肌萎缩性侧索硬化症中基于毛链的元素生物动力学失调。

IF 10.8 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
EBioMedicine Pub Date : 2025-09-01 Epub Date: 2025-09-02 DOI:10.1016/j.ebiom.2025.105907
Vishal Midya, Ghalib Bello, Angeline S Andrew, Diane B Re, Elijah W Stommel, Manish Arora
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引用次数: 0

摘要

背景:肌萎缩性侧索硬化症(ALS)是一种罕见的运动神经退行性疾病,主要在老年人中诊断。必需元素和有毒元素水平的改变与ALS病理生理有关;然而,对于ALS患者中这些元素的纵向生物动力学模式知之甚少。方法:使用一根单独的头发,我们从美国的一个国家收集和一个区域中心收集als阳性病例和als阴性对照的17个元素强度,以大约2到4小时的分辨率生成400-800个时间点的时间序列数据(总共391个样本,其中295个病例和96个对照,头发收集时的中位年龄超过60岁)。元素包括Li、Mg、P、S、Ca、Cr、Mn、Fe、Co、Ni、Cu、Zn、As、Sr、Sn、Ba和Pb。我们使用激光烧蚀-电感耦合等离子体质谱法分析了单根发丝的生长增量,以沿发丝产生元素暴露和强度的时间分辨信号。采用两种互补的信息理论方法,交叉递归量化分析和基于传递熵的网络分析,生成时间分辨特征,量化多元素生物动力学的同步性。结果:男性als阳性患者Cu-Zn时间生物动力学同向性明显低于als阴性对照组(复发率:log(β) = -1.64, p值< 0.001,q值= 0.03)。女性als阳性患者Cr-Ni时间生物动力学同向性低于als阴性对照组(复发率:log(β) = -1.59, p值< 0.001,q值= 0.46)。在男性和女性中,als阳性病例中Cu的多重中心性测量(量化Cu在所有元素强度网络中的重要性)显著低于als阴性对照[男性中,Cu的接近中心性:log(β) = -0.64, p值= 0.002,q值= 0.04;在女性中,Cu的特征向量中心性:log(β) = -0.53, p值= 0.02,q值= 0.97]。解释:我们证明,与als阴性对照相比,als阳性病例在元素生物动力学同步方面的崩溃几率明显更高,铜基网络的连通性也更差。资助:美国国立卫生研究院(P30ES023515, R01ES026033, U2CES030859, U2CES026561, R35ES030435, UL1TR004419, 1OT2NS136938-01, 1R01ES034133-01)和CDC/ATSDR (R01TS000331, R01TS000324和R01TS000285)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dysregulation of hair-strand-based elemental biodynamics in amyotrophic lateral sclerosis.

Dysregulation of hair-strand-based elemental biodynamics in amyotrophic lateral sclerosis.

Dysregulation of hair-strand-based elemental biodynamics in amyotrophic lateral sclerosis.

Dysregulation of hair-strand-based elemental biodynamics in amyotrophic lateral sclerosis.

Background: Amyotrophic lateral sclerosis (ALS) is a rare motor neurodegenerative disorder and is predominantly diagnosed in older adults. Altered levels of essential and toxic elements have been implicated in ALS pathophysiology; however, little is known about the longitudinal biodynamic patterns of these elements in patients with ALS.

Methods: Using a single individual hair strand, we generated time series data of 400-800 time points approximately at 2 to 4 hourly resolution on 17 elemental intensities in ALS-positive cases and ALS-negative controls from a national collection and a regional centre in the US (on a total sample of 391, with 295 cases and 96 controls, with median age at hair collection over 60 years). The elements included were Li, Mg, P, S, Ca, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Sr, Sn, Ba, and Pb. We analysed the growth increments in single hair strands using laser ablation-inductively coupled plasma-mass spectrometry to create time-resolved signals of elemental exposure and intensity along the hair strand. Two complementary information-theoretic methods, cross-recurrence quantification analysis and transfer entropy-based network analysis, were employed to generate time-resolved features that quantify the synchronisation of multi-element biodynamics.

Findings: Male ALS-positive cases had significantly lower synchronicity in Cu-Zn temporal biodynamics than ALS-negative controls (recurrence: log(β) = -1.64, p-value < 0.001, q-value = 0.03). Female ALS-positive cases had lower synchronicity in Cr-Ni temporal biodynamics than ALS-negative controls (recurrence: log(β) = -1.59, p-value < 0.001, q-value = 0.46). In both males and females, multiple centrality measures of Cu (that quantify the importance of Cu within a network of all elemental intensities) were significantly lower in ALS-positive cases than in ALS-negative controls [in males, closeness centrality of Cu: log(β) = -0.64, p-value = 0.002, q-value = 0.04; in females, eigenvector centrality of Cu: log(β) = -0.53, p-value = 0.02, q-value = 0.97].

Interpretation: We demonstrate that ALS-positive cases have significantly higher odds of collapse in the synchronisation of elemental biodynamics and worse connectedness in copper-based networks compared to ALS-negative controls.

Funding: US National Institutes of Health (P30ES023515, R01ES026033, U2CES030859, U2CES026561, R35ES030435, UL1TR004419, 1OT2NS136938-01, 1R01ES034133-01) and CDC/ATSDR (R01TS000331, R01TS000324 and R01TS000285).

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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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