Genetics of otitis media

Advances in Oto-Rhino-Laryngology

Volumn 70, Issue , 2011, Pages 135-140

  Post, Christopher ^a  

^a ALLEGHENY GENERAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; ARTICLE; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC PREDISPOSITION; GENETIC SCREENING; GENETICS; HUMAN; OTITIS MEDIA; PEDIGREE; TWINS;

ANIMALS; DISEASES IN TWINS; GENETIC PREDISPOSITION TO DISEASE; GENETIC TESTING; GENOME-WIDE ASSOCIATION STUDY; HUMANS; OTITIS MEDIA; PEDIGREE; POLYMORPHISM, GENETIC;

EID: 79952365534     PISSN: 00653071     EISSN: None     Source Type: Book Series    
DOI: 10.1159/000322489     Document Type: Article

References (26)

1. Gultekin E, Develioǧlu ON, Yener M, Ozdemir I, Külekci M: Prevalence and risk factors for persistent otitis media with effusion in primary school children in Istanbul, Turkey. Auris Nasus Larynx. In press.
2. Trune DR, Zheng QY: Mouse models for human otitis media. Brain Res 2009; 1277:90-103.
3. Depreux FF, Darrow K, Conner DA, et al: Eya4- deficient mice are a model for heritable otitis media. J Clin Invest 2008; 118:471-474.
4. Hernandez M, Leichtle A, Pak K, et al: Myeloid differentiation primary response gene 88 is required for the resolution of otitis media. J Infect Dis 2008; 198:1862-1869.
5. Casselbrandt ML, Mandel EM: The genetics of otitis media. Curr Allergy Asthma Rep 2001;1:353-357.
6. Casselbrandt ML, Mandel EM: Genetic susceptibility to otitis media. Curr Opin Allergy Clin Immunol 2005;5:1-4. (Pubitemid 40175488)
7. Casselbrandt ML, Mandel EM, Fall PA, et al: The heritability of otitis media: a twin and triplet study. JAMA 1999;282: 2125-2130.
8. Casselbrandt ML, Mandel EM, Rockette HE, et al: The genetic component of middle ear disease in the first 5 years of life. Arch Otolaryngol Head Neck Surg 2004;130:273-278. (Pubitemid 38314224)
9. Kvestad E, Kværner KJ, Røysamb E, et al: Otitis media: genetic factors and sex differences. Twin Res 2004;7:239-244. (Pubitemid 38915566)
10. Rovers M, Haggard M, Gannon M, Koeppen- Schomerus G, Plomin R: Heritability of symptom domains in otitis media: a longitudinal study of 1,373 twin pairs. Am J Epidemiol 2002;155: 958-964. (Pubitemid 34517853)
11. Lijnen HR: Pleiotropic functions of plasminogen activator inhibitor- 1. J Thromb Haemost 2005;3:35-45. (Pubitemid 41647113)
12. Emonts M, Wiertsma SP, Veenhoven RH, et al: The 4G/4G plasminogen activator inhibitor- 1 genotype is associated with frequent recurrence of acute otitis media. Pediatrics 2007;120:e317-e323. (Pubitemid 47219482)
13. Patel JA, Nair S, Revai K, et al: Association of proinflammatory cytokine gene polymorphisms with susceptibility to otitis media. Pediatrics 2006;118:2273-2279. (Pubitemid 46397564)
14. Revai K, Patel JA, Grady JJ, et al: Association between cytokine gene polymorphisms and risk for upper respiratory tract infection and acute otitis media. Clin Infect Dis 2009;49:257-261.
15. Alper CM, Winther B, Hendley JO, Doyle WJ: Cytokine polymorphisms predict the frequency of otitis media as a complication of rhinovirus and RSV infections in children. Eur Arch Otorhinolaryngol 2009;266:199-205.
16. Kalm O, Johnson U, Prellner K, Ninn K: HLA frequency in patients with recurrent acute otitis media. Arch Otolaryngol Head Neck Surg 1991;117:1296-1299.
17. Kalm O, Johnson U, Prellner K: HLA frequency in patients with chronic secretory otitis media. Int J Pediatr Otorhinolaryngol 1994;30:151-157. (Pubitemid 24183878)
18. Ruskamp JM, Hoekstra MO, Rovers MM, Schilder AG, Sanders EA: Mannosebinding lectin and upper respiratory tract infections in children and adolescents: a review. Arch Otolaryngol Head Neck Surg 2006;132:482-486. (Pubitemid 43742564)
19. Rantala A, Lajunen T, Juvonen R, et al: Mannose- binding lectin concentrations, MBL2 polymorphisms, and susceptibility to respiratory tract infections in young men. J Infect Dis 2008;198:1247-1253.
20. Chen J, Xu Z, Ou X, et al: Mannosebinding lectin polymorphisms and recurrent respiratory tract infection in Chinese children. Eur J Pediatr 2009; 168:1305-1313.
21. Madsen HO, Garred P, Thiel S, et al: Interplay between promoter and structural gene variants control basal serum level of mannan- binding protein. J Immunol 1995;155:3013-3020.
22. Daly KA, Brown WM, Segade F, et al: Chronic and recurrent otitis media: a genome scan for susceptibility loci. Am J Hum Genet 2004;75:988-997. (Pubitemid 39532069)
23. Casselbrandt ML, Mandel EM, Jung J, et al: Otitis media: a genome- wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions. BMC Med Genetics 2009;10:85.
24. Avanzini AM, Castellazzi AM, Marconi M, et al: Children with recurrent otitis show defective IFN gamma- producing cells in adenoids. Pediatr Allergy Immunol 2008;19:523-526.
25. Schousboe LP, Rasumussen LM, Ovesen T: RANTES in otitis media with effusion: presence, role and correlation with cytokines and microbiology. APMIS 2001;109:441-446. (Pubitemid 32701849)
26. Brien MA, Prosser LA, Paradise JL, et al: New vaccines against otitis media: projected benefits and cost- effectiveness. Pediatrics 2009;123:1452-1463.