TY - JOUR
T1 - ATLANTIC DIP
T2 - Simplifying the follow-up of women with previous gestational diabetes
AU - Noctor, E.
AU - Crowe, C.
AU - Carmody, L. A.
AU - Avalos, G. M.
AU - Kirwan, B.
AU - Infanti, J. J.
AU - O'Dea, A.
AU - Gillespie, P.
AU - Newell, J.
AU - McGuire, B.
AU - O'Neill, C.
AU - O'Shea, P. M.
AU - Dunne, F. P.
PY - 2013/11
Y1 - 2013/11
N2 - Objective: Previous gestational diabetes (GDM) is associated with a significant lifetime risk of type 2 diabetes. In this study, we assessed the performance of HbA1c and fasting plasma glucose (FPG) measurements against that of 75 g oral glucose tolerance testing (OGTT) for the follow-up screening of women with previous GDM. Methods: Two hundred and sixty-six women with previous GDM underwent the follow-up testing (mean of 2.6 years (S.D. 1.0) post-index pregnancy) using HbA1c (100%), and 75 g OGTT (89%) or FPG (11%). American Diabetes Association (ADA) criteria for abnormal glucose tolerance were used. Design, cohort study, and results: The ADA HbA1c high-risk cut-off of 39 mmol/mol yielded sensitivity of 45% (95% CI 32, 59), specificity of 84% (95% CI 78, 88), negative predictive value (NPV) of 87% (95% CI 82, 91) and positive predictive value (PPV) of 39% (95% CI 27, 52) for detecting abnormal glucose tolerance. ADA high-risk criterion for FPG of 5.6 mmol/l showed sensitivity of 80% (95% CI 66, 89), specificity of 100% (95% CI 98, 100), NPVof 96% (95% CI 92, 98) and PPVof 100% (95% CI 91, 100). Combining HbA1c ≥39 mmol/mol with FPG≥5.6 mmol/l yielded sensitivity of90%(95% CI 78, 96), specificity of 84% (95% CI 78, 88), NPVof 97% (95% CI 94, 99) and PPVof 56% (95% CI 45, 66). Conclusions: Combining test cut-offs of 5.6 mmol/l and HbA1c 39 mmol/mol identifies 90% of women with abnormal glucose tolerance post-GDM (mean 2.6 years (S.D.1.0) post-index pregnancy). Applying this follow-up strategy will reduce the number of OGTT tests required by 70%, will be more convenient forwomen and their practitioners, and is likely to lead to increased uptake of long-term retesting by these women whose risk for type 2 diabetes is substantially increased.
AB - Objective: Previous gestational diabetes (GDM) is associated with a significant lifetime risk of type 2 diabetes. In this study, we assessed the performance of HbA1c and fasting plasma glucose (FPG) measurements against that of 75 g oral glucose tolerance testing (OGTT) for the follow-up screening of women with previous GDM. Methods: Two hundred and sixty-six women with previous GDM underwent the follow-up testing (mean of 2.6 years (S.D. 1.0) post-index pregnancy) using HbA1c (100%), and 75 g OGTT (89%) or FPG (11%). American Diabetes Association (ADA) criteria for abnormal glucose tolerance were used. Design, cohort study, and results: The ADA HbA1c high-risk cut-off of 39 mmol/mol yielded sensitivity of 45% (95% CI 32, 59), specificity of 84% (95% CI 78, 88), negative predictive value (NPV) of 87% (95% CI 82, 91) and positive predictive value (PPV) of 39% (95% CI 27, 52) for detecting abnormal glucose tolerance. ADA high-risk criterion for FPG of 5.6 mmol/l showed sensitivity of 80% (95% CI 66, 89), specificity of 100% (95% CI 98, 100), NPVof 96% (95% CI 92, 98) and PPVof 100% (95% CI 91, 100). Combining HbA1c ≥39 mmol/mol with FPG≥5.6 mmol/l yielded sensitivity of90%(95% CI 78, 96), specificity of 84% (95% CI 78, 88), NPVof 97% (95% CI 94, 99) and PPVof 56% (95% CI 45, 66). Conclusions: Combining test cut-offs of 5.6 mmol/l and HbA1c 39 mmol/mol identifies 90% of women with abnormal glucose tolerance post-GDM (mean 2.6 years (S.D.1.0) post-index pregnancy). Applying this follow-up strategy will reduce the number of OGTT tests required by 70%, will be more convenient forwomen and their practitioners, and is likely to lead to increased uptake of long-term retesting by these women whose risk for type 2 diabetes is substantially increased.
UR - https://www.scopus.com/pages/publications/84886242426
U2 - 10.1530/EJE-13-0491
DO - 10.1530/EJE-13-0491
M3 - Article
SN - 0804-4643
VL - 169
SP - 681
EP - 687
JO - European Journal of Endocrinology
JF - European Journal of Endocrinology
IS - 5
ER -