The association of increased total glycosylated hemoglobin levels with delayed age at menarche in young women with type 1 diabetes

被引:57
作者
Danielson, KK [1 ]
Palta, M [1 ]
Allen, C [1 ]
D'Alessio, DJ [1 ]
机构
[1] Univ Wisconsin, Dept Populat Hlth Sci, Madison, WI 53726 USA
关键词
D O I
10.1210/jc.2005-0349
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Delayed menarche is associated with subsequent reproductive and skeletal complications. Previous research has found delayed growth and pubertal maturation with type 1 diabetes and poor glycemic control. The effect of diabetes management on menarche is important to clarify, because tighter control might prevent these complications. Objective: The objective of this study was to investigate age at menarche in young women with type 1 diabetes and examine the effect of diabetes management [e.g. total glycosylated hemoglobin (GHb) level, number of blood glucose checks, insulin therapy intensity, and insulin dose] on age at menarche in those diagnosed before menarche. Design: The Wisconsin Diabetes Registry Project is a follow-up study of a type 1 diabetes population-based incident cohort initially enrolled between 1987 and 1992. Setting: This study was performed in 28 counties in south-central Wisconsin. Patients or Other Participants: The study participants were recruited through referrals, self-report, and hospital/clinic ascertainment. Individuals with newly diagnosed type 1 diabetes, less than 30 yr old, were invited to participate. Of 288 young women enrolled, 188 reported menarche by 2002; 105 were diagnosed before menarche. Interventions: There were no interventions. Main Outcome Measure: The main outcome measure was age at menarche. Results: Mean age at menarche was 12.78 yr, compared with 12.54 yr in the United States (P = 0.01). Ages at menarche and diagnosis were not associated. For those diagnosed before menarche, age at menarche was delayed 1.3 months with each 1% increase in mean total GHb level in the 3 yr before menarche. Conclusions: Age at menarche was moderately delayed in young women with type 1 diabetes. Delayed menarche could potentially be minimized with improved GHb levels.
引用
收藏
页码:6466 / 6471
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]   Risk of irregular menstrual cycles and low peak bone mass during early adulthood associated with age at menarche [J].
Anai, T ;
Miyazaki, F ;
Tomiyasu, T ;
Matsuo, T .
PEDIATRICS INTERNATIONAL, 2001, 43 (05) :483-488
[3]   Relative weight and race influence average age at menarche: Results from two nationally representative surveys of US girls studied 25 years apart [J].
Anderson, SE ;
Dallal, GE ;
Must, A .
PEDIATRICS, 2003, 111 (04) :844-850
[4]  
BERGQVIST N, 1954, ACTA ENDOCRINOL-COP, V19, P3
[5]   MENARCHE, CYCLING AND FERTILITY IN DIABETIC WOMEN [J].
BURKART, W ;
FISCHERGUNTENHONER, E ;
STANDL, E ;
SCHNEIDER, HPG .
GEBURTSHILFE UND FRAUENHEILKUNDE, 1989, 49 (02) :149-154
[6]   PERIMENSTRUAL SYMPTOMS IN WOMEN WITH DIABETES-MELLITUS AND THE RELATIONSHIP TO DIABETIC CONTROL [J].
CAWOOD, EHH ;
BANCROFT, J ;
STEEL, JM .
DIABETIC MEDICINE, 1993, 10 (05) :444-448
[7]   Predictors of glycemic control in children with Type 1 diabetes - The importance of race [J].
Chalew, SA ;
Gomez, R ;
Butler, A ;
Hempe, J ;
Compton, T ;
Mercante, D ;
Rao, J ;
Vargas, A .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2000, 14 (02) :71-77
[8]   Age at menarche and racial comparisons in US girls [J].
Chumlea, WC ;
Schubert, CM ;
Roche, AF ;
Kulin, HE ;
Lee, PA ;
Himes, JH ;
Sun, SS .
PEDIATRICS, 2003, 111 (01) :110-113
[9]   CLINICAL AND HORMONAL CHARACTERISTICS IN WOMEN WITH ANOVULATION AND INSULIN-TREATED DIABETES-MELLITUS [J].
DJURSING, H ;
NYHOLM, HC ;
HAGEN, C ;
CARSTENSEN, L ;
PEDERSEN, LM .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1982, 143 (08) :876-882
[10]   SERUM SEX-HORMONE CONCENTRATIONS IN INSULIN DEPENDENT DIABETIC WOMEN WITH AND WITHOUT AMENORRHEA [J].
DJURSING, H ;
HAGEN, C ;
ANDERSEN, AN ;
SVENSTRUP, B ;
BENNETT, P ;
PEDERSEN, LM .
CLINICAL ENDOCRINOLOGY, 1985, 23 (02) :147-154