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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04469283
Other study ID # APHP200193
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 15, 2020
Est. completion date July 15, 2021

Study information

Verified date June 2020
Source Assistance Publique - Hôpitaux de Paris
Contact Aurélie MENERET, MD
Phone 1 42 16 24 61
Email aurelie.meneret@aphp.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Heterozygous mutations in ADCY5 induce hyperactivity of striatal adenylate cyclase type 5 (AC5), manifesting as early-onset hyperkinetic movement disorders. Numerous treatments have been tried without much efficacy thus far. Two patients from the same family reported efficacy of caffeine on paroxysmal episodes, both to prevent episodes and to reduce their duration (efficacy estimated to be around 80%), which was specific to caffeine as it was reproduced with caffeine citrate capsules. Interestingly, there is a rationale underlying this observation. Indeed, caffeine is an antagonist of adenosine A2A receptors (A2AR), which activate AC5 and are localized preferentially in striatal neurons that express dopamine receptors D2 .Caffeine therefore likely induces AC5 inhibition, and thus clinical improvement in patients with hyperactivity of this protein. This observation has been recently published in2019.

The investigators will collect preliminary data by interviewing our neurologist and neuropediatric colleagues, in France and abroad since it is a rare disease, on the effect of caffeine on motor symptoms and global clinical status in their ADCY5 patients.


Description:

Heterozygous mutations in ADCY5 induce hyperactivity of striatal adenylate cyclase type 5 (AC5) manifesting as early-onset hyperkinetic movement disorders. The phenotype combines chorea, dystonia and/or myoclonus with frequent facial involvement, axial hypotonia, fluctuations and/or episodes of paroxysmal dyskinesia which can be nocturnal and/or painful, generally without intellectual deficiency, epilepsy or cerebellar syndrome . It is a very rare disease, affecting around twenty patients in France.

Scientific context of the research:

Numerous treatments have been tried without much efficacy thus far.

Scientific justification for the study:

Two patients from the same family reported efficacy of caffeine on paroxysmal episodes, both to prevent episodes and to reduce their duration (efficacy estimated to be around 80%), which was specific to caffeine as it was reproduced with caffeine citrate capsules. Interestingly there is a rationale underlying this situation. Indeed, caffeine is an antagonist of adenosine A2A receptors (A2AR), which activate AC5 and are localized preferentially in striatal neurons that express dopamine receptors D2. Caffeine therefore likely induces inhibition of AC5, and thus clinical improvement in patients with hyperactivity of this protein. This observation has been recently published in 2019 HYPOTHESIS Our hypothesis is that most patients with ADCY5-related dyskinesia respond well to caffeine.

This study is a multicentric retrospective study, which will be conducted in neurology and neuropediatric departments across the world.

Participants will be recruited by their own physician. This research will take place over 18 months in total: 12 month to collect all patients' data and 6 months to analyse data.

The number of participants will be between 5 and 20, depending on colleagues replies.

This research will take place over 18 months in total: 12 month to collect all patients' data and 6 months to analyse data.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date July 15, 2021
Est. primary completion date July 15, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion criteria

- Proven genetic diagnosis of ADCY5-related dyskinesia

- Adults or children without age limits

- Past or present caffeine intake

- Non-opposition by the patient (adults) or the legal representatives (minors) in France, and patient information according to each country's legislation in other countries.

4.2. Exclusion criteria None.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
caffeine and movement disorders
Caffeine efficacy on movement disorders in patients with ADCY5-related dyskinesia.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

References & Publications (1)

Méneret A, Gras D, McGovern E, Roze E. Caffeine and the Dyskinesia Related to Mutations in the ADCY5 Gene. Ann Intern Med. 2019 Sep 17;171(6):439. doi: 10.7326/L19-0038. Epub 2019 Jun 11. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of responders to caffeine the response being defined as an improvement of overall involuntary movements of 40% or more. 12 months
Secondary Global improvement of involuntary movements, Global change of involuntary movements ranging from 0 (no change) to 10 (disappearance of involuntary movements) 12 MONTHS
Secondary Global clinical change Global clinical change ranging from 0 (no change) to 10 (normalization of the global clinical state) 12 months
Secondary Duration of paroxysmal episodes of movement disorders Change of the duration of paroxysmal episodes of movement disorders with caffeine 12 months
See also
  Status Clinical Trial Phase
Recruiting NCT05136495 - Assessment of ADCY5-related Movement Disorders With Motion SENSors N/A