Moreira Ana Paula Boroni, Alves Raquel Duarte Moreira, Teixeira Tatiana Fiche Salles, Macedo Viviane Silva, de Oliveira Leandro Licursi, Costa Neuza Maria Brunoro, Bressan Josefina, do Carmo Gouveia Peluzio Maria, Mattes Richard, de Cássia Gonçalves Alfenas Rita
Departamento de Nutrição, Universidade Federal de Juiz de Fora, Bairro Martelos, s/n, Juiz de Fora, Minas Gerais, CEP 36036-330, Brazil.
Department of Nutrition and Health, Universidade Federal de Viçosa, Viçosa, Brazil.
Eur J Nutr. 2015 Dec;54(8):1363-70. doi: 10.1007/s00394-014-0817-6. Epub 2014 Dec 18.
Lipopolysaccharide (LPS) from the outer membrane of gram-negative bacteria might be an inflammation trigger in adipose tissue. It has recently been proposed that there is a link between adipose tissue distribution and blood LPS. However, the number of studies on this topic is scarce, and further investigation in humans is required. In this study, we explored the association between plasma LPS concentrations and body fat distribution, as well as the biochemical parameters that may indicate the presence of metabolic disorders.
Sixty-seven young adult men with body mass index of 26-35 kg/m(2) were evaluated. Anthropometry, body composition and body fat distribution, blood pressure, energy expenditure, physical activity level, dietary intake, and biochemical parameters were assessed.
Men with median plasma LPS ≥ 0.9 EU/mL presented higher sagittal abdominal diameter, trunk fat percentage, and android fat percentage, and mass, insulin and alanine aminotransferase concentrations, homeostasis model assessment of insulin resistance (HOMA-IR), and beta cell dysfunction (HOMA-B) than those with lower plasma LPS. LPS correlated positively with the trunk fat percentage, and android fat percentage, and mass, insulin, aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase concentrations, as well as HOMA-IR and HOMA-B.
Our results suggest that a higher plasma LPS concentration is associated with a less favorable phenotype as characterized by higher central adiposity, higher values of HOMA-IR, and beta cell function impairment in overweight/obese men.
革兰氏阴性菌外膜的脂多糖(LPS)可能是脂肪组织中的炎症触发因素。最近有人提出脂肪组织分布与血液LPS之间存在联系。然而,关于该主题的研究数量稀少,需要在人体中进行进一步调查。在本研究中,我们探讨了血浆LPS浓度与体脂分布之间的关联,以及可能表明存在代谢紊乱的生化参数。
对67名体重指数为26 - 35 kg/m²的年轻成年男性进行评估。评估了人体测量学、身体成分和体脂分布、血压、能量消耗、身体活动水平、饮食摄入和生化参数。
血浆LPS中位数≥0.9 EU/mL的男性比血浆LPS较低的男性具有更高的腹径、躯干脂肪百分比、男性型脂肪百分比、体重、胰岛素和丙氨酸转氨酶浓度、胰岛素抵抗稳态模型评估(HOMA-IR)和β细胞功能障碍(HOMA-B)。LPS与躯干脂肪百分比、男性型脂肪百分比、体重、胰岛素、天冬氨酸转氨酶、丙氨酸转氨酶和碱性磷酸酶浓度以及HOMA-IR和HOMA-B呈正相关。
我们的结果表明,较高的血浆LPS浓度与不太理想的表型相关,其特征为超重/肥胖男性的中心性肥胖程度更高、HOMA-IR值更高以及β细胞功能受损。