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Effects of a Multimodal Lifestyle Intervention on Cardiometabolic Markers in People with Progressive Multiple
Arturo S Martinez1, Alyanne J Bastian1, Farnoosh Shemirani1
1Department of Internal Medicine, University of Iowa, 200 Hawkins Dr, Iowa City, IA 52242, USA.
Insights
A 12-month lifestyle intervention for people with progressive multiple sclerosis (PwPMS) showed no significant changes in cardiometabolic biomarkers. Further research is needed to confirm potential benefits for managing comorbidities in PwPMS.
Area of Science:
- Neurology
- Cardiology
- Metabolic Health
Background:
- Cardiometabolic comorbidities are prevalent in multiple sclerosis (MS).
- Lifestyle interventions are effective for managing cardiometabolic conditions in the general population.
- Evidence for lifestyle interventions in MS patients is limited.
Purpose of the Study:
- To assess the impact of a multimodal lifestyle intervention on serum apolipoproteins (Apo), creatine kinase (CK), glucose, and insulin.
- To evaluate cardiometabolic health markers in people with progressive MS (PwPMS).
Main Methods:
- A 12-month multimodal lifestyle intervention was implemented.
- Intervention components included diet, exercise, neuromuscular electrical stimulation, supplements, and stress reduction.
- Serum biomarkers (ApoA1, B, E, CK, glucose, insulin) were measured at baseline and 12 months.
Main Results:
- A marginally significant decrease in apolipoprotein B (ApoB) was observed (p=0.06).
- No significant changes were found in ApoA1, ApoE, CK, HOMA-IR, or HOMA-β.
- An initial association between increased insulin resistance and fatigue was not sustained after outlier exclusion.
Conclusions:
- The multimodal lifestyle intervention did not negatively affect glycemic and lipid profiles in PwPMS.
- Observed improvements in serum biomarkers were not statistically significant.
- Larger, controlled studies are required to validate cardiometabolic health benefits in PwPMS.
Abstract:
Background: Cardiometabolic comorbidities are common in multiple sclerosis (MS), and lifestyle interventions are effective in managing these conditions in the general population, though evidence in the MS patient population is limited. Objective: To evaluate the effect of a multimodal lifestyle intervention on serum apolipoproteins (Apo), creatine kinase (CK), glucose, and insulin in people with progressive MS (PwPMS). Methods: This study included n = 19 PwPMS who participated in a 12-month multimodal lifestyle intervention (including a modified Paleolithic diet, exercise, neuromuscular electrical stimulation, supplements, and stress reduction). Lipid profile (ApoA1, B, and E), CK, glucose, and insulin were obtained at baseline and after 12 months under fasting conditions. Results: At 12 months, there was a marginally significant decrease in ApoB (mean change: -7.17 mg/dL; 95% CI: -14.4, 0.12; p = 0.06), while no significant changes were observed for ApoA1 (mean change: -1.28 mg/dL; 95% CI: 12.33, 9.76; p = 0.80), ApoE (mean change: +0.12 mg/dL; 95% CI: -0.27, 0.52; p = 0.51), CK (mean change: +13.19 U/L; 95% CI: -32.72, 59.11; p = 0.55), Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) (mean change: -0.44; 95% CI: -1.11, 0.22; p = 0.17), and HOMA-β (mean change: +45.62; 95% CI: -95.6, 186.9; p = 0.50). A positive association was observed between changes in HOMA-IR and fatigue changes at 12 months (β = 0.81, p = 0.02), suggesting that an increase in HOMA-IR was linked to increased fatigue, which was no longer significant following the exclusion of outliers (β = 0.71, p = 0.16). Conclusions: A multimodal lifestyle intervention did not negatively impact glycemic and lipid profiles. While improvements were observed in serum biomarkers, these changes were not statistically significant, highlighting the need for stronger evidence from larger, controlled studies to confirm the cardiometabolic health benefits in PwPMS.
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