RESUMO
Resumo Fundamento Embora os ácidos graxos poli-insaturados ômega-3 e ômega-6 (AGPIs n-3 e n-6) tenham efeitos bem conhecidos sobre os fatores de risco de doenças cardiovasculares (DCV), ainda existe um conhecimento limitado sobre como eles afetam os indicadores de qualidade da LDL. Objetivo Avaliar as associações dos AGPIs n-3 e n-6 de hemácias com o tamanho da partícula da LDL, LDL-c pequena e densa (sdLDL-c) e com LDL eletronegativa [LDL(-)] em adultos com fatores de risco para DCV. Métodos Estudo transversal com 335 homens e mulheres de 30 a 74 anos com, pelo menos, um fator de risco cardiovascular. Foram realizadas análises de parâmetros bioquímicos, como glicose, insulina, HbA1c, proteína C reativa (PCR), perfil lipídico, subfrações de lipoproteínas, partícula eletronegativa de LDL [LDL(-)] e seu autoanticorpo, e os AGPIs n-3 e n- 6 de hemácias. Os testes t independente/teste de Mann-Whitney, ANOVA unidirecional/teste de Kruskal-Wallis e regressões lineares múltiplas foram aplicados. Todos os testes foram bilaterais e um valor de p inferior a 0,05 foi considerado estatisticamente significativo. Resultados A relação n-6/n-3 de hemácias foi associada ao aumento dos níveis de LDL(-) (β = 4,064; IC de 95% = 1,381 - 6,748) e sdLDL-c (β = 1,905; IC de 95% = 0,863 - 2,947), e redução do tamanho das partículas de LDL (β = -1,032; IC de 95% = -1,585 − -0,478). Individualmente, os AGPIs n-6 e n-3 apresentaram associações opostas com esses parâmetros, realçando os efeitos protetores do n-3 e evidenciando os possíveis efeitos adversos do n-6 na qualidade das partículas de LDL. Conclusão O AGPI n-6, presente nas hemácias, foi associado ao aumento do risco cardiometabólico e à aterogenicidade das partículas de LDL, enquanto o AGPI n-3 foi associado a melhores parâmetros cardiometabólicos e à qualidade das partículas de LDL.
Abstract Background While Omega-3 and omega-6 polyunsaturated fatty acids (n-3 and n-6 PUFAs) have established effects on cardiovascular disease (CVD) risk factors, little is known about their impacts on LDL quality markers. Objective To assess the associations of n-3 and n-6 PUFA within red blood cells (RBC) with LDL particle size, small dense LDL-c (sdLDL-c), and electronegative LDL [LDL(-)] in adults with CVD risk factors. Methods Cross-sectional study involving 335 men and women aged 30 to 74 with at least one cardiovascular risk factor. Analyses were conducted on biochemical parameters, such as glucose, insulin, HbA1c, C-reactive protein (CRP), lipid profile, lipoprotein subfractions, electronegative LDL particle [LDL(-)] and its autoantibody, and RBC n-3 and n-6 PUFAs. Independent t-test/Mann-Whitney test, one-way ANOVA/Kruskal-Wallis test, and multiple linear regressions were applied. All tests were two-sided, and a p-value of less than 0.05 was considered statistically significant. Results The RBC n-6/n-3 ratio was associated with increased LDL(-) (β = 4.064; 95% CI = 1.381 - 6.748) and sdLDL-c (β = 1.905; 95% CI = 0.863 - 2.947) levels, and reduced LDL particle size (β = -1.032; 95% CI = -1.585 − -0.478). Separately, n-6 and n-3 PUFAs had opposing associations with those parameters, reinforcing the protective effects of n-3 and showing the potential negative effects of n-6 on LDL particle quality. Conclusion RBC n-6 PUFA was associated with increased cardiometabolic risk and atherogenicity of LDL particles, while n-3 PUFA was associated with better cardiometabolic parameters and LDL particle quality.
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A peri-implantite é uma condição patológica associada ao biofilme peri-implantar que ocorre nos tecidos ao redor do implante dentário, caracterizado por inflamação e perda óssea progressiva. A peri-implantite desenvolve um infiltrado inflamatório intenso, oxidando partículas de lipoproteínas de baixa densidade (ox-LDL), conhecida por ter comportamento aterogênico. O objetivo da pesquisa foi fazer uma revisão sistemática sobre o papel do receptor 1 de LDL oxidado do tipo lectina (LOX-1) na patogênese da peri-implantite. Uma busca eletrônica sem restrição de idioma ou data de publicação foi realizada nas bases de dados MEDLINE|Pubmed, Cochrane CENTRAL e Embase, registros de protocolos e outras fontes até abril de 2023. A questão clínica e a estratégia de busca foram formuladas usando o método PECOD. Os critérios de elegibilidade incluíram estudos observacionais que avaliam o papel da LOX-1 na patogênese da peri-implantite. A qualidade dos estudos primários foi avaliada por "JBI Critical Appraisal Tools for Analytical Cross-Sectional Studies". A síntese dos resultados qualitativos seguiu a diretriz de relatórios SWiM e o GRADE foi usado para avaliar a qualidade das respostas nesta revisão sistemática (RS). Esta RS foi estruturada de acordo com a declaração PRISMA 2020. Foram selecionados 6 artigos, envolvendo 152 indivíduos, conforme os critérios de elegibilidade apresentando como resultados, o aumento e a participação do receptor 1 de LDL oxidado tipo lectina (LOX-1) em pacientes com periimplantite, além de mediar a expressão de metaloproteinase de matriz 2, contribuindo para a destruição tecidual progressiva na peri-implantite. Esta RS fornece evidências preliminares sobre a associação entre LOX-1 e peri-implantite. Reconhecendo as limitações deste estudo, observamos que a LOX-1 está envolvida na patogênese, além de ser um alvo potencial para o manejo da peri-implantite. (AU)
Peri-implantitis is a pathological condition associated with the peri-implant biofilm that occurs in the tissues around the dental implant, characterized by inflammation and progressive bone loss. Peri-implantitis develops an intense inflammatory infiltrate, oxidizing low-density lipoprotein particles (oX-LDL), known to have an atherogenic behavior. The objective of this research was to carry out a systematic review on the role of the lectin-type oxidized LDL receptor 1 (LOX-1) in the pathogenesis of peri-implantitis. An electronic search with no restriction on language or publication date was performed on MEDLINE|Pubmed, Cochrane CENTRAL, and Embase databases, protocol registries, and other sources through April 2023. The clinical question and search strategy were formulated using the method PECOD. Eligibility criteria included observational studies evaluating the role of LOX-1 in the pathogenesis of periimplantitis. The quality of the primary studies was assessed using the "JBI Critical Appraisal Tools for Analytical Cross-Sectional Studies". The synthesis of qualitative results followed the SWiM reporting guideline and GRADE was used to assess the quality of responses in this systematic review (SR). This SR was structured in accordance with the PRISMA 2020 statement. Six articles, involving 152 individuals, were selected according to the eligibility criteria, presenting as results, the increase and participation of oxidized lectin-type LDL receptor 1 (LOX-1) in patients with peri-implantitis, in addition to mediating the expression of matrix metalloproteinase 2, contributing to the progressive tissue destruction in periimplantitis. This SR provides preliminary early evidence on the association between LOX-1 and peri-implantitis. Recognizing the limitations of this study, we observed that LOX-1 is involved in the pathogenesis, in addition to being a potential target for the management of periimplantitis. (AU)
Assuntos
Lectinas Tipo C , Peri-Implantite/tratamento farmacológico , Peri-Implantite/etiologia , Revisões Sistemáticas como AssuntoRESUMO
Nuts consumption has been associated with a protective effect against cardiovascular diseases and oxidative stress-related disorders. We aimed to perform a systematic review with clinical trials to assess the impact of chronic nuts consumption on oxidative stress and the possible mechanisms involved. Studies were identified by searching in three electronic databases: PubMed/MEDLINE, Scopus, and LILACS, and selected following PRISMA guidelines. Two authors perform searching and data extraction. A total of 16 articles were included (12 randomized clinical trials and 4 one or two-arm clinical trials). Nut doses were generally high (> 30 g/d), except for Brazil nuts (5-13 g/d). The follow-up time ranges between four weeks and six months, and the oxidized low-density lipoprotein (ox-LDL) was the most assessed biomarker. Eight articles reported improvement in oxidative stress biomarkers after nuts supplementation. Pathways regulated by selenium (e.g. glutathione peroxidase activity and nuclear factor-E2-related factor 2 (Nrf2) regulation), monounsaturated fatty acids (e.g. reduction of LDL oxidation), and bioactive compounds (e.g. antioxidant activity) were described as mechanisms involved in these beneficial effects. No studies reported harmful effects of nut consumption, even in high doses. The chronic consumption of nuts seemed to be effective to change some oxidative stress biomarkers, however, this topic remains controversial because the benefits depends on nut type, nut dose, and population characteristics.
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Doenças Cardiovasculares , Selênio , Antioxidantes , Humanos , Nozes , Estresse OxidativoRESUMO
BACKGROUND AND AIMS: The transition of macrophage to foam cells is a major hallmark of early stage atherosclerotic lesions. This process is characterized by the accumulation of large cytoplasmic lipid droplets containing large quantities of cholesterol esters (CE), triacylglycerol (TAG) and phospholipid (PL). Although cholesterol and CE metabolism during foam cell formation has been broadly studied, little is known about the role of the glycerolipids (TAG and PL) in this context. Here we studied the contribution of glycerolipid synthesis to lipid accumulation, focusing specifically on the first and rate-limiting enzyme of the pathway: glycerol-3-phosphate acyltransferase (GPAT). METHODS: We used RAW 264.7 cells and bone marrow derived macrophages (BMDM) treated with oxidized LDL (oxLDL). RESULTS: We showed that TAG synthesis is induced during the macrophage to foam cell transition. The expression and activity of GPAT3 and GPAT4 also increased during this process, and these two isoforms were required for the accumulation of cell TAG and PL. Compared to cells from wildtype mice after macrophage to foam cell transition, Gpat4-/- BMDM released more pro-inflammatory cytokines and chemokines, suggesting that the activity of GPAT4 could be associated with a decrease in the inflammatory response, probably by sequestering signaling precursors into lipid droplets. CONCLUSIONS: Our results provide evidence that TAG synthesis directed by GPAT3 and GPAT4 is required for lipid droplet formation and the modulation of the inflammatory response during the macrophage-foam cell transition.
Assuntos
Células Espumosas , Gotículas Lipídicas , 1-Acilglicerol-3-Fosfato O-Aciltransferase/genética , Animais , Glicerol , Glicerol-3-Fosfato O-Aciltransferase/genética , Lipoproteínas LDL , Macrófagos , Camundongos , Fosfatos , TriglicerídeosRESUMO
Inflammatory signals associated with cardiac diseases trigger trans-differentiation of cardiac fibroblasts to cardiac myofibroblasts. Cardiac myofibroblasts are the main cell type involved in the development of cardiac fibrosis, a diffuse and disproportionate accumulation of collagen in the myocardium. Although the role of the scavenger like-lectin receptor LOX-1 was previously investigated in cardiac fibroblasts and fibrosis, the involvement of the LOX-1 ligand -oxidized low-density lipoprotein (oxLDL)- on cardiac myofibroblast function still remains unexplored. In the present work, we investigated the effect of oxLDL/LOX-1 on fibrotic markers and cardiac myofibroblast function. Our in vitro results showed that oxLDL increased cardiac myofibroblast proliferation, triggered an increase in the synthesis of collagen type I and fibronectin containing extra domain A, and stimulated collagen type I secretion. oxLDL also decreased cardiac myofibroblast migration, collagen gel contraction and cell area, without modifying α-smooth muscle actin protein levels. These effects were dependent on LOX-1, because LOX-1 knockdown abolished oxLDL effects. Collectively these data showed that oxLDL has important modulatory effects on cardiac myofibroblast function.
Assuntos
Lipoproteínas LDL/metabolismo , Miocárdio/patologia , Miofibroblastos/patologia , Animais , Movimento Celular , Proliferação de Células , Colágeno Tipo I/metabolismo , Matriz Extracelular/metabolismo , Fibrose , Ratos Sprague-Dawley , Receptores Depuradores Classe E/metabolismoRESUMO
Plasma membrane repair (PMR) is an important process for cell homeostasis, especially for cells under constant physical stress. Repair involves a sequence of Ca2+-dependent events, including lysosomal exocytosis and subsequent compensatory endocytosis. Cholesterol sequestration from plasma membrane causes actin cytoskeleton reorganization and polymerization, increasing cell stiffness, which leads to exocytosis and reduction of a peripheral pool of lysosomes involved in PMR. These changes in mechanical properties are similar to those observed in cells exposed to oxidized Low Density Lipoprotein (oxLDL), a key molecule during atherosclerosis development. Using a human umbilical vein endothelial cell line (EAhY926) we evaluated the influence of mechanical modulation induced by oxLDL in PMR and its effect in endothelial fragility. Similar to MßCD (a drug capable of sequestering cholesterol) treatment, oxLDL exposure led to actin reorganization and de novo polymerization, as well as an increase in cell rigidity and lysosomal exocytosis. Additionally, for both MßCD and oxLDL treated cells, there was an initial increase in endocytic events, likely triggered by the peak of exocytosis induced by both treatments. However, no further endocytic events were observed, suggesting that constitutive endocytosis is blocked upon treatment and that the reorganized cytoskeleton function as a mechanical barrier to membrane traffic. Finally, the increase in cell rigidity renders cells more prone to mechanical injury. Together, these data show that mechanical modulation induced by oxLDL exposure not only alters membrane traffic in cells, but also makes them more susceptible to mechanical injury, which may likely contribute to the initial steps of atherosclerosis development.
Assuntos
Membrana Celular/metabolismo , Lipoproteínas LDL/metabolismo , Actinas/metabolismo , Membrana Celular/fisiologia , Movimento Celular , Células Cultivadas , Colesterol/metabolismo , Citoesqueleto/metabolismo , Endocitose/fisiologia , Células Endoteliais/metabolismo , Endotélio Vascular/metabolismo , Exocitose/fisiologia , Células Endoteliais da Veia Umbilical Humana , Humanos , Lipoproteínas LDL/fisiologia , Lisossomos/metabolismo , Membranas/metabolismo , Transporte ProteicoRESUMO
The electronegative low-density lipoprotein, LDL (-), is an endogenously modified LDL subfraction with cytotoxic and proinflammatory actions on endothelial cells, monocytes, and macrophages contributing to the progression of atherosclerosis. In this study, epitopes of LDL (-) were mapped using a phage display library of peptides and monoclonal antibodies reactive to this modified lipoprotein. Two different peptide libraries (X6 and CX8C for 6- and 8-amino acid-long peptides, respectively) were used in the mapping. Among all tested peptides, two circular peptides, P1A3 and P2C7, were selected based on their high affinities for the monoclonal antibodies. Small-angle X-ray scattering analysis confirmed their structures as circular rings. P1A3 or P2C7 were quickly internalized by bone marrow-derived murine macrophages as shown by confocal microscopy. P2C7 increased the expression of TNFα, IL-1 ß and iNOS as well as the secretion of TNFα, CCL2, and nitric oxide by murine macrophages, similar to the responses induced by LDL (-), although less intense. In contrast, P1A3 did not show pro-inflammatory effects. We identified a mimetic epitope associated with LDL (-), the P2C7 circular peptide, that activates macrophages. Our data suggest that this conformational epitope represents an important danger-associated molecular pattern of LDL (-) that triggers proinflammatory responses.
Assuntos
Epitopos/metabolismo , Inflamação/metabolismo , Lipoproteínas LDL/metabolismo , Epitopos/sangue , Epitopos/isolamento & purificação , Humanos , Lipoproteínas LDL/sangue , Lipoproteínas LDL/isolamento & purificação , Macrófagos/metabolismo , Óxido Nítrico/análiseRESUMO
The accumulation of oxidized ApoB-100-containing lipoproteins in the vascular intima and its subsequent recognition by macrophages results in foam cell formation and inflammation, key events during atherosclerosis development. Agents targeting this process are considered potentially atheroprotective. Since natural biflavonoids exert antioxidant and anti-inflammatory effects, we evaluated the atheroprotective effect of biflavonoids obtained from the tropical fruit tree Garcinia madruno. To this end, the pure biflavonoid aglycones morelloflavone (Mo) and volkensiflavone (Vo), as well as the morelloflavone's glycoside fukugiside (Fu) were tested in vitro in primary macrophages, whereas a biflavonoid fraction with defined composition (85% Mo, 10% Vo, and 5% Amentoflavone) was tested in vitro and in vivo. All biflavonoid preparations were potent reactive oxygen species (ROS) scavengers in the oxygen radical absorbance capacity assay, and most importantly, protected low-density lipoprotein particle from both lipid and protein oxidation. In biflavonoid-treated macrophages, the surface expression of the oxidized LDL (oxLDL) receptor CD36 was significantly lower than in vehicle-treated macrophages. Uptake of fluorescently labeled oxLDL and cholesterol accumulation were also attenuated in biflavonoid-treated macrophages and followed a pattern that paralleled that of CD36 surface expression. Fu and Vo inhibited oxLDL-induced ROS production and interleukin (IL)-6 secretion, respectively, whereas all aglycones, but not the glucoside Fu, inhibited the secretion of one or more of the cytokines IL-1ß, IL-12p70, and monocyte chemotactic protein-1 (MCP-1) in lipopolysaccharide (LPS)-stimulated macrophages. Interestingly, in macrophages primed with low-dose LPS and stimulated with cholesterol crystals, IL-1ß secretion was significantly and comparably inhibited by all biflavonoid preparations. Intraperitoneal administration of the defined biflavonoid fraction into ApoE-/- mice was atheroprotective, as evidenced by the reduction of the atheromatous lesion size and the density of T cells and macrophages infiltrating the aortic root; moreover, this treatment also lowered the circulating levels of cholesterol and the lipid peroxidation product malondialdehyde. These results reveal the potent atheroprotective effects exerted by biflavonoids on key events of the oxLDL-macrophage interphase: (i) atheroligand formation, (ii) atheroreceptor expression, (iii) foam cell transformation, and (iv) prooxidant/proinflammatory macrophage response. Furthermore, our results also evidence the antioxidant, anti-inflammatory, hypolipemiant, and atheroprotective effects of Garcinia madruno's biflavonoids in vivo.
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LOX-1 es un receptor endotelial de la familia de las lectinas. Su actividad biológica tiene un fuerte impacto en los fenómenos inflamatorios, oxidativos y aterogénicos endoteliales. Cuando se conoció el receptor de la lipoproteína de baja densidad (RLDL) y su regulación, se afirmó el papel aterogénico del colesterol transportado en esta lipoproteína (C-LDL). Este papel de las lipoproteínas fue la base de la denominación de dislipoproteinemias en reemplazo de dislipemias. En condiciones post-prandiales, las lipoproteínas ricas en triglicéridos, como quilomicrones y lipoproteínas de muy baja densidad (VLDL), son degradadas por la lipoproteína lipasa (LPL) de la pared vascular, produciéndose remanentes de quilomicrones (RQ) y lipoproteínas de densidad intermedia (IDL), respectivamente, que en conjunto se denominan lipoproteínas remanentes (RLPs). Dependiendo del estrés oxidativo las RLPs son oxidables y pueden unirse al LOX-1. También se liberan ácidos grasos que injurian células endoteliales y contribuyen a abrir brechas en el endotelio, que en condiciones fisiológicas es una barrera de células con uniones estrechas. El dominio intracelular de LOX-1 regula el reconocimiento de lipoproteínas de baja densidad oxidadas (LDLOX) y de RLPs. Además, posee un efecto dependiente de los radicales reactivos de oxígeno (ROS). Su dominio transmembrana actúa en el pasaje de LDLOX y monocitos al subendotelio. La inhibición de LOX-1 con anticuerpos específicos impide su unión con LDLOX, restableciendo la barrera entre el lumen vascular y el subendotelio. En cambio, las LDLOX unidas al dominio transmembrana, producen apoptosis de las células endoteliales y suprimen uniones estrechas intercelulares en el endotelio, facilitando la actividad de las moléculas de adhesión leucocitarias que promueven el pasaje al subendotelio de los elementos del lumen, tales como monocitos, plaquetas, LDLOX, RLPs oxidables y lipoproteínas (a) (Lp(a)) semejantes al plasminógeno. Las LDLOX subendoteliales aumentan la movilidad de células musculares lisas. Los monocitos subendoteliales se establecen como residentes, e incorporan LDLOX, convirtiéndose sucesivamente en macrófagos, células espumosas y lesiones aterogénicas. Sin embargo, desde Assmann G y su estudio PROCAM no puede ignorarse el papel de los triglicéridos y colesterol de lipoproteínas de alta densidad (C-HDL) como componentes del cuadro de riesgo en ECV.
LOX-1 is an endothelial receptor belonging to the family of lectins. Its biological activity has a strong impact on inflammatory, oxidative and atherogenic phenomena in endothelium. When Low Density Lipoprotein receptor (RLDL) and its regulation were known, the atherogenic role of the cholesterol transported in LDL (LDL-C) was confirmed. This lipoprotein role in atherosclerosis was the base to use the term dyslipoproteinemia instead of dyslipidemia. In post-prandial conditions, triglyceride-rich lipoproteins like chylomicrons and very low-density lipoproteins (VLDL), are degraded by lipoprotein lipase (LPL) on the vascular wall, with the resultant formation of chylomicron remnants (CR) and intermediate density lipoproteins (IDL) respectively, which as a whole are called remnant lipoproteins (RLPs). Depending on oxidative stress, RLPs are oxidized and then they can bind the LOX-1. In this process, fatty acids are also released, injuring endothelial cells and contributing to open gaps in endothelium, which under physiological conditions, is a barrier of cells with tight junctions. The intracellular domain of LOX-1 regulates the recognition of oxidized LDL (oxLDL) and RLPs, and its effect depends on reactive oxygen species (ROS). LOX-1 transmembrane domain acts in the passage of oxLDL and monocytes to the sub-endothelium. Inhibition of LOX-1 by specific antibodies prevents its binding with OxLDL, restoring the barrier between the vascular lumen and sub-endothelium. By contrast, the oxLDL, attached to the transmembrane domain, produce apoptosis of endothelial cells and the suppression of narrow intercellular junctions in the endothelium. Thus, enabling the activity of leucocyte adhesion molecules that promote the transfer to subendothelial elements lumen of monocytes, platelets, oxLDL, oxidized RLPs and lipoprotein (a) (Lp (a)), similar to plasminogen such as. Sub-endothelial OxLDL increase the mobility of smooth muscle cells. Sub-endothelial monocytes establish as resident, up-take oxLDL and successively become into macrophages, foam cells and atherosclerotic lesions. However, since Assman’s PROCAM study, the role of triglycerides and High Density Lipoprotein-cholesterol (HDL-C), as components of cardiovascular risk, cannot be ignored.
LOX-1 é um receptor endotelial da família das lectinas. Sua atividade biológica tem um importante impacto nos fenômenos inflamatórios, oxidativos e aterogênicos endoteliais. Quando foi conhecido o receptor da lipoproteína de baixa densidade (RLDL) e sua regulação, afirmou-se o papel aterogênico do colesterol transportado nesta lipoproteína (C-LDL). Este papel das lipoproteínas foi a base da denominação de dislipoproteinemias em substituição de dislipidemias. Em condições pós-prandiais, as lipoproteínas ricas em triglicérides como quilomícrons e Lipoproteínas de muito baixa densidade (VLDL) são degradadas pela lipoproteína lipase (LPL) da parede vascular, produzindo remanescentes de quilomícrons (RQ) e lipoproteínas de densidade intermediária (IDL) respectivamente, que em conjunto são chamadas lipoproteínas remanescentes (RLPs). Dependendo do estresse oxidativo, as RLPs são oxidáveis e podem se ligar ao LOX-1. Também são liberados ácidos graxos que injuriam células endoteliais e contribuem na abertura de fendas no endotélio, que em condições fisiológicas é uma barreira de células com uniões estreitas. O domínio intracelular de LOX-1 regula o reconhecimento de lipoproteínas de baixa densidade oxidativa (LDLOX) e de RLPs. Também possui um efeito dependente dos radicais reativos de oxigênio (ROS). Seu domínio transmembrana atua na passagem de LDLOX e monócitos para o subendotélio. A inibição de LOX-1 com anticorpos específicos impede sua união com LDLOX restabelecendo a barreira entre o lúmem vascular e o subendotélio. Entretanto, as LDLOX ligadas ao domínio transmembrana produzem apoptose das células endoteliais e suprimem estreitas junções intercelulares no endotélio, facilitando a atividade das moléculas de adesão leucocitária que promovem a passagem para o subendotélio de elementos do lúmem, tais como monócitos, plaquetas, LDLOX, RLPs oxidáveis e lipoproteínas (a) [Lp(a)] semelhantes ao plasminogênio. As LDLOX subendoteliais aumentam a mobilidade das células musculares lisas. Os monócitos subendoteliais se estabelecem como residentes, e incorporam LDLOX, virando sucessivamente em macrófagos, células espumosas e lesões aterogênicas. No entanto, desde Assman G e seu estudo PROCAM, não pode se ignorar o papel dos triglicérides e do colesterol de lipoproteínas de alta densidade (C-HDL) como componentes do evento de risco em ECV.
Assuntos
Endotélio , Inflamação , Lectinas , Estresse Oxidativo , Lipoproteínas LDL , Receptores de LDL OxidadoRESUMO
OBJECTIVE: Obstructive sleep apnea (OSA) has been linked to increased oxidative stress, lipid peroxidation and worsening atherosclerosis. This study investigated oxidized low-density lipoprotein (oxLDL) as a marker of lipid peroxidation, and total LDL cholesterol (direct LDL-C), as a marker of the lipid profile among individuals with OSA, and its association with hypertension (HYP) and dyslipidemia (DYS). The impact of one year of continuous positive airway pressure (CPAP) was also assessed. METHODS: Blood was collected after 12 h of fasting from 99 consecutive patients who were diagnosed with OSA via polysomnography, and were also diagnosed with both HYP and DYS via clinical and laboratory studies. The patients were classified into the following three groups: GI [OSA with comorbidities (HYP or DYS)], GII [OSA without comorbidities], and GIII [control]. Thirty-five patients with an apnea/hypopnea index >20 per hour of sleep were randomized to groups that received either Sham-CPAP or CPAP treatments over 12 months. RESULTS: In a binary regression controlled for sex, age, body mass index, and glycemia, model 1 which analyzed direct LDL-C, demonstrated significant levels of risk in the setting of DYS but not in the settings of HYP and OSA. In model 2, which analyzed oxLDL, DYS (p = 0.01), HYP (p = 0.032), and OSA (p = 0.039) were statistically significant. Significant alterations were observed in only the sleep parameters following one year of CPAP. CONCLUSIONS: Based on the statistical regression model, only the presence of DYS (p = 0.001) was associated with the levels of direct LDL-C. The remaining comorbidities (OSA and HYP) were not significantly related to the levels of direct LDL-C. Regarding oxLDL, OSA, HYP and DYS each added significant score values to the levels of oxLDL. These findings are suggestive of the importance of assessing oxLDL among patients presenting with OSA, both with and without comorbidities.
Assuntos
Pressão Positiva Contínua nas Vias Aéreas , Dislipidemias/sangue , Hipertensão/sangue , Lipoproteínas LDL/sangue , Apneia Obstrutiva do Sono/sangue , Apneia Obstrutiva do Sono/terapia , Adulto , Anti-Hipertensivos/uso terapêutico , Biomarcadores/sangue , Pressão Sanguínea/efeitos dos fármacos , Brasil/epidemiologia , Comorbidade , Dislipidemias/diagnóstico , Dislipidemias/epidemiologia , Feminino , Humanos , Hipertensão/diagnóstico , Hipertensão/tratamento farmacológico , Hipertensão/epidemiologia , Hipertensão/fisiopatologia , Peroxidação de Lipídeos , Masculino , Pessoa de Meia-Idade , Estresse Oxidativo , Fatores de Risco , Apneia Obstrutiva do Sono/diagnóstico , Apneia Obstrutiva do Sono/epidemiologia , Fatores de Tempo , Resultado do Tratamento , Regulação para CimaRESUMO
Background: Rheumatoid arthritis (RA) is a chronic inflammatory disease, with progressive joint destruction, leading to disability. In half of patients, mortality is associated to coronary events, caused by classical risk factors (RF) and/or the inflammatory process. Objectives: To explore the relevance of systemic inflammatory milieu in RA without the burden of traditional RF. Methods: Women with RA and free of traditional RF (n = 30) were compared against healthy women (n = 31). Body mass index, blood pressure, glycemia, serum creatinine, total cholesterol (TC), high density lipoprotein (HDL-c), low-density lipoprotein cholesterol (LDL-c), triglycerides (TG) and oxidized LDL (oxLDL), erythrocyte sedimentation rate, high-sensitivity C reactive protein (hsCRP), lipid quotients for assessing risk (TC/HDLc, LDLc/HDLc, oxLDL/non HDL cholesterol, TG/HDLc), and ultrasonographic carotid intima media thickness (IMT) were estimated or measured. Results: hsCRP and oxLDL were significantly higher in RA patients. IMT values were among normality, but thickness was slightly increased in left carotid, suggesting early atherosclerotic changes. In RA patients inflammation is associated to a higher concentration of oxLDL. No atherosclerosis was proven but a slight greater thickness in left carotid foretells the development of the disease. Conclusions: In RA patients without vascular RF, a special follow up must be implemented to halt atherosclerosis development.
Antecedentes: La artritis reumatoide (AR) es una enfermedad inflamatoria crónica, con destrucción progresiva de las articulaciones, que lleva a la discapacidad. En la mitad de lospacientes, la mortalidad se asocia con eventos coronarios, causados por factores de riesgo (FR) clásicos y/o el proceso inflamatorio. Objetivo: Explorar la relevancia del medio inflamatorio sistémico en la AR sin la carga de FR tradicionales. Métodos: Las mujeres con AR, sin los FR tradicionales (n = 30) fueron comparados contra mujeres sanas (n = 31). El índice de masa corporal, presión arterial, glucemia, creatinina sérica, colesterol total (CT), lipoproteínas de alta densidad (HDL-c), colesterol de lipoproteínas de baja densidad (LDL-c), triglicéridos (TG) y LDL oxidada (LDLox), velocidad de sedimentación de los eritrocitos, proteína C reactiva de alta sensibilidad (PCR-us), cocientes de lípidos para la evaluación de riesgos (TC/HDLc, LDLc/HDLc, colesterol LDLox/noHDL, TG/HDLc), y el espesor ultrasonográfico de la capa íntima-media carotídea (IMT), fueron estimados o medidos. Resultados: hsCRP y LDLox fueron significativamente mayores en los pacientes con AR. Los valores de IMT estaban dentro de la normalidad, pero el espesor se incrementó ligeramente en la carótida izquierda, lo que sugiere cambios ateroscleróticos tempranos. En los pacientes con AR la inflamación está asociada con una mayor concentración de oxLDL. No se comprobó aterosclerosis pero un espesor ligeramente mayor en la carótida izquierda, los hace propensos a desarrollar la enfermedad. Conclusiones: En los pacientes con AR sin FR vascular, un seguimiento especial debe ser implementado para frenar el desarrollo de la aterosclerosis.
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BACKGROUND: During a session of prolonged and exhaustive exercise, such as a marathon race, large quantities of free radicals are produced and can oxidise (ox) several molecules, such as low-density lipoprotein (LDL). To prevent oxidative damage, athletes present higher antioxidant levels. However, the effect of marathon running on the natural IgM or IgG anti-oxLDL autoantibodies is not understood. Thus, we investigated the effect of a marathon race on oxidative stress and the mechanisms of control of this stress. METHODS: Blood samples of 20 marathon runners were collected 24 hours before, immediately and 72 hours after a marathon race to evaluate: plasma lipid profile; serum levels of oxLDL and anti-oxLDL autoantibodies (IgM and IgG isotype) and total antioxidant capacity (TAC). Maximum oxygen uptake (VO2max) was also determined. RESULTS: Immediately after the race, oxLDL and TAC levels decreased in comparison to the basal levels; however, the IgM or IgG anti-oxLDL levels remain unchanged. Whereas no differences were observed in the IgM or IgG anti-oxLDL levels 72h after the marathon, the oxLDL and TAC levels returned to the basal values. Significant positive correlations were observed between oxLDL and LDL-cholesterol before, and 72h after the marathon. Significant negative correlations were observed between oxLDL and VO2max immediately after the marathon and 72 h later, as well as between oxLDL and TAC 72 h after the race. CONCLUSIONS: Athletes with a higher VO2max and total antioxidant activity presented reduced LDL oxidation. The levels of IgM or IgG anti-oxLDL autoantibodies were not affected by running the marathon.
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BACKGROUND: The influence of diet on metabolic syndrome and oxidative stress are not completely known. DESIGN: This cross-sectional study assessed the association of red meat and white meat consumption with metabolic syndrome, insulin resistance and lipid peroxidation in Brazilian middle-aged men. METHODS: A total of 296 subjects (age: 50.5 ± 5.0 years, body mass index: 25.8 ± 3.5 kg/m(2)) were evaluated. Anthropometry, lifestyle features, blood biochemical parameters, diagnosis of metabolic syndrome, homeostatic model assessment for insulin resistance, a lipid peroxidation marker (oxidized low-density lipoprotein) and triglycerides:high-density lipoprotein cholesterol ratio were assessed. Dietary intake was estimated by a food frequency questionnaire. RESULTS: The subjects included in the highest tertile red meat (≥81.5 g/d) and saturated fatty acid from red meat consumption (≥4.3 g/d) had higher occurrence of central obesity (nearly 60%, p < 0.01), hypertriglyceridaemia (nearly 43%, p < 0.01) and metabolic syndrome (35%, p < 0.01). They also had higher values of homeostatic model assessment for insulin resistance, oxidized low-density lipoprotein, and triglycerides:high-density lipoprotein cholesterol ratio, regardless of interfering factors. There were no associations of highest white meat tertile (≥39.4 g/d) and saturated fatty acid from white meat (≥1.0 g/d) consumption with the assessed parameters (p > 0.05). CONCLUSIONS: Red meat consumption was cross-sectionally associated with the occurrence of central obesity, hypertriglyceridaemia, and metabolic syndrome as well as with higher homeostatic model assessment for insulin resistance, oxidized low-density lipoprotein concentrations and triglycerides:high-density lipoprotein cholesterol ratio. The content of saturated fatty acid from red meat consumption may be a factor that contributed to this relationship, while white meat consumption was not associated with metabolic syndrome and the assessed biomarkers.
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Dieta/efeitos adversos , Resistência à Insulina/fisiologia , Peroxidação de Lipídeos/fisiologia , Carne/efeitos adversos , Síndrome Metabólica/etiologia , Animais , Brasil , Estudos Transversais , Humanos , Hipertrigliceridemia/etiologia , Masculino , Pessoa de Meia-Idade , Obesidade Abdominal/etiologia , Estresse OxidativoRESUMO
Elevated levels of oxidized low density lipoprotein (oxLDL) are considered to be one of the major risk factors for atherosclerosis and cardiovascular morbidity. The early stages of atherosclerosis are initiated by the accumulation of oxLDL and the induction of toxic effects on endothelial cells, resulting in endothelial dysfunction. The aim of this study was to investigate how diphenyl diselenide (DD), an organoselenium compound, protect vascular endothelial cells against the toxic effects of oxLDL in vitro. Our data showed that the treatment of bovine endothelial aortic cells (BAEC) with DD (0.1-1 µM) for 24 h protected from oxLDL-induced reactive species (RS) production and reduced glutathione (GSH) depletion. Moreover, DD (1 µM) per se improved the maximal mitochondrial respiratory capacity and prevented oxLDL-induced mitochondrial damage. In addition, DD could prevent apoptosis induced by oxLDL in BAEC. Results from this study may provide insight into a possible molecular mechanism underlying DD suppression of oxLDL-mediated vascular endothelial dysfunction.
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Aterosclerose/tratamento farmacológico , Derivados de Benzeno/administração & dosagem , Células Endoteliais/efeitos dos fármacos , Compostos Organosselênicos/administração & dosagem , Substâncias Protetoras/administração & dosagem , Animais , Apoptose/efeitos dos fármacos , Aterosclerose/etiologia , Aterosclerose/metabolismo , Bovinos , Sobrevivência Celular/efeitos dos fármacos , Células Endoteliais/patologia , Glutationa/metabolismo , Humanos , Lipoproteínas LDL/metabolismo , Lipoproteínas LDL/toxicidade , Mitocôndrias/efeitos dos fármacos , Estresse Oxidativo/efeitos dos fármacos , Substâncias Protetoras/metabolismo , Espécies Reativas de Oxigênio/metabolismoRESUMO
OBJECTIVE: The aim of this cross-sectional study was to assess the potential relationships between fruit and vegetable (FV) intake and oxidative stress markers in middle-aged men, with an emphasis on vitamin C, fiber, and magnesium content. METHODS: The study was conducted with 296 healthy men, age 50.5 ± 5.0 y, and body mass index (BMI) of 25.8 ± 3.5 kg/m(2). Dietary intake, anthropometry, blood pressure, lifestyle features, and blood and urine biochemical data were assessed with validated procedures. The oxidative stress markers selected were plasma oxidized low-density lipoprotein (ox-LDL), urinary 8-iso-prostaglandin F2 α (8-iso-PGF2 α) and 8-hydroxy-2'-deoxyguanosine (8-OHdG). RESULTS: The men included in the highest tertile of FV intake (≥341.1 g/d) displayed lower concentrations of ox-LDL, 8-iso-PGF2 α and 8-OHdG (P for trend < 0.05), regardless of confounding factors. Concentrations of ox-LDL were negatively associated with fiber from the FV intake (P for trend < 0.05) regardless of confounding factors. ox-LDL and 8-OHdG concentrations tended to be lower in the higher tertile of magnesium (P for trend = 0.06) and vitamin C from FV intake (P for trend = 0.05), respectively. Additionally, concentrations of 8-iso-PGF2 α were lower in men in the highest tertile of fiber (≥6.5 g/d; P for trend = 0.034), vitamin C (≥98.0 mg/d; P for trend = 0.007), and magnesium (≥48.9 mg/d; P for trend = 0.018) from the FV-group intake. CONCLUSIONS: Greater FV intake was independently associated with reduced ox-LDL, 8-OHdG, and 8-iso-PGF2 α in middle-aged men. Fiber, vitamin C, and magnesium from FV seem to contribute to this beneficial relationship.
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Biomarcadores/sangue , Biomarcadores/urina , Frutas , Micronutrientes/administração & dosagem , Estresse Oxidativo/fisiologia , Verduras , 8-Hidroxi-2'-Desoxiguanosina , Pressão Sanguínea , Índice de Massa Corporal , Estudos Transversais , Desoxiguanosina/análogos & derivados , Desoxiguanosina/urina , Dinoprosta/análogos & derivados , Dinoprosta/urina , Voluntários Saudáveis , Humanos , Estilo de Vida , Lipoproteínas LDL/sangue , Masculino , Pessoa de Meia-IdadeRESUMO
AIMS: To compare the effects of two of the most effective lipid-lowering therapies with similar LDL-cholesterol reduction capacity on the innate and adaptive immune responses through the evaluation of autoantibodies anti-oxidized LDL (anti-oxLDL Abs) and electronegative LDL [LDL(-)] levels. MAIN METHODS: We performed a prospective, randomized, open label study, with parallel arms and blinded endpoints. One hundred and twelve subjects completed the study protocol and received rosuvastatin 40 mg or ezetimibe/simvastatin 10/40 mg for 12 weeks. Lipids, apolipoproteins, LDL(-), and anti-oxLDL Abs (IgG) were assayed at baseline and end of study. KEY FINDINGS: Main clinical and laboratory characteristics were comparable at baseline. Lipid modifications were similar in both treatment arms, however, a significant raise in anti-oxLDL Abs levels was observed in subjects treated with rosuvastatin (p=0.026 vs. baseline), but not in those receiving simvastatin/ezetimibe. (p=0.233 vs. baseline), thus suggesting modulation of adaptive immunity by a potent statin. Titers of LDL(-) were not modified by the treatments. SIGNIFICANCE: Considering atherosclerosis as an immune disease, this study adds new information, showing that under similar LDL-cholesterol reduction, the choice of lipid-lowering therapy can differently modulate adaptive immune responses.
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Anticorpos/metabolismo , Azetidinas/uso terapêutico , Fluorbenzenos/uso terapêutico , Hiperlipidemias/tratamento farmacológico , Hiperlipidemias/imunologia , Hipolipemiantes/uso terapêutico , Pirimidinas/uso terapêutico , Sulfonamidas/uso terapêutico , Anticorpos/sangue , Azetidinas/farmacologia , LDL-Colesterol/sangue , Ezetimiba , Fluorbenzenos/farmacologia , Antígenos HLA-D/imunologia , Humanos , Hipolipemiantes/farmacologia , Sistema Imunitário/efeitos dos fármacos , Pirimidinas/farmacologia , Rosuvastatina Cálcica , Sulfonamidas/farmacologiaRESUMO
BACKGROUND: Oxidative stress has a pivotal role in the onset of obesity-related chronic diseases. This study assessed potential gender differences in the associations of adiposity (total vs. central) with oxidative stress markers in healthy young adults. METHODS: This cross-sectional study enrolled 272 subjects (97 males, 175 females; 22 ± 3 years, body mass index 22.0 ± 2.8 kg/m(2)). Body composition, cardiometabolic and lifestyle features, oxidized low-density lipoprotein cholesterol (ox-LDL) concentrations, plasma total antioxidant capacity (TAC), and glutathione peroxidase (GPx) activity in erythrocytes were determined by validated procedures. RESULTS: Compared to women, men had statistically higher concentrations of ox-LDL (61.7 vs. 53.5 U/l, p = 0.022). In analyses with the whole sample, those individuals included in the highest tertile of central adiposity indicators (waist circumference, WC, or waist-to-hip ratio, WHR) presented higher ox-LDL and lower TAC values (p < 0.01), while no statistical differences were found across tertiles of total body fat. WHR values were more strongly associated with ox-LDL and TAC concentrations, compared to other adiposity indicators, with higher slopes for women. Sex differences in ox-LDL concentrations were abolished (p > 0.05) after individual pairing of men and women for WC (53.8 vs. 61.6 U/l, p = 0.225) or WHR (56.1 vs. 56.3 U/l, p = 0.471). No differences were found in GPx values concerning gender or adiposity indicators. CONCLUSIONS: Plasma ox-LDL and TAC values were more strongly influenced by central adiposity indicators (WHR and WC) in women than in men, suggesting that the change of the gynoid to android pattern phenotype among young women could lead to a steeper unfavourable redox status compared to men.
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Adiposidade/fisiologia , Antioxidantes/metabolismo , Glutationa Peroxidase/sangue , Lipoproteínas LDL/sangue , Obesidade/metabolismo , Estresse Oxidativo/fisiologia , Adulto , Biomarcadores/sangue , Composição Corporal , Estudos Transversais , Feminino , Humanos , Masculino , Fatores Sexuais , Adulto JovemRESUMO
OBJECTIVE: Previous reports have indicated that subjects with chronic spinal cord injury (SCI) exhibit increased cardiovascular risk compared to able-bodied individuals. This study investigated the relationship between plasmatic oxidized low-density lipoprotein (OxLDL), matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs (TIMPs) levels and vascular remodeling in SCI subjects and the role of physical activity in this regard. METHODS: We studied 42 men with chronic (≥2 years) SCI [18 sedentary (S-SCI) and 24 physically active (PA-SCI)] and 16 able-bodied men by clinical, anthropometric, laboratory, and carotid intima-media thickness (IMT) analysis. All enrolled subjects were normotensive, non-diabetics, non-smokers and normolipemic. Plasmatic OxLDL, MMP-2, MMP-8, MMP-9, TIMP-1 and TIMP-2 levels were determined by enzyme-linked immunosorbent assay. RESULTS: Carotid IMT, IMT/diameter ratio and OxLDL levels of PA-SCI and able-bodied subjects were statistically similar. Conversely, S-SCI subjects exhibited higher IMT, IMT/diameter ratio and OxLDL levels compared to PA-SCI (p < 0.01, p < 0.001 and p = 0.01, respectively) and able-bodied (p < 0.001 for all) individuals. Results of bivariate correlation analysis including all injured subjects showed that carotid IMT and IMT/diameter ratio only correlated with OxLDL, MMP-8 and MMP-8/TIMP-1 ratio. Further stepwise regression analysis adjusted for the presence or not of physical activity and age showed that OxLDL was associated with carotid IMT and IMT/diameter ratio, while MMP-8 was associated with IMT/diameter ratio in SCI individuals. CONCLUSIONS: Plasmatic OxLDL and MMP-8 levels are associated with carotid atherosclerosis and there is an interaction among physical inactivity, atherosclerosis and OxLDL in SCI individuals.
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Artérias Carótidas/patologia , Doenças das Artérias Carótidas/sangue , Lipoproteínas LDL/sangue , Metaloproteinase 8 da Matriz/sangue , Traumatismos da Medula Espinal/sangue , Adulto , Artérias Carótidas/diagnóstico por imagem , Doenças das Artérias Carótidas/complicações , Doenças das Artérias Carótidas/patologia , Espessura Intima-Media Carotídea , Estudos de Casos e Controles , Exercício Físico , Humanos , Masculino , Metaloproteinase 2 da Matriz/sangue , Metaloproteinase 9 da Matriz/sangue , Paraplegia/sangue , Paraplegia/complicações , Quadriplegia/sangue , Quadriplegia/complicações , Risco , Comportamento Sedentário , Traumatismos da Medula Espinal/complicações , Inibidor Tecidual de Metaloproteinase-1/sangue , Inibidor Tecidual de Metaloproteinase-2/sangueRESUMO
We identified different lipemic and metabolic responses after the ingestion of a standardized meal by healthy adults and related them to atherosclerotic markers. Samples from 60 normolipidemic adults were collected before and after a liquid meal (40 g fat/m² body surface) at 0, 2, 4, 6, and 8 h for measurements of lipids, free fatty acids (FFA), insulin, cholesteryl ester transfer protein (CETP), autoantibodies to epitopes of oxidized LDL (oxLDL Ab), lipolytic activities, and apolipoprotein E polymorphism. Mean carotid intima-media thickness (cIMT) was determined by Doppler ultrasound. The volunteers were classified into early (N = 39) and late (N = 31) triacylglycerol (TAG) responders to the test meal. Late responders showed lower HDL cholesterol concentration at fasting and in the TAG peak, lower insulin and higher FFA concentrations compared to early responders. Multivariate regression analyses showed that mean cIMT was associated with gender (male) and age in early responders and by cholesterol levels at the 6th hour in late responders. oxLDL Ab were explained by lipoprotein lipase and negatively by hepatic lipase and oxLDL Ab (fasting period) by CETP (negative) and FFA (positive). This study is the first to identify a postalimentary insulin resistance state, combined with a reduced CETP response exclusively among late responders, and the identification of the regulators of postalimentary atherogenicity. Further research is required to determine the metabolic mechanisms described in the different postalimentary phenotypes observed in this study, as well as in different pathological states, as currently investigated in our laboratory.
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Adolescente , Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Arteriosclerose/etiologia , Gorduras na Dieta/administração & dosagem , Arteriosclerose/sangue , Arteriosclerose/metabolismo , Índice de Massa Corporal , Biomarcadores/sangue , Espessura Intima-Media Carotídea , Gorduras na Dieta/metabolismo , HiperlipidemiasRESUMO
Objetivo: Establecer si el aumento de ácido úrico sérico se asocia a niveles más elevados de LDL oxidada (LDLox), anticuerpos contra LDLox (anti LDLox) e índices de oxidación de la LDL, en mujeres con exceso de peso. Método: Estudio transversal que incluyó 114 mujeres con índice de masa corporal > 25 kg/m². Se determinó peso, talla, circunferencia abdominal, presión arterial, glicemia, ácido úrico, perfil lipídico, creatinina, apolipoproteína B (ApoB), LDLox, anti LDLox e insulina. Se estimó resistencia a la insulina mediante HOMA. Se calcularon índice de masa corporal, ApoB asociada a LDL, índices de oxidación de la LDL y terciles de ácido úrico. Se diagnosticó síndrome metabólico según criterios del NCEP/ATP III. Resultados: De las mujeres estudiadas, 51.8% mostró sobrepeso y el resto fueron obesas; 66.7% presentó síndrome metabólico. En el grupo con sobrepeso y en el grupo total de mujeres, sólo el índice LDLox/HDLc fue significativamente mayor en el último tercil de ácido úrico. Las concentraciones séricas de LDLox y los índices LDLox/colesterol total, LDLox/HDLc, LDLox/ApoB y LDLox/ApoB asociada a LDL fueron significativamente mayores entre las obesas ubicadas en el tercil más elevado de ácido úrico. Las concentraciones de anti LDLox y el índice LDLox/Anti LDLox no se relacionaron con ácido úrico. Los niveles séricos de ácido úrico y ApoB predijeron la elevación de la LDLox. Conclusión: El aumento del ácido úrico sérico se asoció con mayor oxidación de la LDL entre mujeres obesas, sugiriendo la importancia que podría tener el control periódico de ácido úrico en mujeres con exceso de peso.
Objective: To establish whether increased serum uric acid is associated with higher levels of oxidized LDL (oxLDL), antibodies against human oxidized LDL (oxLDL Ab) and ratios of LDL oxidation in overweight women. Methods: Cross-sectional study that included 114 women with body mass index > 25 kg/m2. We determined weight, height, waist circumference, blood pressure, glycemia, uric acid, lipid profile, creatinine, Apolipoprotein B (ApoB), oxLDL, oxLDL Ab, insulin and insulin resistance was estimated using HOMA. Body mass index, LDL-associated ApoB, rates of LDL oxidation and tertiles of uric acid were calculated. Metabolic syndrome was defined using NCEP/ATP III criteria. Results: Of the women studied 51.8% were overweight and the rest was classified as obese; 66.7% had metabolic syndrome. In the total group and overweight group, only the oxLDL/HDL cholesterol ratio was significantly higher in the last tertile of uric acid. The serum levels of circulanting oxLDL and oxLDL/cholesterol, oxLDL/HDL cholesterol, oxLDL/ApoB and oxLDL/ LDL-associated ApoB ratios were significantly higher among obese women located in the highest tertile of uric acid. Concentrations of oxLDL Ab and oxLDL/oxLDL Ab were not related to the uric acid. Serum uric acid and ApoB predicted the elevation of oxLDL. Conclusion: Increased serum uric acid was associated with more oxidation of LDL among obese women. This suggests the importance of regular monitoring of uric acid in overweight women. Prospective research should be conducted.