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生活方式干预对非酒精性脂肪性肝病患者巨噬细胞活化标志物可溶性CD163的影响。

Effects of lifestyle intervention on soluble CD163, a macrophage activation marker, in patients with non-alcoholic fatty liver disease.

作者信息

Rødgaard-Hansen Sidsel, St George Alexis, Kazankov Konstantin, Bauman Adrian, George Jacob, Grønbæk Henning, Jon Møller Holger

机构信息

a Department of Clinical Biochemistry , Aarhus University Hospital , Aarhus , Denmark.

b Storr Liver Centre, Westmead Institute for Medical Research , University of Sydney and Westmead Hospital , Australia.

出版信息

Scand J Clin Lab Invest. 2017 Nov;77(7):498-504. doi: 10.1080/00365513.2017.1346823. Epub 2017 Jul 17.

Abstract

OBJECTIVE

Liver macrophages play an important role in the pathogenesis of non-alcoholic fatty liver disease (NAFLD). Soluble CD163 (sCD163), a macrophage-specific biomarker, reflects disease activity in the range of liver diseases. The impact of lifestyle intervention on sCD163 in adult NAFLD patients has not been investigated.

MATERIAL AND METHODS

We assessed 126 NAFLD patients participating in a lifestyle intervention study for sCD163 concentrations at baseline, after the three-month intervention period, and at long-term follow-up after 12 and 24 months.

RESULTS

The median sCD163 concentration at baseline was 2.59 mg/L (IQR = 1.78-3.63 mg/L). There was a significant decrease in sCD163 from baseline to three months follow-up (-0.64 mg/L, p < .001) with no difference between the four study groups (p = .6). At 12 and 24 months follow-up, the sCD163 concentrations had returned to baseline level (p = .3 and p = .1). Baseline sCD163 correlated with liver biomarkers and metabolic variables. There was a significantly greater decrease in sCD163 in patients who had a decrease in alanine aminotransferase (ALT) compared with patients with unchanged or increased ALT (-0.76 mg/L vs. -0.41 mg/L, p = .02), and in patients with a decrease in HOMA-IR compared with individuals with no decrease (-0.86 mg/L vs. -0.55 mg/L, p = .03).

CONCLUSION

sCD163 is associated with markers of liver necro-inflammation and glucose homoeostasis in NAFLD. Participation in a lifestyle intervention programme resulted in a significant reduction in sCD163. Our data support the utility of sCD163 as a biomarker for monitoring the efficacy of therapeutic interventions in NAFLD.

摘要

目的

肝巨噬细胞在非酒精性脂肪性肝病(NAFLD)的发病机制中起重要作用。可溶性CD163(sCD163)是一种巨噬细胞特异性生物标志物,可反映肝脏疾病范围内的疾病活动情况。尚未研究生活方式干预对成年NAFLD患者sCD163的影响。

材料与方法

我们评估了126名参与生活方式干预研究的NAFLD患者在基线、三个月干预期后以及12个月和24个月长期随访时的sCD163浓度。

结果

基线时sCD163浓度中位数为2.59mg/L(四分位间距=1.78 - 3.63mg/L)。从基线到三个月随访时sCD163显著降低(-0.64mg/L,p <.001),四个研究组之间无差异(p =.6)。在12个月和24个月随访时,sCD163浓度已恢复到基线水平(p =.3和p =.1)。基线sCD163与肝脏生物标志物和代谢变量相关。与丙氨酸氨基转移酶(ALT)未改变或升高的患者相比,ALT降低的患者sCD163降低幅度显著更大(-0.76mg/L对-0.41mg/L,p =.02),与胰岛素抵抗稳态模型评估(HOMA-IR)未降低的个体相比,HOMA-IR降低的患者sCD163降低幅度更大(-0.86mg/L对-0.55mg/L,p =.03)。

结论

sCD163与NAFLD中的肝脏坏死性炎症和葡萄糖稳态标志物相关。参与生活方式干预计划导致sCD163显著降低。我们的数据支持sCD163作为监测NAFLD治疗干预疗效的生物标志物的实用性。

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