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Shh Signaling in Brain AVMs: Novel Player & Therapeutic Target (SHAM)

24 de junio de 2026 actualizado por: Pola Roberto, Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Sonic Hedgehog Signaling: Novel Player and Potential Therapeutic Target in Brain Arteriovenous Malformations

The present study, entitled "SHAM Study," is a prospective observational translational study aimed at investigating the molecular mechanisms underlying brain arteriovenous malformations (AVMs). In particular, the study seeks to explore the role of the Sonic Hedgehog (Shh) signaling pathway, which has recently been hypothesized as a potential key player in pathological angiogenesis and in the maintenance of the malformative nidus.

The study will be conducted through the analysis of brain tissues obtained exclusively as residual material from neurosurgical procedures performed for clinical indications. Under no circumstances will additional procedures be carried out or modifications made to the patients' therapeutic pathway for research purposes. Samples will include tissues from adult patients undergoing AVM resection and, as controls, non-pathological brain tissues derived from surgeries performed for other indications, such as drug-resistant epilepsy.

The methodological approach involves the isolation of endothelial cells from collected samples and their characterization using multi-omics techniques, including transcriptomic analysis, microRNA profiling, and quantitative proteomics. The resulting data will be integrated through advanced bioinformatics analyses in order to identify specific molecular patterns, altered pathways, and potential biomarkers. Particular attention will be given to the evaluation of Shh pathway activation and its interactions with other signaling systems involved in AVM pathogenesis.

The collected biological material may also be used, subject to specific informed consent, for preclinical studies conducted on animal models, with the aim of further investigating the identified pathogenetic mechanisms and assessing their functional relevance. Such activities will be carried out in compliance with current regulations on animal experimentation and subject to approval by the relevant authorities.

The primary objective of the study is to identify significant differences in gene expression between endothelial cells derived from AVMs and control brain tissue. Secondary objectives include the identification of integrated molecular profiles (RNA, microRNA, and proteins), the correlation of these profiles with patients' clinical and radiological characteristics, and the identification of potential therapeutic targets.

The study is designed so as not to entail additional risks for participants, as it is based exclusively on the use of biological material that would otherwise be discarded. All subjects will be enrolled only after providing written informed consent. Data will be processed in pseudonymized form in compliance with current regulations on personal data protection.

The total expected duration is 36 months, and the study is part of a targeted research project aimed at generating new knowledge with potential translational impact, laying the groundwork for the future development of targeted therapeutic strategies.

Study duration and number of patients:

The overall duration of the study will be 36 months. Enrollment will begin immediately after ethical approval and will be completed by month 24.

A total of 30-45 adult patients are expected to be enrolled, including 20-30 undergoing resection of brain arteriovenous malformations and 10-15 patients undergoing neurosurgical procedures for drug-resistant epilepsy, from whom non-pathological cortical tissue will be obtained.

Descripción general del estudio

Estado

Aún no reclutando

Tipo de estudio

De observación

Inscripción (Estimado)

45

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Rome
      • Rome, Rome, Italia, 00168
        • Fondazione Policlinico Universitario Agostino Gemelli IRCCS
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

N/A

Método de muestreo

Muestra no probabilística

Población de estudio

Adults ≥18 years undergoing neurosurgical intervention with resection of AVM or non-pathological cortical tissue (controls).

Descripción

Inclusion Criteria:

  • Adult patients aged 18 years or older undergoing neurosurgical resection who provide written informed consent for research use of residual tissue.

Exclusion Criteria:

  • Tissue with extensive necrosis or contamination, lack of valid consent, or known infectious agents that preclude safe handling.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
AVM group (cases)
Adult patients undergoing neurosurgical resection of brain arteriovenous malformations for clinically indicated reasons. Residual AVM tissue obtained during surgery will be used for molecular analyses.
Control group
Adult patients undergoing neurosurgical procedures for drug-resistant epilepsy or other clinical indications, from whom non-pathological brain tissue is resected as part of standard care. Residual tissue will be used as control.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Differential endothelial gene expression between AVM and control tissues.
Periodo de tiempo: Up to 34 months
Endothelial differential gene expression measured as log2 fold change and adjusted p value from bulk RNA seq.
Up to 34 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
MicroRNA and proteomic profiles, pathway activity scores, histological markers, and clinical correlations.
Periodo de tiempo: Up to 34 months
MicroRNA abundance (normalized counts); protein abundance (LFQ intensity); pathway activity scores (Shh, Notch, VEGF, TGF β/ALK1, MAPK); histological metrics (percent positive area; mean staining intensity for Shh, Gli1, CD31, α SMA).
Up to 34 months

Otras medidas de resultado

Medida de resultado
Medida Descripción
Periodo de tiempo
Single-cell analyses, integrated biomarkers, and potential therapeutic targets.
Periodo de tiempo: Up to 36 months

Identification of single-cell transcriptional clusters and inferred cell-type composition, where single-cell data are available.

Identification of integrated multi-omics biomarker panels based on concordant transcriptomic and proteomic signals.

Identification of candidate druggable targets prioritized through network centrality analyses and cross-platform validation.

Up to 36 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de agosto de 2026

Finalización primaria (Estimado)

1 de junio de 2029

Finalización del estudio (Estimado)

1 de agosto de 2029

Fechas de registro del estudio

Enviado por primera vez

24 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

24 de junio de 2026

Publicado por primera vez (Actual)

30 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

30 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

24 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 27587

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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