Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.
Welch Center for Prevention, Epidemiology, and Clinical Research, Johns Hopkins University, Baltimore, MD, USA.
Diabetologia. 2023 Aug;66(8):1442-1449. doi: 10.1007/s00125-023-05930-7. Epub 2023 May 24.
AIMS/HYPOTHESIS: The aim of this work was to evaluate whether the association of prediabetes with dementia is explained by the intervening onset of diabetes.
Among participants of the Atherosclerosis Risk in Communities (ARIC) study we defined baseline prediabetes as HbA 39-46 mmol/mol (5.7-6.4%) and subsequent incident diabetes as a self-reported physician diagnosis or use of diabetes medication. Incident dementia was ascertained via active surveillance and adjudicated. We quantified the association of prediabetes with dementia risk before and after accounting for the subsequent development of diabetes among ARIC participants without diabetes at baseline (1990-1992; participants aged 46-70 years). We also evaluated whether age at diabetes diagnosis modified the risk of dementia.
Among 11,656 participants without diabetes at baseline, 2330 (20.0%) had prediabetes. Before accounting for incident diabetes, prediabetes was significantly associated with the risk of dementia (HR 1.12 [95% CI 1.01, 1.24]). After accounting for incident diabetes, the association was attenuated and non-significant (HR 1.05 [95% CI 0.94, 1.16]). Earlier age of onset of diabetes had the strongest association with dementia: HR 2.92 (95% CI 2.06, 4.14) for onset before 60 years; HR 1.73 (95% CI 1.47, 2.04) for onset at 60-69 years; and HR 1.23 (95% CI 1.08, 1.40) for onset at 70-79 years.
CONCLUSIONS/INTERPRETATION: Prediabetes is associated with dementia risk but this risk is explained by the subsequent development of diabetes. Earlier age of onset of diabetes substantially increases dementia risk. Preventing or delaying progression of prediabetes to diabetes will reduce dementia burden.
目的/假设:本研究旨在评估糖尿病前期与痴呆之间的关联是否可以用糖尿病的发生来解释。
在动脉粥样硬化风险社区(ARIC)研究的参与者中,我们将基线时的糖尿病前期定义为 HbA 39-46mmol/mol(5.7-6.4%),随后发生的糖尿病定义为自我报告的医生诊断或使用糖尿病药物。通过主动监测和裁决确定痴呆的发病情况。我们量化了在 ARIC 研究中没有基线糖尿病(1990-1992 年;年龄 46-70 岁)的参与者中,在考虑到随后发生的糖尿病后,糖尿病前期与痴呆风险的关联。我们还评估了糖尿病诊断年龄是否改变了痴呆的风险。
在基线时没有糖尿病的 11656 名参与者中,有 2330 人(20.0%)患有糖尿病前期。在没有考虑到新发糖尿病之前,糖尿病前期与痴呆风险显著相关(HR 1.12 [95%CI 1.01, 1.24])。在考虑到新发糖尿病后,这种关联减弱且无统计学意义(HR 1.05 [95%CI 0.94, 1.16])。糖尿病发病年龄越早与痴呆的关联越强:发病年龄在 60 岁之前的 HR 为 2.92(95%CI 2.06, 4.14);发病年龄在 60-69 岁的 HR 为 1.73(95%CI 1.47, 2.04);发病年龄在 70-79 岁的 HR 为 1.23(95%CI 1.08, 1.40)。
结论/解释:糖尿病前期与痴呆风险相关,但这种风险可以用随后发生的糖尿病来解释。糖尿病发病年龄越早,痴呆风险越大。预防或延缓糖尿病前期向糖尿病的进展将降低痴呆的负担。