In April 2016 Manchester eScholar was replaced by the University of Manchester’s new Research Information Management System, Pure. In the autumn the University’s research outputs will be available to search and browse via a new Research Portal. Until then the University’s full publication record can be accessed via a temporary portal and the old eScholar content is available to search and browse via this archive.

Vascular Risk Factors in the Aetiology of Idiopathic Sudden Sensorineural Hearing Loss in Young Adults.

Freeman, Simon

[Thesis]. Manchester, UK: The University of Manchester; 2011.

Access to files

Abstract

Objective:To investigate the frequency of vascular risk factors in unilateral idiopathic sudden sensorineural hearing loss (ISSHL) in young adults.Materials and Methods:Twenty patients aged 18-50 years when suffering a unilateral ISSHL and 20 age and sex matched controls were examined with contrast-enhanced transcranial doppler to identify venous to arterial circulation shunts (v-aCS), flow mediated dilation of the brachial artery to identify endothelial dysfunction and blood tests for a thrombophilia screen, full blood count, fasting plasma lipids, p-selectin and soluble glycoprotein V.Results:There were no significant differences between cases and controls for any of the investigations performed. There was no difference at all between the larger (“significant” or “major”) v-aCS and ISSHL (25% vs 25%). There was a limited association for “small” v-aCS with ISSHL (35% vs 25%; p=0.77); between the presence of v-aCS and severity of hearing loss (no v-aCS 49.0+/- 26 dBHL vs v-aCS 73.4 +/- 34dBHL, p=0.11); for endothelial dysfunction with ISSHL (5.9 +/- 3.2% vs 7.2 +/- 3.2%; p=0.32); and for platelet hypereactivity with ISSHL (glycoprotein V: 67.0+/-22.3ng/ml vs 64.2+/-21.5ng/ml, p=0.605; p-selectin: 81.7+/-40.2ng/ml vs 75.8+/-45.6ng/ml, p=0.590). Only 1 case had an inherited thrombophilia compared with 2 controls. No cases had positive antiphospholipid antibodies. High fibrinogen levels were more prevalent in cases: two cases and one control had hyperfibrinogenaemia with a further 5 cases and 4 controls in the upper quartile range. Hyperlipidaemia was more prevalent in controls.Conclusions:Paradoxical embolism and venous thrombosis are unlikely to be important causes of unilateral ISSHL in young adults. Mildly raised cardiovascular arterial risk factors such as endothelial dysfunction, hyperfibrinogenaemia and p-selectin suggest a possible vascular dysfunction in these patients that may warrant further study. The cause of ISSHL remains a mystery.

Bibliographic metadata

Type of resource:
Content type:
Form of thesis:
Type of submission:
Degree type:
Master of Philosophy
Degree programme:
MPhil Medicine (Biomedicine)
Publication date:
Location:
Manchester, UK
Total pages:
71
Abstract:
Objective:To investigate the frequency of vascular risk factors in unilateral idiopathic sudden sensorineural hearing loss (ISSHL) in young adults.Materials and Methods:Twenty patients aged 18-50 years when suffering a unilateral ISSHL and 20 age and sex matched controls were examined with contrast-enhanced transcranial doppler to identify venous to arterial circulation shunts (v-aCS), flow mediated dilation of the brachial artery to identify endothelial dysfunction and blood tests for a thrombophilia screen, full blood count, fasting plasma lipids, p-selectin and soluble glycoprotein V.Results:There were no significant differences between cases and controls for any of the investigations performed. There was no difference at all between the larger (“significant” or “major”) v-aCS and ISSHL (25% vs 25%). There was a limited association for “small” v-aCS with ISSHL (35% vs 25%; p=0.77); between the presence of v-aCS and severity of hearing loss (no v-aCS 49.0+/- 26 dBHL vs v-aCS 73.4 +/- 34dBHL, p=0.11); for endothelial dysfunction with ISSHL (5.9 +/- 3.2% vs 7.2 +/- 3.2%; p=0.32); and for platelet hypereactivity with ISSHL (glycoprotein V: 67.0+/-22.3ng/ml vs 64.2+/-21.5ng/ml, p=0.605; p-selectin: 81.7+/-40.2ng/ml vs 75.8+/-45.6ng/ml, p=0.590). Only 1 case had an inherited thrombophilia compared with 2 controls. No cases had positive antiphospholipid antibodies. High fibrinogen levels were more prevalent in cases: two cases and one control had hyperfibrinogenaemia with a further 5 cases and 4 controls in the upper quartile range. Hyperlipidaemia was more prevalent in controls.Conclusions:Paradoxical embolism and venous thrombosis are unlikely to be important causes of unilateral ISSHL in young adults. Mildly raised cardiovascular arterial risk factors such as endothelial dysfunction, hyperfibrinogenaemia and p-selectin suggest a possible vascular dysfunction in these patients that may warrant further study. The cause of ISSHL remains a mystery.
Thesis main supervisor(s):
Thesis co-supervisor(s):
Thesis advisor(s):
Language:
en

Institutional metadata

University researcher(s):

Record metadata

Manchester eScholar ID:
uk-ac-man-scw:123737
Created by:
Freeman, Simon
Created:
31st May, 2011, 20:26:46
Last modified by:
Freeman, Simon
Last modified:
21st June, 2011, 12:28:26

Can we help?

The library chat service will be available from 11am-3pm Monday to Friday (excluding Bank Holidays). You can also email your enquiry to us.