School of Public Health, The Second Affiliated Hospital, The Key Laboratory of Intelligent Preventive Medicine of Zhejiang Province, Zhejiang University School of Medicine, Hangzhou 310058, Zhejiang, China.
Department of Neurobiology, Department of Orthopedics, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, Zhejiang, China; NHC and CAMS Key Laboratory of Medical Neurobiology, MOE Frontier Science Center for Brain Research and Brain-Machine Integration, School of Brain Science and Brain Medicine, Zhejiang University, Hangzhou 310058, Zhejiang, China; Department of Rehabilitation Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, Zhejiang, China.
Exp Gerontol. 2023 Jul;178:112225. doi: 10.1016/j.exger.2023.112225. Epub 2023 Jun 3.
Adults without diabetes are not completely healthy; they are probably heterogeneous with several potential health problems. The management of hemoglobin A1c (HbA1c) is crucial among patients with diabetes; but whether similar management strategy is needed for adults without diabetes is unclear. Thus, this study aimed to investigate the associations of visit-to-visit HbA1c variability with incident dementia and hippocampal volume among middle-aged and older adults without diabetes, providing potential insights into this question.
We conducted a prospective analysis for incident dementia in 10,792 participants (mean age 58.9 years, 47.8 % men) from the UK Biobank. A subgroup of 3793 participants (mean age 57.8 years, 48.6 % men) was included in the analysis for hippocampal volume. We defined HbA1c variability as the difference in HbA1c divided by the mean HbA1c over the 2 sequential visits ([latter - former]/mean). Dementia was identified using hospital inpatient records with ICD-9 codes. T1-structural brain magnetic resonance imaging was conducted to derive hippocampal volume (normalized for head size). The nonlinear and linear associations were examined using restricted cubic spline (RCS) models, Cox regression models, and multiple linear regression models.
During a mean follow-up (since the second round) of 8.4 years, 90 (0.8 %) participants developed dementia. The RCS models suggested no significant nonlinear associations of HbA1c variability with incident dementia and hippocampal volume, respectively (All P > 0.05). Above an optimal cutoff of HbA1c variability at 0.08, high HbA1c variability (increment in HbA1c) was associated with an increased risk of dementia (Hazard Ratio, 1.88; 95 % Confidence Interval, 1.13 to 3.14, P = 0.015), and lower hippocampal volume (coefficient, -96.84 mm, P = 0.037), respectively, in models with adjustment of covariates including age, sex, etc. Similar results were found for a different cut-off of 0. A series of sensitivity analyses verified the robustness of the findings.
Among middle-aged and older adults without diabetes, increasing visit-to-visit HbA1c variability was associated with an increased dementia risk and lower hippocampal volume. The findings highlight the importance of monitoring and controlling HbA1c fluctuation in apparently healthy adults without diabetes.
非糖尿病成年人并非完全健康;他们可能存在多种潜在健康问题,具有异质性。糖化血红蛋白(HbA1c)的管理对于糖尿病患者至关重要;但对于非糖尿病成年人是否需要类似的管理策略尚不清楚。因此,本研究旨在探讨非糖尿病成年人随访间 HbA1c 变异性与痴呆和海马体积之间的关联,为这一问题提供潜在的见解。
我们对来自英国生物库的 10792 名参与者(平均年龄 58.9 岁,47.8%为男性)进行了前瞻性痴呆分析。3793 名参与者(平均年龄 57.8 岁,48.6%为男性)被纳入海马体积分析。我们将 HbA1c 变异性定义为两次连续就诊之间 HbA1c 的差异除以平均 HbA1c([后者-前者]/平均)。痴呆症是通过 ICD-9 代码的医院住院记录确定的。T1 结构磁共振成像用于获得海马体积(按头部大小归一化)。使用受限立方样条(RCS)模型、Cox 回归模型和多元线性回归模型分别检查非线性和线性关联。
在平均(自第二轮以来)随访 8.4 年期间,90 名(0.8%)参与者发生了痴呆。RCS 模型表明,随访间 HbA1c 变异性与痴呆症和海马体积之间均无显著的非线性关联(均 P>0.05)。在 HbA1c 变异性的最佳截断值 0.08 以上,HbA1c 变异性升高(HbA1c 增加)与痴呆风险增加相关(危险比,1.88;95%置信区间,1.13 至 3.14,P=0.015),并且在调整年龄、性别等混杂因素的模型中,海马体积降低(系数,-96.84mm,P=0.037)。在截断值为 0.08 时,也得到了相似的结果。一系列敏感性分析验证了研究结果的稳健性。
在非糖尿病的中老年成年人中,随访间 HbA1c 变异性增加与痴呆风险增加和海马体积降低相关。这些发现强调了监测和控制非糖尿病成年人 HbA1c 波动的重要性。