胆碱酯酶抑制剂在路易体痴呆中的应用模式和预测因素

IF 6.8 Q1 CLINICAL NEUROLOGY
Rachel J. Heo, Ahmed Negida, Kathryn A. Wyman-Chick, James R. Bateman, Federico Rodriguez-Porcel, Brian D. Berman, Nitai Mukhopadhyay, Matthew J. Barrett
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引用次数: 0

摘要

目前的证据支持使用胆碱酯酶抑制剂(ChEIs)作为改善路易体痴呆(DLB)认知的一线对症治疗。目前对DLB患者chei的处方模式知之甚少。本研究旨在确定美国DLB患者ChEI处方的模式和预测因素。方法:使用TriNetX数据库,我们确定了2004年至2024年间诊断为DLB的20,643名年龄在45至90岁之间的美国患者。我们只包括那些有不止一种诊断记录的患者。分析了多奈哌齐、利瓦斯汀、加兰他明和美金刚的处方数据和模式。我们使用多元逻辑回归模型来估计基于人口统计学因素的ChEI处方的几率。结果51.9%的DLB患者曾接受过ChEI治疗,且接受过ChEI治疗的患者有较长的诊断间隔。开具ChEIs的患者更有可能是西班牙裔(比值比[OR] 1.36, 95%可信区间[CI]: 1.15, 1.59)和居住在中西部(OR 1.93, 95% CI: 1.76, 2.13),而黑人患者较少可能开具ChEIs (OR 0.80, 95% CI: 0.71, 0.91)。在服用ChEIs的患者中,首次用药至最后一次用药的中位时间为13.4个月(四分位数差1.1 ~ 32.9),其中以多奈哌齐最常见(76.9%),其次是利瓦斯汀(35.6%)和加兰他明(3.9%)。在20年的研究期间,ChEIs的处方率逐渐增加,个体ChEIs的处方频率保持相对稳定。结论:尽管有证据支持ChEIs的耐受性和疗效,但在美国DLB患者中,ChEIs的处方不足,而且在处方上存在种族、民族和地区的差异。有必要了解DLB中ChEIs处方不足的原因,因此可以开发专注于增加使用的干预措施。尽管胆碱酯酶抑制剂(ChEIs)已被证明具有耐受性和有效性,但在路易体痴呆(DLB)中,胆碱酯酶抑制剂(ChEIs)的处方不足。人种、民族和地区显著影响ChEI处方的几率。有必要增加对DLB患者的ChEI处方。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Patterns and predictors of cholinesterase inhibitor use in dementia with Lewy bodies

Patterns and predictors of cholinesterase inhibitor use in dementia with Lewy bodies

INTRODUCTION

Current evidence supports the use of cholinesterase inhibitors (ChEIs) as the first-line symptomatic treatment for improving cognition in dementia with Lewy bodies (DLB). Little is known about current prescribing patterns of ChEIs in DLB. This study aimed to identify the patterns and predictors of ChEI prescribing in patients with DLB in the United States.

METHODS

Using the TriNetX database, we identified 20,643 US patients ages 45 to 90 who were diagnosed with DLB between 2004 and 2024. We only included those with more than one documented diagnosis. Prescription data and patterns for donepezil, rivastigmine, galantamine, and memantine were analyzed. We used multivariate logistic regression models to estimate the odds of ChEI prescription based on demographic factors.

RESULTS

We found that 51.9% of DLB patients were ever prescribed a ChEI, and those who were prescribed a ChEI had a greater diagnosis interval. Patients who were prescribed ChEIs were more likely to be Hispanic (odds ratio [OR] 1.36, 95% confidence interval [CI]: 1.15, 1.59) and reside in the Midwest (OR 1.93, 95% CI: 1.76, 2.13), while Black patients were less likely to be prescribed ChEIs (OR 0.80, 95% CI: 0.71, 0.91). Of patients prescribed ChEIs, the median time between the first and last prescription was 13.4 months (interquartile range: 1.1, 32.9), and donepezil was the most commonly prescribed (76.9%) followed by rivastigmine (35.6%) and galantamine (3.9%). Over the 20-year study period, there was a gradual increase in the rate of prescribing of ChEIs, and the prescribing frequency of individual ChEIs remained relatively stable.

CONCLUSION

Despite evidence supporting their tolerability and efficacy, ChEIs are under-prescribed in DLB patients within the United States, and there are differences in prescribing based on race, ethnicity, and region. There is a need to understand the reasons for under-prescribing ChEIs in DLB, so interventions focused on increasing use can be developed.

Highlights

  • Despite proven tolerability and efficacy, cholinesterase inhibitors (ChEIs) are under-prescribed in dementia with Lewy bodies (DLB).
  • Race, ethnicity, and region significantly affected the odds of ChEI prescription.
  • There is a need to increase ChEI prescribing for DLB patients.
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来源期刊
CiteScore
10.10
自引率
2.10%
发文量
134
审稿时长
10 weeks
期刊介绍: Alzheimer''s & Dementia: Translational Research & Clinical Interventions (TRCI) is a peer-reviewed, open access,journal from the Alzheimer''s Association®. The journal seeks to bridge the full scope of explorations between basic research on drug discovery and clinical studies, validating putative therapies for aging-related chronic brain conditions that affect cognition, motor functions, and other behavioral or clinical symptoms associated with all forms dementia and Alzheimer''s disease. The journal will publish findings from diverse domains of research and disciplines to accelerate the conversion of abstract facts into practical knowledge: specifically, to translate what is learned at the bench into bedside applications. The journal seeks to publish articles that go beyond a singular emphasis on either basic drug discovery research or clinical research. Rather, an important theme of articles will be the linkages between and among the various discrete steps in the complex continuum of therapy development. For rapid communication among a multidisciplinary research audience involving the range of therapeutic interventions, TRCI will consider only original contributions that include feature length research articles, systematic reviews, meta-analyses, brief reports, narrative reviews, commentaries, letters, perspectives, and research news that would advance wide range of interventions to ameliorate symptoms or alter the progression of chronic neurocognitive disorders such as dementia and Alzheimer''s disease. The journal will publish on topics related to medicine, geriatrics, neuroscience, neurophysiology, neurology, psychiatry, clinical psychology, bioinformatics, pharmaco-genetics, regulatory issues, health economics, pharmacoeconomics, and public health policy as these apply to preclinical and clinical research on therapeutics.
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