Risk of hypoglycemia in youth with type 2 diabetes on insulin

被引:6
作者
Shahid, Madhia [1 ]
Shaibi, Gabriel Q. [1 ,2 ]
Baines, Hayley [3 ]
Garcia-Filion, Pamela [4 ]
Gonzalez-Garcia, Zoe [5 ,6 ]
Olson, Micah [1 ,2 ]
机构
[1] Phoenix Childrens Hosp, Div Endocrinol & Diabet, 1920 East Cambridge Ave,Suite 301, Phoenix, AZ 85016 USA
[2] Arizona State Univ, Coll Nursing & Hlth Innovat, Ctr Hlth Promot & Dis Prevent, Phoenix, AZ USA
[3] Oregon Hlth & Sci Univ, Doernbecher Childrens Hosp, Div Endocrinol & Diabet, Portland, OR 97201 USA
[4] Univ Arizona, Coll Med Phoenix, Dept Biomed Informat, Phoenix, AZ USA
[5] Univ Nebraska, Div Endocrinol & Diabet, Childrens Hosp, Omaha, NE 68182 USA
[6] Univ Nebraska, Med Ctr, Omaha, NE USA
关键词
hypoglycemia; insulin; type; 2; diabetes; BETA-CELL FUNCTION; GLYCEMIC CONTROL; CLINICAL-TRIAL; THERAPY; MELLITUS; ADOLESCENTS; ASSOCIATION; RESISTANCE; CANCER; HYPERTENSION;
D O I
10.1515/jpem-2018-0014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The objective of this study was to ascertain the risk of hypoglycemia among youth with type 2 diabetes (T2D) on insulin therapy. Methods: Twenty-two youth with T2D on insulin therapy (M = 12, F = 10, age = 14.4 +/- 4.0 years) were enrolled from a single pediatric endocrine practice. They were followed-up for 3 months with weekly phone calls and monthly inperson visits to review blood glucose logs and document any signs or symptoms of hypoglycemia (defined as finger stick glucose of <= 70 mg/dL). Episodes of hypoglycemia were categorized into five categories: severe, documented symptomatic, asymptomatic, probable symptomatic and relative hypoglycemia. In addition to examining the risk of hypoglycemia, the degree to which hypoglycemia was associated with patient demographics (e.g. age, gender and body mass index [BMI]) or clinical factors (i.e. duration of diabetes, duration of insulin treatment, glycemic control or insulin dose and regimen) was determined. Results: Nine hypoglycemic events occurred during the study period in five patients with an incidence rate of nine events per 5.3 patient-years. Of the hypoglycemic events, five were symptomatic and four were asymptomatic. No severe hypoglycemic events occurred. Hypoglycemia was not associated with age, ethnicity, duration of insulin treatment, insulin dose or initial hemoglobin (HbA(1c)). However, a significant difference in BMI was noted, with T2D youth who experienced hypoglycemia having a lower BMI than those who did not experience hypoglycemia. Conclusions: The results of this study suggest that the risk of hypoglycemia in youth with T2D on insulin therapy is low.
引用
收藏
页码:625 / 630
页数:6
相关论文
共 41 条
[1]  
[Anonymous], 2013, FRONT ENDOCRINOL
[2]   Increased cancer-related mortality for patients with type 2 diabetes who use sulforrylureas or insulin [J].
Bowker, SL ;
Majumdar, SR ;
Veugelers, P ;
Johnson, JA .
DIABETES CARE, 2006, 29 (02) :254-258
[3]  
Childs BP, 2005, DIABETES CARE, V28, P1245
[4]  
Cryer PE, 2009, NEW ENGL J MED, V360, P129
[5]  
Cryer PE., 2009, HYPOGLYCEMIA DIABETE
[6]  
Dabelea D, 2007, JAMA-J AM MED ASSOC, V297, P2716, DOI 10.1001/jama.297.24.2716
[7]   From the Triumvirate to the Ominous Octet: A New Paradigm for the Treatment of Type 2 Diabetes Mellitus [J].
DeFronzo, Ralph A. .
DIABETES, 2009, 58 (04) :773-795
[8]   Impaired activation of phosphoinositide 3-kinase by insulin in fibroblasts from patients with severe insulin resistance and pseudoacromegaly - A disorder characterized by selective postreceptor insulin resistance [J].
Dib, K ;
Whitehead, JP ;
Humphreys, PJ ;
Soos, MA ;
Baynes, KCR ;
Kumar, S ;
Harvey, T ;
O'Rahilly, S .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (05) :1111-1120
[9]   Antidiabetic therapy and increased risk of hepatocellular carcinoma in chronic liver disease [J].
Donadon, Valter ;
Balbi, Massimiliano ;
Ghersetti, Michela ;
Grazioli, Silvia ;
Perciaccante, Antonio ;
Della Valentina, Giovanni ;
Gardenal, Rita ;
Dal Mas, Maria ;
Casarin, Pietro ;
Zanette, Giorgio ;
Miranda, Cesare .
WORLD JOURNAL OF GASTROENTEROLOGY, 2009, 15 (20) :2506-2511
[10]  
Felszeghy E, 2008, J PEDIATR ENDOCR MET, V21, P847