Patterns of Glycemia in Normal Pregnancy
Should the current therapeutic targets be challenged?
- Teri L. Hernandez, PHD, RN1,2⇓,
- Jacob E. Friedman, PHD3,
- Rachael E. Van Pelt, PHD4 and
- Linda A. Barbour, MD, MSPH1,5
- 1Department of Medicine, Division of Endocrinology, Metabolism, and Diabetes, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado
- 2College of Nursing, Division of Women, Children, and Family Health, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado
- 3Department of Pediatrics, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado
- 4Division of Geriatric Medicine, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado
- 5Division of Obstetrics and Gynecology, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado
- Corresponding author: Teri L. Hernandez, .
Despite the well-known influence of maternal glucose on infant birth weight (BW), the prevalence of large for gestational age (LGA) infants (≥90th percentile for age) has been increasing steadily over decades, particularly in pregnancies complicated by pregestational or gestational diabetes mellitus (1). Although the overall prevalence of macrosomia (BW ≥4,000 g) is 17–29% in women with untreated gestational diabetes, the majority of macrosomic infants are born to women with obesity but no gestational diabetes (2,3). Moreover, epidemiologic data show that a higher BW is associated with higher BMI and glucose intolerance later in life (4,5), suggesting life-long metabolic implications for offspring.
Recent data from the Hyperglycemia and Adverse Pregnancy Outcomes (HAPO) study suggested that concentrations of maternal glucose below the previously accepted diagnostic thresholds for gestational diabetes are predictive of LGA and fetal hyperinsulinemia (6). On the basis of this landmark study, the International Association of Diabetes in Pregnancy Study Group and the American Diabetes Association (ADA) recommended new lower diagnostic criteria for gestational diabetes (7,8). However, a significant number of women with gestational diabetes whose glucose values are within the current targeted therapeutic ranges deliver macrosomic infants (9). Although glucose plays a major role in fetal growth, this paradox underscores the likely role of other nutrients in fetal growth, but also the need to critically reexamine our definition of “normal” maternal patterns of glycemia and the effects on fetal growth. The new diagnostic criteria recommended by the International Association of Diabetes in Pregnancy Study Group and ADA are expected to increase the prevalence of gestational diabetes to 18%. Thus, treatment targets may need to be reevaluated.
Historically, the treatment goal in pregnancies complicated by diabetes has been to mimic patterns of glycemia in normal pregnancy (1). Although the HAPO study better defined abnormal glycemic thresholds for the diagnosis of gestational diabetes based on fetal outcomes, the current clinical guidelines for defining treatment targets (10–13) are less rigorous given that optimal therapeutic targets remain untested in randomized trials (14). Further, there has been a reluctance to compare descriptive data in “normal” pregnant women because of the difficulty of comparing major differences in study design, patient characteristics, and methodology. Nevertheless, ∼5 decades of research have helped define “normal” maternal glucose metabolism. The intent of this review is to offer the clinician 1) a clear graphic representation of available glucose data collected in “normal” pregnancy (i.e., a pooled analysis of weighted averages across 12 studies involving nonobese patients); 2) a full discussion of study methodologies and limitations; and 3) a proposal of more aggressive therapeutic targets that may be prospectively tested for the prevention of fetal macrosomia.
RESEARCH DESIGN AND METHODS
Literature search strategy and inclusion of evidence
PubMed was searched broadly using keywords such as pregnancy, glycemia, glucose, diurnal patterns, and gestational diabetes. Reference lists in review papers, original manuscripts, and expert reports were compared with findings in PubMed. Data were included if they provided information on glycemic patterns in normal pregnancy, excluding type 1 or 2 diabetes or gestational diabetes. Patterns needed to have been established using diurnal profiling techniques such as hospital admission with frequent blood sampling, serial measures of self-monitored blood glucose (SMBG), or a continuous glucose monitoring system (CGMS). The patterns of glycemia required characterization during controlled or ad libitum dietary intake to include the effect of incretin hormones and the enteroinsular axis (15). Thus, investigations using a glucose challenge or glucose infusion were not considered.
Graphic portrayal of data and weighted averages
Exact data were plotted as reported in text or tables by the original authors. When data were only shown in figures, the mean and variance were taken from the graphs. In some cases, complete patterns of glycemia were not reported between meals. For graphic purposes, if a premeal value was not reported, the 24-h mean was used as the between-meal glucose concentration. In the graphs, postprandial (PP) spikes are 1 h (60–70 min) and 2 h after a meal as reported.
Because test statistics were not uniformly reported and methodologies for measuring glucose concentrations were variable, a formal meta-analysis was not possible. Thus, this is a pooled analysis of 12 studies that met our inclusion criteria. Weighted means and SDs were calculated as the product of the mean reported value and sample size for each study. The sum of the products across studies was then calculated and divided by the total number of study participants. In addition, mean 1- and 2-h PP glucose concentrations were calculated across three meals (breakfast, lunch, and dinner). Data are presented as weighted mean ± SD.
Twelve studies met the criteria for inclusion with a total of 255 pregnant women with normal weight and glucose tolerance (Table 1). Table 2 reports data from the included studies, and Fig. 1A graphically depicts the patterns of glycemia. The mean gestational week of study was 33.8 ± 2.3 weeks (range 24–40.8 ± 0.09–8.1 weeks). Most of the women had a BMI <25 kg/m2, although prepregnancy BMI versus BMI at the time of study was variably reported and specific BMI ranges were often unreported. On average, fasting blood glucose (FBG) was 70.9 ± 8 mg/dL (n = 195) (Table 2). The weighted mean pattern of glycemia (including FBG, 1- and 2-h PP, and 24-h mean glucose) is shown in Fig. 1B.
In Table 2, the data from five inpatient studies (16–20), one SMBG study (21), and six CGMS studies (22–27) are reported. The inpatient studies were conducted decades earlier than the CGMS studies, and women were admitted to a metabolic ward. The average FBG concentrations were similar across all of the studies, with the exception of the single SMBG study (21) (Fig. 1A). Across studies, the 24-h mean glucose ranged from 77.4 ± 4.7 to 97 ± 9 mg/dL. The single SMBG study reported the lowest glucose concentrations compared with all other studies. However, by excluding these data, the weighted means changed minimally and these data were included because of the structured study design and controlled variance. One-h PP glucose excursions were higher in the inpatient studies compared with the SMBG and CGMS studies (115.2 ± 13.4 compared with 101.8 ± 3.8 and 110.5 ± 17.7 mg/dL, respectively). However, 2-h PP glucose concentrations were similar for inpatient and CGMS studies (103 ± 13 vs. 102.2 ± 12.2 mg/dL, respectively) but were lower in the SMBG study (92.6 ± 4.7 mg/dL). With all studies included, the average 1- and 2-h PP glucose concentrations across meals were 108.9 ± 12.9 and 99.3 ± 10.2 mg/dL, respectively (n = 160–192; Fig. 1B). The ±1 SD range above the weighted mean for a 1-h PP was 96.0–121.8 mg/dL, and the ±2 SD range was 83.1–134.7 mg/dL. For the 2-h PP target, ±1 SD above the weighted mean ranged from 89.1 to 109.5 mg/dL, and ±2 SDs above the weighted mean ranged from 78.9 to 119.7 mg/dL. Time to peak glucose concentration after a meal, based on the CGMS articles (22,24,25), was an average of 69.4 ± 23.9 min (n = 102).
Review of evidence and discussion
The most compelling finding from our review of the available literature is that glucose concentrations during normal pregnancy in the absence of obesity are lower than the current suggested normal therapeutic targets. As depicted in Fig. 1B, the weighted mean pattern of glycemia reveals an FBG of 71 ± 8 mg/dL, followed by 1- and 2-h PP glucose concentrations of 109 ± 13 and 99 ± 10 mg/dL, respectively, and a 24-h glucose of 88 ± 10 mg/dL. These weighted mean values are appreciably lower than the currently recommended therapeutic targets of ≤95 mg/dL for FBG, <140 and <120 mg/dL at 1- and 2-h PP, respectively (13). Although HAPO provided rigorous outcome data to determine the thresholds appropriate for the diagnosis of gestational diabetes, there are a paucity of data on appropriate therapeutic targets for women with diabetes or gestational diabetes. Until prospective outcome data are generated by examining the most appropriate therapeutic targets to minimize both LGA and small for gestational age (SGA) infants (infants <10th percentile for gestational age), mimicking patterns of normal glycemia in pregnancy, in women without obesity, remains a reasonable goal. The data presented would argue that lower targets be tested in future prospective trials.
Differences in methodology
There has been a reluctance to compare data characterizing glycemia in pregnancy, largely because of differences in study design and methodologies. Studies in women admitted to a hospital have been criticized because of the highly controlled nature of the design (28), the lack of repeated measures throughout pregnancy, and the small numbers of participants (21). These studies removed women from the free-living environment, which changed their physical activity pattern. However, dietary carbohydrate intake was controlled and a liberal amount (190–275 g/day) was administered (Table 1). The controlled physical activity and liberal carbohydrate intake may explain, in part, the somewhat higher PP peaks, particularly by Phelps et al. (20) (Table 2, Fig. 1). Nevertheless, the patterns of glycemia across inpatient studies remain remarkably similar. The CGMS studies may be criticized for opposite reasons. With the exception of one study (27), investigations using CGMS tended to poorly control for the week of pregnancy, with variance up to ±8 weeks reported (22). This makes glucose concentrations difficult to compare because of the variably increasing insulin resistance with each passing week of the third trimester (29,30). Also, with the one exception (27), no effort was made to control dietary intake or physical activity. Further, the methods for interpreting the large volume of data points generated by CGMS are not well described in regard to how FBG and PP values were defined.
There has been further reluctance to compare data among studies because of variations in the methodologies used to measure glucose concentrations. Glucose is unstable in whole blood, including capillary blood. Compared with serum or plasma, glucose concentrations are 11–12% lower in whole blood because of erythrocyte metabolism of glucose via glycolysis. Moreover, compared with plasma, serum glucose concentrations can decrease ∼0.6 mmol/L/h as the result of glycolysis during sample preparation (31). Since 1987 (32), glucometers have been standardized (31) to report plasma-adjusted glucose values (within ±15%) (33). Current CGMS technology measures glucose concentrations in interstitial fluid, which are highly correlated with glucometer-derived plasma-corrected glucose measures (34,35). Thus, although capillary and interstitial glucose concentrations are not recommended for diagnostic purposes (7,33,34), they seem reliable for determination of glucose trends (33,34).
On the basis of our detailed review of the published studies, we think the pooled studies for our analyses were comparable according to the following criteria. First, the inpatient studies reported laboratory-derived glucose concentrations measured in plasma (glucose oxidase) (16,18–20) or serum (photoelectric) (17) (Table 1). None used whole blood measurements, which would have produced lower glucose concentrations. Second, the single SMBG study (21) used a reflectance photometry-based glucometer that reported plasma-corrected values comparable (<10% error) to the standard laboratory glucose oxidase method (36). Thus, the lower glucose concentrations in the SMBG study (21) cannot be explained by use of this glucometer. Third, the CGMS interstitial glucose concentrations are correlated with now standardized glucometer-derived, plasma-corrected glucose measures (34,35). Therefore, although there is undoubtedly a degree of variance among methodologies, it is reasonable to compare the data for therapeutic purposes.
Early descriptive studies of glycemia in pregnancy
The earliest study of glucose metabolism in pregnancy revealed that PP glucose concentrations were higher despite higher insulin levels (37), implying a degree of maternal insulin resistance. These early observations were confirmed in later studies (16–18,20,37) (Tables 1 and 2). Gillmer et al. (16) showed that during normal pregnancy, mean diurnal glucose concentrations increased only 4 mg/dL and rarely exceeded 100 mg/dL. Cousins et al. (18) demonstrated that a lower 24-h glucose area under the curve could be explained by relative nocturnal hypoglycemia. In addition, third-trimester, 2-h postmeal glucose excursions were higher compared with those at 22 to 26 weeks’ gestation.
Studies using SMBG
Parretti et al. (21) published the only study in which SMBG was used to characterize patterns of glycemia (51 pregnancies) controlling for gestational age. Women measured their blood glucose every 2 h throughout the day and night and ate their meals within defined time periods. This structured study tried to approach what had previously been possible only during hospital admission. However, glucose concentrations were far lower than those in any other study (Table 2, Fig. 1A). Although the glucometer used does not seem to explain the lower concentrations, it is possible the women in this study were more physically active or consumed less simple carbohydrates compared with other studies. Furthermore, the women were not blinded to the glucometer measurements, and it is possible that they changed their behavior on the basis of their SMBG concentrations.
Studies using CGMS
The advent of CGMS made it possible to measure continuous patterns of glycemia over a 24-h period, rather than hourly. By using CGMS, it was recognized that women with gestational diabetes had occult periods of hyperglycemia not captured using SMBG (38). Moreover, the glucose peak occurred 90 min PP (rather than 70 min) with the tendency to remain elevated for 3 h without returning to baseline (39). In another CGMS study, obese pregnant (BMI >27 kg/m2) women were shown to have higher preprandial and PP glucose, compared with normal-weight control subjects, and the PP peak was delayed 15 min (22). Unexpectedly, these obese women also had lower nocturnal glycemia compared with control subjects (22). In contrast, Porter et al. (23) did not observe differences in nocturnal glycemia between women with and without a history of macrosomia (Table 1). The former study is the most highly cited study (22) in support of current clinical practice for PP glucose monitoring (13). However, the week of pregnancy during which CGMS was worn varied between 21 and 37 weeks of gestation, diet was not controlled (or reported), and the CGMS analysis of the data was generally not well described (22). Thus, interpretation of the data is limited.
Other groups using CGMS have attempted to control sources of variance (24), but even women with normal pregnancies seem to have a wide range of glucose concentrations (Table 1) (26). In the most controlled CGMS study to date (27), PP blood glucose concentrations increased up to 36 weeks of gestation despite a self-reported constant caloric intake; macronutrient composition of the diet was not reported. Because the study was well controlled for the week of pregnancy, this report provides perhaps the best interpretable data from CGMS yet published.
In summary, the inpatient studies were less “real-world,” but the physical activity and dietary intake were highly controlled, so they likely best captured the normal physiology of pregnancy. On the other hand, the CGMS studies, although less controlled, better depict free-living conditions. Both types of studies require careful interpretation but provide important information. Taken together, the data reveal a range of glycemia in glucose-tolerant women, yet a remarkably similar pattern among studies (Fig. 1A).
Basis for the currently recommended therapeutic targets
The current clinical recommendations for treatment targets in pregnancies complicated by diabetes are not uniform internationally or primarily based on the studies listed in Table 1. Although the therapeutic targets were chosen to attenuate the risk for fetal macrosomia, they have never been prospectively tested compared with lower targets (12,13). Even when current glucose targets are achieved in the pregnancy affected by diabetes, macrosomia still occurs and in utero programming may have a lasting metabolic impact on the offspring (40,41).
The current therapeutic targets of ≤95 mg/dL for FBG, <140 mg/dL for 1-h PP glucose, and <120 mg/dL for 2-h PP glucose (13) were established on the basis of data from women with pregestational and gestational diabetes. In 1986, Willman et al. (42) reported data in 95 women with medication-treated gestational diabetes (A2 gestational diabetes) that indicated a mean 24-h blood glucose concentration >130 mg/dL was associated with a high risk of fetal macrosomia. In 1992, Combs et al. (43) reported that in pregnant women with class B through RF diabetes, a 1-h PP target equal to 130 mg/dL during gestational weeks 29–32 suggested a reduction in macrosomia incidence without increasing the incidence of SGA. Previously, it had been thought that monitoring preprandial versus PP glucose concentrations were equally effective in preventing macrosomia (44). However, data from women with pregestational diabetes (45,46) and later with gestational diabetes (44) established the relation between PP glucose and infant body weight/fetal macrosomia, as well as other infant outcomes (47). The randomized study of de Veciana et al. in 1995 (44) demonstrated that targeting a 1-h PP glucose (compared with preprandial) in women with gestational diabetes was superior in the reduction of macrosomia incidence. In this study, an FBG threshold of <105 mg/dL and a 1-h PP threshold of <140 mg/dL were used, but they were not compared with any other threshold. In 1998, this evidence was cited as the basis for 1- and 2-h PP thresholds of <140 and <120 mg/dL, respectively (14). As a result, these targets were used in most studies published after the year 2000 (21,48–50). As recognized by others (13,51), these cutoffs are not based on randomized studies of alternate treatment targets. In the most recent guidelines from the ADA 5th International Conference on Gestational Diabetes, two studies were cited to support maintaining the current therapeutic targets (21,22) without citation of the inpatient (16–20) or other CGMS studies (23–26).
Although the prevention of macrosomia is clearly an important target for therapy during the pregnancy complicated by diabetes, it is equally important to consider the risk for SGA when testing lower therapeutic targets. Langer and Mazze (52) and Langer et al. (53) observed that a range of 87–104 mg/dL for mean 24-h blood glucose can minimize both SGA and LGA incidence. It has further been observed that overtreatment of pregnant women with diabetes with insulin can cause SGA (54). However, the considerations for type 1, type 2, and gestational diabetes may be different. In long-standing type 1 diabetes, placental perfusion may be compromised to a variable degree because of abnormal placentation from underlying vascular disease or hypertension that may limit glucose availability to the fetus (55). Thus, if glucose concentrations are too low in pregnant women with long-standing diabetes accompanied by vascular disease or placental insufficiency, the glucose gradient to the fetus may be further compromised. This is unlikely to be the case with uncomplicated gestational diabetes. It is also critical to acknowledge that increasing evidence suggests other factors, such as free fatty acids and triglycerides, are extremely important in influencing fetal growth (56,57) as are prepregnancy BMI and, to a lesser extent, gestational weight gain (58). None of the trials that have examined therapeutic glycemic targets to prevent macrosomia have controlled for these significant confounders.
Challenge to reconsider current therapeutic targets
In this critical review and pooled analysis of 12 studies (n = 255 women), we have for the first time graphically compiled patterns of glycemia in normal pregnancy (Fig. 1A and B) and derived weighted means and SDs for clinical application. As seen in Table 2 and Fig. 1A, despite the differences in study design and methodology for measuring glucose, the data fall into a remarkably similar range. The weighted average for FBG was 70.9 ± 7.8 mg/dL (n = 195), well below the current therapeutic target of ≤95 mg/dL (13) and below the HAPO-based diagnostic threshold of <92 mg/dL (7,8). The weighted average for 1- and 2-h PP glucose concentrations across meals were 108.9 ± 12.9 and 99.3 ± 10.2 mg/dL, respectively, also far below the current targets of <140 and <120 mg/dL. Finally, the weighted mean 24-h glucose was 88 ± 10 mg/dL, on the lower end of the observed 87–104 mg/dL range that is thought to minimize SGA and LGA incidence (52,53).
The HAPO study documented a mean FBG of 80.9 mg/dL in >25,000 women with an average BMI of 28 kg/m2 and determined that LGA and a cord C-peptide ≥90th percentile were 1.75 times higher at an FBG ≥92 mg/dL (6). Thus, there are strong data to support that this fasting diagnostic threshold might be adopted as an FBG therapeutic target. However, there are no equivalent data for PP targets. On the basis of our pooled analysis, we suggest prospective controlled studies are needed to test more aggressive therapeutic targets for PP glycemia in pregnancies affected by diabetes, uncomplicated by underlying vascular disease, hypertension, or smoking, and controlled for BMI and gestational age. On the basis of the weighted means, the ±1 SD above the weighted mean for a 1-h PP glucose ranges from 96 to 122 mg/dL and the ±2 SD ranges from 83 to 135 mg/dL. For the 2-h PP target, ±1 SD above the weighted mean ranges from 89 to 110 mg/dL, and ±2 SDs above the weighted mean ranges from 79 to 119 mg/dL. Although the glucose targets 2 SDs above the weighted means (135 mg/dL for 1 h and 119 mg/dL for 2 h) are similar to the current therapeutic targets, it is important to keep in mind that these values are the high end of the SD range. Thus, if a woman with gestational diabetes consistently demonstrates a glucose concentration at or ∼135 mg/dL 1 h after a meal, her average value will significantly exceed the population mean of 110 mg/dL. Although observing that +2 SD values are helpful for understanding normality in a population, it is possible that targeting the mean or the +1 SD range of values will result in a lower risk of macrosomia and, more important, excess neonatal adiposity (59). Therefore, we suggest testing PP targets at +1 SD above the calculated weighted means, 122 and 110 mg/dL (120 and 110 mg/dL, rounded for clinical use) for 1 and 2 h, respectively (Fig. 1B), in women without significant risks for placental insufficiency. We also strongly recommend that recent data supporting a role for maternal lipids as a significant contributor to excess fetal growth be concurrently evaluated in such future studies (60).
The results of 45 years of data characterizing glycemia in normal pregnancy strongly support the need for future prospective studies that specifically test lower therapeutic PP glycemic targets for gestational diabetes, and possibly obese patients, to potentially limit a looming epidemic of fetal macrosomia.
No potential conflicts of interest relevant to this article were reported.
T.L.H. researched and analyzed data and wrote the manuscript. J.E.F. contributed to discussion and reviewed and edited the manuscript. R.E.V. contributed to discussion and data interpretation and reviewed and edited the manuscript. L.A.B. assisted in data analysis, contributed to discussion and data interpretation, and reviewed and edited the manuscript.
- Received February 7, 2011.
- Accepted April 4, 2011.
- © 2011 by the American Diabetes Association.
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