Single Nucleotide Polymorphisms in Apolipoprotein B, Apolipoprotein E, and Methylenetetrahydrofolate Reductase Are Associated With Serum Lipid Levels in Northern Chilean Subjects. A Pilot Study

被引:5
|
作者
Galvez, Anita S. [1 ]
Ramirez, Hugo [1 ]
Placencia, Pablo [1 ]
Rojas, Claudio [1 ]
Urzua, Ximena [1 ]
Kalergis, Alexis M. [2 ,3 ]
Salazar, Luis A. [4 ]
Escobar-Vera, Jorge [1 ]
机构
[1] Univ Antofagasta, Fac Ciencias Salud, Dept Biomed, Lab Genet, Antofagasta, Chile
[2] Pontificia Univ Catolica Chile, Dept Genet Mol & Microbiol, Fac Ciencias Biol, Millennium Inst Immunol & Immunotherapy MIII, Santiago, Chile
[3] Pontificia Univ Catolica Chile, Fac Med, Dept Endocrinol, Santiago, Chile
[4] Univ La Frontera, Fac Med, Dept Ciencias Basicas, Ctr Biol Mol & Farmacogenet, Temuco, Chile
关键词
Lipid levels; genetic variants; Apo B; Apo E; MTHFR; polymorphism; DENSITY-LIPOPROTEIN CHOLESTEROL; CARDIOVASCULAR-DISEASE; MTHFR; 677C-GREATER-THAN-T; MYOCARDIAL-INFARCTION; C677T POLYMORPHISM; GENE POLYMORPHISMS; CHINESE PATIENTS; E GENOTYPE; HIGH-RISK; POPULATION;
D O I
10.3389/fgene.2021.640956
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Characterization of allelic variants is relevant to demonstrate associations among genetic background and susceptibility to develop cardiovascular diseases, which are the main cause of death in Chile. Association of APOB, APOE, and MTHFR polymorphisms with higher lipid levels and the risk of developing hypertension and cardiovascular diseases have been described. Thus, the aim of this study was to assess genotype distribution and relative allelic frequency of ApoB rs693, ApoE rs7412, ApoE rs429358, MTHFR rs1801131, and MTHFR rs1801133 allelic variants and their effects on lipid profile in young healthy men and women from Northern Chile. A group of 193 healthy subjects were enrolled for this study. Genotyping of rs693 (APOB), rs7412 and rs429358 (APOE), and rs1801131 and rs1801133 (MTHFR) polymorphisms were performed by real time PCR. In addition, lipid profiles were determined and associated to genetic data. The genotype distribution was APOB rs693 (CC = 37%, CT = 41%, and TT = 22%), APOE rs7412/rs429358 (E4 = 0.06, E3 = 0.91, and E2 = 0.03), MTHFR rs1801131 (AA = 57%, AC = 30%, and CC = 13%), and MTHFR rs1801133 (CC = 20%, CT = 47%, and TT = 33%). The association of the genetic variants with plasma lipid levels showed that women, but not men, carrying APOB mutated allele (T) and Apo E4 allele presented lower values of total cholesterol when compared with C/C homozygous genotype or E3 allele, respectively (p < 0.05). In addition, a subgroup analysis revealed that ApoB C/C homozygous women exhibited higher values of HDL-C when compared with men carrying identical genotype (p < 0.01). On the other hand, women carrying E4 allele exhibited lower values of triglycerides when compared with male carrying identical genotype (p < 0.05). Finally, women carrying mutate allele (C) for MTHFR rs1801131 showed lower levels of triglycerides when compared with A/A homozygous genotype (p < 0.05) and lower levels of LDL-C for MTHFR rs1801133 in females carrying (T) allele when compared with males carrying identical genotype (p < 0.05). In summary, the present data showed that APOB, APOE, and MTHFR single nucleotide polymorphisms are associated to lipid levels in a gender-dependent manner among healthy subjects from Northern Chile, especially in women.
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页数:10
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共 27 条
  • [21] Metabolic Analysis of Methylenetetrahydrofolate Reductase Single Nucleotide Polymorphisms (MTHFR 677C<T and MTHFR 1298A<C), Serum Folate and Vitamin B12 in Neural Tube Defects
    Mohammed H. Hassan
    Mohamed A. Raslan
    Mena Tharwat
    Hala M. Sakhr
    Eslam El-Sayed El-Khateeb
    Shimaa Fathy Sakr
    Hesham H. Ameen
    Ali R. Hamdan
    [J]. Indian Journal of Clinical Biochemistry, 2023, 38 : 305 - 315
  • [22] Prevalence of C677T Single Nucleotide Polymorphism of Methylenetetrahydrofolate Reductase Gene and its Relationship With Serum Levels of Homocysteine, Vitamin B12, Folate, and Cholesterol in Alzheimer's Patients
    Amani, Sanaz
    Mirzajani, Ebrahim
    Goodarzi, Mohammad Taghi
    Ghayeghran, Amir Reza
    [J]. CRESCENT JOURNAL OF MEDICAL AND BIOLOGICAL SCIENCES, 2024, 11 (03): : 121 - 127
  • [23] Metabolic Analysis of Methylenetetrahydrofolate Reductase Single Nucleotide Polymorphisms (MTHFR 677C&lt;T and MTHFR 1298A&lt;C), Serum Folate and Vitamin B12 in Neural Tube Defects
    Hassan, Mohammed H.
    Raslan, Mohamed A.
    Tharwat, Mena
    Sakhr, Hala M.
    El-Khateeb, Eslam El-Sayed
    Sakr, Shimaa Fathy
    Ameen, Hesham H.
    Hamdan, Ali R.
    [J]. INDIAN JOURNAL OF CLINICAL BIOCHEMISTRY, 2023, 38 (03) : 305 - 315
  • [24] SINGLE NUCLEOTIDE POLYMORPHISMS ASSOCIATED WITH ELEVATED SERUM VIRAL LOAD OF HEPATITIS B VIRUS IN PATIENTS WITH CHRONIC HEPATITIS B: A GENOME-WIDE ASSOCIATION STUDY IN TAIWAN
    Yang, H. -I.
    Chien, Y. -C.
    Ho, T. -N.
    Jen, C. -L.
    Lee, C. -Y.
    Lin, Y. -R.
    Lee, M. -H.
    Liu, J.
    Chen, C. -H.
    Chen, C. -J.
    [J]. JOURNAL OF HEPATOLOGY, 2011, 54 : S361 - S361
  • [25] Analysis of the APOB Gene and Apolipoprotein B Serum Levels in a Mexican Population with Acute Coronary Syndrome: Association with the Single Nucleotide Variants rs1469513, rs673548, rs676210, and rs1042034
    Aceves-Ramirez, Maricela
    Valle, Yeminia
    Casillas-Munoz, Fidel
    Martinez-Fernandez, Diana Emilia
    Parra-Reyna, Brenda
    Lopez-Moreno, Victor Arturo
    Flores-Salinas, Hector Enrique
    Valdes-Alvarado, Emmanuel
    Munoz-Valle, Jose Francisco
    Garcia-Garduno, Texali
    Padilla-Gutierrez, Jorge Ramon
    [J]. GENETICS RESEARCH, 2022, 2022
  • [26] Population-Based Genome-Wide Association Study to Identify Potential Single Nucleotide Polymorphisms Associated with the Serum Levels of Alanine Aminotransferase among Asymptomatic Chronic Hepatitis C Patients
    Lee, Mei-Hsuan
    Yang, Hwai-I
    Lu, Sheng-Nan
    Lin, Yu-Ju
    Liu, Pao-Jen
    Chien, Yu-Chuan
    Jen, Chin-Lan
    You, San-Lin
    Wang, Li-Yu
    Yuan, Yong
    L'Italien, Gilbert
    Chen, Chien-Jen
    [J]. HEPATOLOGY, 2013, 58 : 907A - 907A
  • [27] Using late-onset Alzheimer's disease (LOAD) as a model to study the application of single nucleotide polymorphisms (SNPs) for complex disease association studies: Genotyping and analysis of 65 SNPs in a 4-megabase region surrounding apolipoprotein E (APOE).
    Vance, JM
    Martin, ER
    Gilbert, JR
    Rogala, AR
    Afshari, A
    Slotterbeck, BD
    Grubber, JM
    Saunders, AM
    Riley, J
    Purvis, I
    Schmechel, DE
    Conneally, PM
    Lai, EH
    Pericak-Vance, MA
    Roses, AD
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A470 - A470