Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis
- PMID: 17990579
Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis
Abstract
The aim of this study was to examine the presence of any association between mannose binding lectin (MBL) gene variants and bacterial meningitis. Codon 54 (B allele) and codon 57 (C allele) polymorphisms in exon 1 of the MBL gene were investigated in 50 healthy controls and 31 patients diagnosed as purulent meningitis. Codon 57 polymorphism was not found in our patient and control groups. B allele frequency was significantly higher in the patient group (22%) compared to the control group (3%). AB genotype was determined in 39% and 6% of patient and healthy control groups, respectively, and the difference was statistically significant. AA genotype was determined in 61% of the patient group and in 94% of the control group, and it was statistically low in the patient group. These results suggest that codon 54 polymorphism in the MBL gene may play a role in susceptibility to bacterial meningitis in children.
Similar articles
-
Structural polymorphisms in the mannose-binding lectin gene are associated with juvenile idiopathic arthritis.J Rheumatol. 2009 Apr;36(4):843-7. doi: 10.3899/jrheum.080681. Epub 2009 Mar 13. J Rheumatol. 2009. PMID: 19286845
-
Mannose binding lectin (+54) exon 1 gene polymorphism in Tunisian kidney transplant patients.Transplant Proc. 2009 Mar;41(2):660-2. doi: 10.1016/j.transproceed.2009.01.030. Transplant Proc. 2009. PMID: 19328949
-
Evidence of an association between mannose binding lectin codon 54 polymorphism and adenoidectomy and/or tonsillectomy in children.Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1157-61. doi: 10.1016/j.ijporl.2007.05.004. Epub 2007 Jun 7. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17559949
-
Mannose-binding lectin and upper respiratory tract infections in children and adolescents: a review.Arch Otolaryngol Head Neck Surg. 2006 May;132(5):482-6. doi: 10.1001/archotol.132.5.482. Arch Otolaryngol Head Neck Surg. 2006. PMID: 16702562 Review.
-
Genetic risk of acute pulmonary infections and sepsis.Expert Rev Respir Med. 2010 Apr;4(2):229-38. doi: 10.1586/ers.10.13. Expert Rev Respir Med. 2010. PMID: 20406089 Review.
Cited by
-
Mannose binding lectin and macrophage migration inhibitory factor gene polymorphisms in Turkish children with cardiomyopathy: no association with MBL2 codon 54 A/B genotype, but an association between MIF -173 CC genotype.Int J Med Sci. 2012;9(6):506-12. doi: 10.7150/ijms.4787. Epub 2012 Aug 22. Int J Med Sci. 2012. PMID: 22927777 Free PMC article.
-
Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (-) patients.Pathog Glob Health. 2022 May;116(3):178-184. doi: 10.1080/20477724.2021.1984726. Epub 2021 Sep 27. Pathog Glob Health. 2022. PMID: 34570692 Free PMC article.
-
Mannose-binding lectin gene polymorphism and chronic hepatitis B infection in children.Saudi J Gastroenterol. 2015 Mar-Apr;21(2):84-9. doi: 10.4103/1319-3767.153825. Saudi J Gastroenterol. 2015. PMID: 25843194 Free PMC article.
-
A Case-Control Study on the Risk Factors for Meningococcal Disease among Children in Greece.PLoS One. 2016 Jun 28;11(6):e0158524. doi: 10.1371/journal.pone.0158524. eCollection 2016. PLoS One. 2016. PMID: 27351742 Free PMC article.
-
Investigation of Monnose-Binding Lectin gene Polymorphism in Patients with Erythema Multiforme, Stevens-Johnson Syndrome and Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Overlap Syndrome.Balkan Med J. 2012 Sep;29(3):310-3. doi: 10.5152/balkanmedj.2012.018. Epub 2012 Sep 1. Balkan Med J. 2012. PMID: 25207021 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Miscellaneous