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二甲双胍的起始使用与新诊断为糖尿病的老年患者发生痴呆症无关。

No association between metformin initiation and incident dementia in older adults newly diagnosed with diabetes.

机构信息

Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada.

Sandra Black Centre for Brain Resilience and Recovery, Hurvitz Brain Sciences Program, Sunnybrook Research Institute, Toronto, Ontario, Canada.

出版信息

J Intern Med. 2024 Jan;295(1):68-78. doi: 10.1111/joim.13723. Epub 2023 Sep 25.

Abstract

BACKGROUND

Metformin has been suggested to reduce dementia risk; however, most epidemiologic studies have been limited by immortal time bias or confounding due to disease severity.

OBJECTIVES

To investigate the association of metformin initiation with incident dementia using strategies that mitigate these important sources of bias.

METHODS

Residents of Ontario, Canada ≥66 years newly diagnosed with diabetes from January 1, 2008 to December 31, 2017 entered this retrospective population-based cohort. To consider the indication for metformin monotherapy initiation, people with hemoglobin A1c of 6.5%-8.0% and estimated glomerular filtration rate ≥45 mL/min/1.73 m were selected. Using the landmark method to address immortal time bias, exposure was grouped into "metformin monotherapy initiation within 180 days after new diabetes diagnosis" or "no glucose-lowering medications within 180 days." To address disease latency, 1-year lag time was applied to the end of the 180-day landmark period. Incident dementia was defined using a validated algorithm for Alzheimer's disease and related dementias. Adjusted hazard ratios (aHR) and confidence intervals (CIs) were estimated from propensity-score weighted Cox proportional hazard models.

RESULTS

Over mean follow-up of 6.77 years from cohort entry, metformin initiation within 180 days after new diabetes diagnosis (N = 12,331; 978 events; 65,762 person-years) showed no association with dementia risk (aHR [95% CI] = 1.05 [0.96-1.15]), compared to delayed or no glucose-lowering medication initiation (N = 22,369; 1768 events; 117,415 person-years).

CONCLUSION

Early metformin initiation was not associated with incident dementia in older adults newly diagnosed with diabetes. The utility of metformin to prevent dementia was not supported.

摘要

背景

二甲双胍被认为可以降低痴呆风险;然而,大多数流行病学研究受到无事件时间偏倚或因疾病严重程度导致的混杂因素的限制。

目的

采用减轻这些重要偏倚来源的策略,研究二甲双胍起始治疗与新发痴呆的相关性。

方法

这项回顾性基于人群的队列研究纳入了 2008 年 1 月 1 日至 2017 年 12 月 31 日期间安大略省年满 66 岁、新诊断为糖尿病的居民。为了考虑二甲双胍单药起始治疗的适应证,选择糖化血红蛋白为 6.5%-8.0%且估算肾小球滤过率≥45ml/min/1.73m2的人群。通过使用 landmark 方法解决无事件时间偏倚,将暴露分为“新诊断糖尿病后 180 天内开始二甲双胍单药治疗”或“180 天内未使用任何降糖药物”。为解决疾病潜伏期问题,在 180 天 landmark 期结束时应用 1 年的滞后时间。采用验证后的阿尔茨海默病和相关痴呆症算法定义新发痴呆。采用倾向评分加权 Cox 比例风险模型估计调整后的风险比(aHR)和置信区间(CI)。

结果

在从队列入组到平均 6.77 年的随访期间,与延迟或未开始使用任何降糖药物相比,新诊断糖尿病后 180 天内开始二甲双胍治疗(N=12331;978 例事件;65762 人年)与痴呆风险无关联(aHR[95%CI]为 1.05[0.96-1.15])。

结论

在新诊断为糖尿病的老年人中,早期起始二甲双胍治疗与新发痴呆无关。二甲双胍预防痴呆的效果不支持这一结论。

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