The significance of autoantibodies against oxidatively modified low-density lipoprotein (LDL) in patients with psoriasis

Citation
A. Orem et al., The significance of autoantibodies against oxidatively modified low-density lipoprotein (LDL) in patients with psoriasis, CLIN CHIM A, 284(1), 1999, pp. 81-88
Citations number
25
Categorie Soggetti
Medical Research Diagnosis & Treatment
Journal title
CLINICA CHIMICA ACTA
ISSN journal
00098981 → ACNP
Volume
284
Issue
1
Year of publication
1999
Pages
81 - 88
Database
ISI
SICI code
0009-8981(19990615)284:1<81:TSOAAO>2.0.ZU;2-J
Abstract
Psoriasis is associated with changes in plasma lipid and lipoproteins, whic h may play a role in the development of occlusive vascular disease. The oxi dation of low-density Lipoprotein (LDL) is considered a key event in the de velopment and progression of atherosclerosis. Autoantibodies against oxidiz ed LDL (auAb-oxLDL) may contribute to understanding the relationship betwee n oxidative processes and development of atherosclerosis. Thirty-three pati ents with psoriasis and 30 matched control subjects were investigated. LDL oxidation was evaluated as the presence of autoantibodies against LDL oxida tively modified with Cu++, by an ELISA system in the patients and control s era. AuAb-ox LDL levels of the patients were found to be significantly incr eased compared with a control group. 42% of the patients and 3.3% of the co ntrol subjects had higher auAb-ox LDL levels than the cut-off point (352 mU /ml). The levels of auAb-ox LDL were found to be correlated with PASI score (r = 0.67, p < 0.01). Also, The antibody level was found to be correlated with polymorphonuclear elastase and alpha-1 antitrypsin levels (r = 0.58, p < 0.05; r = 0.51, p < 0.05, respectively). It was concluded that increased levels of auAb-oxLDL in the psoriatic patients may be a consequence of the interaction between imbalance of oxidant-antioxidant system and lipoprotei ns, and the measurement of auAb-oxLDL in the patients may mirror in vivo oc currence of oxidative processes. (C) 1999 Elsevier Science B.V. All rights reserved.