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Ketogenic diet and fasting diet as Nutritional Approaches in Multiple Sclerosis (NAMS): protocol of a randomized controlled study
Multiple sclerosis (MS) is the most common inflammatory disease of the central nervous system in young adults that may lead to progressive disability. Since pharmacological treatments may have substantial side effects, there is a need for complementary treatment options such as specific dietary appr...
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Published in: | Current controlled trials in cardiovascular medicine 2020-01, Vol.21 (1), p.3-3, Article 3 |
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description | Multiple sclerosis (MS) is the most common inflammatory disease of the central nervous system in young adults that may lead to progressive disability. Since pharmacological treatments may have substantial side effects, there is a need for complementary treatment options such as specific dietary approaches. Ketone bodies that are produced during fasting diets (FDs) and ketogenic diets (KDs) are an alternative and presumably more efficient energy source for the brain. Studies on mice with experimental autoimmune encephalomyelitis showed beneficial effects of KDs and FDs on disease progression, disability, cognition and inflammatory markers. However, clinical evidence on these diets is scarce. In the clinical study protocol presented here, we investigate whether a KD and a FD are superior to a standard diet (SD) in terms of therapeutic effects and disease progression.
This study is a single-center, randomized, controlled, parallel-group study. One hundred and eleven patients with relapsing-remitting MS with current disease activity and stable immunomodulatory therapy or no disease-modifying therapy will be randomized to one of three 18-month dietary interventions: a KD with a restricted carbohydrate intake of 20-40 g/day; a FD with a 7-day fast every 6 months and 14-h daily intermittent fasting in between; and a fat-modified SD as recommended by the German Nutrition Society. The primary outcome measure is the number of new T2-weighted MRI lesions after 18 months. Secondary endpoints are safety, changes in relapse rate, disability progression, fatigue, depression, cognition, quality of life, changes of gut microbiome as well as markers of inflammation, oxidative stress and autophagy. Safety and feasibility will also be assessed.
Preclinical data suggest that a KD and a FD may modulate immunity, reduce disease severity and promote remyelination in the mouse model of MS. However, clinical evidence is lacking. This study is the first clinical study investigating the effects of a KD and a FD on disease progression of MS.
ClinicalTrials.gov, NCT03508414. Retrospectively registered on 25 April 2018. |
doi_str_mv | 10.1186/s13063-019-3928-9 |
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This study is a single-center, randomized, controlled, parallel-group study. One hundred and eleven patients with relapsing-remitting MS with current disease activity and stable immunomodulatory therapy or no disease-modifying therapy will be randomized to one of three 18-month dietary interventions: a KD with a restricted carbohydrate intake of 20-40 g/day; a FD with a 7-day fast every 6 months and 14-h daily intermittent fasting in between; and a fat-modified SD as recommended by the German Nutrition Society. The primary outcome measure is the number of new T2-weighted MRI lesions after 18 months. Secondary endpoints are safety, changes in relapse rate, disability progression, fatigue, depression, cognition, quality of life, changes of gut microbiome as well as markers of inflammation, oxidative stress and autophagy. Safety and feasibility will also be assessed.
Preclinical data suggest that a KD and a FD may modulate immunity, reduce disease severity and promote remyelination in the mouse model of MS. However, clinical evidence is lacking. This study is the first clinical study investigating the effects of a KD and a FD on disease progression of MS.
ClinicalTrials.gov, NCT03508414. Retrospectively registered on 25 April 2018.</description><identifier>ISSN: 1745-6215</identifier><identifier>EISSN: 1745-6215</identifier><identifier>DOI: 10.1186/s13063-019-3928-9</identifier><identifier>PMID: 31898518</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Alzheimer's disease ; Analysis ; Anti-inflammatory diet ; Autophagy ; Body mass index ; Brain research ; Calories ; Carbohydrates ; Central nervous system ; Chief financial officers ; Clinical trials ; Cognition ; Development and progression ; Diagnostic imaging ; Diet ; Diet therapy ; Dietary intervention ; Disabilities ; Diseases ; Encephalomyelitis ; Fasting ; Glucose ; Inflammation ; Informed consent ; Insulin resistance ; Intermittent fasting ; Ketogenic diet ; Medical research ; Metabolism ; Multiple sclerosis ; Nervous system ; Neurodegeneration ; Nutrition ; Nutrition research ; Oils & fats ; Oxidative stress ; Patients ; Quality of life ; Recurrence (Disease) ; Review boards ; Study Protocol</subject><ispartof>Current controlled trials in cardiovascular medicine, 2020-01, Vol.21 (1), p.3-3, Article 3</ispartof><rights>COPYRIGHT 2020 BioMed Central Ltd.</rights><rights>The Author(s). 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s). 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-d5f0e8a47699aa98622e8a64cdb7208697e3640d6c97c2fab04531a32b21ee423</citedby><cites>FETCH-LOGICAL-c560t-d5f0e8a47699aa98622e8a64cdb7208697e3640d6c97c2fab04531a32b21ee423</cites><orcidid>0000-0002-3904-5789</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941322/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6941322/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31898518$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bahr, Lina Samira</creatorcontrib><creatorcontrib>Bock, Markus</creatorcontrib><creatorcontrib>Liebscher, Daniela</creatorcontrib><creatorcontrib>Bellmann-Strobl, Judith</creatorcontrib><creatorcontrib>Franz, Liane</creatorcontrib><creatorcontrib>Prüß, Alexandra</creatorcontrib><creatorcontrib>Schumann, Dania</creatorcontrib><creatorcontrib>Piper, Sophie K</creatorcontrib><creatorcontrib>Kessler, Christian S</creatorcontrib><creatorcontrib>Steckhan, Nico</creatorcontrib><creatorcontrib>Michalsen, Andreas</creatorcontrib><creatorcontrib>Paul, Friedemann</creatorcontrib><creatorcontrib>Mähler, Anja</creatorcontrib><title>Ketogenic diet and fasting diet as Nutritional Approaches in Multiple Sclerosis (NAMS): protocol of a randomized controlled study</title><title>Current controlled trials in cardiovascular medicine</title><addtitle>Trials</addtitle><description>Multiple sclerosis (MS) is the most common inflammatory disease of the central nervous system in young adults that may lead to progressive disability. Since pharmacological treatments may have substantial side effects, there is a need for complementary treatment options such as specific dietary approaches. Ketone bodies that are produced during fasting diets (FDs) and ketogenic diets (KDs) are an alternative and presumably more efficient energy source for the brain. Studies on mice with experimental autoimmune encephalomyelitis showed beneficial effects of KDs and FDs on disease progression, disability, cognition and inflammatory markers. However, clinical evidence on these diets is scarce. In the clinical study protocol presented here, we investigate whether a KD and a FD are superior to a standard diet (SD) in terms of therapeutic effects and disease progression.
This study is a single-center, randomized, controlled, parallel-group study. One hundred and eleven patients with relapsing-remitting MS with current disease activity and stable immunomodulatory therapy or no disease-modifying therapy will be randomized to one of three 18-month dietary interventions: a KD with a restricted carbohydrate intake of 20-40 g/day; a FD with a 7-day fast every 6 months and 14-h daily intermittent fasting in between; and a fat-modified SD as recommended by the German Nutrition Society. The primary outcome measure is the number of new T2-weighted MRI lesions after 18 months. Secondary endpoints are safety, changes in relapse rate, disability progression, fatigue, depression, cognition, quality of life, changes of gut microbiome as well as markers of inflammation, oxidative stress and autophagy. Safety and feasibility will also be assessed.
Preclinical data suggest that a KD and a FD may modulate immunity, reduce disease severity and promote remyelination in the mouse model of MS. However, clinical evidence is lacking. This study is the first clinical study investigating the effects of a KD and a FD on disease progression of MS.
ClinicalTrials.gov, NCT03508414. Retrospectively registered on 25 April 2018.</description><subject>Alzheimer's disease</subject><subject>Analysis</subject><subject>Anti-inflammatory diet</subject><subject>Autophagy</subject><subject>Body mass index</subject><subject>Brain research</subject><subject>Calories</subject><subject>Carbohydrates</subject><subject>Central nervous system</subject><subject>Chief financial officers</subject><subject>Clinical trials</subject><subject>Cognition</subject><subject>Development and progression</subject><subject>Diagnostic imaging</subject><subject>Diet</subject><subject>Diet therapy</subject><subject>Dietary intervention</subject><subject>Disabilities</subject><subject>Diseases</subject><subject>Encephalomyelitis</subject><subject>Fasting</subject><subject>Glucose</subject><subject>Inflammation</subject><subject>Informed consent</subject><subject>Insulin resistance</subject><subject>Intermittent fasting</subject><subject>Ketogenic diet</subject><subject>Medical research</subject><subject>Metabolism</subject><subject>Multiple sclerosis</subject><subject>Nervous system</subject><subject>Neurodegeneration</subject><subject>Nutrition</subject><subject>Nutrition research</subject><subject>Oils & fats</subject><subject>Oxidative stress</subject><subject>Patients</subject><subject>Quality of life</subject><subject>Recurrence (Disease)</subject><subject>Review boards</subject><subject>Study 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cardiovascular medicine</jtitle><addtitle>Trials</addtitle><date>2020-01-02</date><risdate>2020</risdate><volume>21</volume><issue>1</issue><spage>3</spage><epage>3</epage><pages>3-3</pages><artnum>3</artnum><issn>1745-6215</issn><eissn>1745-6215</eissn><abstract>Multiple sclerosis (MS) is the most common inflammatory disease of the central nervous system in young adults that may lead to progressive disability. Since pharmacological treatments may have substantial side effects, there is a need for complementary treatment options such as specific dietary approaches. Ketone bodies that are produced during fasting diets (FDs) and ketogenic diets (KDs) are an alternative and presumably more efficient energy source for the brain. Studies on mice with experimental autoimmune encephalomyelitis showed beneficial effects of KDs and FDs on disease progression, disability, cognition and inflammatory markers. However, clinical evidence on these diets is scarce. In the clinical study protocol presented here, we investigate whether a KD and a FD are superior to a standard diet (SD) in terms of therapeutic effects and disease progression.
This study is a single-center, randomized, controlled, parallel-group study. One hundred and eleven patients with relapsing-remitting MS with current disease activity and stable immunomodulatory therapy or no disease-modifying therapy will be randomized to one of three 18-month dietary interventions: a KD with a restricted carbohydrate intake of 20-40 g/day; a FD with a 7-day fast every 6 months and 14-h daily intermittent fasting in between; and a fat-modified SD as recommended by the German Nutrition Society. The primary outcome measure is the number of new T2-weighted MRI lesions after 18 months. Secondary endpoints are safety, changes in relapse rate, disability progression, fatigue, depression, cognition, quality of life, changes of gut microbiome as well as markers of inflammation, oxidative stress and autophagy. Safety and feasibility will also be assessed.
Preclinical data suggest that a KD and a FD may modulate immunity, reduce disease severity and promote remyelination in the mouse model of MS. However, clinical evidence is lacking. This study is the first clinical study investigating the effects of a KD and a FD on disease progression of MS.
ClinicalTrials.gov, NCT03508414. Retrospectively registered on 25 April 2018.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>31898518</pmid><doi>10.1186/s13063-019-3928-9</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-3904-5789</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer's disease Analysis Anti-inflammatory diet Autophagy Body mass index Brain research Calories Carbohydrates Central nervous system Chief financial officers Clinical trials Cognition Development and progression Diagnostic imaging Diet Diet therapy Dietary intervention Disabilities Diseases Encephalomyelitis Fasting Glucose Inflammation Informed consent Insulin resistance Intermittent fasting Ketogenic diet Medical research Metabolism Multiple sclerosis Nervous system Neurodegeneration Nutrition Nutrition research Oils & fats Oxidative stress Patients Quality of life Recurrence (Disease) Review boards Study Protocol |
title | Ketogenic diet and fasting diet as Nutritional Approaches in Multiple Sclerosis (NAMS): protocol of a randomized controlled study |
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