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Caffeine Efficacy in ADCY5-related Dyskinesia

Study of Caffeine Efficacy in ADCY5-related Dyskinesia - a Retrospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04469283
Acronym
ADCY5-CAF
Enrollment
20
Registered
2020-07-14
Start date
2020-07-15
Completion date
2021-07-15
Last updated
2020-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ADCY5-related Dyskinesia

Keywords

ADCY5, dyskinesia, caffeine

Brief 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.

Detailed 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.

Interventions

OTHERcaffeine and movement disorders

Caffeine efficacy on movement disorders in patients with ADCY5-related dyskinesia.

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of responders to caffeine12 monthsthe response being defined as an improvement of overall involuntary movements of 40% or more.

Secondary

MeasureTime frameDescription
Global improvement of involuntary movements,12 MONTHSGlobal change of involuntary movements ranging from 0 (no change) to 10 (disappearance of involuntary movements)
Global clinical change12 monthsGlobal clinical change ranging from 0 (no change) to 10 (normalization of the global clinical state)
Duration of paroxysmal episodes of movement disorders12 monthsChange of the duration of paroxysmal episodes of movement disorders with caffeine

Contacts

Primary ContactAurélie MENERET, MD
aurelie.meneret@aphp.fr1 42 16 24 61

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026