Ebert T, Hindricks J, Kralisch S, Lossner U, Jessnitzer B, Richter J, Blüher M, Stumvoll M, Fasshauer M
Department of Endocrinology and Nephrology, University of Leipzig, Leipzig, Germany; IFB AdiposityDiseases, Leipzig University Medical Center, Leipzig, Germany.
Diabet Med. 2014 Aug;31(8):1014-7. doi: 10.1111/dme.12451. Epub 2014 Apr 16.
Fractalkine has recently been introduced as an adipokine that improves glucose tolerance. Regulation of fractalkine in gestational diabetes, as well as its association with markers of obesity, glucose and lipid metabolism, inflammation and renal function, has not been elucidated.
Circulating fractalkine was quantified by enzyme-linked immunosorbent assay in 74 women with gestational diabetes and 74 healthy, pregnant control subjects matched for age, BMI, and gestational age.
Median (interquartile range) levels of fractalkine were not significantly different between the two groups [gestational diabetes: 2.24 (2.16) μg/l; control: 2.45 (1.38) μg/l] (P = 0.461). In multivariate linear regression analysis, fractalkine remained independently associated with homeostasis model assessment of insulin resistance (β = -0.253, P = 0.002) and the proinflammatory adipokine progranulin (β = 0.218, P = 0.007).
Circulating fractalkine is not different between women with gestational diabetes and control subjects, but the adipokine is independently associated with markers of insulin resistance and proinflammatory progranulin in pregnancy.
趋化因子最近被作为一种改善糖耐量的脂肪因子引入。妊娠期糖尿病中趋化因子的调节及其与肥胖、糖脂代谢、炎症和肾功能标志物的关联尚未阐明。
采用酶联免疫吸附测定法对74例妊娠期糖尿病女性和74例年龄、体重指数及孕周相匹配的健康妊娠对照者的循环趋化因子进行定量分析。
两组间趋化因子的中位数(四分位间距)水平无显著差异[妊娠期糖尿病组:2.24(2.16)μg/l;对照组:2.45(1.38)μg/l](P = 0.461)。在多变量线性回归分析中,趋化因子仍与胰岛素抵抗的稳态模型评估独立相关(β = -0.253,P = 0.002)以及促炎脂肪因子颗粒蛋白前体独立相关(β = 0.218,P = 0.007)。
妊娠期糖尿病女性与对照者之间的循环趋化因子无差异,但该脂肪因子与妊娠期间胰岛素抵抗和促炎颗粒蛋白前体的标志物独立相关。