Related Experiment Video
Updated: Aug 5, 2026

09:50
Real-time Quaking-induced Conversion Assay for Detection of CWD Prions in Fecal Material
Published on: September 29, 2017
Variant Creutzfeldt-Jakob disease
Esther A Croes1, Cornelia M van Duijn
1Genetic Epidemiology Unit, Department of Epidemiology and Biostatistics, Erasmus MC, Rotterdam, The Netherlands. e.croes@erasmusmc.nl
European Journal of Epidemiology
|August 12, 2003
Summary
Variant Creutzfeldt-Jakob disease (vCJD) impacts Europe. This review covers vCJD causes, bovine spongiform encephalopathy links, treatment, prevention, and research challenges.
Area of Science:
- Neurology
- Epidemiology
- Public Health
Background:
- Variant Creutzfeldt-Jakob disease (vCJD) has emerged as a significant public health concern in Europe.
- The disease is linked to the consumption of products contaminated with bovine spongiform encephalopathy (BSE) prions.
Purpose of the Study:
- To provide a comprehensive review of the aetiology of vCJD.
- To discuss the relationship between vCJD and BSE.
- To explore treatment options, transmission prevention strategies, and future research directions.
Main Methods:
- Literature review of epidemiological studies, scientific publications, and public health reports.
- Analysis of the transmission pathways and risk factors associated with vCJD.
- Synthesis of current knowledge on disease management and prevention.
Main Results:
- The aetiology of vCJD is strongly associated with the bovine spongiform encephalopathy agent.
- Transmission is primarily linked to dietary exposure to contaminated beef products.
- Current treatment options are limited, emphasizing the importance of preventive measures.
Conclusions:
- Understanding the aetiology and transmission of vCJD is crucial for effective public health interventions.
- Continued research is needed to develop treatments and overcome epidemiological study limitations.
- Strict control measures are essential to prevent further transmission of vCJD.
Related Concept Videos
Arboviral Encephalitis
Arboviral encephalitis refers to brain inflammation caused by arthropod-borne viruses, particularly those transmitted through mosquito vectors. Among these, West Nile virus (WNV), a member of the Flaviviridae family, is a significant public health concern. WNV is an enveloped, positive-sense, single-stranded RNA virus. Human infection typically begins when an infected mosquito introduces the virus into the dermis during feeding. The primary transmission cycle involves birds as amplifying hosts...
Cytomegalovirus Disease
Cytomegalovirus (CMV) disease is caused by human cytomegalovirus, a double-stranded DNA virus of the Herpesviridae family. While primary CMV infection is often asymptomatic in immunocompetent individuals, the virus can cause severe disease in neonates and immunocompromised patients. CMV is the most common cause of congenital viral infection in the United States, and a major pathogen in solid organ and hematopoietic stem cell transplant recipients.CMV is transmitted via bodily fluids, sexual...
Cryptococcal Meningitis
Cryptococcal meningitis is a life-threatening opportunistic infection predominantly associated with HIV/AIDS, accounting for over 100,000 deaths annually worldwide. However, it also affects individuals with other forms of immunosuppression, including those undergoing immunosuppressive therapy, organ transplant recipients, patients with innate immunodeficiencies, and individuals with hematological disorders. The infection is caused mainly by Cryptococcus neoformans and Cryptococcus gattii,...
Encephalitis ll: Pathophysiology
Encephalitis is inflammation of the brain parenchyma caused by direct viral invasion or immune-mediated mechanisms triggered by infections or tumors. Both processes lead to neuronal injury, disrupted neurotransmission, and diverse neurological symptoms, often with overlapping clinical and pathological features.Autoimmune EncephalitisIn autoimmune encephalitis, antibodies target neuronal antigens on cell surfaces, synapses, or within neurons. A key example is anti-NMDAR encephalitis, which can...
Alzheimer Disease ll: Pathophysiology
Alzheimer disease involves structural changes in the brain that begin long before symptoms appear. The most distinctive features are extracellular neuritic plaques and intracellular neurofibrillary tangles.Neuritic plaques form in the cerebral cortex and around blood vessels. These plaques contain a dense core of beta-amyloid (Aβ)—a toxic protein fragment that clumps outside neurons. The core is surrounded by damaged neuronal extensions, as well as reactive astrocytes and microglia. Abnormal...
Huntington Disease l: Introduction
Huntington disease or HD is a progressive, fatal neurodegenerative disorder inherited in an autosomal dominant pattern.PathophysiologyIt is caused by expansion of the CAG trinucleotide repeat in the HTT gene on chromosome 4 (4p16.3), producing an abnormal huntingtin protein with an expanded polyglutamine tract. This misfolded protein disrupts cellular function, leading to neuronal death. Normal alleles have ≤26 repeats, 27–35 are intermediate (risk of expansion), 36–39 show reduced penetrance,...

