Angiotensin‐converting enzyme gene insertion/deletion polymorphism and family history in severe acne vulgaris
Journal of Cosmetic Dermatology • 2019
Publication Information
Authors
Neveen E. Sorour MD | Amany I. Mustafa MD | 31Naglaa F. Alhusseni MD |Eman Fawzy PhD | Aml G. Amer MBBCH
Keywords
acne vulgaris, angiotensin‐converting enzyme, gene polymorphism
Journal
Journal of Cosmetic Dermatology
Publisher
Wiley Periodicals, Inc.
Volume
18
Issue
Not Available
Pages
1992–1997
publication.type
International
Paper Link
Not Available
Supplementary Materials
Not Available
Abstract
Background: Acne vulgaris is an inflammatory disorder with a profound heteroge‐ nous aetio‐pathophysiology. ACE gene I/D polymorphism affects angiotensin‐con‐ verting enzyme activities that play a role in inflammation. However, there are no molecular genetic studies investigating the contribution of ACE gene insertion/dele‐ tion polymorphism in the genetic background of acne vulgaris.
Aims: The aim of this work was to reveal the relation between the ACE gene I/D poly‐ morphism and acne vulgaris development among a sample of patients.
Patients and Methods: This study included 100 acne vulgaris patients in addition to 120 matched control subjects. The ACE gene I/D polymorphism was analyzed using polymerase chain reaction (PCR).
Results: The distribution of DD, ID genotypes, and D allele showed higher frequency in AV patients than in controls (P < 0.001 for all). Moreover, positive family history and ACEI/D gene polymorphism (DD + ID genotypes) were considered as independ‐ ent predictors for severe acne grades (P ≤ 0.001 and 0.046, respectively) in multivari‐ ate analysis.
Conclusions: The current study results suggest that the D allele of the ACE I/D gene polymorphism might confer risk to AV among the studied patients. Moreover, ACE I/D gene polymorphism and positive family history were considered as independent predictors of severe AV.
Aims: The aim of this work was to reveal the relation between the ACE gene I/D poly‐ morphism and acne vulgaris development among a sample of patients.
Patients and Methods: This study included 100 acne vulgaris patients in addition to 120 matched control subjects. The ACE gene I/D polymorphism was analyzed using polymerase chain reaction (PCR).
Results: The distribution of DD, ID genotypes, and D allele showed higher frequency in AV patients than in controls (P < 0.001 for all). Moreover, positive family history and ACEI/D gene polymorphism (DD + ID genotypes) were considered as independ‐ ent predictors for severe acne grades (P ≤ 0.001 and 0.046, respectively) in multivari‐ ate analysis.
Conclusions: The current study results suggest that the D allele of the ACE I/D gene polymorphism might confer risk to AV among the studied patients. Moreover, ACE I/D gene polymorphism and positive family history were considered as independent predictors of severe AV.
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