Mechanisms of Erythropoietin Action in the Cardiorenal Syndrome

• ClinicalTrials.gov Identifier: NCT00356733
• Recruitment Status: Completed
• First Posted: July 26, 2006
• Last Update Posted: December 2, 2011
• Sponsor: UMC Utrecht
• Collaborator: Dutch Heart Foundation
• Information provided by (Responsible Party): G.B. Braam, University of Alberta

Study Description

Brief Summary:

Erythropoietin (EPO) treatment in patients with the severe cardiorenal syndrome increases cardiac performance and decreases progression of renal failure by dampening the main driving forces of the cardiorenal syndrome in part via non-erythropoietic pathways.

I. Does EPO administration to patients with the severe cardiorenal syndrome increase cardiac performance and decrease progression of renal disease?

II. Does EPO treatment affect the main driving forces of the cardiorenal connection, that is, dampen the activated renin-angiotensin system (RAS), attenuate increased reactive oxygen species (ROS), normalize increased sympathetic activity, and decrease inflammation?

III. Does EPO treatment positively affect the cell function of patients with the cardiorenal syndrome:

1. are gene expression signatures of leukocytes positively influenced by EPO treatment,
2. does EPO shift the Jak/STAT pathway to a less pro-inflammatory profile in monocytes, and
3. are function and number of endothelial progenitor cells (EPCs) affected by treatment with EPO in the cardiorenal syndrome?

IV. Can the direct actions of EPO be differentiated from the effects on hemoglobin levels?

Condition or disease	Intervention/treatment	Phase
Heart Failure, Congestive; Renal Insufficiency, Chronic	Drug: Erythropoietin administration	Phase 3

Detailed Description:

The combination of renal and cardiac failure is associated with an extraordinary cardiovascular morbidity and mortality. We propose that the severe cardiorenal syndrome (SCRS), the pathophysiological condition in which there is combined cardiac and renal dysfunction, amplifies the progression of the failure of the individual organ. Central in the pathogenesis of the cardiorenal syndrome is enhanced oxidative stress, inflammation and enhanced activation of the renin-angiotensin and sympathetic nervous system. Chronic renal failure is further accompanied by anemia due to a gradual decline in erythropoietin (EPO) formation by the diseased kidneys and/or by EPO resistance. Recently, the interest in EPO is increasing since it serves not only as a hematopoietic factor, but also has been shown to increase the number of endothelial progenitor cells (EPCs) in end-stage renal disease (ESRD) patients. Moreover, EPO is involved in signaling via Akt to support NO release and may act as an anti-apoptotic. Some evidence supports the idea that EPO improves cardiac and renal function in the syndrome; however, no information is available about the mechanisms. The hypothesis of the present proposal is that EPO treatment in patients with the severe cardiorenal syndrome increases cardiac performance and decreases progression of renal failure in part via non-erythropoietic pathways. The questions are whether EPO administration to patients with the severe cardiorenal syndrome:

1. increases cardiac performance and decreases progression of renal disease,
2. dampens the activated RAS and sympathetic nervous system, attenuates increased ROS and decreases signs of inflammation and
3. positively influences cell function of leukocytes (assessed by gene expression signatures), of monocytes (shifts to a less pro-inflammatory Jak/Stat signaling) and of EPC (number and function).

This will be addressed in a two-part clinical study in patients with combined moderate chronic renal failure and heart failure (New York Heart Association [NYHA] II-III). First, patients will be treated with EPO for 12 months, and hemoglobin levels will be kept constant at initial levels or will be allowed to increase; another group will be left untreated. Besides cardiac and renal function, the RAS, the SNS, and ROS/NOS balance and inflammatory parameters will be assessed. Furthermore, cell function of leukocytes (gene expression signatures), monocytes (Jak/STAT activation) and EPCs (number and function) will be studied. Taken together, central in the proposal is that combined heart-kidney failure is accompanied by relative or absolute EPO dysfunction, disproportional to the degree of renal failure and that treatment with EPO improves cardiac performance and renal function.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 62 participants
• Allocation: Randomized
• Intervention Model: Factorial Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: Mechanisms of Erythropoietin Action in the Cardiorenal Syndrome
• Study Start Date: January 2007
• Actual Primary Completion Date: July 2011
• Actual Study Completion Date: July 2011

Arms and Interventions

Arm	Intervention/treatment
Experimental: EPO rise; EPO administration	Drug: Erythropoietin administration; 50 IU/kg/week EPO to a target haemoglobin level of 13.7 g/dL for men and 13.4 g/dL for women (group A) or to a target comparable to starting hemoglobin level (group B)
Experimental: EPO stable; EPO and stable Hemoglobin	Drug: Erythropoietin administration; 50 IU/kg/week EPO to a target haemoglobin level of 13.7 g/dL for men and 13.4 g/dL for women (group A) or to a target comparable to starting hemoglobin level (group B)
No Intervention: control; standard treatment

Outcome Measures

Primary Outcome Measures :

1. changes in gene-arrays, EPC and biomarkers panels [ Time Frame: 14 days, 6 and 12 months ]

Secondary Outcome Measures :

1. cardiac performance and renal function [ Time Frame: 6 and 12 months ]
2. QoL [ Time Frame: 6 and 12 months ]

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 80 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Patients with moderate renal failure (glomerular filtration rate [GFR] by Cockroft formula of 20-70 ml/min)
• Patients with heart failure NYHA class II-III-IV
• Hemoglobin (Hb) between 6.4 - 7.8 mmol/L in men and between 6.0 - 7.4 mmol/L in women
• Age > 18 years, < 80 years
• Written informed consent must be obtained from the subject or legally accepted representative before study-specific procedures, including screening procedures, are performed.

Exclusion Criteria:

• Therapy within 1 year before randomisation or any planned erythropoietic therapy between randomisation and study day 1
• Known intolerance to EPO administration
• Previously suspected of or confirmed to have neutralizing antibodies to recombinant human erythropoietin (rHuEPO)
• Uncontrolled hypertension (RR > 160 systolic, >100 diastolic)
• Forms of secondary hypertension other than renal hypertension
• Uncontrolled diabetes (HbA1c > 8.0 %)
• Primary dyslipidemia
• Kidney transplantation
• Proteinuria > 3.5 g/L
• Acute renal failure or rapidly progressive glomerulonephritis
• Hyperparathyroidism (parathyroid hormone [PTH] > 40)
• Bleeding or haemolysis as a cause of anaemia
• Deficiency of iron, folate, and/or vitamin B12
• Presence of chronic inflammatory disease or clinically significant infection
• Haematologic malignancy or solid tumour < 5 years ago
• Chronic liver disease
• Haemoglobinopathies
• Alcohol and/or drug abuse
• Enrolment in another study
• Child bearing potential (pre-menopausal woman who is not using adequate contraceptive precautions)
• Any kind of disorder that compromises the ability of the subject to give written informed consent and/or to comply with study procedures

Contacts and Locations

Locations

Netherlands

Meander Medical Center Amersfoort

Amersfoort, Utrecht, Netherlands, 3800 BM

Univ. Medical Center Utrecht

Utrecht, Netherlands, 3508 GA

Sponsors and Collaborators

UMC Utrecht

Dutch Heart Foundation

Investigators

• Principal Investigator: Branko Braam, MD, PhD; UMC Utrecht, The Netherlands
• Principal Investigator: Carlo AJ Gaillard, MD, PhD; Meander Medical Center Amersfoort, The Netherlands
• Study Director: Pieter AF Doevendans, MD, PhD; UMC Utrecht, The Netherlands

More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Eisenga MF, Emans ME, van der Putten K, Cramer MJ, Diepenbroek A, Velthuis BK, Doevendans PA, Verhaar MC, Joles JA, Bakker SJL, Nolte IM, Braam B, Gaillard CAJM. Epoetin Beta and C-Terminal Fibroblast Growth Factor 23 in Patients With Chronic Heart Failure and Chronic Kidney Disease. J Am Heart Assoc. 2019 Aug 20;8(16):e011130. doi: 10.1161/JAHA.118.011130. Epub 2019 Aug 17.

Emans ME, van der Putten K, Velthuis BK, de Vries JJ, Cramer MJ, America YG, Hillege HL, Meiss L, Doevendans PA, Braam B, Gaillard CA. Atherosclerotic renal artery stenosis is prevalent in cardiorenal patients but not associated with left ventricular function and myocardial fibrosis as assessed by cardiac magnetic resonance imaging. BMC Cardiovasc Disord. 2012 Sep 18;12:76. doi: 10.1186/1471-2261-12-76.

van der Putten K, Jie KE, Emans ME, Verhaar MC, Joles JA, Cramer MJ, Velthuis BK, Meiss L, Kraaijenhagen RJ, Doevendans PA, Braam B, Gaillard CA. Erythropoietin treatment in patients with combined heart and renal failure: objectives and design of the EPOCARES study. J Nephrol. 2010 Jul-Aug;23(4):363-8.

• Responsible Party: G.B. Braam, Associate Professor of Medicine, University of Alberta
• ClinicalTrials.gov Identifier: NCT00356733
• Other Study ID Numbers: NHS-2005B192
• First Posted: July 26, 2006
• Last Update Posted: December 2, 2011
• Last Verified: November 2011

Keywords provided by G.B. Braam, University of Alberta:

cardiorenal syndrome; erythropoietin; Heart Failure, Congestive; Renal Insufficiency, Chronic

Additional relevant MeSH terms:

Renal Insufficiency; Renal Insufficiency, Chronic; Cardio-Renal Syndrome; Heart Failure; Pathologic Processes; Heart Diseases; Cardiovascular Diseases; Kidney Diseases; Urologic Diseases; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Male Urogenital Diseases; Chronic Disease; Disease Attributes; Epoetin Alfa; Hematinics