首页 > 最新文献

Journal of the Neurological Sciences最新文献

英文 中文
Functional imaging reveals cerebral microvascular dysfunction in primary antiphospholipid syndrome: Pathophysiologic insights and translational implications 功能成像揭示原发性抗磷脂综合征的脑微血管功能障碍:病理生理学见解和翻译意义。
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-09 DOI: 10.1016/j.jns.2026.125750
A. Mameli , L. Indovina , F. Cocciolillo , A. Serra , F. Marongiu , D. Barcellona
Primary antiphospholipid syndrome (PAPS) is an autoimmune thromboinflammatory disorder primarily characterized by recurrent arterial and venous thromboses and persistently elevated antiphospholipid antibodies (aPL). Beyond its classical vascular manifestations, an expanding spectrum of neuropsychiatric symptoms—including cognitive impairment, mood disturbances, and attention deficits—has been reported in PAPS, often in the absence of overt ischemic lesions on structural neuroimaging. In this study, we present original data from a cohort of 25 well-defined PAPS patients who underwent brain single-photon emission computed tomography (SPECT) imaging with Statistical Parametric Mapping (SPM) analysis. Compared to age- and sex-matched controls, PAPS patients demonstrated a consistent pattern of cerebral hypoperfusion involving bilateral frontoparietal cortices, independent of clinical neurological manifestations or MRI findings. These abnormalities suggest functional microvascular impairment potentially mediated by chronic endothelial dysfunction, complement activation, and aPL-induced neuroinflammatory cascades. Our findings support the hypothesis that cerebral involvement in PAPS extends beyond thrombotic injury to include immune-mediated microvascular and neuroglial dysregulation. This study highlights the value of functional imaging in uncovering subclinical cerebral dysfunction and proposes a neuroimmunological framework for understanding and managing cognitive and psychiatric symptoms in PAPS. Early identification of such changes may offer a window for therapeutic intervention before irreversible neuronal damage occurs.
原发性抗磷脂综合征(PAPS)是一种自身免疫性血栓炎性疾病,主要特征是动脉和静脉血栓复发和持续升高的抗磷脂抗体(aPL)。除了其典型的血管表现外,PAPS中还报道了一系列神经精神症状,包括认知障碍、情绪障碍和注意力缺陷,通常在结构神经影像学上没有明显的缺血性病变。在这项研究中,我们提供了来自25名定义明确的PAPS患者的原始数据,这些患者接受了脑单光子发射计算机断层扫描(SPECT)成像和统计参数映射(SPM)分析。与年龄和性别匹配的对照组相比,PAPS患者表现出涉及双侧额顶叶皮质的一致的脑灌注不足模式,独立于临床神经学表现或MRI结果。这些异常提示微血管功能损伤可能由慢性内皮功能障碍、补体激活和apl诱导的神经炎症级联反应介导。我们的研究结果支持了脑参与PAPS的假设,包括免疫介导的微血管和神经胶质失调,而不仅仅是血栓性损伤。这项研究强调了功能成像在发现亚临床脑功能障碍方面的价值,并提出了一个神经免疫学框架来理解和管理PAPS的认知和精神症状。在不可逆的神经元损伤发生之前,早期识别这些变化可能为治疗干预提供一个窗口。
{"title":"Functional imaging reveals cerebral microvascular dysfunction in primary antiphospholipid syndrome: Pathophysiologic insights and translational implications","authors":"A. Mameli ,&nbsp;L. Indovina ,&nbsp;F. Cocciolillo ,&nbsp;A. Serra ,&nbsp;F. Marongiu ,&nbsp;D. Barcellona","doi":"10.1016/j.jns.2026.125750","DOIUrl":"10.1016/j.jns.2026.125750","url":null,"abstract":"<div><div>Primary antiphospholipid syndrome (PAPS) is an autoimmune thromboinflammatory disorder primarily characterized by recurrent arterial and venous thromboses and persistently elevated antiphospholipid antibodies (aPL). Beyond its classical vascular manifestations, an expanding spectrum of neuropsychiatric symptoms—including cognitive impairment, mood disturbances, and attention deficits—has been reported in PAPS, often in the absence of overt ischemic lesions on structural neuroimaging. In this study, we present original data from a cohort of 25 well-defined PAPS patients who underwent brain single-photon emission computed tomography (SPECT) imaging with Statistical Parametric Mapping (SPM) analysis. Compared to age- and sex-matched controls, PAPS patients demonstrated a consistent pattern of cerebral hypoperfusion involving bilateral frontoparietal cortices, independent of clinical neurological manifestations or MRI findings. These abnormalities suggest functional microvascular impairment potentially mediated by chronic endothelial dysfunction, complement activation, and aPL-induced neuroinflammatory cascades. Our findings support the hypothesis that cerebral involvement in PAPS extends beyond thrombotic injury to include immune-mediated microvascular and neuroglial dysregulation. This study highlights the value of functional imaging in uncovering subclinical cerebral dysfunction and proposes a neuroimmunological framework for understanding and managing cognitive and psychiatric symptoms in PAPS. Early identification of such changes may offer a window for therapeutic intervention before irreversible neuronal damage occurs.</div></div>","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125750"},"PeriodicalIF":3.2,"publicationDate":"2026-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145966565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The ongoing debate about the association between benzodiazepines and dementia 关于苯二氮卓类药物和痴呆之间关系的持续争论。
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-09 DOI: 10.1016/j.jns.2026.125737
Diego Legrand , Pasquale Roberge , Christian Bocti
{"title":"The ongoing debate about the association between benzodiazepines and dementia","authors":"Diego Legrand ,&nbsp;Pasquale Roberge ,&nbsp;Christian Bocti","doi":"10.1016/j.jns.2026.125737","DOIUrl":"10.1016/j.jns.2026.125737","url":null,"abstract":"","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125737"},"PeriodicalIF":3.2,"publicationDate":"2026-01-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146018995","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Methodological considerations on benzodiazepine exposure and dementia risk: Commentary on Legrand et al. 苯二氮卓类药物暴露与痴呆风险的方法学考虑:对Legrand等人的评论。
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-08 DOI: 10.1016/j.jns.2026.125736
Tian Ruan , Tao Yu , Fang Zhao , Yaohua Tang
{"title":"Methodological considerations on benzodiazepine exposure and dementia risk: Commentary on Legrand et al.","authors":"Tian Ruan ,&nbsp;Tao Yu ,&nbsp;Fang Zhao ,&nbsp;Yaohua Tang","doi":"10.1016/j.jns.2026.125736","DOIUrl":"10.1016/j.jns.2026.125736","url":null,"abstract":"","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125736"},"PeriodicalIF":3.2,"publicationDate":"2026-01-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146018976","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Letter to the editor: Association between benzodiazepines and dementia: A case-control study from Canadian health surveys and medico-administrative databases 致编辑的信:苯二氮卓类药物与痴呆之间的关系:来自加拿大健康调查和医学管理数据库的病例对照研究
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-07 DOI: 10.1016/j.jns.2026.125738
Zhiyi Chen , Longyao Zhang , Xuezhu Zhang
{"title":"Letter to the editor: Association between benzodiazepines and dementia: A case-control study from Canadian health surveys and medico-administrative databases","authors":"Zhiyi Chen ,&nbsp;Longyao Zhang ,&nbsp;Xuezhu Zhang","doi":"10.1016/j.jns.2026.125738","DOIUrl":"10.1016/j.jns.2026.125738","url":null,"abstract":"","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125738"},"PeriodicalIF":3.2,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145940313","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of corticosteroid use on comorbidities in patients with myasthenia gravis in the US National Veterans Affairs Health Network 美国国家退伍军人事务健康网络中使用皮质类固醇对重症肌无力患者合并症的影响
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-07 DOI: 10.1016/j.jns.2025.125716
Cynthia Z. Qi , Yilu Lin , Yuebing Li , Tuan Vu , Deborah Gelinas , Alexis A. Lizarraga , Cécile Blein , Femke De Ruyck , Lizheng Shi

Background

Corticosteroid use may increase the risk of common comorbidities in patients with myasthenia gravis (MG); however, limited longitudinal data are available to evaluate this risk over time.

Methods

This retrospective cohort study used electronic medical record data from the National Veterans Affairs Health Care Network database (January 1999–March 2024) to evaluate the impact of corticosteroid use on the development of selected comorbidities in patients with and without generalized MG. Index date was the first MG diagnosis for the MG cohort and a randomly chosen date for a propensity score-matched non-MG cohort; patients were followed until disenrollment, end-of-study, or death.

Results

In total, 10,632 patients with MG and 10,632 matched controls were included; mean follow-up was 7.8 years. Corticosteroids were received by 51.6% of MG and 21.2% of non-MG patients. Both MG and non-MG patients who received corticosteroids had a higher incidence of new-onset comorbidities during follow-up than MG and non-MG patients without corticosteroid use (p < 0.0001). Among MG patients, multivariate analyses showed statistically significant increases in the annualized risk of new-onset diabetes (hazard ratios 1.32–1.76), infections (1.19–1.25), osteoporosis (1.33–1.69), and cardiovascular disease (1.19–1.31) across medium- and high-dose intensities (p < 0.05). Statistically significant increases in annualized risk were observed for glaucoma (hazard ratio 1.81 at high dose; p < 0.05) and depression (1.22 at medium dose; p < 0.05).

Conclusions

Increased risks for the development of key comorbidities among patients with MG were associated with corticosteroid use, particularly at higher-dose intensities. Our findings support strategies to minimize corticosteroid usage in MG.
背景:使用皮质类固醇可能会增加重症肌无力(MG)患者常见合并症的风险;然而,有限的纵向数据可用于评估这种风险随时间的变化。方法本回顾性队列研究使用国家退伍军人事务卫生保健网络数据库(1999年1月至2024年3月)的电子病历数据,评估皮质类固醇使用对有和无全身性MG患者选定合并症发展的影响。指标日期为MG队列的首次MG诊断,为倾向评分匹配的非MG队列的随机选择日期;随访患者直至受试者退出、研究结束或死亡。结果共纳入MG患者10632例,对照组10632例;平均随访7.8年。51.6%的MG患者和21.2%的非MG患者接受了皮质类固醇治疗。接受皮质类固醇治疗的MG和非MG患者在随访期间新发合并症的发生率均高于未使用皮质类固醇的MG和非MG患者(p < 0.0001)。在MG患者中,多因素分析显示,在中、高剂量组中,新发糖尿病(危险比1.32-1.76)、感染(危险比1.19-1.25)、骨质疏松(危险比1.33-1.69)和心血管疾病(危险比1.19-1.31)的年化风险增加具有统计学意义(p < 0.05)。青光眼(高剂量时风险比为1.81,p < 0.05)和抑郁症(中剂量时风险比为1.22,p < 0.05)的年化风险显著增加。结论:MG患者发生主要合并症的风险增加与皮质类固醇的使用有关,特别是在高剂量强度下。我们的研究结果支持在MG患者中减少皮质类固醇使用的策略。
{"title":"Impact of corticosteroid use on comorbidities in patients with myasthenia gravis in the US National Veterans Affairs Health Network","authors":"Cynthia Z. Qi ,&nbsp;Yilu Lin ,&nbsp;Yuebing Li ,&nbsp;Tuan Vu ,&nbsp;Deborah Gelinas ,&nbsp;Alexis A. Lizarraga ,&nbsp;Cécile Blein ,&nbsp;Femke De Ruyck ,&nbsp;Lizheng Shi","doi":"10.1016/j.jns.2025.125716","DOIUrl":"10.1016/j.jns.2025.125716","url":null,"abstract":"<div><h3>Background</h3><div>Corticosteroid use may increase the risk of common comorbidities in patients with myasthenia gravis (MG); however, limited longitudinal data are available to evaluate this risk over time.</div></div><div><h3>Methods</h3><div>This retrospective cohort study used electronic medical record data from the National Veterans Affairs Health Care Network database (January 1999–March 2024) to evaluate the impact of corticosteroid use on the development of selected comorbidities in patients with and without generalized MG. Index date was the first MG diagnosis for the MG cohort and a randomly chosen date for a propensity score-matched non-MG cohort; patients were followed until disenrollment, end-of-study, or death.</div></div><div><h3>Results</h3><div>In total, 10,632 patients with MG and 10,632 matched controls were included; mean follow-up was 7.8 years. Corticosteroids were received by 51.6% of MG and 21.2% of non-MG patients. Both MG and non-MG patients who received corticosteroids had a higher incidence of new-onset comorbidities during follow-up than MG and non-MG patients without corticosteroid use (<em>p</em> &lt; 0.0001). Among MG patients, multivariate analyses showed statistically significant increases in the annualized risk of new-onset diabetes (hazard ratios 1.32–1.76), infections (1.19–1.25), osteoporosis (1.33–1.69), and cardiovascular disease (1.19–1.31) across medium- and high-dose intensities (<em>p</em> &lt; 0.05). Statistically significant increases in annualized risk were observed for glaucoma (hazard ratio 1.81 at high dose; <em>p</em> &lt; 0.05) and depression (1.22 at medium dose; <em>p</em> &lt; 0.05).</div></div><div><h3>Conclusions</h3><div>Increased risks for the development of key comorbidities among patients with MG were associated with corticosteroid use, particularly at higher-dose intensities. Our findings support strategies to minimize corticosteroid usage in MG.</div></div>","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125716"},"PeriodicalIF":3.2,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145979232","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A 12-month observational study on the safety, efficacy on migraine-associated symptoms and satisfaction of CGRP monoclonal antibodies in Japanese patients with migraine 日本偏头痛患者服用CGRP单克隆抗体的安全性、偏头痛相关症状的有效性和满意度的12个月观察研究
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-07 DOI: 10.1016/j.jns.2026.125751
Shungo Imai , Keiko Ihara , Nobuyuki Takahashi , Seiya Ohtani , Narumi Watanabe , Chisato Iba , Kei Ishizuchi , Ryo Takemura , Jin Nakahara , Satoko Hori , Tsubasa Takizawa

Introduction

Calcitonin gene-related peptide monoclonal antibodies (CGRP mAbs) are effective in clinical trials and real-world settings. However, data other than headache frequency remains limited in East Asia. Thus, we investigated long-term efficacy, tolerability, and patient-reported satisfaction of CGRP mAbs in clinical practice.

Methods

This single-center observational study included patients with migraine who were administered one of three CGRP mAbs (erenumab, galcanezumab, and fremanezumab) between August 2021 and February 2023. Baseline demographic and headache characteristics were recorded, and treatment outcomes, adverse events, migraine-associated symptoms, and satisfaction levels were assessed over time.

Results

We enrolled 150 patients with episodic (n = 81) or chronic migraine (n = 69), including 40 with migraine aura. At six and twelve months, 36/67 (54%) and 22/42 (52%) patients achieved at least 50% reduction in monthly migraine days. Multivariate logistic regression showed that among differences in demographic and headache characteristics between responders and non-responders, the response rate at 3 months was associated with the 6-month response. Migraine-associated symptoms and aura showed improving trends until 5 months after CGRP mAbs initiation. As for safety, injection site reaction was seen in 35/146 (24%), 14/57 (25%), and 4/37 (11%) at 1, 6, and 12 months, respectively. Regarding satisfaction, 74%, 92%, and 94% answered “very satisfied” or “somewhat satisfied” at 1, 6, and 12 months, respectively.

Conclusion

This study highlighted the role of early response in predicting the long-term response to CGRP mAbs. We also emphasized the importance of documenting satisfaction, migraine aura frequency, in addition to migraine frequency, for deeper insights into migraine pathophysiology.
降钙素基因相关肽单克隆抗体(CGRP mab)在临床试验和现实环境中是有效的。然而,除了头痛频率以外,东亚地区的数据仍然有限。因此,我们在临床实践中调查了CGRP单克隆抗体的长期疗效、耐受性和患者报告的满意度。该单中心观察性研究纳入了在2021年8月至2023年2月期间接受三种CGRP单抗(erenumab, galcanezumab和fremanezumab)之一治疗的偏头痛患者。记录基线人口统计学和头痛特征,并随时间评估治疗结果、不良事件、偏头痛相关症状和满意度。结果我们纳入了150例发作性偏头痛(n = 81)或慢性偏头痛(n = 69)患者,包括40例偏头痛先兆患者。在6个月和12个月时,36/67(54%)和22/42(52%)患者每月偏头痛天数减少至少50%。多因素logistic回归分析显示,在缓解者和无缓解者人口学特征和头痛特征的差异中,3个月时的缓解率与6个月时的缓解率相关。偏头痛相关症状和先兆在CGRP单克隆抗体启动后5个月有改善趋势。安全性方面,1个月、6个月和12个月时,分别有35/146(24%)、14/57(25%)和4/37(11%)出现注射部位反应。在满意度方面,74%、92%和94%分别在1个月、6个月和12个月时回答“非常满意”或“比较满意”。结论本研究强调了早期反应在预测CGRP单抗长期反应中的作用。我们还强调了记录满意度、偏头痛先兆频率以及偏头痛频率的重要性,以便更深入地了解偏头痛的病理生理学。
{"title":"A 12-month observational study on the safety, efficacy on migraine-associated symptoms and satisfaction of CGRP monoclonal antibodies in Japanese patients with migraine","authors":"Shungo Imai ,&nbsp;Keiko Ihara ,&nbsp;Nobuyuki Takahashi ,&nbsp;Seiya Ohtani ,&nbsp;Narumi Watanabe ,&nbsp;Chisato Iba ,&nbsp;Kei Ishizuchi ,&nbsp;Ryo Takemura ,&nbsp;Jin Nakahara ,&nbsp;Satoko Hori ,&nbsp;Tsubasa Takizawa","doi":"10.1016/j.jns.2026.125751","DOIUrl":"10.1016/j.jns.2026.125751","url":null,"abstract":"<div><h3>Introduction</h3><div>Calcitonin gene-related peptide monoclonal antibodies (CGRP mAbs) are effective in clinical trials and real-world settings. However, data other than headache frequency remains limited in East Asia. Thus, we investigated long-term efficacy, tolerability, and patient-reported satisfaction of CGRP mAbs in clinical practice.</div></div><div><h3>Methods</h3><div>This single-center observational study included patients with migraine who were administered one of three CGRP mAbs (erenumab, galcanezumab, and fremanezumab) between August 2021 and February 2023. Baseline demographic and headache characteristics were recorded, and treatment outcomes, adverse events, migraine-associated symptoms, and satisfaction levels were assessed over time.</div></div><div><h3>Results</h3><div>We enrolled 150 patients with episodic (<em>n</em> = 81) or chronic migraine (<em>n</em> = 69), including 40 with migraine aura. At six and twelve months, 36/67 (54%) and 22/42 (52%) patients achieved at least 50% reduction in monthly migraine days. Multivariate logistic regression showed that among differences in demographic and headache characteristics between responders and non-responders, the response rate at 3 months was associated with the 6-month response. Migraine-associated symptoms and aura showed improving trends until 5 months after CGRP mAbs initiation. As for safety, injection site reaction was seen in 35/146 (24%), 14/57 (25%), and 4/37 (11%) at 1, 6, and 12 months, respectively. Regarding satisfaction, 74%, 92%, and 94% answered “very satisfied” or “somewhat satisfied” at 1, 6, and 12 months, respectively.</div></div><div><h3>Conclusion</h3><div>This study highlighted the role of early response in predicting the long-term response to CGRP mAbs. We also emphasized the importance of documenting satisfaction, migraine aura frequency, in addition to migraine frequency, for deeper insights into migraine pathophysiology.</div></div>","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125751"},"PeriodicalIF":3.2,"publicationDate":"2026-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145979231","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The impact of adding optical coherence tomography in MS diagnostic criteria on the classification of tumefactive demyelination 在MS诊断标准中加入光学相干断层扫描对肿瘤性脱髓鞘分类的影响。
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-06 DOI: 10.1016/j.jns.2026.125739
Fiorella S. Guido , John J. Chen , Paul A. Decker , Mahboubeh Fereidan-Esfahani , Kevin D. Chodnicki , Deena A. Tajfirouz , Eoin P. Flanagan , Orhun H. Kantarci , B. Mark Keegan , Sean J. Pittock , Jan-Mendelt Tillema , Claudia F. Lucchinetti , Jeanette E. Eckel-Passow , W. Oliver Tobin

Background

De novo tumefactive demyelination (TD) poses a diagnostic challenge, with lower rates of cerebrospinal fluid (CSF) oligoclonal bands and lower female-to-male ratio than typical onset multiple sclerosis (MS). Only about half fulfill the 2017 McDonald diagnostic criteria for MS at presentation. Therefore, our aim was to assess optic nerve involvement by optical coherence tomography (OCT) in patients with TD. Further, whether the presence of abnormalities on OCT would allow additional TD patients to be diagnosed with MS when the optic nerve is added as a fifth topography to the Barkhof criteria or 2017 McDonald criteria.

Methods

Observational retrospective chart review of patients seen at a tertiary referral center from 1/1/1990 to 2/21/2024 with TD. Inclusion criteria were: 1) brain MRI showing an active TD lesion; 2) medical records with at least one available clinical assessment by a neurologist; 3) available Cirrus OCT data to review. Exclusion criteria were: 1) patients with final diagnosis of vasculitis, abscess, CNS malignancies, or MOGAD; 2) presence of confounding ocular disease.

Results

OCT was available in 68 patients with TD. The tumefactive attack was the first demyelinating event in 45 (67 %) patients. At presentation, 29/68 (43 %) fulfilled 3 of 4 Barkhof criteria, and 34/68 (50 %) fulfilled the 2017 McDonald criteria for the diagnosis of MS. A clinical history of optic neuritis was present in 9/68 (13 %) patients and OCT was abnormal in 9/9 (100 %) of those patients. Regardless of clinical history, OCT was abnormal in 22/68 (32 %) patients. Therefore, OCT identified abnormalities suggestive of prior optic neuritis in 13/59 (22 %) TD patients without a clinical history of optic neuritis. If the optic nerve, as a firth topography, was assessed by OCT 39/68 (57 %) would fulfill McDonald criteria.

Conclusions

OCT in patients presenting with TD lesions can frequently identify both clinical and subclinical optic neuritis. The addition of the optic nerve as a fifth topography assessed by OCT to fulfill dissemination in space criteria would allow additional TD patients to be diagnosed with MS.
背景:与典型发病的多发性硬化症(MS)相比,新生肿瘤性脱髓鞘(TD)的脑脊液(CSF)寡克隆带率较低,男女比例较低,这给诊断带来了挑战。只有大约一半的患者符合2017年麦当劳多发性硬化症的诊断标准。因此,我们的目的是通过光学相干断层扫描(OCT)评估TD患者的视神经受累情况。此外,当视神经作为第五个地形添加到Barkhof标准或2017 McDonald标准中时,OCT异常的存在是否会允许额外的TD患者被诊断为MS。方法:对1990年1月1日至2024年2月21日在三级转诊中心就诊的TD患者进行观察性回顾性分析。纳入标准为:1)脑MRI显示活动性TD病变;2)医疗记录,至少有一份由神经科医生进行的临床评估;3)可利用的卷云OCT数据进行审查。排除标准为:1)最终诊断为血管炎、脓肿、中枢神经系统恶性肿瘤或MOGAD的患者;2)存在混淆性眼病。结果:68例TD患者行OCT检查。45例(67%)患者的首次脱髓鞘事件为肿瘤性发作。就诊时,29/68(43%)符合Barkhof 4项诊断标准中的3项,34/68(50%)符合2017年诊断ms的McDonald标准。9/68(13%)患者有视神经炎的临床病史,9/9(100%)患者OCT异常。无论临床病史如何,68例患者中有22例(32%)OCT异常。因此,OCT在13/59(22%)无视神经炎临床史的TD患者中发现提示既往视神经炎的异常。如果视神经,作为第一个地形,通过OCT 39/68评估(57%),将满足McDonald标准。结论:视神经病变患者的OCT可以经常识别临床和亚临床视神经炎。视神经作为OCT评估的第五个地形,以满足空间传播标准,将允许更多的TD患者被诊断为多发性硬化症。
{"title":"The impact of adding optical coherence tomography in MS diagnostic criteria on the classification of tumefactive demyelination","authors":"Fiorella S. Guido ,&nbsp;John J. Chen ,&nbsp;Paul A. Decker ,&nbsp;Mahboubeh Fereidan-Esfahani ,&nbsp;Kevin D. Chodnicki ,&nbsp;Deena A. Tajfirouz ,&nbsp;Eoin P. Flanagan ,&nbsp;Orhun H. Kantarci ,&nbsp;B. Mark Keegan ,&nbsp;Sean J. Pittock ,&nbsp;Jan-Mendelt Tillema ,&nbsp;Claudia F. Lucchinetti ,&nbsp;Jeanette E. Eckel-Passow ,&nbsp;W. Oliver Tobin","doi":"10.1016/j.jns.2026.125739","DOIUrl":"10.1016/j.jns.2026.125739","url":null,"abstract":"<div><h3>Background</h3><div>De novo tumefactive demyelination (TD) poses a diagnostic challenge, with lower rates of cerebrospinal fluid (CSF) oligoclonal bands and lower female-to-male ratio than typical onset multiple sclerosis (MS). Only about half fulfill the 2017 McDonald diagnostic criteria for MS at presentation. Therefore, our aim was to assess optic nerve involvement by optical coherence tomography (OCT) in patients with TD. Further, whether the presence of abnormalities on OCT would allow additional TD patients to be diagnosed with MS when the optic nerve is added as a fifth topography to the Barkhof criteria or 2017 McDonald criteria.</div></div><div><h3>Methods</h3><div>Observational retrospective chart review of patients seen at a tertiary referral center from 1/1/1990 to 2/21/2024 with TD. Inclusion criteria were: 1) brain MRI showing an active TD lesion; 2) medical records with at least one available clinical assessment by a neurologist; 3) available Cirrus OCT data to review. Exclusion criteria were: 1) patients with final diagnosis of vasculitis, abscess, CNS malignancies, or MOGAD; 2) presence of confounding ocular disease.</div></div><div><h3>Results</h3><div>OCT was available in 68 patients with TD. The tumefactive attack was the first demyelinating event in 45 (67 %) patients. At presentation, 29/68 (43 %) fulfilled 3 of 4 Barkhof criteria, and 34/68 (50 %) fulfilled the 2017 McDonald criteria for the diagnosis of MS. A clinical history of optic neuritis was present in 9/68 (13 %) patients and OCT was abnormal in 9/9 (100 %) of those patients. Regardless of clinical history, OCT was abnormal in 22/68 (32 %) patients. Therefore, OCT identified abnormalities suggestive of prior optic neuritis in 13/59 (22 %) TD patients without a clinical history of optic neuritis. If the optic nerve, as a firth topography, was assessed by OCT 39/68 (57 %) would fulfill McDonald criteria.</div></div><div><h3>Conclusions</h3><div>OCT in patients presenting with TD lesions can frequently identify both clinical and subclinical optic neuritis. The addition of the optic nerve as a fifth topography assessed by OCT to fulfill dissemination in space criteria would allow additional TD patients to be diagnosed with MS.</div></div>","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125739"},"PeriodicalIF":3.2,"publicationDate":"2026-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145966568","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Digital biomarkers in early Alzheimer's disease from wearable or portable technology: A scoping review 可穿戴或便携式技术在早期阿尔茨海默病中的数字生物标志物:范围综述
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-06 DOI: 10.1016/j.jns.2026.125734
Mathias Holsey Gramkow , Helena Sophia Coley Gleerup , Anja Hviid Simonsen , Gunhild Waldemar , Kristian Steen Frederiksen

Background

The pursuit of accurate biomarkers for early detection and disease monitoring of Alzheimer's disease (AD) has driven a growing interest in digital biomarkers. We aimed to map the research landscape of digital biomarkers in early AD obtained with wearable or portable digital health technologies (DHTs).

Methods

In our scoping review, we included original research on portable or wearable DHTs where digital biomarkers were measured in populations of early AD (mild cognitive impairment (MCI) or mild dementia). We searched MEDLINE, Web of Science and EMBASE with a wide search strategy with independent review and data extraction by two review team members. We charted data in tabular/graphical form.

Results

After deduplication and screening of 8893 records, we included 109 studies describing a wide array of wearable or portable DHTs that obtained digital biomarkers. The study population consisted of 3019 individuals with MCI due to AD (54 % female, weighted mean age 73 years), and 1942 individuals with mild AD (55 % female, weighted mean age 73 years). The most studied biomarkers were rest/activity (39 %), speech (17 %), and gait (14 %), with most studies focusing on one domain. Few studies reported outcomes associated with diagnosis (16 %) and prognosis (3 %).

Conclusion

We identified a growing evidence base investigating digital biomarkers in early AD. There is a paucity of studies examining diagnostic and prognostic properties, representing a knowledge gap. This overview may help to guide future research efforts to bridge the gap between the development and clinical implementation of digital biomarkers in early Alzheimer's disease.
对阿尔茨海默病(AD)早期检测和疾病监测的准确生物标志物的追求推动了对数字生物标志物的兴趣日益浓厚。我们的目标是绘制可穿戴或便携式数字健康技术(dht)获得的早期AD数字生物标志物的研究图景。在我们的范围综述中,我们纳入了便携式或可穿戴dht的原始研究,其中在早期AD(轻度认知障碍(MCI)或轻度痴呆)人群中测量数字生物标志物。我们对MEDLINE, Web of Science和EMBASE进行了广泛的检索,由两名评审小组成员独立评审和数据提取。我们以表格的形式绘制数据。在对8893份记录进行重复数据删除和筛选后,我们纳入了109项研究,这些研究描述了一系列获得数字生物标志物的可穿戴或便携式dht。研究人群包括3019例由AD引起的轻度认知障碍患者(54%为女性,加权平均年龄73岁)和1942例轻度AD患者(55%为女性,加权平均年龄73岁)。研究最多的生物标志物是休息/活动(39%),语言(17%)和步态(14%),大多数研究集中在一个领域。很少有研究报告结果与诊断(16%)和预后(3%)相关。结论:我们发现了越来越多的证据基础来研究早期AD的数字生物标志物。检查诊断和预后特性的研究缺乏,这代表了知识差距。这一综述可能有助于指导未来的研究工作,以弥合早期阿尔茨海默病数字生物标志物的开发和临床实施之间的差距。
{"title":"Digital biomarkers in early Alzheimer's disease from wearable or portable technology: A scoping review","authors":"Mathias Holsey Gramkow ,&nbsp;Helena Sophia Coley Gleerup ,&nbsp;Anja Hviid Simonsen ,&nbsp;Gunhild Waldemar ,&nbsp;Kristian Steen Frederiksen","doi":"10.1016/j.jns.2026.125734","DOIUrl":"10.1016/j.jns.2026.125734","url":null,"abstract":"<div><h3>Background</h3><div>The pursuit of accurate biomarkers for early detection and disease monitoring of Alzheimer's disease (AD) has driven a growing interest in digital biomarkers. We aimed to map the research landscape of digital biomarkers in early AD obtained with wearable or portable digital health technologies (DHTs).</div></div><div><h3>Methods</h3><div>In our scoping review, we included original research on portable or wearable DHTs where digital biomarkers were measured in populations of early AD (mild cognitive impairment (MCI) or mild dementia). We searched MEDLINE, Web of Science and EMBASE with a wide search strategy with independent review and data extraction by two review team members. We charted data in tabular/graphical form.</div></div><div><h3>Results</h3><div>After deduplication and screening of 8893 records, we included 109 studies describing a wide array of wearable or portable DHTs that obtained digital biomarkers. The study population consisted of 3019 individuals with MCI due to AD (54 % female, weighted mean age 73 years), and 1942 individuals with mild AD (55 % female, weighted mean age 73 years). The most studied biomarkers were rest/activity (39 %), speech (17 %), and gait (14 %), with most studies focusing on one domain. Few studies reported outcomes associated with diagnosis (16 %) and prognosis (3 %).</div></div><div><h3>Conclusion</h3><div>We identified a growing evidence base investigating digital biomarkers in early AD. There is a paucity of studies examining diagnostic and prognostic properties, representing a knowledge gap. This overview may help to guide future research efforts to bridge the gap between the development and clinical implementation of digital biomarkers in early Alzheimer's disease.</div></div>","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125734"},"PeriodicalIF":3.2,"publicationDate":"2026-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145940311","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comments on ZILU25: Real-world efficacy of Zilucoplan in generalized myasthenia gravis 评价ZILU25: Zilucoplan治疗广泛性重症肌无力的实际疗效
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-06 DOI: 10.1016/j.jns.2026.125741
Bowen Zheng
{"title":"Comments on ZILU25: Real-world efficacy of Zilucoplan in generalized myasthenia gravis","authors":"Bowen Zheng","doi":"10.1016/j.jns.2026.125741","DOIUrl":"10.1016/j.jns.2026.125741","url":null,"abstract":"","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125741"},"PeriodicalIF":3.2,"publicationDate":"2026-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145940312","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Methodological and clinical considerations on the association between COVID-19 vaccination and ischemic stroke COVID-19疫苗接种与缺血性脑卒中相关性的方法学和临床研究
IF 3.2 3区 医学 Q1 CLINICAL NEUROLOGY Pub Date : 2026-01-06 DOI: 10.1016/j.jns.2026.125742
Yi Yang
{"title":"Methodological and clinical considerations on the association between COVID-19 vaccination and ischemic stroke","authors":"Yi Yang","doi":"10.1016/j.jns.2026.125742","DOIUrl":"10.1016/j.jns.2026.125742","url":null,"abstract":"","PeriodicalId":17417,"journal":{"name":"Journal of the Neurological Sciences","volume":"481 ","pages":"Article 125742"},"PeriodicalIF":3.2,"publicationDate":"2026-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146018964","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of the Neurological Sciences
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1