Jr. Kaplan et al., DOMINANT SOCIAL-STATUS AND CONTRACEPTIVE HORMONE-TREATMENT INHIBIT ATHEROGENESIS IN PREMENOPAUSAL MONKEYS, Arteriosclerosis, thrombosis, and vascular biology, 15(12), 1995, pp. 2094-2100
The stress of social subordination is associated with exacerbation of
coronary artery atherosclerosis in premenopausal cynomolgus monkeys, p
ossibly as a result of the ovarian dysfunction that reliably accompani
es subordinate social status. The primary objective of the current stu
dy was to determine whether treatment with an oral contraceptive (OC)
provides relative protection from development of atherosclerotic plaqu
es, especially among animals made vulnerable to atherosclerosis by soc
ial subordination, In the present study, 193 adult female monkeys (Mac
aca fascicularis) were placed in social groups of 5 or 6 animals each.
Half of the animals were then fed an atherogenic diet to which had be
en added a triphasic OC, while the remainder received only the atherog
enic diet. At the end of 26 months, atherosclerosis was measured in an
iliac artery biopsy taken from each monkey. The results demonstrated
that among untreated animals subordinate individuals developed signifi
cantly more atherosclerosis than did their dominant counterparts (P<.0
1); however, OC treatment inhibited atherosclerosis in subordinate ani
mals (P<.05) and eliminated the difference between dominant and subord
inate animals that was observed in the untreated condition. Subordinat
e social status and OC treatment were both associated with reduced pla
sma concentrations of HDL cholesterol (P<.01 for both), and subordinat
e monkeys also had elevations in LDL cholesterol plus VLDL cholesterol
(P<.01). Nonetheless, the interaction between social status and OC tr
eatment remained significant even after covariance adjustment for vari
ation in plasma lipids. Taken together, these results suggest that soc
ial subordination worsens, whereas OC treatment inhibits, atherosclero
sis, and that these effects are independent of concomitant variability
in plasma lipids.