Measuring time saved in Alzheimer's disease: What is a meaningful slowing of progression?

IF 4.9 Q1 CLINICAL NEUROLOGY
Krista Lanctot, Linus Jönsson, Alireza Atri, Russ Paulsen, Soeren Mattke, Julie Hviid Hahn-Pedersen, Pepa Polavieja, Thomas Maltesen, Teresa León, Anders Gustavsson, Alzheimer's Disease Neuroimaging Initiative
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引用次数: 0

Abstract

INTRODUCTION

Minimal clinically important differences (MCIDs) for Alzheimer's disease (AD) have previously been estimated using clinician-based anchors. However, MCIDs have been criticized for not reflecting the preferences of people living with AD (PLWAD). Furthermore, interpretations of clinical trial results have been criticized for conflating within-person meaningfulness thresholds and between-group differences. Here, we simulate scenarios of disease slowing and compare those to published MCIDs.

METHODS

Scenarios of 5%–95% disease slowing were simulated using Alzheimer's Disease Neuroimaging Initiative (ADNI) data. Time saved and point differences on the Clinical Dementia Rating scale—Sum of Boxes (CDR-SB) were estimated for these scenarios and compared to published MCIDs.

RESULTS

Scenario analyses resulted in estimates of time saved at ∼3 weeks–17 months and mean changes at 0.08–1.5 CDR-SB points over 18 months. The often referenced MCID for mild cognitive impairment (0.98) thereby corresponded to 11 months slowing, whereas the MCID for mild dementia (1.63) corresponded to >17 months slowing.

DISCUSSION

Translating trial endpoints to estimates of time saved supports that often-referenced MCIDs may not be aligned with realistic and meaningful slowing of clinical progression.

Highlights

  • AD slowing of clinical progression by 5%–95% resulted in 0.74–17 months saved and 0.08–1.5 CDR-SB points change at 18 months.
  • Slowing of at least 60% or 11 months of time saved over 18 months met an often-cited MCID threshold of 0.98 points for mild cognitive impairment.
  • For mild AD dementia, an MCID of 1.63 meant that even an 18-month delay over 18 months would be considered only borderline meaningful—a face invalid and unrealistic proposition.

Abstract Image

测量阿尔茨海默病节省的时间:什么是有意义的进展减缓?
阿尔茨海默病(AD)的最小临床重要差异(MCIDs)先前已经使用基于临床的锚定来估计。然而,MCIDs因未能反映AD患者(PLWAD)的偏好而受到批评。此外,对临床试验结果的解释因混淆了个人意义阈值和组间差异而受到批评。在这里,我们模拟疾病减缓的情景,并将其与已发表的MCIDs进行比较。方法使用阿尔茨海默病神经影像学倡议(ADNI)数据模拟5%-95%疾病减缓的情景。对这些情景的临床痴呆评定量表-盒和量表(CDR-SB)上节省的时间和点数差异进行估计,并与已发表的mcid进行比较。结果:情景分析得出在~ 3周- 17个月期间节省的时间估计,18个月期间平均变化为0.08-1.5 CDR-SB点。因此,经常被引用的轻度认知障碍的MCID(0.98)相当于11个月的减缓,而轻度痴呆的MCID(1.63)相当于17个月的减缓。将试验终点转换为节省时间的支持估计,通常引用的MCIDs可能与现实和有意义的临床进展减缓不一致。AD临床进展减缓5%-95%,节省0.74-17个月,18个月时CDR-SB积分变化0.08-1.5。减缓至少60%或在18个月内节省11个月的时间符合经常被引用的轻度认知障碍的MCID阈值0.98分。对于轻度阿尔茨海默氏症,MCID为1.63意味着即使延迟18个月超过18个月,也只会被认为是有意义的边缘——这是一个无效和不现实的命题。
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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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