PMID- 23282800 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20130104 LR - 20230404 IS - 1939-4551 (Print) IS - 1939-4551 (Electronic) IS - 1939-4551 (Linking) VI - 3 IP - 9 DP - 2010 Sep TI - Association of BDNF gene polymorphism with asthma in polish children. PG - 235-8 LID - 10.1097/WOX.0b013e3181eedb68 [doi] AB - Allergic asthma is associated with changes in neuronal control in the airways that modulate inflammation and airway hyperresponsiveness. The link between inflammation and neuronal dysfunction is provided mainly by neurotrophins, in particular Brain Derived Neurotrophic Factor (BDNF). In humans, significantly higher serum BDNF levels have been observed in asthmatic patients when compared with healthy subjects. BDNF levels are also significantly higher in untreated asthmatic patients in comparison to those treated with inhaled glucocorticoids and nonasthmatic controls. Allergic inflammation increases local BDNF production and its concentration correlates with clinical parameters of allergic airway dysfunction. The aim of this study was to analyze the possible association of BDNF gene polymorphism with susceptibility to asthma and disease severity. We analyzed 146 children diagnosed with asthma and 227 children from the control group. Genotyping of 4 BDNF polymorphisms (rs12273363, rs7124442, rs6265, and rs2030324) was done with use of PCR-RFLP and TaqMan SNP genotyping assay. Genetic association analysis was performed in Statistica. Linkage disequilibrium was determined with Haploview. Single marker analysis revealed a significant association of C allele of rs2030324 polymorphism with asthma susceptibility (P = 0.048). However, BDNF polymorphism was not associated with severe asthma. Strong linkage disequilibrium was observed between all of the BDNF polymorphisms analyzed grouped in one haplotype block. We found a significant association of TTGC haplotype with asthma (P = 0.025). Our results suggest that genetic variation in the BDNF gene may contribute to asthma susceptibility in case of rs2030324 polymorphism and TTGC haplotype, however it does not influence asthma severity. FAU - Szczepankiewicz, Aleksandra AU - Szczepankiewicz A AD - From the 1Laboratory of Cellular and Molecular Analysis, Department of Pediatric Pulmonology, Allergy and Clinical Immunology, IIIrd Department of Pediatrics, Poznan University of Medical Sciences, Poland; 2Department of Pediatric Pulmonology, Allergy and Clinical Immunology, IIIrd Department of Pediatrics, Poznan University of Medical Sciences, Poland. FAU - Breborowicz, Anna AU - Breborowicz A FAU - Sobkowiak, Paulina AU - Sobkowiak P FAU - Popiel, Anna AU - Popiel A LA - eng PT - Journal Article PL - United States TA - World Allergy Organ J JT - The World Allergy Organization journal JID - 101481283 PMC - PMC3651092 EDAT- 2010/09/01 00:00 MHDA- 2010/09/01 00:01 PMCR- 2010/09/01 CRDT- 2013/01/04 06:00 PHST- 2013/01/04 06:00 [entrez] PHST- 2010/09/01 00:00 [pubmed] PHST- 2010/09/01 00:01 [medline] PHST- 2010/09/01 00:00 [pmc-release] AID - S1939-4551(19)30485-5 [pii] AID - 1939-4551-3-9-235 [pii] AID - 10.1097/WOX.0b013e3181eedb68 [doi] PST - ppublish SO - World Allergy Organ J. 2010 Sep;3(9):235-8. doi: 10.1097/WOX.0b013e3181eedb68.