Adiponectin, Insulin Sensitivity, β-Cell Function, and Racial/Ethnic Disparity in Treatment Failure Rates in TODAY

被引:32
作者
Arslanian, Silva [1 ]
El Ghormli, Laure [2 ]
Bacha, Fida [3 ]
Caprio, Sonia [4 ]
Goland, Robin [5 ]
Haymond, Morey W. [3 ]
Levitsky, Lynne [6 ]
Nadeau, Kristen J. [7 ]
White, Neil H. [8 ]
Willi, Steven M. [9 ]
机构
[1] Childrens Hosp Pittsburgh, Pittsburgh, PA 15213 USA
[2] George Washington Univ, Ctr Biostat, Rockville, MD 20052 USA
[3] Texas Childrens Hosp, Baylor Coll Med, Houston, TX 77030 USA
[4] Yale Univ, Sch Med, New Haven, CT USA
[5] Columbia Univ, New York, NY USA
[6] Massachusetts Gen Hosp Children, Boston, MA USA
[7] Univ Colorado, Anschutz Med Campus, Aurora, CO USA
[8] Washington Univ St Louis, St Louis, MO USA
[9] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
GLUCOSE-TOLERANCE; OBESE ADOLESCENTS; LIFE-STYLE; ETHNIC-DIFFERENCES; RACIAL-DIFFERENCES; METFORMIN; YOUTH; RESISTANCE; CHILDREN; PLASMA;
D O I
10.2337/dc16-0455
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE The Treatment Options for type 2 Diabetes in Adolescents and Youth (TODAY) study demonstrated that glycemic failure rates in the three treatments combined-metformin plus rosiglitazone, metformin alone, and metformin plus lifestyle-were higher in non-Hispanic blacks (NHB; 52.8%) versus non-Hispanic whites (NHW; 36.6%) and Hispanics (H; 45.0%). Moreover, metformin alone was less effective in NHB versus NHW versus H youth. This study describes treatment-associated changes in adiponectin, insulin sensitivity, and b-cell function over time among the three racial/ethnic groups to understand potential mechanism(s) responsible for this racial/ethnic disparity. RESEARCH DESIGN AND METHODS TODAY participants underwent periodic oral glucose tolerance tests to determine insulin sensitivity, C-peptide index, and oral disposition index (oDI), with measurements of total and high-molecular-weight adiponectin (HMWA). RESULTS At baseline NHB had significantly lower HMWA than NHW and H and exhibited a significantly smaller increase (17.3% vs. 33.7% vs. 29.9%, respectively) during the first 6 months overall. Increases in HMWA were associated with reductions in glycemic failure in the three racial/ethnic groups combined (hazard ratio 0.61, P < 0.0001) and in each race/ethnicity separately. Over time, HMWA was significantly lower in those who failed versus did not fail treatment, irrespective of race/ethnicity. There were no differences in treatment-associated temporal changes in insulin sensitivity, C-peptide index, and oDI among the three racial/ethnic groups. CONCLUSIONS HMWA is a reliable biomarker of treatment response in youth with type 2 diabetes. The diminutive treatment-associated increase in HMWA in NHB (similar to 50% lower) compared with NHW and H may explain the observed racial/ethnic disparity with higher therapeutic failure rates in NHB in TODAY.
引用
收藏
页码:85 / 93
页数:9
相关论文
共 42 条
[1]
Hyperinsulinemia in African-American children - Decreased insulin clearance and increased insulin secretion and its relationship to insulin sensitivity [J].
Arslanian, SA ;
Saad, H ;
Lewy, V ;
Danadian, K ;
Janosky, J .
DIABETES, 2002, 51 (10) :3014-3019
[2]
Effects of Metformin, Metformin Plus Rosiglitazone, and Metformin Plus Lifestyle on Insulin Sensitivity and β-cell Function in TODAY [J].
Arslanian, Silva ;
Pyle, Laura ;
Payan, Marisa ;
Bacha, Fida ;
Caprio, Sonia ;
Haymond, Morey W. ;
Levitsky, Lynne L. ;
Goland, Robin ;
White, Neil H. ;
Willi, Steven M. .
DIABETES CARE, 2013, 36 (06) :1749-1757
[3]
Does adiponectin explain the lower insulin sensitivity and hyperinsulinemia of African-American children? [J].
Bacha, F ;
Saad, R ;
Gungor, N ;
Arslanian, SA .
PEDIATRIC DIABETES, 2005, 6 (02) :100-102
[4]
Adiponectin in youth -: relationship to visceral adiposity, insulin sensitivity, and β-cell function [J].
Bacha, F ;
Saad, R ;
Gungor, N ;
Arslanian, SA .
DIABETES CARE, 2004, 27 (02) :547-552
[5]
Type 2 diabetes in youth: are there racial differences in β-cell responsiveness relative to insulin sensitivity? [J].
Bacha, Fida ;
Gungor, Neslihan ;
Lee, Sojung ;
Arslanian, Silva A. .
PEDIATRIC DIABETES, 2012, 13 (03) :259-265
[6]
Short-term metabolic and cardiovascular effects of metformin in markedly obese adolescents with normal glucose tolerance [J].
Burgert, Tania S. ;
Duran, Elvira J. ;
Goldberg-Gell, Rachel ;
Dziura, James ;
Yeckel, Catherine W. ;
Katz, Stuart ;
Tamborlane, William V. ;
Caprio, Sonia .
PEDIATRIC DIABETES, 2008, 9 (06) :567-576
[7]
Adiponectin is lower among African Americans and is independently related to insulin sensitivity in children and adolescents [J].
Bush, NC ;
Darnell, BE ;
Oster, RA ;
Goran, MI ;
Gower, BA .
DIABETES, 2005, 54 (09) :2772-2778
[8]
Metformin in combination with structured lifestyle intervention improved body mass index in obese adolescents, but did not improve insulin resistance [J].
Clarson, Cheril L. ;
Mahmud, Farid H. ;
Baker, Janet E. ;
Clark, Helen E. ;
Mckay, Wendy M. ;
Schauteet, Vicki D. ;
Hill, David J. .
ENDOCRINE, 2009, 36 (01) :141-146
[9]
Characteristics of Adolescents and Youth with Recent-Onset Type 2 Diabetes: The TODAY Cohort at Baseline [J].
Copeland, Kenneth C. ;
Zeitler, Philip ;
Geffner, Mitchell ;
Guandalini, Cindy ;
Higgins, Janine ;
Hirst, Kathryn ;
Kaufman, Francine R. ;
Linder, Barbara ;
Marcovina, Santica ;
McGuigan, Paul ;
Pyle, Laura ;
Tamborlane, William ;
Willi, Steven .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2011, 96 (01) :159-167
[10]
COX DR, 1972, J R STAT SOC B, V34, P187