Etiological Approach to Characterization of Diabetes Type The SEARCH for Diabetes in Youth Study

被引:149
作者
Dabelea, Dana [1 ]
Pihoker, Catherine [2 ]
Talton, Jennifer W. [3 ]
D'Agostino, Ralph B., Jr. [3 ]
Fujimoto, Wilfred [4 ]
Klingensmith, Georgeanna J. [5 ,6 ]
Lawrence, Jean M. [7 ]
Linder, Barbara [8 ]
Marcovina, Santica M. [9 ]
Mayer-Davis, Elizabeth J. [10 ,11 ]
Imperatore, Giuseppina [12 ]
Dolan, Lawrence M. [13 ]
机构
[1] Univ Colorado Denver, Colorado Sch Publ Hlth, Dept Epidemiol, Aurora, CO 80045 USA
[2] Univ Washington, Dept Washington, Seattle, WA 98195 USA
[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Biostat Sci, Winston Salem, NC 27109 USA
[4] Kuakini Med Ctr, Honolulu, HI USA
[5] Univ Colorado Denver, Barbara Davis Ctr, Sch Med, Aurora, CO USA
[6] Univ Colorado Denver, Dept Pediat, Sch Med, Aurora, CO USA
[7] Kaiser Permanente So Calif, Dept Res & Evaluat, Pasadena, CA USA
[8] NIDDK, NIH, Bethesda, MD USA
[9] Univ Washington, Dept Med, Seattle, WA USA
[10] Univ N Carolina, Dept Nutr, Chapel Hill, NC USA
[11] Univ N Carolina, Dept Med, Chapel Hill, NC USA
[12] Ctr Dis Control & Prevent, Div Diabet Translat, Atlanta, GA USA
[13] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati Childrens Hosp, Cincinnati, OH USA
关键词
BETA-CELL FUNCTION; CHILDREN; GENOTYPES; MELLITUS; INSULIN; AUTOIMMUNITY; ADULTS; RISK;
D O I
10.2337/dc10-2324
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-To describe an etiologic approach to classification of diabetes types in youth based on the 1997 American Diabetes Association (ADA) framework, using data from the SEARCH for Diabetes in Youth Study. RESEARCH DESIGN AND METHODS-SEARCH conducted a comprehensive assessment of 2,291 subjects aged <20 years with recently diagnosed diabetes. Using autoimmunity (at least one of two diabetes autoantibodies) and insulin sensitivity (equation validated against hyperinsulinemic-euglycemic clamps) as the main etiologic markers, we described four categories along a bidimensional spectrum: autoimmune plus insulin-sensitive (IS), autoimmune plus insulin-resistant (IR), nonautoimmune plus IS, and nonautoimmune plus IR. We then explored how characteristics, including genetic susceptibility to autoimmunity (HLA genotypes), insulin deficiency, and clinical factors varied across these four categories. RESULTS-Most subjects fell into either the autoimmune plus IS (54.5%) or nonautoimmune plus IR categories (15.9%) and had characteristics that align with traditional descriptions of type 1 or type 2 diabetes. The group classified as autoimmune plus IR (19.5%) had similar prevalence and titers of diabetes autoantibodies and similar distribution of HLA risk genotypes to those in the autoimmune plus IS group, suggesting that it includes individuals with type 1 diabetes who are obese. The group classified as nonautoimmune plus IS (10.1%) likely includes individuals with undetected autoimmunity but may also include those with monogenic diabetes and thus requires further testing. CONCLUSIONS-The SEARCH study offers researchers and clinicians a practical application for the etiologic classification of diabetes type and at the same time identifies a group of youths who would benefit from further testing.
引用
收藏
页码:1628 / 1633
页数:6
相关论文
共 25 条
[1]   HLA-DQB1 genotypes, islet antibodies and beta cell function in the classification of recent-onset diabetes among young adults in the nationwide Diabetes Incidence Study in Sweden [J].
Bakhtadze, E. ;
Borg, H. ;
Stenstrom, G. ;
Fernlund, P. ;
Arnqvist, H. J. ;
Ekbom-Schnell, A. ;
Bolinder, J. ;
Eriksson, J. W. ;
Gudbjornsdottir, S. ;
Nystrom, L. ;
Groop, L. C. ;
Sundkvist, G. .
DIABETOLOGIA, 2006, 49 (08) :1785-1794
[2]   Harmonization of Glutamic Acid Decarboxylase and Islet Antigen-2 Autoantibody Assays for National Institute of Diabetes and Digestive and Kidney Diseases Consortia [J].
Bonifacio, Ezio ;
Yu, Liping ;
Williams, Alastair K. ;
Eisenbarth, George S. ;
Bingley, Polly J. ;
Marcovina, Santica M. ;
Adler, Kerstin ;
Ziegler, Anette G. ;
Mueller, Patricia W. ;
Schatz, Desmond A. ;
Krischer, Jeffrey P. ;
Steffes, Michael W. ;
Akolkar, Beena .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2010, 95 (07) :3360-3367
[3]   A quantitative scale of acanthosis nigricans [J].
Burke, JP ;
Hale, DE ;
Hazuda, HP ;
Stern, MP .
DIABETES CARE, 1999, 22 (10) :1655-1659
[4]   Development, validation and use of an insulin sensitivity score in youths with diabetes: the SEARCH for Diabetes in Youth study [J].
Dabelea, D. ;
D'Agostino, R. B., Jr. ;
Mason, C. C. ;
West, N. ;
Hamman, R. F. ;
Mayer-Davis, E. J. ;
Maahs, D. ;
Klingensmith, G. ;
Knowler, W. C. ;
Nadeau, K. .
DIABETOLOGIA, 2011, 54 (01) :78-86
[5]   Type 2 diabetes mellitus in minority children and adolescents - An emerging problem [J].
Dabelea, D ;
Pettitt, DJ ;
Jones, KL ;
Arslanian, SA .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1999, 28 (04) :709-+
[6]  
Dabelea D, 2007, JAMA-J AM MED ASSOC, V297, P2716, DOI 10.1001/jama.297.24.2716
[7]   HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: Analysis of the Type 1 Diabetes Genetics Consortium families [J].
Erlich, Henry ;
Valdes, Ana Maria ;
Noble, Janelle ;
Carlson, Joyce A. ;
Varney, Mike ;
Concannon, Pat ;
Mychaleckyj, Josyf C. ;
Todd, John A. ;
Bonella, Persia ;
Fear, Anna Lisa ;
Lavant, Eva ;
Louey, Anthony ;
Moonsamy, Priscilla .
DIABETES, 2008, 57 (04) :1084-1092
[8]   Waist circumference percentiles in nationally representative samples of African-american, European-American, and Mexican-American children and adolescents [J].
Fernández, JR ;
Redden, DT ;
Pietrobelli, A ;
Allison, DB .
JOURNAL OF PEDIATRICS, 2004, 145 (04) :439-444
[9]   The rising incidence of type 1 diabetes is accounted for by cases with lower-risk human leukocyte antigen genotypes [J].
Fourlanos, Spiros ;
Varney, Michael D. ;
Tait, Brian D. ;
Morahan, Grant ;
Honeyman, Margo C. ;
Colman, Peter G. ;
Harrison, Leonard C. .
DIABETES CARE, 2008, 31 (08) :1546-1549
[10]   Declassifying diabetes [J].
Gale, E. A. M. .
DIABETOLOGIA, 2006, 49 (09) :1989-1995