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Identification of Senescence-Related Biomarkers and Regulatory Networks in Intracerebral Hemorrhage. 鉴定脑出血中与衰老相关的生物标记物和调控网络
IF 1.1 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-07-01 DOI: 10.1097/NRL.0000000000000548
Yan Wang, Ling Chen

Objectives: Intracerebral hemorrhage (ICH) is a severe neurological disorder with substantial societal implications. Cellular senescence plays a critical role in ICH pathogenesis. This study aims to identify senescence-related biomarkers in ICH for diagnostic and therapeutic purposes.

Methods: Raw data from GSE24265 in Gene Expression Omnibus was downloaded. Senescence-related genes were acquired from CellAge. Differential gene analysis was done between patients with ICH and controls. The intersection of ICH differentially expressed genes and senescence-related genes for senescence-related ICH genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were performed. Protein-protein interaction network was constructed through the Search Tool for the Retrieval of Interacting Genes. Single sample gene set enrichment analysis was done for immune cell infiltration and function evaluation in control and ICH groups. miRWalk2.0 database was used for microRNA predictions targeting ICH biomarkers. Transcriptional regulatory relationships unraveled by sentence-based text mining database was employed to predict transcription factors regulating identified biomarkers.

Results: Thirteen senescence-related ICH genes were identified. They were primarily enriched in the positive regulation of angiogenesis and the Advanced Glycation End Product -Receptor for AGE signaling pathway in diabetic complications. Validation in the GSE149317 data set and receiver operating characteristic analysis highlighted Caveolin 1, C-X-C Motif Chemokine Ligand 1, ETS proto-oncogene 1, transcription factor, and Serpin Family E Member 1 as potential ICH biomarkers. Single sample gene set enrichment analysis revealed increased Type 2 T helper cell 2_cells, Treg cells, and immune functions like Antigen-presenting cells_co_stimulation in patients with ICH. Fourteen microRNA, including has-miR-6728-3p, were predicted to regulate these biomarkers. transcription factors such as PPARG, RARA, HMGA1, and NFKB1 were identified as potential regulators of the ICH biomarkers.

Conclusion: Caveolin 1, C-X-C Motif Chemokine Ligand 1, ETS proto-oncogene 1, transcription factor, and Serpin Family E Member 1 may serve as valuable biomarkers in ICH. Targeting these genes could contribute to ICH prevention and treatment.

目的:脑出血(ICH)是一种严重的神经系统疾病,具有重大的社会影响。细胞衰老在 ICH 发病机制中起着关键作用。本研究旨在鉴定 ICH 中与衰老相关的生物标记物,以用于诊断和治疗:方法:下载基因表达总库(Gene Expression Omnibus)中 GSE24265 的原始数据。衰老相关基因来自 CellAge。对 ICH 患者和对照组进行差异基因分析。ICH 差异表达基因与衰老相关基因的交叉点为衰老相关的 ICH 基因。进行了基因本体和京都基因与基因组百科全书的富集分析。通过检索相互作用基因的搜索工具构建了蛋白质-蛋白质相互作用网络。利用 miRWalk2.0 数据库预测了针对 ICH 生物标志物的 microRNA。基于句子的文本挖掘数据库揭示了转录调控关系,用于预测调控已识别生物标志物的转录因子:结果:发现了 13 个与衰老相关的 ICH 基因。结果:发现了 13 个与衰老相关的 ICH 基因,它们主要富集于血管生成的正向调控和糖尿病并发症中的高级糖化终产物-AGE 受体信号通路。GSE149317 数据集和接收器操作特征分析的验证结果表明,Caveolin 1、C-X-C Motif Chemokine Ligand 1、ETS 原癌基因 1、转录因子和 Serpin 家族 E 成员 1 是潜在的 ICH 生物标志物。单样本基因组富集分析显示,ICH 患者的 2 型 T 辅助细胞 2_细胞、Treg 细胞以及抗原递呈细胞协同刺激等免疫功能增加。包括has-miR-6728-3p在内的14种microRNA被预测为可调控这些生物标志物,PPARG、RARA、HMGA1和NFKB1等转录因子被确定为ICH生物标志物的潜在调控因子:结论:Caveolin 1、C-X-C Motif Chemokine Ligand 1、ETS 原癌基因 1、转录因子和 Serpin 家族 E 成员 1 可作为有价值的 ICH 生物标志物。以这些基因为靶标可有助于 ICH 的预防和治疗。
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引用次数: 0
Cerebral Tumefactive Inflammatory Lesion Occurrence During Ixekizumab Treatment in a Patient With Active Psoriatic Arthritis. 一名活动性银屑病关节炎患者在伊克珠单抗治疗期间出现脑肿瘤性炎症病变
IF 1.1 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-07-01 DOI: 10.1097/NRL.0000000000000551
Antonio Marangi, Francesco Benvenuti, Linda Mazzai, Giulio Riva, Diana Polo, Ilaria Franceschetti, Pierino De Sandre, Mariano Agostino Zanusso, Giovanni Scanelli, Francesco Perini

Introduction: Ixekizumab is an anti-interleukin-17A (IL-17A) humanized monoclonal antibody approved for the treatment of moderate-to-severe plaque psoriasis, active psoriatic arthritis, and ankylosing spondylitis. Central nervous system inflammatory manifestations are atypical during therapy with IL-17A inhibitors, with only one case of myelitis described to date.

Case report: A 72-year-old man with a medical history of active psoriatic arthritis was admitted to our department owing to the acute onset of left face numbness 1 month after the first ixekizumab administration. Magnetic resonance imaging of the brain displayed a large T2-hyperintense infratentorial lesion involving the root of the fifth and seventh left cranial nerves. A thorough laboratoristic and instrumental work-up did not show elements suggestive of extracerebral neoplasms or infections. Therefore, neuronavigation-assisted brain biopsy was performed, and histologic analysis of the lesion revealed the presence of wide aggregates of foamy histiocytes diffusely infiltrating the brain parenchyma, in the absence of malignant tissue or histologic elements suggestive of central nervous system infections or primary histiocytoses. Steroid treatment (dexamethasone 8 mg/daily) was then administered with subsequent clinical amelioration. One month after hospital discharge, a brain magnetic resonance imaging showed a nearly complete resolution of the lesion.

Conclusion: This is the first case of a cerebral inflammatory lesion occurring during treatment with ixekizumab. Although very rare, neurological complications may occur during anti-IL-17A therapies, thus leading to the need for careful monitoring of patients exposed to these drugs.

简介伊克珠单抗是一种抗白细胞介素-17A(IL-17A)的人源化单克隆抗体,已被批准用于治疗中重度斑块状银屑病、活动性银屑病关节炎和强直性脊柱炎。在使用 IL-17A 抑制剂治疗期间,中枢神经系统炎症表现并不典型,迄今为止仅有一例脊髓炎病例:病例报告:一名 72 岁的男性患者,有活动性银屑病关节炎病史,在首次使用 ixekizumab 1 个月后因左脸麻木急性发作入住我科。脑部磁共振成像显示,其脑室下T2-高密度病变累及左侧第五颅神经根和第七颅神经根。全面的实验室和仪器检查未发现提示脑外肿瘤或感染的因素。因此,在神经导航辅助下进行了脑活检,病变组织学分析表明,脑实质内弥漫性浸润着广泛聚集的泡沫组织细胞,但没有恶性组织或提示中枢神经系统感染或原发性组织细胞病的组织学因素。随后,患者接受了类固醇治疗(地塞米松 8 毫克/天),临床症状随之好转。出院一个月后,脑磁共振成像显示病灶几乎完全消退:这是首例在使用伊克珠单抗治疗期间出现脑部炎症病变的病例。尽管非常罕见,但在抗IL-17A疗法期间可能会出现神经系统并发症,因此需要对接触此类药物的患者进行仔细监测。
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引用次数: 0
Predictive Value of Serum Inflammatory Factors and FT3 for Stroke-Associated Pneumonia in Patients With Acute Ischemic Stroke. 急性缺血性脑卒中患者血清炎症因子和 FT3 对脑卒中相关肺炎的预测价值
IF 1.2 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-06-10 DOI: 10.1097/NRL.0000000000000570
Xin Li, Xiaomei Xie, Shenju Cheng, Shan Luo, Yancui Zhu, Kun Wu

Objective: The ability of serum inflammatory factors and free triiodothyronine (FT3) in predicting the occurrence of stroke-associated pneumonia (SAP) in patients with acute ischemic stroke (AIS) was assessed in this study.

Methods: A retrospective analysis was conducted on 285 consecutive patients with AIS initially diagnosed and admitted to our hospital from January to December 2022. Patients were categorized into SAP and non-SAP groups based on the presence of SAP. Both groups were compared in terms of baseline characteristics, including National Institute of Health Stroke Scale (NIHSS) score, SAP risk assessment (A2DS2), TOAST classification. Independent risk factors for SAP were identified using multivariate logistic regression analysis, and the predictive value of inflammatory markers was evaluated through ROC curves.

Results: Among 285 patients with AIS, 40 (14.03%) were found to have developed SAP. Higher NIHSS and A2DS2 scores, elevated serum IL-1β, IL-8, and IL-33 levels, increased age, atrial fibrillation, swallowing difficulties, and a higher proportion of patients with low FT3 levels were observed in the SAP group compared with the non-SAP group (all P<0.05). Significant risk factors for SAP in patients with AIS were identified through multivariate logistic regression analysis, including age, swallowing difficulties, NIHSS, A2DS2 , IL-1β , IL-8 , IL-33, and FT3 (P<0.05). The highest predictive values were observed for A2DS2, FT3, and IL-8 with AUC values of 0.854, 0.844, and 0.823, respectively.

Conclusion: SAP can be highly predicted by A2DS2, FT3, and IL-8, enabling the early identification of patients with high-risk SAP and facilitating timely intervention and treatment.

目的本研究评估了血清炎症因子和游离三碘甲状腺原氨酸(FT3)预测急性缺血性卒中(AIS)患者卒中相关肺炎(SAP)发生的能力:方法:本研究对2022年1月至12月期间本院收治的285例急性缺血性脑卒中(AIS)患者进行了回顾性分析。根据是否存在 SAP,将患者分为 SAP 组和非 SAP 组。比较两组患者的基线特征,包括美国国立卫生研究院卒中量表(NIHSS)评分、SAP风险评估(A2DS2)和TOAST分类。通过多变量逻辑回归分析确定了SAP的独立风险因素,并通过ROC曲线评估了炎症标志物的预测价值:结果:在285名AIS患者中,有40人(14.03%)发展为SAP。与非 SAP 组相比,SAP 组患者的 NIHSS 和 A2DS2 评分更高,血清 IL-1β、IL-8 和 IL-33 水平升高,年龄增大,存在心房颤动、吞咽困难,FT3 水平低的患者比例更高(均为 PC):A2DS2、FT3和IL-8可高度预测SAP,从而能早期识别高危SAP患者,并促进及时干预和治疗。
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引用次数: 0
HaNDL Syndrome: The Innocent Lymphocytic Pleocytosis. HaNDL综合征:单纯淋巴细胞增多症。
IF 1.1 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-05-01 DOI: 10.1097/NRL.0000000000000546
Kadriye Güleda Keskin, Irem Carus, Isil Kalyoncu Aslan, Eren Gözke

Introduction: HaNDL syndrome is a transient and rare condition that presents with neurological deficit and headache accompanied by lymphocytosis on cerebrospinal fluid (CSF) analysis. It is usually characterized by spontaneous recovery without neurological sequelae. This is a benign condition, which has not yet been adequately defined and includes many diseases in the differential diagnosis. We indicated 2 different cases that applied with acute neurological findings.

Case report: Two patients who were admitted to our hospital with transient neurological deficits and headaches were evaluated. There was no significant pathology in cranial imaging and EEG reports. Lymphocytic pleocytosis was observed in CSF. Patients were followed up with attacks but were discharged without deficits. We diagnosed the patients with HaNDL syndrome with clinical features, imaging, and laboratory findings.

Conclusion: HaNDL is an underdiagnosed syndrome and it should be considered especially for young patients with headaches is prominent without a risk factor for ischemia, recurrent episodes with neurological symptoms, CSF pleocytosis, and normal imaging findings.Therefore, we wanted to raise awareness for the existence of this rare disease which is a waste of time by performing unnecessary tests and therapies during the diagnosis period.

简介:HaNDL综合征是一种短暂的、罕见的疾病,表现为神经功能缺损和头痛,并伴有脑脊液(CSF)淋巴细胞增多。它通常以自发恢复为特征,无神经系统后遗症。这是一种尚未得到充分定义的良性疾病,包括许多疾病的鉴别诊断。我们指出了2个不同的病例,适用于急性神经学表现。病例报告:我们评估了两名因短暂性神经功能障碍和头痛而入院的患者。颅成像和脑电图报告未见明显病理变化。脑脊液淋巴细胞增多。患者随访发作,出院无缺陷。我们根据临床特征、影像学和实验室结果诊断患者为HaNDL综合征。结论:HaNDL是一种未被诊断的综合征,特别是年轻的头痛患者,在没有缺血、反复发作并伴有神经系统症状、脑脊液多细胞增多、影像学正常等危险因素的情况下,应予以重视。因此,我们希望提高人们对这种罕见疾病存在的认识,因为在诊断期间进行不必要的检查和治疗是浪费时间。
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引用次数: 0
Mechanical Thrombectomy in Anticoagulated Patients With Acute Ischemic Stroke: A Meta-Analysis. 急性缺血性脑卒中抗凝患者机械取栓:荟萃分析
IF 1.2 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-05-01 DOI: 10.1097/NRL.0000000000000542
HaoLiang Zhang, Shiqin Chen, QianYuan Zhu, ZongShan Li, Tian Lv, Chengjiang Liu

Background: According to a previous studies, mechanical thrombectomy(MT) is safe for anticoagulated patients. However, the safety and prognosis of direct oral anticoagulants (DOACs) and vitamin K antagonists (VKA) have not been compared with those of MT.This meta-analysis aimed at determining the efficacy of DOACs or VKA for patients after MT.

Review summary: We searched PubMed, Embase, Web of Science databases, and Cochrane from their inception to Aug 2022. Revman 5.3 served for the meta-analysis. The meta-analysis included 12 studies that covered 3571 patients, finding that after MT treatment, DOACs significantly decreased the symptomatic intracerebral hemorrhage [odd ratio (OR)=0.49, 95% CI 0.30-0.80, P =0.004] and mortality (OR=0.63, 95% CI 0.48-0.83, P =0.001) compared with VKA. Meanwhile, no obvious differences were found between DOACs and VKA after MT treatment in terms of in any hemorrhagic transformation (OR=1.07, 95% CI 0.84-1.37, P =0.59), good functional outcome (OR=1.06, 95% CI 0.88-1.27, P =0.53), and successful arterial recanalization (OR=1.24, 95% CI 1.00-1.53, P =0.05).

Conclusions: This meta-analysis demonstrates that the application of DOACs in MT treatment for anticoagulated patients with acute ischemic stroke is safer than that in the VKA group. However, further studies are necessary to confirm these results.

背景:根据以往的研究,机械取栓(MT)对抗凝患者是安全的。然而,直接口服抗凝剂(DOACs)和维生素K拮抗剂(VKA)的安全性和预后尚未与mt进行比较。这项荟萃分析旨在确定DOACs或VKA对mt后患者的疗效。综述摘要:我们检索了PubMed, Embase, Web of Science数据库和Cochrane,从他们成立到2022年8月。meta分析采用Revman 5.3。meta分析纳入12项研究,涵盖3571例患者,发现与VKA相比,MT治疗后DOACs显著降低症状性脑出血[奇比(OR)=0.49, 95% CI 0.30-0.80, P=0.004]和死亡率(OR=0.63, 95% CI 0.48-0.83, P=0.001)。同时,在MT治疗后,DOACs与VKA在任何出血转化(OR=1.07, 95% CI 0.84-1.37, P=0.59)、良好的功能结局(OR=1.06, 95% CI 0.88-1.27, P=0.53)、动脉再通成功(OR=1.24, 95% CI 1.00-1.53, P=0.05)方面均无明显差异。结论:本荟萃分析表明,DOACs在抗凝急性缺血性脑卒中患者MT治疗中的应用比VKA组更安全。然而,需要进一步的研究来证实这些结果。
{"title":"Mechanical Thrombectomy in Anticoagulated Patients With Acute Ischemic Stroke: A Meta-Analysis.","authors":"HaoLiang Zhang, Shiqin Chen, QianYuan Zhu, ZongShan Li, Tian Lv, Chengjiang Liu","doi":"10.1097/NRL.0000000000000542","DOIUrl":"10.1097/NRL.0000000000000542","url":null,"abstract":"<p><strong>Background: </strong>According to a previous studies, mechanical thrombectomy(MT) is safe for anticoagulated patients. However, the safety and prognosis of direct oral anticoagulants (DOACs) and vitamin K antagonists (VKA) have not been compared with those of MT.This meta-analysis aimed at determining the efficacy of DOACs or VKA for patients after MT.</p><p><strong>Review summary: </strong>We searched PubMed, Embase, Web of Science databases, and Cochrane from their inception to Aug 2022. Revman 5.3 served for the meta-analysis. The meta-analysis included 12 studies that covered 3571 patients, finding that after MT treatment, DOACs significantly decreased the symptomatic intracerebral hemorrhage [odd ratio (OR)=0.49, 95% CI 0.30-0.80, P =0.004] and mortality (OR=0.63, 95% CI 0.48-0.83, P =0.001) compared with VKA. Meanwhile, no obvious differences were found between DOACs and VKA after MT treatment in terms of in any hemorrhagic transformation (OR=1.07, 95% CI 0.84-1.37, P =0.59), good functional outcome (OR=1.06, 95% CI 0.88-1.27, P =0.53), and successful arterial recanalization (OR=1.24, 95% CI 1.00-1.53, P =0.05).</p><p><strong>Conclusions: </strong>This meta-analysis demonstrates that the application of DOACs in MT treatment for anticoagulated patients with acute ischemic stroke is safer than that in the VKA group. However, further studies are necessary to confirm these results.</p>","PeriodicalId":49758,"journal":{"name":"Neurologist","volume":" ","pages":"194-203"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138452960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Intracranial Hypertension Associated With Poly-Cranio-Radicular-Neuropathies: A Case Report and Review of the Literature. 与多发性颅脊髓神经病相关的颅内高血压:病例报告和文献综述。
IF 1.2 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-05-01 DOI: 10.1097/NRL.0000000000000559
James E Eaton, Ipek Oguz, Habeeb Kazimuddin, Francesca Bagnato

Introduction: We present the case of a gentleman who developed rapidly progressive vision loss, ophthalmo-paresis, and flaccid quadriparesis in the context of severe intracranial hypertension. We reviewed the available cases in the literature to increase awareness of this rare clinical entity.Case Report:A 36-year-old man developed rapidly progressive vision loss, ophthalmo-paresis, and flaccid quadriparesis. He had an extensive workup, only notable for severe intracranial hypertension, >55 cm of H 2 O. No inflammatory features were present, and the patient responded to CSF diversion. Few similar cases are available in the literature, but all show markedly elevated intracranial pressure associated with extensive neuroaxis dysfunction. Similarly, these patients improved with CSF diversion but did not appear to respond to immune-based therapies.

Conclusions: We term this extensive neuroaxis dysfunction intracranial hypertension associated with poly-cranio-radicular-neuropathy (IHP) and distinguish it from similar immune-mediated clinical presentations. Clinicians should be aware of the different etiologies of this potentially devastating clinical presentation to inform appropriate and timely treatment.

导言:我们介绍了一名男性患者的病例,该患者在严重颅内高压的背景下出现了快速进展性视力下降、眼球震颤和弛缓性四肢瘫。我们回顾了现有文献中的病例,以提高人们对这一罕见临床实体的认识。病例报告:一名 36 岁的男子出现了快速进展性视力下降、眼球震颤和弛缓性四肢瘫。他接受了广泛的检查,唯一值得注意的是严重的颅内高压,>55 cm H2O。没有炎症特征,患者对脑脊液引流术反应良好。类似病例在文献中很少见,但都显示颅内压明显升高,伴有广泛的神经轴功能障碍。同样,这些患者在接受脑脊液转移治疗后病情有所好转,但似乎对基于免疫的疗法没有反应:我们将这种广泛的神经轴功能障碍称为颅内高压伴多颅神经病(IHP),并将其与类似的免疫介导型临床表现区分开来。临床医生应了解这种具有潜在破坏性的临床表现的不同病因,以便为适当和及时的治疗提供依据。
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引用次数: 0
Short-Term Exposure to Air Pollution and the Incidence and Mortality of Stroke: A Meta-Analysis. 短期空气污染暴露与中风的发病率和死亡率:一项荟萃分析。
IF 1.2 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-05-01 DOI: 10.1097/NRL.0000000000000544
Wenjian Lin, Jie Pan, Jiahe Li, Xiaoyu Zhou, Xueyuan Liu

Background: The relationship between short-term exposure to various air pollutants [particulate matter <10 μm (PM 10 ), particulate matter <2.5 μm (PM 2.5 ), nitrogen dioxide (NO 2 ), sulfur dioxide (SO 2 ), carbon monoxide, and ozone (O 3 )] and the incidence and mortality of stroke remain unclear.

Review summary: We conducted a comprehensive search across databases, including PubMed, Web of Science, and others. A random-effects model was employed to estimate the odds ratios (OR) and their 95% CIs. Short-term exposure to PM 10 , PM 2.5 , NO 2 , SO 2 , and O 3 was associated with increased stroke incidence [per 10 μg/m 3 increase in PM 2.5 : OR = 1.005 (95% CI: 1.004-1.007), per 10 μg/m 3 increase in PM 10 : OR = 1.006 (95% CI: 1.004-1.009), per 10 μg/m 3 increase in SO 2 : OR = 1.034 (95% CI: 1.020-1.048), per 10 μg/m 3 increase in NO 2 : OR = 1.029 (95% CI: 1.015-1.043), and O 3 for per 10 μg/m 3 increase: OR: 1.006 (95% CI: 1.004-1.007)]. In addition, short-term exposure to PM 2.5 , PM 10 , SO 2, and NO 2 was correlated with increased mortality from stroke [per 10 μg/m 3 increase in PM 2.5 : OR = 1.010 (95% CI: 1.006-1.013), per 10 μg/m 3 increase in PM 10 : OR = 1.004 (95% CI: 1.003-1.006), per 10 μg/m 3 increase in SO 2 : OR = 1.013 (95% CI: 1.007-1.019) and per 10 μg/m 3 increase in NO 2 : OR = 1.012 (95% CI: 1.008-1.015)].

Conclusion: Reducing outdoor air pollutant levels may yield a favorable outcome in reducing the incidence and mortality associated with strokes.

背景:短期暴露于各种空气污染物之间的关系综述摘要:我们在数据库中进行了全面的搜索,包括PubMed, Web of Science等。采用随机效应模型估计比值比(OR)及其95% ci。短期暴露于PM10、PM2.5、NO2、SO2和O3与卒中发病率增加相关[PM2.5每增加10 μg/m3: OR = 1.005 (95% CI: 1.004-1.007), PM10每增加10 μg/m3: OR = 1.006 (95% CI: 1.004-1.009), SO2每增加10 μg/m3: OR = 1.034 (95% CI: 1.020-1.048), NO2每增加10 μg/m3: OR = 1.029 (95% CI: 1.015-1.043), O3每增加10 μg/m3: OR: 1.006 (95% CI: 1.004-1.007)]。此外,短期暴露于PM2.5、PM10、SO2和NO2与卒中死亡率增加相关[PM2.5每增加10 μg/m3: OR = 1.010 (95% CI: 1.006-1.013), PM10每增加10 μg/m3: OR = 1.004 (95% CI: 1.003-1.006), SO2每增加10 μg/m3: OR = 1.013 (95% CI: 1.007-1.019), NO2每增加10 μg/m3: OR = 1.012 (95% CI: 1.008-1.015)]。结论:减少室外空气污染水平可能对降低卒中相关的发病率和死亡率产生有利的结果。
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引用次数: 0
Neurological Diagnosis: Artificial Intelligence Compared With Diagnostic Generator. 神经学诊断:人工智能与诊断生成器的比较。
IF 1.2 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-05-01 DOI: 10.1097/NRL.0000000000000560
Pasquale F Finelli

Objective: Artificial intelligence has recently become available for widespread use in medicine, including the interpretation of digitized information, big data for tracking disease trends and patterns, and clinical diagnosis. Comparative studies and expert opinion support the validity of imaging and data analysis, yet similar validation is lacking in clinical diagnosis. Artificial intelligence programs are here compared with a diagnostic generator program in clinical neurology.

Methods: Using 4 nonrandomly selected case records from New England Journal of Medicine clinicopathologic conferences from 2017 to 2022, 2 artificial intelligence programs (ChatGPT-4 and GLASS AI) were compared with a neurological diagnostic generator program (NeurologicDx.com) for diagnostic capability and accuracy and source authentication.

Results: Compared with NeurologicDx.com, the 2 AI programs showed results varying with order of key term entry and with repeat querying. The diagnostic generator yielded more differential diagnostic entities, with correct diagnoses in 4 of 4 test cases versus 0 of 4 for ChatGPT-4 and 1 of 4 for GLASS AI, respectively, and with authentication of diagnostic entities compared with the AI programs.

Conclusions: The diagnostic generator NeurologicDx yielded a more robust and reproducible differential diagnostic list with higher diagnostic accuracy and associated authentication compared with artificial intelligence programs.

目的:人工智能近来已广泛应用于医学领域,包括解读数字化信息、跟踪疾病趋势和模式的大数据以及临床诊断。比较研究和专家意见支持成像和数据分析的有效性,但在临床诊断中却缺乏类似的验证。本文将人工智能程序与临床神经学诊断生成器程序进行比较:使用从 2017 年至 2022 年《新英格兰医学杂志》临床病理会议中非随机抽取的 4 个病例记录,将 2 个人工智能程序(ChatGPT-4 和 GLASS AI)与神经学诊断生成程序(NeurologicDx.com)进行了诊断能力和准确性以及来源认证方面的比较:结果:与NeurologicDx.com相比,这两个人工智能程序的结果随关键术语输入顺序和重复查询的不同而变化。诊断生成器产生了更多的鉴别诊断实体,4 个测试案例中有 4 个诊断正确,而 ChatGPT-4 和 GLASS AI 则分别为 4 个和 1 个:结论:与人工智能程序相比,诊断生成器 NeurologicDx 生成的鉴别诊断列表更稳健、更可重复,诊断准确率更高,相关认证也更高。
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引用次数: 0
Characteristics of Cerebral Venous Sinus Thrombosis Due to Autoimmune Diseases: A Single-Center Retrospective Observational Study. 自身免疫性疾病导致的脑静脉窦血栓的特征:一项单中心回顾性观察研究
IF 1.2 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-05-01 DOI: 10.1097/NRL.0000000000000555
Furkan Saridas, Gizem Mesut, Yasemin Dinc, Emine Rabia Koc, Rifat Ozpar, Bahattin Hakyemez, Omer Faruk Turan

Objectives: Cerebral venous sinus thrombosis (CVST) is a cerebrovascular disease characterized by thrombosis of the cerebral venous or dural sinuses. Autoimmune diseases (AD) are important causes of CVST. This study aims to reveal the differences between CVST associated with autoimmune diseases compared with other causes (OCs) and Behcet's syndrome (BS) compared with other ADs.

Methods: This is a single-center retrospective study in which the medical records of 187 patients we followed with a diagnosis of CVST between 2008 and 2023 were collected retrospectively. Four neurologists collected data on initial symptoms, neurological examinations, and laboratory findings. Findings on magnetic resonance imaging and magnetic resonance venography performed on all patients (thrombosis localizations, hemorrhagic or ischemic complications, and collateralization) were re-evaluated by 2 radiologists. The results were compared with AD, other ADs, and OCs groups.

Results: There were 28 cases of CVST associated with AD. Of these, 18 were BS, and 10 were other AD. Subacute-chronic onset, headache, and transverse sinus involvement were more common in AD-related patients than in OCs. However, collateralization, venous infarction, hemorrhagic transformation, and bleeding were less common. BS-related patients had earlier age, more frequent transverse sinus, less frequent cortical vein thrombosis, and better collateralization than other ADs.

Conclusion: CVST is one of the rare complications in autoimmune diseases. It has a more subacute-chronic onset. Since headaches are more common, it is essential to make a differential diagnosis of CVST in autoimmune diseases with chronic headaches. Transverse sinus thrombosis is more common. Collateralization, venous infarction, and hemorrhagic transformation are less.

目的:脑静脉窦血栓形成(CVST)是一种以脑静脉或硬脑膜窦血栓形成为特征的脑血管疾病。自身免疫性疾病(AD)是导致 CVST 的重要原因。本研究旨在揭示与自身免疫性疾病相关的 CVST 与其他病因(OCs)相比的差异,以及白塞氏综合征(BS)与其他 ADs 相比的差异:这是一项单中心回顾性研究,我们对 2008 年至 2023 年间诊断为 CVST 的 187 名患者的病历进行了回顾性收集。四位神经科医生收集了有关初始症状、神经系统检查和实验室检查结果的数据。所有患者的磁共振成像和磁共振静脉造影结果(血栓定位、出血或缺血并发症以及侧支)均由两名放射科医生重新评估。结果与 AD 组、其他 AD 组和 OC 组进行了比较:结果:与 AD 相关的 CVST 有 28 例。结果:与 AD 相关的 CVST 有 28 例,其中 18 例为 BS,10 例为其他 AD。与 OCs 相比,AD 相关患者中亚急性慢性起病、头痛和横窦受累更为常见。然而,侧支、静脉梗塞、出血性转化和出血则较少见。与其他 ADs 相比,BS 相关患者的年龄更早、横窦更常见、皮质静脉血栓形成更少、侧支化更好:结论:CVST 是自身免疫性疾病中罕见的并发症之一。结论:CVST 是自身免疫性疾病中罕见的并发症之一。由于头痛更为常见,因此对伴有慢性头痛的自身免疫性疾病进行 CVST 鉴别诊断至关重要。横窦血栓形成更为常见。侧支、静脉梗塞和出血性转化则较少见。
{"title":"Characteristics of Cerebral Venous Sinus Thrombosis Due to Autoimmune Diseases: A Single-Center Retrospective Observational Study.","authors":"Furkan Saridas, Gizem Mesut, Yasemin Dinc, Emine Rabia Koc, Rifat Ozpar, Bahattin Hakyemez, Omer Faruk Turan","doi":"10.1097/NRL.0000000000000555","DOIUrl":"10.1097/NRL.0000000000000555","url":null,"abstract":"<p><strong>Objectives: </strong>Cerebral venous sinus thrombosis (CVST) is a cerebrovascular disease characterized by thrombosis of the cerebral venous or dural sinuses. Autoimmune diseases (AD) are important causes of CVST. This study aims to reveal the differences between CVST associated with autoimmune diseases compared with other causes (OCs) and Behcet's syndrome (BS) compared with other ADs.</p><p><strong>Methods: </strong>This is a single-center retrospective study in which the medical records of 187 patients we followed with a diagnosis of CVST between 2008 and 2023 were collected retrospectively. Four neurologists collected data on initial symptoms, neurological examinations, and laboratory findings. Findings on magnetic resonance imaging and magnetic resonance venography performed on all patients (thrombosis localizations, hemorrhagic or ischemic complications, and collateralization) were re-evaluated by 2 radiologists. The results were compared with AD, other ADs, and OCs groups.</p><p><strong>Results: </strong>There were 28 cases of CVST associated with AD. Of these, 18 were BS, and 10 were other AD. Subacute-chronic onset, headache, and transverse sinus involvement were more common in AD-related patients than in OCs. However, collateralization, venous infarction, hemorrhagic transformation, and bleeding were less common. BS-related patients had earlier age, more frequent transverse sinus, less frequent cortical vein thrombosis, and better collateralization than other ADs.</p><p><strong>Conclusion: </strong>CVST is one of the rare complications in autoimmune diseases. It has a more subacute-chronic onset. Since headaches are more common, it is essential to make a differential diagnosis of CVST in autoimmune diseases with chronic headaches. Transverse sinus thrombosis is more common. Collateralization, venous infarction, and hemorrhagic transformation are less.</p>","PeriodicalId":49758,"journal":{"name":"Neurologist","volume":" ","pages":"152-157"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139514295","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"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
Anticonvulsant Agents for Treatment of Restless Legs Syndrome: A Case Report With Lamotrigine and a Review of the Literature. 抗惊厥药物治疗不安腿综合征:使用拉莫三嗪的病例报告和文献综述。
IF 1.2 4区 医学 Q4 CLINICAL NEUROLOGY Pub Date : 2024-05-01 DOI: 10.1097/NRL.0000000000000552
Jawad Al-Kassmy, Mohammed Alsalmi, Woojin Kang, Philippe Huot

Introduction: Restless Legs Syndrome (RLS) is a neurological disorder primarily treated with pregabalin and gabapentin, followed by dopamine agonists later in the process due to the risk of augmenting RLS symptoms. In addition, clinical reports have disclosed varying degrees of success employing other agents in patients unresponsive to traditional agents. Here, we present a patient who had success in the reduction of RLS symptoms with lamotrigine, a broad-spectrum anticonvulsant. Previously, lamotrigine had been used in 2 trials with successful treatment of RLS.

Case report: We present a 58-year-old right-handed lady with long-standing history of smoking, hypertension, dyslipidaemia, prediabetes, gastro-esophageal reflux disease, asthma, strabismus, uterine cancer, severe and debilitating course of RLS accompanied by unexplained deterioration. The patient initially demonstrated abnormal sensation in all her limbs, which worsened with radiotherapy treatment, and was eventually diagnosed with RLS based on the diagnostic criteria. Subsequent examinations were unremarkable and revealed no further explanation for the deterioration of the RLS symptoms. While the complexity of the patient's medical history had exposed her to a variety of medications, she reported that only lamotrigine, in addition to her original regimen of methadone and pramipexole, offered significant symptomatic relief. It must be noted that no adverse side effects, including impulse-control disorder, were reported by the patient.

Conclusions: We present a case of a woman whose deteriorating symptoms of RLS were successfully alleviated by the administration of lamotrigine. This is only the third case in the literature to have successfully utilized lamotrigine as a treatment option for RLS.

简介:多动腿综合征(RLS)是一种神经系统疾病,主要采用普瑞巴林和加巴喷丁治疗,由于有加重 RLS 症状的风险,因此在治疗过程的后期会使用多巴胺受体激动剂。此外,临床报告显示,对传统药物无反应的患者使用其他药物也取得了不同程度的成功。在此,我们介绍了一位使用拉莫三嗪(一种广谱抗惊厥药)成功减轻 RLS 症状的患者。此前,拉莫三嗪曾在两项试验中成功治疗了 RLS:我们为您介绍一位 58 岁的右撇子女士,她有长期吸烟史、高血压、血脂异常、糖尿病前期、胃食管反流病、哮喘、斜视、子宫癌、严重和衰弱的 RLS 病程以及不明原因的病情恶化。患者最初表现为四肢感觉异常,放疗后症状加重,最终根据诊断标准被确诊为 RLS。随后的检查没有发现异常,也无法进一步解释 RLS 症状恶化的原因。虽然患者病史复杂,曾接受过多种药物治疗,但她表示,除了美沙酮和普拉克索这两种药物外,只有拉莫三嗪能明显缓解症状。必须指出的是,患者没有报告任何不良副作用,包括冲动控制障碍:结论:我们介绍了一例女性患者的病例,通过服用拉莫三嗪,她不断恶化的 RLS 症状得到了成功缓解。这是文献中第三例成功利用拉莫三嗪治疗 RLS 的病例。
{"title":"Anticonvulsant Agents for Treatment of Restless Legs Syndrome: A Case Report With Lamotrigine and a Review of the Literature.","authors":"Jawad Al-Kassmy, Mohammed Alsalmi, Woojin Kang, Philippe Huot","doi":"10.1097/NRL.0000000000000552","DOIUrl":"10.1097/NRL.0000000000000552","url":null,"abstract":"<p><strong>Introduction: </strong>Restless Legs Syndrome (RLS) is a neurological disorder primarily treated with pregabalin and gabapentin, followed by dopamine agonists later in the process due to the risk of augmenting RLS symptoms. In addition, clinical reports have disclosed varying degrees of success employing other agents in patients unresponsive to traditional agents. Here, we present a patient who had success in the reduction of RLS symptoms with lamotrigine, a broad-spectrum anticonvulsant. Previously, lamotrigine had been used in 2 trials with successful treatment of RLS.</p><p><strong>Case report: </strong>We present a 58-year-old right-handed lady with long-standing history of smoking, hypertension, dyslipidaemia, prediabetes, gastro-esophageal reflux disease, asthma, strabismus, uterine cancer, severe and debilitating course of RLS accompanied by unexplained deterioration. The patient initially demonstrated abnormal sensation in all her limbs, which worsened with radiotherapy treatment, and was eventually diagnosed with RLS based on the diagnostic criteria. Subsequent examinations were unremarkable and revealed no further explanation for the deterioration of the RLS symptoms. While the complexity of the patient's medical history had exposed her to a variety of medications, she reported that only lamotrigine, in addition to her original regimen of methadone and pramipexole, offered significant symptomatic relief. It must be noted that no adverse side effects, including impulse-control disorder, were reported by the patient.</p><p><strong>Conclusions: </strong>We present a case of a woman whose deteriorating symptoms of RLS were successfully alleviated by the administration of lamotrigine. This is only the third case in the literature to have successfully utilized lamotrigine as a treatment option for RLS.</p>","PeriodicalId":49758,"journal":{"name":"Neurologist","volume":" ","pages":"173-178"},"PeriodicalIF":1.2,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139514291","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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