Assessment of long-term risks for living related kidney donors by 24-h blood pressure monitoring and testing for microalbuminuria

Clin Transplant. 1997 Oct;11(5 Pt 1):415-9.


Our aim was to assess the long-term risks for kidney donors of developing arterial hypertension and hypertension-associated diseases or hyperfiltration injury of the remaining solitary kidney. We conducted a cross-sectional study in which 29 donors who were nephrectomized at our center between October 1973 and March 1990 were enrolled. At the time of evaluation median age was 54 (37-70) yr. Since kidney donation an average time interval of 11.1 +/- 3.8 yr had elapsed. Body weight, casual blood pressure, S-creatinine and proteinuria were recorded. In 28/29 donors 24-h blood pressure monitoring was performed; all 29 were tested for microalbuminuria (MAU). The patient history was checked for treatment with antihypertensives, coronary heart disease and diabetes mellitus. From all 29 kidney donors surveyed up to 19.8 yr none developed marked renal insufficiency: median S-creatinine was 1.0 mg/dl (range 0.7-1.6), only 3 donors had a S-creatinine > 1.3 mg/dl. Glomerular filtration rate (GFR) decreased in an age-dependent manner. While all donors had been normotensive without an antihypertensive treatment at time of nephrectomy, actually 29% proved to be hypertensive with average values > 130/80 mmHg in the 24-h assessment. 5/29 donors received antihypertensives, 3 of whom nevertheless were hypertensive. Day-night profile was lost in 2 patients. After donation one patient developed coronary heart disease. 7/29 donors (24%) displayed positive testing for MAU, furthermore one had proteinuria (approx. 300 mg/l). MAU was associated in one case with slightly elevated S-creatinine (1.3 mg/dl) and in 3 cases with arterial hypertension. In the long-term course living related kidney donors do not seem to be at risk for developing hypertensive disorders more often than the general population. The prevalence of MAU in the 29 cases studied was higher than so far described for healthy subjects. This may reflect subclinical hyperfiltration damage of the glomerulus. Progressive renal insufficiency with clinical relevant function loss of the remaining solitary organ, however, was not observed up to 19.8 yr after kidney donation.

MeSH terms

  • Adult
  • Age Factors
  • Aged
  • Albuminuria / etiology*
  • Albuminuria / urine
  • Antihypertensive Agents / therapeutic use
  • Blood Pressure*
  • Body Weight
  • Coronary Disease / etiology
  • Creatinine / blood
  • Cross-Sectional Studies
  • Diabetes Mellitus / etiology
  • Female
  • Follow-Up Studies
  • Glomerular Filtration Rate
  • Humans
  • Hypertension / drug therapy
  • Hypertension / etiology
  • Kidney Diseases / etiology
  • Kidney Transplantation*
  • Living Donors*
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Monitoring, Ambulatory
  • Nephrectomy
  • Proteinuria / urine
  • Renal Insufficiency / etiology
  • Retrospective Studies
  • Risk Assessment*


  • Antihypertensive Agents
  • Creatinine