Impact of COVID-19 Lockdown on the Metabolic Control Parameters in Patients with Diabetes Mellitus: A Systematic Review and Meta-Analysis

Article information

Diabetes Metab J. 2022;46(2):260-272
Publication date (electronic) : 2022 March 8
doi : https://doi.org/10.4093/dmj.2021.0125
1Faculty of Medicine, Airlangga University, Surabaya, Indonesia
2Department of Public Health and Preventive Medicine, Airlangga University, Surabaya, Indonesia
3Department of Internal Medicine, Airlangga University, Surabaya, Indonesia
Corresponding author: Hermina Novida https://orcid.org/0000-0001-5899-1589 Department of Internal Medicine, Airlangga University, Jalan Mayjen Prof. Dr. Moestopo No.47, Surabaya 60131, Indonesia, E-mail: hermina-n@fk.unair.ac.id
*Ifan Ali Wafa, Nando Reza Pratama, and Nurizzah Farahiyah Sofia contributed equally to this study as first authors.
Received 2021 June 14; Accepted 2021 September 10.

Abstract

Background

Abrupt implementation of lockdowns during the coronavirus disease 2019 (COVID-19) pandemic affected the management of diabetes mellitus in patients worldwide. Limited access to health facilities and lifestyle changes potentially affected metabolic parameters in patients at risk. We conducted a meta-analysis to determine any differences in the control of metabolic parameters in patients with diabetes, before and during lockdown.

Methods

We performed searches of five databases. Meta-analyses were carried out using random- or fixed-effect approaches to glycaemic control parameters as the primary outcome: glycosylated hemoglobin (HbA1c), random blood glucose (RBG), fasting blood glucose (FBG), time-in-range (TIR), time-above-range (TAR), time-below-range (TBR). Mean difference (MD), confidence interval (CI), and P value were calculated. Lipid profile was a secondary outcome and is presented as a descriptive analysis.

Results

Twenty-one studies enrolling a total of 3,992 patients with type 1 or type 2 diabetes mellitus (T1DM or T2DM) were included in the study. Patients with T1DM showed a significant improvement of TIR and TAR (MD=3.52% [95% CI, 0.29 to 6.74], I2=76%, P=0.03; MD=−3.36% [95% CI, −6.48 to −0.25], I2=75%, P=0.03), while FBG among patients with T2DM significantly worsened (MD=3.47 mg/dL [95% CI, 1.22 to 5.73], I2=0%, P<0.01). No significant difference was found in HbA1c, RBG, and TBR. Use of continuous glucose monitoring in T1DM facilitated good glycaemic control. Significant deterioration of lipid parameters during lockdown, particularly triglyceride, was observed.

Conclusion

Implementation of lockdowns during the COVID-19 pandemic did not worsen glycaemic control in patients with diabetes. Other metabolic parameters improved during lockdown, though lipid parameters, particularly triglyceride, worsened.

INTRODUCTION

Ever since coronavirus disease 2019 (COVID-19) first emerged in China, lockdowns have been implemented in numerous countries as an attempt to reduce the spread of disease [1]. Lockdowns resulted in significant changes to daily life, from decreased physical activity, dietary changes, alterations in psychological and emotional states, and appetite dysregulation in individuals [24]. During lockdown, vulnerable populations, such as patients with diabetes mellitus, encountered restrictions in healthcare access that resulted in substandard care for patients [4]. Moreover, routine monitoring of metabolic control parameters, including glycaemic and lipid control, decreased significantly, resulting in an overall worsening of the assessment of patients with diabetes [4,5].

In an attempt to tackle the limitations on face-to-face meetings, several solutions using advanced technology were proposed as monitoring alternatives for maintaining good glycaemic control [6]. Before the COVID-19 pandemic, technological solutions for continuous glucose monitoring (CGM) and telemedicine were used to a limited extent [7]. CGM usage was associated with improved clinical outcomes of overall care [7,8]. With social restrictions due to COVID-19, CGM is a critical tool for remote glucose monitoring in patients with diabetes. Therefore, the benefits of CGM in monitoring diabetes during the COVID-19 pandemic needs to be further evaluated.

With this systematic review and meta-analysis, we aim to (1) provide an overview of the correlation between lockdowns and metabolic control and (2) evaluate the association between current medical practices during the lockdown and proper glycaemic control in patients with diabetes.

METHODS

This study was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 reporting guideline [9]. The study protocol has been registered in the international prospective register of systematic reviews database (PROSPERO) (CRD42021252321).

Search strategy

A comprehensive electronic-based literature search was conducted in PubMed, ScienceDirect, Cochrane Library, Journal Storage (JSTOR), and Directory of Open Access Journals (DOAJ) databases from 19 to 26 April 2021, for studies published in English. Medical Subject Heading (MeSH) terms were used in combination with the Boolean operator (AND/OR) and the following keywords: (COVID) AND [(pandemic) OR (lockdown) OR (quarantine)] AND (diabetes mellitus [MeSH Terms]) AND [(glycaemic control) OR (glucose level) OR (lipid profile)]. The authors also performed manual searches to retrieve potentially relevant articles from the reference list of retrieved articles.

Study selection

Title and abstract screening were carried out on each article, after removing duplicates using the Mendeley reference manager. Two authors (I.A.W. and N.R.P.) independently conducted the screening based on the following eligibility criteria: observational studies (cross-sectional, case-control, or cohort), published between 2020 and 2021, including patients of any age with type 1 or type 2 diabetes mellitus (T1DM or T2DM), that reported glycaemic control parameters and/or lipid profile as primary or secondary outcomes, and assessed comparisons of metabolic control among diabetic patients during and before lockdown. We excluded studies with the following criteria: experimental studies, non-English language articles, studies that included other types of diabetes or involved patients with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) comorbid infections, and those studies that did not reported the glycaemic control and/or lipid profile during lockdown. The search, selection, and screening processes were recorded and are documented in the PRISMA flow diagram (Fig. 1).

Fig. 1

Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram of study selection process [9].

Data extraction

Three independent authors (I.A.W., N.R.P., and N.F.S.) used a standardised form to extract the data. Any discrepancies were resolved by discussion among the authors until a consensus was reached. The following data were extracted: first author name, year of publication, the country setting, study design, sample size, study period, age, and types of diabetes. Glycaemic control parameters (glycosylated hemoglobin [HbA1c] or estimated A1c [eA1c], random blood glucose [RBG], fasting blood glucose [FBG], time-in-range [TIR], time-above-range [TAR], and time-below-range [TBR]), lipid control parameters (total cholesterol, low-density lipoprotein cholesterol [LDL-C], high-density lipoprotein cholesterol [HDL-C], and triglyceride), measurement methods, and comparison of metabolic control before and during COVID-19 lockdowns were also extracted. HbA1c data obtained from laboratory assessment, and eA1c, data from CGM, are defined as HbA1c.

Quality assessment

Quality assessment was performed independently by two authors (I.A.W. and N.F.S.). Any discrepancies were resolved by discussion among authors until a consensus was reached. Quality assessment of the studies included in the meta-analysis was performed with the Effective Public Health Practice Project (EPHPP) tool, consisting of six components: (1) selection bias, (2) study design, (3) confounders, (4) blinding, (5) data collection method, and (6) withdrawals and dropouts. Each component was rated as 1 (strong), 2 (moderate), or 3 (weak). Based on the number of components with a weak rating, the global rating of the quality of each study was assigned as either strong, moderate, or weak [10].

Operational definitions

TIR, TAR, and TBR are defined as the percentage of time per day an individual spent at various blood glucose levels, respectively, in the target range (70 to 180 mg/dL [3.9 to 10.0 mmol/L]), above range (>180 mg/dL), and below range (<70 mg/dL) [11].

Data synthesis and analysis

The primary outcomes of this study were the differences identified in the following glycaemic control parameters, before and during lockdown: HbA1c, RBG, and FBG; along with other glycaemic control parameters obtained from CGM or flash glucose monitoring (FGM) device: TIR, TAR, and TBR. Secondary outcomes were the differences in lipid control parameters during and before the lockdown of the following: total cholesterol, LDL-C, HDL-C, and triglyceride. The mean and standard deviation of the glycaemic control parameters and lipid profile data from each study were extracted. Any outcomes presented as a median and interquartile range were not included in the meta-analysis. The comparison of glycaemic control parameters and lipid profile during and before the lockdown were analysed as continuous variables using the mean difference (MD) and summarised with their corresponding 95% confidence interval (CI). The overall effect (Z test) was considered significant if the P value was <0.05. Heterogeneity was assessed using the Q statistic and I2 test. The I2 test presents the variability percentage of the analysis due to clinical or methodological heterogeneity, rather than sampling error. The random-effects model was used when the I2 was >50% or the P value was <0.10; otherwise, the fixed-effect model was preferred. Potential publication bias was observed visually using Begg’s funnel plots. We pre-planned to perform subgroup analyses for all outcomes based on the study design. Sensitivity analyses were also performed based on the quality of the studies. All statistical analyses were performed using Review Manager version 5.4 (The Cochrane Collaboration, London, UK).

RESULTS

The search strategy yielded 166 articles from primary databases and manual searching after removing four duplications using Mendeley reference manager. After titles and abstracts were screened, 45 articles were selected for full-text evaluation. Of those, 21 studies with a total of 3,992 participants met the eligibility criteria and were included in this study (Fig. 1). Quality assessment resulted in 12 “strong” quality articles, eight “moderate” quality articles, and one “weak” quality article based on the EPHPP tool (Supplementary Table 1). Funnel plot asymmetry was obtained in HbA1c, RBG, TIR, and TAR outcomes (Supplementary Figs. 14) but not in FBG and TBR (Supplementary Figs. 5 and 6).

All studies included were observational studies and consisted of 13 cohort studies, five case-control studies, and three cross-sectional studies. Most studies were conducted in Italy, with others conducted in Spain, France, Greece, the Netherlands, Israel, Saudi Arabia, Turkey, and India. The characteristics of the included studies are presented in Table 1.

Characteristics of the included study

According to the findings in these 21 studies, seven studies reported negative impacts and a deterioration in glycaemic control during lockdown, while others reported no significant differences. However, some studies showed significant improvements in glycaemic control among patients with diabetes during lockdown. Due to insufficient outcome data, only 17 studies were included in the meta-analysis. The lipid control parameters were analysed as secondary outcomes and are presented as descriptive analyses since only two available studies reported this outcome.

Primary outcomes

HbA1c

Eleven studies [1222] with a total of 1,357 pre-lockdown and 1,325 lockdown participants, comprised of patients with either T1DM or T2DM, reported mean levels of HbA1c and eA1c which was obtained either from CGM or FGM (Supplementary Fig. 7). A pooled estimate showed that lockdown did not significantly result in changes to HbA1c (MD=0.06% [95% CI, −0.10 to 0.23], I2=77%, random-effects). All HbA1c subgroup analyses in cohort studies. found no significant differences of HbA1c between pre-lockdown and lockdown (MD=−0.01% [95% CI, −0.17 to 0.14], I2=65%, random-effects), case-control (MD=0.00% [95% CI, −0.32 to 0.32], I2=75%, random-effects), and cross-sectional studies (MD=0.56% [95% CI, −0.67 to 1.78], I2=95%, random-effects).

Random blood glucose

Twelve studies [13,15,17,1927] in patients with T1DM reported MDs of RBG with a total of 2,162 pre-lockdown and 2,210 lockdown participants (Supplementary Fig. 8). Pooled estimates showed no significant differences in RBG level between pre-lockdown and during lockdown periods (MD=0.91 mg/dL [95% CI, −4.52 to 6.34], I2=88%, random-effects). RBG subgroup analysis showed no significant differences in cohort studies (MD=−0.71 mg/dL [95% CI, −7.64 to 6.22], I2=0.64%, random-effects), case-control studies (MD=−2.47 mg/dL [95% CI, −8.91 to 3.98], I2=75%, random-effects), and cross-sectional studies (MD=23.61 mg/dL [95% CI, −15.32 to 62.54], I2=93%, random-effects).

Fasting blood glucose

Mean FBG level was reported in two cohort studies [14,28] of patients with T2DM with a total of 257 participants in each arm (Fig. 2). Meta-analysis showed a significant deterioration in FBG control from pre-lockdown to the lockdown period (MD=3.47 mg/dL [95% CI, 1.22 to 5.73], I2=0%, fixed-effect).

Fig. 2

Forest plots of meta-analysis for fasting blood glucose. SD, standard deviation; IV, inverse variance; CI, confidence interval.

Time-in-range

Data on the mean level of TIR was reported in eight studies [13,15,17,19,20,2426] among patients with T1DM, with a total of 580 participants in each arm (Fig. 3). A significant improvement of TIR from pre-lockdown to during the lockdown period was observed (MD=3.52% [95% CI, 0.29 to 6.74], I2=76%, random-effects). However, pooled estimates of subgroup analysis did not show significant improvement in TIR during lockdown in both cohort studies (MD=4.61% [95% CI, −0.55 to 9.78], I2=87%, random-effects) and case-control studies (MD=2.24% [95% CI, −0.43 to 4.90], I2=0%, fixed-effect).

Fig. 3

Forest plots of meta-analysis for time-in-range. SD, standard deviation; IV, inverse variance; CI, confidence interval.

Time-above-range

Data on the mean level of TAR was reported in eight studies [13,15,17,19,20,2426] among patients with T1DM, with a total of 580 participants in each arm (Fig. 4). The pooled effect showed that TAR significantly improved from the pre-lockdown to the lockdown period (MD=−3.36% [95% CI, −6.48 to −0.25], I2=75%, random-effects). However, when subgroup analysis was performed, the pooled effects failed to reach statistical significance in both cohorts (MD=−4.44% [95% CI, −9.83 to 0.94], I2=86%, random-effects) and case-control studies (MD=−2.20% [95% CI, −4.66 to 0.27], I2=0%, fixed-effect).

Fig. 4

Forest plots of meta-analysis for time-above-range. SD, standard deviation; IV, inverse variance; CI, confidence interval.

Time-below-range

Data on the mean level of TBR was reported in eight studies [13,15,17,19,20,2426] among patients with T1DM, with a total of 580 participants in each arm (Supplementary Fig. 9). TBR was not significantly affected during the lockdown period (MD=−0.05% [95% CI, −0.38 to 0.28], I2=0%, fixed-effect). Subgroup analysis was performed and insignificant changes in TBR were found in both cohort studies (MD=−0.11% [95% CI, −0.52 to 0.29], I2=0%, fixed-effect) and case-control studies (MD=0.08% [95% CI, −0.49 to 0.64], fixed-effect).

Sensitivity analysis

Heterogeneity of variance was found in HbA1c, RBG, TIR, and TAR analysis; therefore, a sensitivity analysis was carried out to identify the source of heterogeneity using the leave-one-out method on moderate-quality studies. Bonora et al. [24] was found to be the source of heterogeneity in both TAR and TIR. Neither the direction of effect nor the statistical significance was changed when this study was excluded from each outcome. Sensitivity analysis on each subgroup analysis of HbA1c and RBG was unable to provide significant results.

Secondary outcomes

Lipid control

Meta-analysis on lipid profiles could not be performed due to the limited data available. An Italian cohort study [14] of 114 Caucasian patients with T2DM reported significant improvements in total cholesterol and LDL-C levels during the lockdown (P<0.05), despite consistent doses and types of medication administered before and during lockdown. In contrast, a Turkish case-control study [18] of 85 patients with T2DM reported a significant increase in triglyceride and body weight (P<0.05). Multinomial logistic regression in Biancalana et al. [14], and multivariate analysis in the Karatas et al. [18] study also revealed disparate outcomes, where one study reported pre-lockdown triglyceride as a predictor of glycaemic control during the lockdown period, and the other reported that duration of diabetes was the independent predictor of both glycaemic control (HbA1c) and lipid profile (triglyceride) (odds ratio, 1.2; 95% CI, 1.1 to 1.8; P=0.032). Karatas et al. [18] reported that increases in body weight, blood glucose, HbA1c, and plasma lipids simultaneously served as factors in the increased risk of cardiovascular diseases.

DISCUSSION

We obtained a total of 21 observational studies with 3,992 participants. The pooled estimates of TIR and TAR among patients with T1DM showed improvements during lockdown, while FBG among patients with T2DM deteriorated. Total cholesterol and LDL-C were improved [14], but triglyceride worsened [18]. The majority of the studies reported that diet, physical activity, and stress management played a primary role in affecting the control of metabolic parameters. However, other factors were found to have an equal effect on worsening control. Social factors including emotional instability, socioeconomic vulnerability, uncertainty in employment status, and difficulty in accessing healthcare and medication aggravated the deterioration of metabolic parameters. In contrast, all arrangements of telemedicine, whether in the form of tele-assistance or use of automated glucose monitoring systems were found to improve the control of diabetic parameters [68,29].

Excessive consumption of high carbohydrate foods, including several types of fruit and vegetables, is a well-known cause of increased triglyceride and blood glucose levels in patients with diabetes [30]. A reduction in physical activity during lockdown may have further contributed to an increase in triglyceride and blood glucose [31]. Refractory glucose fluctuations, shown by unchanged TBR in patients with T1DM and worsening FBG in patients with T2DM, despite improvements in other parameters, could indeed be heightened by several risk factors such as gender, younger age, higher body mass index, higher HbA1c, and current treatment strategies; in particular, triple combination or insulin therapy [32]. Nevertheless, poor dietary practices and physical inactivity were still the main contributors to adverse outcomes in the control of diabetes. Despite the downsides, we found that glycaemic parameters were still well-controlled, possibly due to the use of appropriate insulin treatments and medications which maintain normal blood glucose levels and prevent hyperglycaemia. Therefore, HbA1c did not deteriorate overall, and TIR and TAR were even found to show improvement. In addition to dietary factors, physical activity, and stress management, adherence to medication was essential in maintaining satisfactory glycaemic control during lockdown.

We observed that individuals who lacked exercise and neglected healthy habits during lockdown were at higher risk of having poor glycaemic control [2,3]. Socioeconomic issues and psychological burden during lockdown had also worsened glycaemic control parameters. This deterioration was evident even among patients with T1DM who previously had appropriate metabolic control [23,33]. These factors led to changes in diet, sleep, and physical activity [2,3,34,35].

Precisely how daily habit changes affected metabolic control were conflicting, however. For example, Ruissen et al. [16] reported an increase in stress, weight gain, and a reduction in exercise, but this study showed improvements in glycaemic control, in contrast to other studies [21,23,28]. Indeed, the population in this study [16] was previously well-controlled and received insulin treatments during lockdown. Meanwhile, another study reported that some patients with previously well-controlled diabetes had worsened parameters in lockdown [14]. Based on these findings, it is possible to infer that other factors, including adherence to medications or insulin treatment, might also have played a pivotal role in the maintenance of metabolic control [36]. In addition, adequate control of diabetes among patients with gestational diabetes was found to be unfavourable during the COVID-19 pandemic lockdown, even when follow-up via telemedicine was facilitated [37]. Without ignoring confounders, the net effect on metabolic control seems to be the result of all factors combined, rather than the effect of a single factor. It seems apparent that adequate diabetic control requires active participation and care from patients themselves.

Most of the studies we included [13,1517,19,20,23,25,26,35, 38,39] used either standalone CGM or CGM with an automated insulin delivery system such as hybrid closed loop for patients monitoring during lockdown. Use of CGM and an automated insulin delivery system as an artificial pancreas that maintains basal insulin levels have recently increased for the management of patients with T1DM [7,8]. Features on some versions of CGM enable the automatic scanning of blood glucose levels and are equipped with an active alarm in real time CGM, while other versions require patients to actively scan blood glucose, as in intermittently scanning CGM [40,41]. CGM can be very helpful in remotely managing diabetes and improving quality of life [42]. In addition to the psychosocial benefits, CGM use for patients with diabetes can improve poor diabetic control, as demonstrated by improvements in HbA1c, TAR, TIR, and TBR [43], and reductions in hypoglycaemia risk [43,44]. The use of auto-mode CGM is associated with improved glycaemic variability (GV) [35].

Improving GV in patients with diabetes is considered crucial in reducing adverse outcomes. Several studies have shown that poor GV is associated with oxidative stress, which could induce endothelial dysfunction, atherosclerosis, and other cardiovascular complications. Glycaemic fluctuations have been shown to promote inflammatory cytokine release, monocyte adhesion to endothelial cells, endothelial cells apoptosis, and epigenetic changes in endothelial and mononuclear cells. These alterations could foster the downregulation of superoxide dismutase, detoxification genes, and free radical scavengers [45]. The most disadvantageous outcome of poor GV is that it has cytotoxic effects on the pancreas, which significantly reduces glucose-mediated insulin secretion, β-cells’ apoptosis, and mitochondrial alterations. Thus, poor GV promotes the vicious cycle of poor glycaemic control and diabetic complications [46].

We noted that most of the worsening events in diabetic parameter control were reported from non-European countries, particularly countries in the Middle East, where cultural influences were highly correlated. According to 2019 Global Burden of Diseases (GBD) data, individuals living in Middle Eastern countries have one of the highest daily mean energy intakes and the lowest level of physical activity worldwide [47]. We propose that both of these factors, in conjunction with changes in habits during lockdown, led to a substantial worsening in metabolic control in patient with diabetes who reside in the Middle East.

Regarding lipid profile findings, a previous observational study observed that a high carbohydrate diet increases fasting triglycerides and is associated with higher mortality rates [30]. Triglycerides are closely related to non-esterified fatty acids and could have hazardous effects on glucose homeostasis due to lipotoxicity [48]. Serum triglycerides could also independently represent a risk factor for cardiovascular and kidney diseases [49].

In summary, the implementation of lockdowns to limit the spread of COVID-19 resulted in lifestyle modifications for many people worldwide. A sedentary lifestyle, unhealthy dietary intake, and poor stress management could be a factor in the poor management of diabetes. However, the application of CGM for some people had a positive effect on diabetic management, such as improving medication adherence. Despite many factors that can directly influence metabolic control parameters, these parameters tended to improve during COVID-19 lockdowns.

As a meta-analysis, this study has some limitations. We included retrospective and prospective studies in this review due to the limited number of studies available. In particular, controlled studies were difficult to conduct during the lockdown period. Diversities in the duration and technical implementation of lockdowns between countries worldwide resulted in a heterogeneity of methods and results in this review, which along with the brief study period, had given rise to limitations in data availability. Thus, some outcomes could not be thoroughly analysed. Further study over an extended time period, larger population, and observation of post-lockdown findings could advance the significance of reviews on similar topics. Analysis of lipid profile should be further deepened in a more focused setting. To the best of our knowledge, until submission of this manuscript, this is the first study that compares glycaemic control parameters and lipid profiles of patients with diabetes before and during COVID-19 lockdown. The inclusion of patients with either T1DM or T2DM and with various types of study designs, including cohort, case-control, and cross-sectional studies from various countries worldwide supports the robust findings in this review.

In conclusion, COVID-19 lockdowns did not have a negative effect on metabolic parameters in patients with diabetes, especially in those individuals who were able to maintain healthy daily habits. A nutritionally balanced diet, regular physical activity, and proper stress management, alongside the use of GCM as a remote diabetic monitoring strategy are recommended for good control of metabolic parameters in patients with diabetes who were unable to access in-person consultations with physicians during lockdown.

SUPPLEMENTARY MATERIALS

Supplementary materials related to this article can be found online at https://doi.org/10.4098/dmj.2021.0125.

Supplementary Table 1.

Effective Public Health Practice Project (EPHPP) quality assessment of included studies

dmj-2021-0125-suppl1.pdf
Supplementary Fig. 1.

Funnel plot for 11 studies of glycosylated hemoglobin. SE, standard error; MD, mean difference.

dmj-2021-0125-suppl2.pdf
Supplementary Fig. 2.

Funnel plot for 12 studies of random blood glucose. SE, standard error; MD, mean difference.

dmj-2021-0125-suppl3.pdf
Supplementary Fig. 3.

Funnel plot for eight studies of timein-range. SE, standard error; MD, mean difference.

dmj-2021-0125-suppl4.pdf
Supplementary Fig. 4.

Funnel plot for eight studies of timeabove-range. SE, standard error; MD, mean difference.

dmj-2021-0125-suppl5.pdf
Supplementary Fig. 5.

Funnel plot for two studies of fasting blood glucose. SE, standard error; MD, mean difference.

dmj-2021-0125-suppl6.pdf
Supplementary Fig. 6.

Funnel plot for eight studies of timebelow-range. SE, standard error; MD, mean difference.

dmj-2021-0125-suppl7.pdf
Supplementary Fig. 7.

Forest plots of meta-analysis for glycosylated hemoglobin. SD, standard deviation; IV, inverse variance; CI, confidence interval.

dmj-2021-0125-suppl8.pdf
Supplementary Fig. 8.

Forest plots of meta-analysis for random blood glucose. SD, standard deviation; IV, inverse variance; CI, confidence interval.

dmj-2021-0125-suppl9.pdf
Supplementary Fig. 9.

Forest plots of meta-analysis for time-below-range. SD, standard deviation; IV, inverse variance; CI, confidence interval.

dmj-2021-0125-suppl10.pdf

ACKNOWLEDGMENTS

Authors would like to thank the Department of Public Health and Preventive Medicine at the Medical Faculty of Universitas Airlangga for their support throughout the writing process.

Notes

CONFLICTS OF INTEREST

No potential conflict of interest relevant to this article was reported.

AUTHOR CONTRIBUTIONS

Conception or design: I.A.W., N.R.P., N.F.S., E.S.A., T.K., M.A.W., M.R.W., L.D., H.N.

Acquisition, analysis, or interpretation of data: I.A.W., N.R.P., N.F.S., E.S.A., T.K., M.A.W., M.R.W.

Drafting the work or revising: I.A.W., N.R.P., N.F.S., E.S.A., T.K., M.A.W., M.R.W.

Final approval of the manuscript: I.A.W., N.R.P., N.F.S., E.S.A., T.K., M.A.W., M.R.W., L.D., H.N.

FUNDING

None

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Article information Continued

Fig. 1

Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram of study selection process [9].

Fig. 2

Forest plots of meta-analysis for fasting blood glucose. SD, standard deviation; IV, inverse variance; CI, confidence interval.

Fig. 3

Forest plots of meta-analysis for time-in-range. SD, standard deviation; IV, inverse variance; CI, confidence interval.

Fig. 4

Forest plots of meta-analysis for time-above-range. SD, standard deviation; IV, inverse variance; CI, confidence interval.

Table 1

Characteristics of the included study

Study Study design Sample size Study period Diabetes type Age, yr Quality assessment Measurement method Outcomes Findings
Al Agha et al. (2021)
Saudi Arabia [21]
CS 150 Apr–Jun 2020 T1DM 12.45±4.62 Strong SMBG RBG, HbA1c Worsen due to decreased physical activity, increased carbohydrates and fast food consumption, and worsening mood.
Alaqeel et al. (2021)
Saudi Arabia [12]
RC 154, 106 1 Mar–30 Jun 2020 T1DM 9.8±0.2 Strong SMBG HbA1c Worsen with increased frequency of DKA.
Aragona et al. (2020)
Italy [13]
RC 63 21 Feb–25 Apr 2020 T1DM 44.0±12.0 Strong FGM, CGM RBG, eA1c, TIR, TAR, TBR Improved due to increased daily routine activities and decreased work-related stress.
Barchetta et al. (2020)
Italy [23]
RC 50 20 Jan–11 Apr 2020 T1DM 40.7±13.5 Moderate FGM, CGM RBG, eA1c, TIR, TAR, TBR Worsen due to work instability.
Biancalana et al. (2021)
Italy [14]
PC 114 9 Mar–4 May 2020 T2DM 69.4±10.3 Strong SMBG HbA1c, FBG, TC, LDL-C, TG Worsen. Pre-lockdown TG is the sole predictor of lockdown glycemic control.
Bonora et al. (2020)
Italy [24]
RC 20 Feb–June 2020 T1DM 36.9±13.4 Moderate FGM RBG, TIR, TAR, TBR Improved due to slow down in daily routine activities, particularly in stay-at-home patients.
Brener et al. (2020)
Israel [25]
RC 102 23 Feb–7 Apr 2020 T1DM 10.9 ± 3.9 Strong CGM RBG, TIR, TAR, TBR Unchanged.
Christoforidis et al. (2020)
Greece [26]
CC 34 18 Feb–1 Apr 2020 T1DM 11.37±4.45 Moderate HCL system RBG, TIR, TAR, TBR Unchanged due to insulin pumps and glucose monitoring sensors usage.
Cotovad-Bellas et al. (2020)
Spain [17]
CC 44 1 Mar–19 Apr 2020 T1DM 37.0±18.0 Moderate FGM, CGM RBG, eA1c, TIR, TAR, TBR Unchanged due to increased time for exercise and home-made cooking.
Di Dalmazi et al. (2020)
Italy [38]
PC 130 20 Feb–30 Mar 2020 T1DM 8.8 (7.7–10.6)
15.6 (14.2–16.8)
45 (29–58.1)
Moderate CGM RBG, eA1c, TIR, TAR, TBR Unchanged due to the use of CGM, physical activity, and stress reduction.
Dover et al. (2021)
United Kingdom [33]
PC 572 11–21 May 2020 T1DM 39 (31–50) Weak FGM RBG, eA1c, TIR, TAR, TBR Unchanged. Socioeconomic status served as risk factors.
Karatas et al. (2021)
Turkey [18]
CC 85 Mar 2019–Oct 2020 T2DM 54.81±10.53 Strong SMBG HbA1c, FBG, LDL-C, HDL-C, TG Worsen. No association with weight gain.
Khare et al. (2020)
India [28]
PC 143 The first 3 weeks of lockdown T2DM 54.68±9.22 Strong SMBG FBG, PPBG Worsen due to lifestyle changes, psychological stress, and difficulties in access to treatments and health care facilities.
Longo et al. (2020)
Italy [35]
RC 30 23 Feb–3 May 2020 T1DM 31.5 (25–42) Moderate HCL system RBG, eA1c, TIR, TAR, TBR Improved due to HCL usage.
Study Study design Sample size Study period Diabetes type Age, yr Quality assessment Measurement method Outcomes Findings
Mesa et al. (2020)
Spain [19]
CC 92 23 Feb–14 Apr 2020 T1DM 42.8±13.9 Strong CGM RBG, eA1c, TIR, TAR, TBR Improved due to strict daily routines at home.
Parise et al. (2021)
Italy [15]
PC 166 10 Mar–3 June 2020 T1DM 40.0±14.0 Strong CGM RBG, eA1c, TIR, TAR, TBR Improved due to structured virtual visits (tele-assistance).
Potier et al. (2021)
France [27]
CS 1,378 23–28 Apr 2020 T1DM 45.6±13.6 Strong FGM RBG Improved due to improved diet, increased physical activity, and increased FGM scans.
Ruissen et al. (2021)
Netherlands [16]
PC 435 24 Feb–7 May 2020 T1DM
T2DM
50.1±14.9
62.5±11.6
Strong FGM, CGM HbA1c, TIR, TAR, TBR Improved due to good control.
Tornese et al. (2020)
France [39]
RC 13 10 Feb–22 Mar 2020 T1DM 14.2 (11.4–15.5) Moderate HCL system RBG, eA1c, TIR, TAR, TBR Improved due to physical activity.
Verma et al. (2020)
India [22]
CS 52 25 Mar–31 May 2020 T1DM 11.9 Moderate SMBG RBG, HbA1c Worsen due to the unavailability of insulin/glucostrips.
Vinals et al. (2021)
Spain [20]
CC 59 23 Feb–14 Apr 2021 T1DM 46.18±13.02 Strong HCL system RBG, eA1c, TIR, TAR, TBR Unchanged due to strict daily routines at home.

Values are presented as mean±standard deviation or median (interquartile range).

CS, cross-sectional; T1DM, type 1 diabetes mellitus; SMBG, self-monitoring blood glucose; RBG, random blood glucose; HbA1c, glycosylated hemoglobin; RC, retrospective cohort; DKA, diabetic ketoacidosis; FGM, flash glucose monitoring; CGM, continuous glucose monitoring; eA1c, estimated A1c; TIR, time-in-range; TAR, time-above-range; TBR, time-below-range; PC, prospective cohort; T2DM, type 2 diabetes mellitus; FBG, fasting blood glucose; TC, total cholesterol; LDL-C, low-density lipoprotein cholesterol; TG, triglyceride; CC, case-control; HCL, hybrid closed loop; HDL-C, high-density lipoprotein cholesterol; PPBG, postprandial blood glucose.