Teenage girls with type 1 diabetes have poorer metabolic control than boys and face more complications in early adulthood

被引:37
作者
Samuelsson, Ulf [1 ]
Anderzen, Johan [2 ]
Gudbjornsdottir, Soffia [3 ]
Steineck, Isabelle [4 ]
Akesson, Karin [2 ,5 ]
Hanberger, Lena [6 ]
机构
[1] Linkoping Univ, Div Paediat, Dept Clin & Expt Med, Linkoping, Sweden
[2] Ryhov Cty Hosp, Dept Paediat, Jonkoping, Sweden
[3] Univ Gothenburg, Dept Med, Sahlgrenska Acad, Gothenburg, Sweden
[4] Copenhagen Univ Hosp, Dept Endocrinol, Hvidovre, Denmark
[5] Jonkoping Cty Council, Futurum Acad Hlth & Care, Gothenburg, Sweden
[6] Linkoping Univ, Div Nursing, Dept Med & Hlth Sci, Linkoping, Sweden
关键词
HbA1c; Type; 1; diabetes; Gender; Microvascular complications; Quality of care; GLYCEMIC CONTROL; CHILDREN; ADOLESCENTS; DIAGNOSIS; GENDER; CHILDHOOD; MORTALITY; ONSET; RISK; SEX;
D O I
10.1016/j.jdiacomp.2016.02.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: To compare metabolic control between males and females with type 1 diabetes during adolescence and as young adults, and relate it to microvascular complications. Methods: Data concerning 4000 adolescents with type 1 diabetes registered in the Swedish paediatric diabetes quality registry, and above the age of 18 years in the Swedish National Diabetes Registry was used. Results: When dividing HbA1c values in three groups; < 7.4% (57 mmol/mol), 7.4-93% (57-78 mmol/mol) and >9.3% (78 mmol/mol), there was a higher proportion of females in the highest group during adolescence. In the group with the highest HbA1c values during adolescence and as adults, 51.7% were females, expected value 46.2%; in the group with low HbA1c values in both registries, 34.2% were females, p < 0.001. As adults, more females had retinopathy, p < 0.05. Females had higher mean HbAlc values at diagnosis, 112 vs. 10.9% (99 vs. 96 mmol/mol), p < 0.03, during adolescence, 8.5 vs. 82% (69 vs. 66 mmol/mol) p < 0.01, but not as young adults. Conclusions: Worse glycaemic control was found in adolescent females, and they had a higher frequency of microvascular complications. Improved paediatric diabetes care is of great importance for increasing the likelihood of lower mortality and morbidity later in life. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:917 / 922
页数:6
相关论文
共 39 条
[1]   Pubertal growth in IDDM is determined by HbA1c levels, sex, and bone age [J].
Ahmed, ML ;
Connors, MH ;
Drayer, NM ;
Jones, JS ;
Dunger, DB .
DIABETES CARE, 1998, 21 (05) :831-835
[2]  
[Anonymous], SWED PAED DIAB QUAL
[3]  
[Anonymous], NAT DIAB REG ANN REP
[4]  
[Anonymous], BR MED J
[5]  
[Anonymous], PEDIAT DIABETES
[6]   Incidence and trends of childhood Type 1 diabetes worldwide 1990-1999 [J].
Bessaoud, K. ;
Boudraa, G. ;
Molinero de Ropolo, M. ;
de Sereday, M. ;
Marti, M. L. ;
Moser, M. ;
Lapertosa, S. ;
Damiano, M. ;
Verge, C. ;
Howard, N. ;
Schober, E. ;
Jordan, O. ;
Weets, I. ;
Gorus, F. ;
Coeckelberghs, M. ;
Rooman, R. ;
Van Gaal, L. ;
Franco, L. J. ;
Ferreira, S. R. G. ;
Lisboa, H. P. K. ;
Kurtz, L. A. ;
Graebin, R. ;
Kutzke, L. ;
Rodriges, C. ;
Savova, R. ;
Christov, V. ;
Iotova, V. ;
Tzaneva, V. ;
Pacaud, D. ;
Toth, E. ;
Tan, M. H. ;
Carrasco, E. ;
Perez, F. ;
Ze, Y. ;
Bo, Y. ;
Chen, S. ;
Fu, L. ;
Deng, L. ;
Shen, S. ;
Teng, K. ;
Wang, C. ;
Jian, H. ;
Ju, J. ;
Yan, C. ;
Ze, Y. ;
Deng, Y. ;
Li, C. ;
Zhang, Y. ;
Liu, Y. ;
Long, X. .
DIABETIC MEDICINE, 2006, 23 (08) :857-866
[7]   Diabetes care provision and glycaemic control in Northern Ireland: a UK regional audit [J].
Cardwell, CR ;
Patterson, CC ;
Allen, M ;
Carson, DJ .
ARCHIVES OF DISEASE IN CHILDHOOD, 2005, 90 (05) :468-473
[8]   Deteriorating diabetic control through adolescence - do the origins lie in childhood? [J].
Dabadghao, P ;
Vidmar, S ;
Cameron, FJ .
DIABETIC MEDICINE, 2001, 18 (11) :889-894
[9]   Hospitalization for vascular complications in childhood onset type 1 diabetes -: effects of gender and age at onset [J].
Dahlquist, G. ;
Mollsten, A. ;
Kallen, B. .
ACTA PAEDIATRICA, 2008, 97 (04) :483-488
[10]   Beneficial effects of intensive therapy of diabetes during adolescence: Outcomes after the conclusion of the Diabetes Control and Complications Trial (DCCT) [J].
Genuth, S ;
Nathan, D ;
Shamoon, H ;
Duffy, H ;
Engel, S ;
Engel, H ;
Dahms, W ;
Mayer, L ;
Pendegras, S ;
Zegarra, H ;
Miller, D ;
Singerman, L ;
Brillion, D ;
Lackaye, M ;
Heinemann, M ;
Rahhal, F ;
Reppuci, V ;
Lee, T ;
Whitehouse, F ;
Kruger, D ;
Carey, JD ;
Bergenstal, R ;
Johnson, M ;
Kendall, D ;
Spencer, M ;
Noller, D ;
Morgan, K ;
Etzwiler, D ;
Jacobson, A ;
Golden, E ;
Soroko, D ;
Sharuk, G ;
Arrigg, P ;
Doyle, J ;
Nathan, D ;
Fritz, S ;
Crowell, S ;
Godine, J ;
McKitrick, C ;
Lou, P ;
Service, J ;
Ziegler, G ;
Pach, J ;
Colwell, J ;
Wood, D ;
Mayfield, R ;
Hermayer, K ;
Szpiech, M ;
Lyons, T ;
Parker, J .
JOURNAL OF PEDIATRICS, 2001, 139 (06) :804-812