ABC Family Arquivos Brasileiros de Cardiologia International Journal of Cardiovascular Sciences ABC Heart Failure & Cardiomyopathy ABC Imagem Cardiovascular
Português English
ABC Family
Português English
  • About
    • About ABC Family
    • Internal Regulation
    • Editorial Board
    • Brazilian Society of Cardiology (SBC)
  • Issues
  • SBC Guidelines
  • Content
    • Videos
    • Podcasts
    • News
  • About
    • About ABC Family
    • Internal Regulation
    • Editorial Board
    • Brazilian Society of Cardiology (SBC)
  • Issues
  • SBC Guidelines
  • Content
    • Videos
    • Podcasts
    • News

ABC Family

  • ABC Family
  • Arquivos Brasileiros de Cardiologia
  • International Journal of Cardiovascular Sciences
  • ABC Heart Failure & Cardiomyopathy
  • ABC Imagem Cardiovascular
Search in

No content found.

Journals
Ordering
Article types
Others

  1. Home
  2. Keyword: genetic markers
DD Genotype and Atherosclerosis in Overweight Menopausal Women
IJCS
Original Article

DD Genotype and Atherosclerosis in Overweight Menopausal Women

José Ramón Lanz-Luces et al. Fernando Alves Costa Luis Fernando Escobar Guzman Antonio Ricardo de Toledo Gagliardi … José Antonio Lanz-Luces José Daniel Lanz-Souquett Leandro Menezes Alves da Costa

Abstract

Background

Sex-specific pathology of coronary artery disease (CAD) has not been recognized. Women with obstructive or nonobstructive CAD associated with traditional risk factors have similar events; no studies have explored both populations in association with genetic markers.

Objective

To evaluate the DD genotype in overweight menopausal women and its association with CAD and traditional risk factors.

Method

This cross-sectional study included 356 menopausal women who underwent coronary angiography as CAD assessment. The patients’ DNA was extracted and polymorphisms were detected with a single polymerase chain reaction assay. Two groups were formed based on luminal lesions (normal [n = 134] or pathological [n = 222]) with a cutoff value > 30%, considering overweight and age. The chi-square test, Student’s t-test, and multivariate logistic regression were performed as appropriate (p < 0.05) using the following variables: overweight, diabetes, hypertension, dyslipidemia, smoking status, sedentary lifestyle, and a family history of CAD.

Results

The mean age of the sample was 63 8 years, and the mean BMI was 28 5 kg/m2. The DD genotype was slightly more prevalent in the pathological group (30.2% vs. 21.6%, p = 0.079), but this significantly changed when BMI > 25 was considered (33% vs. 18%, p = 0.012). In multivariate analysis with two threshold levels (> 50 and > 60 years), diabetes was significantly associated with CAD in both models (p = 0.021 vs. 0.009) but the genotype was only associated with younger age (p = 0.034).

Conclusion

These data support an association between atherosclerosis and the renin–angiotensin system in overweight menopausal women that is dependent on the age at which the ischemic event occurs.

  • Coronary Artery Disease
  • DD Genotype
  • genetic markers
  • Menopause
  • Overweight
Read Full Article
Creative Commons Attribution (CC BY) Creative Commons license
16/07/2021 DOI: 10.36660/ijcs.20200400 Views 2
ABC
Editorial

New Markers of Carotid Thickening in Hypertension

Rui Póvoa

Arterial hypertension was considered an important cardiovascular risk factor only after the Framingham studies, as it was believed that it was a necessary “good” for good tissue perfusion. These emblematic long-term cohort studies about the cardiovascular system brought data that allowed the evaluation of the interaction with several other diseases, such as dyslipidemias and diabetes, for the atheromatous plaque formation, which is the initial step for cardiovascular complications. A time when clinical examination was essential to detect markers of atherosclerotic disease.

However, with the evolution of knowledge, clinical biological markers were no longer sufficient to predict risk, as we increasingly need to articulate preventive measures as early as possible, for more effective treatment and better prevention. Additionally, the interaction between the environment, with all its risk factors and genetics proved to be interactive and of crucial importance in the development of the atherosclerotic plaque. Regarding hypertension, the genetic component with an estimated inheritance of 15-40% became clear, so much so that the brothers have a risk agreement rate for the disease ranging from 1.2 to 1.7.,

[…]

  • genetic markers
  • Hypertension/epidemiology
  • Monocytes
  • mRNA, Carotid Intima-Media Thickness
Read Full Article
Creative Commons Attribution (CC BY) Creative Commons license
03/02/2021 DOI: 10.36660/abc.20201335 Views 1
22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype
ABC
Artigo Original

22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype

Sintia Iole Nogueira Belangero et al. Fernanda T.S. Bellucco Leslie Domenici Kulikowski Denise M. Christofolini … Mirlene C. S. P. Cernach Maria Isabel Melaragno

BACKGROUND: The 22q11.2 deletion syndrome is the most frequent human microdeletion syndrome. The phenotype is highly variable, being characterized by conotruncal heart defect, facial dysmorphisms, velopharyngeal insufficiency, learning difficulties and mental retardation. OBJECTIVE: The objective of this study was to investigate the frequency of deletion 22q11.2 in a Brazilian sample of individuals with isolated conotruncal heart defect and 22q11.2 deletion syndrome phenotype. METHODS: Twenty-nine patients were studied by classical cytogenetics, by fluorescence in situ hybridization (FISH), and by molecular techniques. RESULTS: Cytogenetic analysis by G-banding revealed a normal karyotype in all patients except one who presented a 47,XX,+idic(22)(q11.2) karyotype. Using molecular techniques, a deletion was observed in 25% of the patients, all exhibiting a 22q11.2 deletion syndrome phenotype. In none of the cases the deletion was inherited from the parents. The frequency of 22q11.2 deletion was higher in patients with the clinical spectrum of the 22q11.2 deletion syndrome than in patients with isolated conotruncal heart defect. CONCLUSION: Investigating the presence of the deletion and its correlation with the patients’ clinical data can help the patients and their families to have a better genetic counseling and more adequate clinical follow-up.

  • Chromosome deletion
  • genetic markers
  • Heart Defects, Congenital
  • Phenotype
Read Full Article
Creative Commons Attribution (CC BY) Creative Commons license
23/06/2009 DOI: 10.1590/S0066-782X2009000400010

How to cite this article

EndNote RIS

Electronic Document Format (Vancouver)

Lanz-Luces JR, Costa FA, Guzman LFE, Gagliardi ART, Lanz-Luces JA, Lanz-Souquett JD, Costa LMA, et al. DD Genotype and Atherosclerosis in Overweight Menopausal Women. International Journal of Cardiovascular Sciences 2021;34(4):411-9.

Electronic Document Format (ABNT)

Lanz-Luces, José Ramón; Costa, Fernando Alves; Guzman, Luis Fernando Escobar; Gagliardi, Antonio Ricardo de Toledo; Lanz-Luces, José Antonio; Lanz-Souquett, José Daniel; Costa, Leandro Menezes Alves da. DD Genotype and Atherosclerosis in Overweight Menopausal Women. International Journal of Cardiovascular Sciences, v. 34, n. 4, p. 411-419, Jul. 2021.

Electronic Document Format (APA)

Lanz-Luces, J. R., Costa, F. A., Guzman, L. F. E., Gagliardi, A. R. T., Lanz-Luces, J. A., Lanz-Souquett, J. D., & Costa, L. M. A. (2021). DD Genotype and Atherosclerosis in Overweight Menopausal Women. International Journal of Cardiovascular Sciences, 34(4), 411-419.

Electronic Document Format (ISO)

Lanz-Luces, José Ramón and Costa, Fernando Alves and Guzman, Luis Fernando Escobar and Gagliardi, Antonio Ricardo de Toledo and Lanz-Luces, José Antonio and Lanz-Souquett, José Daniel and Costa, Leandro Menezes Alves da. DD Genotype and Atherosclerosis in Overweight Menopausal Women. International Journal of Cardiovascular Sciences [online]. 2021, vol. 34, n. 4, [cited 2026-10-14], pp. 411-419. Available from: <https://journals.cardiol.br/en/article/dd-genotype-and-atherosclerosis-in-overweight-menopausal-women/>. ISSN 2359-4802

EndNote RIS

Electronic Document Format (Vancouver)

Póvoa R. New Markers of Carotid Thickening in Hypertension. Arquivos Brasileiros de Cardiologia 2021;116(1):66-7.

Electronic Document Format (ABNT)

Póvoa, Rui. New Markers of Carotid Thickening in Hypertension. Arquivos Brasileiros de Cardiologia, v. 116, n. 1, p. 66-67, Feb. 2021.

Electronic Document Format (APA)

Póvoa, R. (2021). New Markers of Carotid Thickening in Hypertension. Arquivos Brasileiros de Cardiologia, 116(1), 66-67.

Electronic Document Format (ISO)

Póvoa, Rui. New Markers of Carotid Thickening in Hypertension. Arquivos Brasileiros de Cardiologia [online]. 2021, vol. 116, n. 1, [cited 2026-10-14], pp. 66-67. Available from: <https://journals.cardiol.br/en/article/new-markers-of-carotid-thickening-in-hypertension/>. ISSN 0066-782X

EndNote RIS

Electronic Document Format (Vancouver)

Belangero SIN, Bellucco FT, Kulikowski LD, Christofolini DM, Cernach MCSP, Melaragno MI. 22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype. Arquivos Brasileiros de Cardiologia 2009;92(4):307-11.

Electronic Document Format (ABNT)

Belangero, Sintia Iole Nogueira; Bellucco, Fernanda T.S.; Kulikowski, Leslie Domenici; Christofolini, Denise M.; Cernach, Mirlene C. S. P.; Melaragno, Maria Isabel. 22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype. Arquivos Brasileiros de Cardiologia, v. 92, n. 4, p. 307-311, Jun. 2009.

Electronic Document Format (APA)

Belangero, S. I. N., Bellucco, F. T., Kulikowski, L. D., Christofolini, D. M., Cernach, M. C. S. P., & Melaragno, M. I. (2009). 22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype. Arquivos Brasileiros de Cardiologia, 92(4), 307-311.

Electronic Document Format (ISO)

Belangero, Sintia Iole Nogueira and Bellucco, Fernanda T.S. and Kulikowski, Leslie Domenici and Christofolini, Denise M. and Cernach, Mirlene C. S. P. and Melaragno, Maria Isabel. 22q11.2 deletion in patients with conotruncal heart defect and del22q syndrome phenotype. Arquivos Brasileiros de Cardiologia [online]. 2009, vol. 92, n. 4, [cited 2026-10-14], pp. 307-311. Available from: <https://journals.cardiol.br/en/article/22q11-2-deletion-in-patients-with-conotruncal-heart-defect-and-del22q-syndrome-phenotype/>. ISSN 0066-782X

  • About ABC Family
  • Internal Regulation
  • Editorial Board
  • Brazilian Society of Cardiology (SBC)

Issues

SBC Guidelines

  • Videos
  • Podcasts
  • News