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Characteristics of Young-onset Diabetes in Sub-Saharan Africa (YODA) Study (YODA)

16 de agosto de 2021 actualizado por: Sobngwi Eugene, Yaounde Central Hospital

Understanding the Characteristics of Young-onset Diabetes in Sub-Saharan Africa

Type 1 diabetes has been poorly characterised, with very sparse information available in the literature about the characteristics of the disease in Africa. Atypical young onset diabetes is often reported by clinicians in sub-Saharan Africa, including patients who have the phenotype of type 1 diabetes but do not appear to have an absolute insulin requirement. The onset of type 1 diabetes in many sub-Saharan African populations seem to occur at later ages (20s to 40s) than what is generally seen in Caucasian populations. The investigators seek to characterise young-onset insulin treated diabetes (clinically diagnosed type 1 diabetes) in sub-Saharan Africa;

Descripción general del estudio

Estado

Reclutamiento

Intervención / Tratamiento

Descripción detallada

The specific objectives will be to; (1) characterise a population with clinically diagnosed type 1 diabetes and to determine the proportion of islet autoantibody positivity rates and to compare with a similar cohort of patients in the UK, (2) to determine the proportion of participants with retained endogenous insulin secretion (C-peptide > 600pmol/l) and whether they have evidence of autoimmunity as assessed by islet autoantibody and the type 1 diabetes genetic risk score

Study setting: This study will be a multi-center cross-sectional study of clinically diagnosed type 1 diabetes patients who are currently on insulin treatment who are being followed-up in existing diabetes care centers in 4 sub-Saharan African countries; Cameroon, Uganda, Tanzania and South Africa. Recruitment will take place at regional diabetes care centers which usually serve as the main diabetes treatment hub for many smaller spoke clinics in the sub-region. In Cameroon, the Yaounde Central Hospital and the Bafoussam Regional Hospital will serve as main clinical sites. In Uganda the clinical sites involved are the Mulago National Referral and Teaching Hospital, St. Francis Hospital Nsambya, all in Kampala and the Masaka Regional Referral Hospital. The Muhimbili National Hospital in Dar Es Salaam will serve as the main clinical site in Tanzania. Cameroon, Uganda and Tanzania will carry out primary data collection over the study period while South Africa (University of Witwatersrand Medical School) will provide secondary data consisting of a minimal dataset and relevant collected samples for analysis. All these centers have existing diabetes care clinics with experienced staff who are used to collecting and providing data for research purposes.

Eligibility: All patients with a clinical diagnosis of type 1 diabetes or young-onset insulin treated diabetes, who were diagnosed before the age of 30 years will be eligible to be enrolled into the study. We estimated a minimum total sample size of 500 participants will have a high precision with 95% confidence intervals of 17-25% around a prevalence of 20% for a clinical or biological characteristics (e.g. retained C-peptide or presence of islet auto-antibodies) and 46-54% around a prevalence of 50%.

Sampling method: We will follow a systematic sampling method, enrolling consecutive eligible participants from the different primary collection clinical sites.

Enrollment: All consented patients will be interviewed using a structured pre-tested questionnaire (Data Collection Form) by a trained study staff to collect relevant information; demographic, socioeconomic, lifestyle, family history, history of diabetes and diabetes complications. The questionnaire used in this study is available in English and has been translated into the major local language(s); the appropriate questionnaire is used according to the participant's preference. After the interview, a short clinical examination will be performed to record anthropometric characteristics (weight, height, waist and hip circumferences) and blood pressure.

Using standardized operating procedures (SOPs), saliva, blood and urine samples will be collected from all study participants for biochemical analysis, and biobanking for future studies. Saliva will be used for DNA extraction and for the determination of type 1 genetic risk score (T1D GRS) using a 67 single nucleotide polymorphism score as described by Sharp et al. 2019. Venous whole blood will be used for full blood count and A1c determination. Plasma will be used for random C-peptide determination on the 801 module of the Cobas 8000 analyser and the measuring range will be truncated to <3pmol/L. Serum creatinine will be measured to assist in the interpretation of the C-peptide result. Islet autoantibodies, GAD, IA2 and ZnT8 will be measured in serum on the RSR Limited ELISA (RSR Limited, Cardiff, U.K.). Dipstick urinalysis will be done, with urinary C-peptide and creatinine measurement for the determination of the urinary C-peptide to creatinine ration (UCPCR). .

Data collected from the different clinical sites using the data collection form will be entered into a centralized data management tool (REDCap). All data will be anonymised before being stored in the data management system.

Ethical consideration: All participants will be required to provide a written informed consent before participating in the study. Refusal to participate will not affect the quality of care of the participants at the clinical sites. The study has received ethical clearance from the National Ethics Committee of Cameroon ( No 2018/12/1252/L/CNERSH/SP), and the Uganda Virus Research Institute (GC/127/19/12/736), Muhimbili National Hospital (MNH/IRB/I/2020/019) and Human Research Ethics Committe, South Africa (M200174).

Tipo de estudio

De observación

Inscripción (Anticipado)

1200

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.

Estudio Contacto

  • Nombre: Eugene Sobngwi, MD, PhD
  • Número de teléfono: +237 675088750
  • Correo electrónico: sobngwieugene@yahoo.fr

Copia de seguridad de contactos de estudio

  • Nombre: Jean-Claude Katte, MD, MSc
  • Número de teléfono: +237 677587929
  • Correo electrónico: jckatte@gmail.com

Ubicaciones de estudio

    • Centre
      • Yaounde, Centre, Camerún
        • Reclutamiento
        • National Obesity Centre, Yaounde Central Hospital
        • Contacto:
    • Gauteng
      • Johannesburg, Gauteng, Sudáfrica
        • Activo, no reclutando
        • School of Pathology, University of Witwatersrand
      • Dar Es Salaam, Tanzania
        • Reclutamiento
        • Muhimbili National Hospital
        • Contacto:
      • Entebbe, Uganda, P.O. Box 49

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

5 años y mayores (Niño, Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

The target population is patients with clinically diagnosed type 1 diabetes or diagnosed with young-onset diabetes who are on permanent insulin therapy and being followed-up at the selected different clinical sites across the three countries. The diagnosis of diabetes must have been made before the age of 30 years.

Descripción

Inclusion Criteria:

  • Clinical diagnosis of type 1 diabetes at age less than 30 years
  • Currently use insulin as a permanent treatment
  • Able to consent to study

Exclusion Criteria:

  • Refusal to provide written informed consent

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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Proportion of retained endogenous insulin secretion
Periodo de tiempo: Baseline
Random non-fasting C-peptide level
Baseline
Islet auto-antibody titre and positivity proportions
Periodo de tiempo: Baseline
GADA, IA-2A, ZnT8A
Baseline

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Type 1 diabetes genetic risk score
Periodo de tiempo: Baseline
Proportion with T1D GRS > 50th centile
Baseline

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Eugene Sobgnwi, MD, PhD, University of Yaounde 1/ Yaounde Central Hospital

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el 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 septiembre de 2019

Finalización primaria (Anticipado)

31 de diciembre de 2021

Finalización del estudio (Anticipado)

31 de marzo de 2022

Fechas de registro del estudio

Enviado por primera vez

16 de agosto de 2021

Primero enviado que cumplió con los criterios de control de calidad

16 de agosto de 2021

Publicado por primera vez (Actual)

19 de agosto de 2021

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

19 de agosto de 2021

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

16 de agosto de 2021

Última verificación

1 de agosto de 2021

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

SÍ

Descripción del plan IPD

A data sharing plan has been developed and validated by all the institutions. All data produced will be anonymized at the clinical site based on pre-existing data codes that have been generated. The data will be kept at a central data hub with all individual principal researchers having access to the data. The data produced during the course of study can be shared upon reasonable request to the Global Health Research Group study committee.

Marco de tiempo para compartir IPD

All data produced during the course of the study are entered and held at the central data management hub with access to all principal study investigators in real time as they are uploaded into the system. The data will be held on the server up to 5 years after the closure of recruitment in 2022.

Criterios de acceso compartido de IPD

Access to the main data hub which is being controlled by the Global Health Research Group at the University of Exeter will be granted to country principal investigators who can remotely access the database from their different locations with their personal secured credentials.

Tipo de información de apoyo para compartir IPD

  • PROTOCOLO DE ESTUDIO
  • SAVIA

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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