Skip to main content

Significance of day-to-day glucose variability in patients after acute coronary syndrome

Abstract

Background

Several studies have recently addressed the importance of glycemic variability (GV) in patients with acute coronary syndrome (ACS). Although daily GV measures, such as mean amplitude of glycemic excursions, are established predictors of poor prognosis in patients with ACS, the clinical significance of day-to-day GV remains to be fully elucidated. We therefore monitored day-to-day GV in patients with ACS to examine its significance.

Methods

In 25 patients with ACS, glucose levels were monitored for 14 days using a flash continuous glucose monitoring system. Mean of daily differences (MODD) was calculated as a marker of day-to-day GV. N-terminal pro-brain natriuretic peptide (NT-proBNP) was evaluated within 4 days after hospitalization. Cardiac function (left ventricular end-diastolic volume, left ventricular ejection fraction, stroke volume) was assessed by echocardiography at 3–5 days after admission and at 10–12 months after the disease onset.

Results

Of the 25 patients, 8 (32%) were diagnosed with diabetes, and continuous glucose monitoring (CGM)-based MODD was high (16.6 to 42.3) in 17 patients (68%). Although MODD did not correlate with max creatine kinase (CK), there was a positive correlation between J-index, high blood glucose index, and NT-proBNP (r = 0.83, p < 0.001; r = 0.85, p < 0.001; r = 0.41, p = 0.042, respectively).

Conclusions

In patients with ACS, MODD was associated with elevated NT-proBNP. Future studies should investigate whether day-to-day GV in ACS patients can predict adverse clinical events such as heart failure.

Peer Review reports

Background

Several studies have recently addressed the importance of glycemic variability (GV) in patients with acute coronary syndrome (ACS) [1,2,3,4]. Continuous glucose monitoring (CGM) systems are an emerging technology that can continuously measure glucose levels, thereby enabling evaluation of GV [5, 6]. Su et al. reported that monitoring GV using CGM can predict mortality and major adverse cardiovascular events in elderly patients after acute myocardial infarction [7]. They also reported that high GV at admission may be closely correlated with in-hospital poor outcomes in diabetes mellitus (DM) patients with non-ST segment elevation ACS following percutaneous coronary intervention (PCI) [8]. Furthermore, using CGM to monitor daily GV parameters such as mean amplitude of glycemic excursions (MAGE) is a predictor of poor prognosis in patients with ACS without severe DM [9]. In-hospital daily GV in the stable phase of ST-elevation myocardial infarction predicts left ventricular remodeling, as determined by cardiac magnetic resonance imaging [10].

However, the clinical significance of day-to-day GV in patients with ACS remains to be fully elucidated. Therefore, we monitored day-to-day GV in patients with ACS to examine its clinical significance.

Methods

Subjects

We enrolled 25 patients who were admitted to the University of Fukui Hospital with ACS between September 2017 and March 2018. Patients with hemodynamic instability, such as those with complications of infection, catecholamine or sedative use, ventilator management, or ventricular arrhythmia, were excluded because of concerns about the effects of infection, drugs, and severe stress on blood glucose levels. Patients on insulin were also excluded because of the possible effect on blood glucose variability.

Smoking is defined as any smoking in the past year. Diabetes was defined based on one or more of the following: self-reported, use of diabetes medications, fasting plasma glucose ≥ 126 mg/dl, or hemoglobin A1c (National Glycohemoglobin Standardization Program) ≥ 6.5%. Clinical histories of the patients were obtained from interviews with patients.

Study protocol

After the purpose and methods of the study were explained to patients, they provided written informed consent for participation in the study. In this study, continuous glucose levels were monitored using a flash glucose monitoring (FGM) system (Free-Style Libre™ or Free-Style Libre Pro, Abbott™, UK). All patients were implanted with sensors of Free-Style Libre™ or Free-Style Libre Pro™ in their left upper arm within 3–5 days after hospitalization. Glucose levels were recorded using the FGM system for up to 14 days, excluding the first 2 days after sensor implantation because of the risk of errors due to inflammatory reactions, which could produce unstable glucose data. After analysis of the CGM data, MAGE, MODD, ADRR (average daily risk range, mg/dl), J-index, M-value (mg/dl), LBGI (low blood glucose index), and HBGI (high blood glucose index) were calculated using EasyGV© software. The formulas for each parameter are based on Nathan et al. [11] Chen et al. reported the MODD of non-diabetic patients is 16.0 ± 5.4 mg/dl [12]. Therefore, a MODD value of 16.0 or higher was chosen as the abnormal value. MODD was calculated by \(\frac{\sum_{t={t}_{1}}^{{t}_{k}}|{G}_{t}-{G}_{t-1440}|}{k}\) (k = number of observations with an observation 24 h ago, G = glucose measured, t = time). To assess cardiac function, patients underwent echocardiography at 3–5 days after admission and at 10–12 months after the disease onset. The patients' diet consisted of a cardiac diet of 30 kcal/kg in ideal body weight in three portions. They did not receive any intravenous catecholamines or antibiotics. This investigation conformed to the principles outlined in the 1975 Declaration of Helsinki and later amendments. This study was approved by the Research Ethics Committee of University of Fukui and informed consent from all patients were obtained, and the follow-up results were registered in the Universal Hospital Medical Information Network Clinical Trials Registry (UMIN 000023837, 30/08/2016).

Measurements of blood samples

Within 4 days after hospitalization, following overnight fasting, blood samples were collected from the peripheral vein of each patient and kept on ice. Plasma was collected with EDTA-2Na as an anti-coagulant, and serum samples were separated by centrifugation within 30 min. Blood parameters were determined using standard methods.

Statistical analysis

All statistical analyses were performed using Statcel2 software (OMS Publishing Inc., Saitama, Japan) and Excel2019 (Microsoft Corporation). Data are presented as frequencies and percentages for categorical variables and mean ± SD for continuously distributed variables. Differences between categorical variables were assessed using the χ2 test. Correlations between continuous variables were determined using Pearson’s correlation coefficient test. A p value of < 0.05 was considered statistically significant.

Results

Patient characteristics

The characteristics of all patients are listed in Table 1. The mean age was 69.7 years, and 84% of patients were male. The study included 25 patients (14 patients with ST-elevated acute myocardial infarction, 6 patients with non-ST-elevated acute myocardial infarction, and 5 patients with unstable angina). In the study, 72% had a medical history of hypertension, and 24% had hypercholesterolemia. DM was observed in 8 patients (32%), and 7 patients (28%) were taking one or more antidiabetes medications. The mean value of peak CK was 1310.1 ± 1293.0 U/l, and NT-pro BNP was 2032.0 ± 2063.3 pg/ml (Table 1).

Table 1 Patient characteristics

Prevalence of MODD and DM

On admission, only 8 patients (32%) were diagnosed with diabetes. On the other hand, as many as 17 of 25 patients (68%) had abnormally high MODD values. The rate of abnormal MODD was significantly higher than the diagnosed rate of DM (32% vs. 68%, p = 0.011) (Fig. 1).

Fig. 1
figure 1

Prevalence of MODD and DM. Detection rate of MODD abnormalities was significantly higher than the diagnosed rate of DM (32% vs. 96%, p < 0.001). DM diabetes mellitus, MODD mean of daily differences

Correlation of MODD and NT-pro BNP

MODD was correlated with MAGE, J-index, and M-value (mg/dl), which are indicators of GV. MODD was also correlated with LBGI, HBGI, and ADRR, which is another indicator of day-to-day GV. There was no correlation between MODD and lipid-related coronary risk factors such as LDL, apoB, and EPA/AA (Table 2). There was no correlation between clinical parameters such as age, renal function, and echocardiography measurements and markers of blood glucose variability, including MODD.

Table 2 Single correlation analysis between MODD and clinical characteristics, other indices of blood glucose fluctuation

A positive correlation was found between MODD and NT-pro BNP (r = 0.409, p = 0.042), although MODD did not correlate with max CK (Table 2, Fig. 2). HBGI was correlated with NT-pro BNP (r = 0.46, p = 0.019) as well as MODD.

Fig. 2
figure 2

Correlation between MODD and NT-proBNP. A positive correlation was found between MODD and NT-proBNP (r = 0.409, p = 0.042). MODD mean of daily differences, NT-proBNP N-terminal pro-brain natriuretic peptide

Using the cut off value of 400 pg/ml, the reference value for heart failure in NT-proBNP, 19 of 25 patients were abnormal. The mean MODD of the group with high NT-proBNP (≥ 400 pg/ml) was 22.2 and the percentage of abnormalities was 73.7%, while the mean MODD of the group with low NT-proBNP was 17.6 and the percentage of abnormalities was 60%, which was not a significant difference. The high MODD group (≥ 16 mg/dl) had a mean NT-proBNP of 2323 pg/ml, 82.4% of abnormalities, while the MODD normal group had a mean NT-proBNP of 1324 pg/ml, 71.4% of abnormalities, also not significantly different.

Discussion

The main findings of the present study were as follows. First, among 25 patients with ACS, the prevalence of abnormal MODD was high (68%) compared to the prevalence of DM (38%). Second, there was an association between MODD, a parameter of day-to-day GV, and NT-pro BNP, a parameter of poor prognosis.

In the present study, 8 patients (32%) were diagnosed with diabetes at or before admission to the hospital. In contrast, MODD assessed by CGM was found to be over the normal level (> 16.0) in 17 (68%) patients. These results suggest that CGM may provide indications of diabetes and glucose intolerance in some patients who were considered normal using previous diagnostic methods. Previous reports have shown that when oral glucose tolerance testing (OGTT) was performed on patients admitted with ACS, 24% were diagnosed as diabetic, 38% as impaired glucose tolerance, and the remaining 38% as normal [13, 14]. Day-to-day assessment of blood glucose using CGM could identify patients with blood glucose variations beyond daily glucose variability.

In this study, we found that many patients with ACS had GV. Previous reports have suggested that high GV is an important factor in coronary plaque vulnerability [15, 16], and our results may also suggest an association between GV and plaque vulnerability.

Although day-to-day GV in the acute phase may differ from day-to-day variability in regular outpatient care [17], it was suggested that incorporating CGM into routine diabetes care and measuring MODD may help to differentiate patients at high risk for ACS who are being impacted by GV.

We also examined the association between various markers of GV calculated from CGM and other indices. HBGI was also abnormal in 4 of 25 patients and correlated with BNP. Despite the lack of correlation between peak CK and MODD, MODD was found to be associated with NT-pro BNP. MODD was not correlated with CK, which reflects the degree of myocardial infarction. In addition, there was no correlation between infarct size and MODD. On the other hand, the fact that MODD associated with NT-pro BNP, a marker of poor prognosis, suggests that patients with abnormal MODD have some factors associated with poor prognosis in addition to the myocardial infarction that led to hospitalization. These results are consistent with previous reports that daily and day-to-day GV increase oxidative stress and inflammation, which cause myocardial damage [18,19,20,21]. Recent investigations suggest that α-glucosidase inhibitor and glucagon-like peptide-1 analogue attenuate GV and inhibit oxidative injury [22, 23]. Therefore, we could potentially improve prognosis using these drugs.

Clinical implications

There have been no studies comparing MODD with traditional BNP or myocardial infarction. The significance of measuring MODD in patients with ACS is that the measurement can predict poor cardiac prognosis beyond those expected based on infarct volume and may serve as a marker for more-intensive anti-cardiac therapy. In addition, CGM in DM routine practice may help in risk stratification of vulnerable patients with ACS.

Limitations

Although some of the patients in this study had high HbA1c levels, these patients may have had less blood glucose variability and been less likely to have MODD abnormalities and therefore should have been omitted from the study, we included them due to the limited number of cases. Therefore, the correlation between MODD and NT-pro BNP in this study may be weak. In addition, OGTT was not used to diagnose diabetes at hospitalization. This may have resulted in a lower rate of diabetes diagnosis. However, the rate of elevated MODD was higher than the number of diagnoses of DM comorbidities and new DM cases on admission for ACS previously reported. NT-pro BNP can be elevated by chronic kidney disease, and it was present in 44% of our patient group. However, there was no correlation between MODD and eGFR values. In this study, all patients with ACS were undergoing inpatient care, and we did not score heart failure symptoms nor evaluate the association between symptoms and NT-pro BNP. All of the patients included in this study had undergone PCI, and although this invasive procedure may affect GV, they all had this procedure in common and did not undergo other invasive procedures such as the use of devices that affect hemodynamics. The blood glucose variability observed in this study may include not only the existing blood glucose variability caused by DM, but also the effect of the stress response of ACS. Therefore, the stress response may have influenced the result of the high MODD abnormality rate relative to the DM patient ratio. However, stress-induced hyperglycemia itself is also said to be a poor prognostic factor [24], and the association between MODD and NT-pro BNP in the present study seems to be consistent with previous reports.

Conclusions

In conclusion, CGM estimations of MODD, a parameter of day-to-day GV, in ACS patients were abnormal at a high rate. In patients with ACS, MODD was associated with elevated NT-proBNP. Future studies should investigate whether day-to-day GV in ACS patients can predict adverse clinical events such as heart failure.

Availability of data and materials

The datasets generated during and analyzed during the current study are not publicly available due to the participants in this study not consenting to the release of their data, but are available from the corresponding author on reasonable request.

Abbreviations

GV:

Glycemic variability

ACS:

Acute coronary syndrome

MODD:

Mean of daily differences

NT-pro BNP:

N-terminal pro-brain natriuretic peptide

CGM:

Continuous glucose monitoring

CK:

Creatine kinase

DM:

Diabetes mellitus

PCI:

Percutaneous coronary intervention

MAGE:

Mean amplitude of glycemic excursions

FGM:

Flash glucose monitoring

ADRR:

Average daily risk range

LBGI:

Low blood glucose index

HBGI:

High blood glucose index

OGTT:

Oral glucose tolerance testing

References

  1. Natsuaki M, Node K. Glycemic variability and cardiac remodeling in patients with acute myocardial infarction. Circ J. 2015;79(5):972–3.

    Article  Google Scholar 

  2. Teraguchi I, Imanishi T, Ozaki Y, et al. Acute-phase glucose fluctuation is negatively correlated with myocardial salvage after acute myocardial infarction. Circ J. 2014;78(1):170–9.

    Article  CAS  Google Scholar 

  3. Issa M, Alqahtani F, Berzingi C, Al-Hajji M, Busu T, Alkhouli M. Impact of acute diabetes decompensation on outcomes of diabetic patients admitted with ST-elevation myocardial infarction. Diabetol Metab Syndr. 2018;10:57.

    Article  Google Scholar 

  4. Yu JH, Han K, Park S, et al. Effects of long-term glycemic variability on incident cardiovascular disease and mortality in subjects without diabetes: a nationwide population-based study. Medicine (Baltimore). 2019;98(29):e16317.

    Article  Google Scholar 

  5. Service FJ. Glucose variability. Diabetes. 2013;62(5):1398–404.

    Article  Google Scholar 

  6. Monnier L, Colette C, Owens DR. Glycemic variability: the third component of the dysglycemia in diabetes. Is it important? How to measure it? J Diabetes Sci Technol. 2008;2(6):1094–100.

    Article  Google Scholar 

  7. Su G, Mi SH, Li Z, Tao H, Yang HX, Zheng H. Prognostic value of early in-hospital glycemic excursion in elderly patients with acute myocardial infarction. Cardiovasc Diabetol. 2013;12:33.

    Article  CAS  Google Scholar 

  8. Su G, Zhang T, Yang H, et al. Admission glycemic variability correlates with in-hospital outcomes in diabetic patients with non-ST segment elevation acute coronary syndrome undergoing percutaneous coronary intervention. Anatol J Cardiol. 2018;19(6):368–73.

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Takahashi H, Iwahashi N, Kirigaya J, et al. Glycemic variability determined with a continuous glucose monitoring system can predict prognosis after acute coronary syndrome. Cardiovasc Diabetol. 2018;17(1):116.

    Article  CAS  Google Scholar 

  10. Gohbara M, Iwahashi N, Kataoka S, et al. Glycemic variability determined by continuous glucose monitoring system predicts left ventricular remodeling in patients with a first ST-segment elevation myocardial infarction. Circ J. 2015;79(5):1092–9.

    Article  CAS  Google Scholar 

  11. Hill NR, Oliver NS, Choudhary P, Levy JC, Hindmarsh P, Matthews DR. Normal reference range for mean tissue glucose and glycemic variability derived from continuous glucose monitoring for subjects without diabetes in different ethnic groups. Diabetes Technol Ther. 2011;13(9):921–8.

    Article  Google Scholar 

  12. Chen T, Xu F, Su JB, et al. Glycemic variability in relation to oral disposition index in the subjects with different stages of glucose tolerance. Diabetol Metab Syndr. 2013;5:38.

    Article  CAS  Google Scholar 

  13. Mokta J, Kumar S, Ganju N, Mokta K, Panda PK, Gupta S. High incidence of abnormal glucose metabolism in acute coronary syndrome patients at a moderate altitude: a sub-Himalayan study. Indian J Endocrinol Metab. 2017;21(1):142–7.

    Article  CAS  Google Scholar 

  14. de Mulder M, Oemrawsingh RM, Stam F, Boersma E, Umans VA. Comparison of diagnostic criteria to detect undiagnosed diabetes in hyperglycaemic patients with acute coronary syndrome. Heart. 2012;98(1):37–41.

    Article  Google Scholar 

  15. Okada K, Hibi K, Gohbara M, et al. Association between blood glucose variability and coronary plaque instability in patients with acute coronary syndromes. Cardiovasc Diabetol. 2015;14:111.

    Article  Google Scholar 

  16. Kataoka S, Gohbara M, Iwahashi N, et al. Glycemic variability on continuous glucose monitoring system predicts rapid progression of non-culprit lesions in patients with acute coronary syndrome. Circ J. 2015;79(10):2246–54.

    Article  CAS  Google Scholar 

  17. Robinson LE, van Soeren MH. Insulin resistance and hyperglycemia in critical illness: role of insulin in glycemic control. AACN Clin Issues. 2004;15(1):45–62.

    Article  Google Scholar 

  18. Lubrano V, Balzan S. Role of oxidative stress-related biomarkers in heart failure: galectin 3, α1-antitrypsin and LOX-1: new therapeutic perspective? Mol Cell Biochem. 2020;464(1–2):143–52.

    Article  CAS  Google Scholar 

  19. Ohara M, Fukui T, Ouchi M, et al. Relationship between daily and day-to-day glycemic variability and increased oxidative stress in type 2 diabetes. Diabetes Res Clin Pract. 2016;122:62–70.

    Article  CAS  Google Scholar 

  20. Meng L, Uzui H, Guo H, Tada H. Role of SGLT1 in high glucose level-induced MMP-2 expression in human cardiac fibroblasts. Mol Med Rep. 2018;17(5):6887–92.

    CAS  PubMed  Google Scholar 

  21. D’Oria R, Schipani R, Leonardini A, et al. The role of oxidative stress in cardiac disease: from physiological response to injury factor. Oxid Med Cell Longev. 2020;2020:5732956.

    PubMed  PubMed Central  Google Scholar 

  22. Shimabukuro M, Tanaka A, Sata M, et al. α-Glucosidase inhibitor miglitol attenuates glucose fluctuation, heart rate variability and sympathetic activity in patients with type 2 diabetes and acute coronary syndrome: a multicenter randomized controlled (MACS) study. Cardiovasc Diabetol. 2017;16(1):86.

    Article  Google Scholar 

  23. Li Q, Lin Y, Wang S, Zhang L, Guo L. GLP-1 inhibits high-glucose-induced oxidative injury of vascular endothelial cells. Sci Rep. 2017;7(1):8008.

    Article  Google Scholar 

  24. Li M, Chen G, Feng Y, He X. Stress induced hyperglycemia in the context of acute coronary syndrome: definitions, interventions, and underlying mechanisms. Front Cardiovasc Med. 2021;8:676892.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors thank Hiromi Nishimura, Motoko Oku, Mari Kurata, and Yoshiko Kurose for providing excellent technical assistance.

Funding

Not applicable.

Author information

Authors and Affiliations

Authors

Contributions

MM collected and analyzed data and wrote the manuscript. HU contributed to conceptualization, investigation, and critical revision. TS, TA, YS, MN, HI, NT, KH, KI, SM contributed to data curation. TM contributed to data curation and formal analysis. HT contributed to supervision. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Hiroyasu Uzui.

Ethics declarations

Ethics approval and consent to participate

This work was partially supported by a research grant from the University of Fukui and a research grant for cardiovascular diseases from the Ministry of Health, Labour and Welfare, Japan (Grant Number 16K09426 to Dr. Hiroyasu Uzui). This investigation conformed to the principles outlined in the 1975 Declaration of Helsinki and later amendments. This study was approved by the Research Ethics Committee of the University of Fukui, and informed consent was obtained from all patients. The follow-up results were registered in the Universal Hospital Medical Information Network Clinical Trials Registry (UMIN 000023837, 30/08/2016).

Consent for publication

Not applicable.

Competing interests

Not applicable.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Miyoshi, M., Uzui, H., Shimizu, T. et al. Significance of day-to-day glucose variability in patients after acute coronary syndrome. BMC Cardiovasc Disord 21, 490 (2021). https://doi.org/10.1186/s12872-021-02303-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12872-021-02303-z

Keywords