Chlamydia pneumoniae seropositivity and the risk of nonarteritic ischemic optic neuropathy
Section snippets
Materials and methods
We studied 71 consecutive patients with NAION who met the inclusion criteria, and 71 controls matched for age and gender. All participants were seen at our department between January 1996 and June 2000 and gave written informed consent before enrollment. The study was approved by the Ethics Committee of the Karl-Franzens University, Graz, Austria.
Criteria for diagnosis of NAION included sudden visual loss, optic disc edema followed by optic atrophy, relative afferent pupillary defect, and
Results
We studied 71 patients (30 females and 41 males) with NAION and 71 age- and gender-matched control subjects. The mean age of patients was 68.1 ± 8.7 years (range, 48–83 years) and 68.3 ± 9.4 years (range, 47–84 years) for controls, respectively. The mean interval between occurrence of NAION and blood sampling for C. pneumoniae analysis was 15.8 months (range, 0–37 months). Within a mean follow-up time of 24.8 months (range, 9–46 months) bilateral NAION was diagnosed in 15 of 71 patients (21.1%).
Discussion
The main finding of our study is that seropositivity for IgG antibodies to C. pneumoniae was significantly more common in patients with NAION than in controls. Subjects with IgG titers ≥1:128 had an approximately twofold risk for NAION. The presence of IgG titers ≥1:256 increased the risk further to fourfold, thus suggesting an association between serologic evidence of C. pneumoniae infection and NAION.
Previous studies have shown that NAION affects both eyes in up to 40% of patients within 5 to
References (27)
- et al.
Clinical profile and long-term implications of anterior ischemic optic neuropathy
Am J Ophthalmol
(1983) - et al.
Systemic diseases associated with nonarteritic anterior ischemic optic neuropathy
Am J Ophthalmol
(1994) - et al.
Hyperhomocystinemia in patients with nonarteritic anterior ischemic optic neuropathy, central retinal artery occlusion, and central retinal vein occlusion
Ophthalmology
(2000) - et al.
Serological evidence of an association of a novel chlamydia, TWAR, with chronic coronary heart disease and acute myocardial infarction
Lancet
(1988) - et al.
Chlamydia pneumoniaerisk factors for seropositivity and association with coronary heart disease
J Infect
(1995) Chronic infection in the aetiology of atherosclerosis - focus on Chlamydia pneumoniae
Atherosclerosis
(1999)- et al.
Anterior ischemic optic neuropathy. VII. Incidence of bilaterality and various influencing factors
Ophthalmology
(1987) Chlamydia pneumoniae, strain TWAR
Chest
(1989)- et al.
Chlamydia pneumoniae multiplies in human endothelial cells in vitro
Microb Pathog
(1994) - et al.
Expression of adhesion molecules on endothelial cells stimulated by Chlamydia pneumoniae
Microb Pathog
(1996)
Randomised trial of roxithromycin in non-Q-wave coronary syndromesROXIS Pilot Study. ROXIS Study Group
Lancet
Fibrinogen, cholesterol and smoking as risk factors for non-arteritic anterior ischaemic optic neuropathy
Eye
Current knowledge on Chlamydia pneumoniae strain TWAR, an important cause of pneumonia and other acute respiratory diseases
Eur J Clin Microbiol Infect Dis
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