ABSTRACT The targets for continuous glucose monitoring (CGM)-derived metrics were recently set; however, studies on CGM data over a long period with stable glycemic control are limited. We

analyzed 194,279 CGM values obtained from 19 adult Japanese patients with type 1 diabetes. CGM data obtained during stable glycemic control over four months were analyzed. CGM-related

metrics of different durations “within 120, 90, 60, 30, and 7 days” were calculated from baseline. Time in range (TIR; glucose 70–180 mg/dL), time above range (TAR; glucose ≥ 181 mg/dL), and

average glucose levels, but not time below range (TBR; glucose ≤ 69 mg/dL), strongly correlated with glycated hemoglobin (HbA1c) values (P < 0.0001). TBR correlated with glucose

patients with type 1 diabetes with stable glycemic control. Glucose CV and TBR complemented the limitation of HbA1c to detect glucose variability and hypoglycemia. Stable glycemic control

with minimal hypoglycemia depended on residual β-cell function. SIMILAR CONTENT BEING VIEWED BY OTHERS SERUM 25-HYDROXYVITAMIN D LEVEL IS ASSOCIATED WITH SHORT-TERM GLYCEMIC VARIABILITY

METRICS DERIVED FROM CONTINUOUS GLUCOSE MONITORING IN T2DM Article Open access 27 October 2023 CONTINUOUS GLUCOSE MONITORING AND INTRAPERSONAL VARIABILITY IN FASTING GLUCOSE Article 08 April

2024 LOG-LINEAR RELATIONSHIP BETWEEN ENDOGENOUS INSULIN SECRETION AND GLYCEMIC VARIABILITY IN PATIENTS WITH TYPE 2 DIABETES ON CONTINUOUS GLUCOSE MONITORING Article Open access 27 April

2021 INTRODUCTION Glycated hemoglobin (HbA1c) is the gold standard for long-term blood glucose monitoring reflecting the mean glucose levels over the last 2–3 months1,2. Many seminal trials

have clarified the relationship between glycemic control and microvascular and macrovascular complications in patients with type 1 and type 2 diabetes using HbA1c3,4,5. However, HbA1c has

several limitations because first, it is affected by genetic, hematological, and other clinical factors unrelated to glycemia, such as disorders affecting red cell turnover,

hemoglobinopathies, and certain anemias etc. Second, HbA1c does not reflect the short-term changes in glycemic control. Third, HbA1c cannot be used to identify the magnitude and frequency of

intra- and inter-day glucose variations1,2 to distinguish between patients with stable glycemic control and those with rapidly changing glycemic levels. Continuous glucose monitoring (CGM)

has been recognized as a "beyond HbA1c" tool1,6. CGM devices, which can measure glucose levels in the subcutaneous interstitial fluid and convert them into the equivalent venous

blood glucose levels, have grown rapidly in recent years, because of their improved sensor accuracy, convenience of use, and reduced user cost. The major advantage of CGM technology is that

the overall daily profile of blood glucose can be captured, particularly, the postprandial and nocturnal blood glucose levels. Many studies have demonstrated considerable benefits of CGM in

patients with diabetes7, particularly those with insulin-depended diabetes and at high hypoglycemia risk2,8. Although the opportunities to use CGM are increasing, the utilization of CGM data

is not adequate in routine clinical practice because of the lack of clear and agreed-upon glycemic targets. Recently, consensus recommendations for the relevant aspects of CGM data

utilization have been reported by the consensus panel in the Advanced Technologies & Treatments for Diabetes (ATTD) Congress in 20192. In the consensus recommendations, several metrics,

such as time in range (TIR), time above range (TAR), time below range (TBR), average glucose, glycemic variability (% coefficient of variation [CV]), were included. Given that long-term

studies on the relationship between these metrics and diabetes complications are required, the guidance on target for these metrics has been shown for various types of diabetes based on

several lines of evidence, which showed correlations between TIR (70–180 mg/dL) and diabetes complications7,9,10 and clarified the relationship between TIR and HbA1c11,12,13. However, most

studies were based on data extracted from published trials or articles for other purposes. In addition, these studies were performed in Western countries and most of the participants were

Caucasian11,13. Considering the impact of the racial factor in the relationship between mean blood glucose and HbA1c14, studies in different populations are necessary. This study aimed to

clarify the relationship between several metrics measured by CGM and data of well-established laboratory parameters, particularly, HbA1c and serum C-peptide (C-peptide immunoreactivity:

CPR), in adult Japanese patients with type 1 diabetes. To ensure data accuracy, CGM data for a sufficiently long period were obtained from patients with stable glycemic control without

conditions leading to variability of HbA1c. This would be beneficial for both, patients with type 1 diabetes and healthcare professionals for the appropriate interpretation of CGM-related

metrics and their use for better management of glycemic control, reducing the incidences of hypoglycemia or hyperglycemia. RESULTS The results of univariate regression analysis between HbA1c

(x-axis) and TIR (y-axis) measured within 120 days from baseline are shown in Fig. 1A. A strong inverse relationship between HbA1c and TIR was observed (P < 0.0001), suggesting that

HbA1c data were sufficient to explain TIR. HbA1c of 7% corresponded to a TIR of approximately 74% (Table 1), and the coordinate (x = 7%, y = 70%) was included within the 95% confidence band

of the best-fit line (Fig. 1A). An increase in TIR of 18% will cause a decrease in HbA1c of 1.0% (Supplementary Fig. 1A). In Fig. 1B, a strong positive relationship was observed between

HbA1c and TAR (P < 0.0001), suggesting that HbA1c data were sufficient to explain TAR. HbA1c of 7% corresponded to a TAR of approximately 20% (Table 1), and the coordinate (x = 7%, y = 

25%) was not included within the 95% confidence band of the best-fit line (Fig. 1B). A decrease of 19% in TAR will cause a decrease in HbA1c of 1.0% (Supplementary Fig. 1B). In Fig. 1C,

unlike TIR and TAR, no significant relationship was observed between HbA1c and TBR (P > 0.05) (Table 1). In Fig. 2A, we observe a strong positive relationship between HbA1c and average

glucose (P < 0.0001), suggesting that HbA1c had sufficient data to explain average glucose. HbA1c of 7% corresponded to an average glucose of approximately 138 mg/dL (7.7 mM) (Table 1). A

decrease of 39 mg/dL (2.6 mM) in average glucose will cause a decrease in HbA1c of 1.0% (Supplementary Fig. 1C), indicating that HbA1c of 6% of the study population corresponded to an

average glucose of approximately 100 mg/dL (5.6 mM). In the remaining CGM-related metrics, glucose SD positively correlated with HbA1c (P < 0.0001) (Fig. 2B), whereas glucose CV and HbA1c

were not related (P > 0.05) (Fig. 2C). The mean of glucose CV was 0.35 (range 0.27–0.47). Glucose CV did not correlate with TIR and TAR (P > 0.05 in both) (Fig. 3A,B) as in the case

of HbA1c (Fig. 2C). However, glucose CV significantly correlated with TBR, indicating that the increase in glucose CV was associated with increase in hypoglycemia (Fig. 3C). Since 2 of the

19 patients (No. 3 and 10 in Tables 2 and 3) had fewer readings (< 70%) for “within 120 days,” we performed an analysis excluding them, but the results were similar to the analysis with

all the patients. As previous studies have indicated serum CPR levels as an essential contributor to glucose variability15,16,17, the relationship between serum CPR and CGM-related metrics

was investigated. Wide variations in TIR and TAR were observed in decreased fasting serum CPR (Fig. 4A,B). Markedly low TIR (Fig. 4A), high TAR (Fig. 4B) and high TBR (Fig. 4C) were observed

in patients with fasting serum CPR < 0.1 ng/mL. In Fig. 5A, a significant inverse relationship was observed between fasting serum CPR and glucose CV (P < 0.005). An increase in

fasting serum CPR was associated with a decrease in glucose CV (P < 0.01, Jonckheere–Terpstra trend test) (Fig. 5B). In addition to the analysis of CGM data “within 120 days” from

baseline described above, we further studied multiple time period measurements from baseline: within 90, 60, 30, and 7 days (Table 1). The results obtained were essentially the same as in

the case of “within 120 days.” TIRs measured within 90 and 60 days from baseline showed strong relationship with HbA1c (coefficient of determination (R2) = 0.8771 and R2 = 0.8851,

respectively) as in the case of within 120 days (R2 = 0.8881); however, TIRs measured within 30 and 7 days showed a slightly weaker correlation with HbA1c (R2 = 0.8489 and R2 = 0.7110,

respectively). TARs and average glucose showed same tendency as TIRs, namely, a strong relationship with HbA1c for longer periods and slightly weaker for shorter periods. As for TBRs, no

significant relationship with HbA1c for any period was observed. Glucose CVs measured within 90, 60, and 30 days from baseline showed strong relationship with fasting serum CPR (R2 = 0.4092,

R2 = 0.3333, and R2 = 0.2250, respectively) as in the case of “within 120 days” (R2 = 0.4203); however, glucose CVs measured within 7 days showed no correlation with fasting serum CPR (R2 =

 0.1405). DISCUSSION The present study was performed to clarify the advantages and disadvantages of CGM-related metrics relative to well-established laboratory-measured parameters, HbA1c and

serum CPR, in type 1 diabetes. TIR, TAR, and average glucose levels, but not TBR, strongly correlated with HbA1c. TBR correlated with glucose CV. Fasting serum CPR was negatively correlated

with glucose CV. HbA1c of approximately 7% corresponded to TIR of 74% and TAR of 20%. The shorter the CGM period, the weaker the relationship between HbA1c and CGM-related metrics. To date,

numerous studies have been published on the relationship between CGM-related metrics and HbA1c11,13. However, most studies have been based on data extracted from published trials or

articles for other purposes and does not exist as studies specified in measurement terms, to investigate for CGM data for a sufficiently long period of time11,13,18. To exactly investigate

the relationship between HbA1c and CGM-related metrics, the measurement periods were fixed as 120, 90, 60, 30, and 7 days from the baseline. To avoid discrepancy due to CGM-related metrics

reflecting short-term glycemic status and HbA1c reflecting long-term glycemic status, only those patients with stable glycemic control and minimal changes in HbA1c four months prior to the

baseline were considered for analysis, thus resulting in less than 15% variation in HbA1c. Despite a relatively small number of patients, a very strong relationship between CGM-related

metrics, TIR, TAR, and particularly average glucose levels, and HbA1c was detected, indicating that CGM-related metrics TIR and TAR could adequately reflect laboratory-measured HbA1c

provided that HbA1c levels have been stable within the past several months. ATTD has indicated three key CGM-related metrics: TIR, TAR, and TBR2. The ATTD report has described that CGM-based

glycemic targets must be personalized to meet the needs of each person with diabetes. In addition, the report had proposed a glycemic range (a target range of 70–180 mg/dL) and targets of

TIR, TAR, and TBR for adults with type 1 or type 2 diabetes (TIR > 70%, TAR < 25%, TBR < 4%) and older/high-risk individuals (TIR > 50%, TAR < 50%, TBR < 1%). Two studies

have reported that TIR of 70% and 50% corresponded to an HbA1c of approximately 7% and 8%11, and 6.7% and 8.3%13, respectively. However, the present study on adult Japanese patients with

type 1 diabetes showed that TIRs of 70% and 50% corresponded to HbA1c of approximately 7.3% and 8.4%, respectively (best-fit line: y = − 0.05412x + 11.06; when x = TIR, y = HbA1c)

(Supplementary Fig. 1A). To achieve HbA1c of 7% and 8%, TIR should be more than 74% and 57%, respectively. TAR matched more with HbA1c compared to TIR or TBR, in our population. TAR of 25%

and 50% corresponded with HbA1c of approximately 7.3% and 8.6%, respectively (best-fit line: y = 0.05211x + 5.969; when x = TAR, y = HbA1c) (Supplementary Fig. 1B). To achieve HbA1c of 7%

and 8%, TAR should be less than 20% and 39%, respectively. TBR showed only marginal correlation with HbA1c. This may be due to a limited TBR compared to TIR and TAR. However, a tendency of

reducing HbA1c with increasing TBR suggests the limitation of HbA1c and the advantage of the differentiation to increase TIR and simultaneously decrease or at least have unchanged TBR. In

addition, as shown in Fig. 3C, a significant relationship between glucose CV and TBR was observed; therefore, higher the glucose CV, higher was TBR (risk of hypoglycemia). These results

demonstrated the need to maintain glucose CV below a certain level (e.g., < 0.3619) to avoid hypoglycemia in patients at an increased risk. However, it is often difficult to regulate

glucose CV in type 1 diabetes, particularly, in the subset of patients with unstable (brittle) diabetes. Even in patients with stable HbA1c in our study, the mean glucose CV was 0.35. One

major factor contributing to glucose CV is residual beta-cell function15,16,17. Wide variations in TIR and TAR in patients with low CPR (Fig. 4A,B) together with the inverse relationship

between glucose CV and serum CPR (Fig. 5A,B) indicate the importance of residual β-cell function on glycemic control stabilization. Our data regarding CGM-derived glucose CV are consistent

with those of previous reports on the negative correlation between serum CPR and glucose variability assessed in pre-CGM era15,16,17. It emphasizes the importance of residual CPR, which is

reported to be associated with the progression of diabetes complications20, on glycemic stability in type 1 diabetes. Most Japanese patients with type 1 diabetes were reported to completely

lose endogenous insulin during the disease duration21; inversely most patients with long-duration type 1 diabetes in Western countries preserved endogenous insulin levels22,23, and treatment

to prevent CPR decline has been reported to inhibit the progression of diabetes complications in patients with residual CPR24. Therefore, CGM-derived TBR and glucose CV together with CPR

are essential metrics supplementing HbA1c in patients with type 1 diabetes, particularly in the Japanese population. Average glucose, rather than other CGM-related metrics, exactly matched

with HbA1c, particularly, in the CGM data collected from the last 60 days or more. CGM data collected “within 7 days” showed a significant but weaker relationship with HbA1c and average

glucose than those from longer periods (Table 1). These results confirmed that HbA1c is an index for long-term monitoring of blood glucose and reflects mean glucose levels during the last 2 

months, as reported previously1,2. This study was designed to use CGM data only in patients with stable glycemic control with minimal changes in HbA1c during the 4 months before the

baseline. Even then, a duration dependency was observed regarding the correlation between CGM-related metrics and HbA1c, shorter duration of CGM-derived data, weaker was the correlation with

HbA1c. The correlation would be even weaker in case CGM-derived data are extracted from clinical trials or articles in which glycemic control changes due to interventions or treatments

resulting in CGM-derived data reflecting short-term glycemic control changes much faster than HbA1c. In fact, only a moderate correlation was reported between CGM-related metrics and HbA1c

with a correlation coefficient of 0.67–0.73 for TIR in 545 patients with type 1 diabetes from 4 randomized trials11. From this point of view, previous studies on the relationship between

HbA1c and CGM-related metrics and estimation of HbA1c from CGM-related metrics using short-term CGM data should be carefully interpreted. Petersson et al. reported the relationship between

HbA1c and CGM-related metrics, focusing on time in target range (TIT) defined as 70–140 mg/dL25; this is the first report to identify a nonlinear relationship between TIT and HbA1c in

pediatric type 1 diabetes. However, in the same paper, there is a description of a linear analysis of TIT 30, 60, and 90 days and HbA1c. All of them showed significant correlations, but the

correlation coefficients (R2: 0.59–0.63) were lower than R2 for TIR in the present study. These differences may be due to the difference in race (Japanese vs. Swedish), subjects (adults vs.

children and adolescents), selection criteria (stable HbA1c population vs. general population), and CGM-metrics (TIR vs. TIT). The relationship between HbA1c and CGM-metrics relative to CGM

duration, which is our main objective in the present study, is unknown because the relationship in shorter (7 days) and longer (120 days) CGM duration is not available in their study. The

main strength of this study is that it was specifically designed to test the correlation between CGM-related metrics and HbA1c; it evaluated the accuracy of CGM-related metrics for different

CGM measurement periods. Moreover, this is the first report on adult Japanese patients with type 1 diabetes, a population prone to insulin depletion. This study had limitations. First, only

a limited number of patients were eligible for investigation because we considered a study design for data collection to increase the accuracy of the results; herein, we selected for each

patient the period with stable glycemic control with small changes in HbA1c. In addition, we excluded patients with clinical conditions unrelated to glycemia but affecting HbA1c levels, such

as unstable blood hemoglobin values, gestational period, surgery, and diagnosis of malignant tumors. Due to the exclusion of subjects with these conditions, the results of the present study

may not apply to patients with type 1 diabetes in general. Second, the relationship between HbA1c and average glucose was studied only with respect to CGM-derived glucose value, but not

with laboratory-measured plasma glucose, as our study was performed under daily life conditions. Considering the recent developments in CGM technology with improvement in sensor accuracy,

the data obtained with CGM for real-life glucose in normal daily use provide information difficult to be obtained with the laboratory-measured glucose, under restricted settings such as

hospitals. Third, as our patients use FreeStyle Libre, which has dual function, CGM and FGM, there may be biases based on patients’ habits. For example, when unexpected high or low glucose

values were detected using FGM, patients willingly compensated their blood glucose, leading to better than the expected TIR levels. Fourth, the analysis of the relationship between glucose

CV and fasting serum CPR was performed using only univariate regression analysis because of the limited number of the subjects in this study. For this reason, the observed relationship can

be indirect and secondary to other unknown factors. Although our data on CGM-derived glucose CV are consistent with those of previous reports of glucose variability estimated using different

methods in pre-CGM era15,16,17, further studies with larger number of participants are required to clarify the observed relationship with the consideration for other confounding factors.

Fifth, although the relationship between glucose CV and TBR was detected in this study, the relationship may be overrated or underrated. This is because residual CPR may potentially affect

both glucose CV and TBR. Additionally, Japanese patients with type 1 diabetes are known to be prone to CPR depletion. In conclusion, this study provided evidence regarding the reliability of

CGM-related metrics in adult Japanese patients with type 1 diabetes in a usual daily life setting. TIR and TAR strongly correlated with HbA1c and complemented or even replaced HbA1c for

short-term monitoring of blood glucose. While TIR, TAR, and HbA1c reflected mean blood glucose, TBR and glucose CV complemented the mean glucose-related metrics by reflecting hypoglycemia.

The negative correlation between glucose CV and fasting CPR suggests the importance of residual β-cell function for stable glycemic control without hypoglycemia, in type 1 diabetes. METHODS

PATIENTS Nineteen patients with type 1 diabetes who regularly visited the Kindai University Faculty of Medicine (Osaka-sayama, Osaka, Japan) once a month for more than 5 months were included

in the study, between December 2018 and December 2019. Patient characteristics are given in Table 2. All patients were adults (age range 30.5–75.8, mean ± SD 53.1 ± 15.2) with type 1

diabetes receiving multiple insulin injections or continuous subcutaneous insulin infusion. The protocols were approved by the Ethics Review Committee of the Kindai University Faculty of

Medicine (approval number: 31-162), and informed consent was obtained from all participants. All methods were performed in accordance with the relevant guidelines and regulations. STUDY

DESIGN Patients’ data were collected in their daily life settings. The patients at their visit to our hospital, brought with them their FreeStyle Libre device (Abbott Japan Diabetes Care

Inc., Tokyo, Japan), which is a flash glucose monitoring (FGM) system that has dual function, CGM and FGM. The FreeStyle Libre data were extracted and stored in a computer solely for this

purpose. CGM measures every 15 min the interstitial fluid glucose and converts it to venous blood glucose; however, in FGM, glucose data are not constantly shown and are available only on

demand. In this study, only CGM data were used for analysis. Patients who met all of the following five criteria were included in the study: (1) stable HbA1c, which was defined as minimum

difference in HbA1c levels for the past 4 months in each patient, and stable blood hemoglobin levels in the past 4 months, (2) no gestational period, (3) no operations within the last 6 

months and no planned operations, (4) no diagnosis for malignant tumors, (5) no clinical conditions unrelated to glycemia but affecting HbA1c levels, such as anemia, renal failure and liver

cirrhosis. HbA1c at baseline and at 1 to 4 months before baseline is shown in Table 3. In our institution, about 200 patients with type 1 diabetes are provided treatment through regular

outpatient clinic visits, and 26 patients used Freestyle Libre during the period of this study. Of these, 7 patients were excluded because of the following reasons: CGM data of less than 4 

months were available, blood data were not available, and/or inclusion criteria were not met. Eventually, 19 patients were included in the analysis. The CGM-related metrics were calculated,

namely TIR (glucose 70–180 mg/dL), TAR (glucose ≥ 181 mg/dL), TBR (glucose ≤ 69 mg/dL), average glucose, glucose standard deviation (SD), and glucose CV for each patient using the CGM data

within 120 days from baseline. Overall, 194,279 CGM values (average 10,225 per patient) were analyzed. In addition, we calculated CGM-related metrics based on CGM data closer to the

baseline, “within 90 days,” “within 60 days,” “within 30 days,” and “within 7 days” from baseline. The number of data analyzed and the percentage mounting time of CGM in the corresponding

period are provided in Table 3. On an average, the percentage mounting time of CGM was over 84%. In addition to the relationship between CGM-related metrics and HbA1c, the relationship

between CGM-related metrics and serum CPR was analyzed to study the effect of residual β-cell function on glycemic control, particularly fluctuation (glucose CV) and hypoglycemia (TBR).

STATISTICAL ANALYSIS Univariate linear regression was used to characterize the relationship between HbA1c and CGM-related metrics, and between fasting serum CPR and glucose CV. The

relationship between the trend of fasting serum CPR improvement and glucose CV was analyzed using the Jonckheere–Terpstra trend test. Statistical tests were performed using GraphPad Prism

(GraphPad software) or Bell Curve for Excel (Social Survey Research Information Co., Ltd.). P < 0.05 was considered statistically significant. REFERENCES * Vigersky, R. A. Going beyond

HbA1c to understand the benefits of advanced diabetes therapies. _J. Diabetes_ 11, 23–31 (2019). Article  Google Scholar  * Battelino, T. _et al._ Clinical targets for continuous glucose

monitoring data interpretation: Recommendations from the international consensus on time in range. _Diabetes Care_ 42, 1593–1603 (2019). Article  Google Scholar  * Nathan, D. M. _et al._ The

effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. _N. Engl. J. Med._ 329, 977–986 (1993).

Article  CAS  Google Scholar  * UK Prospective Diabetes Study (UKPDS) Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of

complications in patients with type 2 diabetes (UKPDS 33). _Lancet_ 352, 837–853 (1998). * Diabetes Control and Complications Trial (DCCT)/Epidemiology of Diabetes Interventions and

Complications (EDIC) Study Research Group. Intensive diabetes treatment and cardiovascular outcomes in type 1 diabetes: The DCCT/EDIC study 30-year follow-up. _Diabetes Care_ 39, 686–693

(2016). * Riddle, M. C., Gerstein, H. C. & Cefalu, W. T. Maturation of CGM and glycemic measurements beyond HbA1c-A turning point in research and clinical decisions. _Diabetes Care_ 40,

1611–1613 (2017). Article  Google Scholar  * Maiorino, M. I. _et al._ Effects of continuous glucose monitoring on metrics of glycemic control in diabetes: A systematic review with

meta-analysis of randomized controlled trials. _Diabetes Care_ 43, 1146–1156 (2020). Article  CAS  Google Scholar  * van Beers, C. A. _et al._ Continuous glucose monitoring for patients with

type 1 diabetes and impaired awareness of hypoglycaemia (IN CONTROL): A randomised, open-label, crossover trial. _Lancet Diabetes Endocrinol._ 4, 893–902 (2016). Article  Google Scholar  *

Beck, R. W. _et al._ Validation of time in range as an outcome measure for diabetes clinical trials. _Diabetes Care_ 42, 400–405 (2019). Article  CAS  Google Scholar  * Lu, J. _et al._

Association of time in range, as assessed by continuous glucose monitoring, with diabetic retinopathy in type 2 diabetes. _Diabetes Care_ 41, 2370–2376 (2018). Article  ADS  CAS  Google

Scholar  * Beck, R. W. _et al._ The relationships between time in range, hyperglycemia metrics, and HbA1c. _J. Diabetes Sci. Technol._ 13, 614–626 (2019). Article  Google Scholar  * Fabris,

C., Heinemann, L., Beck, R., Cobelli, C. & Kovatchev, B. Estimation of hemoglobin A1c from continuous glucose monitoring data in individuals with type 1 diabetes: Is time in range all we

need?. _Diabetes Technol. Ther._ 22, 501–508 (2020). Article  CAS  Google Scholar  * Vigersky, R. A. & McMahon, C. The relationship of hemoglobin A1C to time-in-range in patients with

diabetes. _Diabetes Technol. Ther._ 21, 81–85 (2019). Article  CAS  Google Scholar  * Bergenstal, R. M. _et al._ Racial differences in the relationship of glucose concentrations and

hemoglobin A1c levels. _Ann. Intern. Med._ 167, 95–102 (2017). Article  Google Scholar  * Fukuda, M. _et al._ Correlation between minimal secretory capacity of pancreatic beta-cells and

stability of diabetic control. _Diabetes_ 37, 81–88 (1988). Article  CAS  Google Scholar  * Gibb, F. W., McKnight, J. A., Clarke, C. & Strachan, M. W. J. Preserved C-peptide secretion is

associated with fewer low-glucose events and lower glucose variability on flash glucose monitoring in adults with type 1 diabetes. _Diabetologia_ 63, 906–914 (2020). Article  CAS  Google

Scholar  * Shibasaki, S., Imagawa, A., Terasaki, J. & Hanafusa, T. Endogenous insulin secretion even at a very low level contributes to the stability of blood glucose control in

fulminant type 1 diabetes. _J. Diabetes Investig._ 1, 283–285 (2010). Article  CAS  Google Scholar  * Toschi, E. _et al._ The relationship between CGM-derived metrics, A1C, and risk of

hypoglycemia in older adults with type 1 diabetes. _Diabetes Care_ 43, 2349–2354 (2020). Article  CAS  Google Scholar  * Lu, J. _et al._ Glycemic variability modifies the relationship

between time in range and hemoglobin A1c estimated from continuous glucose monitoring: A preliminary study. _Diabetes Res. Clin. Pract._ 161, 108032 (2020). Article  CAS  Google Scholar  *

Jeyam, A. _et al._ Clinical impact of residual C-peptide secretion in type 1 diabetes on glycemia and microvascular complications. _Diabetes Care_ https://doi.org/10.2337/dc2320-0567 (2020).

Article  PubMed  Google Scholar  * Uno, S. _et al._ Complete loss of insulin secretion capacity in type 1A diabetes patients during long-term follow up. _J. Diabetes Investig._ 9, 806–812

(2018). Article  CAS  Google Scholar  * Keenan, H. A. _et al._ Residual insulin production and pancreatic β-cell turnover after 50 years of diabetes: Joslin medalist study. _Diabetes_ 59,

2846–2853 (2010). Article  CAS  Google Scholar  * Oram, R. A. _et al._ The majority of patients with long-duration type 1 diabetes are insulin microsecretors and have functioning beta cells.

_Diabetologia_ 57, 187–191 (2014). Article  CAS  Google Scholar  * Lachin, J. M., McGee, P., Palmer, J. P. & Group, D. E. R. Impact of C-peptide preservation on metabolic and clinical

outcomes in the Diabetes Control and Complications Trial. _Diabetes_ 63, 739–748 (2014). Article  Google Scholar  * Petersson, J., Akesson, K., Sundberg, F. & Sarnblad, S. Translating

glycated hemoglobin A1c into time spent in glucose target range: A multicenter study. _Pediatr Diabetes_ 20, 339–344 (2019). Article  CAS  Google Scholar  Download references

ACKNOWLEDGEMENTS This study was supported by the Japan Society for the Promotion of Science, Grants-in-Aid for Scientific Research (JSPS KAKENHI) Grant Number JP17K09852, JP18K08493,

JP18K08530. We thank Yayoi Kibayashi for her help. We thank Editage (www.editage.com) for English language editing. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department of Endocrinology,

Metabolism and Diabetes, Kindai University Faculty of Medicine, 377-2 Ohno-higashi, Osaka-sayama, Osaka, 589-8511, Japan Naru Babaya, Shinsuke Noso, Yoshihisa Hiromine, Yasunori Taketomo, 

Fumimaru Niwano, Sawa Yoshida, Sara Yasutake, Yumiko Kawabata & Hiroshi Ikegami Authors * Naru Babaya View author publications You can also search for this author inPubMed Google Scholar

* Shinsuke Noso View author publications You can also search for this author inPubMed Google Scholar * Yoshihisa Hiromine View author publications You can also search for this author

inPubMed Google Scholar * Yasunori Taketomo View author publications You can also search for this author inPubMed Google Scholar * Fumimaru Niwano View author publications You can also

search for this author inPubMed Google Scholar * Sawa Yoshida View author publications You can also search for this author inPubMed Google Scholar * Sara Yasutake View author publications

You can also search for this author inPubMed Google Scholar * Yumiko Kawabata View author publications You can also search for this author inPubMed Google Scholar * Hiroshi Ikegami View

author publications You can also search for this author inPubMed Google Scholar CONTRIBUTIONS N.B. collected and analyzed the data and drafted the manuscript. S.N., Y.H., Y.T., F.N., S.Y.,

S.Y., Y.K. contributed with data collection. H.I. contributed to the study concept and design and revised the writing of the paper. All authors read and approved the final manuscript.

CORRESPONDING AUTHOR Correspondence to Hiroshi Ikegami. ETHICS DECLARATIONS COMPETING INTERESTS The authors declare no competing interests. ADDITIONAL INFORMATION PUBLISHER'S NOTE

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ARTICLE Babaya, N., Noso, S., Hiromine, Y. _et al._ Relationship of continuous glucose monitoring-related metrics with HbA1c and residual β-cell function in Japanese patients with type 1

diabetes. _Sci Rep_ 11, 4006 (2021). https://doi.org/10.1038/s41598-021-83599-x Download citation * Received: 28 July 2020 * Accepted: 04 February 2021 * Published: 17 February 2021 * DOI:

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