Literature DB >> 16936573

Conductive hearing loss in patients with active acromegaly.

Borivoj B Babic1, Milan S Petakov, Vojko B Djukic, Sanja I Ognjanovic, Nenad A Arsovic, Tatjana V Isailovic, Jovica D Milovanovic, Djuro Macut, Svetozar S Damjanovic.   

Abstract

OBJECTIVE: There have been rare conflicting results reported concerning possible higher frequency of hearing loss in acromegalic patients. Our goal was to determine whether there is higher frequency of conductive hearing loss in acromegalics and what may cause it if there is any. STUDY
DESIGN: Prospective study.
SETTING: Tertiary referral center. PATIENTS: Thirty previously untreated patients with acromegaly were compared with 20 age- and sex-matched healthy control subjects.
INTERVENTIONS: In all subjects: Otomicroscopy, tuning fork tests, audiometry tympanometry, cochleostapedial reflex, otoacoustic emissions. In acromegalics: endocrinologic assessment, MRI and if necessary, epipharyngoscopy. MAIN OUTCOME MEASURES: We searched for: 1) Signs of ossicle fixation: absence of stapedial reflex in the presence of normal tympanogram, conductive hearing loss, and absence of or grossly disturbed OAE; 2) Disturbances of middle ear ventilation: excessive negative pressure (tympanogram type C), or middle ear effusion (tympanogram type B).
RESULTS: The only statistically significant difference between untreated acromegalics and healthy subjects was the presence of middle ear ventilation problem: 7/30 acromegalics (23%) in comparison to none out of 20 healthy controls (0%), p = 0.033. The acromegalics with middle ear ventilation problem were significantly older, had longer duration of the disease, and lower mean growth hormone (GH) levels in comparison with acromegalics without this problem (51.6 +/- 1.7 vs. 44.4 +/- 2.5 years, 11.6 +/- 2.4 vs. 7.7 +/- 0.4 years, 21.68 +/- 4.89 vs. 49.98 +/- 12.54 microg/L respectively).
CONCLUSION: Patients with active acromegaly have more frequent middle ear ventilation problem than normal population, especially those with longer duration of the disease. Possible causes are discussed.

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Year:  2006        PMID: 16936573     DOI: 10.1097/01.mao.0000201429.57746.1b

Source DB:  PubMed          Journal:  Otol Neurotol        ISSN: 1531-7129            Impact factor:   2.311


  5 in total

1.  Auditory changes in acromegaly.

Authors:  S Tabur; H Korkmaz; E Baysal; E Hatipoglu; I Aytac; E Akarsu
Journal:  J Endocrinol Invest       Date:  2016-12-29       Impact factor: 4.256

2.  Thyroid hormone receptors control developmental maturation of the middle ear and the size of the ossicular bones.

Authors:  Emily A Cordas; Lily Ng; Arturo Hernandez; Masahiro Kaneshige; Sheue-Yann Cheng; Douglas Forrest
Journal:  Endocrinology       Date:  2012-01-17       Impact factor: 4.736

Review 3.  Challenges in the diagnosis and management of acromegaly: a focus on comorbidities.

Authors:  Alin Abreu; Alejandro Pinzón Tovar; Rafael Castellanos; Alex Valenzuela; Claudia Milena Gómez Giraldo; Alejandro Castellanos Pinedo; Doly Pantoja Guerrero; Carlos Alfonso Builes Barrera; Humberto Ignacio Franco; Antônio Ribeiro-Oliveira; Lucio Vilar; Raquel S Jallad; Felipe Gaia Duarte; Mônica Gadelha; Cesar Luiz Boguszewski; Julio Abucham; Luciana A Naves; Nina Rosa C Musolino; Maria Estela Justamante de Faria; Ciliana Rossato; Marcello D Bronstein
Journal:  Pituitary       Date:  2016-08       Impact factor: 4.107

Review 4.  Hearing Loss in Acromegaly - A Review.

Authors:  Liane Sousa Teixeira; Isabelle Braz de Oliveira Silva; Andre Luiz Lopes Sampaio; Carlos Augusto Pires de Oliveira; Fayez Bahamad Júnior
Journal:  Int Arch Otorhinolaryngol       Date:  2017-06-16

5.  Sensorineural hearing loss in acromegalic patients under treatment.

Authors:  Marcelo Alexandre Carvalho; Renan Magalhães Montenegro Júnior; Marcos Rabelo de Freitas; Lúcio Vilar; Alessandra Teixeira Bezerra de Mendonça; Renan Magalhães Montenegro
Journal:  Braz J Otorhinolaryngol       Date:  2012 Jul-Aug
  5 in total

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