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Published on: November 7, 2017
[Angiotensin converting enzyme and left ventricular hypertrophy in uremic patients: correlation and therapeutic
Senija Rasić1, Amra Catović, Jasmin Huskić
1Institut za nefrologiju, Klinicki centar Univerziteta Sarajevo, Sarajevo, Bosna i Hercegovina.
Insights
Anemia treatment with erythropoietin in hemodialysis patients reduced left ventricular hypertrophy and angiotensin-converting enzyme activity. This suggests a link between renal anemia, cardiac remodeling, and ACE levels.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Context:
- Anemia is a common complication of chronic kidney disease and a contributor to left ventricular hypertrophy (LVH).
- The renin-angiotensin-aldosterone system, particularly angiotensin-converting enzyme (ACE), plays a role in cardiac remodeling.
- Erythropoietin therapy is standard for anemia in hemodialysis patients.
Purpose:
- To investigate the association between serum ACE activity and LVH in hemodialysis patients with anemia.
- To evaluate the effect of human recombinant erythropoietin (rHuEpo) treatment on serum ACE activity and LV geometry over six months.
Summary:
- Serum ACE activity was significantly higher in hemodialysis patients with LVH compared to those with normal LV mass.
- A positive correlation was observed between ACE activity and LV mass index.
- Six months of rHuEpo treatment led to significant reductions in both LV mass index and serum ACE activity.
Impact:
- Serum ACE activity levels are linked to left ventricular geometry in hemodialysis patients.
- rHuEpo therapy may offer a dual benefit by improving renal anemia, reducing LV mass, and modulating ACE activity.
Introduction:
Anemia has been shown to be a key component of renal failure, as well as of the occurrence of left ventricular hypertrophy (LVH), with special attention paid to the paracrine mechanism of left ventricular remodelling.
Aim:
The aim of the study was to analyze possible association of serum angiotensin-converting enzyme (ACE) activity and LVH in hemodialysis patients with anemia treated with human recombinant erythropoietin (rHuEpo) during six months.
Method:
LV geometry was determined by echocardiographic analysis in 20 hemodialysis patients before and after erythropoietin treatment. Serum ACE activity was measured by spectrophotometric method using hippyril-l-histidyl-l-leucin as a substrate.
Results:
Serum ACE activity increased to 47.3% in hemodialysis patients with LVH as compared to patients with normal LV mass. A significant positive correlation was found between the level of ACE activity and LV mass index (p=0.004). Six-month erythropoietin treatment of anemia led to a significant reduction of LV mass index (p<0.008) and serum ACE activity (p=0.003) from the initial values.
Conclusion:
The levels of serum ACE activity are associated with LV geometry. Our findings suggested the possibility of simultaneous and modest modulation of LV mass and serum ACE activity with rHuEpo correction of renal anemia.
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