Glycemic Targets in the Second and Third Trimester of Pregnancy for Women With Type 1 Diabetes

被引:123
|
作者
Maresh, Michael J. A. [1 ]
Holmes, Valerie A. [2 ]
Patterson, Christopher C. [2 ]
Young, Ian S. [2 ]
Pearson, Donald W. M. [3 ]
Walker, James D. [4 ]
McCance, David R. [5 ]
机构
[1] Cent Manchester Univ Hosp NHS Fdn Trust, St Marys Hosp, Manchester Acad Hlth Sci Ctr, Dept Obstet, Manchester, Lancs, England
[2] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Ctr Publ Hlth, Belfast, Antrim, North Ireland
[3] Aberdeen Royal Infirm, Dept Diabet, Aberdeen, Scotland
[4] St Johns Hosp Howden, Dept Diabet, Livingston, West Lothian, Scotland
[5] Royal Victoria Hosp, Reg Ctr Endocrinol & Diabet, Belfast BT12 6BA, Antrim, North Ireland
基金
英国惠康基金;
关键词
GESTATIONAL-AGE INFANTS; BIRTH-WEIGHT; PREPREGNANCY CARE; METABOLIC-CONTROL; FETAL MACROSOMIA; GLUCOSE-LEVELS; HEMOGLOBIN; MELLITUS; HYPERTENSION; HBA(1C);
D O I
10.2337/dc14-1755
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE To assess the relationship between second and third trimester glycemic control and adverse outcomes in pregnant women with type 1 diabetes, as uncertainty exists about optimum glycemic targets. RESEARCH DESIGN AND METHODS Pregnancy outcomes were assessed prospectively in 725 women with type 1 diabetes from the Diabetes and Pre-eclampsia Intervention Trial. HbA(1c) (A1C) values at 26 and 34 weeks' gestation were categorized into five groups, the lowest, <6.0% (42 mmol/mol), being the reference. Average pre- and postprandial results from an eight-point capillary glucose profile the previous day were categorized into five groups, the lowest (preprandial <5.0 mmol/L and postprandial <6.0 mmol/L) being the reference. RESULTS An A1C of 6.0-6.4% (42-47 mmol/mol) at 26 weeks' gestation was associated with a significantly increased risk of large for gestational age (LGA) (odds ratio 1.7 [95% CI 1.0-3.0]) and an A1C of 6.5-6.9% (48-52 mmol/mol) with a significantly increased risk of preterm delivery (odds ratio 2.5 [95% CI 1.3-4.8]), preeclampsia (4.3 [1.7-10.8]), need for a neonatal glucose infusion (2.9 [1.5-5.6]), and a composite adverse outcome (3.2 [1.3-8.0]). These risks increased progressively with increasing A1C. Results were similar at 34 weeks' gestation. Glucose data showed less consistent trends, although the risk of a composite adverse outcome increased with preprandial glucose levels between 6.0 and 6.9 mmol/L at 34 weeks (3.3 [1.3-8.0]). CONCLUSIONS LGA increased significantly with an A1C >= 6.0 (42 mmol/mol) at 26 and 34 weeks' gestation and with other adverse outcomes with an A1C >= 6.5% (48 mmol/mol). The data suggest that there is clinical utility in regular measurement of A1C during pregnancy.
引用
收藏
页码:34 / 42
页数:9
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