Kathryn A Wyman-Chick, Matthew J Barrett, Michael J Miller, Lana Sargent, Ella A B Chrenka, Joseph P M Kane, Samuel J Crowley, Jennifer L Kuntz, Sotirios A Parashos, John T Schousboe, Huong Nguyen, Ann M Werner, Rebecca C Rossom
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Logistic regression was used to estimate the association between ACB and odds of frailty.</p><p><strong>Results: </strong>Compared to controls (<i>n</i> = 525), a diagnosis of DLB (<i>n</i> = 175; adjusted odds ratio [aOR]: 15.1, 95% confidence interval [CI]: 7.0-33.9) or Alzheimer's disease (AD: <i>n </i>= 525; aOR = 7.7, 95% CI: 4.4-13.7) was associated with an increased odds of frailty. Patients with DLB had greater prescriptions for anticholinergic medications than patients with AD (<i>p</i> <sub>B</sub> < 0.001; 23% vs 9.7%). ACB was positively correlated with frailty for all groups (<i>r</i> = 0.30 to 0.47, <i>p</i> < 0.001).</p><p><strong>Discussion: </strong>Cumulative anticholinergic burden may be a modifiable predictor of frailty among older adults, including those newly diagnosed with dementia.</p><p><strong>Highlights: </strong>Patients with newly diagnosed dementia with Lewy bodies (DLB) are more likely to have prescriptions for anticholinergic medications relative to patients newly diagnosed with Alzheimer's disease (AD) and older adults without documented cognitive impairment.In the year prior to a documented dementia diagnosis, 74% of patients with DLB and 66% of patients with AD had evidence of frailty.Anticholinergic medication burden was associated with frailty among all older adults in the study, including those without a dementia diagnosis.</p>","PeriodicalId":53226,"journal":{"name":"Alzheimer''s and Dementia: Diagnosis, Assessment and Disease Monitoring","volume":"16 4","pages":"e70034"},"PeriodicalIF":4.0000,"publicationDate":"2024-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11645712/pdf/","citationCount":"0","resultStr":"{\"title\":\"The relationship between anticholinergic burden and frailty in the year preceding a diagnosis of dementia with Lewy bodies.\",\"authors\":\"Kathryn A Wyman-Chick, Matthew J Barrett, Michael J Miller, Lana Sargent, Ella A B Chrenka, Joseph P M Kane, Samuel J Crowley, Jennifer L Kuntz, Sotirios A Parashos, John T Schousboe, Huong Nguyen, Ann M Werner, Rebecca C Rossom\",\"doi\":\"10.1002/dad2.70034\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>Little is known regarding the relationship between anticholinergic medications and frailty in dementia with Lewy bodies (DLB).</p><p><strong>Methods: </strong>Anticholinergic Cognitive Burden Scale (ACB) and Claims-based Frailty Index scores were calculated for 12 months prior to the dementia diagnosis using electronic medical record and claims data. Logistic regression was used to estimate the association between ACB and odds of frailty.</p><p><strong>Results: </strong>Compared to controls (<i>n</i> = 525), a diagnosis of DLB (<i>n</i> = 175; adjusted odds ratio [aOR]: 15.1, 95% confidence interval [CI]: 7.0-33.9) or Alzheimer's disease (AD: <i>n </i>= 525; aOR = 7.7, 95% CI: 4.4-13.7) was associated with an increased odds of frailty. Patients with DLB had greater prescriptions for anticholinergic medications than patients with AD (<i>p</i> <sub>B</sub> < 0.001; 23% vs 9.7%). 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引用次数: 0
摘要
导言:关于抗胆碱能药物与路易体痴呆(DLB)虚弱之间的关系,我们知之甚少。方法:使用电子病历和索赔数据计算痴呆诊断前12个月的抗胆碱能认知负担量表(ACB)和基于索赔的衰弱指数评分。Logistic回归用于估计ACB与虚弱几率之间的关系。结果:与对照组(n = 525)相比,诊断为DLB的患者(n = 175;校正优势比[aOR]: 15.1, 95%可信区间[CI]: 7.0-33.9)或阿尔茨海默病(AD: n = 525;(aOR = 7.7, 95% CI: 4.4-13.7)与虚弱的几率增加有关。DLB患者比AD患者有更多的抗胆碱能药物处方(p r = 0.30至0.47,p)。讨论:累积抗胆碱能负担可能是老年人虚弱的可变预测因子,包括那些新诊断为痴呆的老年人。亮点:与新诊断为阿尔茨海默病(AD)的患者和无记录认知障碍的老年人相比,新诊断为路易体痴呆(DLB)的患者更有可能开抗胆碱能药物处方。在记录在案的痴呆诊断前一年,74%的DLB患者和66%的AD患者有虚弱的迹象。抗胆碱能药物负担与研究中所有老年人的虚弱有关,包括那些没有痴呆诊断的老年人。
The relationship between anticholinergic burden and frailty in the year preceding a diagnosis of dementia with Lewy bodies.
Introduction: Little is known regarding the relationship between anticholinergic medications and frailty in dementia with Lewy bodies (DLB).
Methods: Anticholinergic Cognitive Burden Scale (ACB) and Claims-based Frailty Index scores were calculated for 12 months prior to the dementia diagnosis using electronic medical record and claims data. Logistic regression was used to estimate the association between ACB and odds of frailty.
Results: Compared to controls (n = 525), a diagnosis of DLB (n = 175; adjusted odds ratio [aOR]: 15.1, 95% confidence interval [CI]: 7.0-33.9) or Alzheimer's disease (AD: n = 525; aOR = 7.7, 95% CI: 4.4-13.7) was associated with an increased odds of frailty. Patients with DLB had greater prescriptions for anticholinergic medications than patients with AD (pB < 0.001; 23% vs 9.7%). ACB was positively correlated with frailty for all groups (r = 0.30 to 0.47, p < 0.001).
Discussion: Cumulative anticholinergic burden may be a modifiable predictor of frailty among older adults, including those newly diagnosed with dementia.
Highlights: Patients with newly diagnosed dementia with Lewy bodies (DLB) are more likely to have prescriptions for anticholinergic medications relative to patients newly diagnosed with Alzheimer's disease (AD) and older adults without documented cognitive impairment.In the year prior to a documented dementia diagnosis, 74% of patients with DLB and 66% of patients with AD had evidence of frailty.Anticholinergic medication burden was associated with frailty among all older adults in the study, including those without a dementia diagnosis.
期刊介绍:
Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.