From the Departments of Epidemiology (F.J.W., H.I.Z., S.L., L.G.M.C., M.K.I., M.W.V., M.A.I.), Neurology (F.J.W., M.K.I., P.J.K.), and Radiology (H.I.Z., L.G.M.C., M.W.V.), Erasmus Medical Center, Rotterdam, the Netherlands.
Neurology. 2019 Aug 27;93(9):e917-e926. doi: 10.1212/WNL.0000000000008003. Epub 2019 Jul 31.
To determine the long-term association of hemoglobin levels and anemia with risk of dementia, and explore underlying substrates on brain MRI in the general population.
Serum hemoglobin was measured in 12,305 participants without dementia of the population-based Rotterdam Study (mean age 64.6 years, 57.7% women). We determined risk of dementia and Alzheimer disease (AD) (until 2016) in relation to hemoglobin and anemia. Among 5,267 participants without dementia with brain MRI, we assessed hemoglobin in relation to vascular brain disease, structural connectivity, and global cerebral perfusion.
During a mean follow-up of 12.1 years, 1,520 individuals developed dementia, 1,194 of whom had AD. We observed a U-shaped association between hemoglobin levels and dementia ( = 0.005), such that both low and high hemoglobin levels were associated with increased dementia risk (hazard ratio [95% confidence interval (CI)], lowest vs middle quintile 1.29 [1.09-1.52]; highest vs middle quintile 1.20 [1.00-1.44]). Overall prevalence of anemia was 6.1%, and anemia was associated with a 34% increased risk of dementia (95% CI 11%-62%) and 41% (15%-74%) for AD. Among individuals without dementia with brain MRI, similar U-shaped associations were seen of hemoglobin with white matter hyperintensity volume ( = 0.03), and structural connectivity (for mean diffusivity, < 0.0001), but not with presence of cortical and lacunar infarcts. Cerebral microbleeds were more common with anemia. Hemoglobin levels inversely correlated to cerebral perfusion ( < 0.0001).
Low and high levels of hemoglobin are associated with an increased risk of dementia, including AD, which may relate to differences in white matter integrity and cerebral perfusion.
确定血红蛋白水平和贫血与痴呆风险的长期关联,并在一般人群中通过脑 MRI 探索潜在的脑内基础。
在人群为基础的鹿特丹研究中,我们测量了 12305 名无痴呆症参与者的血清血红蛋白(平均年龄 64.6 岁,57.7%为女性)。我们确定了血红蛋白和贫血与痴呆和阿尔茨海默病(AD)(截至 2016 年)的风险关系。在 5267 名无痴呆症且有脑 MRI 的参与者中,我们评估了血红蛋白与血管性脑疾病、结构连通性和全脑灌注之间的关系。
在平均 12.1 年的随访期间,1520 人发生了痴呆,其中 1194 人为 AD。我们观察到血红蛋白水平与痴呆之间存在 U 型关联( = 0.005),即低和高血红蛋白水平均与痴呆风险增加相关(风险比[95%置信区间(CI)],最低与中间五分位数相比为 1.29[1.09-1.52];最高与中间五分位数相比为 1.20[1.00-1.44])。总的贫血患病率为 6.1%,贫血与痴呆风险增加 34%相关(95%CI 11%-62%),与 AD 增加 41%相关(15%-74%)。在没有脑 MRI 的无痴呆症的参与者中,血红蛋白与脑白质高信号体积( = 0.03)和结构连通性(对于平均扩散系数,<0.0001)也存在类似的 U 型关联,但与皮质和腔隙性梗死的存在无关。贫血时脑微出血更常见。血红蛋白水平与脑灌注呈负相关(<0.0001)。
低和高血红蛋白水平与痴呆风险增加相关,包括 AD,这可能与脑白质完整性和脑灌注的差异有关。