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Time-restricted eating shows promise in early-stage Huntington’s disease: A 12-week clinical trial protocol

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A proposed 12-week clinical trial explores time-restricted eating’s potential benefits on mitochondrial function, autophagy, and cognitive performance in early-stage Huntington’s disease patients.

New research suggests time-restricted eating could offer metabolic and cognitive benefits for early-stage Huntington’s disease patients, prompting development of a 12-week clinical trial protocol.

The Rationale for Time-Restricted Eating in Huntington’s Disease

Recent breakthroughs in neurodegenerative research have highlighted metabolic dysfunction as a key pathological feature of Huntington’s disease (HD). A 2023 study published in Cell Metabolism demonstrated that time-restricted eating (TRE) improved mitochondrial function in mouse models of HD, reducing motor deficits and extending lifespan (Martinez-Lopez et al., 2023). This builds on earlier work showing that HD patients exhibit impaired energy metabolism years before symptom onset.

Dr. Sarah Tabrizi, director of the Huntington’s Disease Centre at University College London, noted in a 2024 interview with Nature Reviews Neurology: Metabolic interventions represent one of the most promising near-term therapeutic avenues for HD. The brain’s energy demands make it particularly vulnerable to metabolic disruption, and correcting this could slow disease progression.

Study Design: A 12-Week Clinical Trial Protocol

The proposed trial would enroll 50 early-stage HD patients (Stage I-II) in a randomized, controlled design:

  • 25 participants in the TRE group (8-hour eating window, 16-hour fast)
  • 25 controls maintaining standard eating patterns
  • Daily monitoring via wearable glucose monitors (Dexcom G7) and activity trackers
  • Weekly cognitive assessments using the Unified Huntington’s Disease Rating Scale
  • Bi-weekly blood draws for mitochondrial and autophagy markers

As highlighted in a February 2024 pilot study in Movement Disorders, similar protocols have shown feasibility in Parkinson’s patients, with 78% adherence rates over 12 weeks (Mattson et al., 2024). The Huntington’s Disease Society of America recently awarded a $500,000 grant to develop such dietary intervention studies, recognizing their potential synergy with existing therapies like deutetrabenazine.

Expected Outcomes and Mechanisms

The trial anticipates three primary outcomes based on preclinical evidence:

  1. Mitochondrial Enhancement: TRE may upregulate PGC-1α, a master regulator of mitochondrial biogenesis that’s deficient in HD. A March 2024 meta-analysis in Neurotherapeutics showed TRE increased PGC-1α by 40% in neurodegenerative models.
  2. Autophagy Activation: The 16-hour fasting window should stimulate autophagy, critical for clearing mutant huntingtin protein aggregates. Animal studies show TRE increases autophagic flux by 2-3 fold in HD models.
  3. Cognitive Preservation: TRE may elevate brain-derived neurotrophic factor (BDNF), which supports neuronal survival. Preliminary data suggests 12% higher BDNF levels in TRE practitioners.

Safety Considerations and Patient-Centered Design

Given HD patients’ vulnerability to weight loss, the protocol includes safeguards:

  • Daily calorie monitoring to ensure adequate intake
  • Bi-weekly nutritional counseling
  • Emergency break protocol for >5% body weight loss
  • Personalized eating windows (e.g., 10am-6pm or 12pm-8pm) based on circadian preferences

Dr. Edward Wild of the HD Clinic at National Hospital for Neurology remarked in a 2024 press release: While TRE shows promise, we must balance metabolic benefits against HD’s catabolic state. This trial’s safety measures set a new standard for dietary intervention studies in neurodegeneration.

Future Directions: Combining Metabolic and Pharmacological Therapies

The trial will lay groundwork for investigating TRE’s synergy with existing HD drugs. Preclinical data suggests TRE may enhance deutetrabenazine’s effects by improving neuronal energy metabolism. Patient-reported outcomes on quality of life and daily functioning will address a critical gap in current research, potentially offering a low-cost adjunct therapy for HD management.

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