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Completed

NCT Number: NCT04351360

Pilot Study on Caffeine Efficiency in ADCY5-related Dyskinesia

Heterozygous mutations in the ADCY5 gene cause involuntary early-onset hyperkinetic movements. In addition, patients may have associated psychiatric disorders.There is currently no treatment. As the pathophysiology is linked to ADCY5 hyperactivity, the investigative team has treated patients with caffeine, an antagonist. The investigator wishes to interview patients on the effect of caffeine on their motor symptoms and their overall clinical condition, and on the possible existence of psychiatric comorbidities using phone questionnaires.

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Key information

Age range

8 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Département de Neurologie Groupe Hospitalier Pitié-Salpêtrière

Paris, 75651 PARIS Cedex 13, France

About this study

Heterozygous mutations in the ADCY5 gene cause involuntary early-onset hyperkinetic movements. 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.

Many treatments have been tried, with no obvious efficacy. Two patients from the same family (a father and daughter) told investigators that caffeine had a dramatic effect on their paroxysmal episodes. They said that taking coffee would prevent episodes and reduce their duration (efficacy estimated at 80%), an effect specific to caffeine since it was reproduced by the ingestion of caffeine citrate capsules. Very interestingly, there is a rationale underlying this phenomenon. Indeed, caffeine is an antagonist of the adenosine A2A receptors (A2AR), receptors which activate ADCY5 and which are localized preferentially in striatal neurons expressing dopamine D2 receptors. As caffeine is an A2AR antagonist, it likely inhibits ADCY5, and therefore induces clinical improvement in patients with hyperactivity of this protein.

In addition, the investigative team noted anxiety in some of its patients, and the question of the presence of psychiatric disorders in ADCY5 patients was recently raised in the literature.

The investigative team wishes to collect standardized preliminary data by questioning patients on the effect of caffeine on their motor symptoms and their overall clinical state, and on the possible existence of psychiatric comorbidities using structured questionnaires which will be carried out by phone.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Proven genetic diagnosis of ADCY5-related dyskinesia
  • Caffeine intake
  • Non opposition by the patient or the legal representatives if the patient is a minor.

No Exclusion Criteria.

Treatment and study plan

Primary outcomes

  1. Percentage of responders to caffeine

    Time frame: one hour

    the response being defined as an improvement of overall involuntary movements of 40% or more.

Secondary outcomes

  1. Global change of involuntary movements ranging from 0 (no change) to 10 (disappearance of involuntary movements)

    Time frame: one hour

    evaluated by patients

  2. Global clinical change ranging from 0 (no change) to 10 (normalization of the global clinical state)

    Time frame: one hour

    evaluated by patients

  3. Change of the duration of paroxysmal episodes of movement disorders with caffeine

    Time frame: one hour

    evaluated by patients

  4. Frequency change of paroxysmal episodes of movement disorders with caffeine

    Time frame: one hour

    evaluated by patients

  5. Presence or absence of psychiatric symptoms

    Time frame: one hour

    according to the MINI (Mini International Neuropsychiatric Interview)

Sponsors and collaborators

Lead sponsor

Institut National de la Santé Et de la Recherche Médicale, France

Other Gov

Registry information

Official study title

Pilot Study on Subjective Efficiency of Caffeine in ADCY5-related Dyskinesia

Acronym: CAF-ADCY5

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Apr 17, 2020
Registry last updated
Dec 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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