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Sleep Apnea, Coronary Atherosclerosis and Heart Failure in Diabetes Patients With Nephropathy (SLEEP)

4 de febrero de 2022 actualizado por: University of Aarhus

Background:

Diabetes, and especially diabetic kidney disease is associated with the development of cardiovascular disease such as calcification in the coronary arteries and heart failure. Sleep apnea is frequent among patients with diabetes and diabetic kidney disease and sleep apnea itself is a solitary risk factor in the development of cardiovascular disease. Nonetheless, sleep apnea is underdiagnosed in diabetes patients because of a discrepancy between sleep apnea severity and actual oxygen deficiency symptoms which makes the diagnosis difficult. For that reason, many diabetics have undiagnosed sleep apnea together with cardiovascular disease. Early discovery of sleep apnea among high risk diabetic patients may therefore be considered crucial before cardiovascular complications develop. For this reason, sleep apnea screening of high-risk diabetics can possibly improve early diagnostics of cardiovascular disease.

Aim:

This study will seek to establish the association between obstructive sleep apnea (OSA) and coronary calcification and heart failure in patients with diabetic kidney disease. The basic hypothesis of the study is that patients with diabetic kidney disease and concurrent OSA have a higher prevalence and severity of coronary calcification and heart failure compared to patients without OSA.

Methods:

Diabetic adult patients with scheduled check-ups at Steno Diabetes Center Aarhus, or Department of Renal Medicine on Aarhus University Hospital will be included in the study.

Firstly, all included patients are screened for sleep apnea with the devices SomnoTouch® and ApneaLink®. Based on the sleep apnea determination; 40 patients with moderate-severe sleep apnea are compared with 40 patients without sleep apnea. In both groups, the patients are examined for calcification in the coronary vessels using a CT-scan while the function of the heart is examined by ultrasound (echocardiography). The stiffness of aorta is measured and performed using radial artery tonometry (SphygmoCor®).

Furthermore, range of blood- and urine samples will be performed

The perspectives are that patients with diabetes should be regularly evaluated for sleep apnea and that patients with moderate/severe sleep apnea should undergo further examination for cardiovascular disease even though the patients don't display any symptoms of either cardiovascular disease or sleep apnea.

Descripción general del estudio

Tipo de estudio

De observación

Inscripción (Actual)

74

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

      • Aarhus, Dinamarca, 8200
        • Aarhus University 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, Adulto Mayor)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

Diabetic adult patients (Type 2) with scheduled check-ups at Steno Diabetes Center Aarhus, or Department of Renal Medicine on Aarhus University Hospital can be included in the study if they satisfy all eligible criteria. Additionally, patients from the GP and within the including area of Aarhus University Hospital were invited to participate in the study.

The study cohort will consist of:

Generel characteristics of both groups:

- Diabetes Mellitus Type 2 with an eGFR between 10-60 ml/min/1,73 m^2

Sleep Apnea:

  1. 40 patients with an apnea/hyponea-index above ≥ 15 per hour.

    Non-Sleep Apnea:

  2. 40 patients with an apnea/hyponea-index below < 5 per hour.

Descripción

Inclusion Criteria:

  • ≥ 18 years.
  • Diabetes Mellitus Type 2 with an eGFR between 10-60 ml/min/1,73 m^2 (Equalling CKD-group 3, 4 and 5 non-dialysis).

Exclusion Criteria:

  • Known sleep apnea in continuous positive airway pressure(CPAP) treatment.
  • Known mild sleep apnea (AHI 5-14) after the sleep apnea measurement.
  • Participants with central apnea (> 50 % of central apnea episodes in the AHI ≥ 15 group.) or Cheyne Stokes after the sleep apnea measurement.
  • < 4 hours of recording (ApneaLink)
  • Known coronary arterial disease with previous revascularization (PCI or CABG)

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
Sleep Apnea (AHI ≥ 15 per hour)
Patients with moderate/severe sleep apnea (Apnea/hypopnea-index ≥ 15 per hour).
Non-Sleep Apnea (AHI < 5 per hour)
Patients without sleep apnea (Apnea/hypopnea-index < 5 per hour).

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The association between sleep apnea and coronary atherosclerosis (Agatston Score) measured with cardiac CT-scan in patients with diabetic nephropathy.
Periodo de tiempo: Cardiac CT-scan will be performed no later than 1 month after inclusion. All Agatston scores will be estimated straight after the cardiac CT-scan.

The degree of atherosclerosis in the coronary artery walls is evaluated by cardiac CT-scan and subsequent quantified by Agatston score. Patients with an estimated glomerular filtration rate (eGFR) ≤ 25 ml/min/1,73 m2 is scanned without contrast whereas patients with an eGFR 26-60 ml/min/1,73 m2 are screened with contrast.

All Agatston scoring will be performed by a cardiologist blinded to information on patient biochemical characteristics and AHI. The only biochemical parameter which the cardiologist is not blinded to is eGFR.

Cardiac CT-scan will be performed no later than 1 month after inclusion. All Agatston scores will be estimated straight after the cardiac CT-scan.
The association between sleep apnea and systolic function in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in the study will undergo transthoracic echocardiography. Systolic function is evaluated by two-dimensional automated evaluation of ejection fraction (2-D auto-EF).

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
The association between sleep apnea and diastolic heart failure in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in the study will undergo transthoracic echocardiography. Diastolic function is evaluated by E/e´.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
The association between sleep apnea and systolic function in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in the study will undergo transthoracic echocardiography. Systolic function is evaluated by Left Ventricular Global Longitudinal Strain (GLS).

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
The association between sleep apnea and coronary plaque volume in patients with diabetic nephropathy.
Periodo de tiempo: Cardiac CT-scan will be performed no later than 1 month after inclusion.

Coronary plaque volume is estimated by a cardiac CT-scan with contrast.

All coronary plaque volume analysing will be performed by a cardiologist blinded to information on patient biochemical characteristics and AHI. The only biochemical parameter which the cardiologist is not blinded to is eGFR.

Cardiac CT-scan will be performed no later than 1 month after inclusion.
Association of sleep apnea and aortic stiffness (defined as Pulse Wave Velocity (PWV)) in patients with diabetic nephropathy.
Periodo de tiempo: PWV is performed the same day as the patient is included.
To get a non-invasive estimate of the aortic stiffness, measurement of Pulse Wave Velocity (PWV) (carotid-femoral and carotid-radial) will be performed. PWV will be recorded with the Sphygmocor® device according to regular protocol. If possible, two acceptable measurements will be conducted for each included patient. Calculation of PWV will be performed automatically by the device using a previously published formula.
PWV is performed the same day as the patient is included.
Association between Matrix Gla Protein (MGP) and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy. MGP, a novel biochemical marker of arterial calcification, will be collected and analysed in all patients.
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between Calcification propensity score (T50test) and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy. Calcification propensity score (T50test) will be collected and analysed in all patients.
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between sRANKL (soluble receptor activator of nuclear factor kappa-B ligand) and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy. sRANKL (soluble receptor activator of nuclear factor kappa-B ligand) will be collected and analysed in all patients.
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between 25-OH-Vitamin D(D3+D2) and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy. 25-OH-Vitamin D(D3+D2) will be collected and analysed in all patients.
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between Fetuin-A(alfa-2-Heremans Schmid glycoprotein; AHSG) and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021.
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy. Fetuin-A(alfa-2-Heremans Schmid glycoprotein; AHSG) will be collected and analysed in all patients
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021.
Association between Sclerostin and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy., Sclerostin will be collected and analysed in all patients
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between osteoprotegerin and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy., osteoprotegerin will be collected and analysed in all patients.
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between BsAP (bone-specific alkaline phosphatase) and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy., BsAP (bone-specific alkaline phosphatase) will be collected and analysed in all patients
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between TRAP5B (tartrate-resistant acid phosphatase 5b) and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy, TRAP5B (tartrate-resistant acid phosphatase 5b) will be collected and analysed in all patients.
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between P1NP (procollagen type 1 N propeptide) and coronary calcification in patients with sleep apnea and diabetic nephropathy.
Periodo de tiempo: Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
To establish a deeper understanding of the pathogenesis of central arterial calcification in patients with sleep apnea and diabetic nephropathy., P1NP (procollagen type 1 N propeptide) will be collected and analysed in all patients
Analysis will be performed as batch-analysis at the end of inclusion of patients summer 2021
Association between LVEDd (Left ventricular end diastolic diameter) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between LVEDs (Left ventricular end systolic diameter) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between IVSd (Interventricular Septal Thickness at Diastole) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between IVSs (Interventricular Septal Thickness at Systole) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between PWTd (Posterior wall thickness at end-diastole) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between PWTs (Posterior wall thickness at end-systole) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between Aorta (sinus valsalva) diameter as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between Aorta (Ascendens) diameter as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between Aorta (Abdominalis) diameter as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between maximum Vena Cava Inferior diameter as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between minimum Vena Cava Inferior diameter as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between Early mitral inflow velocity (E) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between Late mitral inflow velocity (A) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between E/A-ratio as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between Deceleration time of early diastolic transmittal flow (dtE) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between Right ventricular diameter (RVD) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus.

The echocardiographic-clinician is blinded to AHI-status.

Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between left atrial volume (LAV) as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus. The echocardiographic-clinician is blinded to AHI-status.
Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
Association between 2D atrial global strain as determined during echocardiography and sleep apnea in patients with diabetic nephropathy.
Periodo de tiempo: Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan
All patients included in this study will undergo echocardiography. In particular systolic and diastolic function will be in focus. The echocardiographic-clinician is blinded to AHI-status.
Transthoracic echocardiography will be performed no later than 1 month after inclusion and prior to cardiac CT-scan

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Silla de estudio: Niels H. Buus, MD PhD DMSc, Department of Renal diseases, Aarhus University Hospital
  • Investigador principal: Sebastian Nielsen, MD student, Department of Renal diseases, Aarhus University Hospital
  • Silla de estudio: Jakob T. Nyvad, MD, The Clinic of Hypertension, Aarhus University Hospital

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 octubre de 2020

Finalización primaria (Actual)

24 de enero de 2022

Finalización del estudio (Actual)

24 de enero de 2022

Fechas de registro del estudio

Enviado por primera vez

8 de septiembre de 2020

Primero enviado que cumplió con los criterios de control de calidad

14 de septiembre de 2020

Publicado por primera vez (Actual)

16 de septiembre de 2020

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

7 de febrero de 2022

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

4 de febrero de 2022

Última verificación

1 de octubre de 2021

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

IPD. pas

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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