Department of Morphology, Surgery and Experimental Medicine and LTTA Centre, University of Ferrara, Via Fossato di Mortara 70, 44121 Ferrara, Italy.
Department of Morphology, Surgery and Experimental Medicine, Section of Obstetrics and Gynecology, University of Ferrara, Via Aldo Moro 8, 44124 Ferrara, Italy.
Mediators Inflamm. 2017;2017:5356020. doi: 10.1155/2017/5356020. Epub 2017 Sep 5.
Tumor necrosis factor- (TNF-) related apoptosis-inducing ligand (TRAIL) is attracting attention for its role in the physiopathology of metabolic disease/diabetes. Evidence suggests that it might protect against metabolic abnormalities driven by obesity-induced dysregulated secretion of adipokines, but this role of TRAIL has not yet been fully established. On this basis, we aimed to investigate the potential association between TRAIL and adipokine levels in a cohort of subjects in which age/gender/hormonal interferences were excluded.
Serum levels of TRAIL and a panel of adipokines were measured in postmenopausal women ( = 147) stratified according to waist circumference measures as normal, overweight, or obese. The panel of adipokines included interleukin- (IL-) 6, IL-8, IL-1, adipsin, lipocalin-2/neutrophil gelatinase-associated lipocalin (ngal), TNF-alpha, monocyte chemoattractant protein-1, plasminogen activator inhibitor-1, hepatocyte growth factor, resistin, leptin, adiponectin, and nerve growth factor.
Low serum TRAIL concentration (deciles I-IV) was significantly and inversely correlated with resistin and lipocalin 2/ngal levels ( = -0.502 and < 0.001 and = -0.360 and < 0.01, resp.). Both associations retained their statistical significance after adjustment for confounding factors, such as waist circumference and age.
Our data indicate a link between low circulating levels of TRAIL and markers of obesity-induced diseases (resistin and lipocalin-2/ngal), highlighting a new potential axis of TRAIL functions.
肿瘤坏死因子相关凋亡诱导配体(TRAIL)因其在代谢疾病/糖尿病的病理生理学中的作用而受到关注。有证据表明,它可能有助于预防由肥胖引起的脂肪因子失调分泌导致的代谢异常,但 TRAIL 的这一作用尚未得到充分证实。在此基础上,我们旨在研究 TRAIL 与排除年龄/性别/激素干扰的受试者队列中的脂肪因子水平之间的潜在关联。
根据腰围测量结果,将绝经后妇女(n=147)分为正常、超重或肥胖组,检测其血清 TRAIL 水平和一组脂肪因子。该脂肪因子组包括白细胞介素(IL)-6、IL-8、IL-1、adipsin、脂联素、脂联素/中性粒细胞明胶酶相关脂质运载蛋白(ngal)、肿瘤坏死因子-α、单核细胞趋化蛋白-1、纤溶酶原激活物抑制剂-1、肝细胞生长因子、抵抗素、瘦素、脂联素和神经生长因子。
低血清 TRAIL 浓度(十位数 I-IV)与抵抗素和脂联素/ngal 水平呈显著负相关( = -0.502 和 < 0.001 和 = -0.360 和 < 0.01,分别)。在调整腰围和年龄等混杂因素后,这两种关联仍然具有统计学意义。
我们的数据表明,循环 TRAIL 水平低与肥胖引起的疾病标志物(抵抗素和脂联素/ngal)之间存在关联,突出了 TRAIL 功能的一个新的潜在轴。