Glycemic Variability: How to Measure and Its Clinical Implication for Type 2 Diabetes

被引:94
|
作者
Umpierrez, Guillermo E. [1 ]
Kovatchev, Boris P. [2 ]
机构
[1] Emory Univ, Sch Med, Div Endocrinol Diabet & Metab, 69 Jesse Hill Jr Dr, Atlanta, GA 30303 USA
[2] Univ Virginia Hlth Syst, Ctr Diabet Technol, Charlottesville, VA USA
来源
AMERICAN JOURNAL OF THE MEDICAL SCIENCES | 2018年 / 356卷 / 06期
关键词
Glycemic control; Glycated hemoglobin A(1c); Glycemic variability; Type; 2; diabetes; GLARGINE PLUS LIXISENATIDE; PLACEBO-CONTROLLED TRIAL; FIXED-RATIO COMBINATION; GLUCOSE VARIABILITY; BLOOD-GLUCOSE; INSULIN GLARGINE; SEVERE HYPOGLYCEMIA; POSTPRANDIAL HYPERGLYCEMIA; CARDIOVASCULAR OUTCOMES; NOCTURNAL HYPOGLYCEMIA;
D O I
10.1016/j.amjms.2018.09.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glycated hemoglobin A(1c) (A1C) levels have traditionally been the gold standard for assessing glycemic control and treatment efficacy in patients with type 2 diabetes. However, A1C does not take into account fluctuations in blood glucose levels known as glycemic variability (GV). In recent years, GV has become increasingly clinically relevant, because of a better understanding of the need to reach target A1C while avoiding hypoglycemia. GV relates to both hyperglycemia and hypoglycemia, and has been associated with poorer quality of life. Diabetes treatments targeting multiple pathophysiological mechanisms are most beneficial in controlling A1C and reducing GV. In clinical trials, a number of metrics are used to measure GV, many of which are not well understood in the clinical practice. Until a gold standard metric for GV is established, the variety of measurements available may confound the choice of an optimal treatment for an individual patient.
引用
收藏
页码:518 / 527
页数:10
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