Kalp cerrahisinden sonra nörokognitif fonksiyon bozukluğu ve biyokimyasal belirteçler

Ameliyat sonrası kognitif fonksiyon bozukluğu, kalp ameliyatından sonra sık görülen bir nörolojik komplikasyondur. En sık görülen nörolojik komplikasyon olmasına karşın, patofizyolojisi halen tam olarak anlaşılamamıştır. Tanıda standartlaşmış klinik değerlendirme testlerinin olmaması ve uygulanan testlerin zaman alıcı olması, genellikle bu sorunun göz ardı edilmesine yol açmaktadır. Ayrıca tedavi maliyetinin de artışına neden olmaktadır. Bu nedenle, kognitif fonksiyon bozukluğunun kan örneklerinin analizi ile belirlenmesi, zaman kaybını azaltabilecektir. Bu makalede, S100ß ve nöron spesifik enolaz başta olmak üzere, ameliyat sonrası kognitif fonksiyon bozukluğunun belirlenmesinde kullanılan biyobelirteçler incelendi.

Neurocognitive dysfunction after cardiac surgery and biochemical markers

The postoperative cognitive dysfunction is typically neurologic complication after cardiac surgery. Although it is the most frequent neurologic complication, its pathophysiology is still poorly understood. The lack of standardized clinical evaluation tests in diagnosis and the fact that the applied tests are time-consuming usually makes it overlooked. It also increases treatment expenditures. Therefore, the determination of the cognitive dysfunction with the analysis of the blood samples may reduce the waste of time. In this article, we examine biomarkers, notably S100ß and neuron-specific enolase, which are used for the determination of the postoperative cognitive dysfunction.

___

  • 1) Hammon JW, Stump DA. Neurocognitive decline following cardiac surgery: Incidence, risk factors, prevention, and outcomes. In: Bonser RS, Pagano D, Haverich A, editors. Brain protection in cardiac surgery. 1st ed. London: Springer; 2011. p. 29-37.
  • 2) Hanning CD. Postoperative cognitive dysfunction. Br J Anaesth 2005;95:82-7.
  • 3) Deiner S, Silverstein JH. Postoperative delirium and cognitive dysfunction. Br J Anaesth 2009;103 Suppl 1:i41-46. doi:10.1093/bja/aep291.
  • 4) Arrowsmith JE, Grocott HP, Reves JG, Newman MF. Central nervous system complications of cardiac surgery. Br J Anaesth 2000;84:378-93.
  • 5) Martin JF, Melo RO, Sousa LP. Postoperative cognitive dysfunction after cardiac surgery. Rev Bras Cir Cardiovasc 2008;23:245-55.
  • 6) Rasmussen LS, Larsen K, Houx P, Skovgaard LT, Hanning CD, Moller JT, et al. The assessment of postoperative cognitive function. Acta Anaesthesiol Scand 2001;45:275-89.
  • 7) Stump DA. Selection and clinical significance of neuropsychologic tests. Ann Thorac Surg 1995;59:1340-4.
  • 8) Yasir AO, Taggart DP. Pitfalls of neuropsychometric assessment and alternative investigative approaches. In: Bonser RS, Pagano D, Haverich A editors. Brain protection in cardiac surgery. 1st ed. London: Springer; 2011. p. 57-65.
  • 9) Ramlawi B, Rudolph JL, Mieno S, Khabbaz K, Sodha NR, Boodhwani M, et al. Serologic markers of brain injury and cognitive function after cardiopulmonary bypass. Ann Surg 2006;244:593-601.
  • 10) Cata JP, Abdelmalak B, Farag E. Neurological biomarkers in the perioperative period. Br J Anaesth 2011;107:844-58. doi:10.1093/bja/aer338.
  • 11) Jensen BØ, Rasmussen LS, Steinbrüchel DA. Cognitive outcomes in elderly high-risk patients 1 year after offpump versus on-pump coronary artery bypass grafting. A randomized trial. Eur J Cardiothorac Surg 2008;34:1016-21. doi: 10.1016/j.ejcts.2008.07.053.
  • 12) Dieleman J, Sauër AM, Klijn C, Nathoe H, Moons K, Kalkman C, et al. Presence of coronary collaterals is associated with a decreased incidence of cognitive decline after coronary artery bypass surgery. Eur J Cardiothorac Surg 2009;35:48-53. doi: 10.1016/j.ejcts.2008.10.004.
  • 13) Selnes OA, Grega MA, Borowicz LM Jr, Royall RM, McKhann GM, Baumgartner WA. Cognitive changes with coronary artery disease: a prospective study of coronary artery bypass graft patients and nonsurgical controls. Ann Thorac Surg 2003;75:1377-84.
  • 14) Takagi H, Tanabashi T, Kawai N, Umemoto T. A metaanalysis of minimally invasive coronary artery bypass versus percutaneous coronary intervention with stenting for isolated left anterior descending artery disease is indispensable. J Thorac Cardiovasc Surg 2007;134:548; author reply 548-9.
  • 15) Marasco SF, Sharwood LN, Abramson MJ. No improvement in neurocognitive outcomes after off-pump versus on-pump coronary revascularisation: a meta-analysis. Eur J Cardiothorac Surg 2008;33:961-70. doi: 10.1016/j. ejcts.2008.03.022.
  • 16) Hudetz JA, Iqbal Z, Gandhi SD, Patterson KM, Byrne AJ, Pagel PS. Postoperative delirium and short-term cognitive dysfunction occur more frequently in patients undergoing valve surgery with or without coronary artery bypass graft surgery compared with coronary artery bypass graft surgery alone: results of a pilot study. J Cardiothorac Vasc Anesth 2011;25:811-6. doi: 10.1053/j.jvca.2010.05.003.
  • 17) Evered L, Scott DA, Silbert B, Maruff P. Postoperative cognitive dysfunction is independent of type of surgery and anesthetic. Anesth Analg 2011;112:1179-85. doi: 10.1213/ ANE.0b013e318215217e.
  • 18) Sweet JJ, Finnin E, Wolfe PL, Beaumont JL, Hahn E, Marymont J, et al. Absence of cognitive decline one year after coronary bypass surgery: comparison to nonsurgical and healthy controls. Ann Thorac Surg 2008;85:1571-8. doi:10.1016/j.athoracsur.2008.01.090.
  • 19) de Tournay-Jetté E, Dupuis G, Bherer L, Deschamps A, Cartier R, Denault A. The relationship between cerebral oxygen saturation changes and postoperative cognitive dysfunction in elderly patients after coronary artery bypass graft surgery. J Cardiothorac Vasc Anesth 2011;25:95-104. doi: 10.1053/j.jvca.2010.03.019.
  • 20) Parra VM, Sadurní M, Doñate M, Rovira I, Roux C, Ríos J, et al. Neuropsychological dysfunction after cardiac surgery: Cerebral saturation and bispectral index: A longitudinal study. Rev Med Chil 2011;139:1553-61. doi: /S0034- 98872011001200004. Epub 2012. [Abstract]
  • 21) Gu XH, Zhang G, Zhang XQ, Song Y, Wang T, Li SX. Clinical values of detection of serum levels of S100B and NSE in diagnosis of brain injuries at early period after cardiopulmonary bypass. Zhonghua Yi Xue Za Zhi 2007;87:975-7. [Abstract]
  • 22) Johnsson P, Lundqvist C, Lindgren A, Ferencz I, Alling C, Ståhl E. Cerebral complications after cardiac surgery assessed by S-100 and NSE levels in blood. J Cardiothorac Vasc Anesth 1995;9:694-9.
  • 23) Ishida K, Gohara T, Kawata R, Ohtake K, Morimoto Y, Sakabe T. Are serum S100beta proteins and neuron-specific enolase predictors of cerebral damage in cardiovascular surgery? J Cardiothorac Vasc Anesth 2003;17:4-9.
  • 24) Ali MS, Harmer M, Vaughan R. Serum S100 protein as a marker of cerebral damage during cardiac surgery. Br J Anaesth 2000;85:287-98.
  • 25) Zimmer DB, Cornwall EH, Landar A, Song W. The S100 protein family: history, function, and expression. Brain Res Bull 1995;37:417-29.
  • 26) Aurell A, Rosengren LE, Karlsson B, Olsson JE, Zbornikova V, Haglid KG. Determination of S-100 and glial fibrillary acidic protein concentrations in cerebrospinal fluid after brain infarction. Stroke 1991;22:1254-8.
  • 27) Isobe T, Takahashi K, Okuyama T. S100a0 (alpha alpha) protein is present in neurons of the central and peripheral nervous system. J Neurochem 1984;43:1494-6.
  • 28) Kato K, Kimura S. S100ao (alpha alpha) protein is mainly located in the heart and striated muscles. Biochim Biophys Acta 1985;842:146-50.
  • 29) Usui A, Kato K, Abe T, Murase M, Tanaka M, Takeuchi E. S-100ao protein in blood and urine during open-heart surgery. Clin Chem 1989;35:1942-4.
  • 30) Jönsson H, Johnsson P, Höglund P, Alling C, Blomquist S. Elimination of S100B and renal function after cardiac surgery. J Cardiothorac Vasc Anesth 2000;14:698-701.
  • 31) Lam AG, Koppal T, Akama KT, Guo L, Craft JM, Samy B, et al. Mechanism of glial activation by S100B: involvement of the transcription factor NFkappaB. Neurobiol Aging 2001;22:765-72.
  • 32) Donato R. S100: a multigenic family of calcium-modulated proteins of the EF-hand type with intracellular and extracellular functional roles. Int J Biochem Cell Biol 2001;33:637-68.
  • 33) Fazeli MS, Errington ML, Dolphin AC, Bliss TV. Extracellular proteases and S100 protein in long-term potentiation in the dentate gyrus of the anaesthetized rat. Adv Exp Med Biol 1990;268:369-75.
  • 34) Karpiak SE, Serokosz M, Rapport MM. Effects of antisera to S-100 protein and to synaptic membrane fraction on maze performance and EEG. Brain Res 1976;102:313-21.
  • 35) Ashraf S, Bhattacharya K, Zacharias S, Kaul P, Kay PH, Watterson KG. Serum S100beta release after coronary artery bypass grafting: roller versus centrifugal pump. Ann Thorac Surg 1998;66:1958-62.
  • 36) Westaby S, Johnsson P, Parry AJ, Blomqvist S, Solem JO, Alling C, et al. Serum S100 protein: a potential marker for cerebral events during cardiopulmonary bypass. Ann Thorac Surg 1996;61:88-92.
  • 37) Gao F, Harris DN, Sapsed-Byrne S. Time course of neuronespecific enolase and S-100 protein release during and after coronary artery bypass grafting. Br J Anaesth 1999;82:266-7.
  • 38) Schmechel D, Marangos PJ, Brightman M. Neurone-specific enolase is a molecular marker for peripheral and central neuroendocrine cells. Nature 1978;276:834-6.
  • 39) Påhlman S, Esscher T, Bergvall P, Odelstad L. Purification and characterization of human neuron-specific enolase: radioimmunoassay development. Tumour Biol 1984;5:127-39.
  • 40) Schaarschmidt H, Prange HW, Reiber H. Neuron-specific enolase concentrations in blood as a prognostic parameter in cerebrovascular diseases. Stroke 1994;25:558-65.
  • 41) Gao F, Harris DN, Sapsed-Byrne S, Sharp S. Neuronespecific enolase and Sangtec 100 assays during cardiac surgery: Part III--Dose haemolysis affect their accuracy? Perfusion 1997;12:171-7.
  • 42) Herrmann M, Ebert AD, Galazky I, Wunderlich MT, Kunz WS, Huth C. Neurobehavioral outcome prediction after cardiac surgery: role of neurobiochemical markers of damage to neuronal and glial brain tissue. Stroke 2000;31:645-50.
  • 43) Dabrowski W. Magnesium supplementation significantly reduces serum S100beta concentrations in patients who have undergone coronary artery bypass surgery. Magnes Res 2009;22:21-31.
  • 44) Gao F, Harris DN, Sapsed-Byrne S, Sharp S. Neuronespecific enolase and Sangtec 100 assays during cardiac surgery: Part I--The effects of heparin, protamine and propofol. Perfusion 1997;12:163-5.
  • 45) Demir T, Demir H, Tansel T, Kalko Y, Tireli E, Dayioglu E, et al. Influence of methylprednisolone on levels of neuron-specific enolase in cardiac surgery: a corticosteroid derivative to decrease possible neuronal damage. J Card Surg 2009;24:397-403. doi: 10.1111/j.1540- 8191.2009.00842.x.
  • 46) Bayram H, Erer D, Iriz E, Zor MH, Gulbahar O, Ozdogan ME. Comparison of the effects of pulsatile cardiopulmonary bypass, non-pulsatile cardiopulmonary bypass and offpump coronary artery bypass grafting on the inflammatory response and S-100beta protein. Perfusion 2012;27:56-64. doi: 10.1177/0267659111424639.
  • 47) Bonacchi M, Prifti E, Maiani M, Bartolozzi F, Di Eusanio M, Leacche M. Does off-pump coronary revascularization reduce the release of the cerebral markers, S-100beta and NSE? Heart Lung Circ 2006;15:314-9.
  • 48) Civelek A, Akgün S, Roth M, Tekeli A, Aksoy N, İşbir S ve ark. Pulsatil akım kardiyopulmoner bypas sonrası S100B protein salınımı azaltmıyor. Turk Gogus Kalp Dama 2003;11:211-5.
  • 49) Kusch B, Vogt S, Sirat AS, Helwig-Rohlig A, Kasseckert S, Moosdorf R. Serum S-100beta protein release in coronary artery bypass grafting: laminar versus pulsatile flow. Thorac Cardiovasc Surg 2001;49:179-83.
  • 50) Basile AM, Fusi C, Conti AA, Paniccia R, Trefoloni G, Pracucci G, et al. S-100 protein and neuron-specific enolase as markers of subclinical cerebral damage after cardiac surgery: preliminary observation of a 6-month follow-up study. Eur Neurol 2001;45:151-9.
  • 51) Rasmussen LS, Christiansen M, Hansen PB, Moller JT. Do blood levels of neuron-specific enolase and S-100 protein reflect cognitive dysfunction after coronary artery bypass? Acta Anaesthesiol Scand 1999;43:495-500.
  • 52) Kanbak M, Saricaoglu F, Avci A, Ocal T, Koray Z, Aypar U. Propofol offers no advantage over isoflurane anesthesia for cerebral protection during cardiopulmonary bypass: a preliminary study of S-100beta protein levels. Can J Anaesth 2004;51:712-7.
  • 53) Anderson RE, Hansson LO, Liska J, Settergren G, Vaage J. The effect of cardiotomy suction on the brain injury marker S100beta after cardiopulmonary bypass. Ann Thorac Surg 2000;69:847-50.
  • 54) Snyder-Ramos SA, Gruhlke T, Bauer H, Bauer M, Luntz AP, Motsch J, et al. Cerebral and extracerebral release of protein S100B in cardiac surgical patients. Anaesthesia 2004;59:1149-50.
  • 55) Ozatik MA, Tarcan O, Kale A, Aşkin GA, Balci M, Undar A, et al. Do S100beta protein level increases due to inflammation during cardiopulmonary bypass occur without any neurological deficit? Perfusion 2002;17:335-8.
  • 56) Kofke WA, Konitzer P, Meng QC, Guo J, Cheung A. The effect of apolipoprotein E genotype on neuron specific enolase and S-100beta levels after cardiac surgery. Anesth Analg 2004;99:1323-5.
  • 57) Rasmussen LS, Christiansen M, Rasmussen H, Kristensen PA, Moller JT. Do blood concentrations of neurone specific enolase and S-100 beta protein reflect cognitive dysfunction after abdominal surgery? ISPOCD Group. Br J Anaesth 2000;84:242-4.
  • 58) Rasmussen LS, Christiansen M, Eliasen K, Sander- Jensen K, Moller JT. Biochemical markers for brain damage after cardiac surgery--time profile and correlation with cognitive dysfunction. Acta Anaesthesiol Scand 2002;46:547-51.
  • 59) Stolz E, Gerriets T, Kluge A, Klövekorn WP, Kaps M, Bachmann G. Diffusion-weighted magnetic resonance imaging and neurobiochemical markers after aortic valve replacement: implications for future neuroprotective trials? Stroke 2004;35:888-92.
  • 60) Georgiadis D, Berger A, Kowatschev E, Lautenschläger C, Börner A, Lindner A, et al. Predictive value of S-100beta and neuron-specific enolase serum levels for adverse neurologic outcome after cardiac surgery. J Thorac Cardiovasc Surg 2000;119:138-47.
  • 61) Isgro F, Schmidt C, Pohl P, Saggau W. A predictive parameter in patients with brain related complications after cardiac surgery? Eur J Cardiothorac Surg 1997;11:640-4.
  • 62) Grocott HP, Croughwell ND, Amory DW, White WD, Kirchner JL, Newman MF. Cerebral emboli and serum S100beta during cardiac operations. Ann Thorac Surg 1998;65:1645-9.
  • 63) Beaudeux JL, Léger P, Dequen L, Gandjbakhch I, Coriat P, Foglietti MJ. Influence of hemolysis on the measurement of S-100beta protein and neuron-specific enolase plasma concentrations during coronary artery bypass grafting. Clin Chem 2000;46:989-90.
  • 64) Ilcol YO, Basagan-Mogol E, Cengiz M, Ulus IH. Elevation of serum cerebral injury markers correlates with serum choline decline after coronary artery bypass grafting surgery. Clin Chem Lab Med 2006;44:471-8.
  • 65) Kumar RA, Cann C, Hall JE, Sudheer PS, Wilkes AR. Predictive value of IL-18 and SC5b-9 for neurocognitive dysfunction after cardiopulmonary bypass. Br J Anaesth 2007;98:317-22.
  • 66) Goetzl EJ, Banda MJ, Leppert D. Matrix metalloproteinases in immunity. J Immunol 1996;156:1-4.
  • 67) Castrén M, Silfvast T, Rubertsson S, Niskanen M, Valsson F, Wanscher M, et al. Scandinavian clinical practice guidelines for therapeutic hypothermia and post-resuscitation care after cardiac arrest. Acta Anaesthesiol Scand 2009;53:280-8. doi: 10.1111/j.1399-6576.2008.01881.x.
  • 68) Gong B, Leznik E. The role of ubiquitin C-terminal hydrolase L1 in neurodegenerative disorders. Drug News Perspect 2007;20:365-70.
  • 69) Hillis LD, Smith PK, Anderson JL, Bittl JA, Bridges CR, Byrne JG, et al. 2011 ACCF/AHA Guideline for Coronary Artery Bypass Graft Surgery: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. Circulation 2011;124:e652-735. doi: 10.1161/CIR.0b013e31823c074e.
Türk Göğüs Kalp Damar Cerrahisi Dergisi-Cover
  • ISSN: 1301-5680
  • Yayın Aralığı: Yılda 4 Sayı
  • Başlangıç: 1991
  • Yayıncı: Bayçınar Tıbbi Yayıncılık
Sayıdaki Diğer Makaleler

Killian-Jamieson diverticulum

Hanifi BAYAROĞULLARI, Muhittin TEMİZ, Tülin YETİM DURGUN, İsmail Güzel MANSUR

An outcome comparison of adenocarcinoma of the esophagus to squamous cell carcinoma after transthoracic esophagectomy

Ömer YILMAZ, Atila EROĞLU, Ali Bilal ULAŞ, Yener AYDIN

Kronik venöz yetmezlik ile bulgu veren kronik arteriyovenöz fistül

Murat UĞUR, Veysel TEMİZKAN, Ahmet Turan YILMAZ, Alper UÇAK, İbrahim ALP

İki taraflı vertebral arterin kıvrımlanma ve dolanma patolojisi: Olgu sunumu

Ali GÜRBÜZ, Cengiz ÖZBEK, Ufuk YETKİN, İsmail YÜREKLİ

Surgical approach to giant pseudoaneurysm of the left ventricle

Ali İhsan PARLAR, Veysel BAŞAR, Utku ÜNAL, Kerem YAY, Ferit ÇİÇEKÇİOĞLU, Salih Fehmi KATIRCIOĞLU

Delayed endovascular repair of a traumatic aortic dissection

Berk ÖZKAYNAK, Adil POLAT, Bora FARSAK, Gülçin HEPGÜL, Funda GÜMÜŞ, Vedat ERENTUĞ, Nihan KAYALAR

Kalp cerrahisinde propofol ve desfluran ile oluşturulan önkoşullamanın miyokard korunması üzerine etkilerinin karşılaştırılması

Nihan YAPICI, Zuhal AYKAÇ, Ceren KÖKSAL, Zeliha TUNCEL, Türkan KUDİSOĞLU, Yasemin ALTUNTAŞ

Endobronşiyal migrasyon gösteren mermi çekirdeğine bağlı bronşektatik akciğer apsesi

Bülent Mustafa YENİGÜN, Murat ŞAHİN, Adem GÜNGÖR, Ali Abbas YILMAZ, Serkan ENÖN

Redo subfasyal endoskopik perforan ven cerrahisi: Gerektiğinde yapılmalı mı?

Mustafa KARAÇELİK, Cengiz ÖZBEK, Namık Selim ÖZENÇ, Cengiz SERT, Hakan KÖKSAL

Açık kalp cerrahisi sonrası tekrarlayıcı transfüzyon ilişkili akut akciğer hasarı: Olgu sunumu

Barış MALBORA, Murat ÇAPANOĞLU, Tolga BAŞ, Onur IŞIK, Ali KUTSAL