Data-Driven Fatigue Trajectories in Multiple Sclerosis and Their Predictors.

IF 8 1区 医学 Q1 CLINICAL NEUROLOGY
Alessandro Cruciani, Emanuele Olivieri, Ronja Christensen, Sarmad Al-Araji, Samih Fourali, Weaam Hamed, Anna He, Baris Kanber, Davide Maccarrone, Suraya Mohamud, Riccardo Nistri, Anestis Passalis, Valeria Pozzilli, Ferran Prados, Charmaine Yam, Marios C Yiannakas, Alan J Thompson, Frederik Barkhof, Ahmed T Toosy, Olga Ciccarelli
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引用次数: 0

Abstract

Background and objectives: Fatigue is one of the most disabling symptoms of multiple sclerosis (MS), yet its longitudinal trajectories and determinants remain poorly characterized. We aimed to identify trajectories of cognitive and physical fatigue in relapsing-remitting MS (RRMS) and to determine baseline clinical and MRI predictors of worsening fatigue.

Methods: We conducted a prospective, single-center cohort study embedded in the Predicting Optimal INdividualised Treatment response in MS (POINT-MS) program at the Queen Square MS Centre (London, United Kingdom). Adults with RRMS initiating a new disease-modifying therapy within 3 months of baseline were enrolled and underwent clinical and MRI assessments at baseline, 6 months, and 18 months. Key inclusion criteria were a diagnosis of RRMS, availability of baseline brain and cervical spinal cord MRI, and completion of at least 3 Modified Fatigue Impact Scale (MFIS) assessments. The primary outcome was the longitudinal change in MFIS cognitive and physical subscale scores. Fatigue trajectories were identified using growth mixture modeling. Baseline predictors included demographic factors, disability, cognitive performance, depression diagnosis, proportion of disease duration on disease-modifying treatments (DMTs), and MRI-derived measures of cervical spinal cord cross-sectional area (C-CSA) and regional brain volumes standardized to healthy-control norms. Predictor importance was assessed with conditional random forests, followed by multivariable modeling.

Results: We enrolled 225 participants. Three distinct fatigue trajectories emerged for both cognitive and physical MFIS subscales, including improving, stable/mild-worsening, and worsening classes. Worsening trajectories showed annualized increases of +3.32 points/year (cognitive) and +3.37 points/year (physical). Smaller baseline C-CSA was the strongest MRI predictor of worsening trajectories. Clinically, the proportion of disease duration spent on DMTs was the most influential predictor.

Discussion: Fatigue in RRMS follows heterogeneous trajectories over short-term follow-up. Smaller cervical spinal cord area was the strongest MRI predictor of worsening fatigue. Damage to ascending somatosensory axons within the cervical cord may reduce afferent input to the thalamus and diminish thalamocortical drive, contributing to both the motor and the cognitive-arousal dimensions of fatigue. These findings support incorporating cervical cord MRI into prognostic models and future fatigue research.

数据驱动的多发性硬化症疲劳轨迹及其预测因子。
背景和目的:疲劳是多发性硬化症(MS)最严重的致残症状之一,但其纵向轨迹和决定因素仍不清楚。我们的目的是确定复发缓解型MS (RRMS)的认知和身体疲劳的轨迹,并确定疲劳恶化的基线临床和MRI预测指标。方法:我们在女王广场多发性硬化症中心(英国伦敦)进行了一项前瞻性、单中心队列研究,该研究嵌入了预测多发性硬化症最佳个体化治疗反应(POINT-MS)项目。在基线3个月内开始新的疾病改善治疗的RRMS成年患者入组,并在基线、6个月和18个月进行临床和MRI评估。主要纳入标准为RRMS的诊断,基线脑和颈脊髓MRI的可用性,以及完成至少3项修正疲劳影响量表(MFIS)评估。主要结果是MFIS认知和身体亚量表得分的纵向变化。使用生长混合模型识别疲劳轨迹。基线预测因素包括人口统计学因素、残疾、认知能力、抑郁诊断、疾病改善治疗(dmt)的疾病持续时间比例,以及颈脊髓横截面积(C-CSA)和标准化为健康对照标准的区域脑容量的mri衍生测量。通过条件随机森林评估预测因子的重要性,然后进行多变量建模。结果:我们招募了225名参与者。在认知和身体的MFIS子量表中出现了三种不同的疲劳轨迹,包括改善、稳定/轻度恶化和恶化等级。恶化轨迹显示年化增长为+3.32点/年(认知)和+3.37点/年(身体)。较小的基线C-CSA是恶化轨迹的最强MRI预测因子。在临床上,花费在dmt上的疾病持续时间的比例是最具影响力的预测因子。讨论:RRMS的疲劳在短期随访中遵循不同的轨迹。颈脊髓面积较小是疲劳加重的最强MRI预测因子。颈髓内上行体感觉轴突的损伤可能会减少丘脑的传入输入,减少丘脑皮质驱动,从而导致疲劳的运动和认知唤醒维度。这些发现支持将脊髓MRI纳入预后模型和未来的疲劳研究。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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