|Year : 2017 | Volume
| Issue : 9 | Page : 1055-1061
Relationship between Modulator Recognition Factor 2/AT-rich Interaction Domain 5B Gene Variations and Type 2 Diabetes Mellitus or Lipid Metabolism in a Northern Chinese Population
Lu-Lu Sun, Si-Jia Zhang, Mei-Jun Chen, Kazakova Elena, Hong Qiao
Department of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150000, China
|Date of Submission||20-Nov-2016|
|Date of Web Publication||21-Apr-2017|
Department of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150000
Source of Support: None, Conflict of Interest: None
Background: Four single nucleotide polymorphisms (SNPs) in the modulator recognition factor 2/AT-rich interaction domain 5B (MRF2/ARID5B) gene located at chromosome 10q21.2 have been shown to be associated with both type 2 diabetes mellitus (T2DM) and coronary artery disease in a Japanese cohort. This study aimed to investigate the relationship between these SNPs (rs2893880, rs10740055, rs7087507, rs10761600) and new-onset T2DM and lipid metabolism in a Northern Chinese population.
Methods: This was a case-control study. The rs2893880, rs10740055, rs7087507, and rs10761600 genetic variants were genotyped by SNPscan and analyzed in relation to T2DM susceptibility in 2000 individuals (999 with newly diagnosed T2DM and 1001 controls without diabetes mellitus). Associations between the MRF2/ARID5B genetic models and T2DM were determined by multivariate logistic regression.
Results: Regarding the rs10740055 SNP, AA was associated with a higher risk of T2DM compared with codominant-type CC (adjusted by sex, age, and body mass index [BMI], P= 0.041, odds ratio [OR] = 1.421, 95% confidence interval [CI] 1.014–1.991). Meanwhile, AA individuals were at increased risk of presenting with T2DM compared with individuals with CC or a single C (adjusted by sex, age, and BMI, P= 0.034, OR = 1.366, 95% CI 1.023–1.824). With respect to rs10761600, AT contributed to a higher risk of T2DM compared with AA (adjusted by sex, age, and BMI, P= 0.013, OR = 1.585, 95% CI 1.101–2.282), while TT also increased the risk of presenting with T2DM compared with AA or A (adjusted by sex, age, and BMI, P= 0.004, OR = 1.632, 95% CI 1.166–2.284). High-density lipoprotein cholesterol (HDL-C) levels were significantly different among the three genotypes of rs7087507 in the controls (P = 0.048) (GG>GA).
Conclusions: The present results identified MRF2/ARID5B as a potential susceptibility gene for new-onset T2DM in a Northern Chinese population, while the rs7087507 SNP was associated with HDL-C levels. Further larger studies are required to validate these findings.
Keywords: Diabetes Mellitus Type 2; Lipid Metabolism; Polymorphism; Single-nucleotide
|How to cite this article:|
Sun LL, Zhang SJ, Chen MJ, Elena K, Qiao H. Relationship between Modulator Recognition Factor 2/AT-rich Interaction Domain 5B Gene Variations and Type 2 Diabetes Mellitus or Lipid Metabolism in a Northern Chinese Population. Chin Med J 2017;130:1055-61
|How to cite this URL:|
Sun LL, Zhang SJ, Chen MJ, Elena K, Qiao H. Relationship between Modulator Recognition Factor 2/AT-rich Interaction Domain 5B Gene Variations and Type 2 Diabetes Mellitus or Lipid Metabolism in a Northern Chinese Population. Chin Med J [serial online] 2017 [cited 2017 May 27];130:1055-61. Available from: http://www.cmj.org/text.asp?2017/130/9/1055/204926
| Introduction|| |
Type 2 diabetes mellitus (T2DM) is a major public health concern. Approximately 382 million (8.3%) patients worldwide are thought to suffer from T2DM, and this number is expected to increase to 592 million by 2035. T2DM is a complex metabolic disorder characterized by hyperglycemia resulting from pancreatic beta-cell dysfunction and insulin resistance. It is associated with abnormal glucose metabolism and is also usually accompanied by abnormal lipid metabolism, both of which significantly increase the risk of coronary artery disease.
At least 75 genetic variants have been identified as associated with T2DM thanks to the advent of genome-wide association studies (GWASs). However, the effects of ethnicity and/or environmental factors mean that the same genetic variants may have different correlations with T2DM in different populations.
Modulator recognition factor-2 (MRF2) is a member of the AT-rich interaction domain (ARID) family of transcription factors (also known as ARID5B or Desrt). The MRF2/ARID5B gene is located at chromosome 10q21.2, which has been identified by GWAS as the most susceptible region for serum lipid levels. Targeted disruption of MRF2/ARID5B in mice resulted in stunted growth and reduced lipid accumulation.,, Furthermore, both in vivo and in vitro studies have indicated that the MRF2/ARID5B gene may affect adipogenesis.,, Research in a Norwegian cohort identified an association between DNA methylation of the ARID5B gene in cord blood and birth weight. These results suggest that MRF2/ARID5B may play an important role in growth and lipid metabolism.
Recent Japanese studies showed that four single nucleotide polymorphisms (SNPs) in the MRF2/ARID5B gene (rs2893880, rs10740055, rs7087507, and rs10761600) associated with susceptibility to coronary artery disease were also associated with T2DM., However, the relationships between these four SNPs and T2DM have only been reported in a Japanese population.
Based on the results of previous studies, we conducted a case-control study to evaluate the associations between these four MRF2/ARID5B SNPs and new-onset T2DM and lipid metabolism in a Northern Chinese population.
| Methods|| |
The study protocol was reviewed and approved by the Ethics Committee of Harbin Medical University. All patients and controls received adequate information about this study and provided written informed consent.
Using a case-control approach, a total of 2000 participants (aged 20–79 years) including 999 patients with newly diagnosed T2DM and 1001 controls were included in our study. None of the participants were genetically related to each other. The patients were recruited from the Endocrinology and Metabolism Department of the Second Affiliated Hospital of Harbin Medical University from March 2013 to May 2015. T2DM was diagnosed in accordance with the World Health Organization criteria. The duration of newly diagnosed T2DM was <6 months. Patients who used oral medications or insulin injections to achieve adequate glucose control and individuals with type 1 diabetes, gestational diabetes, or other special types of diabetes were excluded from the case group. Patients with acute diabetic complications or other serious metabolic diseases that might raise glucose levels were also excluded from the study.
Controls with a fasting plasma glucose (FPG) concentration <5.1 mmol/L and hemoglobin A1c (HbA1c) <6.0% and no family history of T2DM were enrolled from the physical examination center or outpatient clinics at the same hospital. Control individuals were required to meet the following criteria: no heart disease, liver dysfunction, malignancy, or other serious systemic disease, and no history of drugs known to influence glucose or lipid metabolism.
Anthropometric and clinical measurements
Anthropometric measurements including height, weight, waist and hip circumferences, and systolic and diastolic blood pressures were measured using standardized procedures. Waist-hip ratio was calculated as waist circumference (cm) divided by hip circumference (cm). Body mass index (BMI) was calculated as body weight in kilograms divided by the square of height in meters. The homeostasis model assessment (HOMA) was used to assess individual insulin resistance (HOMA-IR). HOMA-IR = (FPG [mmol/L] × FIN [mU/L])/22.5, FIN represents fasting insulin. HOMA-β was used to assess islet beta-cell secretion function. HOMA-β = FIN × 20/(FPG − 3.5).,
Peripheral venous blood samples were collected in tubes from all participants during the fasting state. Plasma insulin levels were measured by double-antibody radioimmunoassay. FPG was quantified by the glucose oxidase-peroxidase procedure (Modular DPP, Roche Diagnostics GmbH, Mannheim, Germany). Serum total cholesterol (TC), triglycerides (TGs), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein (LDL) levels were measured using an automatic biochemical analyzer (Modular DPP, Roche Diagnostics GmbH). HbA1c levels were measured using a high-performance liquid chromatography system (Bio-Rad DIA-MAT glycosylated hemoglobin analyzer system, Bio-Rad, Hercules, CA, USA).
Peripheral blood samples were collected in tubes containing Na2 EDTA and stored at −20°C for further analysis. Genomic DNA was extracted from peripheral blood leukocytes using a TIANamp Genomic DNA Kit (Tiangen Biotech Co., Ltd., Beijing, China) according to the standard procedure. Four SNPs were genotyped, rs2893880, rs10740055, rs7087507, and rs10761600, using a custom-by-design 48-Plex SNPscan™ kit (Genesky Biotechnologies Inc., Shanghai, China). This kit was developed based on multiplex fluorescence polymerase chain reaction according to patented technology elaborated by Genesky Biotechnologies Inc. The accuracy of the genotyping using the SNPscan™ Kit was validated by genotyping of a random sample of 5% of cases and controls twice for all SNPs, by different people. Specifically, 100 pairs of blind duplicates were performed with a concordance rate >98%. Moreover, these variants exhibited allelic frequencies >15% in Han Chinese (National Center for Biotechnology Information dbSNP database: https://www.ncbi.nlm.nih.gov/snp/).
Deviation from the Hardy–Weinberg equilibrium was assessed by exact tests (http://ihg.gsf.de/). Continuous parameters were compared using Student's t-tests (normal distribution) or nonparametric tests (nonnormal distribution), and categorical variables were compared using Chi-square tests. Data were described as mean ± standard deviation for normally distributed data or median (interquartile range) for nonnormally distributed data. A P < 0.05 was considered statistically significant for all data. Statistical evaluations of the associations between the case–control status and each individual SNP were measured as odds ratios (OR s) and 95% confidence intervals (CI s), estimated using unconditional logistic regression after adjusting for age, gender, and BMI. Quantitative traits among different genotypes were examined by analysis of variance (ANOVA). Associated statistical analyses were performed using SPSS software (version 17.0; SPSS, Chicago, IL, USA). We examined the degree of linkage disequilibrium (LD) between the polymorphisms and determined if the haplotype block associated with T2D using Haploview version 4.2 (http://www.broad.mit.edu/mpg/haploview).
| Results|| |
Clinical and biochemical characteristics of the study participants
The study participants comprised 999 new-onset T2DM patients and 1001 controls. The clinical and biochemical characteristics of the study groups are summarized in [Table 1]. There were no significant differences between the cases and controls with respect to sex (P = 0.232) and serum LDL cholesterol levels (P = 0.742). However, the new-onset T2DM patients had higher age, BMI, waist-hip ratio, FPG, HbA1c, fasting insulin, HOMA-IR, TC, TG, and blood pressure but lower serum HDL-C levels and HOMA-β (all P < 0.001) compared with controls.
Associations between modulator recognition factor 2/AT-rich interaction domain 5B variants and type 2 diabetes mellitus
The genotypes of some samples were not detected because of problems with the SNP detection technology or the quality of the experimental samples. Genotyping of SNP rs2893880, rs10740055, and rs10761600 was successful for 996 T2DM patients and 977 controls and of rs7087507 for 995 T2DM patients and 975 controls. The genotype distributions of the four SNPs were in Hardy–Weinberg equilibrium in both cases and controls. The genotype distributions of the four variants of MRF2/ARID5B are shown in [Table 2]. Analysis of rs2893880 found no differences in the frequency distributions of the GC and CC genotypes compared with the GG genotype between the cases and controls (P > 0.05). Likewise, rs10740055, rs7087507, and rs10761600 were not associated with T2DM.
|Table 2: The genotype distributions of the four variants in MRF2/ARID5B (n (%))|
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We further analyzed the effects of the four SNPs under three different genetic models by logistic tests [Table 3]. rs10740055 and rs10761600 were associated with T2DM risk according to both the additive and recessive models after adjusting for sex, age, and BMI (P < 0.05). For the rs10740055 SNP, AA seemed to increase the risk of T2DM compared with wild-type CC (adjusted P = 0.041, OR = 1.421, 95% CI 1.014–1.991). Meanwhile, AA individuals were at increased risk of T2DM compared with those with CC or a single C (recessive model, Akaike information criterion value = 1839; adjusted P = 0.034, OR = 1.366, 95% CI 1.023–1.824). With respect to rs10761600, TT seemed to increase the risk of presenting with T2DM compared with AA (adjusted P = 0.013, OR = 1.585, 95% CI 1.101–2.282) and carrying TT increased the risk of T2DM compared with AA or a single A (recessive model Akaike information criterion value = 1843; adjusted P = 0.004, OR = 1.632, 95% CI 1.166–2.284). However, there was no association in any genetic models for the SNPs rs7087507 and rs2893880 (P > 0.05).
|Table 3: Association between MRF2/ARID5B genetic models and T2DM with multivariable logistic regression|
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Linkage disequilibrium analysis of the constructed haplotype block with type 2 diabetes mellitus
The combined effect of the four SNPs was evaluated by haplotype analysis using Haploview. Pairwise LD D' values between SNPs and the reconstructed LD plots of the four SNPs are shown in [Figure 1]. Two SNPs (rs7087507and rs10761600) were in strong LD with each other and therefore formed a haplotype block [Figure 1]. However, the haplotype distributions were not significantly different between the cases and controls (data not shown).
|Figure 1: LD patterns of four genotyped SNPs in a Northern Chinese population. The LD between the SNPs is measured as D’ and shown in the diamond at the intersection of the diagonals from each SNP. Numbers in the red square indicating strong LD (|D’| > 0.8) and a logarithm of odds score ≥2.0. The analysis track at the top shows the SNPs according to chromosomal location. One haplotype block (outlined in bold black line) indicating markers that are in high LD are shown. SNPs: Single nucleotide polymorphisms; LD: Linkage disequilibrium.|
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Associations between modulator recognition factor 2/AT-rich interaction domain 5B single nucleotide polymorphisms and serum lipid levels in controls
We further analyzed the relationships between serum lipid metabolism and SNPs in the controls. Serum HDL-C levels were significantly different among the three genotypes in normal individuals (P = 0.048) as shown by ANOVA [Table 4], and serum HDL-C levels were significantly higher in individuals harboring the rs7087507 GG genotype compared with the GA genotype (P = 0.037). However, none of the SNPs were significantly associated with quantitative traits related to glucose or other lipid-related traits in the control population (P > 0.05).
|Table 4: The association analysis of MRF2/ARID5B variants and serum lipid level in control subjects (n = 1001)|
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| Discussion|| |
We evaluated the association between four SNPs of the MRF2/ARID5B gene and susceptibility to new-onset T2DM in a hospital-based case-control study of a Northern Chinese population. Two variants (rs10740055, rs10761600) were significantly associated with T2DM risk, and SNP rs7087507 was associated with serum HDL-C levels.
Previous studies by Japanese researchers found that rs2893880, rs10740055, rs7087507, and rs10761600 variants in the MRF2/ARID5B gene were associated with T2DM, with C, A, A, and T being the respective risk alleles. The four variants were also associated with higher HbA1c and FPG levels. In the present study, participants who harbored the MRF2/ARID5B rs10740055AA genotype had a higher incidence of T2DM, and the risk of T2DM was also increased in subjects harboring the T allele of rs10761600, consistent with the results of the previous study. The rs10740055 and rs10761600 SNPs thus appear to be common loci for T2DM susceptibility among Asian populations. However, we found no association between either rs2893880 or rs7087507 SNP and T2DM in the current sample of a Northern Chinese population. This apparent inconsistency may be the result of genetic heterogeneity, different geographic locations, different genetic origins, or differences in gene structure caused by gene–environment interactions. We also found no significant associations between these SNPs and fasting glucose levels or HbA1C in our study, suggesting that these genetic variations may affect the incidence but not severity of T2DM in Chinese.
The precise role of MRF2/ARID5B with regard to T2DM risk is still under investigation. The MRF2/ARID5B gene encodes a member of a novel class of DNA-binding proteins known as the ARID family. rs10761600 and rs10740055 are located within the second and third intron regions of MRF2/ARID5B, which region may give rise to alternatively spliced mRNAs and thus affect mRNA stability or processing, with possible impacts on MRF2/ARID5B function. Gene variants in this region may affect gene function and thus increase disease risk.
Several studies, including in mice lacking the MRF2/ARID5B gene ,, and other in vivo and in vitro research,,, as well as evidence from epigenetic results, implicate the MRF2/ARID5B gene in diabetes through its regulation of adipogenesis. These results support a direct relationship between MRF2/ARID5B and lipid metabolism and insulin resistance and a critical role in the pathogenesis of T2DM.
MRF2/ARID5B is located at chromosome region 10q21.2, which has been identified by GWAS as the most susceptible region for serum lipid levels. Although we found no association between rs7087507 and T2DM, our results revealed that the rs7087507 SNP was related to serum HDL-C levels (P = 0.048, F = 3.055) (GG>GA) and that HDL-C levels were lower in diabetic patients compared with controls (mean HDL-C 1.21 ± 0.32 vs. 1.48 ± 0.37). Furthermore, a Japanese haplotype analysis revealed that the haplotype G (rs2893880)-C (rs10740055)-G (rs7087507)-A (rs10761600) was negatively associated with susceptibility to coronary artery disease (P = 0.049). Several studies of genetic animal models have proven that increased serum HDL-C levels may protect against atherosclerosis,,, while other researchers have also demonstrated that low HDL-C levels are a well-defined risk factor for the development of cardiovascular diseases.
Wang et al. showed that individuals with haplotype CAAT constructed from the four tested MRF2/ARID5B SNPs were associated with a 1.86-fold increase in the prevalence of T2DM compared with individuals with GCGA (OR 1.86, 95% CI 1.43–2.41). Nevertheless, although two SNPs (rs7087507 and rs10761600) were in strong LD with each other and formed a haplotype block in our study, we found no significant difference in haplotype distributions between cases and controls. It is possible that some causal variants may be ethnic-specific or could be present elsewhere in the same or nearby genes. Differences in the patterns of LD between these SNPs and functional variants at these loci could underlie these disparate findings.
The strengths of our study included the fact that all individuals were of the same ethnicity. Most inhabitants of Harbin have lived there for at least three generations,, and the gene pool of the Harbin Han Chinese population is thus relatively stable. It has been suggested that the strong LD in the haplotype block constructed in our study reflected the characteristics of our cohort. The current study also had some limitations. First, we did not classify both T2DM and low HDL as necessary distinctions between cases and controls, which may have resulted in selection bias. However, the fact that all the controls had attended for routine physical examinations and were not hospitalized patients with specific diseases increased the likelihood that the controls were more representative of the general population. Further well-designed investigations with larger sample sizes are warranted to confirm our findings.
In summary, our results indicate that the MRF2/ARID5B gene is associated with new-onset T2DM in a Northern Chinese population. Among the four MRF2/ARID5B SNPs screened, rs10761600 and rs10740055 are associated with T2DM, while rs7087507 is associated with serum HDL-C levels. Further well-designed studies with larger samples are required to validate these findings.
Financial support and sponsorship
This work was supported by grants from the National Natural Science Foundation of China (No. 81172742 and 81473053), the Natural Science Foundation of Heilongjiang Province (No. ZD201220), and the 973 Project (No. 2014CB542401).
Conflicts of interest
There are no conflicts of interest.
| References|| |
L'Heveder R, Nolan T. International Diabetes Federation. Diabetes Res Clin Pract 2013;101:349-51. doi: 10.1016/j.diabres.2013.08.003.
Basile KJ, Johnson ME, Xia Q, Grant SF. Genetic susceptibility to type 2 diabetes and obesity: Follow-up of findings from genome-wide association studies. Int J Endocrinol 2014;2014:769671. doi: 10.1155/2014/769671.
Sanghera DK, Been LF, Ralhan S, Wander GS, Mehra NK, Singh JR, et al.
Genome-wide linkage scan to identify loci associated with type 2 diabetes and blood lipid phenotypes in the Sikh Diabetes Study. PLoS One 2011;6:e21188. doi: 10.1371/journal.pone.0021188.
Whitson RH, Tsark W, Huang TH, Itakura K. Neonatal mortality and leanness in mice lacking the ARID transcription factor Mrf-2. Biochem Biophys Res Commun 2003;312:997-1004. doi: 10.1016/j.bbrc.2003.11.026.
Lahoud MH, Ristevski S, Venter DJ, Jermiin LS, Bertoncello I, Zavarsek S, et al.
Gene targeting of desrt, a novel ARID class DNA-binding protein, causes growth retardation and abnormal development of reproductive organs. Genome Res 2001;11:1327-34. doi: 10.1101/gr.168801.
Ristevski S, Tam PP, Kola I, Hertzog P. Desrt, an AT-rich interaction domain family transcription factor gene, is an early marker for nephrogenic mesoderm and is expressed dynamically during mouse limb development. Mech Dev 2001;104:139-42. doi: 10.1016/S0925-4773(01)00370-7.
Yamakawa T, Sugimoto K, Whitson RH, Itakura K. Modulator recognition factor-2 regulates triglyceride metabolism in adipocytes. Biochem Biophys Res Commun 2010;391:277-81. doi: 10.1016/j.bbrc.2009.11.049.
Dong J, Ishimori N, Paigen B, Tsutsui H, Fujii S. Role of modulator recognition factor 2 in adipogenesis and leptin expression in 3T3-L1 cells. Biochem Biophys Res Commun 2008;366:551-5. doi: 10.1016/j.bbrc.2007.12.002.
Yamakawa T, Whitson RH, Li SL, Itakura K. Modulator recognition factor-2 is required for adipogenesis in mouse embryo fibroblasts and 3T3-L1 cells. Mol Endocrinol 2008;22:441-53. doi: 10.1210/me.2007-0271.
Engel SM, Joubert BR, Wu MC, Olshan AF, Håberg SE, Ueland PM, et al.
Neonatal genome-wide methylation patterns in relation to birth weight in the Norwegian Mother and Child Cohort. Am J Epidemiol 2014;179:834-42. doi: 10.1093/aje/kwt433.
Wang G, Watanabe M, Imai Y, Hara K, Manabe I, Maemura K, et al.
Associations of variations in the MRF2/ARID5B gene with susceptibility to type 2 diabetes in the Japanese population. J Hum Genet 2012;57:727-33. doi: 10.1038/jhg.2012.101.
Wang G, Watanabe M, Imai Y, Hara K, Manabe I, Maemura K, et al.
Genetic variations of Mrf-2/ARID5B confer risk of coronary atherosclerosis in the Japanese population. Int Heart J 2008;49:313-27. doi: 10.1536/ihj.49.313.
Alberti KG, Zimmet PZ. Definition, diagnosis and classification of diabetes mellitus and its complications. Part 1: Diagnosis and classification of diabetes mellitus provisional report of a WHO consultation. Diabet Med 1998;15:539-53. doi: 10.1002/(SICI) 1096-9136(199807)15:7<539:AID-DIA668>3.0.CO;2-S.
Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC. Homeostasis model assessment: Insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985;28:412-9. doi: 10.1007/BF00280883.
Sun XF, Xiao XH, Zhang ZX, Liu Y, Xu T, Zhu XL, et al.
Positive association between type 2 diabetes risk alleles near CDKAL1 and reduced birthweight in Chinese Han individuals. Chin Med J 2015;128:1873-8. doi: 10.4103/0366-6999.160489.
] [Full text]
Li TT, Qiao H, Tong HX, Zhuang TW, Wang TT. Association of common genetic variants in mitogen-activated protein kinase kinase kinase kinase 4 with Type 2 diabetes mellitus in a Chinese Han population. Chin Med J 2016;129:1179-84. doi: 10.4103/0366-6999.181969.
] [Full text]
Whitson RH, Huang T, Itakura K. The novel Mrf-2 DNA-binding domain recognizes a five-base core sequence through major and minor-groove contacts. Biochem Biophys Res Commun 1999;258:326-31. doi: 10.1006/bbrc.1999.0643.
Qiao L, Maclean PS, Schaack J, Orlicky DJ, Darimont C, Pagliassotti M, et al.
C/EBPalpha regulates human adiponectin gene transcription through an intronic enhancer. Diabetes 2005;54:1744-54. doi: 10.2337/diabetes.54.6.1744.
Besler C, Heinrich K, Rohrer L, Doerries C, Riwanto M, Shih DM, et al.
Mechanisms underlying adverse effects of HDL on eNOS-activating pathways in patients with coronary artery disease. J Clin Invest 2011;121:2693-708. doi: 10.1172/JCI42946.
Calabresi L, Gomaraschi M, Simonelli S, Bernini F, Franceschini G. HDL and atherosclerosis: Insights from inherited HDL disorders. Biochim Biophys Acta 2015;1851:13-8. doi: 10.1016/j.bbalip.2014.07.015.
Rosenson RS, Brewer HB Jr., Ansell BJ, Barter P, Chapman MJ, Heinecke JW, et al.
Dysfunctional HDL and atherosclerotic cardiovascular disease. Nat Rev Cardiol 2016;13:48-60. doi: 10.1038/nrcardio.2015.124.
Karadag MK, Akbulut M. Low HDL levels as the most common metabolic syndrome risk factor in heart failure. Int Heart J 2009;50:571-80. doi: 10.1536/ihj.50.571.
Jin L, Su B. Natives or immigrants: Modern human origin in East Asia. Nat Rev Genet 2000;1:126-33. doi: 10.1038/35038565.
Qin P, Li Z, Jin W, Lu D, Lou H, Shen J, et al
. A panel of ancestry informative markers to estimate and correct potential effects of population stratification in Han Chinese. Eur J Hum Genet 2014;22:248-53. doi: 10.1038/ejhg.2013.111.
[Table 1], [Table 2], [Table 3], [Table 4]