Why the study?
Are serum ACE activities increased in diabetes mellitus and do they correlate with diabetic vascular disease or metabolic control?
Are serum ACE activities increased in diabetes mellitus and do they correlate with diabetic vascular disease or metabolic control?
Serum ACE activity is elevated in a subset of diabetic patients, particularly those with retinopathy, but does not broadly correlate with metabolic control or other diabetic vascular diseases.
ACE elevation associates with retinopathy independent of control; hypothesis-generating and requires longitudinal studies before any clinical role.
Serum angiotensin-converting enzyme activities were measured in 41 type 1 diabetics (16.4 +/- 4.0 U/ml), in 40 type 2 diabetics (15.0 +/- 5.2 U/ml) and in 52 controls (13.0 +/- 2.7 U/ml, mean +/- SD). Twenty six (32%) of 81 patients presented with serum angiotensin-converting enzyme activities above the normal range. No relation between serum angiotensin-converting enzyme activities and the presence or lack of diabetic vascular diseases in type 1 and type 2 diabetics could be detected. No significant differences in serum angiotensin-converting enzyme activities were found when comparing various types of diabetic vascular disease (retinopathy, neuropathy, renal failure, arterial vascular disease, diabetic vascular disease, coronary artery disease). However, mean serum angiotensin-converting enzyme activities were significantly increased in diabetics with retinopathy when compared with controls (p less than 0.0005). Correlation between metabolic long term control as determined by measuring glycohaemoglobin (HbA1) concentrations and serum angiotensin-converting enzyme activities could not be established. Serum angiotensin-converting enzyme activities did not show any correlations with duration of diabetes, age or sex of patients. A representative number of diabetics (32%) showed elevated serum angiotensin-converting enzyme activities, but a correlation with diabetic vascular disease, metabolic control or type of disease could not be established.
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Schernthaner et al. (1984) studied this question.
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