Circulation, Vol 80, 1617-1626, Copyright © 1989 by American Heart Association
H Ogawa, H Yasue, S Oshima, K Okumura, K Matsuyama and K Obata
Plasma levels of fibrinopeptide A (FPA), beta-thromboglobulin (BTG), and
platelet factor 4 (PF4) were examined on venous plasma samples taken every
4 hours for 24 hours in 20 patients with variant angina and 20 patients
with stable exertional angina together with 24-hour Holter recordings. The
mean plasma FPA levels (ng/ml) at 2:00 PM, 6:00 PM, 10:00 PM, 2:00 AM, 6:00
AM, and 10:00 AM were 4.6 +/- 1.0, 3.1 +/- 0.5, 6.1 +/- 1.6, 9.9 +/- 2.4,
8.7 +/- 1.4, and 4.2 +/- 0.8 in patients with variant angina (p less than
0.01) and 1.8 +/- 0.2, 2.3 +/- 0.3, 1.9 +/- 0.3, and 2.3 +/- 0.2 in those
with stable exertional angina. In seven patients with variant angina, we
also examined the effects of heparin (3,000 units), given subcutaneously at
6:00 PM, 10:00 PM, and 2:00 AM, on the plasma FPA levels and the anginal
attacks. Although heparin suppressed the elevation and circadian variation
of plasma FPA levels, it did not suppress the attacks and their circadian
variation in these patients. Plasma FPA levels increased significantly from
3.7 +/- 0.5 to 12.5 +/- 2.7 ng/ml during or immediately after an attack in
the seven patients with no heparin. On the other hand, the plasma levels of
BTG and PF4 were increased in patients with variant angina as compared with
those with stable exertional angina but did not show a significant
circadian variation in both groups. We conclude that 1) plasma levels of
FPA, BTG, and PF4 were increased in patients with variant angina as
compared with those with stable exertional angina; 2) there was a
significant circadian variation in the plasma levels of FPA in parallel
with that of the frequency of the attacks with the peak level occurring
from midnight to early morning in patients with variant angina; and 3)
elevated levels of plasma FPA are the result and not the cause of coronary
spasm.
ARTICLES
Circadian variation of plasma fibrinopeptide A level in patients with variant angina
Division of Cardiology, Kumamoto University Medical School, Japan.
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