2Endocrinology and diabetes unit, internal medicine department, Faculty of Medicine, Beni suif University
3Endocrinology and diabetes unit, internal medicine department, Faculty of Medicine, Elfayoum University
4Endocrinology and diabetes unit, internal medicine department, Faculty of Medicine, Zagazig University
5Gynaecology and Obstetrics department, Faculty of Medicine, Assiut university
6Clinical Pharmacy Department, Faculty of Medicine, Assiut university
*7Internal Medicine Department, Faculty of Medicine, Cairo University
Objective: This study aims to determine the prevalence and risk factors of GDM among pregnant women in Upper Egypt and to evaluate the foetal and maternal outcomes of this disease.
Methods: This prospective cohort study was conducted between July 2014 and July 2018. Universal screening for GDM among all pregnant women attending primary health care clinics was done using Diabetes in Pregnancy Study Group of India (DIPSI) criteria. Those with GDM were followed up until the end of purpureum. Maternal and foetal outcomes were recorded.
Results: GDM was diagnosed in 956 out of 7141 pregnant women (13.4%). Previous history of GDM, macrosomic babies, and family history of diabetes were all significantly higher in GDM women (P<0.001 each). However, no definite risk factors were observed in about half of the GDM women. 29% of GDM women responded to medical nutrition therapy (MNT) alone. When the oral glucose tolerance test (OGTT) was repeated Postpartum, diagnosis of DM was established in 14.3% of the cohort, while 25.7% had impaired glucose tolerance.
Conclusions: The prevalence of GDM is relatively high in Upper Egypt. Half of GDM cases lack risk factors. Universal screening using OGTT should be routinely performed to all attendant pregnant ladies. Discrete MNT is not an enough management in most of GDM cases.
Keywords: GDM; Postpartum OGTT; diabetes; MNT; foetal outcome; maternal outcome.
• The study disclosed a high prevalence of GDM (13.4%) dictating the necessity of the universal screening and early detection of GDM using OGTT.
• This screening test should be applied to all pregnant women even those lacking any of the risk factor known.
• The rising trend of GDM among the Egyptian pregnant women should be checked by increased awareness of the community and encouragement of married women to maintain average weight.
• Further large-scale studies are needed to have a clear perception of the prevalence of GDM in Egypt.
The prevalence of GDM is enhanced by many habits in the community. Urbanization and overconsumption of junk food, even among the low socioeconomic population, often lead to obesity. Unfortunately, overweight is erroneously considered a sign of beauty and good health among Egyptian ladies. Furthermore, the huge work burden posed on low socioeconomic Egyptian women either indoor or outdoor hinders them from suitably prioritizing their health.
GDM documented prevalence varies substantially worldwide, ranging from 1% to >14% [6]. Complexity and controversy have shadowed the diagnosis of GDM among health care providers owing to the lack of consensus and uniformity in the screening standards and diagnostic criteria of GDM [7]. Furthermore, it is challenging to compare the prevalence across countries and regions. The diagnosis of GDM offers a unique opportunity to identify individuals who are susceptible to develop type 2 diabetes mellitus (T2DM). These cases will get the benefit of early lifestyle modification and therapeutic intervention that would delay or even prevent the onset T2DM.
So far, the actual prevalence rate of GDM in Egypt is unknown. The universal screening for GDM was selected in the current study thanks to its high sensitivity. We chose the Diabetes in Pregnancy Study Group of India (DIPSI) criteria for diagnosis of GDM thanks to its simplicity; only one sample of blood is taken, besides the non-necessity for fasting [8-10].
Treatment of GDM aims at minimizing the risk of perinatal outcomes such as macrosomia, birth trauma, neonatal metabolic abnormalities, and the need for caesarean section [2,11]. Lifestyle modification is the first-line treatment and includes medical nutrition therapy (MNT), exercise, and glucose monitoring.
Pharmacological treatment generally consists of insulin, glyburide, or metformin [4,11-13]. Insulin is the preferred pharmacological treatment for the management of GDM if lifestyle modification is insufficient in achieving euglycemia [11-13]. The present study aims to determine the prevalence and risk factors of GDM among pregnant women in Upper Egypt governorates and to evaluate both maternal and foetal outcomes.
Intervention
Eligible participants signed a written consent after adequate counselling and reading the patient information sheet. Participants were given 75 g of glucose anhydrous dissolved in 200 ml of water. All participants were not fasting before the test. Blood samples for glucose estimation were collected after two hours using DIPSI criteria. Blood sugar level ≥ 140 mg/dl was diagnostic for GDM. Blood sugar values ≥ 200 mg/dl indicated the pre-existence of diabetes [4] and therefore were excluded from the study.
Medical nutrition therapy was advised to all GDM cases. If the blood glucose level didn’t reach the target (FBG <92mg/dl, one hour <140mg/dl, and two hours <120mg/dl) after two weeks, insulin was added. Metformin was the alternative in cases incapable to afford or refusing insulin.
Follow up
Women with GDM were followed by regular visits every two weeks until delivery and monthly for one year afterwards. The modes of delivery as well as any obstetric or medical complications were reported. At each visit, complete physical assessment, including weight and blood pressure monitoring was done. Check for the self-monitored blood glucose levels were also accomplished. Foetal assessment, including foetal movement, was assessed by an obstetrician and then by paediatrician post-partum.
Six to twenty-four weeks after delivery, OGTT was repeated for GDM women to detect cases that had frank T2DM.
Statistical analysis Data were collected and analyzed using SPSS (Statistical Package for the Social Science, version 20, IBM, and Armonk, New York). Continuous data were expressed in the form of mean ± standard deviation, while nominal data were represented in frequency (percentage). Student’s t-test and Chi-square test were used to check the significance. Multivariate regression analysis was performed to evaluate the risk factors for GDM development. P-value was considered statistically significant if <0.05.
Ethical considerations
The Assiut Faculty of Medicine Ethical Review Board had approved the study protocol and guaranteed that confidentiality would be maintained and ethical principles would be followed all through the study. Patients who met the eligibility criteria were informed, and their written consent was obtained before the start of the study.
719 (75.2%) of the GDM cases versus 3772 (61%) of the remaining cases were older than 25 years (p<0001). 68% of the GDM were from urban areas, and 64.4% were not working. In addition, 40.2% of the GDM women were multiparous (have 3 or more conceptions) in comparison to 27.2% of those without GDM (P<0.001). Furthermore, most of the studied cohort had either increased body weight or were obese (42.8% and 44.6%, respectively), while normal pre-conception body mass index (BMI) was observed in only 12.7% of cases. BMI was significantly higher in GDM women (30.91 ± 5.95 vs. 29.40 ± 5.54 Kg/m2, p<0.001) (Figure 1).
39.7% of GDM cases have a positive family history of diabetes, and 10.5% have a previous history of a macrocosmic baby. Polycystic ovary syndrome (PCOS) and twin pregnancy were significantly higher in GDM cases (9% vs. 6%, p<0.001 and 6.5% vs. 3.5% respectively, p<0.001in both). On the other hand, no definite risk factors were demonstrated in about half of the GDM women (49.4%). Both systolic (SBP) and diastolic blood pressure (DBP) were significantly higher in GDM women; (118.09 ± 12.55 vs. 115.39 ± 11.55, and 74.97 ± 9.40 vs. 72.98 ± 8.71 for SBP and DBP respectively, p<0.001 in both).
29% of GDM women were controlled with MNT only, while 31% of them needed the addition of metformin to MNT, and 40% were controlled after the addition of insulin to MNT (Figure 2).
As regards the maternal outcome of GDM cases, 39.3% developed preeclampsia, 81.5% delivered by cesarean section (CS), and 17 % had preterm labour. As regards the foetal outcome of GDM babies, 74.3% had persistent physiologic jaundice, 52.1% needed neonatal intensive care unit (NICU) admission, 20.9% developed hypoglycaemia, 14.3% were macrosomic, 3.6% had congenital cardiac problems, and 7.1% died (Table 1).
After delivery, only 560 out of 956 (58.6%) continued regular follow up. Oral glucose tolerance test (OGTT) performed four to twentyfour weeks postpartum disclosed normal test in 60%, impaired glucose tolerance in 25.7%, and frank T2DM in 14.3% (Fig. 3)
MNT= medical nutrition treatment
Parameter |
P value |
Odd ratio |
95% confidence interval |
|
Lower |
Upper |
|||
Age: (years) |
|
|
|
|
25 - < 30 years |
0.011* |
1.292 |
1.062 |
1.573 |
≥ 30 years |
0.000* |
1.604 |
1.293 |
1.989 |
Parity: |
0.033 |
|
|
|
Para 1 – 3 |
0.400 |
1.310 |
0.698 |
2.460 |
Para > 3 |
0.138 |
1.635 |
0.854 |
3.127 |
Working |
0.000* |
1.624 |
1.401 |
1.884 |
Age at marriage (≥ 20 years) |
0.002* |
1.295 |
1.104 |
1.519 |
History of GDM |
0.000* |
2.558 |
1.828 |
3.580 |
History of Macrosomic baby |
0.000* |
1.604 |
1.238 |
2.078 |
Polycystic ovary |
0.148 |
1.210 |
0.934 |
1.567 |
Twin pregnancy |
0.007* |
1.524 |
1.125 |
2.065 |
Family history of diabetes |
0.000* |
1.576 |
1.360 |
1.827 |
About half of our cohort had no risk factors of GDM. The same was true in a previous study of a nearby geographic area in Assiut (31.8%) [16]. This finding was similar to a Malaysian study where 23.8% of women diagnosed to have GDM were without any Known risk factor [28]. This finding would encourage the universal screening for GDM among all pregnant women. However, there is uncertainty as to whether or not to use universal screening versus selective ones. WHO (2006) recommended universal screening while the American Diabetes Association (ADA, 2019) and the American College of Obstetricians and Gynecologists (ACOG ,2018) recommend screening for GDM in high-risk women [29-31].
Worldwide, there are many guidelines with recommendations for appropriate management strategies for GDM once lifestyle modifications have been instituted and failed to achieve control. Pharmacologic treatment of GDM remains controversial; while ACOG (2018) is firmly recommending insulin as the preferred first-line, ADA (2019) dictated that most women with GDM could achieve normoglycemia with nutritional therapy alone [30,31]. In the current study, we found that onl 29% of the GDM women responded to MNT, while 31% needed the addition of metformin to MNT, and 40% needed insulin addition. These data match the observations of other investigators [16, 32], while others found that insulin was needed in only 20 and 8% of GDM women, respectively [33,34].
Women with GDM are more likely to develop T2DM and require lifelong diabetes screening [35]. Within 5–16 years after pregnancy, up to 65% of women with previous GDM present with T2DM [36]. Unfortunately, Loss of health coverage after pregnancy limits access to follow-up care. For this reason, there are no large registries for tracking postpartum T2DM among women in under-resourced communities. These women face challenges with access to care after pregnancy [35]. In the present study, only 560 women attended the scheduled postpartum OGTT. 60% of the women tested (n=336) had normal OGTT and 40% (n=224) had abnormal test as either impaired glucose tolerance in 25.7% (n=144) or frank diabetes in 14.3% (n= 80). These results were slightly inconsistent with a previous study from Upper Egypt, which demonstrated that 52.7% of GDM women postpartum returned to normal, 12.7% had overt diabetes, 21.3% had impaired fasting glucose, and 13.3% had impaired glucose tolerance [37]. Also, another earlier studies done in Brazil and Iran demonstrated that overt postpartum diabetes mellitus and IGT were 8.1% and 21.4%, respectively, while 70.5% restored normoglycemic state [38,39]. However, some other studies reported a lower prevalence rate of diabetes that ranged from 2-8% [40-42].
Study limitations
Lack of structured dietitians explaining the role of MNT in the management of GDM and the noncompliance of pregnant women to MNT may explain the decreased response to MNT. Another limitation was that considerable number of GDM women missed the post-partum follow-up. This miss is likely due to the lack of motivation.
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