A genetic polymorphism in GCKR may be associated with low high-density lipoprotein cholesterol phenotype among Filipinos: A case-control study.
- Author:
Rody G. Sy
1
;
Jose B. Nevado, Jr.
2
;
Eddieson M. Gonzales
1
;
Adrian John P. Bejarin
2
,
3
;
Aimee Yvonne Criselle L. Aman
2
,
3
;
Elmer Jasper B. Llanes
1
;
Jose Donato A. Magno
1
;
Deborah Ignacia D. Ona
1
;
Felix Eduardo R. Punzalan
1
;
Paul Ferdinand M. Reganit
1
;
Lourdes Ella G. Santos
1
;
Richard Henry P. Tiongco II
1
;
Jaime Alfonso M. Aherrera
1
;
Lauro L. Abrahan IV
1
;
Charlene F. Agustin
1
;
Eva Maria C. Cutiongco - de la Paz
2
,
3
Author Information
- Publication Type:Journal Article
- Keywords: GCKR
- MeSH: Cardiovascular Diseases; Dyslipidemias; Genetics; Polymorphism, Single Nucleotide
- From: Acta Medica Philippina 2022;56(10):49-56
- CountryPhilippines
- Language:English
-
Abstract:
Background. Low levels of high-density lipoprotein cholesterol (HDL-c) is a well-recognized risk factor in the development of cardiovascular diseases. Associated gene variants for low HDL-c have already been demonstrated in various populations. Such associations have yet to be established among Filipinos who reportedly have a much higher prevalence of low HDL-c levels compared to other races.
Objective. To determine the association of selected genetic variants and clinical factors with low HDL-c phenotype in Filipinos.
Methods. An age- and sex-matched case-control study was conducted among adult Filipino participants with serum HDL-c concentration less than 35 mg/dL (n=61) and those with HDL-c levels of more than 40 mg/dL (n=116). Genotyping was done using DNA obtained from blood samples. Candidate variants were correlated with the low HDL-c phenotype using chi-squared test and conditional logistic regression analysis.
Results. Twelve single nucleotide polymorphisms (SNPs) were associated with low HDL-c phenotype among Filipinos with univariate regression analysis. The variant rs1260326 of glucokinase regulator (GCKR) (CT genotype: adjusted OR=5.17; p-value=0.007; TT genotype: adjusted OR=6.28; p-value=0.027) remained associated with low HDL-c phenotype, together with hypertension and elevated body mass index, after multiple regression analysis.
Conclusion. The variant rs1260326 near GCKR is associated with low HDL-c phenotype among Filipinos. Its role in the expression of low HDL-c phenotype should be further investigated prior to the development of possible clinical applications.
- Full text:2350-Article Text-29854-2-10-20220614.pdf