Primary care blood tests show lipid profile changes in pre-symptomatic amyotrophic lateral sclerosis.

Brain Communications Pub Date : 2023-07-28 eCollection Date: 2023-01-01 DOI:10.1093/braincomms/fcad211
Alexander G Thompson, Rachael Marsden, Kevin Talbot, Martin R Turner
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Abstract

Multiple sources of evidence suggest that changes in metabolism may precede the onset of motor symptoms in amyotrophic lateral sclerosis. This study aimed to seek evidence for alterations in the levels of blood indices collected routinely in the primary care setting prior to the onset of motor symptoms in amyotrophic lateral sclerosis. Premorbid data, measured as part of routine health screening, for total cholesterol, high-density and low-density lipoprotein cholesterol, triglyceride, glycated haemoglobin A1c and creatinine were collected retrospectively from (i) a cohort of amyotrophic lateral sclerosis patients attending a specialist clinic (n = 143) and (ii) from primary care-linked data within UK Biobank. Data were fitted using linear mixed effects models with linear b-splines to identify inflection points, controlling for age and sex. In specialist amyotrophic lateral sclerosis clinic cases, models indicated decreasing levels of total and low-density lipoprotein cholesterol prior to an inflection point in the years before symptom onset (total cholesterol 3.25 years, low-density lipoprotein cholesterol 1.25 years), after which they stabilized or rose. A similar pattern was observed in amyotrophic lateral sclerosis cases within UK Biobank, occurring several years prior to diagnosis (total cholesterol 7 years, low-density lipoprotein cholesterol 7.25 years), differing significantly from matched controls. High-density lipoprotein cholesterol followed a similar pattern but was less robust to sensitivity analyses. Levels of triglyceride remained stable throughout. Glycated haemoglobin temporal profiles were not consistent between the clinic and biobank cohorts. Creatinine level trajectories prior to amyotrophic lateral sclerosis did not differ significantly from controls but decreased significantly in the symptomatic period after an inflection point of 0.25 years after symptom onset (clinic cohort) or 0.5 years before diagnosis (UK Biobank). These data provide further evidence for a pre-symptomatic period of dynamic metabolic change in amyotrophic lateral sclerosis, consistently associated with alterations in blood cholesterols. Such changes may ultimately contribute to biomarkers applicable to population screening and for pathways guiding the targeting of preventative therapy.

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初级保健血液检测显示症状前肌萎缩性脊髓侧索硬化症患者的血脂变化。
多种证据表明,肌萎缩性脊髓侧索硬化症患者在出现运动症状之前,新陈代谢可能会发生变化。本研究旨在寻找证据,证明在肌萎缩侧索硬化症患者出现运动症状之前,在基层医疗机构常规收集的血液指标水平会发生变化。病前数据是常规健康检查的一部分,包括总胆固醇、高密度和低密度脂蛋白胆固醇、甘油三酯、糖化血红蛋白 A1c 和肌酐,这些数据是通过回顾性方式收集的,数据来源于:(i) 在专科门诊就诊的肌萎缩侧索硬化症患者队列(n = 143);(ii) 英国生物库中与初级保健相关的数据。在控制年龄和性别的前提下,使用线性混合效应模型对数据进行拟合,并使用线性 b-样条来识别拐点。在肌萎缩侧索硬化症专科门诊病例中,模型显示总胆固醇和低密度脂蛋白胆固醇水平在症状发作前几年出现拐点之前不断下降(总胆固醇为 3.25 年,低密度脂蛋白胆固醇为 1.25 年),之后趋于稳定或上升。在英国生物库中的肌萎缩侧索硬化症病例中也观察到类似的模式,在确诊前数年出现(总胆固醇 7 年,低密度脂蛋白胆固醇 7.25 年),与匹配的对照组有显著差异。高密度脂蛋白胆固醇的变化规律与之相似,但在敏感性分析中表现不佳。甘油三酯的水平在整个过程中保持稳定。糖化血红蛋白的时间曲线在诊所和生物库队列中并不一致。肌萎缩性脊髓侧索硬化症发病前的肌酸酐水平轨迹与对照组无明显差异,但在症状发作后 0.25 年(诊所队列)或诊断前 0.5 年(英国生物库)出现拐点后,症状期的肌酸酐水平显著下降。这些数据进一步证明了肌萎缩侧索硬化症患者在症状出现前的动态代谢变化时期,始终与血液胆固醇的变化相关联。这些变化最终可能有助于开发出适用于人群筛查的生物标志物,以及指导预防性治疗目标的途径。
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