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Assessment of ADCY5-related Movement Disorders With Motion SENSors (SENSeo-ADCY5)

A

Assistance Publique - Hôpitaux de Paris

Status

Enrolling

Conditions

ADCY5-related Dyskinesia

Treatments

Other: caffeinated coffee - decaffeinated coffee

Study type

Interventional

Funder types

Other

Identifiers

NCT05136495
2021-A00994-37 (Other Identifier)
APHP201439

Details and patient eligibility

About

ADCY5-related movement disorders are caused by dominant mutations in the ADCY5 gene. This rare neurogenetic disease is characterized by childhood-onset generalized hyperkinetic movements. Currently, the only tools available to rate the severity of movement disorders observed in ADCY5-patients are clinical rating scales of abnormal movements. These scales use the investigators' judgement to rate globally the severity of movements observed in various body parts of the patient. This protocol proposes to investigate a multimodal approach, combining a clinical scale assessment with ViconTM's objective movement measurement. A secondary objective of the study is to assess the effect of coffee on ADCY5-patients.

Full description

ADCY5-related movement disorders are caused by dominant mutations in the ADCY5 gene. This rare neurogenetic disease is characterized by childhood-onset generalized hyperkinetic movements. The abnormal movements typically comprise a combination of dystonia, myoclonus and chorea occurring on a background of axial hypotonia, with superimposed disabling episodes of paroxysmal dyskinesia. The causing mutations are located in the ADCY5 gene coding for the Adenylate Cyclase 5 (AC5). AC5 is highly expressed in the striatal projection neurons of the striatum, a region involved in the control of movements. No effective treatment has been found. Currently, the only tools available to rate the severity of movement disorders observed in ADCY5-patients are clinical rating scales of abnormal movements. These scales use the investigators' judgement to globally rate movements severity in various body parts. This leads to inter-raters' scoring variability. An objective assessment through refined and comprehensive quantification of movements is needed. A motion capture system, such as ViconTM, could better reflect the global and focal variations of abnormal movements. This would be critical for the evaluation of responses to potential treatments. This protocol proposes to investigate a multimodal approach, combining a clinical scale assessment with ViconTM's objective movement measurement. A secondary objective of the study is to assess the effect of coffee on ADCY5-patients. The caffeine contained in coffee acts as a nonselective adenosine receptor antagonist, with a strong affinity for A2A receptors. By blocking A2A receptors, caffeine reduces the enzymatic activity of the altered mutated AC5 protein coded by the mutated ADCY5 gene. This effect could modulate the abnormal movements observed in patients.

Enrollment

10 estimated patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ADCY5 mutation carriers
  • Age > 15 years old and 3 months
  • Informed consent from the patient or/ and a legal representative when appropriate
  • Affiliated with a social security system or beneficiary of such a regime or by waiver from CPP ( french ethic committee) for patients outside the European union ( EU)
  • daily caffeine consumer

Exclusion criteria

  • Hypersensitivity to caffeine or to xanthine derivatives
  • Heart condition contraindicating coffee intake
  • Liver failure
  • Impaired comprehension interfering with an informed consent
  • Positive pregnancy test for women of childbearing potential
  • Patient treated by Enoxacin, Ciprofloxacin, Norfloxacin (Noroxin), Cimetidine, Phenytoin β-adrenergic drugs (β2 mimetics) at inclusion.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

10 participants in 2 patient groups

Caffeinated coffee
Experimental group
Description:
Drink caffeinated coffee one morning and drink decaffeinated coffee the other morning
Treatment:
Other: caffeinated coffee - decaffeinated coffee
Decaffeinated coffee
Experimental group
Description:
Drink decaffeinated coffee one morning and drink caffeinated coffee the other morning
Treatment:
Other: caffeinated coffee - decaffeinated coffee

Trial contacts and locations

1

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Central trial contact

louise laure MARIANI, MD, PhD

Data sourced from clinicaltrials.gov

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