Adiponectin, insulin sensitivity, β-cell function, and racial/ethnic disparity in treatment failure rates in TODAY

Silva Arslanian, Laure El Ghormli, Fida Bacha, Sonia Caprio, Robin Goland, Morey W. Haymond, Lynne Levitsky, Kristen J. Nadeau, Neil H. White, Steven M. Willi

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

OBJECTIVE The Treatment Options for type 2 Diabetes in Adolescents and Youth (TODAY) study demonstrated that glycemic failure rates in the three treatments combineddmetformin plus rosiglitazone, metformin alone, and metformin plus lifestyledwere 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 HMWAthan NHWand 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 (∼50% lower) compared with NHWand H may explain the observed racial/ethnic disparity with higher therapeutic failure rates in NHB in TODAY.

Original languageEnglish
Pages (from-to)85-93
Number of pages9
JournalDiabetes care
Volume40
Issue number1
DOIs
StatePublished - Jan 1 2017

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