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1.
J Med Genet ; 58(7): 442-452, 2021 07.
Artigo em Inglês | MEDLINE | ID: mdl-32709676

RESUMO

BACKGROUND: Otitis media (OM) susceptibility has significant heritability; however, the role of rare variants in OM is mostly unknown. Our goal is to identify novel rare variants that confer OM susceptibility. METHODS: We performed exome and Sanger sequencing of >1000 DNA samples from 551 multiethnic families with OM and unrelated individuals, RNA-sequencing and microbiome sequencing and analyses of swabs from the outer ear, middle ear, nasopharynx and oral cavity. We also examined protein localisation and gene expression in infected and healthy middle ear tissues. RESULTS: A large, intermarried pedigree that includes 81 OM-affected and 53 unaffected individuals cosegregates two known rare A2ML1 variants, a common FUT2 variant and a rare, novel pathogenic variant c.1682A>G (p.Glu561Gly) within SPINK5 (LOD=4.09). Carriage of the SPINK5 missense variant resulted in increased relative abundance of Microbacteriaceae in the middle ear, along with occurrence of Microbacteriaceae in the outer ear and oral cavity but not the nasopharynx. Eight additional novel SPINK5 variants were identified in 12 families and individuals with OM. A role for SPINK5 in OM susceptibility is further supported by lower RNA counts in variant carriers, strong SPINK5 localisation in outer ear skin, faint localisation to middle ear mucosa and eardrum and increased SPINK5 expression in human cholesteatoma. CONCLUSION: SPINK5 variants confer susceptibility to non-syndromic OM. These variants potentially contribute to middle ear pathology through breakdown of mucosal and epithelial barriers, immunodeficiency such as poor vaccination response, alteration of head and neck microbiota and facilitation of entry of opportunistic pathogens into the middle ear.


Assuntos
Microbiota , Otite Média/genética , Otite Média/microbiologia , Inibidor de Serinopeptidase do Tipo Kazal 5/genética , Adulto , Animais , Bactérias/classificação , Bactérias/genética , Criança , Suscetibilidade a Doenças/microbiologia , Orelha Externa/microbiologia , Orelha Média/microbiologia , Exoma , Feminino , Predisposição Genética para Doença , Humanos , Masculino , Camundongos , Boca/microbiologia , Nasofaringe/microbiologia , Linhagem , Análise de Sequência de DNA , Análise de Sequência de RNA
2.
Otolaryngol Head Neck Surg ; 155(5): 856-862, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27484237

RESUMO

OBJECTIVE: To identify genetic and environmental risk factors for otitis media in an indigenous Filipino population. STUDY DESIGN: Cross-sectional study. SETTING: Indigenous Filipino community. SUBJECTS AND METHODS: Clinical history and information on breastfeeding, tobacco smoke exposure, and swimming were obtained from community members. Heads of households were interviewed for family history and personal beliefs on ear health. Height and weight were measured. Otoscopic findings were described for the presence and character of perforation or discharge. An A2ML1 duplication variant that confers otitis media susceptibility was Sanger sequenced in all DNA samples. Co-occurrence of middle ear bacteria detected by 16S rRNA gene sequencing was determined according to A2ML1 genotype and social cluster. RESULTS: The indigenous Filipino population has a ~50% prevalence of otitis media. Young age was associated with otitis media (4 age strata; P = .004); however, age was nonsignificant as a bistratal or continuous variable. There was no association between otitis media and sex, body mass index, breastfeeding, tobacco exposure, or deep swimming. In multivariate analyses, A2ML1 genotype is the strongest predictor of otitis media, with an odds ratio of 3.7 (95% confidence interval: 1.3-10.8; P = .005). When otitis media diagnoses were plotted across ages, otitis media was observed within the first year of life, and chronic otitis media persisted up to adulthood, particularly in A2ML1-variant carriers. CONCLUSION: Among indigenous Filipinos, A2ML1 genotype is the primary risk factor for otitis media and main determinant of disease progression, although age, the middle ear microbiome, and social clusters might modulate the effect of the A2ML1 genotype.


Assuntos
Exposição Ambiental/efeitos adversos , Otite Média/epidemiologia , Otite Média/genética , alfa-Macroglobulinas/genética , Adolescente , Adulto , Criança , Pré-Escolar , Estudos Transversais , Feminino , Predisposição Genética para Doença , Genótipo , Humanos , Masculino , Microbiota , Otite Média/microbiologia , Otoscopia , Filipinas/epidemiologia , Prevalência , Fatores de Risco
3.
Auris Nasus Larynx ; 35(1): 115-20, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17826931

RESUMO

This paper presents a case of a 28-year-old male with a seizure episode and a 4-year history of intermittent tinnitus on the left ear. On computed tomography and magnetic resonance imaging, a density with rim enhancement was found at the temporal lobe, associated with mastoid tegmen destruction and middle ear mass, indicating cholesteatoma with complicating brain abscess. Evacuation of the brain abscess was performed with a combined otolaryngologic and neurosurgical procedures (canal wall-down mastoidectomy and temporal craniotomy). The pathology turned out to be infestation with Echinococcus granulosus.


Assuntos
Abscesso Encefálico/diagnóstico , Infecções Parasitárias do Sistema Nervoso Central/diagnóstico , Otopatias/diagnóstico , Orelha Média , Equinococose/diagnóstico , Echinococcus granulosus , Echinococcus multilocularis , Lobo Temporal , Adulto , Animais , Audiometria de Tons Puros , Abscesso Encefálico/patologia , Abscesso Encefálico/cirurgia , Infecções Parasitárias do Sistema Nervoso Central/patologia , Infecções Parasitárias do Sistema Nervoso Central/cirurgia , Colesteatoma da Orelha Média/diagnóstico , Craniotomia , Diagnóstico Diferencial , Otopatias/patologia , Otopatias/cirurgia , Orelha Média/patologia , Orelha Média/cirurgia , Equinococose/patologia , Equinococose/cirurgia , Humanos , Imageamento por Ressonância Magnética , Masculino , Processo Mastoide/patologia , Processo Mastoide/cirurgia , Prótese Ossicular , Otoscopia , Lobo Temporal/patologia , Lobo Temporal/cirurgia , Tomografia Computadorizada por Raios X
4.
Artigo em Inglês | MEDLINE | ID: mdl-17539266

RESUMO

The objectives of this study were to determine the agreement between the ear examination findings of the otorhinolaryngologist (trainer) and the elementary school nurse (trainee) after training with the use of a penlight and to determine the mean sound pressure level (SPL) produced by school nurses as a standard parameter for hearing screening using a 512 tuning fork after training on tuning fork testing by the otorhinolaryngologist. Training workshops in ear examination using a penlight and hearing screening using a 512 tuning fork were conducted for school nurses. Data for assessment of ear examination skills and production of SPL were collected by questionnaire and observation of performance. Kappa statistics were used to assess agreement between trainees' and trainer's responses. Mean and standard deviation were determined for the assessment of the SPL produced. Results showed an excellent agreement between the school nurses' and otorhinolaryngologist's observations on ear examination. These included observations of the ear canal, visualization of the tympanic membrane and identification of unusual findings such as wax and discharge. The majority of nurses responded positively in terms of the ease and confidence in performance of the procedure. Regarding tuning fork testing, the nurses were able to produce significant SPL. The mean SPL produced by the nurses using a 512 tuning fork was 56.316 dB.


Assuntos
Educação , Perda Auditiva/diagnóstico , Testes Auditivos/métodos , Programas de Rastreamento/métodos , Otolaringologia/educação , Serviços de Enfermagem Escolar/educação , Competência Clínica , Coleta de Dados , Humanos , Filipinas
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