Research Article
BibTex RIS Cite

Platelet-to-lymphocyte ratio predicts contrast-induced nephropathy in acute myocardial infarction

Year 2017, , 97 - 104, 01.06.2017
https://doi.org/10.18663/tjcl.277964

Abstract

Aim: Contrast-induced nephropathy
(CIN) is responsible for an increased mortality rate and correlates with
increases in hospital stays and the risk of cardiovascular complications. The
platelet to lymphocyte ratio (PLR) was introduced as a potential marker to determine
the balance between thrombosis and inflammation and was associated with
increased cardiovascular morbidity and mortality. We investigated whether PLR
on admission is an independent risk factor that predicts the development of CIN
in patients with ST-segment elevation myocardial infarction (STEMI) underwent
primary percutaneous coronary intervention (pPCI).

Material
and Methods:
1348 consecutive patients with acute STMI who were
admitted to our institution and underwent pPCI were retrospectively evaluated.
Data obtained from hospital files and computer records. CIN development was
accepted as the endpoint.

Results: A total of 127 (9.4%)
patients experienced CIN. 16 patients underwent renal replacement theraphy.
In-hospital mortality rate was found 2.7% (n = 37). Patients were divided into
two groups based on development of CIN. Age (P = 0.001), baseline GFR (P < 0.001),
grade 3 and more chronic kidney disease (P < 0.001), baseline creatinin (P <
0.001), EF (P < 0.001), presence of DM (P < 0.001) were different between
groups. In multivariate analyses, PLR (odds ratio [OR] 1.012, 95% confidence
interval [CI] 1.006-1.017, P < 0.001) was independently predicted CIN
development.







Conclusion: PLR is
easily available, widely used, and relatively cheap biomarker, and is an
independent predictor of CIN development in patients with STEMI undergoing
pPCI.

References

  • 1. McCullough PA, Adam A, Becker CR, et al. CIN Consensus Working Panel. Epidemiology and prognostic implications of contrast induced nephropathy. Am J Cardiol. 2006; 98: 5-13.
  • 2. Lazaros G, Tsiachris D, Tousoulis D, et al. In-hospital worsening renal function is an independent predictor of one-year mortality in patients with acute myocardial infarction. Int J Cardiol 2012; 155: 97-101.
  • 3. Temiz A, Gazi E, Gungor O, et al. Platelet/lymphocyte ratio and risk in-hospital mortality in patients with ST-elevated myocardial infarction. Med Sci Monit 2014; 22: 660-5.
  • 4. Levey AS, Bosch JP, Lewis JB, et al. A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group. Ann Intern Med 1999; 130: 461-470.
  • 5. Stone NJ, Robinson JG, Lichtenstein AH, et al. 2013 ACC/AHA guideline on the treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2014; 63: 2889-934.
  • 6. Mehran R, Nikolsky E. Contrast-induced nephropathy: definition, epidemiology, and patients at risk. Kidney Int Suppl 2006; 100: 11e15.
  • 7. Chen YL, Fu NK, Xu J, et al. A simple preprocedural score for risk of contrast-induced acute kidney injury after percutaneous coronary intervention, Catheter Cardiovasc Interv. 2014; 83:8-16.
  • 8. Abaci O, Arat Ozkan A, Kocas C, et al. Impact of Rosuvastatin on contrast-induced acute kidney injury in patients at high risk for nephropathy undergoing elective angiography. Am J Cardiol. 2015; 115: 867-71.
  • 9. Kocas C, Yildiz A, Abaci O, et al. Platelet-to-Lymphocyte Ratio Predicts Contrast-Induced Nephropathy in Patients with Non-ST-Segment Elevation Acute Coronary Syndrome. Angiology. 2015; 66: 964-8.
  • 10. Wong PC, Li Z, Guo J, Zhang A. Pathophysiology of contrast-induced nephropathy, Int J Cardiol 2012; 158: 186-192.
  • 11. Liu Y, Tan N, Zhou YL, et al. High sensitivity C-reactive protein predicts contrast-induced nephropathy after primary percutaneous coronary intervention. J Nephrol 2012; 25: 332-340.
  • 12. Ruparelia N, Digby JE, Jefferson A, et al. Myocardial infarction causes inflammation and leukocyte recruitment at remote sites in the myocardium and in the renal glomerulus. Inflamm Res. 2013; 62: 515-25.
  • 13. Cicek G, Acıkgoz SK, Bozbay M, et al. Neutrophil-lymphocyte ratio and plateletlymphocyte ratio combination can predict prognosis in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention. Angiology 2015; 66: 441-7.
  • 14. Gawaz M, Langer H, May AE. Platelets in inflammation and atherogenesis. J Clin Invest 2005; 115: 3378-84.
  • 15. Nyman U, Aspelin P, Jakobsen J, et al. Controversies in Contrast Material-induced Acute Kidney Injury: Propensity Score Matching of Patients with Different Dose/Absolute Glomerular Filtration Rate Ratios. Radiology. 2015; 277: 633-7.
  • 16. Akbas EM, Demirtas L, Ozcicek A, et al. Association of epicardial adipose tissue, neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio with diabetic nephropathy. Int J Clin Exp Med. 2014,15:1794-801.

Akut miyokard infarktüsünde trombosit/lenfosit oranı kontrast nefropatisini öngörür

Year 2017, , 97 - 104, 01.06.2017
https://doi.org/10.18663/tjcl.277964

Abstract

Amaç:
Kontrast madde nefropatisi (CIN) uzamış hastanede yatış süresi, artmıs
kardiyovasküler komplikasyonlar ve mortalite ile ilişkilidir.
Trombosit/lenfosit oranı (PLR) tromboz ve inflamasyon arasındaki dengeyi
gösteren potansiyel bir belirteç olarak tanımlanmış ve artan kardiyovasküler
morbidite ve mortalite ile ilişkili bulunmuştur. Biz bu çalışmada PLR’nin
primer perkütan koroner girişim (pPCI) yapılan ST yükselmeli miyokard infarktüsü
(STEMI) hastalarda CIN gelişimini tahmin etmede bağımsız bir risk faktörü olup
olmadığı araştırdık.

Gereç
ve Yöntemler:
Kurumumuza akut STEMI ile başvuran ve pPCI yapılan
1348 hasta geriye dönük olarak değerlendirildi. Hastane dosya ve bilgisayar kayıtlarından
veriler elde edildi. CIN gelişimi sonlanım noktası olarak kabul edildi.

Bulgular: 127 (%9.4) hastada CIN
gelişmişti. 16 hastaya renal replasman tedavisi uygulandı. Hastane içi
mortalite oranı %2,7(n = 37) bulunmuştur. Hastalar CIN gelişimine göre iki
gruba ayrıldı. Yaş (P = 0,001), bazal GFR (P < 0,001), grade 3 ve üzeri
kronik böbrek hastalığı (P < 0,001), bazal kreatinin (P < 0,001), EF (P <
0,001), DM varlığı (P < 0,001) gruplar arasında farklı idi. Çok değişkenli
analizlerde, PLR (odds ratio [OR] 1.012, %95 güven aralığı [CI] 1,006-1,017, P
< 0,001) CIN gelişimini bağımsız olarak öngördü.







Sonuçlar: PLR, kolay ulaşılabilir
yaygın olarak kullanılan ve nispeten ucuz biyomarkerdir ve STEMI nedeniyle pPCI
uygulanan hastalarda CIN gelişiminin bağımsız bir belirleyicisidir.

References

  • 1. McCullough PA, Adam A, Becker CR, et al. CIN Consensus Working Panel. Epidemiology and prognostic implications of contrast induced nephropathy. Am J Cardiol. 2006; 98: 5-13.
  • 2. Lazaros G, Tsiachris D, Tousoulis D, et al. In-hospital worsening renal function is an independent predictor of one-year mortality in patients with acute myocardial infarction. Int J Cardiol 2012; 155: 97-101.
  • 3. Temiz A, Gazi E, Gungor O, et al. Platelet/lymphocyte ratio and risk in-hospital mortality in patients with ST-elevated myocardial infarction. Med Sci Monit 2014; 22: 660-5.
  • 4. Levey AS, Bosch JP, Lewis JB, et al. A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation. Modification of Diet in Renal Disease Study Group. Ann Intern Med 1999; 130: 461-470.
  • 5. Stone NJ, Robinson JG, Lichtenstein AH, et al. 2013 ACC/AHA guideline on the treatment of blood cholesterol to reduce atherosclerotic cardiovascular risk in adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2014; 63: 2889-934.
  • 6. Mehran R, Nikolsky E. Contrast-induced nephropathy: definition, epidemiology, and patients at risk. Kidney Int Suppl 2006; 100: 11e15.
  • 7. Chen YL, Fu NK, Xu J, et al. A simple preprocedural score for risk of contrast-induced acute kidney injury after percutaneous coronary intervention, Catheter Cardiovasc Interv. 2014; 83:8-16.
  • 8. Abaci O, Arat Ozkan A, Kocas C, et al. Impact of Rosuvastatin on contrast-induced acute kidney injury in patients at high risk for nephropathy undergoing elective angiography. Am J Cardiol. 2015; 115: 867-71.
  • 9. Kocas C, Yildiz A, Abaci O, et al. Platelet-to-Lymphocyte Ratio Predicts Contrast-Induced Nephropathy in Patients with Non-ST-Segment Elevation Acute Coronary Syndrome. Angiology. 2015; 66: 964-8.
  • 10. Wong PC, Li Z, Guo J, Zhang A. Pathophysiology of contrast-induced nephropathy, Int J Cardiol 2012; 158: 186-192.
  • 11. Liu Y, Tan N, Zhou YL, et al. High sensitivity C-reactive protein predicts contrast-induced nephropathy after primary percutaneous coronary intervention. J Nephrol 2012; 25: 332-340.
  • 12. Ruparelia N, Digby JE, Jefferson A, et al. Myocardial infarction causes inflammation and leukocyte recruitment at remote sites in the myocardium and in the renal glomerulus. Inflamm Res. 2013; 62: 515-25.
  • 13. Cicek G, Acıkgoz SK, Bozbay M, et al. Neutrophil-lymphocyte ratio and plateletlymphocyte ratio combination can predict prognosis in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention. Angiology 2015; 66: 441-7.
  • 14. Gawaz M, Langer H, May AE. Platelets in inflammation and atherogenesis. J Clin Invest 2005; 115: 3378-84.
  • 15. Nyman U, Aspelin P, Jakobsen J, et al. Controversies in Contrast Material-induced Acute Kidney Injury: Propensity Score Matching of Patients with Different Dose/Absolute Glomerular Filtration Rate Ratios. Radiology. 2015; 277: 633-7.
  • 16. Akbas EM, Demirtas L, Ozcicek A, et al. Association of epicardial adipose tissue, neutrophil-to-lymphocyte ratio and platelet-to-lymphocyte ratio with diabetic nephropathy. Int J Clin Exp Med. 2014,15:1794-801.
There are 16 citations in total.

Details

Subjects Health Care Administration
Journal Section Orıgınal Artıcle
Authors

Regayip Zehir

Taner Sarak

Sinan Zehir

Publication Date June 1, 2017
Published in Issue Year 2017

Cite

APA Zehir, R., Sarak, T., & Zehir, S. (2017). Akut miyokard infarktüsünde trombosit/lenfosit oranı kontrast nefropatisini öngörür. Turkish Journal of Clinics and Laboratory, 8(3), 97-104. https://doi.org/10.18663/tjcl.277964
AMA Zehir R, Sarak T, Zehir S. Akut miyokard infarktüsünde trombosit/lenfosit oranı kontrast nefropatisini öngörür. TJCL. October 2017;8(3):97-104. doi:10.18663/tjcl.277964
Chicago Zehir, Regayip, Taner Sarak, and Sinan Zehir. “Akut Miyokard infarktüsünde trombosit/Lenfosit Oranı Kontrast Nefropatisini öngörür”. Turkish Journal of Clinics and Laboratory 8, no. 3 (October 2017): 97-104. https://doi.org/10.18663/tjcl.277964.
EndNote Zehir R, Sarak T, Zehir S (October 1, 2017) Akut miyokard infarktüsünde trombosit/lenfosit oranı kontrast nefropatisini öngörür. Turkish Journal of Clinics and Laboratory 8 3 97–104.
IEEE R. Zehir, T. Sarak, and S. Zehir, “Akut miyokard infarktüsünde trombosit/lenfosit oranı kontrast nefropatisini öngörür”, TJCL, vol. 8, no. 3, pp. 97–104, 2017, doi: 10.18663/tjcl.277964.
ISNAD Zehir, Regayip et al. “Akut Miyokard infarktüsünde trombosit/Lenfosit Oranı Kontrast Nefropatisini öngörür”. Turkish Journal of Clinics and Laboratory 8/3 (October 2017), 97-104. https://doi.org/10.18663/tjcl.277964.
JAMA Zehir R, Sarak T, Zehir S. Akut miyokard infarktüsünde trombosit/lenfosit oranı kontrast nefropatisini öngörür. TJCL. 2017;8:97–104.
MLA Zehir, Regayip et al. “Akut Miyokard infarktüsünde trombosit/Lenfosit Oranı Kontrast Nefropatisini öngörür”. Turkish Journal of Clinics and Laboratory, vol. 8, no. 3, 2017, pp. 97-104, doi:10.18663/tjcl.277964.
Vancouver Zehir R, Sarak T, Zehir S. Akut miyokard infarktüsünde trombosit/lenfosit oranı kontrast nefropatisini öngörür. TJCL. 2017;8(3):97-104.


e-ISSN: 2149-8296

The content of this site is intended for health care professionals. All the published articles are distributed under the terms of

Creative Commons Attribution Licence,

which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.