能水平下认知功能障碍的因素。