Diverse phenotype of Ménière's disease associated with family history, thyroid disorder, migraine and associated disorders

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dc.contributor.author Pyykko, Ilmari
dc.contributor.author Gupta, Vinay
dc.contributor.author Zou, Jing
dc.contributor.author Vetkas, Artur
dc.contributor.author Manchaiah, Vinaya
dc.date.accessioned 2025-03-28T05:52:42Z
dc.date.available 2025-03-28T05:52:42Z
dc.date.issued 2024-10
dc.description.abstract OBJECTIVE: To better understand the clinical phenotype of Ménière's disease (MD), we examined family history, thyroid disorder, migraine, and associated disorders in complaints of people living with MD. METHOD: We designed the study as a retrospective and examined data gathered from 912 participants with MD. Their data were originally collected by the Finnish Ménière Federation (FMF). The survey data included individual case histories for environmental factors, comorbidities, disease-specific complaints, impact-related questions, cognitive complaints, health-related quality of life (HRQoL), and sense of coherence (SOC). RESULTS: We observed significant differences between those with and without sporadic occurrence, family history, thyroid disorder, and migraine-associated complaints. Family history explained 20% of variability in patient complaints. Patients with a family history of MD whose disease started at younger age experienced balance problems, more severe vertigo spells, more severe vestibular drop attacks (VDA), and less nausea, although they had good SOC. Thyroid disorder explained 14% of variability in patient complaints. MD patients with a thyroid disorder comorbidity suffered more often from constant dizziness, balance problems, greater impact of hearing problems, cognitive complaints, and poor HRQoL. Migraine explained 12% of variability in patients’ complaints and was associated with poor SOC and cognitive balance problems. MD patients with both thyroid disorder and migraine used antidepressants more often than other groups. Logistic regression analysis showed comorbidities of ischemic brain disorder (among 7.1%), kidney insufficiency (among 1.2%), and diabetes (among 7.3%) had statistically significant but restricted association with balance and gait problems, VDA, and reduced HRQoL. CONCLUSIONS: Family history of MD and thyroid disorder or migraine comorbidities in MD influence the complaint pattern and partially explain complex symptom profiles, including symptoms of cognitive problems. Confounders play a minimal role in complaint profile and impact of MD whereas comorbidities influence the complaint structure and partly explain the complex symptom profile in MD. en_US
dc.description.department Speech-Language Pathology and Audiology en_US
dc.description.sdg SDG-03:Good heatlh and well-being en_US
dc.description.sdg SDG-09: Industry, innovation and infrastructure en_US
dc.description.uri https://www.sciencedirect.com/journal/journal-of-otology en_US
dc.identifier.citation Pyykko, I., Vinay, Z., Jing, Vetkas, A. & Manchaiah, V. 2024, 'Diverse phenotype of Ménière's disease associated with family history, thyroid disorder, migraine and associated disorders', Journal of Otology, vol. 19, no. 4, pp. 185-192, doi: 10.1016/j.joto.2024.07.005. en_US
dc.identifier.issn 1672-2930 (print)
dc.identifier.issn 2524-1753 (online)
dc.identifier.other 10.1016/j.joto.2024.07.005
dc.identifier.uri http://hdl.handle.net/2263/101778
dc.language.iso en en_US
dc.publisher Elsevier en_US
dc.rights © 2024 PLA General Hospital Department of Otolaryngology Head and Neck Surgery. Production and hosting by Elsevier (Singapore) Pte Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies. This is an Open Access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). en_US
dc.subject Meniere’s disease en_US
dc.subject Migraine en_US
dc.subject Thyroid en_US
dc.subject Family history en_US
dc.subject Hereditary en_US
dc.subject SDG-03: Good health and well-being en_US
dc.subject SDG-09: Industry, innovation and infrastructure en_US
dc.title Diverse phenotype of Ménière's disease associated with family history, thyroid disorder, migraine and associated disorders en_US
dc.type Article en_US


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