Medical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, Germany.
Clinic for Visceral, Transplantation and Thorax and Vascular Surgery, University Hospital Leipzig, Leipzig, Germany.
Int J Obes (Lond). 2021 Feb;45(2):331-336. doi: 10.1038/s41366-020-00667-4. Epub 2020 Sep 1.
BACKGROUND/OBJECTIVES: People with metabolically healthy obesity (MHO) may still have an increased risk for cardiovascular mortality compared to metabolically healthy lean (MHL) individuals. However, the mechanisms linking obesity to cardiovascular diseases are not entirely understood. We therefore tested the hypothesis that circulating cell adhesion molecules (CAMs) are higher in MHO compared to MHL individuals.
SUBJECTS/METHODS: Serum concentrations of soluble intercellular adhesion molecule-1 (sICAM-1), soluble vascular adhesion molecule-1 (sVCAM-1), E-selectin and P-selectin were measured in age- and sex-matched groups of MHL (n = 32), MHO categorized into BMI-matched insulin sensitive (IS, n = 32) or insulin resistant (IR) obesity (n = 32) and people with metabolically unhealthy obesity (MUO, n = 32).
Indeed, individuals with MHO have significantly higher sICAM-1, E-selectin, and P-selectin serum concentrations compared to MHL people. However, these CAMs are still significantly lower in IS compared to IR MHO. There was no difference between the groups in sVCAM-1 serum concentrations. Compared to all other groups, circulating adhesion molecules were significantly higher in individuals with MUO.
These findings suggest that obesity-related increased cardiovascular risk is reflected and may be mediated by significantly higher CAMs. The mechanisms causing elevated adhesion molecules even in the absence of overt cardio-metabolic risk factors and whether circulating CAMs could predict cardiovascular events need to be explored.
背景/目的:与代谢健康的瘦人(MHL)相比,代谢健康肥胖(MHO)患者的心血管死亡率可能仍然较高。然而,将肥胖与心血管疾病联系起来的机制尚不完全清楚。因此,我们检验了这样一个假设,即循环细胞黏附分子(CAMs)在 MHO 中比在 MHL 中更高。
受试者/方法:在年龄和性别匹配的 MHL 组(n=32)、BMI 匹配的胰岛素敏感(IS,n=32)或胰岛素抵抗(IR)肥胖(n=32)以及代谢不健康肥胖(MUO,n=32)的 MHO 中,测量了可溶性细胞间黏附分子-1(sICAM-1)、可溶性血管细胞黏附分子-1(sVCAM-1)、E-选择素和 P-选择素的血清浓度。
事实上,与 MHL 人群相比,MHO 患者的 sICAM-1、E-选择素和 P-选择素血清浓度显著更高。然而,与 IR MHO 相比,IS MHO 中这些 CAMs 仍然显著较低。各组间 sVCAM-1 血清浓度无差异。与所有其他组相比,MUO 个体的循环黏附分子明显更高。
这些发现表明,肥胖相关的心血管风险增加反映在并可能通过显著更高的 CAMs 来介导。即使在没有明显的心血管代谢危险因素的情况下,导致黏附分子升高的机制以及循环 CAMs 是否可以预测心血管事件,仍需要进一步探索。