Evidence map›Paper›PMID 41926293›Full record

ReviewCurrent neurovascular research2026

Neurosyphilis and Parkinsonism: Overlapping Pathophysiology and Emerging Therapeutic Insights.

Shruti, Zuber Khan, Mustak Ahamed, Sidharth Mehan, Mumtaz, Abdul Rahim, Injamamul Haque, Sumedha Gupta, Aysha Bano

Abstract readReview
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In one paragraph

Review in Current neurovascular research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

ShrutiDepartment of Pharmacy Practice, ISF College of Pharmacy (An Autonomous College), Moga, 142001, Punjab, India.
Zuber KhanDivision of Neuroscience, Department of Pharmacology, ISF College of Pharmacy (An Autonomous College), Moga, 142001, Punjab, India.
Mustak AhamedDepartment of Pharmacy Practice, ISF College of Pharmacy (An Autonomous College), Moga, 142001, Punjab, India.
Sidharth MehanDivision of Neuroscience, Department of Pharmacology, ISF College of Pharmacy (An Autonomous College), Moga, 142001, Punjab, India.
MumtazDepartment of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi, 110062, India.
Abdul RahimDepartment of Pharmacy Practice, ISF College of Pharmacy (An Autonomous College), Moga, 142001, Punjab, India.
Injamamul HaqueDepartment of Pharmacy Practice, ISF College of Pharmacy (An Autonomous College), Moga, 142001, Punjab, India.
Sumedha GuptaDivision of Neuroscience, Department of Pharmacology, ISF College of Pharmacy (An Autonomous College), Moga, 142001, Punjab, India.
Aysha BanoDepartment of Translation and Clinical Research, Jamia Hamdard, New Delhi, 110062, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNeurosyphilis, caused by Treponema pallidum, is a complex neurological condition arising from untreated syphilis and can present with diverse manifestations, including Parkinsonism-like motor dysfunction. Its pathophysiology involves Blood-Brain Barrier (BBB) disruption, dopaminergic neuronal loss, and neuroinflammatory cascades that resemble mechanisms seen in idiopathic Parkinson's Disease (PD).

methodsA literature review from PubMed, ScienceDirect, Scopus, and Google Scholar (2014- 2025) explored studies on neurosyphilis, dopaminergic degeneration, BBB dysfunction, neuroinflammation, diagnostics, and treatments, including antibiotics, neuroprotective agents, nanocarriers, and vaccines. A narrative synthesis was conducted due to the variation in study designs.

resultsThe decreased BBB permeability, extracellular matrix degradation, TLR activation, reactive microglia, and neuronal cell death are mechanisms linking syphilis and idiopathic PD. Neurologists differentiate between neurosyphilis and idiopathic PD through neuroimaging and cerebrospinal fluid analysis (CSF). Treatment for neurosyphilis primarily involves penicillin, with alternatives such as ceftriaxone and doxycycline. Emerging evidence suggests that β-lactam antibiotics and nanoparticle systems targeting neuroinflammatory pathways may offer neuroprotective effects. DISCUSSION: These findings exhibit considerable mechanistic overlap between neurosyphilis and PD, particularly concerning BBB dysfunction, dopaminergic neurodegeneration, and neuroinflammation. These common pathways lead to symptoms similar to those of PD and complicate clinical manifestation. Neuroimaging and CSF analyses are still very important for making an accurate diagnosis. Further study is needed to clarify disease mechanisms and to evaluate novel therapeutic approaches.

conclusionNeurosyphilis may present with Parkinsonian features due to PD-like neurodegenerative mechanisms. Early diagnosis and timely antimicrobial therapy are crucial to prevent irreversible neurological damage, while emerging neuroprotective strategies warrant further investigation.

Indexed as

NeurosyphilisParkinsonian DisordersAnimalsAnti-Bacterial AgentsBlood-Brain BarrierHumansNeuroinflammatory DiseasesNeuroprotective AgentsAnti-Bacterial AgentsNeuroprotective Agentsbasal ganglia dysfunctionblood-brain barrier (bbb)neuroinflammationNeurosyphilis parkinsonismpenetrationT. pallidum

Identifiers

PMID41926293

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.