Mechanisms of Neurosyphilis-Induced Dementia: Insights into Pathophysiology.

IF 3.2 Q2 CLINICAL NEUROLOGY Neurology International Pub Date : 2024-12-02 DOI:10.3390/neurolint16060120
Aya Fadel, Hussain Hussain, Robert J Hernandez, Amanda Marie Clichy Silva, Amir Agustin Estil-Las, Mohammad Hamad, Zahraa F Saadoon, Lamia Naseer, William C Sultan, Carla Sultan, Taylor Schnepp, Arumugam R Jayakumar
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Abstract

Neurosyphilis-induced dementia represents a severe manifestation of tertiary syphilis, characterized by cognitive and neuropsychiatric impairments. This condition arises from the progression of syphilis to the central nervous system, where the spirochete causes damage through invasion, chronic inflammation, and neurodegeneration. The pathophysiology involves chronic inflammatory responses, direct bacterial damage, and proteinopathies. Treponema pallidum triggers an inflammatory cascade, resulting in neuronal injury and synaptic dysfunction. Abnormal protein accumulations, including TAR DNA-binding protein 43 (TDP-43) and tau, contribute to neuronal loss and cognitive decline. Seizures, psychiatric symptoms, and motor deficits further complicate the progression of dementia. Diagnosis includes clinical assessment, cerebrospinal fluid analysis, and neuroimaging. Diagnostic tests include CSF-VDRL, FTA-ABS, and neuroimaging techniques such as MRI and PET scans, which help detect structural changes and confirm neurosyphilis. Management of neurosyphilis-induced dementia involves antibiotic therapy and psychotropic medications to address both infectious and symptomatic components. While penicillin remains the cornerstone of treatment, psychotropic agents, including haloperidol, risperidone, quetiapine, and divalproex sodium, can manage psychiatric symptoms. However, careful monitoring is required due to potential side effects and interactions with ongoing treatment. Overall, early diagnosis and comprehensive management are crucial for mitigating the cognitive and neuropsychiatric impairments associated with neurosyphilis-induced dementia.

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神经梅毒诱发痴呆的机制:病理生理学的见解。
神经梅毒诱发痴呆是三期梅毒的一种严重表现,以认知和神经精神障碍为特征。这种情况源于梅毒发展到中枢神经系统,螺旋体通过侵入、慢性炎症和神经退行性变造成损害。病理生理包括慢性炎症反应、直接细菌损伤和蛋白质病变。梅毒螺旋体引发炎症级联反应,导致神经元损伤和突触功能障碍。包括TAR dna结合蛋白43 (TDP-43)和tau在内的异常蛋白积累可导致神经元丧失和认知能力下降。癫痫发作、精神症状和运动缺陷使痴呆症的进展进一步复杂化。诊断包括临床评估、脑脊液分析和神经影像学。诊断测试包括CSF-VDRL、FTA-ABS和神经成像技术,如MRI和PET扫描,这些技术有助于发现结构变化并确认神经梅毒。神经性梅毒性痴呆的治疗包括抗生素治疗和精神药物治疗,以解决感染性和症状性因素。虽然青霉素仍然是治疗的基础,但精神药物,包括氟哌啶醇、利培酮、喹硫平和双丙戊酸钠,也可以控制精神症状。然而,由于潜在的副作用和与正在进行的治疗的相互作用,需要仔细监测。总之,早期诊断和综合治疗对于减轻与神经性梅毒引起的痴呆相关的认知和神经精神障碍至关重要。
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来源期刊
Neurology International
Neurology International CLINICAL NEUROLOGY-
CiteScore
3.70
自引率
3.30%
发文量
69
审稿时长
11 weeks
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