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High prevalence of prolonged QTc interval among individuals in ambulatory diabetic care in southwestern Uganda

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Abstract

Background

Heart rate-corrected QT (QTc) interval is associated with increased risk for cardiovascular events and mortality among individuals with diabetes mellitus (DM). Little is known about the epidemiology of prolonged QTc among people with DM in resource-limited settings.

Methods

We conducted a cross-sectional study among adults with diabetes in ambulatory care at the Mbarara Regional Referral Hospital, from November 2018 to April 2019. Twelve-lead ECG recordings were performed on all participants. We collected clinical and laboratory data related to diabetes disease status and treatment control. We estimated QTc using Bazett’s formula and categorized it according to standardized sex-adjusted thresholds. Linear regression analysis was performed to identify correlates of QTc.

Results

We recruited 299 participants with a mean age of 50.1 years (SD±9.8) and mean HbA1c of 9.7 % (SD±2.6), and 69.6% were female. We detected prolonged and borderline QTc in 6.4% (19/299, 95% CI: 3.9–9.7%) and 23.4% (70/299, 95% CI: 18.7–28.6%) of participants, respectively. In multivariate models, factors associated with increasing QTc interval were mean arterial pressure (β=0.34; 95% CI: 0.07–0.63, p=0.019) and female sex (β=15.26; 95% CI: 7.58–22.94, p<0.001).

Conclusions

The prevalence of abnormal QTc among individuals in routine diabetes care in southwestern Uganda was high. Female sex and mean arterial pressure were correlated with QTc interval. Given these findings, future studies should explore the clinical impact of abnormal QTc in this patient population.

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References

  1. Organization, W.H. Global report on diabetes: World Health Organization; 2016.

  2. Schernthaner G, Lotan C, Baltadzhieva-Trendafilova E, Ceponis J, Clodi M, Ducena K, et al. Unrecognised cardiovascular disease in type 2 diabetes: is it time to act earlier? Cardiovasc Diabetol. 2018;17(1):145.

    Article  Google Scholar 

  3. Cardoso CR, Salles GF, Deccache W. QTc interval prolongation is a predictor of future strokes in patients with type 2 diabetes mellitus. Stroke. 2003;34(9):2187–94.

    Article  Google Scholar 

  4. Veglio M, Sivieri R, Chinaglia A, Scaglione L, Cavallo-Perin P. QT interval prolongation and mortality in type 1 diabetic patients: a 5-year cohort prospective study. Neuropathy Study Group of the Italian Society of the Study of Diabetes, Piemonte Affiliate. Diabetes Care. 2000;23(9):1381–3.

    Article  CAS  Google Scholar 

  5. Okin PM, Devereux RB, Lee ET, Galloway JM, Howard BV, Strong Heart Study. Electrocardiographic repolarization complexity and abnormality predict all-cause and cardiovascular mortality in diabetes: the strong heart study. Diabetes. 2004;53(2):434–40.

    Article  CAS  Google Scholar 

  6. Rossing P, Breum L, Major-Pedersen A, Sato A, Winding H, Pietersen A, et al. Prolonged QTc interval predicts mortality in patients with type 1 diabetes mellitus. Diabet Med. 2001;18(3):199–205.

    Article  CAS  Google Scholar 

  7. Salles GF, Bloch KV, Cardoso CR. Mortality and predictors of mortality in a cohort of Brazilian type 2 diabetic patients. Diabetes Care. 2004;27(6):1299–305.

    Article  Google Scholar 

  8. Li X, Ren H, Xu ZR, Liu YJ, Yang XP, Liu JQ. Prevalence and risk factors of prolonged QTc interval among Chinese patients with type 2 diabetes. Exp Diabetes Res. 2012;2012:1–6.

    Google Scholar 

  9. Veglio M, et al. Prevalence of increased QT interval duration and dispersion in type 2 diabetic patients and its relationship with coronary heart disease: a population-based cohort. J Intern Med. 2002;251(4):317–24.

    Article  CAS  Google Scholar 

  10. Yang X-h, et al. The relationship between insulin sensitivity and heart rate-corrected QT interval in patients with type 2 diabetes. Diabetol Metab Syndr. 2017;9(1):69.

    Article  Google Scholar 

  11. Sivieri R, Veglio M, Chinaglia A, Scaglione P, Cavallo-Perin P, For the Neuropathy Study Group of the Italian Society for the Study of Diabetes, Piemonte affiliate. Prevalence of QT prolongation in a type 1 diabetic population and its association with autonomic neuropathy. Diabet Med. 1993;10(10):920–4.

    Article  CAS  Google Scholar 

  12. Migisha R, et al. Prevalence and correlates of cardiovascular autonomic neuropathy among patients with diabetes in Uganda: a hospital-based cross-sectional study. Glob Heart. 2020;15(1).

  13. Goldenberg I, Moss AJ, Zareba W. QT interval: how to measure it and what is “normal”. J Cardiovasc Electrophysiol. 2006;17(3):333–6.

    Article  Google Scholar 

  14. Ukpabi OJ, Onwubere BJ. QTc prolongation in Black diabetic subjects with cardiac autonomic neuropathy. Afr Health Sci. 2017;17(4):1092–100.

    Article  Google Scholar 

  15. Mahwi TO, Hasan RM, Faraj HI. Incidence of QTc prolongation in type 2 diabetes mellitus and its relation to cardiac autonomic neuropathy. J Med J. 2014;48(2):102–11.

    Google Scholar 

  16. Magodoro IM, et al. Population prevalence and correlates of prolonged QT interval: cross-sectional, population-based study from rural Uganda. Glob Heart. 2018.

  17. Tesfamariam B, Cohen RA. Free radicals mediate endothelial cell dysfunction caused by elevated glucose. Am J Phys Heart Circ Phys. 1992;263(2):H321–6.

    CAS  Google Scholar 

  18. Fiorentini A, Perciaccante A, Valente R, Paris A, Serra P, Tubani L. The correlation among QTc interval, hyperglycaemia and the impaired autonomic activity. Auton Neurosci. 2010;154(1-2):94–8.

    Article  Google Scholar 

  19. Wartenberg M, Ling FC, Schallenberg M, Bäumer AT, Petrat K, Hescheler J, et al. Down-regulation of intrinsic P-glycoprotein expression in multicellular prostate tumor spheroids by reactive oxygen species. J Biol Chem. 2001;276(20):17420–8.

    Article  CAS  Google Scholar 

  20. Roden DM, Yang T. Protecting the heart against arrhythmias: potassium current physiology and repolarization reserve. 2005. Am Heart Assoc.

  21. Satpathy S, Satpathy S, Nayak PK. Correlation of blood pressure and QT interval. Natl J Physiol Pharm Pharmacol. 2018;8(2):207–10.

    Google Scholar 

  22. Sun G-Z, Zhou Y, Ye N, Wu SJ, Sun YX. Independent influence of blood pressure on QTc interval: results from a general Chinese population. Biomed Res Int. 2019;2019:1–8.

    Google Scholar 

  23. Peng S, Yu Y, Hao K, Xing H, Li D, Chen C, et al. Heart rate–corrected QT interval duration is significantly associated with blood pressure in Chinese hypertensives. J Electrocardiol. 2006;39(2):206–10.

    Article  Google Scholar 

  24. Matsumura K, et al. Association of QT interval with blood pressure in 80-year-old subjects. Hypertens Res. 2004;27(6):387–91.

    Article  Google Scholar 

  25. Klimas J, Stankovicova T, Kyselovic J, Bacharova L. Prolonged QT interval is associated with blood pressure rather than left ventricular mass in spontaneously hypertensive rats. Clin Exp Hypertens. 2008;30(7):475–85.

    Article  Google Scholar 

  26. Oikarinen L, Nieminen MS, Toivonen L, Viitasalo M, Wachtell K, Papademetriou V, et al. Relation of QT interval and QT dispersion to regression of echocardiographic and electrocardiographic left ventricular hypertrophy in hypertensive patients: the Losartan Intervention for Endpoint Reduction (LIFE) study. Am Heart J. 2003;145(5):919–25.

    Article  Google Scholar 

  27. Marfella R, Gualdiero P, Siniscalchi M, Carusone C, Verza M, Marzano S, et al. Morning blood pressure peak, QT intervals, and sympathetic activity in hypertensive patients. Hypertension. 2003;41(2):237–43.

    Article  CAS  Google Scholar 

  28. Giunti S, Bruno G, Lillaz E, Gruden G, Lolli V, Chaturvedi N, et al. Incidence and risk factors of prolonged QTc interval in type 1 diabetes: the EURODIAB Prospective Complications Study. Diabetes Care. 2007;30(8):2057–63.

    Article  Google Scholar 

  29. Griffin M, Lee HW, Zhao L, Eghbali-Webb M. Gender-related differences in proliferative response of cardiac fibroblasts to hypoxia. Mol Cell Biochem. 2000;215(1-2):21–30.

    Article  CAS  Google Scholar 

  30. Montanez A, Ruskin JN, Hebert PR, Lamas GA, Hennekens CH. Prolonged QTc interval and risks of total and cardiovascular mortality and sudden death in the general population: a review and qualitative overview of the prospective cohort studies. Arch Intern Med. 2004;164(9):943–8.

    Article  Google Scholar 

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Acknowledgment

We thank the study participants, the staff, and management of the Mbarara Regional Referral Hospital who contributed in several ways towards the success of this study. We are very thankful to members of the Technical Advisory Committee (TAC) of the Mbarara University Research Training Initiative (MURTI) for their technical input into the study. We also acknowledge Dr. Sam Ruvuma and Dr. Kwagga Teddy of the Ophthalmology Department of the Mbarara University of Science and Technology for their technical support.

Availability of data and materials

The datasets generated and analyzed during the study are available from the corresponding author on request.

Funding

This research was supported by the Fogarty International Center and co-founding partners (NIH Common Fund, Office of Strategic Coordination, Office of the Director (OD/OSC/CF/NIH); Office of AIDS Research, Office of the Director (OAR/NIH); National Institute of Mental Health (NIMH/NIH); and National Institute of Neurological Disorders and Stroke (NINDS/NIH)) of the National Institutes of Health under Award Number D43TW010128.

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Authors and Affiliations

Authors

Contributions

R.M., A.M., D.C.A, S.L.M, and M.S conceived the study, contributed to discussion, and reviewed, edited, and wrote the manuscript. G.K. and D.C.A. reviewed the ECG recordings. R.M and M.S. analyzed the data. R.M. is the guarantor of this research work and, as such, had full access to all the data for the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Richard Migisha.

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Ethics approval and consent to participate

The study got an approval from the institutional ethics review board of the Mbarara University of Science and Technology (MUST-REC). We also received approval for the study from the Uganda National Council of Science and Technology (UNCST) and from the Research Secretariat in the Office of the President of Uganda, in accordance with the national guidelines. All study participants provided written informed consent before recruitment and participation. Participants who could not write gave consent with a thumbprint.

Conflict of interests

The authors declare no competing interests.

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Migisha, R., Agaba, D.C., Katamba, G. et al. High prevalence of prolonged QTc interval among individuals in ambulatory diabetic care in southwestern Uganda. Int J Diabetes Dev Ctries 41, 614–620 (2021). https://doi.org/10.1007/s13410-021-00944-6

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