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The role of stress in the pathogenesis of Alopecia Areata: an objective assessment via hair cortisol level

BACKGROUND The pathogenesis of alopecia areata (AA) is poorly understood and multifactorial. There seems to be a strong belief, but conflicting evidence that stress causes or exacerbates AA. Hair cortisol measurement has been proven to be a reliable biological marker for cumulative prior stress. Thi...

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Main Author: Fick, Louis Jean
Other Authors: Khumalo, N P
Format: Thesis
Language:English
Published: Division of Dermatology 2019
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access_status_str Open Access
author Fick, Louis Jean
author2 Khumalo, N P
author_browse Fick, Louis Jean
Khumalo, N P
author_facet Khumalo, N P
Fick, Louis Jean
author_sort Fick, Louis Jean
collection Thesis
description BACKGROUND The pathogenesis of alopecia areata (AA) is poorly understood and multifactorial. There seems to be a strong belief, but conflicting evidence that stress causes or exacerbates AA. Hair cortisol measurement has been proven to be a reliable biological marker for cumulative prior stress. This measurement has up to date not been used in AA cases and may provide convincing evidence in the debate of stress and AA. OBJECTIVES: The primary aim of this project was to determine whether stress triggers onset of hair loss (OOHL) in AA by analysing the relationship between hair cortisol concentrations (HCCs) pre-OOHL in cases vs controls. Three secondary objectives were identified: • To determine whether there is a difference in HCC of lesional skin versus perilesional skin in cases. • To determine whether there is a correlation between disease activity (as determined by the hair pull test) and HCC. • To determine whether validated stress questionnaires correlate with HCC. METHODS A case control study was performed. Fourteen patients, fulfilling the inclusion criteria were recruited from the GSH and RXH outpatient departments. For each case consent was obtained, a data sheet was filled out, stress questionnaire(s) and two strands of hair, one lesional and one peri-lesional, were collected. Next, 14 healthy controls were recruited from whom a hair strand each was collected. On the hair samples, the position of onset of hair loss (OOHL) was determined by measuring one centimetre per month after OOHL, from the proximal (scalp near) end. Then three sections of three centimetres each were cut, two distally (representing the six-month period before OOHL) and one proximally (representing the three months post OOHL). In six of these cases a fourth or “current” section was obtained. This represented the section on the scalp and thus reflected current stress by measuring the most recent HCC. Next, the HCC’s of these sections were measured using the Salivary ELISA Cortisol kit©. An additional 44 cases, not meeting the inclusion criteria, were recruited for acquisition of additional stress questionnaires and data sheets. RESULTS HCC’s on average were higher in cases than in controls (before, during and after OOHL). The difference in HCC’s, however, was not statistically significant. There was no statistical difference between HCC’s in lesional and peri-lesional scalp samples. Distal section HCC’s were the highest. HCC’s correlated positively with disease activity, but was nonsignificant. There was no statistically significant relationship between HCC’s and stress questionnaires. CONCLUSIONS: Although the result was not statistically significant, likely due to small sample size, stress as measured by HCC may trigger OOHL in AA. HCC does not play a role in whether an area of the scalp is affected or not. Disease activity may be cause for stress. A larger study is warranted to validate these findings.
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language eng
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license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2019
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spelling oai:open.uct.ac.za:11427/29387 The role of stress in the pathogenesis of Alopecia Areata: an objective assessment via hair cortisol level Fick, Louis Jean Khumalo, N P Ngwanya, R. M. Van Wyk, J Dermatology BACKGROUND The pathogenesis of alopecia areata (AA) is poorly understood and multifactorial. There seems to be a strong belief, but conflicting evidence that stress causes or exacerbates AA. Hair cortisol measurement has been proven to be a reliable biological marker for cumulative prior stress. This measurement has up to date not been used in AA cases and may provide convincing evidence in the debate of stress and AA. OBJECTIVES: The primary aim of this project was to determine whether stress triggers onset of hair loss (OOHL) in AA by analysing the relationship between hair cortisol concentrations (HCCs) pre-OOHL in cases vs controls. Three secondary objectives were identified: • To determine whether there is a difference in HCC of lesional skin versus perilesional skin in cases. • To determine whether there is a correlation between disease activity (as determined by the hair pull test) and HCC. • To determine whether validated stress questionnaires correlate with HCC. METHODS A case control study was performed. Fourteen patients, fulfilling the inclusion criteria were recruited from the GSH and RXH outpatient departments. For each case consent was obtained, a data sheet was filled out, stress questionnaire(s) and two strands of hair, one lesional and one peri-lesional, were collected. Next, 14 healthy controls were recruited from whom a hair strand each was collected. On the hair samples, the position of onset of hair loss (OOHL) was determined by measuring one centimetre per month after OOHL, from the proximal (scalp near) end. Then three sections of three centimetres each were cut, two distally (representing the six-month period before OOHL) and one proximally (representing the three months post OOHL). In six of these cases a fourth or “current” section was obtained. This represented the section on the scalp and thus reflected current stress by measuring the most recent HCC. Next, the HCC’s of these sections were measured using the Salivary ELISA Cortisol kit©. An additional 44 cases, not meeting the inclusion criteria, were recruited for acquisition of additional stress questionnaires and data sheets. RESULTS HCC’s on average were higher in cases than in controls (before, during and after OOHL). The difference in HCC’s, however, was not statistically significant. There was no statistical difference between HCC’s in lesional and peri-lesional scalp samples. Distal section HCC’s were the highest. HCC’s correlated positively with disease activity, but was nonsignificant. There was no statistically significant relationship between HCC’s and stress questionnaires. CONCLUSIONS: Although the result was not statistically significant, likely due to small sample size, stress as measured by HCC may trigger OOHL in AA. HCC does not play a role in whether an area of the scalp is affected or not. Disease activity may be cause for stress. A larger study is warranted to validate these findings. 2019-02-06T13:12:01Z 2019-02-06T13:12:01Z 2018 2019-02-06T07:40:18Z Master Thesis Masters MMed http://hdl.handle.net/11427/29387 eng application/pdf Division of Dermatology Faculty of Health Sciences University of Cape Town
spellingShingle Dermatology
Fick, Louis Jean
The role of stress in the pathogenesis of Alopecia Areata: an objective assessment via hair cortisol level
thesis_degree_str Master's
title The role of stress in the pathogenesis of Alopecia Areata: an objective assessment via hair cortisol level
title_full The role of stress in the pathogenesis of Alopecia Areata: an objective assessment via hair cortisol level
title_fullStr The role of stress in the pathogenesis of Alopecia Areata: an objective assessment via hair cortisol level
title_full_unstemmed The role of stress in the pathogenesis of Alopecia Areata: an objective assessment via hair cortisol level
title_short The role of stress in the pathogenesis of Alopecia Areata: an objective assessment via hair cortisol level
title_sort role of stress in the pathogenesis of alopecia areata an objective assessment via hair cortisol level
topic Dermatology
url http://hdl.handle.net/11427/29387
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