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1.
Otol Neurotol ; 39(8): e726-e730, 2018 09.
Article in English | MEDLINE | ID: mdl-30113565

ABSTRACT

HYPOTHESIS: Variants in SLC26A4 are an important cause of congenital hearing impairment in the Philippines. BACKGROUND: Cochlear implantation is a standard rehabilitation option for congenital hearing impairment worldwide, but places a huge cost burden in lower-income countries. The study of risk factors such as genetic variants that may help determine genetic etiology of hearing loss and also predict cochlear implant outcomes is therefore beneficial. METHODS: DNA samples from 29 GJB2-negative Filipino cochlear implantees were Sanger-sequenced for the coding exons of SLC26A4. Exome sequencing was performed to confirm results. RESULTS: Four cochlear implantees with bilaterally enlarged vestibular aqueducts (EVA) were homozygous for the pathogenic SLC26A4 c.706C>G (p.Leu236Val) variant, which has a minor allele frequency of 0.0015 in Filipino controls. In patients with the SLC26A4 variant there was no association between cochlear implant outcome and age at implantation or duration of implant. There was also no association between the occurrence of the SLC26A4 variant and postsurgical audiometric thresholds and parents' evaluation of aural/oral performance of children (PEACH) scores. On the other hand, the SLC26A4 variant increased presurgical median audiometric thresholds (p = 0.01), particularly at 500 to 2000 Hz. CONCLUSION: The SLC26A4 c.706C>G (p.Leu236Val) variant is a frequent cause of congenital hearing impairment in Filipinos and is associated with bilateral EVA and increased presurgical audiometric thresholds, but does not adversely affect post-implant outcomes.


Subject(s)
Cochlear Implantation , Cochlear Implants , Hearing Loss/genetics , Mutation , Sulfate Transporters/genetics , Adolescent , Alleles , Child , Child, Preschool , Exons , Female , Gene Frequency , Hearing Loss/surgery , Humans , Infant , Male , Philippines
2.
Infect Dis Poverty ; 5(1): 97, 2016 Nov 01.
Article in English | MEDLINE | ID: mdl-27799062

ABSTRACT

BACKGROUND: Previously rare A2ML1 variants were identified to confer otitis media susceptibility in an indigenous Filipino community and in otitis-prone US children. The goal of this study is to describe differences in the middle ear microbiome between carriers and non-carriers of an A2ML1 duplication variant that increases risk for chronic otitis media among indigenous Filipinos with poor health care access. METHODS: Ear swabs were obtained from 16 indigenous Filipino individuals with chronic otitis media, of whom 11 carry the A2ML1 duplication variant. Ear swabs were submitted for 16S rRNA gene sequencing. RESULTS: Genotype-based differences in microbial richness, structure, and composition were identified, but were not statistically significant. Taxonomic analysis revealed that the relative abundance of the phyla Fusobacteria and Bacteroidetes, and genus Fusobacterium were nominally increased in carriers compared to non-carriers, but were non-significant after correction for multiple testing. We also detected rare bacteria including Oligella that was reported only once in the middle ear. CONCLUSIONS: These findings suggest that A2ML1-related otitis media susceptibility may be mediated by changes in the middle ear microbiome. Knowledge of middle ear microbial profiles according to genetic background can be potentially useful for therapeutic and prophylactic interventions for otitis media and can guide public health interventions towards decreasing otitis media prevalence within the indigenous Filipino community.


Subject(s)
DNA, Bacterial/genetics , Ear, Middle/microbiology , Genes, Duplicate/genetics , Microbiota , Otitis Media/genetics , RNA, Ribosomal, 16S/genetics , alpha-Macroglobulins/genetics , Adolescent , Child , Child, Preschool , Female , Humans , Male , Otitis Media/microbiology , Philippines , Population Groups , Sequence Analysis, DNA , Young Adult , alpha-Macroglobulins/metabolism
3.
Otolaryngol Head Neck Surg ; 155(5): 856-862, 2016 11.
Article in English | MEDLINE | ID: mdl-27484237

ABSTRACT

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.


Subject(s)
Environmental Exposure/adverse effects , Otitis Media/epidemiology , Otitis Media/genetics , alpha-Macroglobulins/genetics , Adolescent , Adult , Child , Child, Preschool , Cross-Sectional Studies , Female , Genetic Predisposition to Disease , Genotype , Humans , Male , Microbiota , Otitis Media/microbiology , Otoscopy , Philippines/epidemiology , Prevalence , Risk Factors
4.
Nat Genet ; 47(8): 917-20, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26121085

ABSTRACT

A duplication variant within the middle ear-specific gene A2ML1 cosegregates with otitis media in an indigenous Filipino pedigree (LOD score = 7.5 at reduced penetrance) and lies within a founder haplotype that is also shared by 3 otitis-prone European-American and Hispanic-American children but is absent in non-otitis-prone children and >62,000 next-generation sequences. We identified seven additional A2ML1 variants in six otitis-prone children. Collectively, our studies support a role for A2ML1 in the pathophysiology of otitis media.


Subject(s)
Gene Duplication , Genetic Predisposition to Disease/genetics , Otitis Media/genetics , alpha-Macroglobulins/genetics , Animals , Base Sequence , Child , Cochlea/metabolism , Cochlea/pathology , Exome/genetics , Family Health , Female , Gene Frequency , Genotype , Haplotypes , Humans , Male , Mice, Inbred C57BL , Models, Molecular , Otitis Media/pathology , Pedigree , Principal Component Analysis , Protein Conformation , Sequence Analysis, DNA , alpha-Macroglobulins/chemistry
5.
Acta Medica Philippina ; : 39-45, 2010.
Article in English | WPRIM (Western Pacific) | ID: wpr-632917

ABSTRACT

OBJECTIVES:To determine the agreement between 1) ear examination findings of the otorhinolaryngologist using an otoscope and trained elementary school nurses using a penlight, 2) hearing screening findings of the otorhinolaryngologist and elementary school nurses, both using the Philippine National Ear Institute (PNEI) Method of 512 Hz Tuning Fork Test (TFT) and 3) PNEI Method of 512 Hz TFT findings and screening audiometry findings.METHODS:In this continuing study, nurses residing in the venue of the study, and previously trained in ear examination using a penlight and hearing screening using the PNEI 512 Hz TFT, conducted these in school children who attended the hearing screening and medical mission. Otoscopy, PNEI Method of 512 Hz TFT, and screening audiometry were then conducted on the children by the otolaryngologist. The nurses and the otolaryngologist performed independent and blinded assessments.RESULTS:Eighteen nurses and ninety children participated in the study. Data subjected to Kappa statistics showed good agreement between nurses and otorhinolaryngologist's findings in the examination of the external canal and tympanic membrane and in PNEI Method of 512 Hz TFTs, and between the PNEI Method of 512 Hz TFT and screening audiometry.CONCLUSION:PNEI methods of penlight ear examination and 512 Hz TFT may be effective tools for early detection of common ear conditions and hearing screening in Filipino school children. These may be conducted in the school setting not only by otorhinolaryngologists but also by adequately trained school nurses.


Subject(s)
Humans , Male , Female , Middle Aged , Adult , Young Adult , Adolescent , Child , Child , Humans , Diagnosis , Nurses , Hearing , Audiometry , Ear Diseases , Early Diagnosis , Otolaryngologists , Otoscopes , Otoscopy , Philippines , Religious Missions , Schools , Tympanic Membrane , Hearing Tests
6.
Article in English | MEDLINE | ID: mdl-17539266

ABSTRACT

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.


Subject(s)
Education , Hearing Loss/diagnosis , Hearing Tests/methods , Mass Screening/methods , Otolaryngology/education , School Nursing/education , Clinical Competence , Data Collection , Humans , Philippines
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