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

Author:

Ong Kwok-Leung12ORCID,Wu Liang13,Januszewski Andrzej S1,O’Connell Rachel1,Xu Aimin45,Scott Russell S6,Sullivan David R17,Rye Kerry-Anne2,Li Huating3,Ma Ronald CW8910,Li Liping1,Gebski Val1,Jenkins Alicia J1,Jia Weiping3,Keech Anthony C111

Affiliation:

1. NHMRC Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia

2. Lipid Research Group, School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia

3. Department of Endocrinology and Metabolism, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Clinical Center of Diabetes, Shanghai Jiao Tong University Affiliated Sixth People’s Hospital, Shanghai, China

4. Department of Medicine, University of Hong Kong, Hong Kong, China

5. State Key Laboratory of Pharmaceutical Biotechnology, University of Hong Kong, Hong Kong, China

6. Lipid and Diabetes Research Group, Christchurch Hospital, Christchurch, New Zealand

7. Department of Chemical Pathology, Royal Prince Alfred Hospital, Sydney, NSW, Australia

8. Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, China

9. Hong Kong Institute of Diabetes and Obesity, The Chinese University of Hong Kong, Hong Kong, China

10. Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, China

11. Department of Cardiology, Royal Prince Alfred Hospital, Sydney, NSW, Australia

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.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

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