2010
DOI: 10.1159/000319310
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Role of Genetic and Acquired Prothrombotic Risk Factors in Genesis of Sudden Sensorineural Hearing Loss

Abstract: The methylenetetrahydrofolate reductase C677T mutation, factor V G1691A (factor V Leiden) mutation, prothrombin G20210A mutation and 8 other laboratory values associated with increased thrombotic risk were analyzed in 40 patients with sudden sensorineural hearing loss (SSHL). The results were compared with those obtained from 120 controls not affected by SSHL. We found a statistically significant higher frequency of hyperhomocysteinemia in the SSHL group compared with controls, and that this was also associate… Show more

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Cited by 29 publications
(28 citation statements)
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“…These findings support the hypothesis of a systemic reaction in these patients that is not only limited to the vestibular organ and supports the idea of a vascular component of the disease, which is similar to what is observed in sudden sensorineural hearing loss [51]. …”
Section: Vascular Theorysupporting
confidence: 87%
“…These findings support the hypothesis of a systemic reaction in these patients that is not only limited to the vestibular organ and supports the idea of a vascular component of the disease, which is similar to what is observed in sudden sensorineural hearing loss [51]. …”
Section: Vascular Theorysupporting
confidence: 87%
“…Many recent studies have explored the cause and pathogenesis of sSNHL, but most cases of sSNHL remain idiopathic. 12,13 This feature indicates a low possibility of definitive neuritis in patients with sSNHL. In a study of 46 patients with sSNHL, 3D-FLAIR MRI obtained precontrast and at 10 minutes after intravenous gadolinium injection showed significant signal-intensity ratio differences.…”
Section: Discussionmentioning
confidence: 97%
“…The etiology for sudden hearing loss has been implicated in some theoretical pathways such as viral infections [27], intracochlear membrane rupture [28,29], immunemediated inner ear disease [30], vascular events [31], thrombotic genetic and acquired factors such as C677T MTHFR, V Leiden G1G91A, prothrombin G20210A, platelet GIyIIIaA1/A2 gene mutations, homocysteinemia, cholesterolemia and fibrinogenemia and etc [32,33].…”
Section: Discussionmentioning
confidence: 99%