Pilot study of a ketogenic diet in relapsing-remitting MS
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作者:
Brenton, J. Nicholas
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Univ Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USAUniv Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
Brenton, J. Nicholas
[1
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Banwell, Brenda
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Univ Penn, Dept Pediat Neurol, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USAUniv Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
Banwell, Brenda
[2
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Bergqvist, A. G. Christina
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Univ Penn, Dept Pediat Neurol, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USAUniv Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
Bergqvist, A. G. Christina
[2
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Lehner-Gulotta, Diana
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Univ Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USAUniv Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
Lehner-Gulotta, Diana
[1
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Gampper, Lauren
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Univ Virginia, Dept Neurol, Charlottesville, VA USAUniv Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
Gampper, Lauren
[3
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Leytham, Emily
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Univ Virginia, Dept Neurol, Charlottesville, VA USAUniv Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
Leytham, Emily
[3
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Coleman, Rachael
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Univ Virginia, Dept Neurol, Charlottesville, VA USAUniv Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
Coleman, Rachael
[3
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Goldman, Myla D.
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Univ Virginia, Dept Neurol, Charlottesville, VA USAUniv Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
Goldman, Myla D.
[3
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机构:
[1] Univ Virginia, Dept Neurol, Div Pediat Neurol, Charlottesville, VA 22903 USA
[2] Univ Penn, Dept Pediat Neurol, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[3] Univ Virginia, Dept Neurol, Charlottesville, VA USA
Objective To assess the safety and tolerability of a modified Atkins diet (KDMAD), a type of ketogenic diet (KD), in subjects with relapsing MS while exploring potential benefits of KDs in MS. Methods Twenty subjects with relapsing MS enrolled into a 6-month, single-arm, open-label study of the KDMAD. Adherence to KDMAD was objectively monitored by daily urine ketone testing. Fatigue and depression scores and fasting adipokines were obtained at baseline and on diet. Brain MRI was obtained at baseline and 6 months. Intention to treat was used for primary data analysis, and a per-protocol approach was used for secondary analysis. Results No subject experienced worsening disease on diet. Nineteen subjects (95%) adhered to KDMAD for 3 months and 15 (75%) adhered for 6 months. Anthropometric improvements were noted on KDMAD, with reductions in body mass index and total fat mass (p < 0.0001). Fatigue (p = 0.002) and depression scores (p = 0.003) were improved. Serologic leptin was significantly lower at 3 months (p < 0.0001) on diet. Conclusions KDMAD is safe, feasible to study, and well tolerated in subjects with relapsing MS. KDMAD improves fatigue and depression while also promoting weight loss and reducing serologic proinflammatory adipokines. Classification of evidence The study is rated Class IV because of the absence of a non-KD control group.