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临床试验/NCT06369571
NCT06369571Enrolling By Invitation1 期

Improving Cardiovascular Health Risks in Adults With Epilepsy on a Modified Atkins Diet

Johns Hopkins University1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2024年10月4日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
Enrolling By Invitation
入组人数
22
试验地点
1
主要终点
Statin Adherence

研究概览

简要总结

Ketogenic diet therapies (KDTs) emphasize high fat and very low carbohydrate intake and help to control seizures in adults who fail to respond to medications. However, KDT use can lead to increased cholesterol levels in some adults with epilepsy (AWE). Treatments that can reverse elevations in cholesterol observed with long-term KDT use without compromising diet adherence and seizure control are needed. The proposed study will explore the feasibility and safety of diet modification and statin use to lower cholesterol in this population. Study findings will help guide doctors utilizing KDTs in adults with epilepsy on how to approach managing elevations in cholesterol.

详细描述

The scientific premise of this proposal is that established or long-term (≥ 12 months) Modified Atkins diet (MAD) use in AWE influences atherosclerotic cardiovascular disease (ASCVD) risk and can be modified to reduce dyslipidemia when observed. Hence, the overarching goals of this proposal are to explore the safety and feasibility of dyslipidemia management strategies to reduce ASCVD risk in AWE on MAD without increasing seizure risk. This study will collect data before and after randomly assigned interventions to reduce LDL in AWE on long-term MAD recruited from patients receiving clinical care in the Johns Hopkins Adult Epilepsy Diet Center.

AWE with dyslipidemia on long-term MAD will be randomized 1:1 to either MAD modification (10% reduction of dietary energy from saturated fat, replaced with poly-unsaturated fat ) or moderate-intensity statin use (atorvastatin 10mg) for 12 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 (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Modified Atkins Diet use ≥ 12 months
  • Dyslipidemia based on American College of Cardiology/American Heart Association guidelines (i.e., LDL ≥190 mg/dL, 10-year ASCVD risk ≥5% with risk enhancers, etc.)
  • 18 years of age or older
  • Body mass index (BMI) > 18.5
  • Stable anti-seizure medication regimen for > 1 month.

排除标准

  • < 18 years of age
  • Body mass index (BMI) < 18.5
  • Changes in anti-seizure medication regimen < 1 month prior to participation
  • Known ASCVD (history of acute coronary syndrome, myocardial infarction, angina, stroke, transient ischemic attack, or peripheral artery disease)
  • Current statin medication use
  • Prior serious adverse response to atorvastatin or other statin medications
  • Uncorrected carnitine deficiency

研究组 & 干预措施

Statin

Active Comparator

Participants will receive 10mg of atorvastatin daily for 12 weeks

干预措施: Atorvastatin 10mg (Drug)

Modified Atkins diet (MAD) Modification

Experimental

Participants will be instructed on how to change their modified Atkins diet for 12 weeks. They will replace 10% of daily dietary energy from saturated fat with poly-unsaturated fat.

干预措施: Modification of dietary fat composition (Other)

结局指标

主要结局

Statin Adherence

时间窗: 12 weeks

Statin adherence will be determined based on pills returned at study completion, with participants labeled adherent if 80% or more of pills were consumed.

Diet adherence as assessed by 3 day food records

时间窗: 12 weeks

Diet adherence will be based on the ability to achieve 10% reduction in dietary energy from saturated fat assessed from 3-day food records, the gold standard for diet intake assessments.

Change in weekly seizure frequency

时间窗: 12 weeks

12-week difference in weekly seizure frequency from baseline

LDL Change

时间窗: 12 weeks

12-week % LDL change from baseline within arms and between arms

Seizure severity questionnaire score

时间窗: 12 weeks

12-week difference in seizure severity questionnaire (SSQ) score (score 1-7, with higher score indicating more severe seizures)

次要结局

  • Blood ketone change(12 weeks)
  • Frequency of adverse events(12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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