Association between monocyte to high-density lipoprotein cholesterol ratio and bicuspid aortic valve degeneration

Association between monocyte to high-density lipoprotein cholesterol ratio and bicuspid aortic valve degeneration

Background/aim: From a pathophysiological point of view, inflammation is thought to be more dominant in bicuspid aortic valve (BAV) stenosis than tricuspid aortic valve (TAV) stenosis. Our study aimed to determine the association between monocyte to highdensity lipoprotein cholesterol (HDL-C) ratio (MHR), a new inflammatory marker, and the speed of progression of stenosis and pathophysiology of BAV stenosis. Materials and methods: A total of 210 severe aortic stenosis patients (70 consecutive BAV patients, 140 matched TAV patients) were retrospectively enrolled in the study. Clinical and echocardiographic data and laboratory results related to our research were collected retrospectively from the patients’ records. MHR was measured as the ratio of the absolute monocyte count to the HDL-C value. Results: Seventy BAV (mean age: 72.0 ± 9.1 years, 42.9% female) and 140 TAV patients (mean age: 77.9 ± 8.3 years, 51.4% female) with severe aortic stenosis were enrolled in this study. There was no difference between the two groups in terms of another baseline demographic or clinic findings except age (P < 0.001). Monocyte count, hemoglobin level, mean platelet volume was significantly higher, and HDL-C level was significantly lower in the BAV group, while other lipid and CBC parameters were found to be similar. In the multivariate analysis, MHR (P = 0.005, 95% CI: 0.90–0.98) and, as expected, age (P = 0.001, 95% CI: 1.02–1.11) were found to be significant as the independent predictor of BAV, after adjusting for other risk factors. Conclusion: Our study showed a significant correlation between increased MHR and BAV. MHR was determined as a significant independent predictor for the speed of progression and diagnosis of severe BAV stenosis in multivariate analysis.

___

  • 1. Benjamin EJ, Muntner P, Alonso A, Bittencourt MS, Callaway CW et al. American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart Disease and Stroke Statistics-2019 Update: A report from the American Heart Association. Circulation 2019; 139 (10): e56-e528. doi: 10.1161/CIR.0000000000000659
  • 2. Michelena HI, Prakash SK, Della Corte A, Bissell MM, Anavekar N et al. BAVCon Investigators. Bicuspid aortic valve: identifying knowledge gaps and rising to the challenge from the International Bicuspid Aortic Valve Consortium (BAVCon). Circulation 2014; 129 (25): 2691-2704. doi: 10.1161/ CIRCULATIONAHA.113.007851
  • 3. Della Corte A, Body SC, Booher AM, Schaefers HJ, Milewski RK et al. International Bicuspid Aortic Valve Consortium (BAVCon) Investigators. Surgical treatment of bicuspid aortic valve disease: knowledge gaps and research perspectives. Journal of Thoracic and Cardiovascular Surgery 2014; 147 (6): 1749-1757. doi: 10.1016/j.jtcvs.2014.01.021
  • 4. Stewart BF, Siscovick D, Lind BK, Gardin JM, Gottdiener JS et al. Clinical factors associated with calcific aortic valve disease. Cardiovascular Health Study. Journal of the American College of Cardiology 1997; 29 (3): 630-634. doi: 10.1016/s0735- 1097(96)00563-3
  • 5. Dweck MR, Boon NA, Newby DE. Calcific aortic stenosis: a disease of the valve and the myocardium. Journal of the American College of Cardiology 2012; 60 (19): 1854-1863. doi: 10.1016/j.jacc.2012.02.093
  • 6. Horne BD, Camp NJ, Muhlestein JB, Cannon-Albright LA. Evidence for a heritable component in death resulting from aortic and mitral valve diseases. Circulation 2004; 110 (19): 3143-3148. doi: 10.1161/01.CIR.0000147189.85636.C3
  • 7. Vollebergh FE, Becker AE. Minor congenital variations of cusp size in tricuspid aortic valves. Possible link with isolated aortic stenosis. British Heart Journal 1977; 39 (9): 1006-1011. doi: 10.1136/hrt.39.9.1006
  • 8. Chan KL, Ghani M, Woodend K, Burwash IG. Case-controlled study to assess risk factors for aortic stenosis in congenitally bicuspid aortic valve. American Journal of Cardiology 2001; 88 (6): 690-693. doi: 10.1016/s0002-9149(01)01820-3
  • 9. Tzemos N, Lyseggen E, Silversides C, Jamorski M, Tong JH et al. Endothelial function, carotid-femoral stiffness, and plasma matrix metalloproteinase-2 in men with bicuspid aortic valve and dilated aorta. Journal of the American College of Cardiology 2010; 55 (7): 660-668. doi: 10.1016/j.jacc.2009.08.080
  • 10. Libby P. Inflammation in atherosclerosis. Arteriosclerosis, Thrombosis, and Vascular Biology 2012; 32 (9): 2045-2051. doi: 10.1161/ATVBAHA.108.17970511
  • 11. Canpolat U, Çetin EH, Cetin S, Aydin S, Akboga MK et al. Association of Monocyte-to-HDL cholesterol ratio with slow coronary flow is linked to systemic inflammation. Clinical and Applied Thrombosis/Hemostasis 2016; 22 (5): 476-482. doi: 10.1177/1076029615594002
  • 12. Michelena HI, Desjardins VA, Avierinos JF, Russo A, Nkomo VT et al. Natural history of asymptomatic patients with normally functioning or minimally dysfunctional bicuspid aortic valve in the community. Circulation 2008; 117 (21): 2776-2784. doi: 10.1161/CIRCULATIONAHA.107.740878
  • 13. Weinberg EJ, Kaazempur Mofrad MR. A multiscale computational comparison of the bicuspid and tricuspid aortic valves in relation to calcific aortic stenosis. Journal of Biomechanics 2008; 41 (16): 3482-3487. doi: 10.1016/j. jbiomech.2008.08.006
  • 14. Wallby L, Janerot-Sjöberg B, Steffensen T, Broqvist M. T lymphocyte infiltration in non-rheumatic aortic stenosis: a comparative descriptive study between tricuspid and bicuspid aortic valves. Heart 2002; 88 (4): 348-351. doi: 10.1136/ heart.88.4.348
  • 15. Manno G, Bentivegna R, Morreale P, Nobile D, A Santangelo et al. Chronic inflammation: A key role in degeneration of bicuspid aortic valve. Journal of Molecular and Cellular Cardiology 2019; 130: 59-64. doi: 10.1016/j.yjmcc.2019.03.013
  • 16. Fernández B, Durán AC, Fernández-Gallego T, Fernández MC, Such M et al. Bicuspid aortic valves with different spatial orientations of the leaflets are distinct etiological entities. Journal of the American College of Cardiology 2009; 54 (24): 2312-2318. doi: 10.1016/j.jacc.2009.07.044
  • 17. Huntley GD, Thaden JJ, Alsidawi S, Michelena HI, Maleszewski JJ et al. Comparative study of bicuspid vs. tricuspid aortic valve stenosis. European Heart Journal - Cardiovascular Imaging 2018; 19 (1): 3-8. doi: 10.1093/ehjci/jex211
  • 18. Ancuta P, Wang J, Gabuzda D. CD16+ monocytes produce IL6, CCL2, and matrix metalloproteinase-9 upon interaction with CX3CL1-expressing endothelial cells. Journal of Leukocyte Biology 2006; 80 (5): 1156-1164
  • 19. Demir V, Samet Y, Akboga MK. Association of lymphocytemonocyte ratio and monocyte-to-high-density lipoprotein ratio with the presence and severity of rheumatic mitral valve stenosis. Biomarkers in Medicine 2017; 11 (8): 657-663. doi: 10.2217/bmm-2017-0036
  • 20. Farb A, Sangiorgi G, Carter AJ, Walley VM, Edwards WD et al. Pathology of acute and chronic coronary stenting in humans. Circulation 1999; 99 (1): 44-52. doi: 10.1161/01.cir.99.1.44
  • 21. Karataş MB, Çanga Y, Özcan KS, İpek G, Güngör B et al. Monocyte to high-density lipoprotein ratio as a new prognostic marker in patients with STEMI undergoing primary percutaneous coronary intervention. American Journal of Emergency Medicine 2016; 34 (2): 240-244. doi: 10.1016/j. ajem.2015.10.049
  • 22. Cetin EH, Cetin MS, Canpolat U, Aydin S, Topaloglu S et al. Monocyte/HDL-cholesterol ratio predicts the definite stent thrombosis after primary percutaneous coronary intervention for ST-segment elevation myocardial infarction. Biomarkers in Medicine 2015; 9 (10): 967-977. doi: 10.2217/bmm.15.74
  • 23. Turhan H, Erbay AR, Yasar AS, Balci M, Bicer A, Yetkin E. Comparison of C-reactive protein levels in patients with coronary artery ectasia versus patients with obstructive coronary artery disease. American Journal of Cardiology 2004; 94 (10): 1303-1306. doi: 10.1016/j.amjcard.2004.07.120
  • 24. Ucar FM. A potential marker of bare metal stent restenosis: monocyte count - to- HDL cholesterol ratio. BMC Cardiovascular Disorders 2016; 16 (1): 186. doi: 10.1186/ s12872-016-0367-3
  • 25. Acikgoz N, Kurtoğlu E, Yagmur J, Kapicioglu Y, Cansel M et al. Elevated monocyte to high-density lipoprotein cholesterol ratio and endothelial dysfunction in Behçet disease. Angiology 2018; 69 (1): 65-70. doi: 10.1177/0003319717704748
  • 26. Cagli K, Tok D, Turak O, Gunertem E, Yayla C et al. Monocyte count-to-high-density lipoprotein-cholesterol ratio is associated with abdominal aortic aneurysm size. Biomarkers in Medicine 2016; 10 (10): 1039-1047. doi: 10.2217/bmm-2016- 0157
  • 27. Demir V, Samet Y, Akboga MK. Association of lymphocytemonocyte ratio and monocyte-to-high-density lipoprotein ratio with the presence and severity of rheumatic mitral valve stenosis. Biomarkers in Medicine 2017; 11 (8): 657-663. doi: 10.2217/bmm-2017-0036
  • 28. Pamukcu HE, Aker M. Association between monocyte to HDL cholesterol ratio and mitral annulus calcification. Journal of Surgery and Medicine 2019; 3 (1): 44-48. doi: 10.28982/ josam.512374
  • 29. Varol E, Arslan A, Yucel H, Ozaydin M, Erdogan D et al. Increased mean platelet volume in patients with aortic stenosis. Clinical and Applied Thrombosis/Hemostasis 2011; 17 (6): E17-20. doi: 10.1177/1076029610379400
  • 30. Bilen E, Tanboga IH, Kurt M, Kocak U, Ayhan H, Durmaz T et al. Mean platelet volume is increased in patients with bicuspid aortic valve. Clinical and Applied Thrombosis/Hemostasis 2012; 18 (4): 351-355. doi: 10.1177/1076029611427439
  • 31. Beppu S, Suzuki S, Matsuda H, Ohmori F, Nagata S et al. Rapidity of progression of aortic stenosis in patients with congenital bicuspid aortic valves. American Journal of Cardiology 1993; 71 (4): 322-327. doi: 10.1016/0002-9149(93)90799-i
  • 32. Moreno PR, Astudillo L, Elmariah S, Purushothaman KR, Purushothaman M et al. Increased macrophage infiltration and neovascularization in congenital bicuspid aortic valve stenosis. Journal of Thoracic and Cardiovascular Surgery 2011; 142 (4): 895-901. doi: 10.1016/j.jtcvs.2011.03.002
Turkish Journal of Medical Sciences-Cover
  • ISSN: 1300-0144
  • Yayın Aralığı: Yılda 6 Sayı
  • Yayıncı: TÜBİTAK
Sayıdaki Diğer Makaleler

Development of albumin macroinitiator for polymers to use in DNA origami coating

Ezgi EMÜL, Necdet SAĞLAM, Aykut BİLİR

What is the impact of PPAR-γ agonist-rosiglitazone on ovarian reserve after hysterectomy? An experimental study

Berna DİLBAZ, Betül DÜNDAR, Ümit GÖKTOLGA, Ömer Lütfi TAPISIZ, Burcu GÜNDOĞDU, Kamil Hakan MÜFTÜOĞLU, Serkan Barış MÜLAZIMOĞLU

Baseline characteristics predicting clinical outcomes and serious adverse events in middle-aged hypertensive women: a subanalysis of the SPRINT in women aged <65 years

Sibel SAKARYA, Mehmet AKMAN, Ahmet AKICI, Volkan AYDIN, Ali Serdar FAK

The triglyceride-glucose index predicts peripheral artery disease complexity

Hüseyin AYHAN, Telat KELEŞ, Bilge DURAN KARADUMAN, Engin BOZKURT

Response to letter to the editor: Radiological approaches to COVID-19 pneumonia

Tevfik ÖZLÜ, Şule AKÇAY, Aydın YILMAZ

Colchicine intolerance in FMF patients and primary obstacles for optimal dosing

Nazife Şule YAŞAR BİLGE, Erdal BODAKÇI, Timuçin KAŞİFOĞLU, Dilek YAPAR, Şeminur HAZNEDAROĞLU, Gözde Kübra YARDIMCI, Nuh ATAŞ, Berna GÖKER, Reyhan BİLİCİ SALMAN, Abdurrahman TUFAN, Hasan SATIŞ, Hakan BABAOĞLU, Berkan ARMAĞAN, Umut KALYONCU, Alper SARI, Levent KILIÇ

Presence of paroxysmal nocturnal hemoglobinuria in patients with idiopathic portal vein thrombosis: a single-center study

Senar EBİNÇ, Cengiz DEMİR, Ömer EKİNCİ

Posttraumatic growth and death anxiety in caregivers of cancer patients: PHOENIX study

Ali ALKAN, Ebru KARCI, Elif Berna KÖKSOY, Aslı ALKAN, Eduardo BRUERA, Filiz ÇAY ŞENLER

Protective effects of apocynin on damaged testes of rats exposed to methotrexate

Yusufhan YAZIR, Melda YARDIMOĞLU YILMAZ, Kübra KAVRAM SARIHAN, Fatma Ceyla ERALDEMİR, Esra ACAR

Alterations in follicular fluid BMP-15 RNA expression in women undergoing controlled ovarian hyperstimulation

Şükriye Derya DEVECİ