Slinin Yelena, Peters Katherine W, Ishani Areef, Yaffe Kristine, Fink Howard A, Stone Katie L, Steffes Michael, Ensrud Kristine E
Department of Medicine, University of Minnesota, Minneapolis. Department of Medicine, Minneapolis VA Health Care System, Minnesota.
California Pacific Medical Center Research Institute, San Francisco.
J Gerontol A Biol Sci Med Sci. 2015 Jun;70(6):771-8. doi: 10.1093/gerona/glu189. Epub 2014 Nov 1.
Results of prospective studies examining the association between cystatin C and incident cognitive impairment have been inconsistent. We tested the hypothesis that there is a U-shaped association in older women between cystatin C and risk of incident cognitive impairment 10 years later.
We conducted a longitudinal analysis of a prospective cohort of 1,332 community-dwelling elderly women without dementia at baseline who had baseline cystatin C and serum creatinine measurements and completed an extended cognitive battery of neuropsychological tests with determination of cognitive status 10 years later. Incident cognitive impairment was defined as either new onset of adjudicated diagnosis of mild cognitive impairment or dementia.
Incident mild cognitive impairment or dementia was identified among 140 (26.0%) women in quartile 1 (Q1), 122 (22.6%) in Q2, 121 (22.5%) in Q3, and 156 (28.9%) in Q4 of cystatin C. In the fully adjusted model, compared to women in Q2-Q3 of cystatin C, adjusted odds ratios (95% CI) for incident cognitive impairment were 1.31 (0.98-1.75) for Q1, and 1.25 (0.94-1.66) for Q4 Compared to women in Q2-Q3 of estimated glomerular filtration rate (eGFRCysC), adjusted odds ratios (95% CI) for incident cognitive impairment after 10 years of follow-up were 1.18 (0.88-1.58) for Q4 (eGFRCysC 76.1-109.4mL/min/1.73 m(2)) and 1.26 (0.94-1.67) for Q1 (eGFRCysC 21.8-55.5mL/min/1.73 m(2)).
These results support a U-shaped association between cystatin C concentration and risk of cognitive impairment or dementia 10 years later, but the association is not independent of potential confounding factors.
关于胱抑素C与新发认知障碍之间关联的前瞻性研究结果并不一致。我们检验了这样一个假设,即老年女性中胱抑素C与10年后新发认知障碍风险之间存在U型关联。
我们对一个前瞻性队列进行了纵向分析,该队列由1332名社区居住的老年女性组成,她们在基线时无痴呆,有基线胱抑素C和血清肌酐测量值,并完成了一套扩展的认知神经心理测试电池,10年后确定认知状态。新发认知障碍定义为经判定诊断为轻度认知障碍或痴呆的新发病例。
在胱抑素C四分位数第1组(Q1)的140名(26.0%)女性、第2组的122名(22.6%)、第3组的121名(22.5%)和第4组的156名(28.9%)女性中发现了新发轻度认知障碍或痴呆。在完全调整模型中,与胱抑素C第2 - 3组的女性相比,第1组新发认知障碍的调整优势比(95%可信区间)为1.31(0.98 - 1.75),第4组为1.25(0.94 - 1.66)。与估计肾小球滤过率(eGFRCysC)第2 - 3组的女性相比,随访10年后新发认知障碍的调整优势比(95%可信区间),第4组(eGFRCysC 76.1 - 109.4mL/min/1.73m²)为1.18(0.88 - 1.58),第1组(eGFRCysC 21.8 - 55.5mL/min/1.73m²)为1.26(0.94 - 1.67)。
这些结果支持胱抑素C浓度与10年后认知障碍或痴呆风险之间存在U型关联,但该关联并非独立于潜在混杂因素。