Role of Ketogenic Diets in Multiple Sclerosis and Related Animal Models: An Updated Review.
Wei-Sheng LinShan-Ju LinPei-Yin LiaoDivya SureshTing-Rong HsuPei-Yu WangPublished in: Advances in nutrition (Bethesda, Md.) (2022)
Prescribing a ketogenic diet (KD) is a century-old dietary intervention mainly used in the context of intractable epilepsy. The classic KD and its variants regained popularity in recent decades, and they are considered potentially beneficial in a variety of neurological conditions other than epilepsy. Many patients with multiple sclerosis (MS) have attempted diet modification for better control of their disease, although evidence thus far remains insufficient to recommend a specific diet for these patients. The results of 3 pilot clinical trials of KD therapy for MS, as well as several related studies, have been reported in recent years. The preliminary findings suggest that KD is safe, feasible, and potentially neuroprotective and disease-modifying for patients with MS. Research on corresponding rodent models has also lent support to the efficacy of KD in the prevention and treatment of experimental autoimmune encephalomyelitis and toxin-induced inflammatory demyelinating conditions in the brain. Furthermore, the animal studies have yielded mechanistic insights into the molecular mechanisms of KD action in relevant situations, paving the way for precision nutrition. Herein we review and synthesize recent advances and also identify unresolved issues, such as the roles of adipokines and gut microbiota, in this field. Hopefully this panoramic view of current understanding can inform future research directions and clinical practice with regard to KD in MS and related conditions.
Keyphrases
- multiple sclerosis
- mass spectrometry
- physical activity
- weight loss
- ms ms
- clinical trial
- white matter
- clinical practice
- end stage renal disease
- primary care
- escherichia coli
- newly diagnosed
- ejection fraction
- cerebral ischemia
- prognostic factors
- copy number
- oxidative stress
- gene expression
- peritoneal dialysis
- high glucose
- endothelial cells
- genome wide
- open label
- study protocol
- stress induced
- adverse drug