What is Neurolathyrism and its Cause?
Neurolathyrism is the specific type of lathyrism associated with the consumption of legumes from the genus Lathyrus, primarily Lathyrus sativus, known commonly as Kesari dal, grass pea, or chickling pea. It is an irreversible neurological disease affecting populations who rely on this hardy crop as a dietary staple, often during food insecurity. The condition is caused by the neurotoxic amino acid β-N-oxalyl-L-α,β-diaminopropionic acid, or β-ODAP.
The Mechanism of the β-ODAP Toxin
When ingested in large quantities over time, β-ODAP acts as an excitotoxin in the central nervous system, mimicking glutamate and overstimulating neuronal receptors. This leads to excessive excitation and cellular damage or death, specifically affecting upper motor neurons and pyramidal tracts in the spinal cord responsible for lower limb movement. The outcome is a progressive loss of motor function, leading to spastic paralysis. β-ODAP also impairs mitochondrial function and increases oxidative stress, contributing to nerve cell degeneration.
Symptoms and Progression of Neurolathyrism
Lathyrism develops gradually after chronic high-level consumption, with symptoms progressing from subtle signs to severe disability.
Stages of Lathyrism
- Early warning signs: Mild leg weakness, muscle cramps (especially in calves after exertion), and a sensation of heaviness.
- Progressive development: Increased muscle stiffness (spasticity), making movement difficult. A characteristic "scissor gait" develops. Lower limb reflexes become exaggerated.
- Advanced lathyrism: Severe paralysis in lower limbs (paraparesis or paraplegia) requiring assistive devices or preventing walking. Muscle wasting (atrophy) and joint contractures may occur. Sensation, mental function, and upper limb movement are typically unaffected.
Risk Factors and Prevention
The main risk is prolonged, heavy consumption of Kesari dal, particularly over 30% of the daily diet, often occurring in drought or famine-stricken areas. Malnutrition can worsen risk. Young adult males may be more susceptible due to higher consumption and exertion.
Methods to Reduce Toxicity
- Proper preparation: Soaking overnight and rinsing can significantly reduce β-ODAP content. Boiling and discarding the water also helps.
- Dietary diversification: Mixing Kesari dal with other foods, especially cereals rich in sulfur-based amino acids, is highly effective.
- Low-toxin varieties: Cultivating and using low-toxin strains of Lathyrus sativus is a long-term solution.
- Public awareness: Educating communities on risks and safe preparation is vital.
Neurolathyrism vs. Osteolathyrism
These are distinct conditions caused by different Lathyrus legumes and toxins, affecting different systems.
| Feature | Neurolathyrism | Osteolathyrism |
|---|---|---|
| Cause | Lathyrus sativus (Kesari dal). | Lathyrus odoratus (sweet peas). |
| Toxin | β-ODAP. | Beta-aminopropionitrile (BAPN). |
| System Affected | Central nervous system, motor neurons. | Connective tissues (bones, blood vessels). |
| Symptoms | Progressive, irreversible lower limb paralysis, spasticity. | Skeletal deformities, hernias, aortic aneurysms. |
The Path Forward
Neurological damage from advanced neurolathyrism is irreversible. Treatment is supportive, focusing on physical therapy and assistive devices. Stopping Kesari dal consumption is crucial to prevent worsening.
Public health initiatives, improved food security, and developing low-toxin varieties are essential for prevention. The situation highlights the challenge of balancing the need for resilient food sources with health risks. Research institutions like the National Institutes of Health continue to investigate this disease.
Conclusion
In conclusion, the disease caused by Kesari dal is lathyrism, a neurodegenerative disorder causing irreversible lower limb paralysis due to the neurotoxin β-ODAP. It primarily affects vulnerable populations relying on the pulse during scarcity. Prevention through proper cooking, dietary diversity, and public awareness is critical, as advanced lathyrism is irreversible, though discontinuing consumption can halt progression.