Antibodies Against β2-Glycoprotein I Complexed With an Oxidised Lipoprotein Relate to Intima Thickening of Carotid Arteries in Primary Antiphospholipid Syndrome. Issue 1 (2006)
- Record Type:
- Journal Article
- Title:
- Antibodies Against β2-Glycoprotein I Complexed With an Oxidised Lipoprotein Relate to Intima Thickening of Carotid Arteries in Primary Antiphospholipid Syndrome. Issue 1 (2006)
- Main Title:
- Antibodies Against β2-Glycoprotein I Complexed With an Oxidised Lipoprotein Relate to Intima Thickening of Carotid Arteries in Primary Antiphospholipid Syndrome
- Authors:
- Ames, P. R. J.
Alves, J. Delgado
Lopez, L. R.
Gentile, F.
Margarita, A.
Pizzella, L.
Batuca, J.
Scenna, G.
Brancaccio, V.
Matsuura, E. - Abstract:
- Abstract : To explore whether antibodies against β2 -glycoprotein I (β2 GPI) complexed to 7-ketocholesteryl-9-carboxynonanoate (oxLig-1) and to oxidised low-density lipoproteins (oxLDL) relate to paraoxonase activity (PONa) and/or intima media thickness (IMT) of carotid arteries in primary antiphospholipid syndrome (PAPS). As many as 29 thrombotic patients with PAPS, 10 subjects with idiopathic antiphospholipid antibodies (aPL) without thrombosis, 17 thrombotic patients with inherited thrombophilia and 23 healthy controls were investigated. The following were measured in all participants: β2 GPI−oxLDL complexes, IgG anti-β2 GPI−oxLig-1, IgG anti-β2 GPI−oxLDL antibodies (ELISA), PONa, (para-nitrophenol method), IMT of common carotid (CC) artery, carotid bifurcation (B), internal carotid (IC) by high resolution sonography. β2 GPI−oxLDL complex was highest in the control group ( p < 0.01), whereas, IgG anti-β2 GPI−oxLig1 and IgG anti-β2 GPI−oxLDL were highest in PAPS ( p < 0.0001). In healthy controls, β2 GPI−oxLDL complexes positively correlated to IMT of the IC ( p = 0.007) and negatively to PONa after correction for age ( p < 0.03). PONa inversely correlated with age ( p = 0.008). In PAPS, IgG anti-2GPI−oxLig-1 independently predicted PONa ( p = 0.02) and IMT of B ( p = 0.003), CC, ( p = 0.03) and of IC ( p = 0.04). In PAPS, PONa inversely correlated to the IMT of B, CC and IC ( p = 0.01, 0.02 and 0.003, respectively). IgG anti-2GPI−oxLig-1 may be involved in PAPS relatedAbstract : To explore whether antibodies against β2 -glycoprotein I (β2 GPI) complexed to 7-ketocholesteryl-9-carboxynonanoate (oxLig-1) and to oxidised low-density lipoproteins (oxLDL) relate to paraoxonase activity (PONa) and/or intima media thickness (IMT) of carotid arteries in primary antiphospholipid syndrome (PAPS). As many as 29 thrombotic patients with PAPS, 10 subjects with idiopathic antiphospholipid antibodies (aPL) without thrombosis, 17 thrombotic patients with inherited thrombophilia and 23 healthy controls were investigated. The following were measured in all participants: β2 GPI−oxLDL complexes, IgG anti-β2 GPI−oxLig-1, IgG anti-β2 GPI−oxLDL antibodies (ELISA), PONa, (para-nitrophenol method), IMT of common carotid (CC) artery, carotid bifurcation (B), internal carotid (IC) by high resolution sonography. β2 GPI−oxLDL complex was highest in the control group ( p < 0.01), whereas, IgG anti-β2 GPI−oxLig1 and IgG anti-β2 GPI−oxLDL were highest in PAPS ( p < 0.0001). In healthy controls, β2 GPI−oxLDL complexes positively correlated to IMT of the IC ( p = 0.007) and negatively to PONa after correction for age ( p < 0.03). PONa inversely correlated with age ( p = 0.008). In PAPS, IgG anti-2GPI−oxLig-1 independently predicted PONa ( p = 0.02) and IMT of B ( p = 0.003), CC, ( p = 0.03) and of IC ( p = 0.04). In PAPS, PONa inversely correlated to the IMT of B, CC and IC ( p = 0.01, 0.02 and 0.003, respectively). IgG anti-2GPI−oxLig-1 may be involved in PAPS related atherogenesis via decreased PON activity. … (more)
- Is Part Of:
- Clinical & developmental immunology. Volume 13:Issue 1(2006)
- Journal:
- Clinical & developmental immunology
- Issue:
- Volume 13:Issue 1(2006)
- Issue Display:
- Volume 13, Issue 1 (2006)
- Year:
- 2006
- Volume:
- 13
- Issue:
- 1
- Issue Sort Value:
- 2006-0013-0001-0000
- Page Start:
- 1
- Page End:
- 9
- Publication Date:
- 2006
- Subjects:
- Developmental immunology -- Periodicals
Clinical immunology -- Periodicals
Immune System -- immunology -- Periodicals
Immune System -- growth & development -- Periodicals
Immune System Diseases -- immunology -- Periodicals
571.9638 - Journal URLs:
- https://www.ncbi.nlm.nih.gov/pmc/journals/499/ ↗
- DOI:
- 10.1080/17402520600554930 ↗
- Languages:
- English
- ISSNs:
- 1740-2522
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.248400
British Library HMNTS - ELD Digital store - Ingest File:
- 10873.xml