Laboratory of Epidemiology and Population Sciences, NIA/NIH/IRP, Baltimore, MD, USA.
Department of Psychology, University of Maryland, Baltimore County, Catonsville, MD, USA.
J Alzheimers Dis. 2021;81(2):711-727. doi: 10.3233/JAD-201386.
Anemia and red cell distribution width (RDW) have been linked to poor cognitive performance, pending studies of underlying mechanisms.
We examined cross-sectional relationships of initial RDW status (v1), RDW change (δ), and anemia with brain structural magnetic resonance imaging (sMRI) markers, including global and cortical brain and hippocampal and white matter lesion (WML) volumes, 5-6 years later.
Data were used from three prospective visits within the Healthy Aging in Neighborhoods of Diversity Across the Life Span (HANDLS) study with complete v1 (2004-2009) and v2 (2009-2013) exposures and ancillary sMRI data at vscan (2011-2015, n = 213, mean v1 to vscan time: 5.7 years). Multivariable-adjusted linear regression models were conducted, overall, by sex, by race, and within non-anemics, correcting for multiple testing with q-values.
In minimally adjusted models (socio-demographics and follow-up time), anemiav1 and RDWv1 were consistently associated with smaller bilateral hippocampal volumes overall, and among females (q < 0.05), without significant sex differences. RDWv1 was related to smaller select regional cortical brain gray and white matter volumes in hematological measure-adjusted models; anemiav1 was associated with larger WML volumes only among whites.
In summary, baseline anemia and RDW were consistently associated with smaller bilateral hippocampal volumes, particularly among females, while anemia was linked to larger WML volume among Whites. In hematological measure-adjusted models, baseline RDW was linked to smaller regional gray and white matter volumes. Pending studies with sMRI repeats, randomized controlled trials are needed, demonstrating associations of anemia and elevated RDW with reduced brain volumes and cognitive dysfunction.
贫血和红细胞分布宽度(RDW)与认知表现不佳有关,但目前仍在研究其潜在机制。
我们研究了初始 RDW 状态(v1)、RDW 变化(δ)和贫血与脑结构磁共振成像(sMRI)标志物之间的横断面关系,这些标志物包括大脑的整体和皮质以及海马和白质病变(WML)体积,这些标志物是在 5-6 年后测量的。
我们使用了来自多样性社区中跨生命周期健康老龄化研究(HANDLS)中的三个前瞻性随访的数据,这些数据包括完整的 v1(2004-2009 年)和 v2(2009-2013 年)暴露情况以及 vscan 时的辅助 sMRI 数据(2011-2015 年,n=213,v1 到 vscan 的平均时间:5.7 年)。采用多变量调整线性回归模型,总体上按性别、种族进行分析,并在非贫血者中进行分析,使用 q 值进行多重检验校正。
在最小调整模型(社会人口统计学和随访时间)中,贫血 v1 和 RDWv1 总体上与双侧海马体体积较小相关,且在女性中更为显著(q<0.05),而性别间无显著差异。RDWv1 与血液学指标调整后的特定皮质脑灰质和白质体积较小相关;贫血 v1 仅与白人的 WML 体积较大相关。
总之,基线贫血和 RDW 与双侧海马体体积较小相关,尤其是在女性中,而贫血与白人中 WML 体积较大相关。在血液学指标调整后的模型中,基线 RDW 与特定的灰质和白质体积较小相关。需要进行 sMRI 重复研究和随机对照试验,以证明贫血和 RDW 升高与脑体积减少和认知功能障碍相关。