open access

Vol 73, No 5 (2022)
Original paper
Submitted: 2022-02-22
Accepted: 2022-03-30
Published online: 2022-07-18
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Association of antithyroid peroxidase antibodies with cardiac function in euthyroid women with type 1 diabetes mellitus — assessment with two-dimensional speckle‑tracking echocardiography

Magdalena Maria Łukawska-Tatarczuk12, Agnieszka Pawlak34, Jakub Zieliński5, Edward Franek24, Leszek Czupryniak1, Beata Mrozikiewicz-Rakowska1
·
Pubmed: 35971937
·
Endokrynol Pol 2022;73(5):812-822.
Affiliations
  1. Department of Diabetology and Internal Diseases, Medical University of Warsaw, Warsaw, Poland
  2. Department of Internal Diseases, Endocrinology, and Diabetology, Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw
  3. Department of Invasive Cardiology, Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, Poland
  4. Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw
  5. Interdisciplinary Centre for Mathematical and Computational Modelling, University of Warsaw, Warsaw, Poland

open access

Vol 73, No 5 (2022)
Original Paper
Submitted: 2022-02-22
Accepted: 2022-03-30
Published online: 2022-07-18

Abstract

Introduction: The presence of diabetes is associated with loss of cardioprotection in premenopausal women; however, the mechanisms involved remain unknown. Autoimmune factors are suspected to play a role in cardiovascular complications, especially in type 1 diabetes (T1DM). The aim of this pilot study was to explore whether antithyroid peroxidase antibody (aTPO) as a marker of increased immune activity is related to cardiac dysfunction in young, asymptomatic women with T1DM.

Material and methods: Eighty-eight euthyroid women (59 with T1DM and 29 healthy controls) underwent physical examination, laboratory tests, thyroid ultrasound, and two-dimensional speckle-tracking echocardiography. According to the antiperoxidase antibodies (aTPO) titre, the T1DM women were divided into an aTPO positive (T1DM aTPO+) (n = 34) and an aTPO negative (T1DM aTPO–) (n = 25) group. The relationship between thyroid autoimmunity parameters and echocardiographic parameters was evaluated.

Results: Global longitudinal strain (GLS) was slightly reduced in the T1DM aTPO+ group compared to T1DM aTPO– and significantly compared to controls (p = 0.051 and p = 0.015, respectively). Although, the lower values of longitudinal strain of left ventricular were found in the majority of segments in the T1DM aTPO+ group in comparison to T1DM aTPO– and controls, significant differences were only found in the two-chamber view (specifically in the anterior segments) between the T1DM aTPO+ and T1DM aTPO– groups (p = 0.030) and in the four-chamber view (specifically in the anterolateral segments) between the T1DM aTPO+ group and controls (p = 0.021). Echocardiographic parameters of diastolic and systolic function of both ventricles were significantly correlated with parameters of thyroid
autoimmunity. A logistic regression analysis showed that Hashimoto’s thyroiditis (HT) duration [odds ratio (OR): 0.997, 95% confidence interval (CI): 0.995–0.999, p = 0.008), the dose of levothyroxine (OR: 0.814, 95% CI: 0.689–0.960, p = 0.013), and reduced echogenicity on thyroid ultrasound (OR: 0.309, 95% CI: 0.120–0.793, p = 0.013) had a significant influence on reduced GLS.

Conclusions: Our results suggest that coexistence of aTPO with T1DM was associated with poorer myocardial function, particularly in the anterior and anterolateral segments, which may be related to an autoimmune factor. The impaired function of these segments is probably the first sign of myocardial systolic dysfunction in women with T1DM, which needs to be confirmed in further studies.

Abstract

Introduction: The presence of diabetes is associated with loss of cardioprotection in premenopausal women; however, the mechanisms involved remain unknown. Autoimmune factors are suspected to play a role in cardiovascular complications, especially in type 1 diabetes (T1DM). The aim of this pilot study was to explore whether antithyroid peroxidase antibody (aTPO) as a marker of increased immune activity is related to cardiac dysfunction in young, asymptomatic women with T1DM.

Material and methods: Eighty-eight euthyroid women (59 with T1DM and 29 healthy controls) underwent physical examination, laboratory tests, thyroid ultrasound, and two-dimensional speckle-tracking echocardiography. According to the antiperoxidase antibodies (aTPO) titre, the T1DM women were divided into an aTPO positive (T1DM aTPO+) (n = 34) and an aTPO negative (T1DM aTPO–) (n = 25) group. The relationship between thyroid autoimmunity parameters and echocardiographic parameters was evaluated.

Results: Global longitudinal strain (GLS) was slightly reduced in the T1DM aTPO+ group compared to T1DM aTPO– and significantly compared to controls (p = 0.051 and p = 0.015, respectively). Although, the lower values of longitudinal strain of left ventricular were found in the majority of segments in the T1DM aTPO+ group in comparison to T1DM aTPO– and controls, significant differences were only found in the two-chamber view (specifically in the anterior segments) between the T1DM aTPO+ and T1DM aTPO– groups (p = 0.030) and in the four-chamber view (specifically in the anterolateral segments) between the T1DM aTPO+ group and controls (p = 0.021). Echocardiographic parameters of diastolic and systolic function of both ventricles were significantly correlated with parameters of thyroid
autoimmunity. A logistic regression analysis showed that Hashimoto’s thyroiditis (HT) duration [odds ratio (OR): 0.997, 95% confidence interval (CI): 0.995–0.999, p = 0.008), the dose of levothyroxine (OR: 0.814, 95% CI: 0.689–0.960, p = 0.013), and reduced echogenicity on thyroid ultrasound (OR: 0.309, 95% CI: 0.120–0.793, p = 0.013) had a significant influence on reduced GLS.

Conclusions: Our results suggest that coexistence of aTPO with T1DM was associated with poorer myocardial function, particularly in the anterior and anterolateral segments, which may be related to an autoimmune factor. The impaired function of these segments is probably the first sign of myocardial systolic dysfunction in women with T1DM, which needs to be confirmed in further studies.

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Keywords

type 1 diabetes mellitus; thyroid autoimmunity; speckle tracking echocardiography; diabetic cardiomyopathy; heart failure

About this article
Title

Association of antithyroid peroxidase antibodies with cardiac function in euthyroid women with type 1 diabetes mellitus — assessment with two-dimensional speckle‑tracking echocardiography

Journal

Endokrynologia Polska

Issue

Vol 73, No 5 (2022)

Article type

Original paper

Pages

812-822

Published online

2022-07-18

Page views

1179

Article views/downloads

524

DOI

10.5603/EP.a2022.0041

Pubmed

35971937

Bibliographic record

Endokrynol Pol 2022;73(5):812-822.

Keywords

type 1 diabetes mellitus
thyroid autoimmunity
speckle tracking echocardiography
diabetic cardiomyopathy
heart failure

Authors

Magdalena Maria Łukawska-Tatarczuk
Agnieszka Pawlak
Jakub Zieliński
Edward Franek
Leszek Czupryniak
Beata Mrozikiewicz-Rakowska

References (50)
  1. Htay T, Soe K, Lopez-Perez A, et al. Mortality and Cardiovascular Disease in Type 1 and Type 2 Diabetes. Curr Cardiol Rep. 2019; 21(6): 45.
  2. Lipes MA, Galderisi A. Cardiac autoimmunity as a novel biomarker, mediator, and therapeutic target of heart disease in type 1 diabetes. Curr Diab Rep. 2015; 15(5): 30.
  3. Hoffman WH, Sharma M, Cihakova D, et al. Cardiac antibody production to self-antigens in children and adolescents during and following the correction of severe diabetic ketoacidosis. Autoimmunity. 2016; 49(3): 188–196.
  4. Łukawska-Tatarczuk M, Mrozikiewicz-Rakowska B, Franek E, et al. Rola autoimmunizacji w rozwoju powikłań cukrzycowych — przegląd badań. Post Hig Med Dośw. 2021; 75(1): 802–814.
  5. Ohkuma T, Komorita Y, Peters SAE, et al. Diabetes as a risk factor for heart failure in women and men: a systematic review and meta-analysis of 47 cohorts including 12 million individuals. Diabetologia. 2019; 62(9): 1550–1560.
  6. Rogers MAM, Wei MY, Kim C, et al. Sex Differences in Autoimmune Multimorbidity in Type 1 Diabetes Mellitus and the Risk of Cardiovascular and Renal Disease: A Longitudinal Study in the United States, 2001-2017. J Womens Health (Larchmt). 2020; 29(4): 511–519.
  7. Nakova VV, Krstevska B, Kostovska ES, et al. The effect of levothyroxine treatment on left ventricular function in subclinical hypothyroidism. Arch Endocrinol Metab. 2018; 62(4): 392–398.
  8. Ahmadi N, Ahmadi F, Sadiqi M, et al. Thyroid gland dysfunction and its effect on the cardiovascular system: a comprehensive review of the literature. Endokrynol Pol. 2020; 71(5): 466–478.
  9. Basu M, Pandit K, Banerjee M, et al. Profile of Auto-antibodies (Disease Related and Other) in Children with Type 1 Diabetes. Indian J Endocrinol Metab. 2020; 24(3): 256–259.
  10. Hensel KO. Subclinical left ventricular systolic and diastolic dysfunction in type 1 diabetic children and adolescents with good metabolic control. Echocardiography. 2018; 35(4): 578–579.
  11. Yoldaş T, Örün UA, Sagsak E, et al. Subclinical left ventricular systolic and diastolic dysfunction in type 1 diabetic children and adolescents with good metabolic control. Echocardiography. 2018; 35(2): 227–233.
  12. Grant PJ, Cosentino F, Cosentino F, et al. ESC Scientific Document Group. 2019 ESC Guidelines on diabetes, pre-diabetes, and cardiovascular diseases developed in collaboration with the EASD. Eur Heart J. 2020; 41(2): 255–323.
  13. 2019 surveillance of diabetes (NICE guidelines NG17, NG18, NG19 and NG28), National Institute for Health and Care Excellence (UK), London 2019. https://www.nice.org.uk/guidance/ng28/resources/2019-surveillance-of-diabetes-nice-guidelines-ng17-ng18-ng19-and-ng28-pdf-8862045321157.
  14. Caturegli P, De Remigis A, Rose NR. Hashimoto thyroiditis: clinical and diagnostic criteria. Autoimmun Rev. 2014; 13(4-5): 391–397.
  15. Trzebińska A, Dobruch-Sobczak K, Jakubowski W, et al. Standardy badań ultrasonografi cznych Polskiego Towarzystwa Ultrasonografi cznego – aktualizacja. Badanie ultrasonografi czne tarczycy oraz biopsja tarczycy pod kontrolą ultrasonografii. J Ultrasonography. 2014; 14(56): 49–60.
  16. Lang RM, Badano LP, Mor-Avi V, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015; 28(1): 1–39.e14.
  17. Lang RM, Badano LP, Mor-Avi V, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015; 28(1): 1–39.e14.
  18. Devereux RB, Alonso DR, Lutas EM, et al. Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol. 1986; 57(6): 450–458.
  19. Knackstedt C, Bekkers SC, Schummers G, et al. Fully Automated Versus Standard Tracking of Left Ventricular Ejection Fraction and Longitudinal Strain: The FAST-EFs Multicenter Study. J Am Coll Cardiol. 2015; 66(13): 1456–1466.
  20. Cameli M, Mandoli GE, Sciaccaluga C, et al. More than 10 years of speckle tracking echocardiography: Still a novel technique or a definite tool for clinical practice? Echocardiography. 2019; 36(5): 958–970.
  21. Beyhoff N, Brix S, Betz IR, et al. Application of Speckle-Tracking Echocardiography in an Experimental Model of Isolated Subendocardial Damage. J Am Soc Echocardiogr. 2017; 30(12): 1239–1250.e2.
  22. Flores-Ramírez R, Azpiri-López JR, González-González JG, et al. Global longitudinal strain as a biomarker in diabetic cardiomyopathy. A comparative study with Gal-3 in patients with preserved ejection fraction. Arch Cardiol Mex. 2017; 87(4): 278–285.
  23. Liu D, Hu K, Nordbeck P, et al. Longitudinal strain bull's eye plot patterns in patients with cardiomyopathy and concentric left ventricular hypertrophy. Eur J Med Res. 2016; 21(1): 21.
  24. Argento LV, Travetto CM, Colicigno Md, et al. Tissue Doppler Imaging and strain rate of the left atrial lateral wall: age related variations and comparison with parameters of diastolic function. Cardiovasc Ultrasound. 2020; 18(1): 38.
  25. M Abd-El Aziz F, Abdelghaffar S, M Hussien E, et al. Evaluation of Cardiac Functions in Children and Adolescents with Type 1 Diabetes. J Cardiovasc Ultrasound. 2017; 25(1): 12–19.
  26. Altun G, Babaoğlu K, Binnetoğlu K, et al. Subclinical Left Ventricular Longitudinal and Radial Systolic Dysfunction in Children and Adolescents with Type 1 Diabetes Mellitus. Echocardiography. 2016; 33(7): 1032–1039.
  27. Sousa GR, Pober D, Galderisi A, et al. Glycemic Control, Cardiac Autoimmunity, and Long-Term Risk of Cardiovascular Disease in Type 1 Diabetes Mellitus. Circulation. 2019; 139(6): 730–743.
  28. El-Shabrawy RM, Ahmed AM, Selim FO, et al. Association between CD4+, CD25+, FOXP3+ Regulatory T-cells and Cardiovascular Complications in Diabetic Patients Type 1. Egyp J Immunol. 2019; 26(1): 129–139.
  29. Janyga S, Marek B, Kajdaniuk D, et al. CD4+ cells in autoimmune thyroid disease. Endokrynol Pol. 2021; 72(5): 572–583.
  30. Sousa GR, Kosiborod M, Bluemke DA, et al. Cardiac Autoimmunity Is Associated With Subclinical Myocardial Dysfunction in Patients With Type 1 Diabetes Mellitus. Circulation. 2020; 141(13): 1107–1109.
  31. Gottumukkala RV, Lv H, Cornivelli L, et al. Myocardial infarction triggers chronic cardiac autoimmunity in type 1 diabetes. Sci Transl Med. 2012; 4(138): 138ra80.
  32. Kajdaniuk D, Marek A, Marek B, et al. Transcriptional activity of TGFβ1 and its receptors genes in thyroid gland. Endokrynol Pol. 2016; 67(4): 375–382.
  33. Frangogiannis NG. Cardiac fibrosis. Cardiovasc Res. 2021; 117(6): 1450–1488.
  34. Siemińska L, Wojciechowska C, Walczak K, et al. Associations between metabolic syndrome, serum thyrotropin, and thyroid antibodies status in postmenopausal women, and the role of interleukin-6. Endokrynol Pol. 2015; 66(5): 394–403.
  35. Ruggeri RM, Vicchio TM, Cristani M, et al. Oxidative Stress and Advanced Glycation End Products in Hashimoto's Thyroiditis. Thyroid. 2016; 26(4): 504–511.
  36. Mikoś H, Mikoś M, Obara-Moszyńska M, et al. The role of the immune system and cytokines involved in the pathogenesis of autoimmune thyroid disease (AITD). Endokrynol Pol. 2014; 65(2): 150–155.
  37. Łukawska-Tatarczuk M, Franek E, Czupryniak L, et al. Sirtuin 1, Visfatin and IL-27 Serum Levels of Type 1 Diabetic Females in Relation to Cardiovascular Parameters and Autoimmune Thyroid Disease. Biomolecules. 2021; 11(8).
  38. Schnelle M, Catibog N, Zhang M, et al. Echocardiographic evaluation of diastolic function in mouse models of heart disease. J Mol Cell Cardiol. 2018; 114: 20–28.
  39. Seferović PM, Paulus WJ. Clinical diabetic cardiomyopathy: a two-faced disease with restrictive and dilated phenotypes. Eur Heart J. 2015; 36(27): 1718–27, 1727a.
  40. Kanamori H, Naruse G, Yoshida A, et al. Morphological characteristics in diabetic cardiomyopathy associated with autophagy. J Cardiol. 2021; 77(1): 30–40.
  41. Kanamori H, Takemura G, Goto K, et al. Autophagic adaptations in diabetic cardiomyopathy differ between type 1 and type 2 diabetes. Autophagy. 2015; 11(7): 1146–1160.
  42. Ferrara F, Rudski LG, Vriz O, et al. Physiologic correlates of tricuspid annular plane systolic excursion in 1168 healthy subjects. Int J Cardiol. 2016; 223: 736–743.
  43. Ahmed TA, Ahmed YA, Arafa AI, et al. Detection of occult right ventricular dysfunction in young Egyptians with type 1 diabetes mellitus by two-dimensional speckle tracking echocardiography. Indian Heart J. 2018; 70(5): 665–671.
  44. Berceanu M, Mirea O, Târtea GC, et al. The Significance of Right Ventricle in Young Subjects with Diabetes Mellitus Type 1. An echocardiographyic study. Curr Health Sci J. 2019; 45(2): 174–178.
  45. Todo S, Tanaka H, Yamauchi Y, et al. Association of left ventricular longitudinal myocardial function with subclinical right ventricular dysfunction in type 2 diabetes mellitus. Cardiovasc Diabetol. 2021; 20(1): 212.
  46. Hu BY, Wang J, Yang ZG, et al. Cardiac magnetic resonance feature tracking for quantifying right ventricular deformation in type 2 diabetes mellitus patients. Sci Rep. 2019; 9(1): 11148.
  47. Łukawska-Tatarczuk M, Mrozikiewicz-Rakowska B, Franek E, et al. Molecular pathogenesis of heart failure in diabetesmellitus — new direction for the therapeutic approach. Post Hig Med Dośw. 2020; 74: 452–463.
  48. Vatan MB, Varım C, Ağaç MT, et al. Echocardiographic Evaluation of Biventricular Function in Patients with Euthyroid Hashimoto's Thyroiditis. Med Princ Pract. 2016; 25(2): 143–149.
  49. Dogdus M, Diker S, Yenercag M, et al. Evaluation of left atrial and ventricular myocardial functions by three-dimensional speckle tracking echocardiography in patients with euthyroid Hashimoto's thyroiditis. Int J Cardiovasc Imaging. 2021; 37(2): 459–465.
  50. Azak E, Uçaktürk SA, Çetin İİ, et al. Subclinical Myocardial Dysfunction Demonstrated by Speckle Tracking Echocardiography in Children with Euthyroid Hashimoto’s Thyroiditis. J Clin Res Pediatr Endocrinol. 2019; 11(4): 410–418.

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