Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD.
Diabetes Care. 2019 Jul;42(7):1248-1254. doi: 10.2337/dc19-0120. Epub 2019 May 21.
We sought to examine associations in older adults among diabetes, glycemic control, diabetes duration, and biomarkers of hyperglycemia with incident mild cognitive impairment (MCI) and incident dementia.
We conducted a prospective analysis of 5,099 participants from the Atherosclerosis Risk in Communities (ARIC) Study who attended the fifth (2011-2013) exam. Cognitive status was assessed during follow-up via telephone calls, death certificate codes, surveillance, and a follow-up examination (2016-2017). We defined incident cognitive impairment as incident MCI or incident dementia in persons dementia-free at the index examination; we also examined each outcome separately. Diabetes was defined using self-report, medications, or HbA ≥6.5%; poor glycemic control in persons with diabetes was defined as HbA ≥7%. We examined the following biomarkers of hyperglycemia: HbA, fructosamine, glycated albumin, and 1,5-anhydroglucitol.
Mean age at baseline was 76 years, 59% were female, and 21% were black. Diabetes (hazard ratio [HR] 1.14 [95% CI 1.00, 1.31]), poor glycemic control in persons with diabetes (HR 1.31 [95% CI 1.05, 1.63]), and longer diabetes duration (≥5 vs. <5 years; HR 1.59 [95% CI 1.23, 2.07]) were significantly associated with incident cognitive impairment. We found a J-shaped association between HbA and incident dementia. Glycated albumin and fructosamine were also associated with incident dementia, independently of HbA. HbA and fructosamine were also associated with incident MCI.
Diabetes status, poor glycemic control, and longer diabetes duration were associated with worse cognitive outcomes over a median follow-up of 5 years.
我们旨在研究老年人中糖尿病、血糖控制、糖尿病病程以及高血糖生物标志物与轻度认知障碍(MCI)和痴呆症发病的相关性。
我们对参加动脉粥样硬化风险社区研究(ARIC)的 5099 名参与者进行了前瞻性分析,这些参与者参加了第五次(2011-2013 年)检查。在随访期间,通过电话、死亡证明代码、监测和后续检查(2016-2017 年)来评估认知状况。我们将认知障碍的发病定义为在基线检查时无痴呆症的患者发生 MCI 或痴呆症;我们还分别检查了每种结果。糖尿病通过自我报告、药物或 HbA ≥6.5%来定义;糖尿病患者血糖控制不佳定义为 HbA ≥7%。我们检查了以下高血糖生物标志物:HbA、果糖胺、糖化白蛋白和 1,5-脱水葡萄糖醇。
基线时的平均年龄为 76 岁,59%为女性,21%为黑人。糖尿病(危险比 [HR] 1.14 [95%CI 1.00, 1.31])、糖尿病患者血糖控制不佳(HR 1.31 [95%CI 1.05, 1.63])和较长的糖尿病病程(≥5 年与<5 年;HR 1.59 [95%CI 1.23, 2.07])与认知障碍发病显著相关。我们发现 HbA 与痴呆症发病之间存在 J 形关联。糖化白蛋白和果糖胺与 HbA 独立相关,也与痴呆症发病相关。HbA 和果糖胺也与 MCI 发病相关。
在中位数为 5 年的随访中,糖尿病状态、血糖控制不佳和较长的糖尿病病程与认知结局恶化相关。