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Published on: November 10, 2021
[Progression factors in chronic kidney disease. Non-immunological mechanisms]
Gema Fernández Fresnedo1, Jaime Sánchez Plumed, Manuel Arias
1Servicio de Nefrología, Hospital Universitario Marqués de Valdecilla, Santander. nefffg@humv.es
Insights
Managing non-immunological factors like high blood pressure and proteinuria is crucial for kidney transplant recipients. Effective treatment of these conditions improves graft survival and patient outcomes.
Area of Science:
- Nephrology
- Transplantation Medicine
- Cardiovascular Medicine
Context:
- Non-immunological factors significantly impact kidney transplant outcomes.
- Arterial hypertension, proteinuria, and dyslipidemia are key contributors to chronic allograft nephropathy and graft loss.
- These factors also increase morbidity and mortality in transplant recipients.
Purpose:
- To outline management strategies for non-immunological factors affecting kidney transplant recipients.
- To provide evidence-based recommendations for controlling blood pressure, proteinuria, and dyslipidemia.
- To emphasize the importance of monitoring and comprehensive treatment plans.
Summary:
- Blood pressure targets are <130/80 mmHg for non-proteinuric and 125/75 mmHg for proteinuric patients.
- Angiotensin receptor antagonists or ACE-inhibitors are recommended for managing proteinuria, with careful monitoring of potassium and creatinine.
- Dyslipidemia management aims for LDL <100 mg/dL, with assessment including a full lipid profile.
Impact:
- Optimizing the control of these non-immunological factors can lead to improved kidney allograft function and long-term survival.
- Proactive management reduces the risk of graft loss and associated patient morbidity and mortality.
- This approach supports better overall health outcomes for kidney transplant recipients.
Abstract:
Non-immunological factors in the progression of kidney disease in transplant patients are the following: high blood pressure, proteinuria, dislypidemia, etc. 1. Arterial hypertension treatment: Blood pressure must be measured periodically in all transplant patients. Similarly to native kidneys, in renal transplant patients arterial hypertension is a risk factor in the progression of kidney disease. Arterial hypertension represent a clinical marker of chronic allograft nephropathy and contributes to graft loss and to the morbid- mortality of these patients (Evidence level C). Blood pressure control should be < 130/80 mm Hg for renal transplant patients without proteinuria and 125/75 mm Hg for proteinuric patients (> 1 g/24 hours). Hypertension and proteinuria are frequently associated in the same patients, a global treatment of both seems more rational (Evidence level C). General measures should be instigated first with pharmacological therapy. All antihypertensive drugs are useful in renal transplant patients and the majority of patients will need two or more drugs. In proteinuric patients an angiotensin receptor antagonist or an ACE-inhibitor should be initiated. It is advisable to monitor the serum potassium and creatinine after the start of this drugs or during the treatment periodically, especially in patients with chronic kidney disease stage IV-V. 2. Proteinuria treatment: Proteinuria has been strongly correlated with reduced function and graft survival. Lowering proteinuria to values as near to normal as possible (< 0.5 g/24 hours). To reduce proteinuria, an angiotensin receptor antagonist, an ACE-inhibitor or a combination of both are required, with serum potassium or creatinine monitoring, especially in patients with chronic kidney disease stage IV-V. 3. Dyslipidemia treatment: For kidney transplant recipients the assessment of dyslipidemias should include a complete fasting lipid profile with total cholesterol, LDL, HDL, and triglycerides. Evidence from the general population indicates that treatment of dyslipidemias reduces cardiovascular disease and evidence in kidney transplant patients suggests that judicious treatment can be safe and effective in improving dyslipidemia. Therapeutic goal must be LDL < 100 mg/dl. (Evidence level C). 4. Others: Cigarette smoking, glucose intolerance or diabetes control and obesity should be assessed.
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