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Low-grade albuminuria and cardiovascular risk : what is the evidence?
Roland E Schmieder1, Joachim Schrader, Walter Zidek
1Medizinische Klinik 4, Nephrologie und Hypertensiologie, Universitätsklinikum Erlangen, Krankenhausstrasse 12, 91054, Erlangen, Germany. roland.schmieder@rzmail.uni-erlangen.de
Abstract:
Microalbuminuria (MA), conventionally defined as a urinary albumin excretion (UAE) of 30-300 mg/day, is recognised as a marker of endothelial dysfunction. Furthermore, it represents an established risk factor for cardiovascular morbidity and mortality and for end-stage renal disease in individuals with an adverse cardiovascular risk profile. It is common in the general population, particularly in patients with diabetes mellitus or arterial hypertension. There is growing evidence from prospective observational trials that UAE levels well below the current MA threshold ("lowgrade MA") are also associated with an increased risk of incident cardiovascular disease and allcause mortality. Even in apparently healthy individuals (without diabetes or hypertension), such an association has been shown. As albuminuria screening assays that are reliable even in the lower ranges are commercially available, there may be an important clinical role for MA in disease screening, comparable to the role of blood pressure and lipid screening. MA is modifiable, and the inhibition of the renin-angiotensin system by ACE inhibitors and AT1 receptor antagonists has been shown to result in a lower incidence of cardiovascular events.
Insights
Microalbuminuria (MA), a marker of endothelial dysfunction, indicates increased cardiovascular and kidney disease risk. Even low-grade MA in healthy individuals signals higher mortality risk, suggesting its screening potential.
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Microalbuminuria (MA), defined as urinary albumin excretion (UAE) of 30-300 mg/day, is a known marker of endothelial dysfunction.
- MA is an established risk factor for cardiovascular morbidity, mortality, and end-stage renal disease, particularly in patients with diabetes mellitus or hypertension.
- Emerging evidence suggests that UAE levels below the current MA threshold ('low-grade MA') also correlate with increased risks.
Purpose of the Study:
- To highlight the clinical significance of microalbuminuria, including low-grade levels, as a predictor of cardiovascular disease and mortality.
- To explore the potential role of MA screening in the general population, analogous to blood pressure and lipid screening.
- To emphasize the modifiable nature of MA and the benefits of renin-angiotensin system inhibition.
Main Methods:
- Review of prospective observational trials examining the association between UAE levels and cardiovascular/all-cause mortality.
- Analysis of evidence supporting the role of MA in apparently healthy individuals.
- Consideration of the availability and reliability of albuminuria screening assays.
Main Results:
- UAE levels below the conventional MA threshold ('low-grade MA') are associated with increased risk of cardiovascular disease and all-cause mortality.
- This association is evident even in individuals without diabetes or hypertension.
- MA is a modifiable risk factor.
Conclusions:
- Microalbuminuria, even at low levels, serves as a critical indicator of endothelial dysfunction and increased disease risk.
- MA screening may hold significant clinical value for disease prediction in broader populations.
- Inhibition of the renin-angiotensin system effectively reduces cardiovascular events in individuals with MA.
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