For debate.Glucose variability and diabetes complication risk: we need to know the answer

被引:36
作者
Kilpatrick, E. S. [1 ]
Rigby, A. S. [3 ]
Atkin, S. L. [2 ]
机构
[1] Hull Royal Infirm, Dept Clin Biochem, Kingston Upon Hull HU3 2JZ, N Humberside, England
[2] Hull York Med Sch, Dept Diabet, Kingston Upon Hull, N Humberside, England
[3] Univ Hull, Acad Dept Cardiol, Kingston Upon Hull HU6 7RX, N Humberside, England
关键词
glucose variability; HbA(1c); microvascular complications; MEAN BLOOD-GLUCOSE; IMPAIRED FASTING GLUCOSE; MICROVASCULAR COMPLICATIONS; POSTPRANDIAL HYPERGLYCEMIA; CARDIOVASCULAR-DISEASE; GLYCEMIC VARIABILITY; OXIDATIVE STRESS; TYPE-2; HBA(1C); FLUCTUATIONS;
D O I
10.1111/j.1464-5491.2010.02929.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P>There is still a debate as to whether or not glucose variability contributes to diabetes complication risk. There is much in vitro laboratory evidence that glycaemic instability gives rise to increased production of reactive oxygen species and has a detrimental effect on endothelial dysfunction. While some in vivo studies have also shown similar findings in patients with or without diabetes, others have been unable to confirm any association. Furthermore, clinical studies which have sought to translate this possible risk into an increased likelihood of developing micro- or macrovascular complications have so far not demonstrated an effect. However, few of these trials were specifically designed to establish any influence of glucose fluctuations. This issue is now one of the largest remaining unanswered questions in diabetes. While this article focuses on the data which do not support a role for glucose variability in the development of complications, it also highlights the need for further studies to be performed which will definitively resolve the matter.
引用
收藏
页码:868 / 871
页数:4
相关论文
共 34 条
[1]   Efficacy and safety of incretin therapy in type 2 diabetes - Systematic review and meta-analysis [J].
Amori, Renee E. ;
Lau, Joseph ;
Pittas, Anastassios G. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 298 (02) :194-206
[2]   Risk of cardiovascular and all-cause mortality in individuals with diabetes mellitus, impaired fasting glucose, and impaired glucose tolerance - The Australian diabetes, obesity, and lifestyle study (AusDiab) [J].
Barr, Elizabeth L. M. ;
Zimmet, Paul Z. ;
Welborn, Timothy A. ;
Jolley, Damien ;
Magliano, Dianna J. ;
Dunstan, David W. ;
Cameron, Adrian J. ;
Dwyer, Terry ;
Taylor, Hugh R. ;
Tonkin, Andrew M. ;
Wong, Tien Y. ;
McNeil, John ;
Shaw, Jonathan E. .
CIRCULATION, 2007, 116 (02) :151-157
[3]   Can glycaemic variability, as calculated from blood glucose self-monitoring, predict the development of complications in type 1 diabetes over a decade? [J].
Bragd, J. ;
Adamson, U. ;
Backlund, L. B. ;
Lins, P. E. ;
Moberg, E. ;
Oskarsson, P. .
DIABETES & METABOLISM, 2008, 34 (06) :612-616
[4]   The pathobiology of diabetic complications - A unifying mechanism [J].
Brownlee, M .
DIABETES, 2005, 54 (06) :1615-1625
[5]   'Glycaemic variability': a new therapeutic challenge in diabetes and the critical care setting [J].
Ceriello, A. ;
Ihnat, M. A. .
DIABETIC MEDICINE, 2010, 27 (08) :862-867
[6]   Postprandial Hyperglycemia and Cardiovascular Disease Is the HEART2D study the answer? [J].
Ceriello, Antonio .
DIABETES CARE, 2009, 32 (03) :521-522
[7]   Is HbA1c affected by glycemic instability? [J].
Derr, R ;
Garrett, E ;
Stacy, GA ;
Saudek, CD .
DIABETES CARE, 2003, 26 (10) :2728-2733
[8]   Glucose Control and Vascular Complications in Veterans with Type 2 Diabetes [J].
Duckworth, William ;
Abraira, Carlos ;
Moritz, Thomas ;
Reda, Domenic ;
Emanuele, Nicholas ;
Reaven, Peter D. ;
Zieve, Franklin J. ;
Marks, Jennifer ;
Davis, Stephen N. ;
Hayward, Rodney ;
Warren, Stuart R. ;
Goldman, Steven ;
McCarren, Madeline ;
Vitek, Mary Ellen ;
Henderson, William G. ;
Huang, Grant D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (02) :129-U62
[9]   Intensive versus Conventional Glucose Control in Critically Ill Patients [J].
Finfer, S. ;
Blair, D. ;
Bellomo, R. ;
McArthur, C. ;
Mitchell, I. ;
Myburgh, J. ;
Norton, R. ;
Potter, J. ;
Chittock, D. ;
Dhingra, V. ;
Foster, D. ;
Cook, D. ;
Dodek, P. ;
Hebert, P. ;
Henderson, W. ;
Heyland, D. ;
McDonald, E. ;
Ronco, J. ;
Schweitzer, L. ;
Peto, R. ;
Sandercock, P. ;
Sprung, C. ;
Young, J. D. ;
Su, S. ;
Heritier, S. ;
Li, Q. ;
Bompoint, S. ;
Billot, L. ;
Crampton, L. ;
Darcy, F. ;
Jayne, K. ;
Kumarasinghe, V. ;
Little, L. ;
McEvoy, S. ;
MacMahon, S. ;
Pandey, S. ;
Ryan, S. ;
Shukla, R. ;
Vijayan, B. ;
Atherton, S. ;
Bell, J. ;
Hadfield, L. ;
Hourigan, C. ;
McArthur, C. ;
Newby, L. ;
Simmonds, C. ;
Buhr, H. ;
Eccleston, M. ;
McGuinness, S. ;
Parke, R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (13) :1283-1297
[10]  
Gerstein HC, 2008, NEW ENGL J MED, V358, P2545, DOI 10.1056/NEJMoa0802743