The relationship of neutrophil elastase and proteinase 3 with risk factors, and chronic complications in type 2 diabetes: A Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) sub-study.

IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Kwok-Leung Ong, Liang Wu, Andrzej S Januszewski, Rachel O'Connell, Aimin Xu, Russell S Scott, David R Sullivan, Kerry-Anne Rye, Huating Li, Ronald Cw Ma, Liping Li, Val Gebski, Alicia J Jenkins, Weiping Jia, Anthony C Keech
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引用次数: 1

Abstract

Introduction: Neutrophil elastase (NE) and proteinase 3 (PR3) are novel inflammation biomarkers. We investigated their associations with chronic complications, determinants of biomarker levels and effects of fenofibrate in patients with type 2 diabetes mellitus (T2DM) from Fenofibrate Intervention and Event Lowering in Diabetes study.

Methods: Plasma NE and PR3 levels were quantified at baseline (n = 2000), and relationships with complications over 5-years assessed. Effects of fenofibrate on biomarker levels (n = 200) were determined at four follow-up visits.

Results: Higher waist-to-hip ratio, homocysteine and C-reactive protein and lower apoA-II were determinants of higher NE and PR3 levels. Higher NE levels were associated with on-trial stroke and cardiovascular mortality, and higher PR3 levels with on-trial stroke, but associations were not significant after adjustment for confounding factors. Although higher NE and PR3 levels were associated with baseline total microvascular disease, only NE levels were associated with on-trial neuropathy or amputation. These associations were not significant after adjusting for multiple comparisons. NE and PR3 levels did not change with fenofibrate.

Conclusions: In T2DM plasma NE and PR3 levels are associated with vascular risk factors, and total microvascular disease at baseline, but on rigorous analyses were not associated with on-trial complications. Levels were not changed by fenofibrate.

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中性粒细胞弹性酶和蛋白酶3与2型糖尿病危险因素和慢性并发症的关系:非诺贝特干预和糖尿病事件降低(FIELD)亚研究
中性粒细胞弹性酶(NE)和蛋白酶3 (PR3)是新型的炎症生物标志物。我们从非诺贝特干预和糖尿病事件降低研究中调查了非诺贝特与慢性并发症、生物标志物水平的决定因素以及非诺贝特对2型糖尿病(T2DM)患者的影响。方法:在基线时定量血浆NE和PR3水平(n = 2000),并评估其与5年内并发症的关系。非诺贝特对生物标志物水平的影响(n = 200)在4次随访中被确定。结果:较高的腰臀比、同型半胱氨酸和c反应蛋白以及较低的apoA-II是NE和PR3水平升高的决定因素。较高的NE水平与试验卒中和心血管死亡率相关,较高的PR3水平与试验卒中相关,但在校正混杂因素后,相关性不显著。虽然较高的NE和PR3水平与基线总微血管疾病相关,但只有NE水平与试验中神经病变或截肢相关。在调整多重比较后,这些关联并不显著。非诺贝特未改变NE和PR3水平。结论:T2DM血浆NE和PR3水平与血管危险因素和基线总微血管疾病相关,但严格分析与试验并发症无关。非诺贝特没有改变其水平。
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来源期刊
Diabetes & Vascular Disease Research
Diabetes & Vascular Disease Research ENDOCRINOLOGY & METABOLISM-PERIPHERAL VASCULAR DISEASE
CiteScore
4.40
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: Diabetes & Vascular Disease Research is the first international peer-reviewed journal to unite diabetes and vascular disease in a single title. The journal publishes original papers, research letters and reviews. This journal is a member of the Committee on Publication Ethics (COPE)
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