Clinical and Research Memory Centre, Lyon Institute For Aging, Charpennes Hospital, Hospices Civils de Lyon, 27 rue Gabriel Péri, Villeurbanne, Lyon, 69100, France.
Heva, Lyon, France.
Alzheimers Res Ther. 2024 Jul 26;16(1):166. doi: 10.1186/s13195-024-01533-5.
The identification of factors involved in the conversion across the different Alzheimer's disease (AD) stages is crucial to prevent or slow the disease progression. We aimed to assess the factors and their combination associated with the conversion across the AD stages, from mild cognitive impairment to dementia, at a mild, moderate or severe stage and to identify profiles associated with earliest/latest conversion across the AD stages.
In this study conducted on the real-life MEMORA cohort data collected from January 1, 2013, and December 31, 2019, three cohorts were selected depending on the baseline neurocognitive stage from a consecutive sample of patients attending a memory center, aged between 50 and 90 years old, with a diagnosis of AD during the follow-up, and with at least 2 visits at 6 months to 1 year of interval. A machine learning approach was used to assess the relationship between factors including socio-demographic characteristics, comorbidities and history of diseases, prescription of drugs, and geriatric hospitalizations, and the censored time to conversion from mild cognitive impairment to AD dementia, from the mild stage of dementia to the moderate or severe stages of AD dementia, and from the moderate stage of AD dementia to the severe stage. Profiles of earliest/latest conversion compared to median time to conversion across stages were identified. The median time to conversion was estimated with a Kaplan-Meier estimator.
Overall, 2891 patients were included (mean age 77±9 years old, 65% women). The median time of follow-up was 28 months for mild cognitive impairment (MCI) patients, 33 months for mild AD dementia and 30 months for moderate AD dementia. Among the 1264 patients at MCI stage, 61% converted to AD dementia (median time to conversion: 25 months). Among the 1142 patients with mild AD dementia, 59% converted to moderate/severe stage (median time: 23 months) and among the 1332 patients with moderate AD dementia, 23% converted to severe stage (Q3 time to conversion: 22 months). Among the studied factors, cardiovascular comorbidities, anxiety, social isolation, osteoporosis, and hearing disorders were identified as being associated with earlier conversion across stages. Symptomatic treatment i.e. cholinesterase inhibitors for AD was associated with later conversion from mild stage of dementia to moderate/severe stages.
This study based on a machine learning approach allowed to identify potentially modifiable factors associated with conversion across AD stages for which timely interventions may be implemented to delay disease progression.
识别与不同阿尔茨海默病(AD)阶段转换相关的因素至关重要,这有助于预防或减缓疾病进展。我们旨在评估与从轻度认知障碍(MCI)到痴呆的 AD 阶段转换相关的因素及其组合,评估发生在轻度、中度或重度阶段的因素及其组合,并确定与 AD 阶段转换最早/最晚相关的特征。
在这项基于 MEMORA 队列的真实数据研究中,我们从 2013 年 1 月 1 日至 2019 年 12 月 31 日收集数据,根据基线神经认知阶段从连续就诊于记忆中心的患者中选择了三个队列,这些患者年龄在 50 至 90 岁之间,在随访期间被诊断为 AD,且在 6 个月至 1 年的随访期间至少进行了 2 次就诊。使用机器学习方法评估了包括社会人口统计学特征、合并症和疾病史、药物处方和老年住院治疗在内的因素与从 MCI 到 AD 痴呆、从轻度痴呆到中度或重度 AD 痴呆以及从中度 AD 痴呆到重度 AD 痴呆的转换时间之间的关系。确定了与各阶段的中位转换时间相比最早/最晚转换的特征。使用 Kaplan-Meier 估计器估计转换的中位时间。
共纳入 2891 例患者(平均年龄 77±9 岁,65%为女性)。MCI 患者的中位随访时间为 28 个月,轻度 AD 痴呆患者为 33 个月,中度 AD 痴呆患者为 30 个月。在 1264 例 MCI 阶段的患者中,61%的患者转化为 AD 痴呆(中位转换时间:25 个月)。在 1142 例轻度 AD 痴呆患者中,59%的患者转化为中重度阶段(中位时间:23 个月),在 1332 例中度 AD 痴呆患者中,23%的患者转化为重度阶段(Q3 转换时间:22 个月)。在研究的因素中,心血管合并症、焦虑、社会孤立、骨质疏松症和听力障碍被确定为与各阶段的早期转换相关的因素。针对 AD 的症状性治疗(即乙酰胆碱酯酶抑制剂)与从轻度痴呆到中度/重度阶段的转换较晚相关。
这项基于机器学习的研究确定了与 AD 阶段转换相关的潜在可改变因素,及时干预这些因素可能有助于延缓疾病进展。