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Published on: March 18, 2022
Diet and Nutrients in Rare Neurological Disorders: Biological, Biochemical, and Pathophysiological Evidence
Marilena Briglia1, Fabio Allia1, Rosanna Avola1
1Department of Medicine and Surgery, "Kore" University of Enna, 94100 Enna, Italy.
Diet and nutrition significantly impact rare neurological diseases, influencing their onset and progression. Research highlights the need for personalized dietary strategies due to genetic and disease variability.
Area of Science:
- Neuroscience
- Genetics
- Nutritional Science
Background:
- Rare diseases encompass diverse, severe conditions affecting multiple systems, often with neurological symptoms.
- Diet and nutrition are crucial factors in the development and progression of neurological disorders.
- Understanding nutritional impacts is vital, especially in rare neurological diseases.
Purpose of the Study:
- To review existing evidence on diet and nutrient intake in rare neurological disorders.
- To link nutritional effects with genetic, biological, and pathophysiological aspects of these diseases.
- To explore nutrition's role as both therapy and risk factor.
Main Methods:
- Comprehensive literature search across major databases (PubMed, Web of Science, DynaMed, Clinicaltrials.gov).
- Systematic review and synthesis of in vitro, in vivo, and clinical data.
- Critical analysis of findings in relation to disease-specific characteristics.
Main Results:
- Nutritional interventions are increasingly recognized alongside pharmacological treatments for rare diseases.
- Standard dietary recommendations are challenged by the genetic heterogeneity and variable manifestations of rare neurological disorders.
- Evidence suggests a complex interplay between diet, genetics, and disease progression.
Conclusions:
- Further research is needed to elucidate molecular mechanisms and long-term effects of nutrition in rare neurological diseases.
- Identifying knowledge gaps can guide future studies for improved therapeutic strategies.
- Personalized nutrition approaches may be essential due to individual disease variability.
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