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Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene

BACKGROUND: /aims: The role of angiotensin-converting enzyme (ACE) gene polymorphism in the development of obesity and hypertension in children has not been widely studied. We aimed to screen Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in the ACE gene. METHODS:...

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Autores principales: El-Kabbany, Zeinab A., Hamza, Rasha T., Shinkar, Dina M., Kamal, Tarek M., Abdelmageed, Reham I., Said, Mina S., Abdel-Hamid, Mennatullah I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: King Faisal Specialist Hospital and Research Centre 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603068/
https://www.ncbi.nlm.nih.gov/pubmed/31304224
http://dx.doi.org/10.1016/j.ijpam.2019.02.008
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author El-Kabbany, Zeinab A.
Hamza, Rasha T.
Shinkar, Dina M.
Kamal, Tarek M.
Abdelmageed, Reham I.
Said, Mina S.
Abdel-Hamid, Mennatullah I.
author_facet El-Kabbany, Zeinab A.
Hamza, Rasha T.
Shinkar, Dina M.
Kamal, Tarek M.
Abdelmageed, Reham I.
Said, Mina S.
Abdel-Hamid, Mennatullah I.
author_sort El-Kabbany, Zeinab A.
collection PubMed
description BACKGROUND: /aims: The role of angiotensin-converting enzyme (ACE) gene polymorphism in the development of obesity and hypertension in children has not been widely studied. We aimed to screen Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in the ACE gene. METHODS: One hundred forty-two children and adolescents were included (70 with simple obesity and 72 controls). Blood pressure was measured, and anthropometric parameters were assessed in all included children and adolescents. Fasting lipid profile, fasting glucose, and insulin were measured. DNA extraction and ACE I/D polymorphism genotyping were also performed. RESULTS: Obese children had a higher frequency of DD genotype (30% in obese versus 11.1% in controls, P = .01) and D alleles (61.8% in obese versus 48.6% in controls, P = .01). Obese children with hypertension and prehypertension had higher frequency of DD genotype than II genotype and higher D alleles than I alleles. DD genotype and D allele were independently associated with hypertension (OR: 9.86 and 11.57, respectively, P < .001), while dyslipidemia and insulin resistance were not associated with the ACE I/D gene polymorphism. CONCLUSION: DD genotype and D-allele of the ACE gene polymorphism were associated with obesity and with hypertension and pre-hypertension in Egyptian children.
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spelling pubmed-66030682019-07-12 Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene El-Kabbany, Zeinab A. Hamza, Rasha T. Shinkar, Dina M. Kamal, Tarek M. Abdelmageed, Reham I. Said, Mina S. Abdel-Hamid, Mennatullah I. Int J Pediatr Adolesc Med Original Research Article BACKGROUND: /aims: The role of angiotensin-converting enzyme (ACE) gene polymorphism in the development of obesity and hypertension in children has not been widely studied. We aimed to screen Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in the ACE gene. METHODS: One hundred forty-two children and adolescents were included (70 with simple obesity and 72 controls). Blood pressure was measured, and anthropometric parameters were assessed in all included children and adolescents. Fasting lipid profile, fasting glucose, and insulin were measured. DNA extraction and ACE I/D polymorphism genotyping were also performed. RESULTS: Obese children had a higher frequency of DD genotype (30% in obese versus 11.1% in controls, P = .01) and D alleles (61.8% in obese versus 48.6% in controls, P = .01). Obese children with hypertension and prehypertension had higher frequency of DD genotype than II genotype and higher D alleles than I alleles. DD genotype and D allele were independently associated with hypertension (OR: 9.86 and 11.57, respectively, P < .001), while dyslipidemia and insulin resistance were not associated with the ACE I/D gene polymorphism. CONCLUSION: DD genotype and D-allele of the ACE gene polymorphism were associated with obesity and with hypertension and pre-hypertension in Egyptian children. King Faisal Specialist Hospital and Research Centre 2019-03 2019-02-25 /pmc/articles/PMC6603068/ /pubmed/31304224 http://dx.doi.org/10.1016/j.ijpam.2019.02.008 Text en © 2019 Publishing services provided by Elsevier B.V. on behalf of King Faisal Specialist Hospital & Research Centre (General Organization), Saudi Arabia. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
El-Kabbany, Zeinab A.
Hamza, Rasha T.
Shinkar, Dina M.
Kamal, Tarek M.
Abdelmageed, Reham I.
Said, Mina S.
Abdel-Hamid, Mennatullah I.
Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene
title Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene
title_full Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene
title_fullStr Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene
title_full_unstemmed Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene
title_short Screening of Egyptian obese children and adolescents for insertion/deletion (I/D) polymorphism in angiotensin-converting enzyme gene
title_sort screening of egyptian obese children and adolescents for insertion/deletion (i/d) polymorphism in angiotensin-converting enzyme gene
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6603068/
https://www.ncbi.nlm.nih.gov/pubmed/31304224
http://dx.doi.org/10.1016/j.ijpam.2019.02.008
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