In Finland in 2021, the average BMI of pregnant women was 25.7 kg/m2 and more than 18% were obese; in 2010 the respective figures were 24 kg/m2 and 12%. Glucose tolerance test was abnormal in 21% in 2018 and in 11% in 2010.
Diagnosis
Screening can be done by performing a 2-hour 75-g glucose tolerance test.
HbA1c is not sufficiently sensitive and should not be used as a diagnostic method.
A glucose tolerance test should primarily be performed in week 24-28 of pregnancy.
A glucose tolerance test is unnecessary in the following cases:
a primigravida aged below 25, BMI below 25 kg/m2 and no type 2 diabetes in close relatives
a multigravida aged below 40 with BMI below 25 kg/m2 , who has not given birth to a macrosomic baby.
A glucose tolerance test should be done in week 12-16 of pregnancy in women:
with GDM in a previous pregnancy
with a BMI ≥30 kg/m2 before pregnancy
with glucosuria in early pregnancy
with type 2 diabetes in close relatives (parents, siblings or children)
taking oral glucocorticoids.
If a glucose tolerance test done in early pregnancy is normal, it should always be repeated in week 24-28 of pregnancy.
Diagnosis is made if the glucose tolerance test shows one or more pathological concentrations (see table T1).
Notice that some national variation exists concerning what is considered normal in glucose tolerance test. Table T1 indicates the threshold concentrations recommended by the International Association of the Diabetes and Pregnancy Study Groups (IADPSG) in 2010 and concentrations used currently in Finland. Further national variation may apply.
If the fasting concentration exceeds 7 mmol/l, the test should not be continued but the mother should be referred to a maternity outpatient clinic for assessment.
If more than one abnormal concentration is obtained in the test, GDM is usually more severe; in one in three of such mothers, medication must be started in addition to dietary treatment.
If diabetes other than gestational diabetes is suspected in early pregnancy, HbA1c can be measured in addition to performing a glucose tolerance test, and the woman can be referred for assessment in specialized care.
There is limited scientific knowledge on the long-term safety of metformin for children. Metformin does not appear to adversely affect the prognosis of the child at 9 years of age.
Follow-up of pregnancy and childbirth
If nutritional therapy is sufficient and the pregnancy is otherwise unproblematic, the risk of perinatal complications is low and the pregnancy can be followed up at a maternal welfare clinic.
If the blood glucose target concentrations are exceeded during nutritional therapy, medication should be started and follow-up carried out in specialized care.
There are no clear recommendations on the frequency of follow-up visits, but visits are recommended every 2-4 weeks with frequency increasing towards the end of pregnancy and with particular attention paid to foetal macrosomia, blood glucose control and blood pressure problems.
It is important to monitor the growth of the uterus and the development of foetal weight in order to be able to detect foetal macrosomia early enough and to be able to plan the time and mode of delivery at the maternity hospital Gestational Diabetes Mellitus and Pregnancy Outcomes.
The definition of macrosomia varies. In many European countries and the USA, the upper limit of normal birthweight in full-term babies is considered to be at 4 000 g, and a neonate weighing more than that is considered macrosomic. Large for gestational age (LGA) is defined as birthweight being greater than the 90th percentile at birth and takes into account the child´s gestational age. In Finland, a neonate is considered macrosomic when birthweight is more than 2 standard deviation (SD) over the average birthweight in the reference population (for a full-term baby 4 500 - 4 600 g).
Macrosomia is about twice as common in foetuses of patients with gestational diabetes receiving insulin treatment than in those receiving dietary treatment.
There are no similar comparisons for metformin-treated patients. Metformin-treated patients have a smaller incidence of macrosomia compared to insulin-treated gestational diabetes patients.
Risk factors for macrosomia include the severity gestational diabetes, maternal obesity, large weight gain during pregnancy, dyslipidaemia (low HDL and high triglyceride concentration) and a history of having had a macrosomic baby Gestational Diabetes Mellitus and Pregnancy Outcomes.
Maternal hyperglycaemia causes foetal hyperinsulinaemia, which has an anabolic effect. In this case, the risk of foetal oxygen deficiency during late pregnancy is increased.
In the foetus of a diabetic mother, the trunk circumference is large compared to the head circumference. In vaginal birth, this increases the risk of shoulder dystocia and brachial plexus injury, of other problems with assisted delivery and of maternal tears.
With lifestyle treatment, pregnancy can usually be allowed to continue for 7-12 days beyond the calculated delivery date if the glucose control is good and there are no other complications associated with the pregnancy.
In the case of pharmacological therapy, the induction of labour is considered after the completion of week 39 of pregnancy, but at the latest around the calculated delivery date, because of the increased risk of asphyxia in late pregnancy.
Delivery is recommended after week 38 of pregnancy if
the foetus is becoming macrosomic (weight estimate +2 SD)
the mother's glucose homeostasis is not optimal or
there are other risk factors associated with the pregnancy.
Delivery according to individual assessment:
Usually vaginally if the child is estimated to weigh below 4 000 g
Usually by caesarean section if the child is estimated to weigh over 4 500 g
National differences may apply.
The accumulation of risk factors related to the mother (obesity, duration and severity of hyperglycaemia) and the foetus (macrosomia) increases neonatal problems in gestational diabetes.
Hypoglycaemia is the most common neonatal problem.
About 30% of neonates of mothers with gestational diabetes have plasma glucose concentrations of < 2.6 mmol/l and 20% < 2.0 mmol/l in the first days.
The child has an approximately 1.5-fold risk of RDS (respiratory distress syndrome) or TTN (transient tachypnoea of the newborn).
Other neonatal findings include polycythaemia, hyperbilirubinaemia, hypocalcaemia and myocardial thickening.
Neonates are 2-4 times more likely to be admitted to the neonatal intensive care unit.
Postnatal glucose tolerance test (reference concentrations: fasting concentration< 6.1 mmol/l and 2-hour concentration< 7.8 mmol/l)
For patients on medication, after 6-12 weeks
For patients on dietary treatment, after about 1 year
In this connection, BMI and blood pressure should be checked and the patient motivated to achieve/maintain normal weight and a healthy, physically active lifestyle.
Subsequently every 1-3 years (depending on the results and the maternal risks)
Glucose tolerance test or HbA1c, BMI, waist circumference, blood pressure, plasma lipids
Gestational diabetes recurs in about 40-60% of the patients. The risk is increased by:
early GDM (before week 24) in the preceding pregnancy
history of pharmacological treatment
born macrosomic baby
maternal overweight or large weight gain between pregnancies
Gestational diabetes, particularly if associated with maternal overweight, increases the risk of subsequent obesity, disturbances of glucose metabolism and the metabolic syndrome in the child. There may also be an increased risk of cardiovascular diseases.
References
Crowther CA, Samuel D, McCowan LME, et al. Lower versus Higher Glycemic Criteria for Diagnosis of Gestational Diabetes. N Engl J Med 2022;387(7):587-598. [PubMed]
Hillier TA, Pedula KL, Ogasawara KK, et al. A Pragmatic, Randomized Clinical Trial of Gestational Diabetes Screening. N Engl J Med 2021;384(10):895-904. [PubMed]
Vounzoulaki E, Khunti K, Abner SC, et al. Progression to type 2 diabetes in women with a known history of gestational diabetes: systematic review and meta-analysis. BMJ 2020;369():m1361. [PubMed]
van Kempen AAMW, Eskes PF, Nuytemans DHGM, et al. Lower versus Traditional Treatment Threshold for Neonatal Hypoglycemia. N Engl J Med 2020;382(6):534-544. [PubMed]