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HbA_1c Levels Are Significantly Lower in Early and Late Pregnancy

¹ Department of Endocrinology, Rigshospitalet, University Hospital of Copenhagen, Copenhagen, Denmark
² Department of Obstetrics, Rigshospitalet, University Hospital of Copenhagen, Copenhagen, Denmark
³ Steno Diabetes Center, Copenhagen, Denmark
⁴ Department of Endocrinology, Odense University Hospital, Odense, Denmark

Address correspondence and reprint requests to Elisabeth Mathiesen, Department of Endocrinology, Rigshospitalet, University Hospital of Copenhagen, Blegdamsvej 9, DK-2100 Copenhagen, Denmark. E-mail: em{at}rh.dk

Abbreviations: DCCT, Diabetes Control and Complications Trial • OGTT, oral glucose tolerance test

	INTRODUCTION

TOP INTRODUCTION RESEARCH DESIGN AND METHODS RESULTS CONCLUSIONS References

 
Strict glycemic control is essential to minimize the maternal and fetal morbidity and mortality of pregnancies complicated by diabetes (1–3). In addition to home blood glucose measurement, which may not always reflect the true average blood glucose level (4), HbA_1c is a useful parameter in metabolic regulation (5–8). Thus, supplementation with HbA_1c, as is common outside pregnancy, seems appropriate.

Before pregnancy, the target for metabolic control in women with diabetes is HbA_1c values near the normal range (9). However, the upper normal range of HbA_1c during normal pregnancy is only sparsely investigated with different methods (10), mainly in late pregnancy (5,6,11,12), and reference ranges are generally established from the nonpregnant state (4). Increased third-trimester HbA_1c levels are associated with an increased risk of preeclampsia (3,13), macrosomia (1), and stillbirth (2), leading to speculations that the target for HbA_1c in pregnancy should be even lower than outside pregnancy to prevent adverse events.

There is a need to establish the reference range of HbA_1c during normal pregnancy with an internationally recognized Diabetes Control and Complications Trial (DCCT)-aligned method. In this study, we evaluated the normal upper range of HbA_1c in early and late pregnancy.

	RESEARCH DESIGN AND METHODS

TOP INTRODUCTION RESEARCH DESIGN AND METHODS RESULTS CONCLUSIONS References

 
From our antenatal clinic, we randomly selected 100 healthy pregnant women without previous gestational diabetes (early pregnancy group). All subjects had a random capillary blood glucose level <7.0 mmol/l at their first antenatal visit at approximately week 14 (range 8–17), and none developed gestational diabetes. A selective screening based on risk factors for gestational diabetes was used (14).

A late pregnancy group was established of 98 healthy pregnant women in week 33 (range 28–37), who, as part of another study (14), had a normal 75-g oral glucose tolerance test (OGTT). HbA_1c was measured on the same day as the OGTT.

The nonpregnant control group consisted of 145 healthy women aged 30 years who were investigated as a part of the population survey Inter 99 (15). All had a normal OGTT.

All women were Nordic Caucasians and had HbA_1c measured in microsamples from the earlobe with the high-performance liquid chromatography DCCT-aligned method (Tosch Automated Glycohemoglobin Analyzer; Tosch Bioscience, Minato, Japan) at the Steno Diabetes Center (8) (normal range 4.1–6.4%, interassay precision coefficient of variation 3.5%). A normal OGTT was defined as a 2-h OGTT value <7.8 mmol/l (16). Random blood glucose measurements were performed using a HemoCue device (Hemocue, Ängelholm, Sweden), which has a coefficient of variation in pregnant women of 2.8–3.7% (17,18).

For calculation of BMI, prepregnancy height and weight were used in the pregnant women. The protocol was approved by the local ethical committee.

Statistical analysis
Data are given as means ± SD. A trend test was used to compare the three groups. When the trend test was significant, unpaired Student’s t tests were used for comparison between the groups using the Bonferroni correction to allow for multiple comparisons. P < 0.05 is considered significant. HbA_1c was regarded as normally distributed. Normal range was calculated as means ± 2 SD.

	RESULTS

TOP INTRODUCTION RESEARCH DESIGN AND METHODS RESULTS CONCLUSIONS References

 
HbA_1c was significantly decreased early in pregnancy and further decreased in late pregnancy compared with age-matched nonpregnant women (Table 1). The normal range of HbA_1c was 4.7–6.3% in nonpregnant women, 4.5–5.7% in early pregnancy, and 4.4–5.6% in late pregnancy. To exclude that the differences in HbA_1c were due to differences in BMI between the groups, women with BMI >25 kg/m² were excluded from all the groups, leaving 106 nonpregnant subjects, 87 early pregnancy subjects, and 85 late pregnancy subjects. Average HbA_1c did not change significantly (control 5.5 ± 0.4, early pregnancy 5.1 ± 0.3, and late pregnancy 5.0 ± 0.3%; P for trend <0.001), whereas BMI was comparable (21.7 ± 2.0, 21.6 ± 1.7, and 21.5 ± 1.9 kg/m²; P = NS).

	CONCLUSIONS

TOP INTRODUCTION RESEARCH DESIGN AND METHODS RESULTS CONCLUSIONS References

Our findings are in agreement with O’Kane et al. (6), who studied 493 healthy women with a DCCT-aligned method, mainly in the third trimester, and with Hartland et al. (5), who investigated 267 pregnant Caucasian and 249 Asian subjects using a latex-enhanced turbidimetric immunoassay. However, nonpregnant women were not included for comparison in these two studies. Our study included a sufficient number of women to detect significant differences, and the importance of using a DCCT-aligned HbA_1c method has been addressed in a consensus statement (8).

In late pregnancy, all women in our study had a documented normal glucose tolerance test. This might explain why we found a further reduction in HbA_1c in late pregnancy in contrast to others (5).

During normal pregnancy, a decrease in fasting blood glucose occurs early in pregnancy, mainly between weeks 6 and 10, and is sustained during the remaining part of pregnancy (19). New erythrocytes formed will therefore be exposed to a lower time-averaged glucose concentration than those of nonpregnant women, and the degree of glycosylation might therefore be less (12). In addition, the erythrocyte lifespan is likely to be decreased in pregnancy, hence also reducing the HbA_1c value (20–22). The Hb level was not measured in this study, and a possible role of anemia could not be accounted for.

Our study, which included nonpregnant, early pregnant, and late pregnant women, demonstrated a decline of the upper normal level of HbA_1c from 6.3 to 5.7% in early pregnancy and to 5.6% in the third trimester of pregnancy, indicating a reduction of HbA_1c during normal pregnancy that is of clinical importance when defining the goal for HbA_1c during pregnancy complicated with diabetes.

	Footnotes

 
C.G. holds stocks in and receives grant support from Novo Nordisk.

Received for publication January 19, 2004. Accepted for publication January 20, 2003.

	References

TOP INTRODUCTION RESEARCH DESIGN AND METHODS RESULTS CONCLUSIONS References

 

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