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Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population

BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disorder with several clinical presentations. This study was undertaken in the Azeri Turkish population in Iran, to investigate gender differences in the age at onset and diagnosis, age of death, and duration of illness of CF. METHODS: The d...

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Autores principales: Vahedi, Leila, Jabarpoor-Bonyadi, Morteza, Ghojazadeh, Morteza, Vahedi, Amir, Rafeey, Mandana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Tuberculosis and Respiratory Diseases 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077730/
https://www.ncbi.nlm.nih.gov/pubmed/27790278
http://dx.doi.org/10.4046/trd.2016.79.4.267
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author Vahedi, Leila
Jabarpoor-Bonyadi, Morteza
Ghojazadeh, Morteza
Vahedi, Amir
Rafeey, Mandana
author_facet Vahedi, Leila
Jabarpoor-Bonyadi, Morteza
Ghojazadeh, Morteza
Vahedi, Amir
Rafeey, Mandana
author_sort Vahedi, Leila
collection PubMed
description BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disorder with several clinical presentations. This study was undertaken in the Azeri Turkish population in Iran, to investigate gender differences in the age at onset and diagnosis, age of death, and duration of illness of CF. METHODS: The data of 331 CF patients from 2001 to 2015 was surveyed. Parameters including age, sex, ΔF508 mutation, age at onset, age at diagnosis, age of death and clinical presentations were evaluated for both sexes, using descriptive analysis. The association of gender with these variables was studied using logistic regression, chi-square test and Mann-Whitney U test by SPSS version 18. Odds ratio with a confidence interval of 95% and p≤0.05 was considered statistically significant. RESULTS: The study included 191 males (57.7%) and 140 females (42.3%), all showing statistically significant difference (p<0.001). Age duration differed between genders. Male and female patients were further under 9 and 4 years, respectively. The occurrence of ΔF508 mutation was 0.51 times more in females than in males. Age, diagnosis and sex were closely associated: males were diagnosed at a significantly later age than females (p=0.05). While this compression performed based on clinical presentations, males with respiratory disease had a later median age at diagnosis than females at lifespan (p=0.001). The risk of infertility in males was approximately two times greater than in females (p=0.02). CONCLUSION: These findings indicate gender differences in CF patients. Future studies are needed to establish other differences and evaluate the causes for the gender variations.
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spelling pubmed-50777302016-10-27 Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population Vahedi, Leila Jabarpoor-Bonyadi, Morteza Ghojazadeh, Morteza Vahedi, Amir Rafeey, Mandana Tuberc Respir Dis (Seoul) Original Article BACKGROUND: Cystic fibrosis (CF) is an autosomal recessive disorder with several clinical presentations. This study was undertaken in the Azeri Turkish population in Iran, to investigate gender differences in the age at onset and diagnosis, age of death, and duration of illness of CF. METHODS: The data of 331 CF patients from 2001 to 2015 was surveyed. Parameters including age, sex, ΔF508 mutation, age at onset, age at diagnosis, age of death and clinical presentations were evaluated for both sexes, using descriptive analysis. The association of gender with these variables was studied using logistic regression, chi-square test and Mann-Whitney U test by SPSS version 18. Odds ratio with a confidence interval of 95% and p≤0.05 was considered statistically significant. RESULTS: The study included 191 males (57.7%) and 140 females (42.3%), all showing statistically significant difference (p<0.001). Age duration differed between genders. Male and female patients were further under 9 and 4 years, respectively. The occurrence of ΔF508 mutation was 0.51 times more in females than in males. Age, diagnosis and sex were closely associated: males were diagnosed at a significantly later age than females (p=0.05). While this compression performed based on clinical presentations, males with respiratory disease had a later median age at diagnosis than females at lifespan (p=0.001). The risk of infertility in males was approximately two times greater than in females (p=0.02). CONCLUSION: These findings indicate gender differences in CF patients. Future studies are needed to establish other differences and evaluate the causes for the gender variations. The Korean Academy of Tuberculosis and Respiratory Diseases 2016-10 2016-10-05 /pmc/articles/PMC5077730/ /pubmed/27790278 http://dx.doi.org/10.4046/trd.2016.79.4.267 Text en Copyright©2016. The Korean Academy of Tuberculosis and Respiratory Diseases. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Original Article
Vahedi, Leila
Jabarpoor-Bonyadi, Morteza
Ghojazadeh, Morteza
Vahedi, Amir
Rafeey, Mandana
Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population
title Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population
title_full Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population
title_fullStr Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population
title_full_unstemmed Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population
title_short Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population
title_sort gender differences in clinical presentations of cystic fibrosis patients in azeri turkish population
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5077730/
https://www.ncbi.nlm.nih.gov/pubmed/27790278
http://dx.doi.org/10.4046/trd.2016.79.4.267
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