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31P-MRS and Huntington Disease

Not Applicable
Completed
Conditions
Huntington Disease
Interventions
Other: 31P-MR spectroscopy
Other: 31P-RMN spectroscopy
Registration Number
NCT01359774
Lead Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Brief Summary

The purpose of this study is to identify and quantify a brain energy deficit in Huntington patients, using 31P-RMN spectroscopy.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • 5<UHDRS<50
  • Age>18 years
  • Ability to undergo MR scanning
  • Covered by french social security
Exclusion Criteria
  • Evidence of psychiatric disorder
  • Attendant neurological disorder
  • Contraindications to MRI (claustrophobia, metallic or material implants)
  • Severe head injury
  • Unable to understand the protocol
  • Pregnancy
  • Failure to give informed consent
  • Subjects with exclusion criteria required by french law (e.g. subjects who require a legally authorized representative to obtain consent)
  • Unwillingness to be informed in case of abnormal MRI

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Healthy volunteers31P-MR spectroscopy-
Huntington patients31P-RMN spectroscopy-
Primary Outcome Measures
NameTimeMethod
Brain energy deficit in Huntington patientsone year

31P-MRS allows quantification of high-energy phosphate metabolites such as ATP and phosphocreatine.

Objective: to look at brain energy metabolism during rest and activation.

Secondary Outcome Measures
NameTimeMethod
Correlating a brain energy deficit with (i) biochemical parameters and (ii) clinical parameters in Huntington patientsone year

Biochemical parameters include metabolites that we previously showed to be biomarkers in HD: branched chain amino acids and IGF1.

Clinical parameters include UHDRS and TFC.

Trial Locations

Locations (1)

Hopital de la Pitié-Salpetrière

🇫🇷

Paris, France

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