Why the study?
Does the cold pressor test elicit different peripheral vascular resistance and thromboxane A2 synthesis responses in patients with various types of angina compared to controls?
Does the cold pressor test elicit different peripheral vascular resistance and thromboxane A2 synthesis responses in patients with various types of angina compared to controls?
Patients with active resting angina exhibit an exaggerated and prolonged peripheral vasoconstrictor response to sympathetic stimulation, which is strongly correlated with increased thromboxane A2 synthesis.
Answers are grounded in this paper and cite their sources.
Exaggerated vasoconstrictor response in active resting angina may link to TxA2; hypothesis-generating and requires prospective validation before clinical consideration.
Peripheral vascular resistance (PVR) and thromboxane A2(TxA2) synthesis after the cold pressor test were investigated in different subsets of patients with angina (10 with stable effort angina, 36 with resting angina [24 in an active phase and 12 in an inactive phase], and five with Prinzmetal's variant angina) and in 41 control subjects of equivalent age and risk factors. Left ventricular end-diastolic pressure, ejection fraction, extent of coronary angiographic lesions, and baseline PVR were not significantly different among the various patient groups. In all patient groups, except those with variant angina, the cold pressor test resulted in a higher increase in PVR than in the control subjects (p less than .001 for all groups). In patients with variant angina the vasoconstrictor response was increased only in proximity (about 1 hr) to ischemic attacks. In patients with active resting angina the vasoconstrictor response was on the average four times longer than that in patients with effort angina and with inactive resting angina (p less than .001). This exaggerated vasoconstrictor response was associated with elevated TxA2 resting levels in plasma and with increased TxA2 synthesis after the cold pressor test. A linear relationship was found between the area of the vascular response and the area of TxA2 production after the cold pressor test in patients with active resting angina (r = .87, p less than .001). The increased TxA2 synthesis and the inappropriate increase of peripheral vascular response to sympathetic stimulation revert back to normal in the inactive phase.(ABSTRACT TRUNCATED AT 250 WORDS)
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Serneri et al. (1986) studied this question.
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