G. Biesenbach et J. Zazgornik, VASCULAR-DISEASE IN TYPE-II DIABETES - PROGRESSION BEFORE AND AFTER COMMENCING HEMODIALYSIS, Nephrology, 3(2), 1997, pp. 195-198
In 20 nephropathic type II-diabetic patients (nine women, 11 men, mean
age 56 +/- 7 years) we compared the progression of macroangiopathic d
amages and the incidence rates of angiopathic complications during the
pre-dialysis phase (mean observation period 70 +/- 26 months) and aft
er start of dialysis treatment (observation period 29 +/- 21 months).
The following parameters were measured at 2-month intervals: HbA1c, se
rum cholesterol and triglycerides, systolic and diastolic blood pressu
re and bodyweight. A fundoscopy, resting electrocardiogram, carotid Du
plex sonography and Doppler sonographic investigations of the lower ex
tremities were performed yearly. In special cases a thallium scintigra
phy and/ or coronary angiography were also performed. The prevalence o
f all cerebrovascular damages increased from 5% at the begin of the st
udy to 50% at the start of haemodialysis and to 70% at the end of the
study. During the same period the prevalence of stroke increased from
0 to 10% and to 50%, respectively. Coronary heart disease was present
in 40% of patients at the beginning of the study, in 80% of patients a
t the start of dialysis treatment, and in 95% patients at the end of o
bservation period. During this time the prevalence of myocardial infar
ction increased from 5 to 25% and at least to 60% at the end of the st
udy. Peripheral vascular disease was be observed in 20% of the patient
s at the time of entry into study, in 65% of patients at the start of
haemodialysis and 85% patients at the end of the study. During the sam
e time the prevalence of amputations of the lower legs increased from
10 to 15% and to 35%, respectively. The incidence of complications in
both observation periods (pre-dialysis and dialysis phase) was: 0.09 v
s 0.08 for cerebrovascular damages (0.02 vs 0.16 for strokes), 0.08 vs
0.06 for cardiovascular diseases (0.04 vs 0.14 for myocardial infarct
ions) and 0.09 vs 0.08 for peripheral vascular diseases (0.01 vs 0.08
for amputations). The increase in the incidence rate of stroke and myo
cardial infarction was significantly (P<0.05) higher during the haemod
ialysis period. In conclusion, the progression of macroangiopathic dis
eases in type II diabetic patients is approximately the same during th
e pre-dialysis and dialysis phase, but the incidence rates of the seve
re macroangiopathic complications stroke and myocardial infarction are
significantly higher during the period of haemodialysis. This increas
e can be explained by the typical dialysis-induced effects on the hear
t and the intravascular volume.