Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association of rs662799 and rs5070 genetic polymorphisms with hypertriglyceridemia and atherogenic dyslipidemia in pediatric patients in Southeast Mexico.

Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis - 1 Jan 2000

Ovando Gómez Valeria, Zavaleta Muñiz Soraya Amalí, Ochoa-Díaz-López Héctor, Hernández Contreras José Armando Camilo, Irecta Nájera Cesar Antonio

Abstract excerpt

BACKGROUND AND AIMS: Triglycerides are the initiators of the metabolic changes that lead to atherogenic dyslipidemia (AD). The APOA5 and APOA1 genes are involved in the response and metabolism of serum lipids and lipoproteins, where single nucleotide polymorphisms (SNP) rs662799 (promoter region) and rs5070 (intronic region) have been associated with the susceptibility to dyslipidemia. Until now, few studies...

Read the complete abstract on PubMed

Topics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share this publication in a Topic to start or enrich a Post.

Share to Apolipoprotein A-V
Share to Atherosclerosis
Share to Child
Share to Dyslipidemias
Share to Gene Frequency
Share to Hypertriglyceridemia
Share to Mexico
Share to Triglycerides

Source

Identifiers

PMID: 35961839
DOI: 10.1016/j.arteri.2022.06.005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of rs662799 and rs5070 genetic polymorphisms with hypertriglyceridemia and atherogenic dyslipidemia in pediatric patients in Southeast Mexico.PMID 35961839Read ↗

APOA5 and APOA1 polymorphisms are associated with triglyceride levels in Mexican children.Semantic proximity Read ↗

Genetic Landscape of Pediatric Dyslipidemia in a Turkish Cohort: Insights From a Single-Center Experience.Semantic proximity Read ↗

Assessment of Pediatric Hypertriglyceridemia Etiology: Insights from Next-Generation Sequencing Panels and Identification of Novel Variants.Semantic proximity Read ↗

Genotypic and phenotypic features of dyslipidemia in a sample of pediatric patients in China.Semantic proximity Read ↗

Triglyceride-raising APOA5 genetic variants are associated with obesity and non-HDL-C in Chinese children and adolescents.Semantic proximity Read ↗

ACE, APOA5, and MTP Gene Polymorphisms Analysis in Relation to Triglyceride and Insulin Levels in Pediatric Patients.Semantic proximity Read ↗

Apolipoprotein A5-1131T>C polymorphism, but not APOE genotypes, increases susceptibility for dyslipidemia in children and adolescents.Semantic proximity Read ↗

Metabolic control, ApoE genotypes, and dyslipidemia in children, adolescents and young adults with type 1 diabetes.Semantic proximity Read ↗

Monogenic pediatric dyslipidemias: classification, genetics and clinical spectrum.Semantic proximity Read ↗

Frequency of rs1051338 and rs116928232 Variants in Individuals from Northwest Mexico.Semantic proximity Read ↗

Implication of the rs670 variant of APOA1 gene with lipid profile, serum adipokine levels and components of metabolic syndrome in adult obese subjects.Semantic proximity Read ↗

Contribution of genetic, biochemical and environmental factors on insulin resistance and obesity in Mexican young adults.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.