According to the American Diabetes Association (ADA), gestational diabetes mellitus (GDM) is “diabetes that is first diagnosed in the second or third trimester of pregnancy that excludes the possibility of pre-existing type 1 or type 2 diabetes” . This disease is a prevalent and potentially serious condition that may lead to adverse outcomes in both mothers and neonates . It is associated with preeclampsia, increased cesarean rates and macrosomia . The detection and adequate treatment of this condition reduces the risks for mothers as well as for babies , , .
The oral glucose tolerance test (OGTT) has been the diagnostic test of choice for diabetes mellitus (DM) in the general population . In the last decades, the diagnostic criteria for GDM have been controversial and a range of recommendations and guidelines to identify women with GDM have been proposed , , , , , .
Up to 2013, the World Health Organization (WHO) recommended that the GDM diagnosis should be based on the same criteria as is used for non-pregnant adults using the 2 h 75 g OGTT . The UK National Institute for Health and Care Excellence (NICE) recommendations  are based on these criteria; however, they recommended a lower cut-off for fasting glucose. More recently, the International Association of the Diabetes in Pregnancy Study Group (IADPSG), after the results of the Hyperglycemia and Adverse Pregnancy Outcomes (HAPO) study, a cohort study with about 25,000 pregnant women; recommended a new diagnostic criterion for GDM also based on 2 h 75 g OGTT but with lowered thresholds for fasting glucose, 1 h and 2 h glucose. GDM is present if one or more results are altered , , . Since 2013, the WHO has adopted these same IADSPG criteria . According to the ADA, GDM diagnosis can be performed by the one-step 2 h 75 g OGTT using the same threshold diagnostic criteria of IADPSG or the two-step strategy with a 1 h 50 g OGTT screen followed by a 3 h 100 g OGTT for those who screen positive .
Although the OGTT is recommended as the diagnostic test for GDM by international organizations, it requires at least 8 h fasting, an extensive patient preparation, lacks reproducibility, it is time-consuming and uncomfortable for pregnant women .
The HbA1c test has been used in clinical practice for monitoring patients with DM since the early 1980s , but its use in diagnosis was established only in 2010 , . Presently, there are more than 100 certified methods/instruments available for routine HbA1c measurement (http://www.ngsp.org/docs/methods.pdf; accessed 14th December 2018). These methods are mainly based on four principles: immunoassays, ion-exchange chromatography (HPLC), affinity chromatography and enzymatic assays. The International Federation of Clinical Chemistry (IFCC) Working Group on HbA1c Standardization developed a reference system for HbA1c  and since the mid 1990s, as well as the National Glycohemoglobin Program (NGSP), work to standardize and align HbA1c methods worldwide , . Despite all these international efforts, there are still many situations that may affect HbA1c results, related or not to assay methods, such as the presence of a variant hemoglobin (Hb), anemia and uremia , . Recently, the role of race/ethnicity on HbA1c values has been raised , . HbA1c values are higher in Blacks, Asians and Latinos when compared to White persons. These factors have limited the use of HbA1c in specific cases.
The cut-off of HbA1c 6.5% (48 mmol/mol) is recommended for DM diagnosis in the general population (Expert Committee 2010), and this cut-off is endorsed by the ADA and WHO , . However, its use for the diagnosis of GDM has not been recommended by any current guidelines yet , , , . Results from the HAPO study showed that HbA1c values, like glycemia levels, were significantly associated with all adverse outcomes, and higher levels of maternal HbA1c were related to greater frequency of adverse outcomes . The HbA1c test would be more receptive to this group of patients because of its convenience when compared to the OGTT. However, due to some physiological and analytical factors that might interfere with HbA1c results, it has not yet been included as a diagnostic tool for GDM , , .
During pregnancy, hemoglobin concentrations change overtime, to accommodate the increasing maternal blood volume and the iron needs of the fetus and also there is a decrease in fasting blood glucose levels . Consequently, HbA1c levels are lower in pregnant women than in non-pregnant women. Due to these factors, different reference values are recommended in pregnancy and HbA1c interpretation should consider these factors . In addition, HbA1c is significantly lower in the first trimesters of gestation and HbA1c trimester-specific reference intervals are required throughout pregnancy . HbA1c values vary from 4.0% (20 mmol/mol) to 6.0% (42 mmol/mol) in pregnant women from different populations .
Some studies have evaluated the diagnostic accuracy of HbA1c in DMG , , , , . In a recent meta-analysis with 2812 patients and 5918 controls, which measured HbA1c in pregnant Chinese women, showed that this test is a useful diagnostic tool to confirm GDM . A large cohort study in New Zealand reported that HbA1c ≥5.9% (41 mmol/mol) at the first antenatal visit identified all cases of GDM and was associated with a two-fold risk of congenital anomalies, preeclampsia, shoulder dystocia and a three-fold risk of perinatal deaths . We also showed that HbA1c levels may be a useful diagnostic tool for GDM in pregnant Brazilian women, the HbA1c cut-off point of 5.8% (40 mmol/mol) was able to diagnose 38% of GDM cases by OGTT and 5% of pregnant women classified as GDM negative by the OGTT were identified according to the HbA1c test . Other studies have also highlighted the potential role of HbA1c in the diagnosis and management of GDM , . In this study we carried out a systematic review and meta-analysis to determine the diagnostic accuracy of the HbA1c test in the diagnosis of GDM in different populations of pregnant women.
Materials and methods
This meta-analysis is in agreement with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis: The PRISMA Statement  and is in accordance with the Cochrane Handbook for Systematic Reviews of Diagnostic Test Accuracy . It was registered in the International Prospective Register of Systematic Reviews (PROSPERO) under the number CRD42018041407.
Search strategy and data sources
We searched PubMed (MEDLINE), Embase, SCOPUS and ClinicalTrials.gov, with assistance from our Institution’s library professionals, for papers published up to October 2018 using search terms related to GDM, HbA1c and diagnosis combined. Details of all search terms are presented in Supplementary Material. From the papers retrieved, a manual search of their references was conducted. Articles published before 1996, duplicate articles and those which were not complete were removed and the remaining articles were assessed for eligibility. The revision of titles was followed by reading the abstracts for relevance. Finally, the identification of eligible studies was carried out, based on a full reading of the articles selected by at least two researchers.
The inclusion criteria were: (1) cross-sectional or cohort studies that assessed the performance of HbA1c (index test) and 75 g OGTT (reference test) for the diagnosis of GDM; (2) the HbA1c method certified by the National Glycohemoglobin Standardization Program (NGSP; http://www.ngsp.org/, 13 December 2017, date last accessed) and/or the International Federation of Clinical Chemistry (IFCC) , ; (3) studies that included pregnant women without DM prior to pregnancy or with GDM already diagnosed. Exclusion criteria were: (1) studies that did not perform the 75 g OGTT for the GDM diagnosis; (2) review articles; (3) comments, letters and/or editorials; (4) studies with a language other than English, Spanish or Portuguese; (5) articles published before 1996, as from this date on was when the standardization for the HbA1c methods started , , . Three independent reviewers (PBR, FCC and JRTT) decided which studies were included based upon the eligibility criteria. First, we screened the titles of all papers resulting from the search to identify potentially relevant articles. Afterwards, we evaluated the abstracts of these studies, and relevant articles had their full-text reviewed. Finally, the reviewers selected articles qualified for inclusion and performed data extraction from all the included reports. Any disagreements concerning study eligibility or data interpretation were resolved through discussion or, if required, a fourth reviewer was consulted (JLC or ALP).
Data collection and analysis
A data extraction form was developed and the following pieces of information were extracted from each report: (1) study details (author, publication year, country of origin); (2) study design; (3) sample size; (4) GDM incidence; (5) participant characteristics (age, gestational age, HbA1c results); (6) test methods (details of methodology and equipment description for the HbA1c test and the OGTT); and (7) test results (true-positive [TP] cases; false-positive [FP] cases; true-negative [TN] cases; and false-negative [FN] cases). We also attempted to contact authors for further information when data to construct a 2×2 table was unclear or additional data were required. When data were not available from the authors, the study was excluded.
At least two reviewers independently assessed the quality of primary studies by evaluating the risk of bias and applicability, using the Quality Assessment of Diagnostic Accuracy Studies tool QUADAS-2, a questionnaire containing 14 questions assessing risk of bias and applicability concerns . Disagreements were resolved by consensus or by involving a third reviewer (JLC or ALP). We also evaluated if the articles were presented according to Standards for Reporting of Diagnostic Accuracy (STARD) initiative guidelines .
Statistical analysis and data synthesis
We followed the standard methods recommended for diagnostic accuracy meta-analysis studies . For each study, 2×2 contingency tables were constructed with data extracted for TP, TN, FP and FN rates. By a bivariate model using a random effects approach  indexes of HbA1c test accuracy were computed: sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR) and diagnostic odds ratio (DOR). PLR >1 for a positive test result is associated with the presence of disease, and NLR <1 for a negative test result is associated with the absence of disease . The DOR is a single indicator that summarizes the diagnostic accuracy of a test, and higher values indicate a better test performance . The overall diagnostic accuracy for the HbA1c test for GDM diagnosis was determined by a summary receiver operating characteristic curve (SROC) for the main cut-off points discussed in each study. Afterwards, hierarchical summary ROC curves (HSROC) were used to summarize the HbA1c performance for specific cut-offs if four or more studies presented data for the same cut-off . The Fagan nomogram was applied, considering a pre-test probability of 18% for GDM, based on external data from the Metzger et al. study , to calculate posttest probabilities for GDM using different HbA1c cut-offs . The heterogeneity among studies was evaluated by chi-square and Cochran Q analysis, I2 (measure of inconsistency, when I2 has a value above 50%, it is considered that there is moderate heterogeneity, 25% is low and 75% is high) and by visual inspection of forest plots. When the studies are reasonably homogeneous, accuracy indexes from individual studies will lie within or near the interval of the pooled accuracy estimate. Deviations may indicate possible heterogeneity or outlier studies , . We also ran the meta-analyses over again while removing studies one at a time to determine whether a particular study accounted for the heterogeneity. In addition, when data was available, we carried out subgroup analysis by specific cut-off points, HbA1c methods and country of origin. The presence of publication bias was tested by using Deeks’ funnel plots . A p-value <0.05 was considered statistically significant in all analyses, except for Deeks’ test, where a value of p<0.1 was considered statistically significant. Analyses were carried out in Meta-Disc Version 1.4 (Universidad Complutense, Madrid, Spain) and Stata Version 12.1 software (Stata, College Station, TX, USA) by METANDI command. The forest plots were constructed using Review Manager Version 5.3 (Cochrane Collaboration, Oxford, UK). All studies selected for this review were previously approved by an Ethical Review Board and consequently ethical approval was not required by this review study.
Study selection and study characteristics
With this strategy 2927 records were identified. Of those, 49 studies were assessed for eligibility. After full-text reading, 40 articles were excluded (one for different language, nine for insufficient data, four for different reference test criterion, three studies performed the diagnostic test in the first gestational trimester and 23 did not meet the research question). Lastly, nine studies met our inclusion criteria , , , , , , , , , and of these, only one article  was excluded from the meta-analysis due to a lack of relevant information to allow a proper extraction of data as it was not clear which diagnostic criterion was used to perform the ROC analysis. Nevertheless, it was included in the qualitative analysis. Eight studies were eligible for systematic review and meta-analysis , , , , , , ,  (Figure 1).
All studies included in this review totaled 6848 pregnant women, who performed the OGTT and HbA1c test in the second or third trimesters of pregnancy for GDM diagnosis, of those 1128 were diagnosed with GDM (15.2%). Table 1 summarizes the characteristics of all selected studies. Three studies had a prospective design , , , one was a retrospective study  and five were cross-sectional studies , , , , . All studies were written in English and published between 2005 and 2017. Four studies were from India, while the Arab Emirates, Australia, Brazil, China and Turkey contributed with one study each.
The quality assessment of the studies by QUADAS-2 criteria is summarized in Table 2. Most studies presented a low risk of bias and applicability concerns. One study  presented a high risk of bias in the patient selection, flow and timing; in this study 1459 pregnant women participated, 33 of which were in the first trimester of pregnancy while the remaining women were in the second trimester of pregnancy. Another study  had a high risk of bias in the reference standard; this study used two different diagnostic criteria for the diagnosis of GDM and it was not clear which criterion was used in the analyses. For this reason, we did not perform the data extraction. One study  presented an unclear risk of bias in flow and timing, as 120 pregnant were diagnosed using the WHO 1999 diagnostic criteria and 142 were diagnosed using the IADPSG criteria. Only one article followed the recommendations and was presented according to the STARD guidelines .
Overall diagnostic accuracy
For this analysis we considered the main HbA1c cut-offs discussed in each article , , , , , , , . HbA1c thresholds ranged from 5.4% (36 mmol/mol) to 6.0% (42 mmol/mol). A total of 6406 pregnant women were included in this analysis, of those, 1044 were diagnosed with GDM. Using data from these eight studies, DOR was 6.97 (95% CI 4.17–11.65) and the area under the curve (AUC) was 0.825 (95% CI 0.751–0.899); indicating a good level of overall accuracy (Figure 2).
Effect of the HbA1c threshold on diagnostic accuracy
The forest plot in Figure 3 shows the sensitivity and specificity of HbA1c for the detection of GDM across all eight included studies. For studies reporting accuracy at more than one threshold, 2×2 tables were built for each cut-off. The cut-offs 5.4% (36 mmol/mol), 5.7% (39 mmol/mol), 5.8% (40 mmol/mol) and 6.0% (42 mmol/mol) were reported by at least four studies and their data were included in the forest plots. Table 3 summarizes the accuracy measures for these cut-offs.
HbA1c ≥5.4% (36 mmol/mol) for the diagnosis of GDM
Four studies evaluated the cut-off of 5.4% (36 mmol/mol) , , , , totaling 2808 pregnant women. The HSROC curve showed an AUC of 0.779 (95% CI 0.739–0.819; Figure 4A). The DOR was 5.20 (95% CI 3.33–8.12; I2=57.6%). Sensitivity ranged from 26% to 86% and specificity from 61% to 96% (Figure 3). The pooled sensitivity for these studies was 50.3% (95% CI 24.8%–75.7%) and the pooled specificity was 83.7% (95% CI 67.5%–92.7%) (Table 3). After re-running the meta-analysis by removing one paper at a time, when removing the study by Bhavadharini et al. , no DOR heterogeneity was found (I2=0%), pooled sensitivity decreased and the pooled specificity was the same (39% [95% CI 33%–44%] and 83% [95% CI 81%–84%]), respectively. However, after carefully reviewing this study, we were unable to explain the reasons why it contributed to the increase in heterogeneity for this cut-off and the results from the primary meta-analysis were considered.
HbA1c ≥5.7 (39 mmol/mol) for the diagnosis of GDM
Five studies presented data for cut-off of 5.7% (39 mmol/mol) , , , , , totaling 3540 pregnant women. The HSROC curve showed an AUC of 0.741 (95% CI 0.675–0.807; Figure 4B). The DOR was 7.03 (95% CI 4.50–10.96; I2=55.7%). Sensitivity ranged from 9% to 73% and specificity from 76% to 100% (Figure 3). The pooled sensitivity for these studies was 24.7% (95% CI 10.3%–48.5%) and the pooled specificity was 95.5% (95% CI 85.7%–98.7%) (Table 3). After re-running the meta-analysis by removing one paper at a time, no article explained the moderate DOR heterogeneity for this cut-off and we were unable to explain the reasons for this heterogeneity.
HbA1c ≥5.8% (40 mmol/mol) for the diagnosis of GDM
Four studies evaluated the threshold of 5.8% (40 mmol/mol) , , , , totaling 4160 pregnant women. The HSROC curve showed an AUC of 0.624 (95% CI 0.482–0.766; Figure 4C. The DOR was 8.54 (95% CI 4.89–14.90; I2=38.3%). Sensitivity ranged from 6% to 27% and specificity from 95% to 100% (Figure 3). The pooled sensitivity for these studies was 10.8% (95% CI 5.7%–19.41%) and the pooled specificity was 98.7% (95% CI 96.2%–99.5%) (Table 3). This meta-analysis showed low heterogeneity thus sensitive analysis was not carried out.
HbA1c ≥6.0% (42 mmol/mol) for the diagnosis of GDM
Five studies reported data at the threshold of 6.0% (42 mmol/mol) , , , , , totaling 3608 pregnant women. The HSROC curve showed an AUC of 0.927 (95% CI 0.840–1.014; Figure 4D). The DOR was 11.40 (95% CI 5.34–24.36; I2=77.0%). Sensitivity ranged from 4% to 47% and specificity from 97% to 100% (Figure 3). The pooled sensitivity for these studies was 12.9% (95% CI 5.5%–27.5%) and the pooled specificity was 98.7% (95% CI 97.6%–99.3%) (Table 3). After re-running the meta-analysis by removing one paper at a time, by removing the Saxena et al.  study, the DOR heterogeneity was 1.4%. After a careful evaluation, this study was the only one using the WHO 1999 criteria to diagnose GDM instead of the IADPSG criteria, this fact could explain the DOR heterogeneity in this subgroup meta-analysis. However, pooled sensitivity and pooled specificity for HbA1c ≥6.0% (42 mmol/mol) after excluding this study were practically unchanged and were 10.2% (95% CI 7.6%–13.2%) and 98.8% (95% CI 98.3%–99.2%), respectively.
Effect of other variables on diagnostic accuracy
We also investigated the effect of different methods of HbA1c measurement and the country of origin of patients to explain the variability among studies. For this analysis, we considered the main HbA1c cut-offs discussed in each article. Four studies used HPLC , , ,  and four used immunoassays , , ,  to measure HbA1c. We observed low variability when we pooled studies with HbA1c results based only on HPLC methods (DOR=5.48 (95% CI 3.78–7.94; I2=38.4%). The variability among studies was high when we pooled only immunoassay methods (DOR=8.38 [95% CI 2.79 – 25.1; I2 =88.6%]), however, when we excluded the study by Saxena et al.  a low heterogeneity was observed (DOR=4.92 [95% CI 3.12–7.75; I2=11.3%]). The heterogeneity was also low when we pooled only studies from Asia , , , , ,  (DOR=4.77 [95% CI 3.55–6.40; I2=38.4%]) and absent when we evaluated non-Asian studies ,  (DOR =7.21 [95% CI 4.15–12.54; I2=0.0%]). There was no data available to investigate the effect of anemia, iron supplementation and presence of variants hemoglobin on results heterogeneity.
Although investigation of reporting bias in diagnostic accuracy data is not well established, we used the method of Deeks , that appears to be most appropriate, which indicated that there was no potential publication bias (p=0.112).
Considering the pre-test probability of 18% for GDM and the PLR and NLR for cut-offs 5.4% (36 mmol/mol), 5.7% (39 mmol/mol), 5.8% (40 mmol/mol) and 6.0% (42 mmol/mol) we calculated the post-test probabilities for GDM applying the Fagan’s nomogram (Figure 5). The post-test probabilities were 40% and 12% for HbA1c ≥5.4% (36 mmol/mol) and <5.4% (36 mmol/mol); 55% and 15% for HbA1c ≥5.7% (39 mmol/mol) and <5.7% (39 mmol/mol); 64% and 17% for HbA1c ≥5.8% (40 mmol/mol) and <5.8% (40 mmol/mol); 69% and 16% for HbA1c ≥6.0%(42 mmol/mol) and <6.0% (42 mmol/mol); respectively.
Summary of the main results
In this meta-analysis we included eight studies, covering 6406 pregnant women, and of those 1044 were diagnosed with GDM. The diagnostic accuracy of the HbA1c test was reported at different thresholds ranging from 5.4% (36 mmol/mol) to 6.0% (42 mmol/mol). The AUC was 0.825 (95% CI 0.751–0.899) with a Q* value of 0.758, indicating a good level of overall accuracy of the HbA1c test. Four studies evaluated the cut-off of 5.4% (36 mmol/mol) , , , , totaling 2808 pregnant women. The pooled sensitivity and specificity for these studies was 50.3% (95% CI 24.8%–75.7%) and 83.7% (95% CI 67.5%–92.7%), respectively. For a cut-off of 5.7% (39 mmol/mol), five studies presented data , , , , , totaling 3540 pregnant women. The pooled sensitivity and specificity for these studies was 24.7% (95% CI 10.3%–48.5%) and 95.5% (95% CI 85.7%–98.7%), respectively. Four studies evaluated the threshold of 5.8% (40 mmol/mol) , , , , totaling 4160 pregnant women yielding a pooled sensitivity and specificity of 10.8% (95% CI 5.7%–19.41%) and 98.7% (95% CI 96.2%–99.5%). Five studies reported data for the threshold of 6.0% (42 mmol/mol) , , , , , totaling 3608 pregnant women. The pooled sensitivity and specificity for these studies was 12.9% (95% CI 5.5%–27.5%) and 98.7% (95% CI 97.6%–99.3%), respectively.
Our results compared with other reports
As far as we know, this is the first meta-analysis including a multi-ethnic population to evaluate the accuracy of the HbA1c test in the diagnosis of GDM. A recent study in pregnant Chinese women  that aimed to establish the overall accuracy of the HbA1c test for the diagnosis of patients with GDM, after a systematic review, included 5918 controls and 2812 patients with GDM. Meta-analyzed data in this report showed sensitivity of 0.762 (95% CI 0.746–0.777), specificity of 0.917 (95% CI 0.910–0.924) and an AUC of 0.93 with a Q* value of 0.841, indicating a high level of overall accuracy for the HbA1c test in the diagnosis of GDM.
In a prospective study that enrolled 1989 pregnant Taiwanese women , the AUC was 0.70 and the optimal HbA1c cut-off point to predict GDM was 5.7% (39 mmol/mol) (sensitivity=45.2% and specificity=84.1%). However, the reference test adopted in this study was two-step OGTT recommended by National Health Institute (NHI). The results are in agreement with this review, showing low sensitivity and relative high specificity for HbA1c to diagnose GDM. Additionally, the study by Li et al.  reported a positive correlation of HbA1c with blood glucose in pregnancy affected by GDM. They showed an AUC for HbA1c of 0.854 (p<0.01). When HbA1c was 5.43% (36 mmol/mol), sensitivity and specificity were 0.832 and 0.764, respectively. Hanna et al.  examined the concordance between different criteria for GDM diagnosis and observed an increased proportion of women with an HbA1c ≥6.0% (42 mmol/mol) in the discordant cases. They then evaluated the performance of this HbA1c threshold in the diagnosis of GDM and found a similar sensitivity and specificity of HbA1c, around 22% and 97%, respectively, irrespective of the criteria used to diagnose GDM. They concluded that the HbA1c test alone is unlikely to replace the OGTT in GDM diagnosis. Indeed, an optimal test to diagnose GDM is still desired. The recent study by Farrar et al.  evaluated through a systematic review a different test strategy for the diagnosis of GDM and concluded that there is insufficient evidence to suggest which strategy is best for diagnosing GDM, although HbA1c data were not included in this study.
Strengths and weaknesses of the review
This study was conducted through an extensive and systematic literature search; we included papers from different countries that analyzed different populations of pregnant women. At least two independent reviewers extracted the data and the overall quality of original studies was checked by a QUADAS-2 tool to perform quality assessments and most studies presented a low risk of bias and applicability concerns. As limitations for this study, we highlight: First, although we only included studies that measured HbA1c with standardized methods, the individual performance of each laboratory was not available. Second, we observed a high heterogeneity among the studies, mainly regarding data for HbA1c sensitivity. Despite our efforts to analyze and exlpain the heterogeneity among studies, scarcity of data regarding interferent factors, such as anemia, iron supplementation and the presence of variants of haemoglobin in the original papers limited our analyses. However, we were able to draw attention to the likely effect of ethnicity and the use of different criteria for OGTT interpretation. One study used the WHO 1999 criteria  and after its exclusion a low heterogeneity was observed. Heterogeneity was also low when we pooled only studies from Asia , , , , ,  and absent when we evaluated non-Asian studies , , pointing to the effect of ethnicity on HbA1c values in different populations , . All these possible interferences might have affected in different ways the HbA1c levels measured by the method used in the primary studies. Third, only one article  followed the recommendations and was presented according to the STARD guidelines  which may have affected the quality of reporting of the other studies.
Applicability of findings to the review question
To make sense of the results of the meta-analysis and to assess the false-error rates, we calculated the post-test probabilities for GDM applying the Fagan’s nomogram, we considered the test performance estimates based on external data from the Metzger et al. study , with a pre-test probability of 18% for GDM and the PLR and NLR for cut-offs 5.4% (36 mmol/mol), 5.7% (39 mmol/mol), 5.8% (40 mmol/mol) and 6.0% (42 mmol/mol). The post-test probabilities for a positive test were 40%, 55%, 64% and 69% for HbA1c ≥5.4% (36 mmol/mol), HbA1c ≥5.7% (39 mmol/mol), HbA1c ≥5.8% (40 mmol/mol) and HbA1c ≥6.0% (42 mmol/mol); respectively. The post-test probabilities for a negative test for these cut-offs were low and ranged from 12 to 17%, like the pre-test probability of 18%. HbA1c results ≥5.4% (36 mmol/mol) increase at least two-fold the probabilitiy for GDM whereas HbA1c results <5.4% (36 mmol/mol) do not alter the initial probability of GDM.
Limited evidence provided by the studies included in this review suggests that HbA1c tests, regardless of the threshold used to diagnose GDM, result in few false-positive GDM cases but very high levels of false negative GDM cases, with a high level of specificity across all the population groups described here. These findings point to the usefulness of HbA1c cut-offs of 5.7% (39 mmol/mol), 5.8 (40 mmol/mol) or 6.0% (42 mmol/mol) as rule-in tests for the diagnosis of GDM. However, it means that irrespective of the cut-off adopted, a negative result will require further investigation through a more sensitive test for confirmation of the diagnosis. The prognostic value of HbA1c for GDM adverse outcomes needs further evaluation by prospective studies and it is beyond the scope of this review.
World Health Organization. Diagnostic criteria and classification of hyperglycaemia first detected in pregnancy. 2013;1–62. http://www.who.int/diabetes/publications/Hyperglycaemia_In_Pregnancy/en/.
Falavigna M, Schmidt MI, Trujillo J, Alves LF, Wendland ER, Torloni MR, et al. Effectiveness of gestational diabetes treatment: a systematic review with quality of evidence assessment. Diabetes Res Clin Pract 2012;98:396–405. PubMedCrossrefGoogle Scholar
Metzger BE, Gabbe SG, Persson B, Buchanan TA, Catalano PA, Damm P, et al. International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care 2010;33:676–82. CrossrefPubMedGoogle Scholar
World Health Organization. Definition, diagnosis and classification of diabetes mellitus and its complications. Report of a WHO consultation. Geneva: World Health Organization, 1999 (WHO Technical Report Series). Google Scholar
Nankervis A, McIntyre HD, Moses R, Ross GP, Callaway L, Porter C, et al. Consensus guidelines for the testing and diagnosis of gestational diabetes mellitus in Australia. The Australasian Diabetes in Pregnancy Society, ADIPS. http://adips.org/downloads/2014ADIPSGDMGuidelinesVJune2014FINALforWEB.pdf.
Commissioned by the National Institute for Health and Care Excellence. Diabetes in pregnancy Management of diabetes and its complications from preconception to the postnatal period. NICE guideline 3 Methods, evidence and recommendations, 2015. https://www.nice.org.uk/guidance/ng3/evidence/full-guideline-pdf-3784285.
International Association of Diabetes and Pregnancy Study Groups. International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care 2010;33:676–82. PubMedGoogle Scholar
Lowe LP, Metzger BE, Dyer AR, Lowe J, McCance DR, Lappin TR, et al. Hyperglycemia and adverse pregnancy outcomes (HAPO) study associations of maternal HbA1c and glucose with pregnancy outcomes. Diabetes Care 2012;35:574–80. CrossrefPubMedGoogle Scholar
Wendland EM, Torloni MR, Falavigna M, Trujillo J, Dode MA, Campos MA, 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 Childbirth 2012;12:23. PubMedCrossrefGoogle Scholar
American Diabetes Association. Standards of medical care in diabetes 2011. Diabetes Care 2011;34 Suppl 1:S11–61. Google Scholar
World Health Organization. Use of glycated hemoglobin (HbA1c) in the diagnosis of diabetes mellitus. Abbreviated report of a WHO consultation 2011. Available: http://www.who.int/diabetes/publications/diagnosis_diabetes2011/en/index.html.
Hoelzel W, Miedema, K. Development of a reference system for the international standardisation of HbA1c/glycohemoglobin determinations. J Int Fed Clin Chem 1996;8:62–4, 66–7. Google Scholar
Jeppsson J-O, Kobold U, Barr J, Finke A, Hoelzel W, Hoshino T, et al. International Federation of Clinical Chemistry and Laboratory Medicine (IFCC). Approved IFCC Reference Method for the measurement of HbA1c in human blood. Clin Chem Lab Med 2002;40:78–89. PubMedGoogle Scholar
Little RR, Rohlfing C, Sacks DB. The National Glycohemoglobin Standardization Program: Over 20 Years of Improving Hemoglobin A1c Measurement. Clin Chem. 2018 Dec 5. pii: clinchem.2018.296962. doi: 10.1373/clinchem.2018.296962. [Epub ahead of print]. PubMedGoogle Scholar
Cavagnolli G, Pimentel AL, Freitas PA, Gross JL,Camargo JL. Effect of ethnicity on HbA1c levels in individuals without diabetes: Systematic review and meta-analysis. PLoS One 2017;12:e0171315. PubMedCrossrefGoogle Scholar
Mosca A, Paleari R, Dalfra MG, Di Cianni G, Cuccuru I, Pellegrini G, et al. Reference intervals for hemoglobin A(1c) inpregnant women: Data from an Italian Multicenter study. Clin Chem 2006;52:1138–43. CrossrefGoogle Scholar
O’Connor C, O’Shea PM, Owens LA, Carmody L, Avalos G, Nestor L, et al. Trimester-specific reference intervals for haemoglobin A1c (HbA1c) in pregnancy. Clin Chem Lab Med 2011;50:905–9. PubMedGoogle Scholar
Tian QW, Xuan C, Wang HW, Zhao JX, Yu WL, Gao G, et al. Diagnostic accuracy of glycosylated hemoglobin in Chinese patients with gestational diabetes mellitus: a meta-analysis based on 2,812 patients and 5,918 controls. Genet Test Mol Biomarkers 2013;17:687–95. CrossrefPubMedGoogle Scholar
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;37:2953–59. CrossrefGoogle Scholar
Moher D, Liberati A, Tetzlaff J, Altman DG, PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med 2009;151:264–9. PubMedCrossrefGoogle Scholar
Higgins JPT, Green S. Cochrane Handbook for Systematic Reviews of Interventions version 5.1.0 [updated March 2011]. The Cochrane Collaboration, 2011. http://handbook.cochrane.org.
Whiting PF, Rutjes AW, Westwood ME, Mallett S, Deeks JJ, Reitsma JB, et al. QUADAS-2 Group. QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med 2011;155:529–536. PubMedCrossrefGoogle Scholar
Bossuyt PM, Reitsma JB, Bruns DE, Gatsonis CA, Glasziou PP, Irwig LM, et al. Towards complete and accurate reporting of studies of diagnostic accuracy: The STARD initiative. Br Med J 2003;326:41–4. CrossrefGoogle Scholar
Deeks JJ, Wisniewski S, Davenport C. Chapter 4: Guide to the contents of a Cochrane Diagnostic Test Accuracy Protocol. In: Deeks JJ, Bossuyt PM, Gatsonis C, editors. Cochrane Handbook for Systematic Reviews of Diagnostic Test Accuracy Version 1.0.0. The Cochrane Collaboration. http://srdta.cochrane.org/ (2013).
Reitsma JB, Glas AS, Rutjes AW, Scholten RJ, Bossuyt PM, Zwinderman AH. Bivariate analysis of sensitivity and specificity produces informative summary measures in diagnostic reviews. J Clin Epidemiol 2005;58:982–90. PubMedCrossrefGoogle Scholar
Devillé WL, Buntinx F, Bouter LM, Montori VM, DeVet HC, Van Der Windt DA, et al. Conducting systematic reviews of diagnostic studies: didactic guidelines. BMC Med Res Methodol 2002;2:9. CrossrefPubMedGoogle Scholar
Deeks JJ, Macaskill P, Irwig L. The performance of tests of publication bias and other sample size effects in systematic reviews of diagnostic test accuracy was assessed. J Clin Epidemiol 2005;58:882–93. CrossrefPubMedGoogle Scholar
Bhavadharini B, Mahalakshmi MM, Deepa M, Harish R, Malanda B, Kayal A, et al. Elevated glycated hemoglobin predicts macrosomia among Asian Indian pregnant women (WINGS-9). Indian J Endocrinol Metab 2017;21:184–9. CrossrefPubMedGoogle Scholar
Khalafallah A, Phuah E, Al-Barazan AM, Nikakis I, Radford A, Clarkson W, et al. Glycosylated haemoglobin for screening and diagnosis of gestational diabetes mellitus. Br Med J Open 2016;6:e011059. Google Scholar
Saxena P, Verma P, Goswami B. Comparison of diagnostic accuracy of non-fasting DIPSI and HbA1c with fasting WHO criteria for diagnosis of gestational diabetes mellitus. J Obstet Gynaecol India 2017;67:337–42. PubMedCrossrefGoogle Scholar
Soumya S, Rohilla M, Chopra S, Dutta S, Bhansali A, Parthan G, et al. HbA1c: A useful screening test for gestational diabetes mellitus. Diabetes Technol Ther 2015;17:899–904. PubMedCrossrefGoogle Scholar
Ye M, Liu Y, Cao X, Yao F, Liu B, Li Y, et al. The utility of HbA1c for screening gestational diabetes mellitus and its relationship with adverse pregnancy outcomes. Diabetes Res Clin Pract 2016;114:43–9. CrossrefPubMedGoogle Scholar
Ho YR, Wang P, Lu MC, Tseng ST, Yang CP, Yan YH. Associations of mid-pregnancy HbA1c with gestational diabetes and risk of adverse pregnancy outcomes in high-risk Taiwanese women. PLoS One 2017;12:e0177563. PubMedCrossrefGoogle Scholar
Li Y, Zhao W, Shi R, Jia J, Li X, Cheng J. The diagnosis value of blood glucose combined glycosylated hemoglobin in gestational diabetes. Int J Clin Exp Med 2017;10:5344–8. Google Scholar
Hanna FW, Duff CJ, Shelley-Hitchen A, Hodgson E, Fryer AA. Diagnosing gestational diabetes mellitus: implications of recent changes in diagnostic criteria and the role of glycated haemoglobin (HbA1c). Clin Med 2017;17:108–13. CrossrefGoogle Scholar
Farrar D, Duley L, Dowswell T, Lawlor DA. Different strategies for diagnosing gestational diabetes to improve maternal and infant health. Cochrane Database Syst Rev 2017;8:CD007122. PubMedGoogle Scholar
The online version of this article offers supplementary material (https://doi.org/10.1515/cclm-2018-1191).
About the article
Published Online: 2019-03-20
Published in Print: 2019-09-25
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: The authors acknowledge the financial support from the Research Incentive Fund from the Hospital de Clínicas de Porto Alegre (FIPE/HCPA, GPPG 140579). PBR and ALP were recipients of a scholarship from Coordenação de Aperfeiçoamento de Pessoal de Ensino Superior (CAPES), FCC was sponsored by the Ministry of Science and Technology, Higher Education and Professional Technician (MCTESTP) of the Republic of Mozambique and JRTT by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq).
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
Registration number: PROSPERO registration-CRD42018 041407.