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QTc interval is associated with C-reactive protein in Novosibirsk residents regardless of cardiometabolic risk factors and coronary artery disease (within the ESSE-RF3 study)

https://doi.org/10.15829/1728-8800-2025-4408

EDN: GZBCQB

Abstract

Aim. To study the association of the QT interval with C-reactive protein (CRP) in combination with cardiometabolic risk factors and coronary artery disease (CAD) in a sample of Novosibirsk residents.

Material and methods. The study included 1042 Novosibirsk residents (men, 510 (48,9%)), aged 35-74 years (as part of the ESSERF3 study). The examination program included blood sampling, collection of demographic and social data, anthropometry, blood pressure measurement, and electrocardiography. CRP threshold value was considered to be ≥5 mg/l. CAD and its categories were established by Rose GA questionnaire and electrocardiogram assessment according to the Minnesota Code. The QT interval was measured in lead V5.

Results. The QTc interval correlates with age, waist circumference, systolic blood pressure, triglycerides, blood glucose, and CRP. The QTc interval was directly and independently associated with age, female sex, blood pressure ≥140/90 mm Hg, fasting plasma glucose ≥6,1 mmol/L, CRP ≥5 mg/L, and CAD. The standardized QTc interval was longer in individuals with CRP ≥5 mg/L than in individuals with CRP <5 mg/L (400,71 [404,43; 397,05] vs, 393,98 [396,17; 391,80] ms).

Conclusion. In Novosibirsk residents, the QTc interval is associated with elevated CRP levels regardless of the presence of CAD and other cardiometabolic risk factors.

About the Authors

E. V. Garbuzova
Research Institute for Therapy and Preventive Medicine — branch of the Federal Research Center Institute of Cytology and Genetics
Russian Federation

Novosibirsk



A. A. Kuznetsov
Research Institute for Therapy and Preventive Medicine — branch of the Federal Research Center Institute of Cytology and Genetics
Russian Federation

Novosibirsk



A. M. Nesterets
Research Institute for Therapy and Preventive Medicine — branch of the Federal Research Center Institute of Cytology and Genetics
Russian Federation

Novosibirsk



A. D. Afanasyeva
Research Institute for Therapy and Preventive Medicine — branch of the Federal Research Center Institute of Cytology and Genetics
Russian Federation

Novosibirsk



V. S. Shramko
Research Institute for Therapy and Preventive Medicine — branch of the Federal Research Center Institute of Cytology and Genetics
Russian Federation

Novosibirsk



A. E. Imaeva
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



G. A. Muromtseva
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



Yu. A. Balanova
National Medical Research Center for Therapy and Preventive Medicine
Russian Federation

Moscow



G. I. Simonova
Research Institute for Therapy and Preventive Medicine — branch of the Federal Research Center Institute of Cytology and Genetics
Russian Federation

Novosibirsk



O. M. Drapkina
Research Institute for Therapy and Preventive Medicine — branch of the Federal Research Center Institute of Cytology and Genetics
Russian Federation

Novosibirsk



References

1. Moss AJ. Prolonged QT-Interval Syndromes. JAMA. 1986;256(21): 2985-7.

2. Cho DH, Choi J, Kim MN, et al. Incremental Value of QT Interval for the Prediction of Obstructive Coronary Artery Disease in Patients with Chest Pain. Sci Rep. 2021;11(1):10513. doi:10.1038/s41598-021-90133-6.

3. Sara JD, Lennon RJ, Ackerman MJ, et al. Coronary Microvascular Dysfunction Is Associated with Baseline QTc Prolongation amongst Patients with Chest Pain and Non-Obstructive Coronary Artery Disease. J Electrocardiol. 2016;49(1):87-93. doi:10.1016/j.jelectrocard.2015.10.006.

4. Sahranavard T, Soflaei SS, Alimi R, et al. Factors Associated with Prolonged QTc Interval in Iranian Population: MASHAD Cohort Study. J Electrocardiol. 2024;84:112-22. doi:10.1016/j.jelectrocard.2024.04.002.

5. Akintunde AA, Oyedeji AT, Familoni OB, et al. QT Interval Prolongation and Dispersion: Epidemiology and Clinical Correlates in Subjects with Newly Diagnosed Systemic Hypertension in Nigeria. J Cardiovasc Dis Res. 2012;3(4):290-5. doi:10.4103/0975-3583.102705.

6. Nikitin YuP, Kuznetsov AA, Malyutina SK. The relationship of some clinical indicators with the duration and variability of the QT and RR intervals (based on the materials of an epidemiological population study). Terapevticheskii arkhiv. 2002;74(3):72-5. (In Russ.)

7. Kuznetsov AA, Voevoda MI, Maksimov VN, et al. The association of the marker of cardiovascular RISK — QTc interval with 64V/64I CCR2 gene polymorphism and metabolic syndrome components in the general male population of Novosibirsk. Ateroscleroz. 2015; 11(4):44-8. (In Russ.)

8. Nikitin YuP, Kuznetsov AA, Maliutina SK, et al. Prognostic value of duration and variability of QT and RR intervals in general population of Novosibirsk. Kardiologiia. 2002;42(2):76-83.

9. Zhang Y, Post WS, Blasco-Colmenares E, et al. Electrocardiographic QT Interval and Mortality: A Meta-Analysis. Epidemiology. 2011;22(5):660-70. doi:10.1097/EDE.0b013e318225768b.

10. Chang KT, Shu HS, Chu CY, et al. Association between C-Reactive Protein, Corrected QT Interval and Presence of QT Prolongation in Hypertensive Patients. Kaohsiung J Med Sci. 2014;30(6):310-15. doi:10.1016/j.kjms.2014.02.012.

11. Isakadze N, Engels MC, Beer D, et al. C-Reactive Protein Elevation Is Associated With QTc Interval Prolongation in Patients Hospitalized With COVID-19. Front Cardiovasc Med. 2022;9:866146. doi:10.3389/fcvm.2022.866146.

12. Kim E, Joo S, Kim J, et al. Association between C-Reactive Protein and QTc Interval in Middle-Aged Men and Women. Eur J Epidemiol. 2006;21(9):653-9. doi:10.1007/s10654-006-9034-9.

13. Lazzerini PE, Acampa M, Capecchi PL, et al. Association between high sensitivity C-reactive protein, heart rate variability and corrected QT interval in patients with chronic inflammatory arthritis. Eur J Intern Med. 2013;24(4):368-74. doi:10.1016/j.ejim.2013.02.009.

14. Viscido A, Capannolo A, Petroni R, et al. Association between Corrected QT Interval and C-Reactive Protein in Patients with Inflammatory Bowel Diseases. Medicina (Kaunas). 2020;56(8): 382. doi:10.3390/medicina56080382.

15. Drapkina OM, Shalnova SA, Imaeva AE et al. Epidemiology of Cardiovascular Diseases in Regions of Russian Federation. Third survey (ESSE-RF-3). Rationale and study design. Cardiovascular Therapy and Prevention. 2022;21(5):3246. (In Russ.) doi:10.15829/1728-8800-2022-3246.

16. Goldenberg I, Moss AJ, Zareba W. QT Interval: How to Measure It and What Is "Normal". J Cardiovasc Electrophysiol. 2006; 17(3):333-6. doi:10.1111/j.1540-8167.2006.00408.x.

17. Postema PG, Wilde AAM. The Measurement of the QT Interval. Curr Cardiol Rev. 2014;10(3):287-94. doi:10.2174/1573403x10666140514103612.

18. Schouten EG, Dekker JM, Meppelink P, et al. QT Interval Pro ongation Predicts Cardiovascular Mortality in an Apparently Healthy Population. Circulation. 1991;84(4):1516-23. doi:10.1161/01.cir.84.4.1516.

19. Karjalainen J, Reunanen A, Ristola P, et al. QT Interval as a Cardiac Risk Factor in a Middle Aged Population. Heart. 1997;77(6): 543-8. doi:10.1136/hrt.77.6.543.

20. Elming H, Holm E, Jun L, et al. The Prognostic Value of the QT Interval and QT Interval Dispersion in All-Cause and Cardiac Mortality and Morbidity in a Population of Danish Citizens. Eur Heart J. 1998;19(9):1391-400. doi:10.1053/euhj.1998.1094.

21. de Bruyne MC, Hoes AW, Kors JA, et al. Prolonged QT Interval Predicts Cardiac and All-Cause Mortality in the Elderly. The Rotterdam Study. Eur Heart J. 1999;20(4):278-84. doi:10.1053/euhj.1998.1276.

22. Noseworthy PA, Peloso GM, Hwang SJ, et al. QT Interval and Long-Term Mortality Risk in the Framingham Heart Study. Ann Noninvasive Electrocardiol. 2012;17(4):340-8. doi:10.1111/j.1542-474X.2012.00535.x.

23. Surawicz B, Childers R, Deal BJ, et al. AHA/ACCF/HRS Recommendations for the Standardization and Interpretation of the Electrocardiogram: Part III: Intraventricular Conduction Disturbances: A Scientific Statement from the American Heart Association Electrocardiography and Arrhythmias Committee, Council on Clinical Cardiology; the American College of Cardiology Foundation; and the Heart Rhythm Society. Endorsed by the International Society for Computerized Electrocardiology. J Am Coll Cardiol. 2009;53(11):976-81. doi:10.1016/j.jacc.2008.12.013.

24. Mach F, Baigent C, Catapano AL, et al. 2019 ESC/EAS Guidelines for the Management of Dyslipidaemias: Lipid Modification to Reduce Cardiovascular Risk. Eur Heart J. 2020;41(1):111-88. doi:10.1093/eurheartj/ehz455.

25. Mychka VB, Vertkin AL, Vardaev LI, et al. Experts’ consensus on the interdisciplinary approach towards the management, diagnostics, and treatment of patients with metabolic syndrome. Cardiovascular Therapy and Prevention. 2013;12(6):41-82. (In Russ.)

26. Nikitin YuP, Voevoda MI, Maksimov VN, et al. Family history and coronary heart disease in Novosibirsk City population (Program WHO-MONICA). Cardiovascular Therapy and Prevention. 2005; 4(4):37-40. (In Russ.)

27. Serova NV, Nikitin YuP. The prevalence of coronary heart disease and its main risk factors among the unorganized urban population of Western Siberia (based on the materials of the Siberian MONICA project). 2016;244-56. In: Monitoring of cardiac mortality, morbidity and their risk factors in different regions of the world (WHO MONICA project). YuP Nikitin (ed); in 2 volumes. Novosibirsk. Academic press "Geo". 2016. 699 p. (In Russ.)

28. Серова Н. В., Никитин Ю. П. Распространенность ишемической болезни сердца и ее основных факторов риска среди неорганизованного городского населения Западной Сибири (по материалам проекта "Сибирская MONICA"). 2016:244-56. ISBN: 978-5-9907634-6-3.

29. Kalinina AM, Shalnova SA, Gambaryan MG, et al. Epidemiological methods for the identification of major chronic noncommunicable diseases and risk factors in mass population surveys. Methodical manual. Boytsov SA (ed). M. 2015. 96 р. (In Russ.)

30. Prineas RJ, Crow RS, Zhang Z. The Minnesota Code Manual of Electrocardiographic Findings; Springer Science & Business Media, 2009; ISBN: 978-1-84882-778-3.

31. Rose GA. The Diagnosis of Ischaemic Heart Pain and Intermittent Claudication in Field Surveys. Bull World Health Organ. 1962; 27(6):645-58.

32. Indraratna P, Tardo D, Delves M, et al. Measurement and Ma nagement of QT Interval Prolongation for General Physicians. J Gen Intern Med. 2020;35(3):865-73. doi:10.1007/s11606-019-05477-7.

33. Lepeschkin E, Surawicz B. The Measurement of the Q-T Interval of the Electrocardiogram. Circulation. 1952;6(3):378-88. doi:10.1161/01.CIR.6.3.378.

34. Bazett H. An Analysis of the Time-Relations Of. Heart. 1920;7:353. Taran LM, Szilagyi N. The Duration of the Electrical Systole (Q-T) in Acute Rheumatic Carditis in Children. Am Heart J. 1947;33(1): 14-26. doi:10.1016/0002-8703(47)90421-3.

35. Molnar J, Weiss JS, Rosenthal JE. The Missing Second: What Is the Correct Unit for the Bazett Corrected QT Interval? Am J Cardiol. 1995;75(7):537-8. doi:10.1016/s0002-9149(99)80603-1.

36. Pokrovskaya MS, Borisova AL, Metelskaya VA, et al. Role of biobanking in managing large-scale epidemiological studies. Cardiovascular Therapy and Prevention. 2021;20(5):2958. (In Russ.) doi:10.15829/17288800-2021-2958.

37. Ma Q, Li Z, Guo X, et al. Prevalence and Risk Factors of Prolonged Cordiovasc Disord. 2019;19(1):276. doi:10.1186/s12872-019-1244-7.

38. Lin N, Zhang H, Li X, et al. The Influence of Different Glucose Tolerance on QTc Interval: A Population-Based Study. BMC Cardiovasc Disord. 2023;23(1):47. doi:10.1186/s12872-023-03081-6.

39. Empana JP, Jouven X, Canouï-Poitrine F, et al. C-Reactive Protein, Interleukin 6, Fibrinogen and Risk of Sudden Death in European Middle-Aged Men: The PRIME Study. Arterioscler Thromb Vasc Biol. 2010;30(10):2047-52. doi:10.1161/ATVBAHA.110.208785.

40. Wu KC, Gerstenblith G, Guallar E, et al. Combined Cardiac Magnetic Resonance Imaging and C-Reactive Protein Levels Identify a Cohort at Low Risk for Defibrillator Firings and Death. Circ Cardiovasc Imaging. 2012;5(2):178-86. doi:10.1161/CIRCIMAGING.111.968024.

41. Lazzerini PE, Capecchi PL, Laghi-Pasini F. Systemic Inflammation and Arrhythmic Risk: Lessons from Rheumatoid Arthritis. Eur Heart J. 2017;38(22):1717-27. doi:10.1093/eurheartj/ehw208.

42. Lazzerini PE, Capecchi PL, El-Sherif N, et al. Emerging Arrhythmic Risk of Autoimmune and Inflammatory Cardiac Channelopathies. J Am Heart Assoc. 2018;7(22):e010595. doi:10.1161/JAHA.118.010595.

43. Lazzerini PE, Acampa M, Laghi-Pasini F, et al. Cardiac Arrest Risk During Acute Infections: Systemic Inflammation Directly Prolongs QTc Interval via Cytokine-Mediated Effects on Potassium Channel Expression. Circ Arrhythm Electrophysiol. 2020;13(8):e008627. doi:10.1161/CIRCEP.120.008627.

44. Lazzerini PE, Capecchi PL, Laghi-Pasini F. Long QT Syndrome: An Emerging Role for Inflammation and Immunity. Front Cardiovasc Med. 2015;2:26. doi:10.3389/fcvm.2015.00026.

45. Lazzerini PE, Laghi-Pasini F, Bertolozzi I, et al. Systemic Inflammation as a Novel QT-Prolonging Risk Factor in Patients with Torsades de Pointes. Heart. 2017;103(22):1821-9. doi:10.1136/heartjnl-2016-311079.

46. Gulletta S, Della Bella P, Pannone L, et al. QTc Interval Prolongation, Inflammation, and Mortality in Patients with COVID-19. J Interv Card Electrophysiol. 2022;63(2):441-8. doi:10.1007/s10840-021-01033-8.


Supplementary files

What is already known about the subject?

  • Corrected QT interval (QTc) prolongation is associated with an increased risk of life-threatening cardiac arrhythmias and sudden death.
  • A number of studies have demonstrated a relationship between QTc interval duration and inflammatory markers, including the level of C-reactive protein.

What might this study add?

  • We showed that the QTc interval is associated with C-reactive protein level regardless of the presence of coronary artery disease and other cardiometabolic risk factors in Russian residents using the example of Novosibirsk.

Review

For citations:


Garbuzova E.V., Kuznetsov A.A., Nesterets A.M., Afanasyeva A.D., Shramko V.S., Imaeva A.E., Muromtseva G.A., Balanova Yu.A., Simonova G.I., Drapkina O.M. QTc interval is associated with C-reactive protein in Novosibirsk residents regardless of cardiometabolic risk factors and coronary artery disease (within the ESSE-RF3 study). Cardiovascular Therapy and Prevention. 2025;24(7):4408. (In Russ.) https://doi.org/10.15829/1728-8800-2025-4408. EDN: GZBCQB

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ISSN 1728-8800 (Print)
ISSN 2619-0125 (Online)