Evidence map›Paper›PMID 41013249›Full record

ArticleBMC cardiovascular disorders2025

Investigation of the characteristics of LDLR gene rs688 polymorphism and its association with dyslipidemia in patients at high to very high cardiovascular risk.

Nguyen Thi Thu Sen, Pham Thi Ngoc Nga, Ngo Hoang Toan, Nguyen Trung Kien

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Article in BMC cardiovascular disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Nguyen Thi Thu SenDepartment of Internal Medicine, Faculty of Medicine, Can Tho University of Medicine and Pharmacy, Can Tho , 90000, Vietnam.
Pham Thi Ngoc NgaDepartment of Biology and Genetics, Faculty of Basic Sciences, Can Tho University of Medicine and Pharmacy, Can Tho, 90000, Vietnam.
Ngo Hoang ToanDepartment of Internal Medicine, Faculty of Medicine, Can Tho University of Medicine and Pharmacy, Can Tho , 90000, Vietnam.
Nguyen Trung KienDepartment of Physiology, Faculty of Medicine, Can Tho University of Medicine and Pharmacy, Can Tho, 90000, Vietnam. ntkien@ctump.edu.vn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe rs688 polymorphism in the LDLR gene has been linked to lipid profile alterations, yet its impact in patients at high to very high cardiovascular risk remains unclear.

objectivesTo investigate the association between the LDLR rs688 polymorphism and dyslipidemia in high to very high cardiovascular risk patients.

methodsThis cross-sectional study included patients classified as high or very high cardiovascular risk and matched controls at Can Tho University of Medicine and Pharmacy Hospital. Blood lipid profiles and LDLR rs688 genotyping were assessed using Realtime-PCR.

resultsAmong 80 patients (mean age 62.36 ± 10.49 years; 35.0% male), CT and TT genotypes were more frequent compared to controls (37.5% vs. 30.6%, and 15.0% vs. 3.8%, respectively). The T allele was also more prevalent (33.8% vs. 19.1%). Dyslipidemia was present in 68.8% of patients. T allele carriers had higher dyslipidemia rates (90.7% vs. 57.5%), higher LDLc (5.42 ± 1.51 mmol/L vs. 3.19 ± 1.37 mmol/L), and lower HDLc (0.70 ± 0.25 mmol/L vs. 1.03 ± 0.32 mmol/L) compared to C allele carriers. Multivariate analysis identified the T allele (OR = 14.18) and diabetes mellitus (OR = 4.85) as independent predictors of dyslipidemia.

conclusionThe LDLR rs688 T allele and diabetes mellitus independently increases dyslipidemia risk among patients at high to very high cardiovascular risk.

Indexed as

Cardiovascular DiseasesDyslipidemiasPolymorphism, Single NucleotideReceptors, LDLAgedBiomarkersCase-Control StudiesCross-Sectional StudiesFemaleGene FrequencyGenetic Association StudiesGenetic Predisposition to DiseaseHeart Disease Risk FactorsHumansLipidsMaleBiomarkersLDLR protein, humanLipidsReceptors, LDLCardiovascular riskDyslipidemiaLDLR rs688

Identifiers

PMID41013249
PMCPMC12465651

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.