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Gestational Diabetes Mellitus: Screening and Outcomes in Southern Italian Pregnant Women

DOI: 10.1155/2013/387495

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Abstract:

Recent Italian guidelines exclude women <35 years old, without risk factors for gestational diabetes mellitus (GDM), from screening for GDM. To determine the effectiveness of these measures with respect to the International Association of the Diabetes and Pregnancy Study Groups (IADPSG) criteria, we evaluated 2,448 pregnant women retrospectively enrolled in Calabria, southern Italy. GDM was diagnosed following the IADPSG 2010 criteria. Among 538 women <35 years old, without risk factors, who would have not been tested according to the Italian guidelines, we diagnosed GDM in 171 (31.8%) pregnants (7.0% of total pregnants). Diagnosis was made at baseline (55.6%), 1 hour (39.8%), or 2 hours (4.7%) during OGTT. Despite of appropriate treatment, GDM represented a risk factor for cesarean section, polyhydramnios, increased birth weight, admission to neonatal intensive care units, and large for gestational age. These outcomes were similar to those observed in GDM women at high risk for GDM. In conclusion, Italian recommendations failed to identify 7.0% of women with GDM, when compared to IADPSG criteria. The risk for adverse hyperglycaemic-related outcomes is similar in low-risk and high-risk pregnants with GDM. To limit costs of GDM screening, our data suggest to restrict OGTT to two steps (baseline and 1 hour). 1. Introduction Gestational diabetes mellitus (GDM) is defined as any degree of glucose intolerance with onset or first recognition during pregnancy [1]. Incidence of GDM is increasing worldwide for recent trends in obesity and advancing maternal age, with huge healthcare and economic costs [2, 3]. Women exposed to GDM are at high risk for pregnancy complications [4–6], future type 2 diabetes mellitus (DM), and cardiovascular disease [7–9]. In particular, several lines of evidence indicate a continuum of risk for adverse pregnancy outcomes for mothers and their offsprings related to increasing maternal glucose levels [10, 11], whereas treatment to reduce maternal glucose levels reduces this risk [12–14]. Based on these evidences, to identify women at risk for adverse pregnancy outcomes and improve prognosis through evidence-based interventions, recent tight diagnostic criteria for GDM have been introduced by the International Association of the Diabetes and Pregnancy Study Groups (IADPSG) [15]. Diagnosis requires a 75?g oral glucose tolerance test (OGTT) carried out between 24 and 28 weeks of gestation in all women not previously found to have overt diabetes or GDM, considering glycaemia of 92?mg/dL at baseline, 180?mg/dL at 1?h, and 153?mg/dL at 2?h

References

[1]  American Diabetes Association, “Diagnosis and classification of diabetes mellitus,” Diabetes Care, vol. 32, supplement 1, pp. S62–S67, 2009.
[2]  K. J. Hunt and K. L. Schuller, “The increasing prevalence of diabetes in pregnancy,” Obstetrics and Gynecology Clinics of North America, vol. 34, no. 2, pp. 173–199, 2007.
[3]  L. L. Lipscombe and J. E. Hux, “Trends in diabetes prevalence, incidence, and mortality in Ontario, Canada 1995–2005: a population-based study,” The Lancet, vol. 369, no. 9563, pp. 750–756, 2007.
[4]  Yogev, Chen, Hod, et al., “Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: preeclampsia,” American Journal of Obstetrics & Gynecology, vol. 3, no. 202, pp. 255.e1–255.e7, 2010.
[5]  O. Verier-Mine, “Outcomes in women with a history of gestational diabetes. Screening and prevention of type 2 diabetes. Literature review,” Diabetes & metabolism, vol. 36, no. 6, part 2, pp. 595–616, 2010.
[6]  O. Langer and R. Mazze, “The relationship between large-for-gestational-age infants and glycemic control in women with gestational diabetes,” American Journal of Obstetrics and Gynecology, vol. 6, no. 159, pp. 1478–1483, 1988.
[7]  L. Bellamy, J. Casas, A. D. Hingorani, and D. Williams, “Type 2 diabetes mellitus after gestational diabetes: a systematic review and meta-analysis,” The Lancet, vol. 373, no. 9677, pp. 1773–1779, 2009.
[8]  S. I. Dawson, “Glucose tolerance in pregnancy and the long-term risk of cardiovascular disease,” Diabetes Research and Clinical Practice, vol. 85, no. 1, pp. 14–19, 2009.
[9]  S. D. Sullivan, J. G. Umans, and R. Ratner, “Gestational diabetes: implications for cardiovascular health,” Current Diabetes Reports, vol. 12, no. 1, pp. 43–52, 2012.
[10]  HAPO Study Cooperative Research Group, “The Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study,” International Journal of Gynecology & Obstetrics, vol. 78, no. 1, pp. 69–77, 2002.
[11]  L. P. Lowe, B. E. Metzger, A. R. Dyer, et al., “Hyperglycemia and adverse pregnancy outcomes,” The New England Journal of Medicine, vol. 358, no. 19, pp. 1991–2002, 2008.
[12]  M. B. Landon, C. Y. Spong, E. Thom et al., “A multicenter, randomized trial of treatment for mild gestational diabetes,” The New England Journal of Medicine, vol. 361, no. 14, pp. 1339–1348, 2009.
[13]  C. A. Crowther, J. E. Hiller, J. R. Moss, A. J. McPhee, W. S. Jeffries, and J. S. Robinson, “Effect of treatment of gestational diabetes mellitus on pregnancy outcomes,” The New England Journal of Medicine, vol. 352, no. 24, pp. 2477–2486, 2005.
[14]  M. Falavigna, M. I. Schmidt, J. Trujillo, et al., “Effectiveness of gestational diabetes treatment: a systematic review with quality of evidence assessment,” Diabetes Research and Clinical Practice, vol. 98, no. 3, pp. 396–405, 2012.
[15]  International Association Of Diabetes And Pregnancy Study Groups Consensus Panel, “International Association of Diabetes and Pregnancy Study Groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy,” Diabetes Care, vol. 33, no. 3, pp. 676–682, 2010.
[16]  E. P. O'Sullivan, G. Avalos, M. O'Reilly, M. C. Dennedy, G. Gaffney, and F. Dunne, “Atlantic Diabetes in Pregnancy (DIP): the prevalence and outcomes of gestational diabetes mellitus using new diagnostic criteria,” Diabetologia, vol. 54, no. 7, pp. 1670–1675, 2011.
[17]  B. S. Buckley, J. Harreiter, P. Damm, et al., “Gestational diabetes mellitus in Europe: prevalence, current screening practice and barriers to screening. A review,” Diabetic Medicine, vol. 29, no. 7, pp. 844–854, 2012.
[18]  O. Kalter-Leibovici, L. S. Freedman, L. Olmer, et al., “Screening and diagnosis of gestational diabetes mellitus: critical appraisal of the new International Association of Diabetes in Pregnancy Study Group recommendations on a national level,” Diabetes Care, vol. 35, no. 9, pp. 1894–1896, 2012.
[19]  D. A. Sacks, D. R. Hadden, M. Maresh, et al., “Frequency of gestational diabetes mellitus at collaborating centers based on IADPSG consensus panel-recommended criteria: the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study,” Diabetes Care, vol. 35, no. 3, pp. 526–528, 2012.
[20]  R. G. Moses, G. J. Morris, P. Petocz, F. Sangil, and D. Garg, “The impact of potential new diagnostic criteria on the prevalence of gestational diabetes mellitus in Australia,” The Medical Journal of Australia, vol. 194, no. 7, pp. 338–340, 2011.
[21]  E. A. Ryan, “Diagnosing gestational diabetes,” Diabetologia, vol. 54, no. 3, pp. 480–486, 2011.
[22]  H. Long, “Diagnosing gestational diabetes: can expert opinions replace scientific evidence?” Diabetologia, vol. 54, no. 9, pp. 2211–2213, 2011.
[23]  R. G. Moses, “Gestational diabetes mellitus: implications of an increased frequency with IADPSG criteria,” Diabetes Care, vol. 35, no. 3, pp. 461–462, 2012.
[24]  T. Cundy, “Proposed new diagnostic criteria for gestational diabetes—a pause for thought?” Diabetic Medicine, vol. 29, no. 2, pp. 176–180, 2012.
[25]  E. M. Wendland, M. R. Torloni, M. Falavigna et al., “Gestational diabetes and pregnancy outcomes—a systematic review of the World Health Organization (WHO) and the International Association of Diabetes in Pregnancy Study Groups (IADPSG) diagnostic criteria,” BMC Pregnancy and Childbirth, vol. 12, article 23, 2012.
[26]  E. F. Werner, C. M. Pettker, L. Zuckerwise, et al., “Screening for gestational diabetes mellitus: are the criteria proposed by the International Association of the Diabetes and Pregnancy Study Groups cost-effective?” Diabetes Care, vol. 35, no. 3, pp. 529–535, 2012.
[27]  American Diabetes Association, “Standards of medical care in diabetes—2011,” Diabetes Care, vol. 34, supplement 1, pp. S4–S10, 2011.
[28]  Committee on Obstetric Practice, “Screening and diagnosis of gestational diabetes mellitus,” Obstetrics & Gynecology, vol. 118, no. 3, pp. 751–753, 2011.
[29]  C. Capula, E. Chiefari, A. Vero, et al., “Predictors of postpartum glucose tolerance testing in Italian women with gestational diabetes mellitus,” ISRN Endocrinology, vol. 2013, Article ID 182505, 6 pages, 2013.
[30]  American Diabetes Association, “Gestational diabetes mellitus,” Diabetes Care, vol. 26, no. supplement 1, pp. S103–S105, 2003.
[31]  G. R. Alexander, M. D. Kogan, and J. H. Himes, “1994–1996 U.S. singleton birth weight percentiles for gestational age by race, Hispanic origin, and gender,” Maternal and Child Health Journal, vol. 3, no. 4, pp. 225–231, 1999.
[32]  C. P. Durnwald, L. Mele, C. Y. Spong et al., “Glycemic characteristics and neonatal outcomes of women treated for mild gestational diabetes,” Obstetrics and Gynecology, vol. 117, no. 4, pp. 819–827, 2011.
[33]  A. Lapolla, M. G. Dalfrà, M. Bonomo et al., “Gestational diabetes mellitus in Italy: a multicenter study,” European Journal of Obstetrics Gynecology and Reproductive Biology, vol. 145, no. 2, pp. 149–153, 2009.
[34]  E. Cosson, A. Benbara, I. Pharisien, et al., “Diagnostic and prognostic performances over 9 years of a selective screening strategy for gestational diabetes mellitus in a cohort of 18, 775 subjects,” Diabetes Care, vol. 36, no. 3, pp. 598–603, 2013.
[35]  G. E. Avalos, L. A. Owens, and F. Dunne, “Applying current screening tools for gestational diabetes mellitus to a European population—is it time for change?” Diabetes Care, 2013.
[36]  P. M. Catalano, H. D. McIntyre, J. K. Cruickshank, et al., “The Hyperglycemia and adverse pregnancy outcome study. Associations of GDM and obesity with pregnancy outcomes,” Diabetes Care, vol. 35, no. 4, pp. 780–786, 2012.
[37]  HAPO Study Cooperative Research Group, “Hyperglycaemia and adverse pregnancy outcome (HAPO) study: associations with maternal body mass index,” BJOG, vol. 117, no. 5, pp. 575–584, 2010.
[38]  A. Lapolla, M. Bonomo, M. G. Dalfrà et al., “Prepregnancy BMI influences maternal and fetal outcomes in women with isolated gestational hyperglycaemia: a multicentre study,” Diabetes and Metabolism, vol. 36, no. 4, pp. 265–270, 2010.
[39]  M. C. Dennedy, G. Avalos, M. W. O'Reilly, E. P. O'Sullivan, G. Gaffney, and F. Dunne, “ATLANTIC-DIP: raised maternal body mass index (BMI) adversely affects maternal and fetal outcomes in glucose-tolerant women according to International Association of Diabetes and Pregnancy Study Groups (IADPSG) criteria,” Journal of Clinical Endocrinology and Metabolism, vol. 97, no. 4, pp. E608–E612, 2012.

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