Literature DB >> 17116177

A Diabetes Outcome Progression Trial (ADOPT): baseline characteristics of Type 2 diabetic patients in North America and Europe.

G Viberti1, J Lachin, R Holman, B Zinman, S Haffner, B Kravitz, M A Heise, N P Jones, M C O'Neill, M I Freed, S E Kahn, W H Herman.   

Abstract

AIMS: To examine baseline characteristics of patients recruited into ADOPT, a multinational trial comparing three oral glucose-lowering monotherapies.
METHODS: Between April 2000 and June 2002, 4360 patients aged 30-75 years with Type 2 diabetes diagnosed for < 3 years and remaining on diet therapy alone with fasting plasma glucose levels (FPG) between 7.0 and 10.0 mmol/l were enrolled by 488 North American and European centres. Medical histories, anthropometric data and laboratory measurements were determined using common methodologies.
RESULTS: The mean (SD) age of the patients was 57 (10) years, body mass index 32.2 (6.4) kg/m(2), HbA(1c) 7.4 (0.9)%; 58% were male, 88% Caucasian and 15% smoked. North American Caucasians (NAC) were younger, more obese, and more insulin resistant than European Caucasians (EUC), but had better pancreatic B-cell function. NAC had lower total, low-density lipoprotein- and high-density liporpotein-cholesterol concentrations with higher triglyceride concentrations and were more often on lipid-lowering treatment. They had lower blood pressure levels but were equally likely to be on antihypertensive treatment. Metabolic syndrome was more frequent and microalbuminuria less frequent in NAC. Within North America, NAC had lower HbA(1c) concentrations than Blacks, Hispanics and Asians despite similar or higher FPG and 30-min postchallenge glucose concentrations.
CONCLUSIONS: Caucasian North American and European ADOPT patients differ with respect to adiposity, insulin resistance and metabolic syndrome prevalence. North American Blacks, Hispanics and Asians had lower HbA(1c) concentrations than NAC despite similar or higher glucose concentrations. These phenotypic differences may influence the progression of Type 2 diabetes and the response to initial oral glucose-lowering monotherapy.

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Year:  2006        PMID: 17116177     DOI: 10.1111/j.1464-5491.2006.02022.x

Source DB:  PubMed          Journal:  Diabet Med        ISSN: 0742-3071            Impact factor:   4.359


  23 in total

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2.  HbA1c for the diagnosis of diabetes and prediabetes: is it time for a mid-course correction?

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Review 4.  Do race and ethnicity impact hemoglobin A1c independent of glycemia?

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5.  Genetic Ancestry Markers and Difference in A1c Between African American and White in the Diabetes Prevention Program.

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Journal:  J Clin Endocrinol Metab       Date:  2019-02-01       Impact factor: 5.958

Review 6.  Biomarkers in diabetes: hemoglobin A1c, vascular and tissue markers.

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7.  Personalizing Second-Line Type 2 Diabetes Treatment Selection: Combining Network Meta-analysis, Individualized Risk, and Patient Preferences for Unified Decision Support.

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Journal:  Med Decis Making       Date:  2019-02-15       Impact factor: 2.583

8.  Implications of the new definition of diabetes for health disparities.

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9.  Glycated haemoglobin A1c for diagnosing diabetes in Chinese population: cross sectional epidemiological survey.

Authors:  Yuqian Bao; Xiaojing Ma; Huating Li; Mi Zhou; Cheng Hu; Haiya Wu; Junling Tang; Xuhong Hou; Kunsan Xiang; Weiping Jia
Journal:  BMJ       Date:  2010-05-17

10.  Are There Clinical Implications of Racial Differences in HbA1c? Yes, to Not Consider Can Do Great Harm!

Authors:  William H Herman
Journal:  Diabetes Care       Date:  2016-08       Impact factor: 19.112

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