CHAPTER 28 Margaret Dziadosz and Ashley S. Roman Department of Obstetrics and Gynecology, NYU School of Medicine, New York University, New York, NY, USA Diabetes mellitus (DM) complicates approximately 6–7% of all pregnancies in the United States. The American Diabetes Association has classified glucose intolerance into three different types (Table 28.1). Gestational diabetes mellitus (GDM), or carbohydrate intolerance with onset or recognition during pregnancy, represents 90% of cases [1]. The White classification is another system for classifying diabetes in pregnancy (Table 28.2). White classification class A1 diabetes (GDMA1) represents pregnant women with gestational diabetes mellitus who are able to maintain glucose control with exercise and diet alterations. White classification class A2 diabetes (GDMA2) represents pregnant women with gestational diabetes who require medication therapy in order to maintain adequate glucose control. Table 28.1 American Diabetes Association three types of glucose intolerance Table 28.2 White classification for diabetes in pregnancy The remaining 10% include both Type 1 and Type 2 diabetes mellitus. This cohort accounts for over eight million women in the US alone at any given time. Type 1 pregestational DM (DM1) occurs as the result of an autoimmune process that destroys pancreatic B cells, leading to a need for insulin therapy [2]. Type 2 pregestational DM (DM2) is characterized by peripheral insulin resistance and insufficiency. The rising epidemic of DM2 is associated with the increasing rate of obesity and metabolic syndrome. Insulin resistance increase in pregnancy is largely related to an increase in placental hormones such as human placental lactogen (promotes lipolysis and decreased glucose uptake), prolactin, cortisol (insulin antagonist), tumor necrosis factor α, leptin, and placental growth hormone. Estrogen and progesterone further disrupt mechanisms of glucose and insulin [3]. Insulin sensitivity is greatest at the end of the first trimester, with the greatest risk of maternal hypoglycemia, and lowest insulin sensitivity in the third trimester, the time of greatest insulin requirement. A decrease in maternal exercise and an increase in caloric intake and altered adipose deposition compound glucose intolerance in pregnancy. All pregnant women who do not have a diagnosis of pregestational diabetes should be routinely screened for gestational diabetes at 24–28 weeks gestation. However, some debate exists over the optimal screening approach. The International Association of Diabetes and Pregnancy Study Groups (IADPSGs) recommend a one‐step testing approach using the 75 g two‐hour oral glucose tolerance test (GTT). A positive test results occurs if any single threshold is abnormal: fasting value 92 mg ml−1, one‐hour value 180 mg dl−1, two‐hour value 152 mg dl−1. The American College of Obstetricians and Gynecologists (ACOG) recommends the two‐step approach. This involves a 50 g oral glucose challenge test (GCT), followed by a 100‐g three‐hour oral GTT in screen positive women (Table 28.3). A threshold of ≥130 mg dl−1 (7.5 mmol l−1) to ≥140 mg dl−1 (7.8 mmol l−1) may be used to determine candidates for the 3‐hour oral GTT dependent on institutional preference [2]. If a patient has a value of ≥200 mg dl−1, they do not require the 3‐hour test for confirmation and are diagnosed with GDM. Table 28.3 Diagnostic criteria for three‐hour 100 g oral GTT For women at high risk of pregestational diabetes but who do not carry this diagnosis upon initiation of prenatal care, consideration should be given to screening for diabetes in the first trimester. Women with risk factors including obesity, known impaired glucose tolerance or a past history of GDM are candidates for early screening [4]. Early screening may include A1C analysis. A value >6.5% (>48 mmol mol−1) is diagnostic of T2DM. In addition, a fasting glucose of >126 mg dl−1 or a GCT of >200 mg dl−1 are also diagnostic of T2DM [5]. Adverse outcomes associated with DM in pregnancy include pre‐eclampsia, hydramnios, macrosomia, or large for gestational age infant, maternal or infant birth trauma, operative delivery, neonatal respiratory problems, and metabolic complications such as hypoglycemia, hyperbilirubinemia, hypocalcemia, and erythremia, and fetal demise. In addition, if a mother is hyperglycemic during organogenesis, there is significantly increased risk of miscarriage and congenital anomalies [6–8].
Diabetes mellitus
Clinical questions
Classification
Mechanism of disease
No insulin required
Insulin required
Insulin required for survival
Type I diabetes mellitus
Immunologic destruction of pancreas
Type II diabetes mellitus
Resistance of pancreatic cells
Gestational diabetes mellitus
Glucose intolerance not present prior to pregnancy
Gestational diabetes mellitus (GDM)
GDM A1
Controlled by diet, exercise
GDM A2
Requires medicotherapy
Pregestational diabetes mellitus
A
Abnormal glucose tolerance at any age or duration treated only by nutritional therapy
B
Onset age ≥ 20 years and duration <10 years
C
Onset age 10–19 years and duration 10–19 years
D
Onset <10 years, duration >20 years, benign retinopathy, or hypertension (not pre‐eclampsia)
D1
Onset <10 years
D2
Duration >20 years
D3
Benign retinopathy (microvascular)
D4
Hypertension (not pre‐eclampsia)
R
Proliferative retinopathy or vitreous hemorrhage
F
Renal nephropathy and >500 mg dl−1 proteinuria
RF
Criteria met for both Type R and F
G
Multiple pregnancy failures
H
Evidence of arteriosclerotic heart disease
T
Prior renal transplantation
Glucose level
Carpenter and Coustan criteria
National Diabetes Data Group criteria
mg dl−1
mmol l−1
mg dl−1
mmol l−1
Fasting
95
5.3
105
5.8
One hour
180
10
190
10.6
Two hours
155
8.6
165
9.2
Three hours
140
7.8
145
8