Schneider A L C, Lutsey P L, Alonso A, Gottesman R F, Sharrett A R, Carson K A, Gross M, Post W S, Knopman D S, Mosley T H, Michos E D
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Eur J Neurol. 2014 Sep;21(9):1211-8, e69-70. doi: 10.1111/ene.12460. Epub 2014 May 21.
Some recent studies in older, largely white populations suggest that vitamin D, measured by 25-hydroxyvitamin D [25(OH)D], is important for cognition, but such results may be affected by reverse causation. Measuring 25(OH)D in late middle age before poor cognition affects behavior may provide clearer results.
This was a prospective cohort analysis of 1652 participants (52% white, 48% black) in the Atherosclerosis Risk in Communities (ARIC) Brain MRI Study. 25(OH)D was measured from serum collected in 1993-1995. Cognition was measured by the delayed word recall test (DWRT), the digit symbol substitution test (DSST) and the word fluency test (WFT). Dementia hospitalization was defined by ICD-9 codes. Adjusted linear, logistic and Cox proportional hazards models were used.
Mean age of participants was 62 years and 60% were female. Mean 25(OH)D was higher in whites than blacks (25.5 vs. 17.3 ng/ml, P < 0.001). Lower 25(OH)D was not associated with lower baseline scores or with greater DWRT, DSST or WFT decline over a median of 3 or 10 years of follow-up (P > 0.05). Over a median of 16.6 years, there were 145 incident hospitalized dementia cases. Although not statistically significant, lower levels of 25(OH)D were suggestive of an association with increased dementia risk [hazard ratio for lowest versus highest race-specific tertile: whites 1.32 (95% confidence interval 0.69, 2.55); blacks 1.53 (95% confidence interval 0.84, 2.79)].
In contrast to prior studies performed in older white populations, our study of late middle age white and black participants did not find significant associations between lower levels of 25(OH)D with lower cognitive test scores at baseline, change in scores over time or dementia risk.
近期针对老年人群(主要为白人)的一些研究表明,通过25-羟基维生素D[25(OH)D]检测的维生素D对认知功能很重要,但此类结果可能受到反向因果关系的影响。在认知功能变差影响行为之前的中年后期测量25(OH)D,可能会得出更清晰的结果。
这是一项对社区动脉粥样硬化风险(ARIC)脑磁共振成像研究中1652名参与者(52%为白人,48%为黑人)进行的前瞻性队列分析。1993 - 1995年采集的血清样本用于检测25(OH)D。认知功能通过延迟单词回忆测试(DWRT)、数字符号替换测试(DSST)和单词流畅性测试(WFT)进行测量。痴呆症住院情况根据国际疾病分类第九版(ICD - 9)编码确定。使用了调整后的线性、逻辑和Cox比例风险模型。
参与者的平均年龄为62岁,60%为女性。白人的平均25(OH)D水平高于黑人(25.5对17.3 ng/ml,P < 0.001)。在中位随访3年或10年期间,较低的25(OH)D水平与较低的基线分数或DWRT、DSST或WFT的更大下降无关(P > 0.05)。在中位16.6年的时间里,有145例新发痴呆症住院病例。虽然无统计学意义,但较低的25(OH)D水平提示与痴呆症风险增加有关[最低与最高种族特异性三分位数的风险比:白人1.32(95%置信区间0.69,2.55);黑人1.53(95%置信区间0.84,2.79)]。
与之前针对老年白人人群的研究不同,我们对中年后期白人和黑人参与者的研究未发现较低水平的25(OH)D与基线认知测试分数较低、分数随时间变化或痴呆症风险之间存在显著关联。