Christina Mueller, Huixian Hong, Ayushe A. Sharma, Hongwei Qin, Etty N. Benveniste, Jerzy P. Szaflarski
{"title":"颞叶癫痫的脑温、脑代谢物和免疫系统表型。","authors":"Christina Mueller, Huixian Hong, Ayushe A. Sharma, Hongwei Qin, Etty N. Benveniste, Jerzy P. Szaflarski","doi":"10.1002/epi4.13082","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Objective</h3>\n \n <p>Epileptogenesis is linked to neuroinflammation. We hypothesized that local heat production caused by neuroinflammation can be visualized non-invasively in vivo via brain magnetic resonance spectroscopic imaging (MRSI) and MRSI-thermometry (MRSI-t) and that there is a relationship in patients with temporal lobe epilepsy (TLE) between MRSI-t and brain metabolites choline and myo-inositol and between neuroimaging and cellular and serum biomarkers of inflammation.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Thirty-six (36) participants, 18 with temporal lobe epilepsy (13 females) and 18 age-matched healthy controls (nine females), were enrolled prospectively and underwent MRSI/MRSI-t; TLE participants also provided blood samples. Temperature was measured using creatine as a reference metabolite. Analysis of Functional NeuroImages <i>3dttest</i>++ tool was used to analyze voxel-level group differences in temperature, choline, and myo-inositol. Associations with immune cell subsets, cytokines, and chemokines related to inflammation were quantified using correlation coefficients with significant relationships as noted.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Patients with TLE showed elevated temperature, choline, and myo-inositol in the temporal lobes. Higher brain temperature was associated with higher levels of cytokines and chemokines, including GM-CSF, TNF, IL-1β, and IL − 12p70, and lower frequency of immune cells including CD3<sup>+</sup> T-cells, CD4<sup>+</sup> T-cells, CD8<sup>+</sup> T-cells, and classical monocytes. Higher choline was associated with higher levels of the cytokines including LT-α, IL-13, and IL-4, and higher myo-inositol was associated with a higher frequency of CD4<sup>+</sup> T-cell and CD19<sup>+</sup> B-cell subsets and higher levels of cytokines and chemokines including LT-α, IL-13, and CCL3.</p>\n </section>\n \n <section>\n \n <h3> Significance</h3>\n \n <p>This study, for the first time, showed that in temporal lobes of patients with TLE temperature and metabolite changes correlate with cellular and serum biomarkers of inflammation. Our results provide support for further development of MRSI-t as a measure of neuroinflammation in epilepsy and potentially other neurological disorders and as an investigative and clinical tool.</p>\n </section>\n \n <section>\n \n <h3> Plain Language Summary</h3>\n \n <p>Neuroinflammation is associated with excessive heat production which can be visualized with magnetic resonance spectroscopic imaging and thermometry (MRSI-t). We prospectively investigated the relationship between MRSI-t and cellular and serum measures of peripheral inflammation in patients with temporal lobe epilepsy (TLE); we compared the results of MRSI-t in patients with TLE to healthy controls. We showed a relationship between the temperature elevations in TLE and elevations of various measures of peripheral inflammation. Our results support further development of MRSI-t as a measure of neuroinflammation in epilepsy and potentially other neurological disorders and as an investigative and clinical tool.</p>\n </section>\n </div>","PeriodicalId":12038,"journal":{"name":"Epilepsia Open","volume":"9 6","pages":"2454-2466"},"PeriodicalIF":2.8000,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633690/pdf/","citationCount":"0","resultStr":"{\"title\":\"Brain temperature, brain metabolites, and immune system phenotypes in temporal lobe epilepsy\",\"authors\":\"Christina Mueller, Huixian Hong, Ayushe A. Sharma, Hongwei Qin, Etty N. Benveniste, Jerzy P. Szaflarski\",\"doi\":\"10.1002/epi4.13082\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Objective</h3>\\n \\n <p>Epileptogenesis is linked to neuroinflammation. We hypothesized that local heat production caused by neuroinflammation can be visualized non-invasively in vivo via brain magnetic resonance spectroscopic imaging (MRSI) and MRSI-thermometry (MRSI-t) and that there is a relationship in patients with temporal lobe epilepsy (TLE) between MRSI-t and brain metabolites choline and myo-inositol and between neuroimaging and cellular and serum biomarkers of inflammation.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Thirty-six (36) participants, 18 with temporal lobe epilepsy (13 females) and 18 age-matched healthy controls (nine females), were enrolled prospectively and underwent MRSI/MRSI-t; TLE participants also provided blood samples. Temperature was measured using creatine as a reference metabolite. Analysis of Functional NeuroImages <i>3dttest</i>++ tool was used to analyze voxel-level group differences in temperature, choline, and myo-inositol. Associations with immune cell subsets, cytokines, and chemokines related to inflammation were quantified using correlation coefficients with significant relationships as noted.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Patients with TLE showed elevated temperature, choline, and myo-inositol in the temporal lobes. Higher brain temperature was associated with higher levels of cytokines and chemokines, including GM-CSF, TNF, IL-1β, and IL − 12p70, and lower frequency of immune cells including CD3<sup>+</sup> T-cells, CD4<sup>+</sup> T-cells, CD8<sup>+</sup> T-cells, and classical monocytes. Higher choline was associated with higher levels of the cytokines including LT-α, IL-13, and IL-4, and higher myo-inositol was associated with a higher frequency of CD4<sup>+</sup> T-cell and CD19<sup>+</sup> B-cell subsets and higher levels of cytokines and chemokines including LT-α, IL-13, and CCL3.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Significance</h3>\\n \\n <p>This study, for the first time, showed that in temporal lobes of patients with TLE temperature and metabolite changes correlate with cellular and serum biomarkers of inflammation. Our results provide support for further development of MRSI-t as a measure of neuroinflammation in epilepsy and potentially other neurological disorders and as an investigative and clinical tool.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Plain Language Summary</h3>\\n \\n <p>Neuroinflammation is associated with excessive heat production which can be visualized with magnetic resonance spectroscopic imaging and thermometry (MRSI-t). We prospectively investigated the relationship between MRSI-t and cellular and serum measures of peripheral inflammation in patients with temporal lobe epilepsy (TLE); we compared the results of MRSI-t in patients with TLE to healthy controls. We showed a relationship between the temperature elevations in TLE and elevations of various measures of peripheral inflammation. Our results support further development of MRSI-t as a measure of neuroinflammation in epilepsy and potentially other neurological disorders and as an investigative and clinical tool.</p>\\n </section>\\n </div>\",\"PeriodicalId\":12038,\"journal\":{\"name\":\"Epilepsia Open\",\"volume\":\"9 6\",\"pages\":\"2454-2466\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-10-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11633690/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Epilepsia Open\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/epi4.13082\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epilepsia Open","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/epi4.13082","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的癫痫的发生与神经炎症有关。我们假设,神经炎症引起的局部产热可通过脑磁共振波谱成像(MRSI)和磁共振波谱成像测温(MRSI-t)在体内无创观察到,而且在颞叶癫痫(TLE)患者中,磁共振波谱成像测温与脑代谢物胆碱和肌醇之间以及神经成像与细胞和血清炎症生物标志物之间存在关系:研究人员前瞻性地招募了 36 名参与者,其中包括 18 名颞叶癫痫患者(13 名女性)和 18 名年龄匹配的健康对照者(9 名女性),他们都接受了 MRSI/MRSI-t 检查;颞叶癫痫患者还提供了血液样本。体温测量以肌酸作为参考代谢物。功能神经图像分析 3dttest++ 工具用于分析温度、胆碱和肌醇的体素水平组间差异。使用相关系数量化了与炎症相关的免疫细胞亚群、细胞因子和趋化因子的关系,并指出了显著的关系:结果:TLE 患者的颞叶温度、胆碱和肌醇均升高。脑温升高与细胞因子和趋化因子(包括 GM-CSF、TNF、IL-1β 和 IL - 12p70)水平升高以及免疫细胞(包括 CD3+ T 细胞、CD4+ T 细胞、CD8+ T 细胞和典型单核细胞)频率降低有关。胆碱越高,细胞因子(包括LT-α、IL-13和IL-4)的水平越高;肌醇越高,CD4+ T细胞和CD19+ B细胞亚群的频率越高,细胞因子和趋化因子(包括LT-α、IL-13和CCL3)的水平越高:这项研究首次表明,TLE 患者颞叶的温度和代谢物变化与细胞和血清中的炎症生物标志物相关。我们的研究结果为进一步开发磁共振波谱成像和温度测量(MRSI-t)提供了支持,MRSI-t可用于测量癫痫和其他潜在神经系统疾病的神经炎症,并可作为一种研究和临床工具。我们前瞻性地研究了颞叶癫痫(TLE)患者的磁共振波谱成像和测温(MRSI-t)与细胞和血清外周炎症指标之间的关系;我们将TLE患者的磁共振波谱成像和测温结果与健康对照组进行了比较。我们发现颞叶癫痫患者的体温升高与各种外周炎症指标的升高之间存在关系。我们的研究结果支持进一步开发 MRSI-t,将其作为癫痫和其他潜在神经系统疾病的神经炎症测量指标,并作为一种研究和临床工具。
Brain temperature, brain metabolites, and immune system phenotypes in temporal lobe epilepsy
Objective
Epileptogenesis is linked to neuroinflammation. We hypothesized that local heat production caused by neuroinflammation can be visualized non-invasively in vivo via brain magnetic resonance spectroscopic imaging (MRSI) and MRSI-thermometry (MRSI-t) and that there is a relationship in patients with temporal lobe epilepsy (TLE) between MRSI-t and brain metabolites choline and myo-inositol and between neuroimaging and cellular and serum biomarkers of inflammation.
Methods
Thirty-six (36) participants, 18 with temporal lobe epilepsy (13 females) and 18 age-matched healthy controls (nine females), were enrolled prospectively and underwent MRSI/MRSI-t; TLE participants also provided blood samples. Temperature was measured using creatine as a reference metabolite. Analysis of Functional NeuroImages 3dttest++ tool was used to analyze voxel-level group differences in temperature, choline, and myo-inositol. Associations with immune cell subsets, cytokines, and chemokines related to inflammation were quantified using correlation coefficients with significant relationships as noted.
Results
Patients with TLE showed elevated temperature, choline, and myo-inositol in the temporal lobes. Higher brain temperature was associated with higher levels of cytokines and chemokines, including GM-CSF, TNF, IL-1β, and IL − 12p70, and lower frequency of immune cells including CD3+ T-cells, CD4+ T-cells, CD8+ T-cells, and classical monocytes. Higher choline was associated with higher levels of the cytokines including LT-α, IL-13, and IL-4, and higher myo-inositol was associated with a higher frequency of CD4+ T-cell and CD19+ B-cell subsets and higher levels of cytokines and chemokines including LT-α, IL-13, and CCL3.
Significance
This study, for the first time, showed that in temporal lobes of patients with TLE temperature and metabolite changes correlate with cellular and serum biomarkers of inflammation. Our results provide support for further development of MRSI-t as a measure of neuroinflammation in epilepsy and potentially other neurological disorders and as an investigative and clinical tool.
Plain Language Summary
Neuroinflammation is associated with excessive heat production which can be visualized with magnetic resonance spectroscopic imaging and thermometry (MRSI-t). We prospectively investigated the relationship between MRSI-t and cellular and serum measures of peripheral inflammation in patients with temporal lobe epilepsy (TLE); we compared the results of MRSI-t in patients with TLE to healthy controls. We showed a relationship between the temperature elevations in TLE and elevations of various measures of peripheral inflammation. Our results support further development of MRSI-t as a measure of neuroinflammation in epilepsy and potentially other neurological disorders and as an investigative and clinical tool.