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Sull, Kim, and Jee: Effects of Obesity and Family History of Diabetes on the Association of CETP rs6499861 with HDL-C Level in Korean Populations
Original Article

Journal of Lipid and Atherosclerosis 2019; 8(2): 252-257.

Published online: 9 September 2019

DOI: https://doi.org/10.12997/jla.2019.8.2.252

Effects of Obesity and Family History of Diabetes on the Association of CETP rs6499861 with HDL-C Level in Korean Populations

Jae Woong Sull1, Soriul Kim2, Sun Ha Jee3

1Department of Biomedical Laboratory Science, College of Health Sciences, Eulji University, Seongnam, Korea.

2Institute for Human Genomic Study, College of Medicine, Korea University, Seoul, Korea.

3Department of Epidemiology and Health Promotion, Institute for Health Promotion, Graduate School of Public Health, Yonsei University, Seoul, Korea.

Correspondence to Sun Ha Jee. Department of Epidemiology and Health Promotion, Graduate School of Public Health, Yonsei University, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 03722, Korea. jsunha@yuhs.ac

Received 2 May 2019       Revised 21 June 2019       Accepted 20 August 2019

Copyright © 2019 The Korean Society of Lipid and Atherosclerosis.

The Korean Society of Lipid and Atherosclerosis

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Objectives

The aim of this study was to examine the associations of cholesterol ester transfer protein (CETP) rs6499861 and rs12708980 with high-density lipoprotein cholesterol (HDL-C) considering obesity and family history of diabetes (FHD) in Korean men and women.

Methods

We analyzed the association of CETP single nucleotide polymorphisms (SNPs) with HDL-C among individuals selected from a hospital (n=4 294) and the Bundang-gu area in Korea (n=2 304).

Results

We found that the CETP SNP rs6499861 was associated with a lower HDL-C level (effect per allele: −2.044 mg/dL, p<0.0001). Individuals with a rs6499861 CG/GG genotype had a 1.45-fold higher risk of an abnormal level of HDL-C (<40 mg/dL) than those with a CC genotype. This genotype-HDL-C association was stronger in women (odds ratio [OR], 1.99; 95% confidence interval [CI], 1.39–2.85) compared with men (OR, 1.33; 95% CI, 1.10–1.61) and in women with a FHD (OR, 4.82; 95% CI, 1.86–12.5; p=0.0012) compared with women without a family history. Relative to individuals with a CC genotype and body mass index (BMI) <25.69 kg/m2, individuals with a CG/GG genotype and BMI ≥25.69 kg/m2 had an OR (95% CI) of 2.61 (1.97–3.47).

Conclusions

These findings indicate that CETP variants are linked to HDL-C level in Koreans and that this link is stronger in obese men and in women who have a FHD.

Graphical Abstract

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Keywords: Cholesterol ester transfer proteins, HDL cholesterol, Physical activity, Genetic polymorphisms

INTRODUCTION

The level of high-density lipoprotein cholesterol (HDL-C) independently predicts cardiovascular disease.123 Previous genome-wide association studies elucidated genes that may directly influence the level of HDL-C, including the gene for cholesterol ester transfer protein (CETP, MIM 118470).45678910 Specifically, previous Swiss and Korean studies show that CETP single nucleotide polymorphisms (SNPs) rs6499861, rs6499863, and rs12708980 are associated with HDL-C level.91011 Another recent study reported that SNP rs6499863 was related to type 2 diabetes and HDL-C.12 Some studies analyzed the association between CETP gene SNP and HDL-C in subjects with other risk factors like obesity.1314 Family history of diabetes (FHD) is also related to lipid levels.1516 In this study, we hypothesized that CETP variants would be linked to HDL-C level in Korean populations. To test this hypothesis, we evaluated the association between HDL-C level and the rs6499861 and rs12708980 CETP gene SNPs in Korean men and women. The relation was also analyzed considering obesity and FHD.

MATERIALS AND METHODS

1. Study population

Individuals were selected from Severance Hospital in Seoul, South Korea from 1994 to 2012 (n=4,294).1017 Among 4,294 participants, 137 participants with lipid-lowering therapy were eliminated, and other subjects were eliminated due to missing data for rs6499861 SNP. Thus, the final subjects included 4,123 individuals. Among 4,123 subjects, 1,715 subjects were cardiovascular disease (CVD) patients identified by the health insurance reimbursement data from the National Health Insurance Corporation.17 Other 2408 subjects were the healthy subjects.
Other 2,304 participants were chosen in 2008 from the Bundang-gu area in Gyeonggi Province in Korea.10 Among them, 27 subjects with lipid-lowering therapy were eliminated, and other individuals were eliminated because of missing data for rs6499861 SNP. Thus, the final subjects involved 2,263 individuals.
The Institutional Review Board of Human Research at Eulji University approved the protocols for this study (IRB No: EURIB2018-74), and written informed consent was acquired from all participants prior to participation.

2. Data collection

Demographic characteristics and cigarette smoking status (current smoker, ex-smoker, or never smoked) were obtained using a structured questionnaire.17 Body mass index (BMI) was calculated as an individual's weight divided by height squared (kg/m2). Serum was isolated from samples of peripheral venous blood after 12 hours of fasting, stored at −70°C, and analyzed for metabolic biomarkers using a Hitachi 7600 analyzer (Hitachi, Ltd., Tokyo, Japan).

3. Genotyping assays

CETP rs6499861 and rs12708980 genotypes that our previous study reported were obtained using TaqMan probes.1018 For quality control, duplicate genotyping was performed for 1%–2.5% of samples.

4. Statistical analysis

Data were expressed as mean±standard deviation. SNPs were examined for possible effects on HDL-C levels under an additive model in PLINK. Multivariate linear regression models and multiple logistic regression analyses were performed using SAS statistical software, version 9.2 (SAS Institute, Cary, NC, USA). Odds ratios (ORs) were calculated to test the relation between the CETP SNP and abnormal HDL-C levels (<40 mg/dL). The joint effect of obesity on the association of CETP SNP with HDL-C levels was also tested. All statistical examinations were two-sided, and the statistical significance was decided as p<0.05.

RESULTS

Most individuals were middle-aged (Table 1), 13.8% had a positive FHD, and 38.8% of men and 3.2% of women were current smokers (data not shown).
Table 1

General characteristics of study population

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Individuals Severance Bundang-gu
No. of patients 4,123 2,263
Men (%) 68.0 54.8
Age (yr) 52.1±10.2 42.8±7.8
Waist circumference (cm) 84.0±9.0 80.0±9.5
BMI (kg/m2) 24.4±2.9 23.4±3.0
Fasting blood sugar (mg/dL) 97.0±22.7 93.6±16.7
Systolic blood pressure (mmHg) 121.9±14.6 117.8±14.2
Diastolic blood pressure (mmHg) 78.4±10.8 76.7±11.9
HDL-C (mg/dL) 50.9±11.6 52.1±12.7
LDL-C (mg/dL) 117.1±31.7 118.1±30.6
Triglycerides (mg/dL) 143.6±97.1 124.3±81.7
Smoking status
Ex-smoker 1,075 (27.9) 490 (21.7)
Current smoker 1,056 (27.4) 528 (23.3)
HDL-C
Normal (≥40 mg/dL) 3,445 (83.6) 1,919 (84.8)
Abnormal (<40 mg/dL) 678 (16.4) 344 (15.2)
FHD
Negative 3,527 (85.5) 1,970 (87.1)
Positive 596 (14.5) 293 (13.2)
Values are expressed as mean±standard deviation or number (%) not otherwise specified.
BMI, body mass index; HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol; FHD, family history of diabetes.
A linear regression model adjusted for age and gender showed that CETP rs6499861 and rs12708980 were related to HDL-C level in the Severance dataset but that only rs6499861 was related to HDL-C level in the Bungdang-gu dataset (Table 2).
Table 2

Association between CETP SNPs and HDL-C level adjusted for age and gender

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SNP Position Severance Bungdang-gu*
MAF β (mg/dL) p MAF β (mg/dL) p
rs6499861 55548996 0.096 −2.044 7.23×10−7 0.096 −1.568 8.91×10−3
rs12708980 55569880 0.096 −2.465 1.54×10−9 0.103 −0.839 0.143
CETP, cholesterol ester transfer protein; SNP, single nucleotide polymorphism; HDL-C, high-density lipoprotein cholesterol; MAF, minor allele frequency.
*Bundang-gu data were previously reported in Sull et al. (2012).10
Individuals with the CG/GG genotype of CETP rs6499861 were more at risk of having an abnormal HDL-C level than individuals with the CC genotype. This association between genotype and HDL-C was stronger in women compared with men (Table 3), in men with a BMI ≥25.69 kg/m2 compared with those with a BMI <25.69 kg/m2 (Table 4), and in women with a positive FHD compared with those with a negative FHD (Table 4). Individuals with the CG/GG genotype and a BMI ≥25.69 kg/m2 were more at risk of having an abnormal HDL-C level than those with the CC genotype or a BMI <25.69 kg/m2 although the interaction effect was not significant (Table 5).
Table 3

Age-adjusted ORs of low HDL-C* in the association with the genotypes of CETP SNP rs6499861 in the merged dataset (Severance and Bundang-gu, n=6 386)

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Individuals Genotype Normal (≥40 mg/dL) No. (%) Abnormal (<40 mg/dL)
No. (%) OR (95% CI) p
All CC 4,425 (82.5) 781 (76.4) 1.00 (reference)
CG/GG 939 (17.5) 241 (23.6) 1.45 (1.22–1.71) <0.0001
Men CC 2,632 (82.3) 659 (77.6) 1.00 (reference)
CG/GG 565 (17.7) 190 (22.4) 1.33 (1.10–1.61) 0.0029
Women CC 1,793 (82.7) 122 (70.5) 1.00 (reference)
CG/GG 374 (17.3) 51 (29.5) 1.99 (1.39–2.85) 0.0002
OR, odds ratio; CI, confidence interval; HDL-C, high-density lipoprotein cholesterol; CETP, cholesterol ester transfer protein; SNP, single nucleotide polymorphism.
*Adjusted for age, gender, and BMI.
Table 4

Age-adjusted ORs of low HDL-C in the association with the genotypes of CETP SNP rs6499861 stratified by gender, BMI, and FHD in the merged dataset (Bundang-gu and Severance, n=6,386)

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Individual Genotype Normal (≥40 mg/dL) No. (%) Abnormal (<40 mg/dL)
No. (%) OR (95% CI) p
Men
BMI<23.55 CC 952 (81.2) 131 (76.2) 1.00 (reference)
CG/GG 220 (18.8) 41 (23.8) 1.34 (0.92–1.97) 0.1246
23.55<BMI≤25.69 CC 864 (82.7) 242 (80.9) 1.00 (reference)
CG/GG 181 (17.3) 57 (19.1) 1.12 (0.81–1.56) 0.4936
BMI≥25.69 CC 816 (83.4) 282 (76.4) 1.00 (reference)
CG/GG 162 (16.6) 87 (23.6) 1.55 (1.15–2.07) 0.0037
Negative FHD CC 2,286 (82.4) 562 (78.4) 1.00 (reference)
CG/GG 490 (17.6) 155 (21.6) 1.29 (1.05–1.58) 0.0153
Positive FHD CC 346 (82.2) 97 (73.5) 1.00 (reference)
CG/GG 75 (17.8) 35 (26.5) 1.66 (1.05–2.64) 0.0301
Women
BMI<21.34 CC 637 (84.2) 17 (85.0) 1.00 (reference)
CG/GG 120 (15.8) 3 (15.0) 0.98 (0.28–3.42) 0.9752
21.34<BMI≤23.82 CC 585 (81.5) 37 (60.7) 1.00 (reference)
CG/GG 133 (18.5) 24 (39.3) 2.89 (1.66–5.02) 0.0002
BMI≥23.82 CC 571 (82.5) 63 (75.0) 1.00 (reference)
CG/GG 121 (17.5) 21 (25.0) 1.59 (0.93–2.70) 0.0903
Negative FHD CC 1,535 (82.9) 112 (73.2) 1.00 (reference)
CG/GG 316 (17.1) 41 (26.8) 1.78 (1.22–2.61) 0.0030
Positive FHD CC 258 (81.7) 10 (50.0) 1.00 (reference)
CG/GG 58 (18.3) 10 (50.0) 4.82 (1.86–12.5) 0.0012
OR, odds ratio; CI, confidence interval; HDL-C, high-density lipoprotein cholesterol; CETP, cholesterol ester transfer protein; SNP, single nucleotide polymorphism; BMI, body mass index; FHD, family history of diabetes.
Table 5

Age-adjusted ORs for HDL-C depending on CETP rs6499861 genotype and BMI in men in the merged dataset (n=4,046)

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Individuals Number by genotype OR (95% CI)
CC CG/GG p for interaction
BMI (kg/m2)
<25.69 2,203/508 1.00 (reference) 1.19 (0.93–1.52) 0.1781
≥25.69 1,088/247 1.69 (1.41–2.01) 2.61 (1.97–3.47)
OR, odds ratio; HDL-C, high-density lipoprotein cholesterol; CETP, cholesterol ester transfer protein; BMI, body mass index.

DISCUSSION

In this study of 6,386 Korean individuals, we found that CETP rs6499861 and rs12708980 were associated with a lower HDL-C level and that rs6499861 was more strongly associated with HDL-C level in women than in men. In several previous studies, a CETP SNP was associated with HDL-C in women but not in men, and CETP SNPs related to HDL-C were linked to type 2 diabetes in women only.512 However, another study reports associations between CETP SNP genotypes and low HDL-C in both women (p<0.0001) and men (p=0.0368).19
We also found that CETP rs6499861 was associated with a higher HDL-C level in obese individuals. Likewise, a previous study reports that a G mutation at the CETP442 locus is related to a higher HDL-C level in obese Chinese individuals.13 Another study reports a significant interaction between obese vs. lean status and genetic risk score on HDL-C.14 Although we found a combined effect of BMI and CETP SNP genotype on abnormal HDL-C level, the interaction was not statistically significant in the multivariate analysis.
In this study, we also found that CETP SNP had a stronger association with HDL-C levels in women subjects with positive FHD than that in women subjects with negative FHD. In a South East Asian study, subjects with a positive FHD had higher HDL-C concentration as compared to subjects with no family history.16 In a Japanese study, low-density lipoprotein cholesterol (LDL-C)/HDL-C ratio was independently associated with maternal family history of type 2 diabetes.15 A study found that a high polyunsaturated fatty acid/saturated fatty acid ratio was related to lower insulin sensitivity and the protective effect of PPARG2 Pro12Ala allele was obvious in subjects with family history of type 2 diabetes.20
In the present study, the association between the SNPs and HDL-C were inconsistent in the Severance data and Bundang-gu data. One of the possible reasons is that the mean age in the Severance data is much higher than the Bundang-gu data. In this study, CETP gene SNP had stronger relation to HDL-C levels in women than in men. It may be due to the different smoking prevalence between men and women. In our study, 38.8% of men participants and 3.2% of women participants were current smokers like the report of Korean national data.21
A limitation of the present study is that we did not categorize type of diabetes. However, type 2 diabetes is more common in Korea, whereas the incidence of type 1 diabetes is very low.2223 In conclusion, although the genetic associations of lipid levels in Asian people may not be comparable to those in European people, we found that CETP SNPs are associated with serum HDL-C level in Korean individuals and that this relationship is most pronounced in obese men and in women with a FHD.

Notes

Funding This study was funded by the Basic Science Research Program of the National Research Foundation of Korea through the Ministry of Education, Science, and Technology (2015R1D1A1A01059651 and 2018R1D1A1B07050834). The funding agency had no role in the design, collection, analysis, or interpretation of data; in the writing of the manuscript; or in the decision to submit the manuscript for publication.

Conflict of Interest The authors have no conflicts of interest to declare.

Author Contributions

  • Conceptualization: Sull JW, Kim S, Jee SH.

  • Data curation: Sull JW.

  • Formal analysis: Sull JW, Jee SH.

  • Funding acquisition: Sull JW.

  • Methodology: Sull JW.

  • Supervision: Jee SH.

  • Validation: Kim S, Jee SH.

  • Writing - original draft: Sull JW.

  • Writing - review & editing: Sull JW, Jee SH.

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ORCID iDs

Jae Woong Sull
https://orcid.org/0000-0002-5178-0065

Soriul Kim
https://orcid.org/0000-0002-6161-1636

Sun Ha Jee
https://orcid.org/0000-0001-9519-3068

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