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Biobank - Investigating the Gut Microbiota, Genetics, Epigenetics and Metabolites

7 de febrero de 2023 actualizado por: Siew Chien NG, Chinese University of Hong Kong

Investigating the Intestinal Microbiota, Epigenetic Markers and Body Fluid Metabolites to Identify Biomarkers for Inflammatory Bowel Diseases

Inflammatory bowel disease (IBD) affects 1 in 500 to 1,000 people in the West. Previously a disease predominantly of the West, there is now a marked increase in the incidence of ulcerative colitis (UC) and Crohn's disease (CD) in Asia, with an estimated prevalence of 1 in 3,000 and 1 in 10,000 respectively[1]. The rapid increase of IBD in Asian raising concern of investigators. Therefore setting up a large scale biobank with comprehensive clinical data is require.

Descripción general del estudio

Estado

Reclutamiento

Descripción detallada

Inflammatory bowel disease (IBD) affects 1 in 500 to 1,000 people in the West. Previously a disease predominantly of the West, there is now a marked increase in the incidence of ulcerative colitis (UC) and Crohn's disease (CD) in Asia, with an estimated prevalence of 1 in 3,000 and 1 in 10,000 respectively [1]. IBD is thought to result from an aberrant immune response to intestinal bacteria in genetically susceptible individuals [2]. Genetic variants have been shown to contribute to an increased IBD risk. Although genetic traits predispose to the development of IBD in Asia, the change in epidemiology that has occurred over only a few decades suggests that other, presumably environmental factors play the major role in the development of disease [10].

IBD patients often rely on medical therapy to achieve remission. Due to the diverse features of severity, phenotypes, clinical courses and responses, personalizing IBD therapy is important to maximize management efficacy, minimize adverse events and decrease cost. Thiopurines is a key component of medications in the treatment of Inflammatory Bowel Disease (IBD). However, achieving an optimal efficacious thiopurine dosing can be difficult, as up to 10% of patients have dose-dependent toxicities and up to 9% of patients are resistant to thiopurine therapy [16, 17]. Such clinical toxicity could be due to inherited genetic variation of certain enzyme, leading to an unusual metabolic pathway, which generates toxic metabolites. On the other hand, few studies have studied the longitudinal changes in the gut microbiome with drug treatment in IBD. Shaw et al. characterized 19 children with CD and 4 with ulcerative colitis (UC), showing that dysbiosis at baseline correlated with the degree of inflammatory burden of luminal disease.Therefore, identification of comprehensive targets for drug monitoring will improve our understanding of the basis for inter-patient variability in drug toxicity and efficacy, and enable more individualized therapy.

Metabolism has an essential role in biological systems; and metabolites represent the end products of this important process from a cell of a certain physiological status. Blood and urine are integrative fluids that incorporates the metabolic outputs at different of the body, and thus providing a metabolic footprint as an end product [4].

Metagenomics which is a study of microbes as communities is also an important approach to study microbiota in human.The interplay between microbiota and genetics gives unique transcription profiles in the gut, and gene expression analyses provide insights into the transcriptional activity and functional molecular pathways underlying disease progression. Therefore, deep sequencing analysis of the colon suggests hypotheses about the pathophysiological processes in IBD patients. Further transcriptomics study and in combination with other meta'omics studies will provide the basis for in-depth understanding of IBD pathogenesis.

Due to the bio-clinical complexity of diseases and microbiota, a long term, large-scale prospective biobank is necessary to carry out meaningful research. This biobank will provide a powerful platform for studying a range of complex factors associated with IBD that are of great relevance to public health. Such biobank may be extended to other diseases including GI diseases and autoimmune disorder, which may possibly provide insight to the role of microbiota in human health.

In conclusion, a comprehensive understanding of the intestinal ecosystem, epigenetic, metabolic and transcription profiles, as well as their mechanisms in the disease pathogenesis in patients with IBD and other diseases may help us identify potential biomarkers. However, our current knowledge about them is still very limited, particularly in Asian patients, who have not been extensively researched. Further investigation in this field is needed. To serve these purposes, we aim to setup a large scale biobank with comprehensive clinical data.

Tipo de estudio

De observación

Inscripción (Anticipado)

6000

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

      • Hong Kong, Hong Kong
        • Reclutamiento
        • Prince of Wales Hospital

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

18 años y mayores (ADULTO, MAYOR_ADULTO)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

Patients with a diagnosis of Crohn's disease or ulcerative colitis defined by endoscopy, radiology and histology

Control will comprise individuals undergoing colonoscopy for polyp or colorectal cancer screening, or investigations of gastrointestinal symptoms, and friends and spouses or partners of patients at Prince of Wales Hospital or Alice Ho Miu Ling Nethersole Hospital, or any individuals who are interested to participate in this study.

Relatives or household members of both patients with IBD or other diseases and controls will be recruited.

Descripción

Inclusion Criteria:

  • Patient ≥18 with a diagnosis of Crohn's disease or ulcerative colitis
  • Informed Consent obtained

Exclusion Criteria:

  • Known current infection with an enteric pathogen
  • Previously been diagnosed with IBD (Control)
  • Have a first of second degree relative with IBD (Control)

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
Inflammatory Bowel Disease Patient
Patient with confirmed diagnosis of Inflammatory Bowel Disease
Healthy control
Controls (non-IBD) will comprise individuals undergoing colonoscopy for polyp or colorectal cancer screening, or investigations of gastrointestinal symptoms, and friends and spouses or partners of patients at Prince of Wales Hospital or Alice Ho Miu Ling Nethersole Hospital, or any individuals who are interested to participate in this study.
Healthy relatives of Inflammatory Bowel Disease patient
Relatives or household members of both patients with IBD or other diseases and controls will be recruited.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Setup a large scale biobank
Periodo de tiempo: 20 años
Configure un biobanco a gran escala para recopilar datos, como datos clínicos completos, como información demográfica y clínica del paciente (p. edad, peso, género, antecedentes familiares de EII, antecedentes de apendicectomía, uso de drogas, etc.)
20 años

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Intestinal microbiota of IBD patient
Periodo de tiempo: 20 years
Study samples will be collected to characterize which microbiota affect severity of IBD by performing metagenomics of gut microbiome in stool and biospy samples
20 years
Genetics and epigenetic markers in IBD
Periodo de tiempo: 20 years
Study samples will be collected from patients with IBD and other diseases for genetic material isolation and gene expression checking by performing PCR.
20 years
Therapeutic drug monitoring
Periodo de tiempo: 20 years
To understand the metabolic pathway leading to the target metabolites and therapeutic drug monitoring during following up by filling in questionniare
20 years
Biomarker of IBD
Periodo de tiempo: 20 years
Study samples will be collected to characterize which microbiota affect severity of IBD by performing metagenomics of gut microbiome in stool and biospy samples
20 years
Pathobionts of IBD
Periodo de tiempo: 20 años
Se recolectarán muestras de estudio para identificar patobiontes específicos que inducen una respuesta inmunitaria innata mediante análisis de resultados de laboratorio (p. análisis de cultivo de tejido celular de toxina específica para células, etc.)
20 años
Microbiota-induced molecular mechanisms
Periodo de tiempo: 20 años
Se recolectarán muestras de estudio para caracterizar qué mecanismos moleculares inducidos por microbiota mediante la realización de metagenómica del microbioma intestinal en muestras de heces y bioespía.
20 años
Disease pathogenesis
Periodo de tiempo: 20 years
Study samples will be collected to characterize which microbiota induces disease by performing metagenomics of gut microbiome in stool and biospy samples
20 years

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 (ACTUAL)

1 de marzo de 2014

Finalización primaria (ANTICIPADO)

1 de febrero de 2034

Finalización del estudio (ANTICIPADO)

1 de julio de 2034

Fechas de registro del estudio

Enviado por primera vez

27 de junio de 2018

Primero enviado que cumplió con los criterios de control de calidad

24 de febrero de 2019

Publicado por primera vez (ACTUAL)

27 de febrero de 2019

Actualizaciones de registros de estudio

Última actualización publicada (ACTUAL)

8 de febrero de 2023

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

7 de febrero de 2023

Última verificación

1 de febrero de 2023

Más información

Términos relacionados con este estudio

Palabras clave

Otros números de identificación del estudio

  • IBD Biobank Study

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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