Murray Anne M, Bell Elizabeth J, Tupper David E, Davey Cynthia S, Pederson Sarah L, Amiot Elizabeth M, Miley Kathleen M, McPherson Lauren, Heubner Brooke M, Gilbertson David T, Foley Robert N, Drawz Paul E, Slinin Yelena, Rossom Rebecca C, Lakshminarayan Kamakshi, Vemuri Prashanthi, Jack Clifford R, Knopman David S
Berman Center for Clinical Research, Minneapolis Medical Research Foundation, Minneapolis, MN; Geriatrics Division, Hennepin County Medical Center, Minneapolis, MN.
Berman Center for Clinical Research, Minneapolis Medical Research Foundation, Minneapolis, MN.
Am J Kidney Dis. 2016 Apr;67(4):593-600. doi: 10.1053/j.ajkd.2015.11.008. Epub 2015 Dec 29.
The Brain in Kidney Disease (BRINK) Study aims to identify mechanisms that contribute to increased risk for cognitive impairment in patients with chronic kidney disease (CKD). We describe the rationale, design, and methods of the study and report baseline recruitment and cognitive function results.
Longitudinal observational cohort study of the epidemiology of cognitive impairment in CKD. The primary aim is to characterize the association between (1) baseline and incident stroke, white matter disease, estimated glomerular filtration rate (eGFR), inflammation, microalbuminuria, and dialysis initiation and (2) cognitive decline over 3 years in a CKD cohort with a mean eGFR<45 mL/min/1.73 m(2).
SETTING & PARTICIPANTS: Community-dwelling participants 45 years or older recruited from 4 health systems into 2 groups: reduced eGFR, defined as eGFR<60 mL/min/1.73 m(2) (non-dialysis dependent), and control, defined as eGFR≥60 mL/min/1.73 m(2).
eGFR group.
Performance on cognitive function tests and structural brain magnetic resonance imaging.
Sequential cognitive and physical function testing, serum and urine biomarker measurement, and brain magnetic resonance images over 3 years.
Of 554 participants, mean age was 69.3 years; 333, 88, and 133 had eGFRs<45 (non-dialysis dependent, nontransplantation), 45 to <60, and ≥60 (controls) mL/min/1.73 m(2), respectively. Mean eGFR in reduced-eGFR participants was 34.3 mL/min/1.73 m(2). Baseline cognitive performance was significantly associated with eGFR in all domains except language. Participants with eGFRs<30 mL/min/1.73 m(2) performed significantly worse than those with eGFRs≥30 mL/min/1.73 m(2) on tests of memory, processing speed, and executive function. Participants with reduced eGFRs overall scored worst on the Immediate Brief Visual-Spatial Memory Test-Revised.
Healthy cohort bias, competing risk for death versus cognitive decline.
Cognitive function was significantly worse in participants with eGFRs<30 mL/min/1.73 m(2). Future BRINK analyses will measure risk factors for cognitive decline using the longitudinal data.
“肾脏疾病中的大脑(BRINK)研究”旨在确定导致慢性肾脏病(CKD)患者认知障碍风险增加的机制。我们描述了该研究的基本原理、设计和方法,并报告了基线招募情况和认知功能结果。
对CKD患者认知障碍流行病学的纵向观察性队列研究。主要目的是描述(1)基线和新发中风、白质疾病、估计肾小球滤过率(eGFR)、炎症、微量白蛋白尿及开始透析之间的关联,以及(2)在平均eGFR<45 mL/min/1.73 m²的CKD队列中3年期间的认知衰退情况。
从4个医疗系统招募年龄在45岁及以上的社区居住参与者,分为2组:eGFR降低组,定义为eGFR<60 mL/min/1.73 m²(非透析依赖),以及对照组,定义为eGFR≥60 mL/min/1.73 m²。
eGFR组。
认知功能测试表现及脑部结构磁共振成像。
3年期间的序贯认知和身体功能测试、血清和尿液生物标志物测量以及脑部磁共振成像。
554名参与者的平均年龄为69.3岁;333人、88人和133人的eGFR分别<45(非透析依赖、非移植)、45至<60以及≥60(对照组)mL/min/1.73 m²。eGFR降低组参与者的平均eGFR为34.3 mL/min/1.73 m²。除语言领域外,所有领域的基线认知表现均与eGFR显著相关。在记忆、处理速度和执行功能测试中,eGFR<30 mL/min/1.73 m²的参与者表现明显比eGFR≥30 mL/min/1.73 m²的参与者差。总体而言,eGFR降低的参与者在即时简短视觉空间记忆测试修订版中的得分最差。
健康队列偏倚、死亡与认知衰退的竞争风险。
eGFR<30 mL/min/1.73 m²的参与者认知功能明显更差。未来BRINK分析将使用纵向数据测量认知衰退的风险因素。