Genetic variation at the BDNF locus: evidence for association with long-term outcome after ischemic stroke

• Published in: PloS one Vol. 9; no. 12; p. e114156
• Main Authors: Stanne, Tara M, Tjärnlund-Wolf, Anna, Olsson, Sandra, Jood, Katarina, Blomstrand, Christian, Jern, Christina
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 03.12.2014; Public Library of Science (PLoS)
• Subjects: Adolescent; Adult; Aged; Alleles; Animal models; Biology and Life Sciences; Brain; Brain Ischemia - complications; Brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - genetics; Case-Control Studies; Female; Gene Frequency; Genetic aspects; Genetic diversity; Genetic factors; Genotype; Genotypes; Humans; Ischemia; Linkage Disequilibrium; Loci; Male; Medicine and Health Sciences; Middle Aged; Neurologi; Neurology; Odds Ratio; Polymorphism, Single Nucleotide; Recovery; Recovery of function; Risk Factors; Severity of Illness Index; Single-nucleotide polymorphism; Stroke; Stroke - etiology; Stroke - genetics; Stroke - pathology; Treatment Outcome; Young Adult; Sweden
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0114156

Rates and extent of recovery after stroke vary considerably between individuals and genetic factors are thought to contribute to post-stroke outcome. Brain-derived neurotrophic factor (BDNF) plays important roles in brain plasticity and repair and has been shown to be involved in stroke severity, recovery, and outcome in animal models. Few clinical studies on BDNF genotypes in relation to ischemic stroke have been performed. The aims of the present study are therefore to investigate whether genetic variation at the BDNF locus is associated with initial stroke severity, recovery and/or short-term and long-term functional outcome after ischemic stroke. Four BDNF tagSNPs were analyzed in the Sahlgrenska Academy Study on Ischemic Stroke (SAHLSIS; 600 patients and 600 controls, all aged 18-70 years). Stroke severity was assessed using the NIH Stroke Scale (NIHSS). Stroke recovery was defined as the change in NIHSS over a 3-month period. Short- and long-term functional outcome post-stroke was assessed using the modified Rankin Scale at 3 months and at 2 and 7 years after stroke, respectively. No SNP was associated with stroke severity or recovery at 3 months and no SNP had an impact on short-term outcome. However, rs11030119 was independently associated with poor functional outcome 7-years after stroke (OR 0.66, 95% CI 0.46-0.92; P =  0.006). BDNF gene variants were not major contributors to ischemic stroke severity, recovery, or short-term functional outcome. However, this study suggests that variants in the BDNF gene may contribute to poor long-term functional outcome after ischemic stroke.