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Abnormal screening glucose challenge test in pregnancy and future risk of diabetes in young women
Aims Pregnant women commonly undergo screening for gestational diabetes mellitus (GDM) using a 50‐g glucose challenge test (GCT), followed by a diagnostic oral glucose tolerance test (OGTT) in those women in whom the GCT is abnormal. Although it has long been recognized that GDM is associated with...
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Published in: | Diabetic medicine 2009-05, Vol.26 (5), p.474-477 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Aims Pregnant women commonly undergo screening for gestational diabetes mellitus (GDM) using a 50‐g glucose challenge test (GCT), followed by a diagnostic oral glucose tolerance test (OGTT) in those women in whom the GCT is abnormal. Although it has long been recognized that GDM is associated with subsequent Type 2 diabetes, it has recently emerged that any degree of abnormal antepartum glucose homeostasis predicts an increased risk of postpartum glucose intolerance. Thus, in this context, we sought to determine whether women who have a pregnancy complicated by an abnormal GCT, but who do not have GDM, are at increased risk of subsequent diabetes, compared with their peers with an abnormal GCT.
Methods A population‐based, retrospective cohort study was conducted. Women referred for an antepartum OGTT indicative of an abnormal GCT (n = 15 381), but without GDM, were matched (for age, region, socioeconomic status, and year of delivery) with up to four other women without such referral (n = 61 237). The two cohorts were followed over a median 6.4 years for the development of diabetes.
Results The rate of incident diabetes was 5.04 cases per 1000 person‐years in the cohort of women who underwent an antepartum OGTT, compared with 1.74 cases per 1000 person‐years in women without an OGTT. The hazard ratio for subsequent diabetes in women with an antepartum OGTT was 2.56 (95% confidence interval 2.28, 2.87) (P |
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ISSN: | 0742-3071 1464-5491 |
DOI: | 10.1111/j.1464-5491.2009.02712.x |