通过多频生物阻抗分析对内脏脂肪面积的简单估计与炎症和心脏代谢疾病的多种生物标志物相关:一项初步研究

Obesities Pub Date : 2023-01-07 DOI:10.3390/obesities3010001
C. Vella, M. C. Nelson
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引用次数: 0

摘要

需要确定估算内脏脂肪的简单技术是否可以准确预测不同人群中的炎症和心脏代谢疾病(CMD)生物标志物。我们旨在确定通过多频生物电阻抗分析(MFBIA)简单估计内脏脂肪面积是否与炎症和CMD的多种生物标志物独立相关。78名男性和女性(平均值±标准差:年龄52.0±10.8岁;内脏脂肪面积105.6±55.0 cm2)自我报告了他们的病史和活动水平。用MFBIA、CMD估计内脏脂肪面积,通过空腹抽血测量炎症生物标志物,并计算胰岛素抵抗的稳态模型评估(HOMA-IR)。使用多变量线性回归评估相关性。在对年龄、性别、身高、种族/民族、糖尿病家族史和吸烟进行调整后,内脏脂肪(55 cm2)的1标准差(1-SD)增加与胰岛素(60.4%)、甘油三酯(43.6%)、C反应蛋白(38.7%)、白细胞介素-6(33.9%)、瘦素(77.9%)和HOMA-IR(51.8%,均p<0.01)水平升高有关。当将体力活动和久坐行为纳入模型时,这些相关性减弱,但仍然显著(p≤0.01)。这些发现表明,通过MFBIA简单估计内脏脂肪面积可能是CMD风险增加的良好指标,并可能在临床实践中有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Simple Estimate of Visceral Fat Area by Multifrequency Bioimpedance Analysis Is Associated with Multiple Biomarkers of Inflammation and Cardiometabolic Disease: A Pilot Study
There is a need for identifying whether simple techniques for estimating visceral fat can accurately predict inflammatory and cardiometabolic disease (CMD) biomarkers in various populations. We aimed to determine whether a simple estimate of visceral fat area by multifrequency bioelectrical impedance analysis (MFBIA) was independently associated with multiple biomarkers of inflammation and CMD. Seventy-eight men and women (mean ± SD: age 52.0 ± 10.8 y; visceral fat area 105.6 ± 55.0 cm2) self-reported their medical histories and activity levels. Visceral fat area was estimated with MFBIA, CMD and inflammatory biomarkers were measured by fasting blood draw, and homeostasis model assessment for insulin resistance (HOMA-IR) was calculated. Associations were assessed using multivariable linear regression. With adjustment for age, sex, height, race/ethnicity, family history of diabetes, and smoking, a 1-standard deviation (1-SD) increase in visceral fat (55 cm2) was associated with higher levels of insulin (60.4%), triglycerides (43.6%), C-reactive protein (38.7%), interleukin-6 (33.9%), leptin (77.9%), and HOMA-IR (51.8%, p < 0.01 for all). These associations were attenuated but remained significant when physical activity and sedentary behavior were entered into the model (p ≤ 0.01). These findings suggest that a simple estimate of visceral fat area by MFBIA may be a good indicator of increased CMD risk and may be useful in clinical practice.
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