Cardiovascular diseases are more common in patients with obstructive s
leep apnea (OSA) than in the general population. We hypothesized that,
severe hypoxemia during sleep in these patients may cause an imbalanc
e between reactive oxygen species and the antioxidant reserve that is
important for the detoxification of these molecules. We tested the hyp
othesis that low-density lipoproteins (LDL) in hypoxic OSA patients ma
y be more susceptible to oxidative stress than LDL of nonhypoxic OSA p
atients and normal controls. Fifteen OSA patients were included in thi
s study, six with severe hypoxia (hypoxic group) who spent more than 1
0 minutes during sleep with SaO(2) <85% (mean 96 minutes), and nine OS
A patients (nonhypoxic group) who spent less than 10 minutes during sl
eep with SaO(2) <85% (mean 1.1 minutes). Six healthy nonsmoking males
of the same age group were included as a control group. The susceptibi
lity of each individual's LDL to oxidative stress was examined after f
ree-radical challenge in vitro by assessing changes in levels of conju
gated dienes. The LDL in OSA patients with severe hypoxia was not more
susceptible to oxidative stress compared to the LDL of nonhypoxic OSA
patients and normal controls. After 6 hours of exposure to an oxidati
ve agent, the changes in the mean conjugated diene were not different
among the three groups (p = 0.75). The time required to reach 50% of m
aximal absorbance was also not different, p = 0.199. Glutathione perox
idase and catalase activities in red blood cells in the hypoxic and no
nhypoxic patient groups were not significantly different. One night of
CPAP therapy in each patient group did not significantly change the l
evel of the antioxidant enzymes. Our results did not show any differen
ce in the susceptibility to oxidative stress between hypoxic and nonhy
poxic OSA patients and normal controls.