Clinical characteristics of children diagnosed with type 1 diabetes through intensive screening and follow-up

被引:138
作者
Barker, JM
Goehrig, SH
Barriga, K
Hoffman, M
Slover, R
Eisenbarth, GS
Norris, JM
Klingensmith, GJ
Rewers, M
机构
[1] Univ Colorado, Hlth Sci Ctr, Barbara Davis Ctr Childhood Diabet, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Prevent Med & Biometr, Denver, CO 80262 USA
关键词
D O I
10.2337/diacare.27.6.1399
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - The objective of this study was to determine whether earlier diagnosis of diabetes in prospectively followed autoantibody-positive children lowered onset morbidity and improved the clinical course after diagnosis. RESEARCH DESIGN AND METHODS - The Diabetes Autoimmunity Study in the Young (DAISY) follows genetically at-risk children for the development of diabetes. Increased genetic risk is identified by family history of type 1 diabetes or expression of diabetes-associated HLA genotypes. Of the 2,140 prospectively followed children, 112 have developed islet auto-antibodies and 30 have progressed to diabetes. Diabetes onset characteristics and early clinical course of these 30 children followed to diabetes were compared with those of 101 age- and sex-matched children concurrently diagnosed with diabetes in the community. RESULTS - Pre-diabetic children followed to diabetes were less often hospitalized than the community cases (3.3 vs. 44%; P < 0.0001). They had a lower mean HbA(1c) at onset (7.2 vs. 10.9%; P < 0.0001) and 1 month after diagnosis (6.9 vs. 8.6%; P < 0.0001) but not after 6 months of diabetes. The mean insulin dose was lower in the DAISY group at 1 (0.30 vs. 0.51 U (.) kg(-1) (.) day(-1); P = 0.003), 6 (0.37 vs. 0.58; P = 0.001), and 12 months (0.57 vs. 0.72; P = 0.03). There was no difference in growth parameters between the two groups. Comparisons limited to children with a family history of type 1 diabetes in both groups showed a similar pattern. 1 CONCLUSIONS - Childhood type 1 diabetes diagnosed through a screening and follow-up program has a less severe onset and a milder clinical course in the first year after diagnosis.
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页码:1399 / 1404
页数:6
相关论文
共 34 条
[1]  
[Anonymous], 1995, DIAB AM
[2]  
BENNETT JS, 1995, DIABETES CARE, V18, P1370
[3]   Prediction of IDDM in the general population - Strategies based on combinations of autoantibody markers [J].
Bingley, PJ ;
Bonifacio, E ;
Williams, AJK ;
Genovese, S ;
Bottazzo, GF ;
Gale, EAM .
DIABETES, 1997, 46 (11) :1701-1710
[4]   Type 1 diabetes mellitus in Czech children diagnosed in 1990-1997:: a significant increase in incidence and male predominance in the age group 0-4 years [J].
Cinek, O ;
Lánská, V ;
Kolousková, S ;
Sumník, Z ;
Snajderová, M ;
Ronningen, KS ;
Vavrinec, J .
DIABETIC MEDICINE, 2000, 17 (01) :64-69
[5]  
Cunniff C, 2000, PEDIATRICS, V106, P1494
[6]  
EISENBARTH GS, 1986, NEW ENGL J MED, V314, P1360
[7]  
Galatzer A, 2001, J PEDIATR ENDOCR MET, V14, P675
[8]   CAN WE PREVENT IDDM [J].
GALE, EAM ;
BINGLEY, PJ .
DIABETES CARE, 1994, 17 (04) :339-344
[9]   Progression to diabetes in relatives with islet autoantibodies - Is it inevitable [J].
Gardner, SG ;
Gale, EAM ;
Williams, AJK ;
Gillespie, KM ;
Lawrence, KE ;
Bottazzo, GF ;
Bingley, PJ .
DIABETES CARE, 1999, 22 (12) :2049-2054
[10]   Rising incidence of insulin dependent diabetes in children aged under 5 years in the Oxford region: time trend analysis [J].
Gardner, SG ;
Bingley, PJ ;
Sawtell, PA ;
Weeks, S ;
Gale, EAM ;
Bell, RAF ;
Dunger, DB ;
Mukhtar, A ;
OMalley, BP ;
Silk, BR ;
Smith, EH ;
Scott, RDM ;
Latham, PJ ;
Lakhani, PK ;
Paton, RC ;
Ackland, FM ;
Fox, CJ ;
Griffin, NK ;
Matthews, DR ;
Neil, HAW ;
Mann, NP ;
Simpson, HCR ;
Brown, RS ;
Knight, AH ;
Cowen, JM ;
Pearce, JC ;
Cheetham, CH ;
Gallen, IW ;
Sandler, L ;
Westcott, T .
BRITISH MEDICAL JOURNAL, 1997, 315 (7110) :713-717