Burke Shanna L, Hu Tianyan, Fava Nicole M, Li Tan, Rodriguez Miriam J, Schuldiner Katie L, Burgess Aaron, Laird Angela
a Robert Stempel College of Public Health & Social Work , School of Social Work, Florida International University , Miami , Florida , USA.
b Department of Health Policy and Management, Robert Stempel College of Public Health & Social Work , Florida International University , Miami , Florida , USA.
J Women Aging. 2019 Mar-Apr;31(2):140-164. doi: 10.1080/08952841.2018.1419476. Epub 2018 Jan 10.
This study examined biological sex differences in the development of mild cognitive impairment (MCI) and probable Alzheimer's disease (AD) development as predicted by changes in the hippocampus or white matter hyperintensities. A secondary data analysis of the National Alzheimer's Coordinating Center Uniform Data Set was conducted. We selected samples of participants with normal cognition at baseline who progressed to MCI (n = 483) and those who progressed to probable AD (n = 211) to determine if hippocampal volume or white matter hyperintensities (WMH) at baseline predicted progression to probable AD or MCI and whether the rate of progression differed between men and women. The survival analyses indicated that changes in hippocampal volumes affected the progression to probable AD (HR = 0.535, 95% CI [0.300-0.953]) only among women. White men had an increased rate of progression to AD (HR = 4.396, CI [1.012-19.08]; HR = 4.665, 95% CI [1.072-20.29]) compared to men in other race and ethnic groups. Among women, increases in hippocampal volume ratio led to decreased rates of progressing to MCI (HR = 0.386, 95% CI [0.166-0.901]). Increased WMH among men led to faster progression to MCI (HR = 1.048. 95% CI [1.011-1.086]). Women and men who were older at baseline were more likely to progress to MCI. In addition, results from longitudinal analyses showed that women with a higher CDR global score, older age at baseline, or more disinhibition symptoms experienced higher odds of MCI development. Changes in hippocampal volumes affect the progression to or odds of probable AD (and MCI) more so among women than men, while changes in WMH affected the progression to MCI only among men.
本研究通过海马体或白质高信号的变化来预测轻度认知障碍(MCI)的发展以及可能的阿尔茨海默病(AD)的发展过程中的生物性别差异。对国家阿尔茨海默病协调中心统一数据集进行了二次数据分析。我们选取了基线时认知正常且进展为MCI的参与者样本(n = 483)以及进展为可能的AD的参与者样本(n = 211),以确定基线时的海马体体积或白质高信号(WMH)是否能预测进展为可能的AD或MCI,以及男女之间的进展速度是否存在差异。生存分析表明,海马体体积的变化仅在女性中影响进展为可能的AD(风险比[HR]=0.535,95%置信区间[CI][0.300 - 0.953])。与其他种族和族裔群体的男性相比,白人男性进展为AD的速度更快(HR = 4.396,CI[1.012 - 19.08];HR = 4.665,95%CI[1.072 - 20.29])。在女性中,海马体体积比的增加导致进展为MCI的速度降低(HR = 0.386,95%CI[0.166 - 0.901])。男性中WMH增加导致进展为MCI的速度更快(HR = 1.048,95%CI[1.011 - 1.086])。基线时年龄较大的女性和男性更有可能进展为MCI。此外,纵向分析结果表明,临床痴呆评定量表(CDR)总体评分较高、基线年龄较大或存在更多去抑制症状的女性发生MCI的几率更高。海马体体积的变化对女性进展为可能的AD(和MCI)的影响比对男性更大,而WMH的变化仅在男性中影响进展为MCI。