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Adipokines and inflammatory markers in elderly subjects with high risk of type 2 diabetes and cardiovascular disease

机译:老年人受试者的adipokines和炎症标志物,具有2型糖尿病和心血管疾病的高风险

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Inflammation plays a significant role in pathogenesis of diabetes and atherosclerosis. Increased adiposity with an upregulation of cytokines in prediabetes has been associated with vascular inflammation and considered a leading causal factor for type 2 diabetes (T2D). Information on adipokines and inflammatory markers in prediabetes, defined by hemoglobin A1C (HbA1c) 5.7–6.4% in addition to impaired fasting glucose (IFG) and impaired glucose tolerance (IGT), are sparse. We conducted a population–based cross-sectional study (part of a follow-up study) of inhabitants of Oulu, Finland, born in 1935. Inflammatory markers and traditional risk markers of 367 subjects were measured. The glucose status was determined by an oral glucose tolerance test (OGTT) and HbA1c. Inflammatory markers and glycemic levels were analysed using analysis of covariance (ANCOVA). Of the participants, 193 were normoglycemic, 82 had prediabetes and 40 T2D. Inflammatory cytokines were significantly higher in subjects with prediabetes as compared to normoglycemic subjects: IL-4 (14.9 vs 5.9?pg/ml, p?=?0.041), IP-10 (251 vs 209?pg/ml, p?=?0.05), TNF-α (10.4 vs 6.9?pg/ml, p?=?0.027), RANTES (43.3 vs 33.1?pg/ml, p?=?0.009), CD40L (3708 vs 1671?pg/ml, p?=?0.010) and VEGF (269 vs 174?pg/ml, p?=?0.013). These inflammatory cytokines remained significant even after adjustment for waist circumference. The differences in inflammatory markers in prediabetic and T2D subjects were not statistically significant. Prediabetes was associated with low-grade inflammation with increased inflammatory cytokine levels, while the levels in prediabetic subjects were comparable to those in T2D subjects. The associations were independent of visceral adiposity.
机译:炎症在糖尿病和动脉粥样硬化的发病机制中起着重要作用。预期肥胖的肥胖增加了前奶油因子的血管因子与血管炎症有关,并且认为2型糖尿病(T2D)的主要因果因素。除血红蛋白A1C(HBA1C)定义的前脂肪因子和炎症标志物的信息除了禁止空腹葡萄糖(IFG)和葡萄糖耐量(IGT)受损的情况下,由血红蛋白A1C(HBA1C)5.7-6.4%稀疏。我们通过1935年出生于1935年的芬兰Oulu居民的基于人口的横断面研究(部分研究)。测量了367名受试者的炎症标志物和传统风险标志。葡萄糖状态由口服葡萄糖耐量试验(OGTT)和HBA1C确定。使用协方差分析分析炎症标记和血糖水平(ANCOVA)。参与者,193年是Normoglycexy,82人有前奶肉和40 T2D。与正常性血糖受试者相比,炎症细胞因子在炎前的炎症性细胞因子显着高:IL-4(14.9 Vs 5.9?pg / ml,p?= 0.041),IP-10(251 vs 209?pg / ml,p?=? 0.05),TNF-α(10.4 Vs 6.9?pg / ml,p?= 0.027),rantes(43.3 Vs 33.1 = pg / ml,p?= 0.009),CD40L(3708 Vs 1671?Pg / ml,p ?=?0.010)和VEGF(269 Vs 174?pg / ml,p?= 0.013)。即使在对腰围的调节后,这些炎症细胞因子仍然有显着性。预测和T2D受试者中炎症标志物的差异在统计学上没有统计学意义。 PrediaBetes与炎症细胞因子水平增加的低级炎症有关,而预脂受试者的水平与T2D受试者的水平相当。协会与内脏肥胖无关。

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