In December 2019, in the Chinese city of Wuhan, a variety of viruses from the Coronavirus group emerged and was named SARS-CoV-2, due to the Severe Acute Respiratory Syndrome Coronavirus. In March 2020, the World Health Organization (WHO) declared a pandemic state in response to the number of infected and killed by COVID-19, a disease caused by the virus [1] [2]. Viral infection induces inflammatory responses through a cascade of cytokines and growth factors, which can damage lung tissue and are responsible for the Acute Respiratory Syndrome [3] [4].

Some conditions predispose to the severe form of the disease. This is possibly due to an impairment of the immune response. Type 2 diabetes mellitus (DM2), in particular, seems to be associated with a worse prognosis once hyperglycemia, in addition to the association with the formation of advanced glycation end products (AGES) result in oxidative stress and inflammatory process that can also favor viral replication [5].

Gestational diabetes (GD), like DM2, is characterized by fasting hyperglycemia as a consequence of resistance to the action of insulin. This resistance occurs due to the production of hyperglycemic hormones and enzymes that degrade insulin, coming from the placenta. During GD, physiological changes, such as immune dysfunction and the promotion of inflammatory factors, make pregnant women even more vulnerable to viral respiratory infections, such as SARS-CoV-2 [6] [7]. For these reasons and due to the restriction of data related to DMG and the involvement by COVID-19, the importance of raising information about these two conditions is evident.

Therefore, this study aimed to perform a literature review about the complications of COVID-19 in patients with GD.

Based on the inclusion and exclusion criteria used for this work, four studies showed the relationship of COVID-19 in DMG patients (Figure 1). Together, these studies included 1101 women aged 15 to 54 years. These studies were carried out in the following countries: China, the United States, France, and Iran. Table 1 shows the characteristics of these studies.

GD: Gestational Diabetes; ICU: Intensive Care Unit.

The review by McIntyre [13] reports that there is insufficient recent evidence to indicate that pregnant women are more susceptible to infection with severe acute respiratory coronavirus syndrome (SARS-Cov-2). Likewise, the case report conducted by Smati et al. [14] narrates about a 36-year-old pregnant woman with GD from the Democratic Republic of Congo hospitalized by COVID-19. Although pregnancy predisposes to an increased chance of diabetic ketoacidosis due to the placenta’s hormonal properties, the study does not clarify whether COVID-19 worsens this condition.

In the same perspective, Gidlöf et al. [15], through the report of a 34-year-old GD woman, sought to establish the maternal-fetal complications implied by COVID-19 manifested by the patient. Although the patient showed some characteristic clinical signs, such as pneumonia, the twins were born in good condition, condition supported by negative nasopharyngeal tests for COVID-19, as well as a sample of breast milk.

One of the hypotheses that explain that vertical transmission of the SARS-CoV-2 virus is unlikely is that the angiotensin-converting enzyme 2 (ECA2), which works as a receptor for the virus, has no significant expression in the cells of the interface maternal-fetal. Moreover, transmission via breastfeeding was also absent due to the virus’s non-detection in breast milk samples. However, infection through contact should not be neglected in these cases, and the distance between mother and baby is safer during the period of transmissibility [16].

The cohort study performed by Pirjani et al. [10] compared possible differences between pregnant women infected with SARS-CoV-2 and uninfected women. Four of the infected patients required care in the ICU, but there was no need for intubation, mechanical ventilation, and they did not have acute respiratory syndrome. Only one baby was infected, but it was not possible to determine the cause of transmission. Therefore, it was not possible to establish differences in prognosis between infected and uninfected women.

On the other hand, the study of Torlone et al. [17] shows that adverse endpoints and mortality are higher in pregnant women with diabetes, precisely because scientific evidence indicates that hyperglycemia promotes immune changes such as the inflammatory state that worsens insulin resistance. Moreover, in the immune response, the most likely infections are viral respiratory infections, which do not have data to confirm the vertical transmission of COVID-19. Therefore, the current pandemic context requires greater care for the diagnosis and treatment of gestational diabetes.

In a study carried out using data from 33 French maternity hospitals, in which in all analyzed cases the women were pregnant and diagnosed with COVID by the RT-PCR test, it was shown that women with diseases such as GD, pre-eclampsia, old age, or age over 35 and obesity, as well as preexisting diabetes, are more likely to have COVID comorbidities [11].

In the study of Panagiotakopoulos et al. [9] performed in eight health centers in the USA, the hospitalization of 105 pregnant women identified with SARS-CoV-2 was evaluated. Among them, 59% were hospitalized for obstetric reasons and 41%, due to COVID-19 and who had no obstetric reasons. In the latter group, a higher prevalence of GD (25.6%) and pre-pregnancy obesity (44.2%) was found among those hospitalized for obstetric reasons. Besides, the prevalence of premature and stillbirth was higher among women with SARS-CoV-2 than in uninfected women.

In another perspective, in an analysis of post-COVID-19 management in the diagnosis of GD in the protocols of the United Kingdom, Canada, and Australia, it is recommended to restrict the Oral Glucose Tolerance Tests (TOTG), performed between 24 and 32 gestational weeks, in order to reduce exposure to COVID-19 in the collection centers, monitoring and guiding pregnant women with alternative resources such as telemedicine [13]. However, the restriction of oral glucose tolerance test (OGTT) would result in a reduction in the frequency of diagnosis of GD in studies, from 81% to 2.5% in the United Kingdom, from 82% to 1.7% in Canada, and from 25% to 12%, 7% in Australia.

A case-control by Sun et al. [9] at Wuhan shows, through laboratory and clinical diagnosis, that the number of neutrophils in GD women with COVID-19 was higher than the pregnant COVID-19 patients without any chronic disease. The data also confirm that lymphocytopenia levels among pregnant women with COVID-19 were higher (43.33%) in relation to the control group (15.83%). Hyperglycemia is a diabetes comorbidity which causes oxidative stress, can increase inflammatory response and compromise the liver’s regeneration [12].

In another study conducted at a London tertiary hospital, the OGTT restriction guidelines published by the Royal College of Obstetricians and Gynecologists during the pandemic impacted the reduction in the rate of detection of GD

Besides that, van Gemert et al. [18] points out that guidelines have been revised to reduce the number of pregnant women with GD exposed to the virus.

In a narrative review of the temporary changes in clinical guidelines performed by Nouhjah et al. (2020), there is a consensus to postpone postpartum screening from 4 to 12 weeks or delay from 6 to 12 months after birth until the end of the COVID-19 crisis. These changes aim to reduce the number of consultations and length of stay in the hospital for pregnant women, in addition to the risks of exposure, since pregnant women with diabetes constitute a population at risk for severe forms of COVID-19 [19] [20] [21] [22]. Also, all women should be encouraged to lead a healthy lifestyle during pregnancy, given the risk that gestational diabetes will not be detected with changes in screening protocols, in addition to maintaining basic precautionary measures such as hand hygiene, wearing masks, and social detachment [23] [24].

Changes in the management of post-COVID-19 GD diagnosis were another aspect discussed in the studies discussed above. Most of these changes prioritize restricting oral glucose tolerance tests, as well as reducing visits to collection centers, and hospital stays in order to deprive patients of exposure to the virus. In this context, it is recommended to adopt healthy lifestyle habits, given the risk that GD will not be detected with changes in screening protocols and telemedicine monitoring.

There are divergences between studies concerning complications related to COVID-19 in patients with GD. Although hyperglycemia and pregnancy are aggravating factors for infections, especially viral respiratory infections, there is no scientific evidence to clarify the mechanisms that promote the severe form of COVID-19 when present with GD. Despite this, some authors have shown no substantial complications in pregnant women infected with SARS-CoV-2 and who had comorbidities such as DMG. In these cases, the severe acute respiratory syndrome was not present. However, clinical conditions, such as pneumonia, were manifested. There was also no evidence of vertical transmission of COVID-19.

Therefore, further studies are needed to elucidate the consequences of the contamination of this virus in GD women.

The authors declare no conflicts of interest regarding the publication of this paper.

Miola, V.F.B., de Oliveira dos Santos, A.R., de Oliveira Zanuso, B., Pinto, M.E.G., Pillon, J.P.G., dos Santos Haber, J.F., de Alvares Goulart, R. and Barbalho, S.M. (2020) COVID-19 and Gestational Diabetes: A Systematic Review. Journal of Diabetes Mellitus, 10, 236-244. https://doi.org/10.4236/jdm.2020.104019