Abstract
Cardiovascular (CV) disease is a continuum, 1 where clinicians can detect 3 main stages characterized by the discovery of CV risk factors in the absence of organ damage or established disease (stage 1), by the detection of some form of target organ damage (stage 2), or by the presence of established disease (stage 3). Classical risk factors present in stage 1 are hypertension and diabetes, which are simultaneously the most frequent causes of end-stage renal disease (ESRD); high serum cholesterol levels; and smoking, which accounts for three quarters of total CV risk. Chronic kidney disease (CKD) constitutes an epidemic for contemporary societies and is accompanied by a significant increase in CV risk. CKD can be initiated as a primary renal disease, eg, chronic glomerulonephritis or polycystic kidney disease, or can develop as a form of target organ damage, through predisposing risk factors (Table). In both cases, the disease progresses through the action of the perpetuating factors seen in the Table. Predisposing and perpetuating factors for CKD are simultaneously the most important promoters of CV disease. Detection of CKD is made by the finding of albuminuria, either microalbuminuria or macroalbuminuria, and ⁄or by an estimated glomerular filtration rate (eGFR) <60 mL ⁄min ⁄1.73 m. Further progression of CV disease is facilitated when CKD appears as a consequence of new CV risk that appear simultaneously with a decrease in renal function, eg, anemia and calcium-phosphate and vitamin D alterations. The finding of target organ damage (stage 2) in a hypertensive patient indicates that CV disease is more advanced and that the time to the potential presentation of a fatal or nonfatal event is shorter than it was in stage 1. In the present issue of The Journal of Clinical Hypertension, Facila and colleagues have investigated the relationship between CKD and CV risk in patients with left ventricular hypertrophy (LVH), detected by electrocardiographic (ECG) criteria. A total of 3962 patients were included in the study and the authors found a higher prevalence of established CV disease in patients with a depressed glomerular filtration rate (68.3% vs 54.9%, P<.001). After adjusting for age, sex, body mass index, diabetes, smoking habits, and systolic and diastolic blood pressures, the stage of renal function was an independent predictor of the presence of CV disease. The authors conclude that the determination of eGFR or estimated creatinine clearance is simple and identifies a progressive and independent increase in CV risk. In other words, the simultaneous finding of LVH and CKD is not infrequent and is characterized by an increased probability of presenting with a CV event or death in the near future. The simultaneous presence of renal and cardiac damage in hypertensive patients has been recognized in recent publications. Early abnormalities of renal function are associated with reduced coronary flow reserve probably as a consequence of an increased left ventricular mass. In fact, the presence of LVH is particularly prevalent in patients with CKD and it has been demonstrated that renal damage of any From the Hypertension Unit, Hospital 12 de Octubre, Madrid, Spain Address for correspondence: Luis M. Ruilope, MD, Hypertension Unit, Hospital 12 de Octubre, Avda de Cordoba s ⁄n, Madrid, Spain E-mail: ruilope@ad-hocbox.com
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