A. Innes et al., CLINICAL-FEATURES OF BENIGN HYPERTENSIVE NEPHROSCLEROSIS AT TIME OF RENAL BIOPSY, Quarterly Journal of Medicine, 86(4), 1993, pp. 271-275
Although hypertension accounts for approximately 15-20% of end-stage r
enal disease and renal impairment occurs in 15% of patients with essen
tial hypertension, there are few data available on the clinical featur
es of patients with benign hypertensive nephrosclerosis, the histologi
cal consequence of hypertension on the kidney. To determine its preval
ence on renal biopsy and its clinical features (including proteinuria
and renal function), we used the U.K. MRC Glomerulonephritis Registry
of 7339 biopsies from 20 centres to define all patients with benign hy
pertensive nephrosclerosis. In patients with no co-existing disease, 1
85 biopsies were classified solely as benign hypertensive nephrosclero
sis (2.5%). Sixty-nine percent of patients were male and 72% aged over
50 years. Sixty-four percent had diastolic blood pressure above 90 mm
Hg and severe hypertension (diastolic > 120 mmHg) was present in 9%. P
rotein excretion of > 1.5 g/day was noted in 40%, with 22% excreting >
3 g/day. Eighteen percent had serum albumin values under 30 g/l. Eigh
ty-one percent had serum creatinine > 120 mumol/l; in 51% this was > 2
50 mumol/l. There was significant correlation between serum creatinine
and systolic blood pressure at time of biopsy (p=0.01) and between se
rum creatinine and serum albumin (p=0.001). Benign hypertensive nephro
sclerosis accounts for 2.5% of all registered biopsies. Significant pr
oteinuria is a common finding and proteinuria within the nephrotic ran
ge does occur. Systolic blood pressure appears to influence serum crea
tinine levels. Hypertensive nephropathy should be considered in all pa
tients with heavy proteinuria and renal impairment.