Abstract
Aim
To evaluate whether the first Covid‐19 lockdown for Italian citizens (March to July 2021) might have altered the incidence of gestational diabetes mellitus (GDM).
Methods
A retrospective single‐center study in a tertiary referral center. Primary outcome was the incidence of GDM among pregnant women. GDM incidence, from June 11, 2019 to December 4, 2020, was compared by dividing the study time as follows: from the beginning of the study to before Covid‐19 lockdown (from June 11, 2019, to March 9, 2020) and lockdown period (from March 10, 2020, to December 4, 2020). GDM was diagnosed with a 75‐g, 2‐h oral glucose tolerance test (OGTT) at 24–28 gestational weeks.
Results
Concerning 1295 women, GDM incidence increased during the lockdown period (9.3% vs. 3.4%, p < 0.001). Higher pregnancy weight gain with an increased body mass index (BMI) at the delivery was reported during the lockdown (31.3 vs. 28.4 kg/m2, p = 0.02 and mean weight gain of 9.3 vs. 6.6 kg, p = 0.007). There was no difference in other comorbidity incidence and OGTT values between the two groups.
Conclusions
Pregnant women during the Covid‐19 lockdown might have experienced higher BMI and pregnancy weight gain with increased GDM diagnoses. This may be related to physical limitations and emotional distress experienced during the lockdown. However, evidence is limited due to restricted study duration and random variations of outcomes across time. More studies are needed to understand the dietary patterns and the physical activity changes during the Covid‐19 lockdown and its impact on fetal outcomes.
Keywords: Covid‐19, diabetes gestational mellitus, gestational diabetes, lockdown, pregnancy, pregnancy outcomes, SARS‐CoV‐2
Introduction
Gestational diabetes mellitus (GDM) is a common disease that typically affects around 5.8% (1.8–22.3%) in European pregnancy. 1 GDM is described as glucose intolerance resulting in hyperglycemia that was diagnosed for the first time during the pregnancy. 2 , 3 , 4 At present, screening for GDM is principally based on the risk factor approach evaluation. 5 The gold standard screening is based on a 75‐g oral glucose tolerance test (OGTT) between 24 and 28 weeks of gestation. However, high‐risk pregnancies, particularly with a prior GDM pregnancy history, are tested early, between 16 and 18 weeks. A positive screening result if a single OGTT value is over the cut‐off. The multicentric trial Hyperglycemia and Adverse Pregnancy Events (HAPO) tested the OGTT validity. 6 Other research described a direct relationship between maternal glucose levels and fetal macrosomia. 7 , 8 , 9 Fetal macrosomia is correlated to more induction of labor rate and an improved risk of intrapartum traumatic lesions and asphyxia. 10 , 11 , 12 Having satisfactory blood glucose levels in GDM reduces maternal and fetal morbidity and reduces the antenatal cardiotocography need. 13 , 14 , 15 It has been reported that diabetes control was not satisfactory during the Covid‐19 pandemic lockdown. 16 Kirchengast and Hartmann analyzed the lockdown period (March to July 2021) in Austria and noted a higher gestational weight gain during the lockdown months but did not investigate the GDM incidence. 17 Different studies explored the Covid‐19 disease impact on pregnancy and remarked the association with increased risks of preeclampsia, preterm birth, and other adverse pregnancy outcomes, 18 , 19 , 20 , 21 but more data are needed to understand the changes that the lockdown restrictions might have had on pregnancy and obstetric care. The Italian lockdown began in March and ended in June 2020, with critical impacts on social life and physical activity. 22 , 23 Therefore, we decided to examine the GDM incidence in our institution before and after the Covid‐19 lockdown periods.
Methods
This was a retrospective single‐center study performed in a tertiary‐care referral center of the University of Campania “Luigi Vanvitelli,” Naples, Italy. Between June 2019 and December 2020, consecutive patients with a singleton low‐risk pregnancy were followed from the first obstetrical examination (6–9 gestational weeks) to term delivery. Term delivery was defined as a vaginal or cesarean delivery at a gestational age of at least 37 weeks, dated by a woman's last menstrual period and confirmed during first trimester ultrasound screening. Women were subdivided in two cohorts based on two‐time intervals as follows: before the Covid‐19 lockdown (from June 11, 2019 to March 9, 2020) and during or after the lockdown period (from March 10, 2020 to December, 42 020).
During the lockdown period, the universal testing for SARS‐CoV‐2 was performed on all women hospitalized in the study site maternity department. Women with pregestational type I or II diabetes, patients affected by Covid‐19 as well as women with other pathologies that could impact the physiological puerperium or postnatal adaptation were excluded.
Concerning the number of patients needed to assess the primary outcome, according to available literature, assuming two unbalanced groups, a sample size of 656 patients achieves 95% of the power with a significance level of 5% to detect a minimum difference of 10% of the anticipated GDM incidence between the two cohorts.
Maternal demographic characteristics, clinical, obstetric, and surgical history, labor and delivery data with neonatal anthropometrical and clinical features were abstracted from patients' charts and evaluated by three researchers (Giuliana Narciso, Ligia Gliubizzi, and Irene Iavarone).
Co‐primary outcomes were the incidence of GDM, body‐mass index (BMI) at the delivery, and mean weight gain.
The GDM diagnosis was made in accordance with previously published criteria and in line with national guidelines. 24 , 25 , 26 GDM is usually diagnosed following the screening made with the one‐step procedure with a 75‐g, 2‐h oral glucose tolerance test (OGTT). 4 The 75‐g, 2‐h OGTT was administered at 16–18 weeks' gestation in high‐risk GDM pregnancies (previous GDM, first‐trimester fasting glucose 100–125 mg/dL, BMI ≥30 kg/m2), while OGTT was recommended at 24–28 weeks' gestation for the pregnant with a risk factor (maternal age ≥ 35 years, BMI ≥25 kg/m2, prior fetal macrosomia, prior GDM with a negative screening at 16–18 weeks, first degree relative with T2DM, high‐risk ethnicity). GDM was diagnosed when a single OGTT value reached or exceeded the normal cut‐off (fasting value, 92 mg/dL; 1‐h value, 180 mg/dL; or 2‐h value, 153 mg/dL). BMI was measured for each patient during the hospitalization for labor. It was calculated using the standardized formula (weight/height2) and categorized as normal weight (18.50–24.99), overweight (25.00–29.99), and obese if ≥30 kg/m2 (according to the World Health Organization criteria). Weight was measured using an electronic scale while an adult stadiometer was used for evaluating the patient's height. Mean weight gain (kg) was evaluated as the difference between the weight measured at first obstetric examination (6–9 weeks of gestation) and weight measured during the hospitalization for labor.
Statistical analysis
Statistical analysis was performed using Statistical Package for Social Sciences (SPSS) v. 20.0 (IBM Inc., Armonk, NY, USA). Data were shown as median with 95% confidence intervals (CI) or number (percentage). In addition, a chi‐square test was conducted for categorical variables and t test for comparison of means of the two groups. All the analyses were performed using a two‐sided model, considering a normal distribution as appropriate. Multiple logistic regression was performed to identify factors that were associated with the incidence of the primary outcome of interest. p‐Value less than 0.05 was considered statistically significant.
Ethics statement
Ethical approval was waived by the Institutional Review Board (IRB) since the study was classified as a hospital audit of current clinical practice. We carried our research according to the Helsinki Declaration of 1975.
All the pregnant women signed a written informed consent before undergoing any study‐specific procedure.
Privacy of the participants of this research was maintained for all the study period. Written informed consent to publication was signed by every woman of this study.
Results
There were a total of 1295 women and subsequent singleton births during the study period divided as follows: 696 in the prepandemic period and 599 in the lockdown period. There were no significant differences in maternal characteristics, including age, pregestational weight, nulliparity, delivery gestational age, ethnicity, and mode of conception (Table 1). The incidence of GDM was significantly higher during the lockdown period (56/599, 9.3% vs. 24/696, 3.4%, p = <0.0001) than before the pandemic (Table 1). The BMI at the delivery was significantly higher during the lockdown period (31.3 kg/m2, 95% CI, 29.9–32.8) than in the prepandemic period (28.4 kg/m2, 95% CI, 26.4–30.5, p = 0.02, Table 1). In addition, the mean weight gain during the pregnancy was significantly higher during the lockdown period (9.3 kg [95% CI 8.0–10.7] vs. 6.6 kg [95% CI 5.0–8.2], p = 0.007, Table 1). There were no differences regarding the maternal comorbidities between the two groups (Table 2). In addition, we evaluated the OGTT values between the two groups. There were no significant differences between women who delivered before and during the lockdown period at 0 (102.1 mg/dL [95% CI, 88.5–115.7 mg/dL] vs 90.7 [87.0–94.5], p = 0.23), 60 (178.2 mg/dL [95% CI, 145.8–210.7 mg/dL] vs. 181.6 mg/dL [95% CI, 168.5–194.6 mg/dL], p = 0.829), and 120 min (151.7 mg/dL [95% CI, 126.5–176.9 mg/dL] vs. 147.1 mg/dL [95% CI, 132.3–162.0 mg/dL], p = 0.28) (Table 3). Moreover, multivariate variable analysis showed that BMI over 25 kg/m2 and a pregnancy weight gain over 9 kg were factors associated with GDM incidence both in the prepandemic and pandemic periods (Table 4).
TABLE 1.
Comparison of maternal and pregnancy characteristics between the prepandemic period and lockdown period
Maternal characteristics | Prepandemic period (n = 696) | Lockdown period (n = 599) | p‐Value |
---|---|---|---|
Age, mean (95% CI), years | 36.3 (34.6–38.0) | 34.5 (33.2–35.9) | 0.10 |
BMI, mean (95% CI), kg/cm2 | 28.4 (26.4–30.5) | 31.3 (29.9–32.8) | 0.02* |
Pregestational weight, median (IQR), kg | 66.8 (60.8–72.7) | 73.0 (68.4–77.6) | 0.09 |
Weight gain during pregnancy, mean (95% CI), kg | 6.6 (5.0–8.2) | 9.3 (8.0–10.7) | 0.007* |
Nulliparity, no. (%) | 13 (54.2) | 34 (60.7) | 0.58 |
Gestational age, median (IQR), weeks | 38.2 (37.1–39.0) | 38.6 (38.2–39.0) | 0.22 |
Race/ethnicity, no. (%) | |||
White | 13 (54.2) | 36 (64.3) | 0.39 |
Afro‐Carribean | 2 (8.3) | 2 (3.6) | 0.37 |
Asian | 7 (29.2) | 13 (23.2) | 0.57 |
Mixed race | 2 (8.3) | 5 (8.9) | 0.93 |
Conception | |||
Assisted reproduction | 3 (12.5) | 2 (3.6) | 0.13 |
Spontaneous | 21 (87.5) | 54 (96.4) | 0.13 |
GDM incidence | 24 (3.4) | 56 (9.3) | <0.001* |
Abbreviations: BMI, body mass index; CI: confidence interval; GDM, gestational diabetes mellitus.
p < 0.05.
TABLE 2.
Comparison of the maternal comorbidities between prepandemic period and lockdown period
Outcomes | Prepandemic period | Pandemic period total | p‐Value |
---|---|---|---|
Comorbidities, no. (%) | |||
PROM | 2 (8.2) | 8 (14.3) | 0.46 |
P‐PROM | 1 (4.2) | 3 (5.4) | 0.82 |
Pregestational diabetes | 0 (0.0) | 2 (3.6) | 0.35 |
Gestational hypertension | 2 (8.3) | 8 (14.3) | 0.46 |
Preeclampsia | 0 (0.0) | 0 (0.0) | |
Multiple pregnancy | 0 (0.0) | 0 (0.0) | |
Stillbirths | 0 (0.0) | 0 (0.0) | |
Fetal growth restriction | 2 (8.2) | 1 (1.8) | 0.16 |
Smoking in pregnancy | 2 (8.3) | 6 (10.7) | 0.74 |
Abbreviations: PROM, premature rupture of membranes; P‐PROM, preterm premature rupture of membranes.
TABLE 3.
Comparison of the maternal OGTT values between prepandemic period and lockdown period
Prepandemic period | Pandemic period | p‐Value | |
---|---|---|---|
OGTT, value. mean (95% CI) | |||
0′ | 102.1 (88.5–115.7) | 90.7 (87.0–94.5) | 0.23 |
60′ | 178.2 (145.8–210.7) | 181.6 (168.5–194.6) | 0.82 |
120′ | 151.7 (126.5–176.9) | 147.1 (132.3–162.0) | 0.28 |
Abbreviation: OGTT, 75‐g oral glucose tolerance test;
TABLE 4.
Multivariate analysis of factors related to increased number of gestational diabetes mellitus diagnosis
Variables | Prepandemic period HR (95% CI) | p‐Value | Pandemic period HR (95% CI) | p‐Value |
---|---|---|---|---|
BMI | ||||
>25 kg/m2 | 1.54 (1.03–1.86) | 0.04 | 1.85 (1.11–2.36) | 0.03 |
Pregnancy weight gain | ||||
>9 kg | 1.77 (1.21–2.04) | 0.03 | 1.91 (1.20–2.47) | 0.03 |
Abbreviations: BMI: body‐mass index; CI: confidence interval; HR: hazard ratio.
Discussion
This study showed a plausible increased rate of GDM diagnosis in the time interval concerning the Covid‐19 lockdown and subsequent months. The Italian national policy to restrict the Covid‐19 infection was rigorous, and outdoor physical activity was strictly limited. 27 The increased pregnancy weight gain during the lockdown period has resulted in a higher BMI at the delivery. 28 These two findings may be related to the increased rate of GDM (Table 4). 29 Other possible explanations include the change in women's physical activity due to lockdown conditions. 30 Many researchers analyzed the Covid‐19 lockdown effect on the dietary patterns and physical activity in nonpregnant women affected by type 2 diabetes mellitus. Ruiz‐Roso et al. showed an increase in sugary food and snack consumption associated with a high rate of physical inactivity during the Covid‐19 lockdown. 31 In another Indian study, type 2 diabetes mellitus patients had an HBA1c level higher during the lockdown period. 32 Additional studies evaluated lockdown's negative impacts on the glucose regulation for GDM and type 2 diabetes mellitus. 33 , 34 , 35 Ghesquière et al. investigated the glycemic balance in GDM patients by practicing capillary blood sugar tests, and the authors noted a lower diabetes control during the Covid‐19 pandemic lockdown. 16 An Indian review about the pandemic effects observed how the travel restriction had caused an increase in snack and meal frequency, correlated with reduced physical activity. 36 Justman et al. evidenced a significant reduction of routine obstetric screenings during the pandemic time. 37 At the same time, another study examined the lockdown impact on the depression rate during the postpartum period. 38 Limitations of this research include its retrospective nature, single‐center setting, short‐time frame (18 months), and partial population agreement to the GDM screening (based on the risk factors presence/absence). Several studies evidenced the link between weight gain, diabetes, and lockdown for nonpregnant patients. Pellegrini et al. underlined changes in weight and nutritional habits in obese adults, and additional studies explored the lockdown consequences on the psychological sphere. 39 , 40 , 41 Nonetheless, literature data on GDM susceptivity due to Covid‐19 lockdown is still lacking, and our study represents a first approach to evaluate such issue.
However, this study shows several limitations that should be considered. First, the study duration, although reporting the outcomes related to a specific time interval (the first Italian lockdown for Covid‐19), is limited to 18 months only, and the differences in weight gain and GDM incidence could be influenced by random variation of evaluated data across time. Second, it is evident that GDM diagnosis has increased in the past 20 years due to a more accurate screening of pregnant women. 1 Moreover, an increasing trend of weight gain and obesity has been observed for the European population. For this reason, the results of this study might also be interfered multiple confounders (higher maternal BMI, increased maternal age, and increased number of GDM diagnoses). 2 An additional limitation is the impossibility to compare the GDM incidence in the lockdown period to the same time interval for the previous year due to the unavailability of data regarding the incidence of GDM before April 2019 in our institution. Moreover, as a retrospective analysis of medical charts, the common limitations related to the study design should be acknowledged, including the possibility of selection and misclassification biases, as well as the inferior level of evidence when compared to prospective or randomized studies, which may affect external and internal validity of the findings.
In conclusion, a plausible increased incidence of GDM together with a higher weight gain was found in pregnant women during Covid‐19 lockdown rather than before. However, due to the limitations of the study methodology, additional research is needed to understand the relationship between dietary patterns, physical activity changes, and GDM onset due to Covid‐19 lockdown restrictions.
Conflict of interest
The authors declare that they have no competing interests.
Data availability statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.
References
- 1. Eades CE, Cameron DM, Evans JM. Prevalence of gestational diabetes mellitus in Europe: a meta‐analysis. Diabetes Res Clin Pract. 2017;129:173–81. [DOI] [PubMed] [Google Scholar]
- 2. Saravanan P, Magee LA, Banerjee A, Coleman MA, Von Dadelszen P, Denison F, et al. Gestational diabetes: opportunities for improving maternal and child health. Lancet Diabetes Endocrinol. 2020;8(9):793–800. [DOI] [PubMed] [Google Scholar]
- 3. Organization WH. Diagnostic criteria and classification of hyperglycaemia first detected in pregnancy. Switzerland: World Health Organization; 2013. [PubMed] [Google Scholar]
- 4. Metzger B, Gabbe S, Persson B, Buchanan T, Catalano P, Damm P, et al. International Association of Diabetes and Pregnancy Study Groups Consensus Panel International association of diabetes and pregnancy study groups recommendations on the diagnosis and classification of hyperglycemia in pregnancy. Diabetes Care. 2010;33(3):676–82. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5. Caughey AB, Sundaram V, Kaimal AJ, Gienger A, Cheng YW, McDonald KM, et al. Systematic review: elective induction of labor versus expectant management of pregnancy. Ann Intern Med. 2009;151(4):252–63. [DOI] [PubMed] [Google Scholar]
- 6. Group HSCR . Hyperglycemia and adverse pregnancy outcomes. N Engl J Med. 2008;358(19):1991–2002. [DOI] [PubMed] [Google Scholar]
- 7. Vasileiou V, Kyratzoglou E, Paschou SA, Kyprianou M, Anastasiou E. The impact of environmental temperature on the diagnosis of gestational diabetes mellitus. Eur J Endocrinol. 2018;178(3):209–14. [DOI] [PubMed] [Google Scholar]
- 8. Hanssen MJ, Hoeks J, Brans B, Van Der Lans AA, Schaart G, Van Den Driessche JJ, et al. Short‐term cold acclimation improves insulin sensitivity in patients with type 2 diabetes mellitus. Nat Med. 2015;21(8):863–5. [DOI] [PubMed] [Google Scholar]
- 9. Symonds ME, Farhat G, Aldiss P, Pope M, Budge H. Brown adipose tissue and glucose homeostasis–the link between climate change and the global rise in obesity and diabetes. Adipocyte. 2019;8(1):46–50. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Persson B, Hanson U. Neonatal morbidities in gestational diabetes mellitus. Diabetes Care. 1998;21:B79. [PubMed] [Google Scholar]
- 11. Mozurkewich E, Chilimigras J, Koepke E, Keeton K, King V. Indications for induction of labour: a best‐evidence review. BJOG. 2009;116(5):626–36. [DOI] [PubMed] [Google Scholar]
- 12. La Verde M, Cobellis L, Torella M, Morlando M, Riemma G, Schiattarella A, et al. Is uterine myomectomy a real contraindication to vaginal delivery? Results from a prospective study. J Investig Surg. 2022;35(1):126–31. [DOI] [PubMed] [Google Scholar]
- 13. Goueslard K, Cottenet J, Mariet A‐S, Sagot P, Petit J‐M, Quantin C. Early screening for type 2 diabetes following gestational diabetes mellitus in France: hardly any impact of the 2010 guidelines. Acta Diabetol. 2017;54(7):645–51. [DOI] [PubMed] [Google Scholar]
- 14. Jeffery T, Petersen R, Quinlivan J. Does cardiotocography have a role in the antenatal management of pregnancy complicated by gestational diabetes mellitus? Aust N Z J Obstet Gynaecol. 2016;56(4):358–63. [DOI] [PubMed] [Google Scholar]
- 15. La Verde M, Riemma G, Torella M, Torre C, Cianci S, Conte A, et al. Impact of Braxton‐Hicks contractions on fetal wellbeing; a prospective analysis through computerised cardiotocography. J Obstet Gynaecol. 2021;1–5. 10.1080/01443615.2021.1929115 [DOI] [PubMed] [Google Scholar]
- 16. Ghesquière L, Garabedian C, Drumez E, Lemaître M, Cazaubiel M, Bengler C, et al. Effects of COVID‐19 pandemic lockdown on gestational diabetes mellitus: a retrospective study. Diabetes Metab. 2021;47(2):101201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17. Kirchengast S, Hartmann B. Pregnancy outcome during the first COVID 19 lockdown in Vienna, Austria. Int J Environ Res Public Health. 2021;18(7):3782. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Wastnedge EA, Reynolds RM, Van Boeckel SR, Stock SJ, Denison FC, Maybin JA, et al. Pregnancy and COVID‐19. Physiol Rev. 2021;101(1):303–18. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Wei SQ, Bilodeau‐Bertrand M, Liu S, Auger N. The impact of COVID‐19 on pregnancy outcomes: a systematic review and meta‐analysis. CMAJ. 2021;193(16):E540–E8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Rasmussen SA, Smulian JC, Lednicky JA, Wen TS, Jamieson DJ. Coronavirus disease 2019 (COVID‐19) and pregnancy: what obstetricians need to know. Am J Obstet Gynecol. 2020;222(5):415–26. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. La Verde M, Riemma G, Torella M, Cianci S, Savoia F, Licciardi F, et al. Maternal death related to COVID‐19: a systematic review and meta‐analysis focused on maternal co‐morbidities and clinical characteristics. Int J Gynecol Obstet. 2021;154(2):212–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. Marziano V, Guzzetta G, Rondinone BM, Boccuni F, Riccardo F, Bella A, et al. Retrospective analysis of the Italian exit strategy from COVID‐19 lockdown. Proc Natl Acad Sci. 2021;118(4):e2019617118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23. Di Renzo L, Gualtieri P, Pivari F, Soldati L, Attinà A, Cinelli G, et al. Eating habits and lifestyle changes during COVID‐19 lockdown: an Italian survey. J Transl Med. 2020;18:1–15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Walker J. NICE guidance on diabetes in pregnancy: management of diabetes and its complications from preconception to the postnatal period. NICE clinical guideline 63. London, March 2008. Diabet Med. 2008;25(9):1025–7. [DOI] [PubMed] [Google Scholar]
- 25. Rudland VL, Price SA, Hughes R, Barrett HL, Lagstrom J, Porter C, et al. ADIPS 2020 guideline for pre‐existing diabetes and pregnancy. Aust N Z J Obstet Gynaecol. 2020;60(6):E18–52. [DOI] [PubMed] [Google Scholar]
- 26. Buchanan TA, Xiang AH. Gestational diabetes mellitus. J Clin Invest. 2005;115(3):485–91. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27. Saglietto A, D'Ascenzo F, Zoccai GB, De Ferrari GM. COVID‐19 in Europe: the Italian lesson. Lancet. 2020;395(10230):1110–1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28. International Weight Management in Pregnancy (i‐WIP) Collaborative Group . Effect of diet and physical activity based interventions in pregnancy on gestational weight gain and pregnancy outcomes: meta‐analysis of individual participant data from randomised trials. BMJ. 2017;358:j3991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29. Egan AM, Simmons D. Lessons learned from lifestyle prevention trials in gestational diabetes mellitus. Diabet Med. 2019;36(2):142–50. [DOI] [PubMed] [Google Scholar]
- 30. Davenport MH, Ruchat S‐M, Poitras VJ, Garcia AJ, Gray CE, Barrowman N, et al. Prenatal exercise for the prevention of gestational diabetes mellitus and hypertensive disorders of pregnancy: a systematic review and meta‐analysis. Br J Sports Med. 2018;52(21):1367–75. [DOI] [PubMed] [Google Scholar]
- 31. Ruiz‐Roso MB, Knott‐Torcal C, Matilla‐Escalante DC, Garcimartín A, Sampedro‐Nuñez MA, Dávalos A, et al. COVID‐19 lockdown and changes of the dietary pattern and physical activity habits in a cohort of patients with type 2 diabetes mellitus. Nutrients. 2020;12(8):2327. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32. Khare J, Jindal S. Observational study on effect of lock down due to COVID 19 on HBA1c levels in patients with diabetes: experience from Central India. Prim Care Diabetes. 2021;S1751‐9918(20):30362–4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33. Önmez A, Gamsızkan Z, Özdemir Ş, Kesikbaş E, Gökosmanoğlu F, Torun S, et al. The effect of COVID‐19 lockdown on glycemic control in patients with type 2 diabetes mellitus in Turkey. Diabetes Metab Syndr Clin Res Rev. 2020;14(6):1963–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34. de Luis Román DA, Jáuregui OI, Primo D, Hoyos EG, Torres BT, Gómez JJL. Effect of lockdown for COVID‐19 on self‐reported body weight gain in a sample of obese patients. Nutr Hosp. 2020;37(6):1232–7. [DOI] [PubMed] [Google Scholar]
- 35. Savas Karatas TY, Beysel S. Impact of lockdown COVID‐19 on metabolic control in type 2 diabetes mellitus and healthy people. Prim Care Diabetes. 2021;15(3):424–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Rawat D, Dixit V, Gulati S, Gulati S, Gulati A. Impact of COVID‐19 outbreak on lifestyle behaviour: a review of studies published in India. Diabetes Metab Syndr Clin Res Rev. 2021;15(1):331–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37. Justman N, Shahak G, Gutzeit O, Ginsberg Y, Solt I, Vitner D, et al. Lockdown with a price: the impact of the COVID‐19 pandemic on prenatal care and perinatal outcomes in a tertiary care center. Isr Med Assoc J. 2020;22(9):533–7. [PubMed] [Google Scholar]
- 38. Oskovi‐Kaplan ZA, Buyuk GN, Ozgu‐Erdinc AS, Keskin HL, Ozbas A, Tekin OM. The effect of COVID‐19 pandemic and social restrictions on depression rates and maternal attachment in immediate postpartum women: a preliminary study. Psychiatry Q. 2021;92(2):675–82. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39. Pellegrini M, Ponzo V, Rosato R, Scumaci E, Goitre I, Benso A, et al. Changes in weight and nutritional habits in adults with obesity during the “lockdown” period caused by the COVID‐19 virus emergency. Nutrients. 2020;12(7):2016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40. Alshareef R, Al Zahrani A, Alzahrani A, Ghandoura L. Impact of the COVID‐19 lockdown on diabetes patients in Jeddah, Saudi Arabia. Diabetes Metab Syndr Clin Res Rev. 2020;14(5):1583–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41. Bonora BM, Morieri ML, Avogaro A, Fadini GP. The toll of lockdown against COVID‐19 on diabetes outpatient care: analysis from an outbreak area in Northeast Italy. Diabetes Care. 2021;44(1):e18–21. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author upon reasonable request.