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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01879267
Other study ID # KEK-ZH-Nr. 2009-0119
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2012
Est. completion date January 2018

Study information

Verified date June 2018
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Huntington's disease (HD) is an incurable and fatal disorder characterised by progressive degeneration of the basal ganglia and the cerebral cortex. Contrary to earlier thinking, HD is associated with abnormalities in peripheral tissues which might even contribute to brain pathology including muscle wasting, mitochondrial abnormalities, and impaired muscle energy metabolism. Mitochondrial impairment and muscle atrophy in human HD patients and murine models of HD are associated with altered expression of PGC-1a, a transcriptional cofactor that seems to regulate many, if not all of the adaptations of muscle fibres to chronic endurance training, and induces improved exercise performance and increased peak oxygen uptake. We aim at investigating whether endurance exercise has the capability of stabilizing and / or reversing PGC-1a dependent alterations of muscle function and structure in HD patients, and whether muscle training ameliorates musculoskeletal and cardiovascular function, as well as motor and cognitive symptoms in HD patients.


Description:

Huntington disease (HD) is an incurable and fatal disorder that affects muscle function and leads to cognitive decline and dementia. HD was long considered a brain disorder but meanwhile it was shown that HD also affects other tissues such as muscle, leading to muscle wasting. Previous studies suggested that the muscle disorder might be caused by an impaired energy metabolism through mitochondrial dysfunction, which also might also contribute to brain pathology.

In muscle tissue of healthy persons, a protein named PGC 1- α seems to regulate many, if not all of the adaptations of muscle metabolism and mitochondrial biogenesis to chronic endurance training. It was shown that PGC 1- α is reduced in muscle tissue of human HD patients and animal models of HD.

We aim investigating whether endurance exercise has the capability of stabilizing and / or reversing PGC-1α dependent decline of muscle function and structure in HD patients, and whether muscle training ameliorates muscular and cardiovascular function, as well as coordination and cognitive decline in HD. To this end, we will train 20 male HD patients using a 6 months progressive endurance exercise program. In order to compare the size effect of exercise between HD patients and healthy individuals, 20 age-matched healthy males will perform the identical exercise regimen as HD patients. Within one week before the training period starts and within one week after it has ended, we will assess metabolic and functional data. In addition, we will analyze muscle tissue samples for muscle fiber structure, metabolic phenotype and cellular pathology. Finally, gene and protein expression analyses will be performed on muscle tissue extracts to gain insights into the molecular regulation of training adaptations in HD.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date January 2018
Est. primary completion date January 2018
Accepts healthy volunteers No
Gender Male
Age group 30 Years to 60 Years
Eligibility Inclusion criteria: Inclusion criteria for HD subjects are:

- Male gender

- Genetically verified diagnosis of HD

- Age 30 to 50 years

- Presence of only mild to moderate neurological, cognitive or muscular impairment allowing the subjects to give their written informed consent and to participate in the endurance training (UHDRS 30 or lower)

For healthy control participants, inclusion criteria are:

- male gender 9

- age 30 to 50 years

- absence of physical or mental illness

Exclusion criteria: Exclusion criteria for HD subjects are:

- Female gender

- Advanced neurological, cognitive or muscular impairment related to HD that does not allow patients to participate in the endurance training and/or to give their written informed consent

- Cardiovascular disease or any other medical condition that might not be compatible with endurance training

- CK levels > 300 U/L

Exclusion criteria for healthy control participants are:

- cardiovascular disease

- any other medical condition that might not be compatible with endurance training

- CK levels > 300 U/L.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Exercise training
6 months of exercise training (2 times 30 min per week) starting one week after a 6-months natural course observation period

Locations

Country Name City State
Switzerland University Hospital Zurich, Division of Neurology Zurich ZH

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Unified Huntington's Disease Rating Scale (UHDRS) Baseline and 6 months
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