Skull Density Ratio as Arm‐Allocation Parameter for a Controlled Focused Ultrasound Trial in Parkinson's Disease

Author:

Pineda‐Pardo José Angel123ORCID,Martínez‐Fernández Raul123,Natera‐Villalba Elena134,Ruiz‐Yanzi Agustina13,Rodríguez‐Rojas Rafael1235ORCID,Del Alamo Marta13,Jiménez‐Castellanos Tamara136,Matarazzo Michele123ORCID,Gasca‐Salas Carmen1237ORCID,Rascol Olivier8ORCID,Obeso José A.1237

Affiliation:

1. HM CINAC MADRID (Centro Integral de Neurociencias Abarca Campal). Hospital Universitario HM Puerta del Sur, HM Hospitales Madrid Spain

2. CIBERNED, Instituto de Salud Carlos III Madrid Spain

3. Instituto de Investigación Sanitaria HM Hospitales Spain

4. PhD Medicine Program Universidad Autonoma de Madrid Madrid Spain

5. Facultad HM de Ciencias de la Salud de la Universidad Camilo José Cela Madrid Spain

6. Department of Preventive Medicine Public Health and Microbiology, Universidad Autónoma de Madrid Madrid Spain

7. Universidad San Pablo‐CEU Madrid Spain

8. Clinical Investigation Center CIC 1436, NS‐Park/F‐CRIN Network and NeuroToul COEN Center; Inserm University of Toulouse 3 and CHU of Toulouse F‐31000 Toulouse France

Abstract

AbstractBackgroundMR‐guided focused ultrasound (FUS) thermoablation is an established therapy for movement disorders. FUS candidates must meet a predefined threshold of skull density ratio (SDR), a parameter that accounts for the efficiency in reaching ablative temperatures. Randomized sham‐controlled trials to provide definitive therapeutic evidence employ pure randomization of subjects into active treatment or control arms. The latter design has several general limitations.ObjectiveTo demonstrate that SDR values are not associated with clinically and demographically relevant variables in patients with Parkinson's disease (PD). This in turn would allow using SDR as an arm‐allocation parameter, separating patients who will receive active FUS treatment and best medical management treatment (BMT).MethodsWe studied a cohort of 215 PD patients who were candidates for FUS subthalamotomy to determine if the SDR was correlated with demographic or clinical variables that could introduce bias for group allocation in a controlled trial.ResultsSDR was unassociated with age, gender, and clinical motor features nor with levodopa daily dose in our cohort of PD patients. A negative association with age was found for the female subgroup.ConclusionsOur results show that in a PD population considered for FUS subthalamotomy treatment, the SDR may be a valid group‐allocation parameter. This could be considered as the basis for a controlled study comparing FUS subthalamotomy vs BMT.

Funder

Instituto de Salud Carlos III

Ministerio de Ciencia e Innovación

Publisher

Wiley

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