Dynamic Neuroimaging Biomarkers in Huntington's Disease (HDeNERGY)

• ClinicalTrials.gov Identifier: NCT02639871
• Recruitment Status: Completed
• First Posted: December 28, 2015
• Last Update Posted: August 8, 2019
• Sponsor: Assistance Publique - Hôpitaux de Paris
• Collaborator: CEA
• Information provided by (Responsible Party): Assistance Publique - Hôpitaux de Paris

Study Description

Brief Summary:

There is no curative treatment available today in Huntington disease (HD) despite the identification of the mutated gene 20 years ago. Nonetheless, safe and promising therapeutic strategies targeting brain energy metabolism are now becoming available.

In view of the small effect sizes of any clinical parameter in HD, robust neuroimaging biomarkers reflecting brain energy metabolism are therefore urgently needed to better assess the potential of therapeutics targeting the mitochondria, and especially the Krebs cycle. Identifying such biomarkers at the presymptomatic phase in HD also provides a unique window for therapeutic intervention, which can be used as a proof-of-concept for the real challenge of tomorrow's medicine: the prevention of neurodegeneration HDeNERGY is an observational study consisting of the transfer of methods from preclinical to clinical studies and their application in HD. HDeNERGY aim at optimizing MRI/MRS methods to study the dynamics of brain energy metabolism. At the CENIR (Centre de neuro-imagerie et de recherche, Paris) the determination of creatine kinase rate will be first validated in healthy volunteers (n=20) and then applied to the selected cohort of early affected HD patients (n=20), presymptomatic individuals (n=20) and controls (n=20) together with the methods previously validated in HD patients (Mochel et al., 2012b) to determine the ratio of inorganic phosphate (Pi)/ phosphocreatine (PCr) during visual stimulation in presymptomatic individuals. The Chemical Exchange Saturation Transfer (CEST) method on the 3T clinical scanner of CENIR will be first validated in healthy volunteers (n=20) and then applied to the selected cohort of early affected HD patients (n=20), presymptomatic individuals (n=20) and controls (n=20).

The cerebral synthesis rate of creatine phosphate and of brain glutamate concentrations and pH values will be compared between controls, HD patients and HD presymptomatic individuals, and correlated with clinical parameters (age, BMI, UHDRS).

Condition or disease
Brain Neuroimaging Biomarkers in Huntington Disease

Detailed Description:

Compelling evidence indicate a key role of energy defects in neurodegenerative diseases (NDs). These defects would constitute extremely informative functional biomarkers of disease states and progression. Such functional biomarkers could be used as readouts for therapeutic efficacy in clinical trials, especially for drugs targeting brain energy metabolism. Magnetic Resonance Imaging (MRI) and Magnetic Resonance Spectroscopy (MRS) are likely the most promising approaches to validate brain biomarkers linked to energy metabolism. However, existing methods allowing "static" measures of metabolites concentrations offer only a fragmented vision of brain energy metabolism in NDs. The validation of novel and "dynamic" methods is urgently needed. Our project addresses this challenge for Huntington disease (HD).

Our study is an observational study consisting of the transfer of methods from preclinical to clinical studies and their application in HD.

This study comprises two period:

• Period 1: transfer of 31P saturation transfer and CEST methods from preclinical to clinical MRS/MRI platforms and the validation of these methods in healthy individuals;
• Period 2: compare brain metabolic markers in early individuals affected by HD, presymptomatic individuals and controls, using 31P saturation transfer and CEST methods.

The primary objectives are:

Using 31P saturation transfer and CEST methods, the primary objective is to compare novel metabolic biomarkers between controls and HD carriers (patients and presymptomatic individuals).

Assessment criterion:

Comparison between controls, HD patients and HD presymptomatic individuals of the cerebral synthesis rate of creatine phosphate and of brain glutamate concentrations and pH values

The secondary objectives are:

• To develop/optimize 31P MRS/CEST methods to study the dynamics of brain energy metabolism in humans
• To improve the understanding and "modeling" the nature of energy deficits in HD
• To look for correlations between brain energy profiles and clinical scores.

Assessment criteria:

• Validation of the 31P MRS and CEST methods in healthy volunteers.
• Combination and integration of the 31P MRS and CEST data in order to obtain a model of energy deficits in HD.
• Correlations between creatine phosphate synthetic rate and clinical parameters (age, BMI, UHDRS); correlations between glutamate concentrations and clinical parameters; correlations between pH values and clinical parameters.

Ancillary studies:

The investigators wish to compare brain energy parameters (creatine phosphate synthetic rate, glutamate concentrations, pH values) with systemic metabolic markers (profiles of plasma metabolites obtained from metabolomic and lipidomic studies).

Study Design

• Study Type: Observational
• Actual Enrollment: 81 participants
• Observational Model: Other
• Time Perspective: Prospective
• Official Title: Validation of Molecular Neuroimaging Biomarkers in Huntington's Disease in View of Therapeutic Trials Targeting the Krebs Cycle
• Actual Study Start Date: June 28, 2016
• Actual Primary Completion Date: June 24, 2019
• Actual Study Completion Date: June 24, 2019

Groups and Cohorts

Group/Cohort
healthy volunteers; 31P-MR Spectroscopy and CEST for Validation of MRI/MRS methods
HD presymptomatic individuals; General medical exam Clinical assessment with illness rating scales: Unified Huntington's Disease Rating Scale Total Motor Score (UHDRS) and Total Functional Capacity (TFC), 31P-MR Spectroscopy and CEST
early affected HD patients; General medical exam Clinical assessment with illness rating scales: UHDRS and TFC, 31P-MR Spectroscopy and CEST
Controls; General medical exam Clinical assessment with illness rating scales: UHDRS and TFC, 31P-MR Spectroscopy and CEST

Outcome Measures

Primary Outcome Measures :

1. Cerebral synthesis rate of creatine phosphate [ Time Frame: 1 day ]
   Comparison between controls, HD patients and HD presymptomatic individuals of the cerebral synthesis rate of creatine phosphate
2. Cerebral brain glutamate concentrations [ Time Frame: 1 day ]
   Comparison between controls, HD patients and HD presymptomatic individuals of brain glutamate concentrations
3. Cerebral pH values. [ Time Frame: 1 day ]
   Comparison between controls, HD patients and HD presymptomatic individuals of pH values

Secondary Outcome Measures :

1. Measure concentration of brain phosphocreatine (PCr) and glutamate using 31P MRS and gluCEST respectively in healthy volunteers [ Time Frame: 1 day ]

   The 31P MRS will allow to measure the synthesis rate of PCr at different time points - rest, visual stimulation and recovery after stimulation. The rate of PCr synthesis will give an indication on the integrity of the rate of creatine-kinase.

   gluCEST will allow to measure the regional distribution of glutamate in the brain in order to create glutamate maps.

2. Data integration of rate of phosphocreatine (PCr) synthesis and gluatamate concentrations. [ Time Frame: 1 day ]
   A model of energy deficit in HD can be created by looking at the correlation between the rate of PCr synthesis, glutamate maps and the disease.
3. Correlations between the ratio of phosphocreatine concentration at different time point and age of participants [ Time Frame: 1 day ]
4. Correlations between the ratio of phosphocreatine concentration at different time points and BMI of participants. [ Time Frame: 1 day ]
5. Correlations between creatine phosphate synthetic rate and UHDRS [ Time Frame: 1 day ]
6. Correlations between glutamate concentrations and age [ Time Frame: inclusion visit ]
7. Correlations between glutamate concentrations and BMI [ Time Frame: inclusion visit ]
8. Correlations between glutamate concentrations and UHDRS [ Time Frame: 1 day ]
9. Correlations between pH values and age [ Time Frame: 1 day ]
10. Correlations between pH values and BMI [ Time Frame: 1 day ]
11. Correlations between pH values and UHDRS [ Time Frame: 1 day ]

Biospecimen Retention:   Samples Without DNA

Plasma

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes
• Sampling Method: Non-Probability Sample

Study Population

Period 1: healthy volunteers; Period 2: presymptomatic individuals, early affected HD patients and controls

Criteria

Inclusion criteria

Healthy Volunteers Period 1:

• At least 18 years of age
• Signature of the informed consent
• Covered by social security

Participants Period 2:

• At least 18 years of age
• Signature of the informed consent
• Covered by social security
• Presymptomatic individuals: Positive genetic test with CAG repeat length > 39 in HTT gene, UHDRS score < 5
• Early affected patients: Positive genetic test with CAG repeat length > 39 in HTT gene and UHDRS score between 5 and 40
• BMI between 18 and 30

Non-inclusion criteria

Healthy Volunteers Period 1:

• Contra-indications to MRI (claustrophobia, metallic or material implants)
• History of severe head injury
• Participation in another trial
• Pregnancy and breastfeeding
• Inability to understand information about the protocol
• Persons deprived of their liberty by judicial or administrative decision
• Adult subject under legal protection or unable to consent.
• Unwillingness to be informed in case of abnormal MRI

Participants Period 2:

• Contra-indications to MRI (claustrophobia, metallic or material implants)
• Additional psychiatric or neurological conditions / Additional major comorbidities
• History of severe head injury
• Participation in another trial
• Pregnancy and breastfeeding
• Inability to understand information about the protocol
• Persons deprived of their liberty by judicial or administrative decision
• Adult subject under legal protection or unable to consent.
• Unwillingness to be informed in case of abnormal MRI
• Treatment with tetrabenazine

Contacts and Locations

Locations

France

APHP - Pitié Salpetriere Hospital

Paris, France

Sponsors and Collaborators

Assistance Publique - Hôpitaux de Paris

CEA

Investigators

• Principal Investigator: Fanny MOCHEL, MD; Assistance Publique - Hôpitaux de Paris

More Information

• Responsible Party: Assistance Publique - Hôpitaux de Paris
• ClinicalTrials.gov Identifier: NCT02639871
• Other Study ID Numbers: P140708; 2015-A00793-46 ( Other Identifier: IDCRB )
• First Posted: December 28, 2015
• Last Update Posted: August 8, 2019
• Last Verified: August 2019

Keywords provided by Assistance Publique - Hôpitaux de Paris:

Huntington disease; Neuroimaging metabolic biomarker

Additional relevant MeSH terms:

Huntington Disease; Basal Ganglia Diseases; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Dementia; Chorea; Dyskinesias; Movement Disorders; Heredodegenerative Disorders, Nervous System; Neurodegenerative Diseases; Genetic Diseases, Inborn; Cognition Disorders; Neurocognitive Disorders; Mental Disorders