Literature DB >> 23241595

Serum levels of IgG antibodies against oxidized LDL and atherogenic indices in HIV-1-infected patients treated with protease inhibitors.

Joel da Cunha1, Luciana Morganti Ferreira Maselli, Arício Treitinger, Andrea Moreira Monteiro, Magnus Gidlund, Raul Cavalcanti Maranhão, Celso Spada, Sérgio Paulo Bydlowski.   

Abstract

BACKGROUND: Antibodies against low-density lipoproteins (LDLs) that have been oxidized are associated with development of atherosclerotic lesions. In individuals infected with human immunodeficiency virus type 1 (HIV-1) with or without therapy, dyslipidemia and increased cardiovascular risk are observed.
METHODS: Serum levels of IgG antibodies against oxidized LDLs (IgG anti-oxLDL Abs) were determined by assay in 151 HIV-1-infected patients. Of these, 42 patients did not receive anti-retroviral therapy (ART-naïve), whereas 109 received highly active anti-retroviral therapy (HAART) consisting of lopinavir/ritonavir (LOP/r; n=50), efavirenz (EFV; n=30) and nevirapine (NVP; n=29) associated with nucleoside reverse transcriptase inhibitors. HIV-1 seronegative individuals (n=43) participated in the study. The following parameters were quantified: total cholesterol and its fractions, atherogenic indices (AIs), apolipoproteins A1 and B100, high sensitivity C-reactive protein, CD4+ and CD8+ T cells, and HIV-1-RNA.
RESULTS: Levels of IgG anti-oxLDL Abs were significantly higher (p<0.05) in the LOP/r group compared with the EFV and/or NVP and the seronegative group: median 0.32 (0.15, 0.58; 95% confidence interval) vs. 0.25 (0.13, 0.53) vs. 0.18 (0.04, 0.38), respectively. HIV-1-infected ART-naïve patients (n=42) presented antibodies levels similar to those observed for the LOP/r group, 0.33 (0.13, 0.63; p>0.05). The levels of IgG anti-oxLDL Abs correlated with an increase in AIs (r=0.216; p=0.036) and triglycerides (r=0.220; p=0.044) in the LOP/r group, and AIs in the ART-naïve group (r=0.300; p=0.046).
CONCLUSIONS: Patients treated with LOP/r showed higher levels of IgG anti-oxLDL Abs compared with patients treated with EFV or NVP regimens, and these levels were associated with an increase in AIs.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23241595     DOI: 10.1515/cclm-2012-0225

Source DB:  PubMed          Journal:  Clin Chem Lab Med        ISSN: 1434-6621            Impact factor:   3.694


  6 in total

Review 1.  Impact of antiretroviral therapy on lipid metabolism of human immunodeficiency virus-infected patients: Old and new drugs.

Authors:  Joel da Cunha; Luciana Morganti Ferreira Maselli; Ana Carolina Bassi Stern; Celso Spada; Sérgio Paulo Bydlowski
Journal:  World J Virol       Date:  2015-05-12

Review 2.  New insights into the emerging effects of inflammatory response on HDL particles structure and function.

Authors:  Xin Su; Guoming Zhang; Ye Cheng; Bin Wang
Journal:  Mol Biol Rep       Date:  2021-07-28       Impact factor: 2.316

3.  Human paraoxonase-1 activity is related to the number of CD4+ T-cells and is restored by antiretroviral therapy in HIV-1-infected individuals.

Authors:  Luciana Morganti Ferreira Maselli; Joel da Cunha; Eliana Battaggia Gutierrez; Raul Cavalcante Maranhão; Celso Spada; Sérgio Paulo Bydlowski
Journal:  Dis Markers       Date:  2014-02-27       Impact factor: 3.434

4.  Reduced IgM levels and elevated IgG levels against oxidized low-density lipoproteins in HIV-1 infection.

Authors:  Aylin Yilmaz; Karin Jennbacken; Linda Fogelstrand
Journal:  BMC Infect Dis       Date:  2014-03-17       Impact factor: 3.090

5.  In vivo assessment of antiretroviral therapy-associated side effects.

Authors:  Eduardo Milton Ramos-Sanchez; Hiro Goto; Dolores Helena Rodriguez Ferreira Rivero; Thais Mauad; Fernando Nogueira de Souza; Andrea Moreira Monteiro; Magnus Gidlund
Journal:  Mem Inst Oswaldo Cruz       Date:  2014-07       Impact factor: 2.743

Review 6.  Paraoxonases Activities and Polymorphisms in Elderly and Old-Age Diseases: An Overview.

Authors:  Débora Levy; Cadiele Oliana Reichert; Sérgio Paulo Bydlowski
Journal:  Antioxidants (Basel)       Date:  2019-05-02
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.