MRC Unit for Lifelong Health and Ageing at UCL, Institute of Cardiovascular Science, University College London, London, UK.
Department of Non-communicable Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK.
Diabetes Obes Metab. 2021 May;23(5):1140-1149. doi: 10.1111/dom.14321. Epub 2021 Feb 14.
To understand the relationship between HbA1c and brain health across the entire glycaemic spectrum.
We used data from the UK Biobank cohort consisting of 500,000 individuals aged 40-69 years. HbA1c and diabetes diagnosis were used to define baseline glycaemic categories. Our outcomes included incident all-cause dementia, vascular dementia (VD), Alzheimer's dementia (AD), hippocampal volume (HV), white matter hyperintensity (WMH) volume, cognitive function and decline. The reference group was normoglycaemic individuals (HbA1c ≥35 & <42 mmol/mol). Our maximum analytical sample contained 449,973 individuals with complete data.
Prediabetes and known diabetes increased incident VD (HR 1.54; 95% CI = 1.04, 2.28 and HR 2.97; 95% CI = 2.26, 3.90, respectively). Known diabetes increased all-cause and AD risk (HR 1.91; 95% CI = 1.66, 2.21 and HR 1.84; 95% CI = 1.44, 2.36, respectively). Prediabetes and known diabetes elevated the risks of cognitive decline (OR 1.42; 1.48, 2.96 and OR 1.39; 1.04, 1.75, respectively). Prediabetes, undiagnosed and known diabetes conferred higher WMH volumes (3%, 22% and 7%, respectively) and lower HV (36, 80 and 82 mm , respectively), whereas low-normal HbA1c had 1% lower WMH volume and 12 mm greater HV.
Both prediabetes and known diabetes are harmful in terms of VD, cognitive decline and AD risks, as well as lower HV. Associations appeared to be somewhat driven by antihypertensive medication, which implies that certain cardiovascular drugs may ameliorate some of the excess risk. Low-normal HbA1c levels, however, are associated with more favourable brain health outcomes and warrant more in-depth investigation.
了解整个血糖范围内 HbA1c 与大脑健康之间的关系。
我们使用了来自英国生物银行队列的 50 万人的数据,年龄在 40-69 岁之间。HbA1c 和糖尿病诊断用于定义基线血糖类别。我们的结果包括新发全因痴呆、血管性痴呆(VD)、阿尔茨海默病性痴呆(AD)、海马体积(HV)、脑白质高信号(WMH)体积、认知功能和下降。参考组为血糖正常者(HbA1c≥35&<42mmol/mol)。我们的最大分析样本包含 449973 名数据完整的个体。
糖尿病前期和已知糖尿病增加了 VD 的发病风险(HR 1.54;95%CI=1.04,2.28 和 HR 2.97;95%CI=2.26,3.90)。已知糖尿病增加了全因和 AD 风险(HR 1.91;95%CI=1.66,2.21 和 HR 1.84;95%CI=1.44,2.36)。糖尿病前期和已知糖尿病增加了认知能力下降的风险(OR 1.42;1.48,2.96 和 OR 1.39;1.04,1.75)。糖尿病前期、未确诊和已知糖尿病导致更高的 WMH 体积(分别为 3%、22%和 7%)和更低的 HV(分别为 36、80 和 82mm),而低正常 HbA1c 的 WMH 体积低 1%,HV 高 12mm。
糖尿病前期和已知糖尿病都会增加 VD、认知能力下降和 AD 风险,以及降低 HV,这表明这两种情况可能在一定程度上与降压药物有关,这意味着某些心血管药物可能会减轻部分额外风险。然而,低正常 HbA1c 水平与更有利的大脑健康结果相关,值得更深入的研究。