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Albuminuria predicts cardiovascular events independently of left ventricular mass in hypertension: a LIFE substudy
M H Olsen1, K Wachtell, J N Bella
1Department of Clinical Physiology and Nuclear Medicine, Glostrup University Hospital, Glostrup, Denmark. mho@dadlnet.dk
Insights
Urine albumin/creatinine ratio (UACR) predicts cardiovascular events and death independently of left ventricular (LV) mass in hypertensive patients. UACR and LV mass together additively predict cardiovascular death, highlighting their importance in risk assessment.
Area of Science:
- Cardiology
- Nephrology
- Hypertension Research
Background:
- Hypertension and diabetes are linked to increased cardiovascular risk.
- Left ventricular (LV) mass and urine albumin/creatinine ratio (UACR) are associated with diabetes and elevated blood pressure.
- Independent predictors of cardiovascular events in hypertensive patients require further investigation.
Purpose of the Study:
- To investigate if urine albumin/creatinine ratio (UACR) and left ventricular (LV) mass independently predict cardiovascular events in hypertensive patients.
- To determine the additive predictive value of UACR and LV mass for cardiovascular death.
Main Methods:
- 960 hypertensive patients with electrocardiographic LV hypertrophy from the LIFE Echo substudy were assessed.
- Urine albumin and creatinine were measured to calculate UACR.
- Patients were followed for composite end points (cardiovascular death, nonfatal stroke, nonfatal myocardial infarction) over 60 months.
Main Results:
- Cardiovascular event incidence increased with higher LV mass in both low and high UACR groups.
- Log UACR independently predicted composite cardiovascular events and cardiovascular death, even after adjusting for Framingham risk score and other factors.
- LV mass did not independently predict composite cardiovascular events but showed an additive effect with UACR for cardiovascular death.
Conclusions:
- Urine albumin/creatinine ratio (UACR) is an independent predictor of cardiovascular events and death in hypertensive patients, irrespective of left ventricular (LV) mass.
- UACR and LV mass contribute additively to the prediction of cardiovascular death, suggesting combined use for risk stratification.
Abstract:
We wanted to investigate whether urine albumin/creatinine ratio (UACR) and left ventricular (LV) mass, both being associated with diabetes and increased blood pressure, predicted cardiovascular events in patients with hypertension independently. After 2 weeks of placebo treatment, clinical, laboratory and echocardiographic variables were assessed in 960 hypertensive patients from the LIFE Echo substudy with electrocardiographic LV hypertrophy. Morning urine albumin and creatinine were measured to calculate UACR. The patients were followed for 60+/-4 months and the composite end point (CEP) of cardiovascular (CV) death, nonfatal stroke or nonfatal myocardial infarction was recorded. The incidence of CEP increased with increasing LV mass (below the lower quartile of 194 g to above the upper quartile of 263 g) in patients with UACR below (6.7, 5.0, 9.1%) and above the median value of 1.406 mg/mmol (9.7, 17.0, 19.0%(***)). Also the incidence of CV death increased with LV mass in patients with UACR below (0, 1.4, 1.3%) and above 1.406 mg/mmol (2.2, 6.4, 8.0%(**)). The incidence of CEP was predicted by logUACR (hazard ratio (HR)=1.44(**) for every 10-fold increase in UACR) after adjustment for Framingham risk score (HR=1.05(***)), history of peripheral vascular disease (HR=2.3(*)) and cerebrovascular disease (HR=2.1(*)). LV mass did not enter the model. LogUACR predicted CV death (HR=2.4(**)) independently of LV mass (HR=1.01(*) per gram) after adjustment for Framingham risk score (HR=1.05(*)), history of diabetes mellitus (HR=2.4(*)) and cerebrovascular disease (HR=3.2(*)). (*)P<0.05, (**)P<0.01, (***)P<0.001. In conclusion, UACR predicted CEP and CV death independently of LV mass. CV death was predicted by UACR and LV mass in an additive manner after adjustment for Framingham risk score and history of CV disease.
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