R. Labiche et al., Presence of Chlamydia pneumoniae in human symptomatic and asymptomatic carotid atherosclerotic plaque, STROKE, 32(4), 2001, pp. 855-860
Background-Chlamydia pneumoniae has been identified in atherosclerotic plaq
ues of patients with cerebrovascular and cardiovascular disease. However, t
he direct causative effect of C pneumoniae infection in the activation of a
therosclerotic plaque to a prothrombotic state remains to be established. T
he aim of the present study is to examine the correlation between intraplaq
ue presence of chlamydiae and symptomatic carotid disease in humans.
Methods-Plaques from 37 symptomatic and 57 asymptomatic consenting patients
undergoing carotid endarterectomy were snap-frozen, and the tissue was pre
pared for polymerase chain reaction analysis for Chlamydia pneumoniae per I
nstitutional Review Board-approved protocol. Blood was drawn from each pati
ent at the time of surgery for serological analysis.
Results-The overall rate of plaques positive for C pneumoniae was 14.82%, w
ith 5 of 37 (13.5%) plaques from symptomatic patients and 9 of 57 (15.8%) f
rom asymptomatic patients, which revealed a definitive presence of the orga
nism. No association existed between C pneumoniae presence and symptomatic
disease (P=1.0), Also, no association existed between presence of C pneumon
iae and severity of stenosis. Finally, seropositivity for antichlamydial Ig
G, IgA, and IgM anti-chlamydial antibodies did not correlate with identific
ation of C pneumoniae in the plaques. However, high-serum anti-chlamydial I
gA levels (greater than or equal to1:128) were associated with occurrence o
f symptomatic disease (P=0.03; odds ratio, 2.86; 95% CI, 1.12 to 7.28).
Conclusions-Presence of C pneumoniae as a single factor does not appear to
be sufficient to explain the occurrence of cerebrovascular symptoms. Low se
nsitivity of seropositivity for IgG, IgA, or IgM associated with PCR-identi
fied C pneumoniae presence in the plaque makes it unlikely to be Valuable a
s the single determining factor for actively infected plaque. Association o
f high-level anti-chlamydial IgA with symptomatic disease suggests that chr
onic or acute chlamydial infection anywhere in the body could play a role i
n atherosclerotic plaque activation and be used as a marker to target popul
ations in future stroke prevention trials.