Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Memory Aging and Cognition Centre, National University Health System, Singapore, Singapore.
Alzheimers Res Ther. 2024 Oct 3;16(1):214. doi: 10.1186/s13195-024-01577-7.
Cognitive impairment is an increasingly recognized comorbidity of diabetes, yet the mechanisms underlying this association remain poorly understood. This knowledge gap has contributed to conflicting findings regarding the impact of diabetes on long-term cognitive outcomes in older adults. The presence of cerebrovascular disease (CeVD) may potentially modify this relationship. However, interactive effect between diabetes and subclinical MRI markers of CeVD on cognitive trajectories and incident dementia remains unexplored.
A total of 654 participants underwent brain MRI at baseline, from whom 614 with at least one follow-up were selected for longitudinal analysis. Cognitive tests were performed annually up to 5 years. CeVD markers of interest were lacunes, white matter hyperintensities (WMHs), cerebral microbleeds (CMBs), cortical microinfarcts (CMIs), intracranial stenosis (ICS), and cortical infarcts. Blood-based Alzheimer biomarkers, including p-tau181 and p-tau181/Aβ42 ratio, were used as indicators of Alzheimer pathology.
At baseline, diabetes was associated with lower cognitive performance and higher burden of CeVD, but not p-tau181 or p-tau181/Aβ42 ratio. Longitudinally, we found an interactive effect of diabetes and WMHs, rather than an independent effect of diabetes, on cognitive decline and dementia risk. Subgroup analyses showed association of diabetes with cognitive outcomes was stronger in participants with high WMHs load but non-significant in those with low WMHs load. Moreover, these associations remained unchanged after adjusting for blood-based Alzheimer biomarkers.
The effect of diabetes on cognitive decline is contingent upon the presence of WMHs and independent of Alzheimer's pathology. This finding raises the possibility of utilizing WMHs as an imaging biomarker to identify diabetic subgroup at greater risk of developing cognitive impairment. Furthermore, therapeutic interventions targeting WMHs may prevent cognitive deterioration in older adults with diabetes.
认知障碍是糖尿病日益被认识到的一种合并症,但这种关联的机制仍知之甚少。这一知识空白导致了关于糖尿病对老年人长期认知结局影响的相互矛盾的发现。脑血管疾病(CeVD)的存在可能会改变这种关系。然而,糖尿病和 CeVD 的亚临床 MRI 标志物对认知轨迹和新发痴呆的交互作用仍有待探索。
共有 654 名参与者在基线时接受了脑部 MRI 检查,其中 614 名至少有一次随访被选中进行纵向分析。认知测试每年进行一次,最长可达 5 年。感兴趣的 CeVD 标志物包括腔隙、脑白质高信号(WMHs)、脑微出血(CMBs)、皮质微梗死(CMIs)、颅内狭窄(ICS)和皮质梗死。阿尔茨海默病相关的血液生物标志物,包括 p-tau181 和 p-tau181/Aβ42 比值,被用作阿尔茨海默病病理的指标。
基线时,糖尿病与认知表现较低和 CeVD 负担较高相关,但与 p-tau181 或 p-tau181/Aβ42 比值无关。纵向研究发现,糖尿病与 WMHs 之间存在交互作用,而不是糖尿病的独立作用,对认知下降和痴呆风险有影响。亚组分析显示,糖尿病与认知结局的关联在 WMHs 负荷较高的参与者中更强,但在 WMHs 负荷较低的参与者中不显著。此外,这些关联在调整了血液阿尔茨海默病生物标志物后仍然不变。
糖尿病对认知下降的影响取决于 WMHs 的存在,与阿尔茨海默病的病理无关。这一发现提出了一种可能性,即利用 WMHs 作为一种影像学生物标志物,来识别糖尿病亚组中认知障碍风险更高的人群。此外,针对 WMHs 的治疗干预可能会预防糖尿病老年患者的认知恶化。