TY - JOUR
T1 - Randomised controlled trial of intermittent calorie restriction in people with multiple sclerosis
AU - Ghezzi, Laura
AU - Tosti, Valeria
AU - Shi, Lisa
AU - Cantoni, Claudia
AU - Mikesell, Robert
AU - Lancia, Samantha
AU - Zhou, Yanjiao
AU - Obert, Kathleen
AU - Dula, Courtney
AU - Sen, Monokesh K.
AU - Ge, Anjie
AU - Tolentino, Miguel
AU - Bollman, Bryan
AU - Don, Anthony S.
AU - Matarese, Giuseppe
AU - Colamatteo, Alessandra
AU - Rocca, Claudia La
AU - Lepore, Maria Teresa
AU - Raji, Cyrus A.
AU - Rahmani, Farzaneh
AU - Wu, Gregory F.
AU - Naismith, Robert T.
AU - Fontana, Luigi
AU - Cross, Anne H.
AU - Salter, Amber
AU - Piccio, Laura
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2024.
PY - 2024
Y1 - 2024
N2 - Background Calorie restriction (CR) ameliorates preclinical models of multiple sclerosis (MS) via multiple mechanisms. These include decreased leptin, a proinflammatory adipokine, but mechanistic studies in humans are lacking. Tests of daily and intermittent CR (iCR) in people with MS (pwMS) showed improvements in fatigue and well-being measures. This trial studied the effects of 12-week iCR on metabolic, immunological, and clinical outcomes in pwMS. Method Relapsing-remitting MS participants were randomised to iCR or a control group. Study visits were conducted at baseline, 6 and 12 weeks. The primary outcome was reduction in serum leptin levels at 12 weeks. Feasibility and safety were assessed by diet adherence and adverse events (AEs). Secondary outcomes included changes in anthropometric and body composition measures, metabolic and immunologic profiling, and clinical measures. Mixed effects linear regression models were used to evaluate outcome differences between and within groups over time. Results Forty-two pwMS were randomised, 34 completed the study (17/group). Leptin serum levels at 12 weeks were significantly lower in the iCR versus the control group (mean decrease −6.98 µg/dL, 95% CI: −28.02 to 14.06; p=0.03). Adherence to iCR was 99.5% and 97.2% at 6 and 12 weeks, respectively, and no serious AEs were reported. An increase in blood CD45RO+ regulatory T-cell numbers was seen after 6 weeks of iCR. Exploratory cognitive testing demonstrated a significant improvement in the Symbol Digit Modality Test Score in the iCR group at 12 weeks. Conclusions iCR has the potential to benefit metabolic and immunologic profiles and is safe and feasible in pwMS.
AB - Background Calorie restriction (CR) ameliorates preclinical models of multiple sclerosis (MS) via multiple mechanisms. These include decreased leptin, a proinflammatory adipokine, but mechanistic studies in humans are lacking. Tests of daily and intermittent CR (iCR) in people with MS (pwMS) showed improvements in fatigue and well-being measures. This trial studied the effects of 12-week iCR on metabolic, immunological, and clinical outcomes in pwMS. Method Relapsing-remitting MS participants were randomised to iCR or a control group. Study visits were conducted at baseline, 6 and 12 weeks. The primary outcome was reduction in serum leptin levels at 12 weeks. Feasibility and safety were assessed by diet adherence and adverse events (AEs). Secondary outcomes included changes in anthropometric and body composition measures, metabolic and immunologic profiling, and clinical measures. Mixed effects linear regression models were used to evaluate outcome differences between and within groups over time. Results Forty-two pwMS were randomised, 34 completed the study (17/group). Leptin serum levels at 12 weeks were significantly lower in the iCR versus the control group (mean decrease −6.98 µg/dL, 95% CI: −28.02 to 14.06; p=0.03). Adherence to iCR was 99.5% and 97.2% at 6 and 12 weeks, respectively, and no serious AEs were reported. An increase in blood CD45RO+ regulatory T-cell numbers was seen after 6 weeks of iCR. Exploratory cognitive testing demonstrated a significant improvement in the Symbol Digit Modality Test Score in the iCR group at 12 weeks. Conclusions iCR has the potential to benefit metabolic and immunologic profiles and is safe and feasible in pwMS.
UR - http://www.scopus.com/inward/record.url?scp=85204222851&partnerID=8YFLogxK
U2 - 10.1136/jnnp-2024-333465
DO - 10.1136/jnnp-2024-333465
M3 - Article
C2 - 39137977
AN - SCOPUS:85204222851
SN - 0022-3050
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
M1 - 333465
ER -