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Polymorphismus des „brain derived neurotrophic factor“ und Erholung nach Schlaganfall

Polymorphism of brain derived neurotrophic factor and recovery of functions after ischemic stroke

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Zusammenfassung

Hintergrund

Die Funktionsrestitution nach einem Schlaganfall wird von vielen Faktoren beeinflusst. Insbesondere das Alter des Patienten, die initiale Ausprägung der Symptomatik, das Vorhandensein kognitiver oder neuropsychologischer Defizite zählen dazu. In dieser Studie wurde untersucht, ob ein Polymorphismus im für den „brain derived neurotrophic factor“ (BDNF) kodierenden Gen Einfluss auf die Verbesserung von motorischen Funktionen und Alltagsaktivitäten nimmt.

Methoden

Patienten mit subakutem ischämischem Hirninfarkt (n = 67) wurden zu Beginn einer stationären neurologischen Rehabilitation, nach 4-wöchiger Behandlung und 6 Monate später mittels Barthel-Index (BI) und Rivermead Motor Assessment (RMA) untersucht. Je nach BDNF-Polymorphismus im Codon 66 erfolgte die Einteilung in Gruppen (Valin [Val]/Valin, Val/Methionin[Met] oder Met/Met).

Ergebnisse

Die 3 Gruppen (Val/Val, n = 34 Patienten; Val/Met, n = 26; Met/Met, n = 7) wiesen im BI und im RMA sowohl nach 4 Wochen als auch nach 6 Monaten eine signifikante Verbesserung zum jeweils vorhergehenden Untersuchungsergebnis auf. BI und RMA waren hoch miteinander korreliert. Es gab keinen Unterschied in Bezug auf den BDNF-Polymorphismus.

Diskussion

Nach Hirninfarkt kommt es über mindestens 6 Monate zu kontinuierlichen Verbesserungen der motorischen Funktionen und der Alltagsfunktionen. Der BDNF-Polymorphismus beeinflusste diese Entwicklung nicht.

Summary

Background

After ischemic stroke, many factors influence the restitution of functions. In particular they include the patient age, the initial stroke severity and the presence of cognitive and neuropsychological deficits. In this study we investigated whether a polymorphism in the gene encoding for brain derived neurotrophic factor (BDNF) influences improvements of motor functions and everyday activities.

Methods

Patients with subacute ischemic stroke (n = 67) were examined at the beginning of an inpatient neurological rehabilitation, after 4 weeks of treatment and after 6 months. The Barthel index (BI) and the Rivermead motor assessment (RMA) were used to measure motor functions and everyday activities. Patients were allocated to three groups (valine [Val]/valine, val/methionine [Met] and Met/Met) depending on the BDNF polymorphism at codon 66.

Results

The 3 groups (Val/Val, n = 34 patients, Val/Met, n = 26 and Met/Met, n = 7) showed significant improvements in BI and RMA after 4 weeks and after 6 months as compared to the preceding measurements. The BI and RMA were positively correlated. The three groups did not differ with respect to the extent of improvement.

Conclusion

After ischemic stroke, motor functions and everyday activities improved continuously over a period of at least 6 months. The BDNF polymorphism did not influence this development.

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Literatur

  1. Cramer SC, Procaccio V, GAIN Americas, GAIN International Study Investigators (2012) Correlation between genetic polymorphisms and stroke recovery: analysis of the GAIN Americas and GAIN International Studies. Eur J Neurol 19(5):718–724

    Article  CAS  PubMed  Google Scholar 

  2. Houlden H, Edwards M, McNeil J, Greenwood R (2006) Use of the Barthel Index and the Functional Independence Measure during early inpatient rehabilitation after single incident brain injury. Clin Rehabil 20:153–159

    Article  PubMed  Google Scholar 

  3. Katzan IL, Spertus J, Bettger JP et al (2014) Risk adjustment of ischemic stroke outcomes for comparing hospital performance: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke 45(3):918–944

    Article  PubMed  Google Scholar 

  4. Kim JM, Stewart R, Park MS et al (2012) Associations of BDNF genotype and promoter methylation with acute and long-term stroke outcomes in an East Asian cohort. PLoS One 7(12):e51280

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Kim WS, Lim JY, Shin JH et al (2013) Effect of the presence of brain-derived neurotrophic factor val(66)met polymorphism on the recovery in patients with acute subcortical stroke. Ann Rehabil Med 37(3):311–319

    Article  PubMed Central  PubMed  Google Scholar 

  6. Kleim JA, Chan S, Pringle E et al (2006) BDNF val66met polymorphism is associated with modified experience-dependent plasticity in human motor cortex. Nat Neurosci 9(6):735–737

    Article  CAS  PubMed  Google Scholar 

  7. Kurtaiş Y, Küçükdeveci A, Elhan A et al (2009) Psychometric properties of the Rivermead Motor Assessment: its utility in stroke. J Rehabil Med 41:1055–1061

    Article  PubMed  Google Scholar 

  8. Laske C, Eschweiler GW (2006) Brain-derived neurotrophic factor: from nerve growth factor to modulator of brain plasticity in cognitive processes and psychiatric diseases. Nervenarzt 77(5):523–537

    Article  CAS  PubMed  Google Scholar 

  9. Liepert J, Heller A, Behnisch G, Schoenfeld A (2013) Catechol-O-methyltransferase polymorphism influences outcome after ischemic stroke: a prospective double-blind study. Neurorehabil Neural Repair 27(6):491–496

    Article  PubMed  Google Scholar 

  10. Manso H, Krug T, Sobral J et al (2012) Evidence for epistatic gene interactions between growth factor genes in stroke outcome. Eur J Neurol 19(8):1151–1153

    Article  CAS  PubMed  Google Scholar 

  11. Medic S, Beslac-Bumbasirevic L, Kisic-Tepavcevic D, Pekmezovic T (2013) Short-term and long-term stroke survival: the belgrade prognostic study. J Clin Neurol 9(1):14–20

    Article  PubMed Central  PubMed  Google Scholar 

  12. Meretoja A, Keshtkaran M, Saver JL et al (2014) Stroke thrombolysis: save a minute, save a day. Stroke 45(4):1053–1058

    Article  PubMed  Google Scholar 

  13. Mirowska-Guzel D, Gromadzka G, Czlonkowski A, Czlonkowska A (2012) BDNF − 270 C>T polymorphisms might be associated with stroke type and BDNF − 196 G>A corresponds to early neurological deficit in hemorrhagic stroke. J Neuroimmunol 249(1–2):71–75

  14. Panja D, Bramham CR (2014) BDNF mechanisms in late LTP formation: a synthesis and breakdown. Neuropharmacology 76 Pt C:664–676

    Article  Google Scholar 

  15. Paolucci S, Di Vita A, Massicci R et al (2012) Impact of participation on rehabilitation results: a multivariate study. Eur J Phys Rehabil Med 48(3):455–466

    CAS  PubMed  Google Scholar 

  16. Qin L, Jing D, Parauda S et al (2014) An adaptive role for BDNF Val66Met polymorphism in motor recovery in chronic stroke. J Neurosci 34(7):2493–2502

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  17. Quinn TJ, Langhorne P, Stott DJ (2011) Barthel index for stroke trials: development, properties, and application. Stroke 42:1146–1151

    Article  PubMed  Google Scholar 

  18. Siironen J, Juvela S, Kanarek K et al (2007) The Met allele of the BDNF Val66Met polymorphism predicts poor outcome among survivors of aneurysmal subarachnoid hemorrhage. Stroke 38(10):2858–2860

    Article  CAS  PubMed  Google Scholar 

  19. Tsai SJ, Cheng CY, Yu YW et al (2003) Association study of a brain-derived neurotrophic factor genetic polymorphism and major depressive disorders, symptomatology and antidepressant response. Am J Med Genet B Neuropsychiatr Genet 123(1):19–22

    Article  Google Scholar 

  20. Vilkki J, Lappalainen J, Juvela S et al (2008) Relationship of the Met allele of the brain-derived neurotrophic factor Val66Met polymorphism to memory after aneurysmal subarachnoid hemorrhage. Neurosurgery 63(2):198–203

    Article  PubMed  Google Scholar 

  21. Westbroek EM, Pawlikowska L, Lawton MT et al (2012) Brain-derived neurotrophic factor Val66Met polymorphism predicts worse functional outcome after surgery in patients with unruptured brain arteriovenous malformation. Stroke 43(8):2255–2257

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  22. Zhao J, Wu H, Zheng L et al (2013) Brain-derived neurotrophic factor G196A polymorphism predicts 90-day outcome of ischemic stroke in Chinese: a novel finding. Brain Res 1537:312–318

    Article  CAS  PubMed  Google Scholar 

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Einhaltung ethischer Richtlinien

Interessenkonflikt. J. Liepert, A. Heller, G. Behnisch und A. Schoenfeld geben an, dass kein Interessenkonflikt besteht.

Alle im vorliegenden Manuskript beschriebenen Untersuchungen am Menschen wurden mit Zustimmung der zuständigen Ethikkommission, im Einklang mit nationalem Recht sowie gemäß der Deklaration von Helsinki von 1975 (in der aktuellen, überarbeiteten Fassung) durchgeführt. Von allen beteiligten Patienten liegt eine Einverständniserklärung vor.

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Liepert, J., Heller, A., Behnisch, G. et al. Polymorphismus des „brain derived neurotrophic factor“ und Erholung nach Schlaganfall. Nervenarzt 86, 1255–1260 (2015). https://doi.org/10.1007/s00115-015-4325-6

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  • DOI: https://doi.org/10.1007/s00115-015-4325-6

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