血浆瘦素水平、阻塞性睡眠呼吸暂停综合征和糖尿病与肥胖相关的外周血单核细胞亚群改变有关。

Svenja Meyhöfer, Armin Steffen, Kirstin Plötze-Martin, Christian Lange, Jens-Uwe Marquardt, Karl-Ludwig Bruchhage, Sebastian M Meyhöfer, Ralph Pries
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引用次数: 0

摘要

肥胖是一种急剧增加的疾病,并伴有心血管疾病和阻塞性睡眠呼吸暂停综合征(OSAS)等合并症。肥胖和OSAS本身都与全身炎症有关。然而,肥胖、OSAS及其伴随疾病对循环单核细胞免疫特性的多因素影响尚未完全解决。使用流式细胞术在全血测量中分析82名肥胖患者的单核细胞亚群的CD14/CD16细胞表面表达模式和不同的单核粘附分子。评估所有患者的血浆脂肪因子脂联素和瘦素水平,并将其与伴随的细胞和临床价值相关联。全血测量显示,肥胖患者中CD14/CD16单核细胞亚群的总体分布显著。单核细胞粘附分子CD11a、CD11b和CX3CR1显著升高。观察到的变化与血浆瘦素水平和糖尿病状况显著相关,这是关键的放大因素。肥胖、糖尿病和OSAS对外周血单核细胞免疫平衡的额外影响需要在治疗、呼吸支持和减肥方面采取协调的方案,以提高这些患者的全身免疫力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets.

Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets.

Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets.

Plasma Leptin Levels, Obstructive Sleep Apnea Syndrome, and Diabetes Are Associated with Obesity-Related Alterations of Peripheral Blood Monocyte Subsets.

Obesity is a dramatically increasing disease, accompanied with comorbidities such as cardiovascular disease and obstructive sleep apnea syndrome (OSAS). Both obesity and OSAS per se are associated with systemic inflammation. However, the multifactorial impact of obesity, OSAS, and its concomitant diseases on the immunological characteristics of circulating monocytes has not yet been fully resolved. Monocyte subsets of 82 patients with obesity were analyzed in whole blood measurements in terms of the CD14/CD16 cell surface expression patterns and different monocytic adhesion molecules using flow cytometry. Plasma levels of adipokines adiponectin and leptin of all patients were evaluated and correlated with accompanying cellular and clinical values. Whole blood measurements revealed a significant overall redistribution of CD14/CD16 monocyte subsets in patients with obesity. Monocytic adhesion molecules CD11a, CD11b, and CX3CR1 were significantly elevated. The observed alterations significantly correlated with plasma leptin levels and diabetes status as crucial amplifying factors. The additive impact of obesity, diabetes, and OSAS on the immunological balance of peripheral blood monocytes requires a coordinated regimen in terms of therapeutic treatment, respiratory support, and weight loss to improve the systemic immunity in these patients.

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