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Circadian Week-to-Week and Physical Exercise-Induced Variation of Serum Microfibrillar-Associated Protein 4

机译:昼夜节日周至周和体育锻炼诱导的血清微纤维结合蛋白4的变异

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摘要

Serum microfibrillar-associated protein 4 (sMFAP4) has been investigated as a biomarker for various diseases and is demonstrated to show significant gradual increase with severity of liver fibrosis. Ideal biomarkers used for disease diagnosis or prognosis should display deviating levels in affected individuals only and be robust to factors unrelated to the disease. Here we show the impact of normal physiological variation of sMFAP4 by characterizing the circadian variation, week-to-week variation, and physical exercise-induced levels. Serum samples from 3 groups of healthy volunteers were drawn: 7 times during a 24-hour period, 5 times during a 3-week period, and before and after a standardized physical exercise challenge. sMFAP4 was determined by AlphaLISA. Statistical analysis was performed using mixed effects modeling of repeated measurements. Circadian variation of sMFAP4 was demonstrated, with time of peak and nadir values depending on age and gender. For males, the peak values were observed during nighttime whereas for females, peak values were observed in the morning. Individual sMFAP4 levels remained stable over a period of 3 weeks and physical exercise inferred a mild negative influence. In conclusion, the circadian sMFAP4 variation was significant, and the levels could be influenced by physical activity. However, these variations were of limited magnitude relative to previously observed disease-induced levels in support of the biomarker potential of sMFAP4.
机译:已经研究了血清微纤维结合的蛋白4(SMFAP4)作为各种疾病的生物标志物,并证明了肝纤维化的严重程度显着增加。用于疾病诊断或预后的理想生物标志物应仅显示受影响的人的偏差水平,并且对与疾病无关的因素具有稳健。在这里,我们通过表征昼夜变异,周到周的变异和体育锻炼水平来显示SMFAP4正常生理变化的影响。从3组健康志愿者进行血清样品:在24小时期间7次,3周期间的5次,在标准化的体育攻击之前和之后。 SMFAP4由alphalisa确定。使用反复测量的混合效应建模进行统计分析。根据年龄和性别,对SMFAP4的昼夜变异进行了演示,随着年龄和性别的峰值和Nadir值。对于雄性,在夜间观察到峰值,而女性,早上观察到峰值。在3周的时间内,个体SMFAP4水平保持稳定,体育锻炼推断出轻度负面影响。总之,昼夜节约SMFAP4变异显着,水平可能受到体力活动的影响。然而,这些变化相对于先前观察到的疾病诱导的水平具有有限的疾病,以支持SMFAP4的生物标志物潜力。

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