Roberts Rosebud O, Christianson Teresa J H, Kremers Walter K, Mielke Michelle M, Machulda Mary M, Vassilaki Maria, Alhurani Rabe E, Geda Yonas E, Knopman David S, Petersen Ronald C
Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota2Department of Neurology, Mayo Clinic, Rochester, Minnesota.
Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
JAMA Neurol. 2016 Jan;73(1):93-101. doi: 10.1001/jamaneurol.2015.2952.
To increase the opportunity to delay or prevent mild cognitive impairment (MCI) or Alzheimer disease (AD) dementia, markers of early detection are essential. Olfactory impairment may be an important clinical marker and predictor of these conditions and may help identify persons at increased risk.
To examine associations of impaired olfaction with incident MCI subtypes and progression from MCI subtypes to AD dementia.
DESIGN, SETTING, AND PARTICIPANTS: Participants enrolled in the population-based, prospective Mayo Clinic Study of Aging between 2004 and 2010 were clinically evaluated at baseline and every 15 months through 2014. Participants (N = 1630) were classified as having normal cognition, MCI (amnestic MCI [aMCI] and nonamnestic MCI [naMCI]), and dementia. We administered the Brief Smell Identification Test (B-SIT) to assess olfactory function.
Mild cognitive impairment, AD dementia, and longitudinal change in cognitive performance measures.
Of the 1630 participants who were cognitively normal at the time of the smell test, 33 died before follow-up and 167 were lost to follow-up. Among the 1430 cognitively normal participants included, the mean (SD) age was 79.5 (5.3) years, 49.4% were men, the mean duration of education was 14.3 years, and 25.4% were APOE ε4 carriers. Over a mean 3.5 years of follow-up, there were 250 incident cases of MCI among 1430 cognitively normal participants. We observed an association between decreasing olfactory identification, as measured by a decrease in the number of correct responses in B-SIT score, and an increased risk of aMCI. Compared with the upper B-SIT quartile (quartile [Q] 4, best scores), hazard ratios (HRs) (95% CI) were 1.12 (0.65-1.92) for Q3 (P = .68); 1.95 (1.25-3.03) for Q2 (P = .003); and 2.18 (1.36-3.51) for Q1 (P = .001) (worst scores; P for trend <.001) after adjustment for sex and education, with age as the time scale. There was no association with naMCI. There were 64 incident dementia cases among 221 prevalent MCI cases. The B-SIT score also predicted progression from aMCI to AD dementia, with a significant dose-response with worsening B-SIT quartiles. Compared with Q4, HR (95% CI) estimates were 3.02 (1.06-8.57) for Q3 (P = .04); 3.63 (1.19-11.10) for Q2 (P = .02); and 5.20 (1.90-14.20) for Q1 (P = .001). After adjusting for key predictors of MCI risk, B-SIT (as a continuous measure) remained a significant predictor of MCI (HR, 1.10 [95% CI, 1.04-1.16]; P < .001) and improved the model concordance.
Olfactory impairment is associated with incident aMCI and progression from aMCI to AD dementia. These findings are consistent with previous studies that have reported associations of olfactory impairment with cognitive impairment in late life and suggest that olfactory tests have potential utility for screening for MCI and MCI that is likely to progress.
为增加延迟或预防轻度认知障碍(MCI)或阿尔茨海默病(AD)痴呆的机会,早期检测标志物至关重要。嗅觉障碍可能是这些疾病的重要临床标志物和预测指标,可能有助于识别风险增加的人群。
研究嗅觉障碍与新发MCI亚型以及从MCI亚型进展为AD痴呆之间的关联。
设计、地点和参与者:2004年至2010年参加基于人群的前瞻性梅奥诊所衰老研究的参与者在基线时以及到2014年每15个月进行一次临床评估。参与者(N = 1630)被分类为认知正常、MCI(遗忘型MCI [aMCI] 和非遗忘型MCI [naMCI])以及痴呆。我们采用简易嗅觉识别测试(B-SIT)评估嗅觉功能。
轻度认知障碍、AD痴呆以及认知表现测量指标的纵向变化。
在嗅觉测试时认知正常的1630名参与者中,33人在随访前死亡,167人失访。在纳入的1430名认知正常参与者中,平均(标准差)年龄为79.5(5.3)岁,49.4%为男性,平均受教育年限为14.3年,25.4%为APOE ε4携带者。在平均3.5年的随访中,1430名认知正常参与者中有250例新发MCI病例。我们观察到,通过B-SIT评分中正确反应数量减少来衡量的嗅觉识别能力下降与aMCI风险增加之间存在关联。与B-SIT四分位数的上四分位数(四分位数 [Q] 4,最佳分数)相比,在按年龄作为时间尺度对性别和教育进行调整后,Q3的风险比(HR)(95% CI)为1.12(0.65 - 1.92)(P = 0.68);Q2为1.95(1.25 - 3.03)(P = 0.003);Q1为2.18(1.36 - 3.51)(P = 0.001)(最差分数;趋势P < 0.001)。与naMCI无关联。在221例现患MCI病例中有64例新发痴呆病例。B-SIT评分还可预测从aMCI进展为AD痴呆,且随着B-SIT四分位数变差存在显著的剂量反应关系。与Q4相比,Q3的HR(95% CI)估计值为3.02(1.06 - 8.57)(P = 0.04);Q2为3.63(1.19 - 11.10)(P = 0.02);Q1为5.20(1.90 - 14.20)(P = 0.001)。在对MCI风险的关键预测因素进行调整后,B-SIT(作为连续测量指标)仍然是MCI的显著预测指标(HR,1.10 [95% CI,1.04 - 1.16];P < 0.001),并改善了模型一致性。
嗅觉障碍与新发aMCI以及从aMCI进展为AD痴呆相关。这些发现与先前报道嗅觉障碍与晚年认知障碍之间关联的研究一致,并表明嗅觉测试在筛查MCI以及可能进展的MCI方面具有潜在效用。