Department of Family Medicine and Public Health, Division of Preventative Medicine, University of California San Diego, La Jolla, CA.
Department of Medicine, Division of Hematology and Oncology, University of Vermont, Burlington, VT.
Med Sci Sports Exerc. 2018 Jul;50(7):1495-1501. doi: 10.1249/MSS.0000000000001570.
Skeletal muscle is the largest regulator of glucose metabolism, but few population-based studies have examined the associations between muscle and inflammation. We studied the relationships between abdominal muscle area and density with selected adiposity-associated inflammatory mediators.
Nearly 2000 subjects underwent computed tomography of the abdomen and had venous fasting blood drawn concomitantly. The computed tomography scans were interrogated for visceral and subcutaneous fat, as well as abdominal lean muscle areas and densities. We then categorized the muscle into locomotion (psoas) and stabilization (rectus, obliques, and paraspinal) groups. Blood samples were assayed for interleukin-6 (IL-6), resistin, C-reactive protein, and TNF-α.
The mean age was 64.7 yr, and 49% were female. Forty percent were white, 26% Hispanic/Latino American, 21% African American, and 13% Chinese American. The mean body mass index was 28.0 kg·m, and 30% were obese (body mass index, >30 kg·m). Using multivariable linear regression models that included adjustment for abdominal muscle area, a 1-SD increment in the mean densities for total, stabilization, and locomotive abdominal muscle were each significantly associated with lower levels of IL-6 (β = -15%, -15%, and -9%, P < 0.01 for all) and resistin (β = -0.11, -0.11, and -0.07 ng·mL, P < 0.02 for all), but not C-reactive protein or TNF-α. Conversely, muscle area was not independently associated with any of the inflammatory mediators studied.
Higher densities of several muscle groups in the abdomen are significantly associated with lower IL-6 and resistin levels, independent of the muscle area in these groups. Techniques that enhance muscle density may reduce levels of adiposity-associated inflammatory mediators.
骨骼肌是调节葡萄糖代谢的最大器官,但很少有基于人群的研究探讨肌肉与炎症之间的关系。我们研究了腹型肌肉面积和密度与选定的与肥胖相关的炎症介质之间的关系。
近 2000 名受试者接受了腹部计算机断层扫描,并同时抽取了空腹静脉血。对 CT 扫描进行了分析,以确定内脏脂肪和皮下脂肪以及腹部的肌肉面积和密度。然后我们将肌肉分为运动(腰大肌)和稳定(腹直肌、斜肌和脊柱旁肌)两组。血液样本用于检测白细胞介素-6(IL-6)、抵抗素、C 反应蛋白和肿瘤坏死因子-α。
平均年龄为 64.7 岁,49%为女性。40%为白人,26%为西班牙裔/拉丁裔美国人,21%为非裔美国人,13%为华裔美国人。平均体重指数为 28.0kg·m,30%为肥胖(体重指数>30kg·m)。使用多元线性回归模型,包括对腹部肌肉面积的调整,平均密度每增加一个标准差,总腹部、稳定和运动腹部肌肉与 IL-6(β=-15%、-15%和-9%,所有 P<0.01)和抵抗素(β=-0.11、-0.11 和-0.07ng·mL,所有 P<0.02)水平降低显著相关,但与 C 反应蛋白或肿瘤坏死因子-α无关。相反,肌肉面积与所研究的任何炎症介质均无独立相关性。
腹部多个肌肉群的密度增加与 IL-6 和抵抗素水平降低显著相关,与这些肌肉群的肌肉面积无关。增强肌肉密度的技术可能会降低与肥胖相关的炎症介质水平。