A. Iaina et al., POSTPRANDIAL INTESTINAL-DERIVED CHYLOMICRON AND CHYLOMICRON REMNANTS IN ESSENTIAL HYPERTENSIVE PATIENTS BEFORE AND AFTER PROLONGED CAPTOPRIL THERAPY, American journal of hypertension, 8(1), 1995, pp. 34-39
The metabolism of the postprandial intestinal-derived lipoproteins, ch
ylomicron and chylomicron remnants, is not known in patients with esse
ntial hypertension. After a fat meal, using the vitamin A test as a ma
rker, retinyl palmitate was measured in the total plasma, chylomicron,
and chylomicron remnant fractions in 14 untreated nondiabetic essenti
al hypertensive patients with normal fasting lipids and lipoproteins.
The vitamin A fat loading test was repeated in eight hypertensive pati
ents after 3 months of captopril therapy. Fifteen matched normotensive
subjects were used as controls. The untreated essential hypertensive
patients had significantly higher chylomicron fraction concentration c
urves (AUC 17,469 +/- 2553 mu g/L/h) P < .001 compared with the contro
l group (AUC 13,208 +/- 1245 mu g/L/h), by two-way analysis of varianc
e with repeated measurements. After 3 months of captopril therapy, the
chylomicron fraction (AUC 9701 +/- 1566 mu g/L/h), and chylomicron re
mnants fraction (AUC 3487 +/- 580 mu g/L/h) were much lower (P < .001)
than before captopril therapy. Oral glucose tolerance tests were bord
erline in five of the eight hypertensives before captopril treatment b
ut returned to normal after 3 months of therapy. In summary, postprand
ial intestinal-derived lipoprotein metabolism is altered in essential
hypertensive patients. Captopril therapy caused significant improvemen
t in the postprandial chylomicron metabolism.