LAUSR

Gestational diabetes (GDM) is one of the most common perinatal complications. As pregnant women have to consume 75 g of glucose during an oral glucose tolerance test (OGTT) in order to diagnose GDM, they have to stay longer in hospitals. Since its outbreak, COVID-19 has spread all over the world. To prevent the COVID-19 infection, patients must minimize hospital visits, avoid spending long periods of time at the hospital, and limit face-to-face contact with healthcare practitioners. As a result, the Japanese Society of Diabetes and Pregnancy published the Japanese GDM diagnostic strategy in the evolving COVID-19 pandemic, on the 10th of April 2020. This strategy is a modification of the United Kingdom and Australian guidelines. With this background, we investigated whether the strategy was suitable for the Japanese GDM population. We retrospectively investigated the records of a cohort of 264 women diagnosed with GDM in their second trimester, using the International Association of Diabetes in Pregnancy Study Group (IADPSG) criteria, who received perinatal care at our hospital between January 2013 and December 2019. We re-classified them retrospectively using the Japanese GDM diagnostic strategy in the evolving COVID-19 pandemic. This strategy in the second trimester was defined as follows: the COVID-19-GDM group, HbA1c ≥ 38 mmol/mol (5.7%), random glucose level (RPG) ≥ 9.0 mmoL/L (162 mg/dL), or fasting plasma glucose (FPG) ≥ 5.1 mmoL/L (92 mg/dL); no further testing (COVID-19-NFT)-group, HbA1c < 38 mmol/mol (5.7%), random glucose level (RPG) < 9.0 mmoL/L (162 mg/dL), or fasting plasma glucose (FPG) < 5.1 mmoL/L (92 mg/dL). This study was approved by the ethical committee of Keio University School of Medicine (No. 20150103). Of the 264 patients, 104 were diagnosed with COVID-19-GDM and 160 GDM patients diagnosed using the IADPSG criteria were reclassified as COVID-19-NFT. In the COVID-19-GDM group, no patients were diagnosed with RPG ≥9.0 mmoL/L (162 mg/dL). A comparison of maternal characteristics between the COVID-19-GDM and COVID19-NFT groups has been shown in the Table 1 below. The incidence of 1 hourand 2 hours-glucose level positives in the COVID-19-NFT group were significantly higher than those in the COVID-19-GDM group (P < .01). There was no difference in the incidence of insulin requirement during pregnancy between the two groups (P = .08). As the Japanese population has lower ability of insulin secretion compared with other ethnicities such as the Caucasians, the Japanese women with GDM has been shown to associate with impaired insulin secretion or beta cell dysfunction in our previous report. In the Japanese GDM diagnostic strategy in the evolving COVID-19 pandemic, which is a modification of criteria from other countries, FPG and HbA1c are listed as important for diagnosing GDM. However, FPG is associated with insulin resistance. Since FPG in Japanese people is lower than that in Caucasians, the 160 patients who were diagnosed using the IADPSG criteria were re-classified as COVID-19-NFT (61%). As 65 patients (41%) in the COVID-19-NFT group required insulin during pregnancy, many patients with GDM who should be treated as such, might not be diagnosed when the Japanese GDM diagnostic strategy in the evolving COVID-19 pandemic is used. Furthermore, according to our results, to diagnose COVID-19-GDM, the cutoff value of RPG might be unsuitable for Japanese GDM because there were no patients who were diagnosed with RPG ≥9.0 mmoL/L (162 mg/dL) in this study. Therefore, further research may be needed based on bigger data sets, to define the cutoff value of RPG to detect Japanese GDM. While the 50-g glucose challenge test (GCT) is not a definitive diagnosis of GDM, the sensitivity of GCT (74%) in the previous report was higher than that in the Japanese GDM diagnostic strategy in the evolving COVID-19 pandemic for diagnosing GDM. While pregnant women have to spend longer periods at the hospital for GCT than those for RPG, if we can create a new strategy such that the pregnant women consume 50 g of glucose for GCT before Received: 12 May 2020 Accepted: 15 May 2020