Genetic, lifestyle and metabolic factors contributing to cardiovascular disease in the Italian population: a literature review

C Ojeda-Granados, E Campisi, M Barchitta… - Frontiers in …, 2024 - frontiersin.org
Cardiovascular diseases (CVD) represent a major health problem worldwide. In Italy,
despite the decline in CVD mortality and disability-adjusted life years recently observed …

Effects of CDKN2B‐AS1 polymorphisms on the susceptibility to coronary heart disease

K Huang, J Zhong, Q Li, W Zhang… - Molecular genetics & …, 2019 - Wiley Online Library
Background Coronary heart disease (CHD) is one of the most severe cardiovascular
diseases. Cyclin‐dependent kinase inhibitor 2B antisense RNA 1 (CDKN2B‐AS1) is a …

[PDF][PDF] The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease.

ŞG Temel, MÇ Ergören - Anatolian Journal of Cardiology …, 2019 - jag.journalagent.com
Objective: Recent genome-wide association studies have established that polymorphisms
within CDKN2B-AS1 of chr9p21. 3 locus increased susceptibility to coronary artery disease …

Single nucleotide polymorphisms in long noncoding RNA, ANRIL, are not associated with severe periodontitis but with adverse cardiovascular events among patients …

S Schulz, L Seitter, K Werdan… - Journal of …, 2018 - Wiley Online Library
Background and Objective Biological plausibility of an association between severe
periodontitis and cardiovascular disease (CVD) has been proven. Genetic characteristics …

New findings in the roles of Cyclin-dependent Kinase inhibitors 2B Antisense RNA 1 (CDKN2B-AS1) rs1333049 G/C and rs4977574 A/G variants on the risk to …

W Yuan, W Zhang, W Zhang, ZB Ruan, L Zhu… - …, 2020 - Taylor & Francis
ABSTRACT The relationship between Cyclin-Dependent Kinase Inhibitors 2B Antisense
RNA 1 (CDKN2B-AS1) variants rs1333049 G/C and rs4977574 A/G and the risk of coronary …

Association between rs3088440 (G> A) polymorphism at 9p21. 3 locus with the occurrence and severity of coronary artery disease in an Iranian population

M Pourgholi, O Abazari, L Pourgholi… - Molecular Biology …, 2021 - Springer
Background Several genome-wide association studies showed that a series of genetic
variants located at the chromosome 9p21 locus are strongly associated with coronary artery …

Analysis of polymorphism rs1333049 (Located at 9P21. 3) in the white population of Western Siberia and associations with clinical and biochemical markers

E Shakhtshneider, P Orlov, S Semaev, D Ivanoshchuk… - Biomolecules, 2019 - mdpi.com
The 9p21. 3 chromosomal region is a marker of the risk of cardiovascular diseases. The aim
of this study was to analyze single-nucleotide polymorphism rs1333049 (chr9: 22125504) in …

Ассоциация вариантов генов АРОЕ, СЕТР и хромосомного региона 9Р21. 3 с ишемической болезнью сердца, инфарктом миокарда и острой сердечной …

СЕ Семаев, ЛВ Щербакова, ПС Орлов… - …, 2024 - ateroskleroz.elpub.ru
Аннотация Актуальной задачей для системы здравоохранения служит выявление
слоев населения, наиболее предрасположенных к сердечно-сосудистым …

[PDF][PDF] Genetics of coronary artery disease: State of the art in the last decade

CR Arce-Sandoval, L Zavala-Romero… - Clin Res, 2021 - researchgate.net
The study of coronary artery disease (CAD) has evolved throughout the years, specially
aiming at the identification of risk factors. Traditional risk factors include high cholesterol …

[PDF][PDF] КАРДИОЛОГИЯ/CARDIOLOGY

ДА Брусенцов, ПА Шестерня - research-journal.org
Аннотация Роль наследственной отягощенности в развитии ишемической болезни
сердца (ИБС) не вызывает сомнений. При этом механизмы реализации данного …