Acute Effects of Medium Chain Triglyceride (MCT) Nutritional Ketosis on Parkinson s Disease (PD) Symptoms and Biomarkers (MCT-PD)
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 21
- 试验地点
- 1
- 主要终点
- Feasibiilty of Ketogenic Diet - Retention (Co-primary Endpoint)
研究概览
简要总结
Background:
The ketogenic diet uses fats as a person's major energy source rather than carbohydrates. There is increasing interest in using this diet to treat neurodegenerative disorders like Parkinson's disease. Researchers want to learn more about the ketogenic diet before recommending this diet in clinical practice.
Objective:
To study the effects of a ketogenic diet for someone with PD.
Eligibility:
People over age 50 with mild to moderate PD.
Design:
Participants will be screened with surveys and a 10-foot walking test. They will have a medical history, physical exam, and blood test.
Participants will be contacted twice in a 1-week period to discuss what they ate over the last 24 hours. They will log data about their daily exercise and activities using an online fitness tracking app.
Participants will stay at NIH Clinical Center for 1 week. They will be put into 1 of 2 groups. One group will follow a ketogenic diet and take MCT oil. The other group will follow a low-fat diet. Their body measurements will be taken. They will meet with a physical therapist and nutritionist.
Participants will have daily respiratory and glucose monitoring. They will have cognitive tests and complete surveys. They will have walking, motor function, and reaction time/finger tapping tests. They will have heart and nerve function tests. They will have electrocardiograms and electroencephalograms. Blood will be taken twice daily.
Participants will follow the ketogenic diet at home for 2 weeks. They will log their activities using the fitness tracking app. Then they will have a follow-up visit at NIH.
Participation in the trial will last for 4 weeks.
详细描述
Study Description:
While three pilot studies of ketogenic diet (KD) in PD have shown either reduction in motor scores (UPDRS) or improved cognition (memory/fluency), there are gaps in knowledge of the time course and mechanisms of reported outcomes. Furthermore, only a standard ketogenic diet was studied while there are variations such as MCT oil supplementation shown to increase keto-induction, and other adaptations may improve tolerability and micronutrient content. It is the goal of this proposed inpatient metabolic study to address the initial question of effect size and time course of ketosis. If suggestive of benefit in PD, this pilot study may lead to a subsequent larger study of long-term feasibility and effects on disease biomarkers and disease progression, which might also compare alternate diets of interest in PD such as Mediterranean diet. Thus, a pilot feasibility study is proposed, targeting retention rate >80% and adherence in the outpatient setting. Recruitment of 32 participants is based upon power analysis of secondary outcome, testing the Timed Up & Go mobility test that has reported validity in fall prediction, additionally plotting continuous and serially repeated direct/indirect ketosis measurements and motor as well as non-motor symptoms / exploratory disease biomarkers. It is hypothesized that, compared to a non-ketogenic, standard American diet (SAD, also referred to interchangeably as usual diet, ketogenic diet supplemented by MCT oil (MCT-KD) will improve mobility tested by Timed Up & Go (TUG), as well as akinesia, tremor, and memory/executive function tasks, and will reduce motor and non-motor fluctuations within the acute period of keto-induction and early ketogenic timepoints due to improved mitochondrial function and neurotransmitter signaling.
Objectives:
The primary objective is to test the hypothesis that nutritional ketosis (NK) supplemented by MCT oil in a PD cohort (MCT-KD) is feasible for a duration of three weeks. The secondary objective is to show that NK improves PD symptomatology in cognition (improved attention, recall, and executive function), mobility (TUG), and motor function (bradykinesia, akinesia and tremor) within three weeks.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 50 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •INCLUSION CRITERIA:
- •In order to be eligible to participate in this study, an individual must meet all of the following criteria:
- •Must be able to speak English
- •Able and willing to provide informed consent
- •Male or female older than age 50 years
- •Clinically probable diagnosis of Parkinson s Disease by UK Brain Bank Criteria, of moderate severity, with ability to safely walk independently for at least a short distance (20 feet) as determined on screening visit
- •BMI > 18.5, to minimize potential risk from expected mild weight loss from ketogenic diet
- •eGFR > 60 by MDRD equation (established on screening visit serum chemistry)
- •MOCA > 20, as well as having in the investigators' assessment the ability and willingness to adhere to either of the study diets
- •Agreement to adhere to Lifestyle Considerations throughout study duration
- •Adhering to Usual Diet (SAD) at baseline, as per investigator determination
排除标准
- •An individual who meets any of the following criteria will be excluded from participation in this study:
- •1. Atypical Parkinsonism or symptoms suggestive of a diagnosis other than PD by clinical criteria
- •2. Family history of early onset PD (\ 8.0% on screening test
- •8. History of kidney stones or gallbladder surgery
- •9. Biliary / liver disease, defined on screening labs, by presence of any of the following: Total bilirubin (TB) \> 2x ULN or \> 2 mg/dL; AST \>3x ULN; or ALT \>5x ULN
- •10. Uncontrolled hypertension, defined as SBP \> 180 mmHg or DBP \> 105 mmHg on screening visit
- •11. Hyperlipidemia defined by LDL \>/= 160 mg/dL as per ATP-III guidelines
- •12. Medical / psychiatric condition identified via clinical assessment in screening visit felt to impede completion of the study\*
- •13. Presence of PD Psychosis or dementia, or other neuropsychiatric or psychiatric illness impeding consent and fidelity to the study intervention and/or measurements
- •14. Dietary or allergy restrictions as determined by research team to be prohibitive for the study
- •15. Inability to communicate and provide informed consent in English
- •16. No history of previous use of ketogenic or similar diet to a degree that could interfere with study blinding
- •* A thorough medical and social history will be performed during the screening visit including questions regarding alcohol and substance abuse. If active alcohol abuse or other current substance abuse is identified which could increase the risk of study participation, then participants will be excluded.
研究组 & 干预措施
Arm A
Ketogenic Diet
干预措施: Liquigen MCT oil (Dietary Supplement)
Arm B
Standard American Diet
干预措施: Standard American Diet (Other)
结局指标
主要结局
Feasibiilty of Ketogenic Diet - Retention (Co-primary Endpoint)
时间窗: Week 3
Analysis of feasibility was determined by 3 co-primary endpoints: retention, adherence, and acceptability, measured at the end of week 3 (outpatient segment). After each co-primary endpoint was calculated, three benchmark criteria were used to determine feasibility. All criteria must be met for feasibility to be positive. Benchmark criteria for Retention was defined as a completion rate at study end (week 3) of \>80%, i.e., \>80% of participants must remain in the study at the 3 week time point.
Feasibility of Ketogenic Diet - Adherence (Co-primary Endpoint)
时间窗: Week 3
Analysis of feasibility was determined by 3 co-primary endpoints: retention, adherence, and acceptability, measured at the end of week 3 (outpatient segment). After each co-primary endpoint was calculated, three benchmark criteria were used to determine feasibility. All criteria must be met for feasibility to be positive. Benchmark criteria for Adherence was defined as a mean net carbohydrate intake of \</=10% during the 2 week outpatient period. Mean net carbohydrate intake was determined using the following calculation: (total carbohydrates minus total dietary fiber) x 4 divided by total calories.
Feasibility of Ketogenic Diet - Acceptability (Co-primary Endpoint)
时间窗: Week 3
Analysis of feasibility was determined by 3 co-primary endpoints: retention, adherence, and acceptability, measured at the end of week 3 (outpatient segment). After each co-primary endpoint was calculated, three benchmark criteria were used to determine feasibility. All criteria must be met for feasibility to be positive. Acceptability was defined via an exit survey (at end of study week 3) using a 4-point Likert scale to indicate how likely the participant would continue the diet on at least an intermittent basis in the future with 1 representing "Very likely" and 4 representing "Very unlikely". The benchmark criteria for Acceptability was defined as at least 2 out of 4 on the Likert scale.
次要结局
- Timed Up and Go (TUG)(Day 7)