Pecht T, Gutman-Tirosh A, Bashan N, Rudich A
Department of Clinical Biochemistry and Pharmacology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel; The National Institute of Biotechnology (NIBN) in the Negev, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Obes Rev. 2014 Apr;15(4):322-37. doi: 10.1111/obr.12133. Epub 2013 Nov 20.
While obesity is clearly accepted as a major risk factor for cardio-metabolic morbidity, it is also apparent that some obese patients largely escape this association, forming a unique obese subphenotype(s). Current approaches to define such subphenotypes include clinical biomarkers that largely reflect already manifested comorbidities, such as markers of dyslipidaemia, hyperglycaemia and impaired regulation of vascular tone, and anthropometric or imaging-based assessment of adipose tissue distribution. Low-grade inflammation, evident both systemically and within adipose tissue (particularly intra-abdominal fat depots), seems to characterize the more cardio-metabolically morbid forms of obesity. Indeed, several systemic inflammatory markers (C-reactive protein), adipokines (retinol-binding protein 4, adiponectin) and cytokines have been shown to correlate in humans with adipose tissue inflammation and with obesity-associated health risks. Circulating leucocytes constitute a diverse group of cells that form a major arm of the immune system. They are both major sources of cytokines and likely also of infiltrating adipose tissue immune cells in obesity. In the present review, we summarize currently available literature on 'classical' blood white cell classes and on more specific leucocyte subclasses present in the circulation in human obesity. We critically raise the possibility that leucocytes may constitute clinically available markers for the more morbidity-associated obesity subphenotype(s), and when available, for intra-abdominal adipose tissue inflammation.
虽然肥胖显然被公认为是心血管代谢疾病的主要危险因素,但很明显,一些肥胖患者在很大程度上避免了这种关联,形成了一种独特的肥胖亚表型。目前定义此类亚表型的方法包括临床生物标志物,这些标志物在很大程度上反映了已经出现的合并症,如血脂异常、高血糖和血管张力调节受损的标志物,以及基于人体测量或成像的脂肪组织分布评估。低度炎症在全身和脂肪组织(特别是腹部脂肪库)中都很明显,似乎是肥胖的心血管代谢疾病更严重形式的特征。事实上,几种全身炎症标志物(C反应蛋白)、脂肪因子(视黄醇结合蛋白4、脂联素)和细胞因子已被证明在人类中与脂肪组织炎症以及与肥胖相关的健康风险相关。循环白细胞是构成免疫系统主要分支的多种细胞群。它们既是细胞因子的主要来源,也可能是肥胖时浸润脂肪组织免疫细胞的来源。在本综述中,我们总结了目前关于人类肥胖中循环中“经典”血液白细胞类别和更特定白细胞亚类的现有文献。我们批判性地提出,白细胞可能构成与疾病关联更强的肥胖亚表型的临床可用标志物,如有可能,也可用于腹部脂肪组织炎症的标志物。