Gretel Sanabria-Diaz PhD, Alessandro Cagol MD, PhD, Po-Jui Lu PhD, Muhamed Barakovic PhD, Mario Ocampo-Pineda PhD, Xinjie Chen MD, Matthias Weigel PhD, Esther Ruberte PhD, Nina de Oliveira S. Siebenborn MD, Riccardo Galbusera MD, Sabine Schädelin MSc, Pascal Benkert PhD, Jens Kuhle MD, PhD, Ludwig Kappos MD, Lester Melie-Garcia PhD, Cristina Granziera MD, PhD
{"title":"髓鞘和轴突体积的高级 MRI 测量可识别多发性硬化症的修复。","authors":"Gretel Sanabria-Diaz PhD, Alessandro Cagol MD, PhD, Po-Jui Lu PhD, Muhamed Barakovic PhD, Mario Ocampo-Pineda PhD, Xinjie Chen MD, Matthias Weigel PhD, Esther Ruberte PhD, Nina de Oliveira S. Siebenborn MD, Riccardo Galbusera MD, Sabine Schädelin MSc, Pascal Benkert PhD, Jens Kuhle MD, PhD, Ludwig Kappos MD, Lester Melie-Garcia PhD, Cristina Granziera MD, PhD","doi":"10.1002/ana.27102","DOIUrl":null,"url":null,"abstract":"<div>\n \n <section>\n \n <h3> Objective</h3>\n \n <p>Pathological studies suggest that multiple sclerosis (MS) lesions endure multiple waves of damage and repair; however, the dynamics and characteristics of these processes are poorly understood in patients living with MS.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>We studied 128 MS patients (75 relapsing–remitting, 53 progressive) and 72 healthy controls who underwent advanced magnetic resonance imaging and clinical examination at baseline and 2 years later. Magnetization transfer saturation and multi-shell diffusion imaging were used to quantify longitudinal changes in myelin and axon volumes within MS lesions. Lesions were grouped into 4 classes (repair, damage, mixed repair damage, and stable). The frequency of each class was correlated to clinical measures, demographic characteristics, and levels of serum neurofilament light chain (sNfL).</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Stable lesions were the most frequent (<i>n</i> = 2,276; 44%), followed by lesions with patterns of “repair” (<i>n</i> = 1,352; 26.2%) and damage (<i>n</i> = 1,214; 23.5%). The frequency of “repair” lesion was negatively associated with disability (β = −0.04; <i>p</i> < 0.001) and sNfL (β = −0.16; <i>p</i> < 0.001) at follow-up. The frequency of the “damage” class was higher in progressive than relapsing–remitting patients (<i>p</i> < 0.05) and was related to disability (baseline: β = −0.078; follow-up: β = −0.076; <i>p</i> < 0.001) and age (baseline: β = −0.078; <i>p</i> < 0.001). Stable lesions were more frequent in relapsing–remitting than in progressive patients (<i>p</i> < 0.05), and in younger patients versus older (β = −0.07; <i>p</i> < 0.001) at baseline. Further, “mixed” lesions were most frequent in older patients (β = 0.004; <i>p</i> < 0.001) at baseline.</p>\n </section>\n \n <section>\n \n <h3> Interpretation</h3>\n \n <p>These findings show that repair and damage processes within MS lesions occur across the entire disease spectrum and that their frequency correlates with patients disability, age, disease duration, and extent of neuroaxonal damage. ANN NEUROL 2025;97:134–148</p>\n </section>\n </div>","PeriodicalId":127,"journal":{"name":"Annals of Neurology","volume":"97 1","pages":"134-148"},"PeriodicalIF":8.1000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11683175/pdf/","citationCount":"0","resultStr":"{\"title\":\"Advanced MRI Measures of Myelin and Axon Volume Identify Repair in Multiple Sclerosis\",\"authors\":\"Gretel Sanabria-Diaz PhD, Alessandro Cagol MD, PhD, Po-Jui Lu PhD, Muhamed Barakovic PhD, Mario Ocampo-Pineda PhD, Xinjie Chen MD, Matthias Weigel PhD, Esther Ruberte PhD, Nina de Oliveira S. Siebenborn MD, Riccardo Galbusera MD, Sabine Schädelin MSc, Pascal Benkert PhD, Jens Kuhle MD, PhD, Ludwig Kappos MD, Lester Melie-Garcia PhD, Cristina Granziera MD, PhD\",\"doi\":\"10.1002/ana.27102\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>Pathological studies suggest that multiple sclerosis (MS) lesions endure multiple waves of damage and repair; however, the dynamics and characteristics of these processes are poorly understood in patients living with MS.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>We studied 128 MS patients (75 relapsing–remitting, 53 progressive) and 72 healthy controls who underwent advanced magnetic resonance imaging and clinical examination at baseline and 2 years later. Magnetization transfer saturation and multi-shell diffusion imaging were used to quantify longitudinal changes in myelin and axon volumes within MS lesions. Lesions were grouped into 4 classes (repair, damage, mixed repair damage, and stable). The frequency of each class was correlated to clinical measures, demographic characteristics, and levels of serum neurofilament light chain (sNfL).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Stable lesions were the most frequent (<i>n</i> = 2,276; 44%), followed by lesions with patterns of “repair” (<i>n</i> = 1,352; 26.2%) and damage (<i>n</i> = 1,214; 23.5%). The frequency of “repair” lesion was negatively associated with disability (β = −0.04; <i>p</i> < 0.001) and sNfL (β = −0.16; <i>p</i> < 0.001) at follow-up. The frequency of the “damage” class was higher in progressive than relapsing–remitting patients (<i>p</i> < 0.05) and was related to disability (baseline: β = −0.078; follow-up: β = −0.076; <i>p</i> < 0.001) and age (baseline: β = −0.078; <i>p</i> < 0.001). Stable lesions were more frequent in relapsing–remitting than in progressive patients (<i>p</i> < 0.05), and in younger patients versus older (β = −0.07; <i>p</i> < 0.001) at baseline. Further, “mixed” lesions were most frequent in older patients (β = 0.004; <i>p</i> < 0.001) at baseline.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Interpretation</h3>\\n \\n <p>These findings show that repair and damage processes within MS lesions occur across the entire disease spectrum and that their frequency correlates with patients disability, age, disease duration, and extent of neuroaxonal damage. ANN NEUROL 2025;97:134–148</p>\\n </section>\\n </div>\",\"PeriodicalId\":127,\"journal\":{\"name\":\"Annals of Neurology\",\"volume\":\"97 1\",\"pages\":\"134-148\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2024-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11683175/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/ana.27102\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ana.27102","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
Advanced MRI Measures of Myelin and Axon Volume Identify Repair in Multiple Sclerosis
Objective
Pathological studies suggest that multiple sclerosis (MS) lesions endure multiple waves of damage and repair; however, the dynamics and characteristics of these processes are poorly understood in patients living with MS.
Methods
We studied 128 MS patients (75 relapsing–remitting, 53 progressive) and 72 healthy controls who underwent advanced magnetic resonance imaging and clinical examination at baseline and 2 years later. Magnetization transfer saturation and multi-shell diffusion imaging were used to quantify longitudinal changes in myelin and axon volumes within MS lesions. Lesions were grouped into 4 classes (repair, damage, mixed repair damage, and stable). The frequency of each class was correlated to clinical measures, demographic characteristics, and levels of serum neurofilament light chain (sNfL).
Results
Stable lesions were the most frequent (n = 2,276; 44%), followed by lesions with patterns of “repair” (n = 1,352; 26.2%) and damage (n = 1,214; 23.5%). The frequency of “repair” lesion was negatively associated with disability (β = −0.04; p < 0.001) and sNfL (β = −0.16; p < 0.001) at follow-up. The frequency of the “damage” class was higher in progressive than relapsing–remitting patients (p < 0.05) and was related to disability (baseline: β = −0.078; follow-up: β = −0.076; p < 0.001) and age (baseline: β = −0.078; p < 0.001). Stable lesions were more frequent in relapsing–remitting than in progressive patients (p < 0.05), and in younger patients versus older (β = −0.07; p < 0.001) at baseline. Further, “mixed” lesions were most frequent in older patients (β = 0.004; p < 0.001) at baseline.
Interpretation
These findings show that repair and damage processes within MS lesions occur across the entire disease spectrum and that their frequency correlates with patients disability, age, disease duration, and extent of neuroaxonal damage. ANN NEUROL 2025;97:134–148
期刊介绍:
Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.