Gemma García-Lluch, Anna Marseglia, Lucrecia Moreno Royo, Juan Pardo Albiach, Mar Garcia-Zamora, Miquel Baquero, Carmen Peña-Bautista, Lourdes Álvarez, Eric Westman, Consuelo Cháfer-Pericás
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Analytical variables were obtained. Antidiabetic prescriptions were recorded in defined daily doses (DDD), according to the ATC/DDD 2021 system, and years of drug exposure duration before lumbar puncture. Logistic regressions were performed to establish the correlations between drug usage and AD biomarker alteration.</p><p><strong>Results: </strong>Among patients with diabetes, Insulin consumption was associated with lower odds of abnormal Aβ<sub>42</sub> levels (OR 0.36 [95% CI 0.15, 0.76]) and tau pathology (OR 0.49 [95% CI 0.24-0.98]). Metformin was related to lower odds of pathological p-tau when diabetes was uncontrolled, acting on t-tau and t-tau/Aβ<sub>42</sub> ratio when it was concomitant with insulin, and patients had controlled diabetes. Lower odds of pathological levels of tau were observed when additional oral antidiabetic drugs were added among metformin users. iSGLT2 was associated with tau pathology.</p><p><strong>Conclusions: </strong>The impact of antidiabetics on AD-related pathological biomarkers may depend on diabetes management.</p>","PeriodicalId":14929,"journal":{"name":"Journal of Alzheimer's Disease","volume":" ","pages":"13872877241304995"},"PeriodicalIF":3.4000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Associations between antidiabetic medications and cerebrospinal fluid biomarkers of Alzheimer's disease.\",\"authors\":\"Gemma García-Lluch, Anna Marseglia, Lucrecia Moreno Royo, Juan Pardo Albiach, Mar Garcia-Zamora, Miquel Baquero, Carmen Peña-Bautista, Lourdes Álvarez, Eric Westman, Consuelo Cháfer-Pericás\",\"doi\":\"10.1177/13872877241304995\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>It has been hypothesized that insulin resistance is pivotal in mediating amyloid and tau dysregulations in Alzheimer's disease (AD).</p><p><strong>Objective: </strong>To investigate the impact of different antidiabetic agents, their daily dosage intake, and treatment duration on cerebrospinal fluid (CSF) AD biomarkers among patients with type 2 diabetes.</p><p><strong>Methods: </strong>This cross-sectional study selected patients between 50 and 80 years with diabetes and CSF AD biomarkers screened between 2017 and 2023 in the VALCODIS Cohort. CSF biomarkers were total tau (t-tau), phosphorylated tau 181 (p-tau), and amyloid-β 42 (Aβ<sub>42</sub>). Analytical variables were obtained. Antidiabetic prescriptions were recorded in defined daily doses (DDD), according to the ATC/DDD 2021 system, and years of drug exposure duration before lumbar puncture. Logistic regressions were performed to establish the correlations between drug usage and AD biomarker alteration.</p><p><strong>Results: </strong>Among patients with diabetes, Insulin consumption was associated with lower odds of abnormal Aβ<sub>42</sub> levels (OR 0.36 [95% CI 0.15, 0.76]) and tau pathology (OR 0.49 [95% CI 0.24-0.98]). Metformin was related to lower odds of pathological p-tau when diabetes was uncontrolled, acting on t-tau and t-tau/Aβ<sub>42</sub> ratio when it was concomitant with insulin, and patients had controlled diabetes. 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引用次数: 0
摘要
背景:人们假设胰岛素抵抗在阿尔茨海默病(AD)中介导淀粉样蛋白和tau蛋白失调中起关键作用。目的:探讨不同降糖药、日剂量和治疗时间对2型糖尿病患者脑脊液(CSF) AD生物标志物的影响。方法:这项横断面研究选择了2017年至2023年在VALCODIS队列中筛选的50至80岁糖尿病患者和CSF AD生物标志物。脑脊液生物标志物为总tau蛋白(t-tau)、磷酸化tau蛋白181 (p-tau)和淀粉样蛋白β42 (a -β 42)。得到了分析变量。根据ATC/DDD 2021系统,记录降糖处方的定义日剂量(DDD),以及腰椎穿刺前的药物暴露时间。通过Logistic回归建立药物使用与AD生物标志物改变之间的相关性。结果:在糖尿病患者中,胰岛素消耗与Aβ42水平异常(OR 0.36 [95% CI 0.15, 0.76])和tau病理(OR 0.49 [95% CI 0.24-0.98])的几率较低相关。当糖尿病不受控制时,二甲双胍与病理性p-tau的发生率较低有关,当与胰岛素合用时,对t-tau和t-tau/ a - β42比值起作用,并且糖尿病已得到控制。当在二甲双胍使用者中添加额外的口服降糖药时,观察到病理水平的tau的几率较低。iSGLT2与tau病理相关。结论:抗糖尿病药物对ad相关病理生物标志物的影响可能取决于糖尿病管理。
Associations between antidiabetic medications and cerebrospinal fluid biomarkers of Alzheimer's disease.
Background: It has been hypothesized that insulin resistance is pivotal in mediating amyloid and tau dysregulations in Alzheimer's disease (AD).
Objective: To investigate the impact of different antidiabetic agents, their daily dosage intake, and treatment duration on cerebrospinal fluid (CSF) AD biomarkers among patients with type 2 diabetes.
Methods: This cross-sectional study selected patients between 50 and 80 years with diabetes and CSF AD biomarkers screened between 2017 and 2023 in the VALCODIS Cohort. CSF biomarkers were total tau (t-tau), phosphorylated tau 181 (p-tau), and amyloid-β 42 (Aβ42). Analytical variables were obtained. Antidiabetic prescriptions were recorded in defined daily doses (DDD), according to the ATC/DDD 2021 system, and years of drug exposure duration before lumbar puncture. Logistic regressions were performed to establish the correlations between drug usage and AD biomarker alteration.
Results: Among patients with diabetes, Insulin consumption was associated with lower odds of abnormal Aβ42 levels (OR 0.36 [95% CI 0.15, 0.76]) and tau pathology (OR 0.49 [95% CI 0.24-0.98]). Metformin was related to lower odds of pathological p-tau when diabetes was uncontrolled, acting on t-tau and t-tau/Aβ42 ratio when it was concomitant with insulin, and patients had controlled diabetes. Lower odds of pathological levels of tau were observed when additional oral antidiabetic drugs were added among metformin users. iSGLT2 was associated with tau pathology.
Conclusions: The impact of antidiabetics on AD-related pathological biomarkers may depend on diabetes management.
期刊介绍:
The Journal of Alzheimer''s Disease (JAD) is an international multidisciplinary journal to facilitate progress in understanding the etiology, pathogenesis, epidemiology, genetics, behavior, treatment and psychology of Alzheimer''s disease. The journal publishes research reports, reviews, short communications, hypotheses, ethics reviews, book reviews, and letters-to-the-editor. The journal is dedicated to providing an open forum for original research that will expedite our fundamental understanding of Alzheimer''s disease.