期刊论文详细信息
BMC Endocrine Disorders
HbA1c as screening for gestational diabetes mellitus in women with polycystic ovary syndrome
Sven Magnus Carlsen4  Eszter Vanky2  Arne Åsberg1  Ingrid Hov Odsæter3 
[1] Department of Clinical Chemistry, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway;Department of Laboratory Medicine, Children’s and Women’s Health, Trondheim, Norway;Department of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway;Unit for Applied Clinical Research, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway
关键词: Birth weight;    Preeclampsia;    HbA1c;    Polycystic ovary syndrome;    Gestational diabetes mellitus;   
Others  :  1222362
DOI  :  10.1186/s12902-015-0039-9
 received in 2015-03-08, accepted in 2015-07-29,  发布年份 2015
PDF
【 摘 要 】

Background

Gestational diabetes mellitus (GDM) is associated with adverse pregnancy outcomes such as preeclampsia and macrosomia. Women with polycystic ovary syndrome (PCOS) are at increased risk of developing GDM. Today, GDM is diagnosed by oral glucose tolerance test (OGTT), a rather cumbersome test for the women and health care system. The objectives of this study were to investigate whether HbA1c in first trimester of pregnancy could be used as a screening test for GDM in first trimester and throughout pregnancy in order to reduce the number of OGTTs, and whether it could predict preeclampsia and macrosomia in women with PCOS.

Methods

Post hoc analyses of data from 228 women from a prospective, randomised, multicenter study comparing metformin to placebo from first trimester to delivery. Fasting and 2-h plasma glucose were measured during a 75 g OGTT in first trimester, gestational week 19 and 32 as well as fasting plasma glucose in gestational week 36. GDM was diagnosed by WHO criteria from 1999 in first trimester and throughout pregnancy and by modified IADPSG criteria (i.e. lacking the 1-h plasma glucose value) in first trimester. The diagnostic accuracy was assessed by logistic regression and ROC curve analysis.

Results

The area under the ROC curve for first trimester HbA1c for screening of GDM diagnosed by WHO criteria in first trimester was 0.60 (95 % CI 0.44-0.75) and 0.56 (95 % CI 0.47-0.65) for GDM diagnosed throughout pregnancy. Only 2.2 % (95 % CI 0.7-5.1 %) of the participants could have avoided OGTT. HbA1c was not statistically significantly associated with GDM diagnosed by modified IADPSG criteria in first trimester. However, first trimester HbA1c was statistically significantly associated with preeclampsia. Both HbA1c and GDM by WHO criteria in first trimester, but not by IADPSG, were negatively associated with birth weight.

Conclusion

First trimester HbA1c can not be used to exclude or predict GDM in women with PCOS, but it might be better to predict preeclampsia than the GDM diagnosis.

【 授权许可】

   
2015 Odsæter et al.

【 预 览 】
附件列表
Files Size Format View
20150820011135770.pdf 454KB PDF download
Fig. 1. 24KB Image download
【 图 表 】

Fig. 1.

【 参考文献 】
  • [1]Diagnostic Criteria and Classification of Hyperglycaemia First Detected in Pregnancy. World Health Organization, Geneva; 2013.
  • [2]Houshmand A, Jensen DM, Mathiesen ER, Damm P. Evolution of diagnostic criteria for gestational diabetes mellitus. Acta Obstet Gynecol Scand. 2013; 92:739-45.
  • [3]International Expert Committee report on the role of the A1C assay in the diagnosis of diabetes. Diabetes Care. 2009; 32:1327-34.
  • [4]Agarwal MM, Hughes PF, Punnose J, Ezimokhai M, Thomas L. Gestational diabetes screening of a multiethnic, high-risk population using glycated proteins. Diabetes Res Clin Pract. 2001; 51:67-73.
  • [5]Agarwal MM, Dhatt GS, Punnose J, Koster G. Gestational diabetes: a reappraisal of HBA1c as a screening test. Acta Obstet Gynecol Scand. 2005; 84:1159-63.
  • [6]O'Shea P, O'Connor C, Owens L, Carmody L, Avalos G, Nestor L et al.. Trimester-specific reference intervals for IFCC standardised haemoglobin A(1c): new criterion to diagnose gestational diabetes mellitus (GDM)? Ir Med J. 2012; 105(5 Suppl):29-31.
  • [7]Aldasouqi SA, Solomon DJ, Bokhari SA, Khan PM, Muneera S, Gossain VV. Glycohemoglobin A1c: a promising screening tool in gestational diabetes mellitus. Int J Diabetes Dev Ctries. 2008; 28:121-4.
  • [8]Rajput R, Yogesh Y, Rajput M, Nanda S. Utility of HbA1c for diagnosis of gestational diabetes mellitus. Diabetes Res Clin Pract. 2012; 98:104-7.
  • [9]Maegawa Y, Sugiyama T, Kusaka H, Mitao M, Toyoda N. Screening tests for gestational diabetes in Japan in the 1st and 2nd trimester of pregnancy. Diabetes Res Clin Pract. 2003; 62:47-53.
  • [10]Sevket O, Sevket A, Ozel A, Dansuk R, Kelekci S. The use of HbA1c as an aid in the diagnosis of gestational diabetes mellitus. J Obstet Gynaecol. 2014; 34:690-2.
  • [11]Fong A, Serra AE, Gabby L, Wing DA, Berkowitz KM. Use of hemoglobin A1c as an early predictor of gestational diabetes mellitus. Am J Obstet Gynecol. 2014; 211:641.e1-7.
  • [12]Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS). Hum Reprod. 2004; 19:41-7.
  • [13]Eilertsen TB, Vanky E, Carlsen SM. Increased prevalence of diabetes and polycystic ovary syndrome in women with a history of preterm birth: a case-control study. BJOG. 2012; 119:266-75.
  • [14]Yildiz BO, Bozdag G, Yapici Z, Esinler I, Yarali H. Prevalence, phenotype and cardiometabolic risk of polycystic ovary syndrome under different diagnostic criteria. Hum Reprod. 2012; 27:3067-73.
  • [15]March WA, Moore VM, Willson KJ, Phillips DI, Norman RJ, Davies MJ. The prevalence of polycystic ovary syndrome in a community sample assessed under contrasting diagnostic criteria. Hum Reprod. 2010; 25:544-51.
  • [16]Moran LJ, Misso ML, Wild RA, Norman RJ. Impaired glucose tolerance, type 2 diabetes and metabolic syndrome in polycystic ovary syndrome: a systematic review and meta-analysis. Hum Reprod Update. 2010; 16:347-63.
  • [17]Ghazeeri GS, Nassar AH, Younes Z, Awwad JT. Pregnancy outcomes and the effect of metformin treatment in women with polycystic ovary syndrome: an overview. Acta Obstet Gynecol Scand. 2012; 91:658-78.
  • [18]Roos N, Kieler H, Sahlin L, Ekman-Ordeberg G, Falconer H, Stephansson O. Risk of adverse pregnancy outcomes in women with polycystic ovary syndrome: population based cohort study. BMJ. 2011; 343:d6309.
  • [19]Kjerulff LE, Sanchez-Ramos L, Duffy D. Pregnancy outcomes in women with polycystic ovary syndrome: a metaanalysis. Am J Obstet Gynecol. 2011; 204:558 e551-556.
  • [20]Boomsma CM, Eijkemans MJ, Hughes EG, Visser GH, Fauser BC, Macklon NS. A meta-analysis of pregnancy outcomes in women with polycystic ovary syndrome. Hum Reprod Update. 2006; 12:673-83.
  • [21]Helseth R, Vanky E, Salvesen O, Carlsen SM. Gestational diabetes mellitus among Norwegian women with polycystic ovary syndrome: prevalence and risk factors according to the WHO and the modified IADPSG criteria. Eur J Endocrinol. 2013; 169:65-72.
  • [22]Metzger BE, Gabbe SG, Persson B, Buchanan TA, Catalano PA et al.. International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care. 2010; 33:676-682.
  • [23]Vanky E, Stridsklev S, Heimstad R, Romundstad P, Skogoy K, Kleggetveit O et al.. Metformin versus placebo from first trimester to delivery in polycystic ovary syndrome: a randomized, controlled multicenter study. J Clin Endocrinol Metab. 2010; 95:E448-55.
  • [24]Definition, Diagnosis and Classification of Diabetes Mellitus and its Complications. Part 1: Diagnosis and Classification of Diabetes Mellitus. World Health Organization, Geneva; 1999.
  • [25]Rolandsson O, Marklund SL, Norberg M, Agren A, Hagg E. Hemoglobin A1c can be analyzed in blood kept frozen at -80 °C and is not commonly affected by hemolysis in the general population. Metabolism. 2004; 53:1496-9.
  • [26]Selvin E, Coresh J, Jordahl J, Boland L, Steffes MW. Stability of haemoglobin A1c (HbA1c) measurements from frozen whole blood samples stored for over a decade. Diabet Med. 2005; 22:1726-30.
  • [27]Barrot A, Dupuy AM, Badiou S, Bargnoux AS, Cristol JP. Evaluation of three turbidimetric assays for automated determination of hemoglobin A1c. Clin Lab. 2012; 58:1171-7.
  • [28]Jeppsson JO, Kobold U, Barr J, Finke A, Hoelzel W, Hoshino T et al.. Approved IFCC reference method for the measurement of HbA1c in human blood. Clin Chem Lab Med. 2002; 40:78-89.
  • [29]Metz CE. Basic principles of ROC analysis. Semin Nucl Med. 1978; 8:283-98.
  • [30]Royston P, Sauerbrei W. Building multivariable regression models with continuous covariates in clinical epidemiology--with an emphasis on fractional polynomials. Methods Inf Med. 2005; 44:561-71.
  • [31]Hughes RC, Moore MP, Gullam JE, Mohamed K, Rowan J. An early pregnancy HbA1c >/=5.9 % (41 mmol/mol) is optimal for detecting diabetes and identifies women at increased risk of adverse pregnancy outcomes. Diabetes Care. 2014; 37:2953-9.
  • [32]Lowe LP, Metzger BE, Dyer AR, Lowe J, McCance DR, Lappin TR et al.. Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study: associations of maternal A1C and glucose with pregnancy outcomes. Diabetes Care. 2012; 35:574-80.
  • [33]Catalano PM, Avallone DA, Drago NM, Amini SB. Reproducibility of the oral glucose tolerance test in pregnant women. Am J Obstet Gynecol. 1993; 169:874-81.
  • [34]Harlass FE, Brady K, Read JA. Reproducibility of the oral glucose tolerance test in pregnancy. Am J Obstet Gynecol. 1991; 164:564-8.
  • [35]Legro RS. Metformin during pregnancy in polycystic ovary syndrome: another vitamin bites the dust. J Clin Endocrinol Metab. 2010; 95:5199-202.
  • [36]Fougner KJ, Vanky E, Carlsen SM. Metformin has no major effects on glucose homeostasis in pregnant women with PCOS: results of a randomized double-blind study. Scand J Clin Lab Invest. 2008; 68:771-6.
  • [37]Helseth R, Salvesen O, Stafne SN, Morkved S, Salvesen KA, Carlsen SM: Gestational diabetes mellitus among Nordic Caucasian women: Prevalence and risk factors according to WHO and simplified IADPSG criteria. Scand J Clin Lab Invest. 2014;74:620-8.
  • [38]Jenum AK, Morkrid K, Sletner L, Vangen S, Torper JL, Nakstad B et al.. Impact of ethnicity on gestational diabetes identified with the WHO and the modified International Association of Diabetes and Pregnancy Study Groups criteria: a population-based cohort study. Eur J Endocrinol. 2012; 166:317-24.
  • [39]Claesson R, Ekelund M, Berntorp K. The potential impact of new diagnostic criteria on the frequency of gestational diabetes mellitus in Sweden. Acta Obstet Gynecol Scand. 2013; 92:1223-6.
  • [40]O'Sullivan EP, Avalos G, O'Reilly M, Dennedy MC, Gaffney G, Dunne F. Atlantic Diabetes in Pregnancy (DIP): the prevalence and outcomes of gestational diabetes mellitus using new diagnostic criteria. Diabetologia. 2011; 54:1670-5.
  • [41]Nallaperumal S, Bhavadharini B, Mahalakshmi MM, Maheswari K, Jalaja R, Moses A et al.. Comparison of the world health organization and the International association of diabetes and pregnancy study groups criteria in diagnosing gestational diabetes mellitus in South Indians. Indian J Endocrinol Metabol. 2013; 17:906-9.
  文献评价指标  
  下载次数:18次 浏览次数:20次