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SYSTEMATIC REVIEW article

Front. Neurol., 23 September 2024
Sec. Neuroinfectious Diseases

The research trend on neurobrucellosis over the past 30 years (1993–2023): a bibliometric and visualization analysis

Lanting Yang,&#x;Lanting Yang1,2Wei Pan&#x;Wei Pan1Qiong CaiQiong Cai1Mingyang AnMingyang An1Chunjie WangChunjie Wang1Xilong Pan
Xilong Pan1*
  • 1Department of Social Medicine and Health Education, School of Public Health, Peking University, Beijing, China
  • 2Faculty of Arts, The University of Melbourne, Melbourne, VIC, Australia

Background: Brucellosis is a zoonotic disease caused by Brucella infection, which is common in pastoral areas. Neurological involvement in brucellosis is relatively rare. But since 1993, continuous studies have been reporting neurological complications of brucellosis, collectively referred to as neurobrucellosis. A bibliometric analysis of existing literature outlines current research progress and gaps and provides guidance for the clinical treatment of neurobrucellosis, promoting patient health in the process of guiding clinical practice, and improving their quality of life.

Methods: CiteSpace and VOSviewer are software tools to visualize research trends and networks. By selecting specific areas of interest and configuring the right parameters, the tools can visualize past research data. The study retrieved the literature from the Web of Science Core Collection Database and downloaded it in plain text file format. Citespace6.1.6, VOSviewer v1.6.20, and Microsoft Excel 16.59 were used for analyzing the following terms: countries, institutions, authors’ cooperation, journals, keywords, and co-citation.

Results: There are eight key results. (1) The publication volume shows a general upward trend. (2) Turkey is the country with the highest publication volume and contributing institutions. (3) Giambartolomei GH, Gul HC, and Namiduru M are the authors with the highest number of publications. (4) Neurology is the journal that published the highest number of related articles (n = 12). (5) “Diagnosis,” “meningitis,” and “features” are the top three frequently occurring keywords. (6) Keyword clusters show “antibiotic therapy” and “cerebrospinal fluid” have future study value. (7) The burst analysis of the keywords also indicates that “cerebrospinal fluid” may become a prominent keyword in future research. (8) The co-citation analysis concludes three categories of the cited articles, which are diagnosis, therapy, and complications, indicating the past research direction.

Conclusion: This study highlights the complexity of neurobrucellosis, presenting the need for advanced diagnostic techniques and multifaceted treatment approaches. While antibiotics remain the cornerstone of therapy, the use of corticosteroids to mitigate inflammatory responses shows promise, albeit with concerns about potential sequelae and relapse. Future research should focus on refining therapeutic strategies that address both the direct effects of infection and the broader immunological impacts to improve patient outcomes and quality of life.

1 Introduction

Brucellosis is one of the most common zoonotic diseases worldwide. It is typically transmitted through direct contact with infected animals or consumption of unpasteurized products. Since 1993, there have been continuous studies reporting neurological complications of brucellosis, collectively referred to as neurobrucellosis, but only approximately 5% of brucellosis patients experience nervous system involvement (1). The pathogenesis of neurobrucellosis involves the invasion of Brucella bacteria into the blood, reaching the meninges and nervous system. The damage to both the peripheral and central nervous systems is predominantly attributed to indirect immune mechanisms (24). Frequent complications involving the central nervous system include acute meningitis, myelitis, strokes, subarachnoid hemorrhages, seizures, and cranial nerve involvement, especially the vestibulocochlear nerve (3, 5, 6). Cognitive disorders, psychiatric symptoms, and pituitary region involvement are rare but documented manifestations (6, 7). Complications involving the peripheral nervous system include Guillain Barre syndrome, sciatica, and polyradiculopathy (811). Clinical manifestations of neurobrucellosis vary widely, including headaches, vision and hearing impairments, confusion, incontinence, behavioral changes, muscle weakness, and neck rigidity (3, 12, 13). Diagnosis relies on a combination of suggestive symptoms, positive cerebrospinal fluid (CSF) culture or Brucella IgG agglutination in blood, lymphocytic pleocytosis, increased CSF protein, and response to specific antibiotics (2). Although there are many detection methods, the diagnosis is challenging due to its variable manifestations and delayed clinical recognition. Neurobrucellosis is usually diagnosed within 2–12 months after the symptom onset (6, 12).

Most existing articles on neurobrucellosis are primarily case reports, and the sample sizes are generally small, with the majority not exceeding 10 cases (1416). These articles typically study manifestations, diagnosis, and treatment therapy of neurobrucellosis. There are also a few articles that focus on the immunopathology of neurobrucellosis, which provide valuable insights into the disease’s pathophysiology, diagnostic biomarkers, and therapeutic strategies (1719). However, there are virtually no comprehensive reviews that integrate and analyze these case studies statistically to track advancements in specific areas such as pathophysiology, diagnostic biomarkers, and treatment therapies. This lack of detailed synthesis contributes to a limited understanding of the existing research gaps in neurobrucellosis.

Web of Science Core Collection Database provides a comprehensive view of scholarly literature. Using this database can ensure the comprehensiveness of literature searches. CiteSpace is a software used for the visualization and analysis of trends and patterns in scientific literature. This study will use CiteSpace and VOSviewer to conduct a bibliometric analysis of the articles related to neurobrucellosis within the Web of Science Core Collection. The aim is to systematically review the existing literature on neurobrucellosis, providing a comprehensive overview that identifies current research trends and gaps. This will guide future studies and provide guidance for the diagnosis and clinical treatment of neurobrucellosis, ultimately aiming to improve the quality of life of patients.

2 Methods

2.1 Data source and search strategy

The researcher retrieved literature on the database, the Web of Science Core collaboration. The searching method is topic searching from January 1, 1993, to October 31, 2023, including search titles, abstracts, author, and keywords. The keywords are Brucellosis, including “Mediterranean fever,” “Undulant fever,” “Malta fever,” and Neurological Disease, including “nervous system disorders,” “Nervous system disease” and “neurological disorders.” To ensure the comprehensiveness of the search, this study also searched for related keywords including “nervous system brucellosis” and “neurobrucellosis.” The search and data were reported on October 31, 2023.

2.2 Inclusion and exclusion criteria

The inclusion and exclusion of studies were based on the filters of the WOS database. The studies that met the following criteria were included: (1) articles published in the period from January 1, 1993, to October 31, 2023; (2) articles about Neurobrucellosis; (3) original Articles, Review articles and book chapters; (4) published in English. Exclusion criteria were: (1) duplicate publications; (2) early access; (3) letters, abstracts, conference presentations, and unpublished manuscripts; (4) articles not related to the topic of neurobrucellosis.

Relevant articles were selected for the final analysis by reviewing the abstracts and titles.

2.3 Data export and standardization

The full record and cited references of selected articles were exported in plain text format and imported to Citespace 6.1.6 and VOSviewer v1.6.20. Keywords with the same meaning were standardized: “nervous system brucellosis” is replaced by “Neurobrucellosis”; “Nervous system diseases” or “Nervous system disorders” are replaced by “neurological disease”; “CNS” is replaced by “Central Nervous System.”

2.4 Bibliometric software

Bibliometric analysis is a research method used to quantitatively analyze scientific literature (20). CiteSpace and VOSviewer are software tools designed for the analysis and visualization of scientific literature and citation data (21). CiteSpace is primarily used to detect critical points and visualize emerging trends of scientific studies in a specific area (22). It is effective for identifying keywords, key authors, and institutions, often represented through cluster analyses and timeline views. VOSviewer specializes in creating network maps of scientific literature, enabling users to visually explore bibliometric networks, including journals, researchers, or individual articles, which helps to illustrate the relationships based on co-authors, co-citations, or bibliographic coupling (23). Users typically import data from databases and then utilize the software’s analytical and visual capabilities to interpret the data and generate insights about how scholarly activities evolve. This study will use Citespace 6.1.6 and VOSviewer v1.6.20 to visualize the development of scientific literature on Neurobrucellosis.

2.5 Data analysis

To analyze the development of neurobrucellosis research, data were systematically collected from selected articles fitting specific inclusion/exclusion criteria. The country and keyword clusters were analyzed in CiteSpace. Co-authorship, keywords co-occurrence, and co-citation analyses were conducted using VOSviewer. The specification settings of CiteSpace are as follows: (1) the Time slicing is from January 1993 to December 2023, with each slice representing 1 year; (2) Text Source includes Title, Abstract, Author Keywords (DE), and Keywords Plus (ID); (3) Node Types include countries for analysis of authors’ countries of origin, and keywords for keyword clusters and burst analysis; (4) Link Strength is set to Cosine, and Link Scope to Within Slices; (5) Selection Criteria employs the g-index in each slice, and the scale factor K is set at 25, which is optimal to present a moderate amount of data clearly, facilitating the identification of significant trends, clusters, and connections within the data. The specification settings for VOSviewer, which differ due to the nature of analyses performed, will be detailed in the sections on co-authorship, keywords co-occurrence, and co-citation, underscoring the distinct configurations necessary for these analyses.

3 Results

3.1 Search results

Figure 1 illustrates the process of searching and filtering. Initially, a database search was conducted in the Web of Science Core Collection using keywords mentioned in 2.1, from January 1, 1993, to October 31, 2023, resulting in 703 articles. These articles were then filtered by document type and language, focusing on articles, review articles, and book chapters written in English, narrowing down the pool to 594 articles. Further screening based on titles and abstracts refined to 438 records, which enters the final analysis stage. Figure 2 shows the number of publications every year from 1993 to 2023. Starting from 1993, papers in this field have been continuously developing, reaching their peak in 2022 and 2023 (n = 26). There was a noticeable decline in 2015 (n = 9), but in the following years, it remained in a fluctuating upward trend.

Figure 1
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Figure 1. Searching flow diagram.

Figure 2
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Figure 2. The number of publications from 1993 to 2023.

3.2 Analysis of authors’ country of origin

Examining the author’s nationality and national collaboration presents the geographical distribution of research and visualizes the extent of international cooperation, enhancing global collaborative networks and helping address geographic disparities in scientific output. In Citespace software, by selecting “Country” as the Node Type, there are 438 articles from 59 countries. Table 1 displays the top 10 countries in terms of the number of published papers. Figure 3 shows the national collaboration graph. Each node represents a country, with larger nodes indicating a higher number of published articles from that country. The lines between nodes signify collaboration among authors from different countries. As the top-ranking country, Turkey’s contribution exceeds 30% (n = 154), followed by Iran (n = 37) and India (n = 33). Turkey leads in research on Brucellosis and Neurological diseases, but its collaboration with other countries is relatively limited. Despite a relatively low publication volume, the United States exhibits the highest level of collaboration with other countries.

Table 1
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Table 1. The ranking of the top 10 contributed countries.

Figure 3
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Figure 3. The map of country cooperation networks.

3.3 Analysis of universities and institutions

The analysis of universities and institutions serves as an indicator of research productivity. It identifies centers of excellence and guides potential collaborations and resource allocation to enhance research, diagnosis, and treatment strategies in this field. A total of 423 institutions have published research about neurobrucellosis. Table 2 shows the top 10 institutions in terms of the number of published papers. Gaziantep University, having published the highest number of articles in this field, has only contributed 12 papers. This suggests that few institutions are conducting in-depth research in this field. Apart from the seventh institution is from Argentina, the remaining nine institutions are all from Turkey.

Table 2
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Table 2. The ranking of the top 10 contributed universities and institutions.

3.4 Analysis of author cooperation

Analyzing author cooperation allows us to observe trends in collaboration frequency over different time periods, providing insights into how research communities evolve and adapt in response to emerging challenges and shifts in scientific focus. In VOSviewer software, choose “co-authorship” as the analysis type, “author” as the unit of analysis, and set the minimum number of documents for an author to be 2. There are a total of 153 authors that meet the criteria. Giambartolomei GH, Gul HC, and Namiduru M have the highest number of publications (n = 9), followed by Erdem H (n = 8), Delpino MV, Demiroglu YZ, and Karsen H (n = 7). Figure 4 shows the authors’ cooperation map. Each node represents an author. And the line that links the two nodes presents the collaboration between the two authors. Authors who have published two or more articles collaborated predominantly between 2009 and 2013, with the majority of collaborations occurring around 2010. Over the past decade, there has been almost no collaboration among authors finishing two or more co-authored articles.

Figure 4
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Figure 4. The map of co-authorship.

3.5 Analysis of publications and journals

The analysis of publications and journals aims to identify the most influential platforms for neurobrucellosis research, helping researchers target journals that maximize the visibility and impact of their work. From 1993, January to 2023, October 31, there were 245 journals publishing articles related to the neurobrucellosis. Table 3 presents the top 10 journals with the most published articles on neurobrucellosis. Except for the fourth and ninth journals, which are relatively broad medical journals, the others are specialized in neurology or infectious diseases. Neurology published the highest number of articles (n = 12), followed by the European Journal of Neurology (n = 9), Clinical Infectious Diseases, Cureus Journal of Medical Science, and International Journal of Infectious Diseases (n = 8).

Table 3
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Table 3. The rank of top publication journals.

3.6 Analysis of co-citation

Co-citation analysis assesses the collective influence of articles by examining their relationships based on co-citation frequency, revealing underlying connections and emerging trends (24). It is significant for identifying key studies and related findings, as well as guiding future research directions. In VOSviewer software, choose “co-citation” as the analysis type, “cited reference” as the unit of analysis, and set the minimum number of citations of a cited reference to be 10. Among the 4,462 cited references, 121 meet the criteria. The c-cited articles are classified into three main clusters, which provide an overview of the previous research directions. Table 4 illustrates representative articles from the three primary clusters.

Table 4
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Table 4. Main co-cited literature information.

Figure 5 shows the map of co-citation. The red nodes represent the first cluster, in which “Neurobrucellosis: Clinical and Therapeutic Feature,” and “Clinical categories of neurobrucellosis. A report on 19 cases” are the most cited articles, all of which describe the therapy of neurobrucellosis. The green dots represent the second cluster, where “Neurobrucellosis: clinical and diagnostic features,” and “Overview of neurobrucellosis: a pooled analysis of 187 cases” are representative articles about the diagnosis of neurobrucellosis. Some of the articles in this cluster overlap with the first cluster. The blue nodes represent the third cluster. “Neurobrucellosis in an Endemic Area of Brucellosis” and “Clinical Manifestations and Complications in 1028 Cases of Brucellosis: A Retrospective Evaluation and Review of the Literature” are two contributed articles providing an overview of Brucellosis and its complications, clinical manifestations, and therapy methods.

Figure 5
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Figure 5. The map of co-citation.

“Overview of neurobrucellosis: a pooled analysis of 187 cases” and “Neurobrucellosis: clinical and diagnostic features” are the two most cited articles on the diagnosis of neurobrucellosis. Gul et al. (1) evaluated 187 cases of neurobrucellosis and found that the main symptoms in patients were headache, fever, sweating, and weight loss, and the major complications included cranial nerve involvement, polyneuropathy, depression, paralysis, stroke, and abscess formation. The low incidence rate and diverse presentations pose a great challenge to the diagnosis of neurobrucellosis (1, 3). Neurological complications of brucellosis could manifest at any stage, but the diagnosis is typically made 2–12 months after symptom onset (12). The study made by Guven et al. (12) indicates that Brucella tube agglutination (TA) with the Coombs test, setting the cutoff greater than or equal to 1:8, is highly sensitive and specific, and it enables the rapid detection of patients with Brucella in the cerebrospinal fluid.

“Neurobrucellosis: Clinical and Therapeutic Feature” and “Clinical categories of neurobrucellosis. A report on 19 cases” are two main cited articles related to the therapy of neurobrucellosis. Shakir et al. (13) described 19 cases of neurobrucellosis and classified them into three groups based on clinical presentations: acute meningoencephalitis presentation, chronic central presentation, and chronic peripheral presentation. The pathology and treatment responses vary among different categories. For example, the acute meningoencephalitis form is marked by severe, acute inflammation of the meninges and brain tissue, often accompanied by cerebral edema and granulomatous inflammation, leading to rapid onset symptoms such as headaches, fever and seizures (2527). In contrast, the chronic central presentation involves prolonged granulomatous inflammation within the central nervous system, resulting in a more insidious onset with cognitive decline and neuropsychiatric disturbances, and a higher risk of relapse (12, 2729). The chronic peripheral form is characterized by less intense inflammation but is often more resistant to standard treatments, presenting with persistent neuropathic symptoms like numbness, tingling, and muscle weakness (30, 31). Proper awareness and serological testing are essential to differentiate neurobrucellosis from other chronic CNS infections, particularly tuberculosis, and neurosyphilis (13). The standard treatment for brucellosis includes streptomycin and tetracycline (5, 7, 32). However due to the limited penetration of these drugs through the blood–brain barrier, additional antimicrobial agents like rifampin and TMP-SMZ, capable of reaching the cerebrospinal fluid (CSF), are necessary for treating central nervous system involvement (32). McLean et al. (32) recommend a combination of three or four antimicrobial agents in curing neurobrucellosis and suggested treatment duration ranges from 2 to 4 months, contingent upon the patient’s clinical and CSF responses.

3.7 Analysis of keyword mapping

Keyword mapping visualizes the relationships between individual keywords, highlighting connections across the research field. In VOSviewer software, by selecting “Co-occurrence” as the type of analysis and “All Keywords” as the unit of analysis and setting the minimum number of occurrences of a keyword as 4, there are 98 keywords. Figure 6 presents the network mapping based on the frequency of keywords. Table 5 shows the top 15 keywords in terms of frequency except the keywords related to the topic like “Brucellosis,” and “neurobrucellosis.”

Figure 6
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Figure 6. The map of keywords co-occurrence.

Table 5
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Table 5. The ranking of the top 15 keywords.

Based on the popular keywords the research focus in this field primarily revolves around diagnosis features and manifestation which reflects that research is more towards reporting the basic information of cases. Meningitis is the most commonly mentioned neurological disease associated with brucellosis

3.8 Analysis of keywords cluster

Keyword clustering organizes the related keywords into thematic groups, offering a more detailed analysis of specific research topics or subfields. While keywords mapping shows how concepts are linked, clustering defines and categorizes these connections into coherent research themes. In CiteSpace software, keywords cluster analysis applies the Log-likelihood ratio (LLR) algorithm. Table 6 shows the basic information of the clusters. The network parameters, Modularity Q = 0.51 > 0.3, Weighted Mean Silhouette S = 0.81 > 0.7, and Harmonic Mean (Q, S value) = 0.62 > 0.5 indicate that the clustering results have a high degree of credibility. Figure 7 shows how nine keywords have evolved from 1993 to 2023. #0 Diagnosis and #4 Cerebrospinal Fluid are popular topics, being the earliest to appear and continuing until recent times. #1 Hearing Loss, #5 Antibiotic Therapy, and #7 Brucella spp. have also continued to appear until recent years. #4 Cerebrospinal Fluid and #5 Antibiotic Therapy clusters have not shown continuous spikes, which may indicate potential future research directions.

Table 6
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Table 6. Keywords clusters information.

Figure 7
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Figure 7. Ridgeline plot for keyword cluster analysis.

3.9 Analysis of burst detection

Keyword burst analysis is conducted to identify periods when specific keywords experience a sudden increase in frequency, indicating emerging trends or shifts in research focus (33). This method helps to pinpoint when certain topics become highly relevant, often correlating with discoveries, technological advancements, or changes in societal concerns. By identifying these “bursts,” researchers can gain insights into the dynamics of a field, track the evolution of interest in specific topics, and predict future research directions. Building on the information from section 3.7, a keyword burst analysis was conducted. Figure 8 displays the top 25 burst keywords for brucellosis and neurological diseases from 1993 to 2023. The keyword with the highest burst strength is “case report” (Str = 3.53), followed by “meningoencephalitis” (Str = 3.01). The keyword with the longest burst duration is “children” (Year = 9), followed by “comparative trial” (Year = 8). “Cerebrospinal fluid” emerged as early as 1993 but experienced a surge starting in 2018. This suggests that prior research on this topic was relatively shallow and not extensive. It will highly likely become a popular keyword for future research.

Figure 8
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Figure 8. The ranking of the top 25 keywords with the strongest citation bursts.

4 Discussion

Neurobrucellosis is a neurological complication of brucellosis and demonstrates diverse neurological manifestations. The most common presentation is acute meningitis, with symptoms such as headache, fever, and neck stiffness (6, 25, 34). Meningoencephalitis is also frequently observed, involving prolonged inflammation of the brain and its membranes (25, 35). Chronic radiculoneuropathy, another syndrome of neurobrucellosis, involves inflammation of the nerve roots and peripheral nerves, leading to pain and sensory disturbances (36). Less common but notable presentations include pseudotumor cerebri, where increased intracranial pressure mimics symptoms of a brain tumor, and myelopathy, which affects the spinal cord leading to motor and sensory impairments (37, 38). These syndromes emphasize the complexity of neurobrucellosis, requiring prompt and effective management strategies.

This research focused on the statistical analysis of the 438 articles from Web of Science Core Collaboration. The existing articles in this field predominantly consist of case reports and most of them have relatively small sample sizes (1416, 39). Researchers found a general upward trend in the articles about neurobrucellosis during the past 30 years. Turkey leads in the number of publications on neurobrucellosis, contributing over 30% of the total articles, with nine out of the top 10 institutions in this field also based in Turkey. However, despite the high volume of research, these Turkish institutions have not conducted in-depth studies in this field. In contrast, the University of Buenos Aires in Argentina has been conducting significant immunopathological research, accounting for 10 of the 11 articles from Argentina (18, 4043). They shed light on neurobrucellosis and contributed valuable insights to the field. Author collaborations, with two or more articles, were mostly concentrated around 2010, with few collaborations in the past decade. The journal “Neurology” published the highest number of articles related to brucellosis and neurological disease. From the analysis of co-citations, articles related to neurobrucellosis are generally categorized into three main groups: therapy methods, diagnosis of neurobrucellosis, and overview of Brucellosis and its complications, which indicated the past research directions. “Diagnosis,” “meningitis,” and “features” are the most frequently occurring keywords, indicating that articles in this field predominantly focus on case reports, and the most frequently reported neurological complication is meningitis. Researchers conducted a cluster analysis of the keywords and found that “Cerebrospinal Fluid and Antibiotic” and “Antibiotic Therapy” have research value, as they have been consistently appearing in recent years, whereas there was no sustained outbreak of these topics in the earlier years. The burst analysis of the keywords also indicated that “cerebrospinal fluid” may become a prominent keyword in future research. The term emerged as early as 1993 but only began to gain prominence in 2018, indicating its research significance.

Cerebrospinal fluid (CSF) is emerging as a focal point for future research, with a primary focus on the detection of neurobrucellosis. Neurobrucellosis poses diagnostic challenges due to non-specific clinical manifestations and inefficient routine culture tests (44). Traditional approaches to detecting neurobrucellosis, such as microbial culture and serological tests, have limitations in application due to low sensitivity or specificity, along with the requirement for a long sample-to-answer turnaround time (4547). Serological tests include RBPT (Rose Bengal plate agglutination tests), STAT (Standard tube agglutination test), and ELISA (Enzyme-linked immunosorbent assay) to identify antibodies in serum and CSF (1, 2). PCR (Polymerase chain reaction) for specific DNA sequences and oligoclonal immunoglobulin G (IgG) tests in cerebrospinal fluid are also traditional methods to confirm neurobrucellosis (4850). Using a combination of diagnostic and clinical methods is recommended for accurate brucellosis detection. Recent research found that Next-generation sequencing (NGS) is a rising method for identifying pathogenic microorganisms based on sequencing, and its utilization is growing in the diagnosis of infectious diseases affecting the central nervous system (CNS) (46, 51). Next-generation sequencing (NGS) is also recommended to be used in diagnosing neurobrucellosis due to its Enhanced Sensitivity and rapid Diagnosis (44, 45, 52). Other research proposed that Metabolites of cerebrospinal fluid (CSF) are biomarkers for neurobrucellosis, representing a potential diagnostic modality for neurobrucellosis (53, 54). CSF samples from neurobrucellosis patients and normal controls were analyzed using liquid chromatography-mass spectrometry (LC–MS) to detect metabolites. The results showed differences in metabolite profiles between neurobrucellosis patients and normal controls, and elevated inflammatory cytokines in CSF further support the utility of metabolomics for diagnosis and treatment insights (53). Although the effectiveness of Next-Generation Sequencing (NGS) and the identification of metabolites of cerebrospinal fluid using LC–MS for detecting neurobrucellosis has been proven, large-scale studies with expanded sample sizes are crucial for further validation (44). Further research into the diagnosis of neurobrucellosis is expected to lead to earlier and more precise identification of the condition, which enables timely and appropriate therapeutic interventions. It is also crucial to validate the efficacy of these diagnostic methods and establish standardized protocols for their use in clinical settings.

Magnetic Resonance Imaging (MRI) can be also instrumental in diagnosing neurobrucellosis. A study classified the MRI features of neruobrucellosis into five types: In meningitis (Type I), MRI often displays equal T1 and high T2 signal intensities, accompanied by meningeal-like enhancement, primarily affecting the frontal and temporal lobes (55). Meningoencephalitis (Type II) is characterized by abnormal signal intensities in the meninges and submeningeal brain regions, presenting with similar T1 and elevated T2 signals. The presence of subtle meningeal enhancements without significant submeningeal tissue alteration further aligns with findings from specialized case studies (55). Inflammatory demyelinating (Type III) features diffuse myelitis, increased intensity in the cerebral white matter, and localized white matter changes (55, 56). These alterations are typically found around critical structures such as the lateral ventricles and spinal cord (5557). Ata et al. (58) also reported that MRI characteristics of demyelination include meningeal enhancement, particularly around the brainstem and along cranial nerves and the lower cranial nerves. The Abscess (Type IV) presents enhancement both in the brain and spinal cord similar to the typical abscess. Pseudotumor (Type V) mimics neoplastic processes with well-defined, enhancing lesions that exhibit low T1 and high T2 signals, demanding meticulous differential diagnosis (55).

Antibiotic therapy is commonly used to treat neurobrucellosis. Shaw et al. (59) advocate for multiagent antibiotic protocols, specifically incorporating ceftriaxone, rifampin, and doxycycline, as the preferred therapeutic approach. They also recommended a treatment duration of 4–6 weeks for ceftriaxone and a minimum of 12 weeks for rifampin and doxycycline, underscoring the pivotal role of strict adherence in mitigating the risk of relapse (59) Many studies have also confirmed the efficacy of antibiotic therapy in various neurological complications of brucellosis. For example, protracted polymicrobial antibiotic therapy and heparin are also proven to be effective in achieving a favorable outcome in patients with neurobrucellosis accompanied by cerebral venous sinus thrombosis (CVST) (60). Antibiotic regimen involving rifampicin, doxycycline, and trimethoprim/sulfamethoxazole is effective for neurobrucellosis complicated with sensorineural hearing loss (SNHL) (15). However, antibiotic therapy may not be permanently effective. Mirza et al. (15) mentioned a previous case report where SNHL persisted even after 6 weeks of antibiotic treatment, which suggested future research about the relationship between neurobrucellosis and SNHL. A documented case of neurobrucellosis with clinical manifestations resembling amyotrophic lateral sclerosis (ALC) reported that the disease-specific antibiotic therapy failed to impede the progression of motor neuron disease, suspecting a causal association between systemic neurobrucellosis and ALS (49).

The primary treatment for neurobrucellosis is antibiotics, but corticosteroids are also used in some situations to mitigate the damaging effects of bacterial toxins, potentially reducing the likelihood of enduring complications (6). Evidence from case reports suggests that corticosteroid therapy can effectively alleviate neurological symptoms such as headaches and vision problems and moderate the inflammatory response in neurobrucellosis patients (61). Despite these benefits, the efficacy of corticosteroids has not been conclusively established through large-scale studies or randomized controlled trials. Recent research indicates a significant concern: corticosteroid therapy was associated with a higher risk of sequelae or relapse (62). It contrasts with outcomes in other conditions like Pneumococcal meningitis, where steroid use is associated with a reduced risk of neurological sequelae, including hearing loss (63). Consequently, while corticosteroids can provide symptomatic relief in neurobrucellosis, the potential risks must be carefully weighed against the benefits.

The relationship between neurobrucellosis and neurological conditions arises from the frequent occurrence of neurological diseases among patients with brucellosis (41). The underlying mechanisms of neurobrucellosis involve direct invasion by Brucella abortus into the Central Nervous System (CNS), primarily facilitated through two routes: the “Trojan horse” mechanism and transcellular traversal of the blood–brain barrier (BBB). B. abortus utilizes infected monocytes to cross the BBB, effectively employing these cells as a means to enter the CNS (64, 65). Once inside, the bacteria can infect brain microvascular endothelial cells (HBMEC), as well as resident CNS cells like astrocytes and microglia (65). The presence of the bacteria triggers an inflammatory response, characterized by the production of cytokines and chemokines, which leads to astrogliosis and potentially to the apoptosis of astrocytes, contributing to the pathology observed in neurobrucellosis (42). The hypothesis is that the bacterial antigens may mimic neuronal antigens (molecular mimicry), leading to an autoimmune response that targets the myelin sheath of nerve cells (6). This could explain the demyelinating-like lesions observed in some patients with neurobrucellosis (66). Both neurobrucellosis and demyelinating disorders such as multiple sclerosis (MS) can present with neurological symptoms like headaches, visual disturbances, ataxia, and sensory or motor deficits (6, 12, 67). MRI findings in neurobrucellosis often include meningeal enhancement, white matter lesions, and other signs of inflammation which are also commonly seen in demyelinating disorders (66, 68). These similarities necessitate a careful differential diagnosis to distinguish between infectious causes and primary demyelinating processes. Neurobrucellosis is also reported to potentially link to psychiatric disorders, a connection supported by its inflammatory and systemic impacts on the central nervous system, which may lead to neuropsychiatric symptoms (69). Studies have shown that patients with neurobrucellosis experience significant emotional disturbances, and exhibit severely impaired cognitive functions, such as mental control, logical memory, and visual reproduction, and score higher on measures of depressive symptoms compared to control subjects (1, 70, 71). Further research needs to clarify these associations and understand the underlying pathophysiological processes, although some reports have recently begun to investigate the pathophysiological processes that associate psychiatric disorders with inflammatory responses elicited by the bacterium (72, 73). Understanding the complex interactions between neurobrucellosis and neurological diseases is crucial for improving diagnostic accuracy and patient outcomes.

This study has certain limitations. It exclusively used the Web of Science Core Collection Database for data analysis and focused on English-language articles during the screening process. This approach might lead to the omission of relevant studies. To counteract these limitations and strengthen the validity of our conclusions, we conducted a thorough review of additional key articles from prominent databases such as PubMed and Scopus in the discussion section, which broadened the scope and enhanced the comprehensiveness of the analysis.

This article employed both CiteSpace and VOSviewer software to make a bibliometric analysis of articles related to neurobrucellosis. By identifying the most active regions, leading institutions, and prevalent themes in current research, this analysis outlines the intellectual landscape and gaps, and guides researchers to develop targeted therapies and interventions that address the most pressing needs in the management of Neurobrucellosis, enhancing clinical outcomes and patients’ quality of life.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Author contributions

LY: Writing – original draft, Visualization, Software, Methodology, Investigation, Formal analysis, Data curation, Conceptualization. WP: Writing – original draft, Conceptualization. QC: Writing – review & editing, Visualization. MA: Writing – review & editing. CW: Writing – review & editing. XP: Writing – review & editing, Supervision, Resources, Project administration, Funding acquisition.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Acknowledgments

We thank the University of Melbourne and Peking University for supporting this study.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Gul, HC, Erdem, H, and Bek, S. Overview of neurobrucellosis: a pooled analysis of 187 cases. Int J Infect Dis. (2009) 13:e339–43. doi: 10.1016/j.ijid.2009.02.015

PubMed Abstract | Crossref Full Text | Google Scholar

2. Bouferraa, Y, Bou Zerdan, M, Hamouche, R, Azar, E, Afif, C, and Jabbour, R. Neurobrucellosis. Neurologist. (2021) 26:248–52. doi: 10.1097/NRL.0000000000000348

Crossref Full Text | Google Scholar

3. Alshalan, A, Yousef, M, and Alsanosi, A. Cochlear implantation in neurobrucellosis: two case reports. Acta Otolaryngol Case Rep. (2022) 7:64–7. doi: 10.1080/23772484.2022.2150629

Crossref Full Text | Google Scholar

4. Zhao, S, Cheng, Y, Liao, Y, Zhang, Z, Yin, X, and Shi, S. Treatment efficacy and risk factors of Neurobrucellosis. Med Sci Monit. (2016) 22:1005–12. doi: 10.12659/MSM.897947

PubMed Abstract | Crossref Full Text | Google Scholar

5. Akbayram, S, Dogan, M, Peker, E, Bektas, MS, Caksen, H, and Karahocagil, M. Evaluation of children with neurobrucellosis. Bratislava Medical Journal. (2012) 113:424–30. doi: 10.4149/BLL_2012_096

PubMed Abstract | Crossref Full Text | Google Scholar

6. Soares, CN, Angelim, AIM, Brandão, CO, Santos, RQ, Mehta, R, and MTT, S. Neurobrucellosis: the great mimicker. Rev Soc Bras Med Trop. (2022) 55:e05672021. doi: 10.1590/0037-8682-0567-2021

PubMed Abstract | Crossref Full Text | Google Scholar

7. Celebi, S, Hacimustafaoglu, M, and Sinirtas, M. Brucellar brain abscess in a child. J Pediatr Infect. (2010) 4:89–91. doi: 10.5152/ced.2010.10

Crossref Full Text | Google Scholar

8. Ertem, G, Kutlu, G, Hatipoğlu, Ç, Bulut, C, and Demiröz, A. A rare presentation of brucellosis: polyradiculopathy and peripheral neuritis. Turk J Med Sci. (2012) 42:23. doi: 10.3906/sag-1007-969

Crossref Full Text | Google Scholar

9. Li, Q, Liu, J, Jiang, W, Jiang, L, Lu, M, Xiao, L, et al. A case of brucellosis-induced Guillain–Barre syndrome. BMC Infect Dis. (2022) 22:72. doi: 10.1186/s12879-021-07025-3

PubMed Abstract | Crossref Full Text | Google Scholar

10. Doya, LJ, Haidar, I, and Sakkour, S. The association between acute brucellosis with a Guillain–Barré syndrome-like presentation: a case report. J Med Case Rep. (2023) 17:25. doi: 10.1186/s13256-022-03740-w

PubMed Abstract | Crossref Full Text | Google Scholar

11. Yuksel, KZ, Senoglu, M, Yuksel, M, and Gul, M. Brucellar spondylo-discitis with rapidly progressive spinal epidural abscess presenting with sciatica. Spinal Cord. (2006) 44:805–8. doi: 10.1038/sj.sc.3101938

PubMed Abstract | Crossref Full Text | Google Scholar

12. Guven, T, Ugurlu, K, Ergonul, O, Celikbas, AK, Gok, SE, Comoglu, S, et al. Neurobrucellosis: clinical and diagnostic features. Clin Infect Dis. (2013) 56:1407–12. doi: 10.1093/cid/cit072

PubMed Abstract | Crossref Full Text | Google Scholar

13. Shakir, R, Asn, A-D, Araj, G, Lulu, A, Mousa, A, and Saadah, M. Clinical categories of neurobrucellosis. Brain. (1987) 110:213–23. doi: 10.1093/brain/110.1.213

PubMed Abstract | Crossref Full Text | Google Scholar

14. Alattas, F, Khojah, O, Mukhtar, A, Khan, R, Jamjoom, M, Halawani, A, et al. Cerebral venous sinus thrombosis secondary to neurobrucellosis: a case report. Cureus. (2022) 14:e32677. doi: 10.7759/cureus.32677

PubMed Abstract | Crossref Full Text | Google Scholar

15. Mirza, B, Kanawi, HM, Alkhatib, T, Bukhari, AF, and Zawawi, F. Neurobrucellosis complicated by sensorineural hearing loss: a case report. Cureus. (2022) 14:e29482. doi: 10.7759/cureus.29482

PubMed Abstract | Crossref Full Text | Google Scholar

16. Qasim, SS, Baharoon, S, and Layqah, L. A case of seronegative pediatric neurobrucellosis presenting with Ataxia. Cureus. (2021) 13:e12540. doi: 10.7759/cureus.12540

Crossref Full Text | Google Scholar

17. Baldi, PC, and Giambartolomei, GH. Pathogenesis and pathobiology of zoonotic brucellosis in humans. Rev Sci Tech. (2013) 32:117–25. doi: 10.20506/rst.32.1.2192

Crossref Full Text | Google Scholar

18. Rodríguez, AM, Delpino, MV, Miraglia, MC, and Giambartolomei, GH. Immune mediators of pathology in Neurobrucellosis: from blood to central nervous system. Neuroscience. (2019) 410:264–73. doi: 10.1016/j.neuroscience.2019.05.018

PubMed Abstract | Crossref Full Text | Google Scholar

19. Baldi, C, and Giambartolomei, G. Immunopathology of Brucella infection. Recent Pat Antiinfect Drug Discov. (2013) 8:18–26. doi: 10.2174/1574891X11308010005

PubMed Abstract | Crossref Full Text | Google Scholar

20. Donthu, N, Kumar, S, Mukherjee, D, Pandey, N, and Lim, WM. How to conduct a bibliometric analysis: an overview and guidelines. J Bus Res. (2021) 133:285–96. doi: 10.1016/j.jbusres.2021.04.070

Crossref Full Text | Google Scholar

21. Ding, X, and Yang, Z. Knowledge mapping of platform research: a visual analysis using VOSviewer and cite space. Electron Commer Res. (2022) 22:787–809. doi: 10.1007/s10660-020-09410-7

Crossref Full Text | Google Scholar

22. Chen, C. Cite space II: detecting and visualizing emerging trends and transient patterns in scientific literature. J Am Soc Inf Sci Technol. (2006) 57:359–77. doi: 10.1002/asi.20317

Crossref Full Text | Google Scholar

23. Bukar, UA, Sayeed, MS, Razak, SFA, Yogarayan, S, Amodu, OA, and Mahmood, RAR. A method for analyzing text using VOSviewer. Methods X. (2023) 11:102339. doi: 10.1016/j.mex.2023.102339

Crossref Full Text | Google Scholar

24. Seduikyte, L, Gražulevičiūtė-Vileniškė, I, Povilaitienė, I, Fokaides, PA, and Lingė, D. Trends and Interdisciplinarity integration in the development of the research in the fields of sustainable, healthy and digital buildings and cities. Buildings. (2023) 13:1764. doi: 10.3390/buildings13071764

Crossref Full Text | Google Scholar

25. Acharya, A, Regmi, A, Manandhar, K, Yaday, J, and Karki, P. Neurobrucellosis presenting with the features of meningoencephalitis: a case report from Nepal. Ann Med Surg. (2022) 80:104278. doi: 10.1016/j.amsu.2022.104278

PubMed Abstract | Crossref Full Text | Google Scholar

26. Altas, M, Evirgen, O, Arica, V, and Tutanc, M. Pediatric neurobrucellosis associated with hydrocephalus. J Pediatr Neurosci. (2010) 5:144–6. doi: 10.4103/1817-1745.76115

PubMed Abstract | Crossref Full Text | Google Scholar

27. Turkoglu, SA, Halicioglu, S, Sirmatel, F, Yildiz, M, Yildiz, N, and Yildiz, S. Vasculitis and neurobrucellosis: evaluation of nine cases using radiologic findings. Brain Behav. (2018) 8:e00947. doi: 10.1002/brb3.947

PubMed Abstract | Crossref Full Text | Google Scholar

28. Bucher, A, Gaustad, P, and Pape, E. Chronic neurobrucellosis due to Brucella melitensis. Scand J Infect Dis. (1990) 22:223–6. doi: 10.3109/00365549009037906

PubMed Abstract | Crossref Full Text | Google Scholar

29. Kim, EJ, Lee, SJ, Ahn, EY, Ryu, DG, Choi, YH, and Kim, TH. Relapsed brucellosis presenting as Neurobrucellosis with cerebral Vasculitis in a patient previously diagnosed with Brucellar spondylitis: a case report. Infect Chemother. (2015) 47:268–71. doi: 10.3947/ic.2015.47.4.268

PubMed Abstract | Crossref Full Text | Google Scholar

30. Solera, J. Update on brucellosis: therapeutic challenges. Int J Antimicrob Agents. (2010) 36:S18–20. doi: 10.1016/j.ijantimicag.2010.06.015

PubMed Abstract | Crossref Full Text | Google Scholar

31. Yakovlev, N, Lyapina, E, Komleva, N, Anisimova, E, and Konnov, V. Polyneuropathy in patients with chronic brucellosis. Case study. Archiv Euromedica. (2022) 12:36–40. doi: 10.35630/2199-885X/2022/12/1.9

Crossref Full Text | Google Scholar

32. McLean, DR, Russell, N, and Khan, MY. Neurobrucellosis: clinical and therapeutic features. Clin Infect Dis. (1992) 15:582–90. doi: 10.1093/clind/15.4.582

Crossref Full Text | Google Scholar

33. Li, H, and Li, B. The state of metaverse research: a bibliometric visual analysis based on cite space. J Big Data. (2024) 11:14. doi: 10.1186/s40537-024-00877-x

Crossref Full Text | Google Scholar

34. Ceran, N, Turkoglu, R, Erdem, I, Inan, A, Engin, D, Tireli, H, et al. Neurobrucellosis: clinical, diagnostic, therapeutic features and outcome. Unusual clinical presentations in an endemic region. Braz J Infect Dis. (2011) 15:52–9. doi: 10.1016/S1413-8670(11)70140-4

PubMed Abstract | Crossref Full Text | Google Scholar

35. Alqwaifly, M, Al-Ajlan, FS, Al-Hindi, H, and Al, SA. Central nervous system brucellosis granuloma and white matter disease in immunocompromised patient. Emerg Infect Dis. (2017) 23:978–81. doi: 10.3201/eid2306.161173

PubMed Abstract | Crossref Full Text | Google Scholar

36. Dar, W, Wani, M, Mir, F, Asimi, R, Yaqoob, A, Raina, A, et al. Isolated neurobrucellosis—characteristic clinical and laboratory features. Acta Neurol Belg. (2022) 122:1469–75. doi: 10.1007/s13760-020-01573-2

PubMed Abstract | Crossref Full Text | Google Scholar

37. Díaz-Vintimilla, JJ, Rosales Hernández, LA, Zapata-Arenas, R, Sánchez-Montes, S, and Becker, I. Subacute transverse myelitis as a clinical presentation of neurobrucellosis. J Infect Dev Ctries. (2021) 15:1359–63. doi: 10.3855/jidc.14753

PubMed Abstract | Crossref Full Text | Google Scholar

38. Sinopidis, X, Kaleyias, J, Mitropoulou, K, Triga, M, Kothare, SV, and Mantagos, S. An uncommon case of pediatric neurobrucellosis associated with intracranial hypertension. Case Rep. Infect Dis. (2012) 2012:1–3. doi: 10.1155/2012/492467

Crossref Full Text | Google Scholar

39. Lakhanpal, V, Singh, D, Bhagwat, K, and Chakravarthy, K. Encephalomyelitis with hearing loss: case report on neurobrucellosis. BMJ Case Rep. (2022) 15:e248226. doi: 10.1136/bcr-2021-248226

PubMed Abstract | Crossref Full Text | Google Scholar

40. Baldi, PC, Araj, GF, Racaro, GC, Wallach, JC, and Fossati, CA. Detection of antibodies to Brucella cytoplasmic proteins in the cerebrospinal fluid of patients with neurobrucellosis. Clin Diagn Lab Immunol. (1999) 6:756–9. doi: 10.1128/CDLI.6.5.756-759.1999

PubMed Abstract | Crossref Full Text | Google Scholar

41. Miraglia, MC, Scian, R, Samartino, CG, Barrionuevo, P, Rodriguez, AM, Ibañez, AE, et al. Brucella abortus induces TNF-α-dependent astroglial MMP-9 secretion through mitogen-activated protein kinases. J Neuroinflammation. (2013) 10:819. doi: 10.1186/1742-2094-10-47

PubMed Abstract | Crossref Full Text | Google Scholar

42. García Samartino, C, Delpino, MV, Pott Godoy, C, Di Genaro, MS, Pasquevich, KA, Zwerdling, A, et al. Brucella abortus induces the secretion of proinflammatory mediators from glial cells leading to astrocyte apoptosis. Am J Pathol. (2010) 176:1323–38. doi: 10.2353/ajpath.2010.090503

PubMed Abstract | Crossref Full Text | Google Scholar

43. Marim, FM, Franco, MMC, Gomes, MTR, Miraglia, MC, Giambartolomei, GH, and Oliveira, SC. The role of NLRP3 and AIM2 in inflammasome activation during Brucella abortus infection. Semin Immunopathol. (2017) 39:215–23. doi: 10.1007/s00281-016-0581-1

Crossref Full Text | Google Scholar

44. Fan, S, Ren, H, Wei, Y, Mao, C, Ma, Z, Zhang, L, et al. Next-generation sequencing of the cerebrospinal fluid in the diagnosis of neurobrucellosis. Int J Infect Dis. (2018) 67:20–4. doi: 10.1016/j.ijid.2017.11.028

PubMed Abstract | Crossref Full Text | Google Scholar

45. Yu, L, Zhang, Z, Zou, Y, Qi, X, Zhang, Y, Bai, K, et al. Next-generation sequencing in the diagnosis of neurobrucellosis: a case series of eight consecutive patients. Ann Clin Microbiol Antimicrob. (2023) 22:44. doi: 10.1186/s12941-023-00596-w

PubMed Abstract | Crossref Full Text | Google Scholar

46. Christopher, S, Umapathy, BL, and Ravikumar, KL. Brucellosis: review on the recent trends in pathogenicity and laboratory diagnosis. J Lab Physicians. (2010) 2:055–60. doi: 10.4103/0974-2727.72149

Crossref Full Text | Google Scholar

47. Mantur, B, Amarnath, S, and Shinde, R. Review of clinical and laboratory features of human brucellosis. Indian J Med Microbiol. (2007) 25:188–202. doi: 10.1016/S0255-0857(21)02105-8

Crossref Full Text | Google Scholar

48. Papadopoulos, VE, Patas, K, Tountopoulou, A, Velonakis, G, Boufidou, F, Chatzipanagiotou, S, et al. Seronegative neurobrucellosis—do we need new neurobrucellosis criteria? Int J Infect Dis. (2021) 111:124–6. doi: 10.1016/j.ijid.2021.08.038

PubMed Abstract | Crossref Full Text | Google Scholar

49. Argyriou, AA, Karanasios, P, Papapostolou, A, Loukopoulou, P, Makridou, A, Marangos, M, et al. Neurobrucellosis presenting as clinically definite amyotrophic lateral sclerosis. Int J Neurosci. (2018) 128:686–8. doi: 10.1080/00207454.2017.1412968

PubMed Abstract | Crossref Full Text | Google Scholar

50. Berek, K, Hegen, H, Auer, M, Zinganell, A, Di Pauli, F, and Deisenhammer, F. Cerebrospinal fluid oligoclonal bands in Neuroborreliosis are specific for Borrelia burgdorferi. PLoS One. (2020) 15:e0239453. doi: 10.1371/journal.pone.0239453

PubMed Abstract | Crossref Full Text | Google Scholar

51. Dreshaj, S, Shala, N, Dreshaj, G, Ramadani, N, and Ponosheci, A. Clinical manifestations in 82 Neurobrucellosis patients from Kosovo. Materia Socio Medica. (2016) 28:408–11. doi: 10.5455/msm.2016.28.408-411

PubMed Abstract | Crossref Full Text | Google Scholar

52. Mongkolrattanothai, K, Naccache, SN, Bender, JM, Samayoa, E, Pham, E, Yu, G, et al. Neurobrucellosis: unexpected answer from metagenomic next-generation sequencing. J Pediatric Infect Dis Soc. (2017) 6:piw066–398. doi: 10.1093/jpids/piw066

PubMed Abstract | Crossref Full Text | Google Scholar

53. Yang, H, Wang, Z, Shi, S, Yu, Q, Liu, M, and Zhang, Z. Identification of cerebrospinal fluid metabolites as biomarkers for neurobrucellosis by liquid chromatography-mass spectrometry approach. Bioengineered. (2022) 13:6996–7010. doi: 10.1080/21655979.2022.2037954

PubMed Abstract | Crossref Full Text | Google Scholar

54. Maji, S, Manjunath, N, Bahubali, VH, Shome, R, Palaniappan, M, Lahiri, S, et al. Neurobrucellosis: a neglected entity? An update from tertiary care Neurocentre of South East Asia. J Neurol Sci. (2020) 411:116683. doi: 10.1016/j.jns.2020.116683

Crossref Full Text | Google Scholar

55. Jiang, C, Shen, L, Feng, Q, Fang, W, Jiang, R, Zhang, W, et al. MRI features and categories of neurobrucellosis: a pooled review. Radiol Infect Dis. (2018) 5:1–6. doi: 10.1016/j.jrid.2018.02.001

Crossref Full Text | Google Scholar

56. Saeed, M, Al Bishri, A, Gammaa, S, Qadir, A, Al-Qahtani, S, and Shat, AA. Neurobrucellosis presenting with features of demyelinating disorder in a pediatric patient. J Coll Physicians Surg Pak. (2022) 32:247–9. doi: 10.29271/jcpsp.2022.02.247

PubMed Abstract | Crossref Full Text | Google Scholar

57. Zhuang, W, He, T, Tuerheng, J, He, G, Wang, BL, Yang, YH, et al. Neurobrucellosis: laboratory features, clinical characteristics, antibiotic treatment, and clinical outcomes of 21 patients. BMC Infect Dis. (2024) 24:485. doi: 10.1186/s12879-024-09308-x

PubMed Abstract | Crossref Full Text | Google Scholar

58. Ata, F, Yousaf, Z, Sharif, MK, and Abdallah, A. Demyelinating steroid-responsive neurobrucellosis. BMJ Case Rep. (2020) 13:e233798. doi: 10.1136/bcr-2019-233798

Crossref Full Text | Google Scholar

59. Shaw, B, Madden, M, Sanchez, E, and Carlan, S. Recurrent neurobrucellosis in a feral swine hunter. Cureus. (2023) 15:e39383. doi: 10.7759/cureus.39383

Crossref Full Text | Google Scholar

60. Ibrahimagić, OĆ, Smajlović, D, Dostović, Z, Iljazović, A, Kojić, B, and Zonić, L. Neurobrucellosis and cerebral venous sinus thrombosis: a case report. Acta Clin Belg. (2017) 72:343–5. doi: 10.1080/17843286.2016.1251385

PubMed Abstract | Crossref Full Text | Google Scholar

61. Alhatou, M, Joudeh, AI, Alhatou, A, and Ghamoodi, M. Neurobrucellosis complicated by primary pyogenic ventriculitis: a case report. Oxf Med Case Rep. (2024) 2024:omad149. doi: 10.1093/omcr/omad149

PubMed Abstract | Crossref Full Text | Google Scholar

62. Fusetti, C, Petri, F, Murad, MH, Merli, S, Giorgi, R, Rizzardini, G, et al. Neurobrucellosis presenting with motor damage or hearing loss, and use of steroids are associated with a higher risk of sequelae or relapse: a systematic review of individual participant data. Neurol Sci. (2024). doi: 10.1007/s10072-024-07621-6

PubMed Abstract | Crossref Full Text | Google Scholar

63. Brouwer, MC, McIntyre, P, Prasad, K, and van de Beek, D. Corticosteroids for acute bacterial meningitis. Cochrane Database Syst Rev. (2015) 2018:CD004405. doi: 10.1002/14651858.CD004405.pub5

Crossref Full Text | Google Scholar

64. Ma, C, Li, H, Lu, S, Li, X, Wang, S, and Wang, W. Ocular lesions in Brucella infection: a review of the literature. Infect Drug Resist. (2022) 15:7601–17. doi: 10.2147/IDR.S394497

PubMed Abstract | Crossref Full Text | Google Scholar

65. Miraglia, MC, Rodriguez, AM, Barrionuevo, P, Rodriguez, J, Kim, KS, Dennis, VA, et al. Brucella abortus traverses brain microvascular endothelial cells using infected monocytes as a Trojan horse. Front Cell Infect Microbiol. (2018) 8:200. doi: 10.3389/fcimb.2018.00200

PubMed Abstract | Crossref Full Text | Google Scholar

66. Ayoobi Yazdi, N, Moosavi, N, Alesaeidi, S, Salahshour, F, and Ghaemi, O. Diffuse Neurobrucellosis of cerebellum, brainstem, spinal cord, and cauda Equina: a case report and literature review. J Radiol Case Rep. (2022) 16:1–9. doi: 10.3941/jrcr.v16i5.3960

PubMed Abstract | Crossref Full Text | Google Scholar

67. Love, S. Demyelinating diseases. J Clin Pathol. (2006) 59:1151–9. doi: 10.1136/jcp.2005.031195

PubMed Abstract | Crossref Full Text | Google Scholar

68. Tillema, JM, and Pirko, I. Neuroradiological evaluation of demyelinating disease. Ther Adv Neurol Disord. (2013) 6:249–68. doi: 10.1177/1756285613478870

PubMed Abstract | Crossref Full Text | Google Scholar

69. Kılıç, F, Temel, E, Sevicin, L, and Ayaz, F. Patient with acute psychosis due to neurobrucellosis: a rare case. Psychiatry Behav Sci. (2019) 9:188–91. doi: 10.5455/PBS.20190612051251

Crossref Full Text | Google Scholar

70. Shehata, GA, Abdel-Baky, L, Rashed, H, and Elamin, H. Neuropsychiatric evaluation of patients with brucellosis. J Neurovirol. (2010) 16:48–55. doi: 10.3109/13550280903586386

PubMed Abstract | Crossref Full Text | Google Scholar

71. Eren, S, Bayam, G, Ergönül, Ö, Çelikbaş, A, Pazvantoğlu, O, Baykam, N, et al. Cognitive and emotional changes in neurobrucellosis. J Infect. (2006) 53:184–9. doi: 10.1016/j.jinf.2005.10.029

PubMed Abstract | Crossref Full Text | Google Scholar

72. Rodríguez, J, De Santis, AJ, Dennis, VA, Rodríguez, AM, and Giambartolomei, GH. Bystander activation of microglia by Brucella abortus-infected astrocytes induces neuronal death via IL-6 trans-signaling. Front Immunol. (2024) 14:14. doi: 10.3389/fimmu.2023.1343503

Crossref Full Text | Google Scholar

73. Rodríguez, AM, Delpino, MV, Miraglia, MC, Costa Franco, MM, Barrionuevo, P, Dennis, VA, et al. Brucella abortus-activated microglia induce neuronal death through primary phagocytosis. Glia. (2017) 65:1137–51. doi: 10.1002/glia.23149

PubMed Abstract | Crossref Full Text | Google Scholar

74. Bodur, H, Erbay, A, Akinci, E, C¸olpan, A, C¸evik, MA, Balaban, N, et al. Neurobrucellosis in an endemic area of brucellosis. Scand J Infect Dis. (2003) 35:94–7.

Google Scholar

75. Buzgan, T, Karahocagil, MK, Irmak, H, Baran, AI, Karsen, H, Evirgen, O, et al. Clinical manifestations and complications in 1028 cases of brucellosis: a retrospective evaluation and review of the literature. IJID. (2010) 14:e469–78.

Google Scholar

Keywords: neurobrucellosis, CiteSpace, VOSviewer, cerebrospinal fluid, antibiotic therapy

Citation: Yang L, Pan W, Cai Q, An M, Wang C and Pan X (2024) The research trend on neurobrucellosis over the past 30 years (1993–2023): a bibliometric and visualization analysis. Front. Neurol. 15:1349530. doi: 10.3389/fneur.2024.1349530

Received: 13 December 2023; Accepted: 02 September 2024;
Published: 23 September 2024.

Edited by:

Heung-No Lee, Gwangju Institute of Science and Technology, Republic of Korea

Reviewed by:

Wang Zhenhai, General Hospital of Ningxia Medical University, China
Guillermo Hernán Giambartolomei, National Scientific and Technical Research Council (CONICET), Argentina
Zhao Wang, The Second Affiliated Hospital of Air Force Medical University, China

Copyright © 2024 Yang, Pan, Cai, An, Wang and Pan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Xilong Pan, xilongp@pku.edu.cn

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.