Insulin resistance in type 2 diabetes youth relates to serum free fatty acids and muscle mitochondrial dysfunction

被引:48
|
作者
Cree-Green, Melanie [1 ,2 ,4 ]
Gupta, Abhinav [1 ,2 ]
Coe, Gregory V. [1 ,2 ]
Baumgartner, Amy D. [1 ,2 ]
Pyle, Laura [3 ,9 ]
Reusch, Jane E. B. [4 ,5 ,6 ]
Brown, Mark S. [7 ]
Newcomer, Bradley R. [8 ]
Nadeau, Kristen J. [1 ,2 ,4 ]
机构
[1] Univ Colorado, Anschutz Med Campus, Div Pediat Endocrinol, Aurora, CO 80045 USA
[2] Childrens Hosp Colorado, Aurora, CO 80045 USA
[3] Univ Colorado, Anschutz Med Campus, Dept Pediat, Aurora, CO USA
[4] Univ Colorado, Anschutz Med Campus, Ctr Womens Hlth Res, Aurora, CO 80045 USA
[5] Univ Colorado, Anschutz Med Campus, Div Endocrinol Metab & Diabet, Aurora, CO 80045 USA
[6] Vet Affairs Med Ctr, Aurora, CO 80012 USA
[7] Univ Colorado, Anschutz Med Campus, Dept Radiol, Aurora, CO 80045 USA
[8] James Madison Univ, Honors Program, Harrisonburg, VA 22807 USA
[9] Colorado Sch Publ Hlth, Dept Biostat & Informat, Aurora, CO 80045 USA
关键词
Type; 2; diabetes; Adolescents; Insulin resistance; Mitochontrial function; Free fatty acids; INTRAMYOCELLULAR LIPID-CONTENT; SKELETAL-MUSCLE; OXIDATIVE CAPACITY; ADP RECOVERY; SENSITIVITY; REDUCTION; SPECTROSCOPY; ADOLESCENTS; CHILDREN; OBESE;
D O I
10.1016/j.jdiacomp.2016.10.014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: Insulin resistance (IR) correlates with mitochondrial dysfunction, free fatty acids (FFAs), and intramyocellular lipid (IMCL) in adults with type 2 diabetes (T2D). We hypothesized that muscle IR would relate to similar factors in T2D youth. Methods: Participants included 17 youth with T2D, 23 normal weight controls (LCs), and 26 obese controls (OBs) of similar pubertal stage and activity level. Results: T2D and OB groups were of similar BMI. T2D youth were significantly more IR and had higher calf IMCL and serum FFA concentrations during hyperinsulinemia. ADP time constant (ADPTC), a blood-flow dependent mitochondrial function measure, was slowed and oxidative phosphorylation rates lower in T2D. In multiple linear regression of the entire cohort, lack of FFA suppression and longer ADPTC, but not IMCL or HbA1c, were independently associated with IR. Conclusion: We found that elevated FFAs and mitochondrial dysfunction are early abnormalities in relatively well-controlled youth with T2D. Further, post-exercise oxidative metabolism appears affected by reduced blood flow, and is not solely an inherent mitochondrial defect. Thus, lowering FFAs and improving mitochondrial function and blood flow may be potential treatment targets in youth with T2D. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:141 / 148
页数:8
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