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Research Article

Joint Effect of Genetic and Lifestyle Risk Factors on Type 2 Diabetes Risk among Chinese Men and Women

  • Raquel Villegas mail,

    raquel.villegas@vanderbilt.edu

    Affiliation: Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America

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  • Ryan Delahanty,

    Affiliation: Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America

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  • Yu-Tang Gao,

    Affiliation: Department of Epidemiology, Shanghai Cancer Institute, Shanghai, Peoples’ Republic of China

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  • Jirong Long,

    Affiliation: Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America

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  • Scott M. Williams,

    Affiliation: Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire, United States of America

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  • Yong-Bing Xiang,

    Affiliation: Department of Epidemiology, Shanghai Cancer Institute, Shanghai, Peoples’ Republic of China

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  • Hui Cai,

    Affiliation: Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America

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  • Hong-Lan Li,

    Affiliation: Department of Epidemiology, Shanghai Cancer Institute, Shanghai, Peoples’ Republic of China

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  • Frank Hu,

    Affiliation: School of Public Health, Harvard University, Boston, Massachusetts, United States of America

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  • Qiuyin Cai,

    Affiliation: Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America

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  • Wei Zheng,

    Affiliation: Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America

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  • Xiao-Ou Shu

    Affiliation: Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America

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  • Published: November 21, 2012
  • DOI: 10.1371/journal.pone.0049464

Abstract

More than 40 genetic susceptibility loci have been reported for type 2 diabetes (T2D). Recently, the combined effect of genetic variants has been investigated by calculating a genetic risk score. We evaluated 36 genome-wide association study (GWAS) identified SNPs in 2,679 T2D cases and 3322 controls in middle-age Han Chinese. Fourteen SNPs were significantly associated with T2D in analysis adjusted for age, sex and BMI. We calculated two genetic risk scores (GRS) (GRS1 with all the 36 SNPs and GRS2 with the 14 SNPs significantly associated with T2D). The odds ratio for T2D with each GRS point (per risk allele) was 1.08 (95% CI: 1.06–1.09) for GRS1 and 1.15 (95% CI: 1.13–1.18) for GRS2. The OR for quintiles were 1.00, 1.26, 1.69, 1.95 and 2.18 (P<0.0001) for GRS1 and 1.00, 1.33, 1.60, 2.03 and 2.80 (P<0.001) for GRS2. Participants in the higher tertile of GRS1 and the higher BMI category had a higher risk of T2D compared to those on the lower tertiles of the GRS1 and of BMI (OR = 11.08; 95% CI: 7.39–16.62). We found similar results when we investigated joint effects between GRS1 and WHR terciles and exercise participation. We finally investigated the joint effect between tertiles of GRSs and a composite high risk score (no exercise participation and high BMI and WHR) on T2D risk. We found that compared to participants with low GRS1 and no high risk factors for T2D, those with high GRS1 and three high risk factors had a higher risk of T2D (OR = 13.06; 95% CI: 8.65–19.72) but the interaction factor was of marginal significance. The association was accentuated when we repeated analysis with the GRS2. In conclusion we found an association between GRS and lifestyle factors, alone and in combination, contributed to the risk of and T2D among middle age Chinese.

Introduction

Type 2 diabetes (T2D) is a complex disease affecting more than a billion people worldwide. Over the last two decades, China, like many other Asian countries, has experienced a dramatic increase in T2D incidence. Both genetic and environmental factors contribute to the development of T2D. Identifying genetic factors that contribute to T2D and their interactions with environmental factors can lead to prevention and lowering incidence of disease.

Through genome-wide association studies (GWAS), several genetic susceptibility loci have been reported for T2D [1][8]. Most of the reported genetic variants have small to moderate effects and account for only a small proportion of the heritability of T2D. Some data is available on the joint effects of common genetic variants on the risk of T2D [9][14]. However, most of these studies have not taken into consideration interactions between genetic risk and environmental factors. Looking at the joint effect between genetic risk and lifestyle factors show a large effect size on associations with T2D might help to identify high risk populations for intervention and to elucidate the biology behind the associations between genes and T2D.

In this report, we evaluated the association between reported SNP from genome-wide association study (GWAS) with T2D using data from a GWAS study of T2D of middle age women and from a nested case control study from two population based cohorts of middle age men and women living in urban Shanghai, China and calculated genetic risk scores (GRSs) with T2D susceptibility markers. We also looked at joint associations between genetic risk score tertiles with tertiles of body mass index (BMI), waist to hip ratio (WHR) and exercise participation and with a composite lifestyle high risk score including high BMI, high WHR and no exercise participation.

Methods

Ethics Statement

The study protocols were approved by the Institutional Review Boards of Vanderbilt University and the Shanghai Cancer Institute, and all participants provided written, informed consent.

Study Design and Population

Participants for the present study come from the Shanghai Diabetes GWAS Study and from a nested case control study of T2D identified from two prospective cohort studies the Shanghai Women’s Health Study (SWHS) and the Shanghai Men’s Health Study (SMHS).

The Shanghai Diabetes GWAS Study (SDGS).

The SDGS includes genome wide scan data of 1,019 diabetes cases and 1,710 controls. Details of the study design have been described elsewhere [5]. Briefly, diabetes cases in the SDGS included 886 incident T2D cases identified in the Shanghai Women’s Health Study (SWHS), a population-based cohort study of 74,941 women [15] and 133 prevalent T2D cases identified from female controls of the Shanghai Breast Cancer Study (SBCS), a population-based case-control study [16]. The 886 diabetes cases identified from the SWHS all met the following criteria: (1) age ≤65 with a self-reported diabetes diagnosed after study enrollment; (2) used diabetes medication; (3) had fasting glucose level >7 mmol/L at least twice, and (4) donated a blood sample. The 133 diabetes cases identified from the controls of SBCS were women who were diagnosed with T2D and were on diabetes medication or had a blood glucose level >7 mmol/L (measured by study). The 1,710 controls used in this GWAS were shared with a GWAS of breast cancer that was recently completed and was based primarily based on the Shanghai Breast Cancer Study (SBCS). Excluded from the control group are women who (1) had a self-reported history of diabetes; or (2) had a blood glucose level between 5.5 and 7 mmol/L and had HbA1C >6.1% or had no HbA1C data.

The SWHS and the SMHS are both population-based, prospective cohort studies based in urban Shanghai, China. The SWHS began first and recruited 74,941 women aged 40–70 years from 1997 to 2000 The SMHS recruited 61,491 men aged 40–74 years from 2002 to 2006 [17]. The validation sample includes 967 incident T2D cases and 913 controls from the SWHS [15] and 733 male incident T2D cases and 734 controls from the SMHS [18].

Anthropometric measurements and exercise participation.

Body weight and height were measured in the SWHS, the SMHS and SBCS using identical protocols. All anthropometric measurements including weight, height, and circumferences of waist and hips were taken twice during the in-person interview according to a standard protocol by trained interviewers who were retired medical professionals [19]. From these measurements, the following variables were created: body mass index (BMI), weight in kg divided by the square of height in meters and waist-hip ratio (WHR), waist circumference divided by hip circumference. Physical activity patterns were assessed during the in-person interviews. Regular exercise and sports participation were evaluated for the past 10 years in the SBCS and for the past 5 years in the SWHS and in the SMHS using validated questionnaires [20], [21].

SNP Selection and Genotyping

The National Human Genome Resource Institute’s (NHGRI) GWAS catalog [Accessed 10/12/2010] [22], was used to identify single nucleotide polymorphisms (SNPs) previously associated with high T2D. We selected 35 SNPs that had been associated with T2D in recent GWAS studies (October 2011) that had a minor allele frequency in Han Chinese (according to HAPMAP CHB group) of at least 5%. The SNPs selected were BCL11A (rs243021), RBMS1, ITGB6 (rs7593730), IRS1 (rs7578326, rs2943641), ADAMTS9 (rs4607103), IGF2BP2 (rs4402960), CDKAL1 (rs7756992, rs10440833), JAZF1 (rs864745), KLF14 (rs972283), TP53INP1 (rs896854), SLC30A8 (rs13266634), CDKN2A, CDKN2B (rs10811661, rs564398), CDC123, CAMK1D (rs12779790), HHEX, IDE (rs5015480, rs1111875), KCNQ1 (rs2237892), KCNJ11 (rs5215), intergenic (rs9300039), MTNR1B (rs1387153), HMGA2 (1531343), TSPAN8, LGRS (rs7961581, rs4760790), C2CD4A, C2CD4B (rs7172432), FTO (rs8050136, rs11642841), SRR (rs391300), HNF1B, TCF2 (rs4430796), DUSP9 (rs5945326), PTPRD (rs17584499), CHCHD9 (rs13292136), CENTD2 (rs1552224), ZFAND6 (rs11634397). In addition, 4 SNPs identified in a meta-analysis of the Asian consortium were also included: KCNK15 (rs3734618), SPRY2 (rs1215468), CMIP (rs12599890) and FITM2-R3HDML-HNF4A (rs6017317).

Genotyping, for the SDGS study and Imputation.

Genotyping was performed using the Affymetrix 6.0 array. The Birdseed v2 algorithm (http://www.broad.mit.edu/mpg/birdsuite/) was used to call genotypes. QC procedures included removal of SNPs with MAFs<0.01, Hardy-Weinberg P-values less than 0.00001, and samples with more than 5% missing genotypes. There were 15 SNPs that had been genotyped and the other SNPs that have been reported to be associated with T2D that were not available were imputed using the program MACH (http://www.sph.umich.edu/csg/abecasis/MA​CH/), using the phased Asian data from HapMap Phase II (release 22) as the reference. Only data with high imputation quality (RSQR>0.3 for MACH) were included in the current analysis.

Genotyping for the nested case control study.

Genotyping for the 39 SNPs included in the SWHS and SMHS sample set was completed using the iPLEX Sequenom MassArray platform. Included in each 96-well plate as quality control samples were two negative controls, two blinded duplicates and two samples included in the HapMap project. There were 2 SNPs that failed analysis (rs231362 and rs1531343), and one SNP was out of Hardy-Weinberg equilibrium HWE (P<10−4); (rs5945326) leaving a total of 36 SNPs for analysis.

Data analyses.

A total of 74 participants with whom data on four or more genotypes were missing were excluded from the analysis leaving 6,001 participants for the analyses. Demographic and lifestyle parameters were compared between cases controls using Mann Whitney rank sum tests for age, as this variable is not normally distributed, or ANOVA, for other continuous variables. Chi-squared statistics were used to evaluate differences between cases and controls for categorical variables. Single-marker association analyses were carried out to the selected SNP associations with T2D risk. Odds Ratios (ORs) and 95% confidence intervals (CI) were estimated using logistic regression models with adjustment for age, gender and BMI. The association between genotype and T2D risk was evaluated based on an additive genetic model, indexing exposure to risk allele reported in literature. To determine our power to detect previously reported effect sizes across a range of allelic frequencies, we used the program PS, to model T2D as a categorical variable with a fixed sample size under an additive model. [23]. To determine our power to detect an effect, we used independent case-control numbers with a ratio of 1.24, reflecting the control: case ratio (3,322 controls to 2,679 cases). We tested our power to detect association at an alpha of 0.05 (two-sided) under the additive model and used using an uncorrected chi-square test.

Genetic risk score.

We calculated two risk scores, one with all the SNPs (GRS1) and one with those SNPs that were significantly associated with T2D in the present study (GRS2). We assumed an additive genetic model for each SNP applying a linear weighting of 0, 1 or 2 to genotypes containing 0, 1 or 2 risk alleles respectively. We also calculated weighted GRS by multiplying the GRS by a weighted factor, calculated as = (number of risk alleles/risk alleles-missing genotypes). We checked the Linkage disequilibrium among SNPs in the same loci to see if the r2 was over 0.80 before calculating the GRSs and found this not the case.

We evaluated the joint effect of the GRSs and obesity categories according to the WHO recommendations [24], WHR categories (tertiles) and exercise participation (yes/no). We also developed a composite lifestyle high risk score by adding the number of risk factors associated with higher risk of T2D: having high BMI, (>25 kg/m2), having a high WHR (>0.85), and no exercise participation. Multiplicative interactions between GRSs and BMI, WHR or exercise participation were examined using the log likelihood ratio test, which compared the model including only the main effect with the model that included both the main effects and the interactive terms. Interaction terms were coded as the product of the genetic and environmental factors under investigation and were considered residual effects after main effects for each SNP. The unknown regression coefficient parameters were estimated using maximum likelihood, conditional on the random variables for genetic, environmental factors, and their products.

All analyses were performed using SAS (version 9.1). All P values presented are based on two-tailed tests. P values presented in this paper were not corrected for multiple testing.

Results

Associations of selected demographic characteristics and risk factors with T2D are shown in Table 1. As expected, cases and controls differed in regards to age, BMI, WHR, exercise participation and combined high risk factor score. Table 2 presents the association of GWAS-identified, T2D-related SNPs with T2D adjusted for BMI, age and sex in our study population. Fourteen variants in twelve gene regions (IGF2BP2, CDKAL1, KCNK15, TP53INP1, SLC30A8, CDKN2A/CDKN2B, CDC123/CAMK1D, HHEX/IDE, KCNQ1, KCNJ11, SPRY2 and HNF1B/TCF2) were significantly associated with T2D. All the SNPs that were significantly associated with T2D in our study (P<0.05), had a direction of association consistent with prior GWAS. Further, 23 of 36 SNPs associated with T2D by GWAS showed a consistent direction of association (as indicated by OR) with T2D in our study population (P = 0.066, binomial sign test).

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Table 1. Characteristics of the study population.

doi:10.1371/journal.pone.0049464.t001
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Table 2. Association of GWAS-Identified T2D-Related SNPs with T2D Risk.

doi:10.1371/journal.pone.0049464.t002

According to our power calculations, we only had 88% power to detect significance (P<0.05) for alleles with MAF of 0.26 (the average MAF in this study) and ORs of 1.2 or greater. The average OR for the 14 SNPs for which we detected significance was 1.18.

We calculated two risk scores, GRS1, based on all thirty six SNPs in unique loci, and GRS2, based on the fourteen SNPs significantly associated with T2D. Risk alleles were defined by previously reported T2D GWAS results for all variants included in GRS1 and GRS2. The associations of GRS1 and GRS2 with T2D were evaluated by logistic regression. Both, GRS1, (OR = 1.08; 95% CI: 1.06–1.09) and GRS2 (OR = 1.15; 95% CI: 1.13–1.18), were significantly associated with a higher risk of T2D in analysis adjusted for age, sex and BMI. The OR for quintiles of the GRS1 were 1.00, 1.26, 1.69, 1.95 and 2.18 (P<0.0001) and 1.00, 1.33, 1.60, 2.03 and 2.80 (P<0.001) for GRS2 (Table 3).

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Table 3. Association between the genetic risk scores and T2D*.

doi:10.1371/journal.pone.0049464.t003

The joint effect of BMI categories, WHR categories, and exercise participation, with GRS1 tertiles on T2D was evaluated (Table 4). We found that individuals in the highest categories of GRS1 and categories of BMI (< = or >25 kg/m2), WHR (< = or >0.85), and no exercise participation, WHR or who had no exercise participation had the highest ORs for risk of T2D compared with those in the lowest categories or GRS1, low BMI, low WHR or participating in exercise. The P value for interaction was only significant for association between GRS1 and WHR. Participants in the highest tertiles of both GRS1 and higher number of risk factors were more likely to have T2D than controls (OR = 13.06, 95% CI = 8.65–19.72) compared with participants with no risk factor and lower GRS1 category. The P value for the multiplicative interaction factor was of marginal significance.

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Table 4. Joint Effects of BMI, WHR, exercise participation and combined lifestyle risk factor with GRS1categories on T2D.

doi:10.1371/journal.pone.0049464.t004

Table 5 shows joint effects between BMI, WHR, exercise participation and lifestyle combined risk factors with GRS2 (tertiles). We found similar results than those with GRS1 and lifestyle factors, with the joint association between GRS2 and lifestyle factors being stronger although the P values for interaction failed to reach significance.

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Table 5. Joint Effects of BMI, WHR, exercise participation and combined lifestyle risk factor with GRS2 categories on T2D.

doi:10.1371/journal.pone.0049464.t005

Discussion

In this study we systematically evaluated the combined effects of a genetic risk score and a lifestyle risk score with T2D risk. Participants with a high GRS and high BMI, high WHR, no exercise participation or of a combination of these high risk factors were at increased risk of developing T2D. We only observed and statistically significant P value for interaction between WHR and GRS1.

Some data is available on GRS and T2D risk in European ancestry populations. In a large nested case-control study of 2,809 T2D cases and 3,501 controls from the Health Professionals Follow-up Study and Nurses’ Health Study (all of European ancestry), a. GRS was calculated with 10 SNPs in 9 loci. The odds ratio for T2D with each point of GRS, corresponding to 1 risk allele, was 1.19 (95% CI, 1.14–1.24) for men and 1.16 (CI, 1.12 to 1.20) for women, (12). In a recent study involving an African American population, the trend of increase in risk for T2D with increasing risk allele load was similar to observations in European-derived populations [9]. Some studies have been conducted in Asian populations and have reported similar results. For example the per-allele odds ratio for the development of T2D was 1.12 (95% CI: 1.00–1.25; P = .049) in a Japanese study [10]. In another study conducted in Pakistani population (from the UK and from Pakistan), the GRS using 30 T2D associated SNPs was also associated with a higher risk of T2D [25].

Two studies in China have evaluated associations between genetic risk scores and T2D. In one of the studies, 19 GWAS SNPS were validated using data from two community based studies, a case control study with subjects with T2D, impaired glucose tolerance and normal glucose and data from a prospective study of 734 non diabetic and 67 T2D incident cases [26]. A GRS was calculated using 4 SNPs in the following loci (CDKAL1, SLC30A8, CDKN2A/CDKN2B an, KCNQ1). The OR for the case control study (comparing T2D with normal glucose tolerance was 1.28 (1.21–1.35) and that comparing GRS in impaired glucose tolerance with normal glucose tolerance was 1.18 (1.11–1.25). In the prospective study the GRS OR was 1.33 (1.08–1.68). Another cross-sectional study conducted in China of 3,210 participants calculated a GRS using 17 GWAS confirmed SNPs and the odds ratio for T2D (per risk allele) was 1.18 (95% CI 1.12–1.23, p<0.0001) [13], which is similar to what we found in our study and they found a multiplicative interactive effect between BMI with fasting glucose and HbA1c but not with T2D. No joint effect with physical activity and the GRS score was found with T2D or fasting glucose.

In our study no statistically significant interactions were observed between the GRS1 and GRS2 and BMI, exercise participation and combined risk factors. Participants with a high GRS1 and GRS2 and high BMI, no exercise participation, high WHR of a combination of high risk factors were at substantially increased risk of developing T2D compared with those with lower GRS and lower lifestyle risks factors (alone or in combination). These findings suggest the potential value of using genetic markers to identify populations at high risk for T2D for targeted prevention. An interaction between WHR and the GRS1 was found. Our results are in agreement with a recent publication from a prevention trial. In an updated GRS using 34 T2D associated loci, in the Diabetes Prevention Program (DPP) conducted in the U.S. population, the ability of the score to predict diabetes incidence or regression to normal glucose tolerance was tested, and a high GRS was associated with increased risk of developing T2D and lower probability of returning to normal glucose tolerance state in high-risk individuals. They found that a lifestyle intervention attenuates this risk [14].

A strength of this study is that we have included a large number of SNPs identified from NHGRI GWAS catalog. A limitation of the study is that most of the SNPs have been identified from non-Asian populations. Other strengths include that this is a population-based epidemiological study that has comprehensively evaluated GWAS-identified T2D markers in association with T2D risk and interactions with modifiable risk factors of T2D including physical activity levels and a combination of risk factors. The vast majority of our study population is of a single ethnicity, reducing the potential effects of population stratification. The relatively large sample size and the detailed exposure information allowed us to evaluate the joint effect of T2D-related genetic markers and lifestyle risk factors on T2D risk.

Our study has some limitations. The linear models we used for the analysis have reduced power for detecting interactions and this might partially explain the marginal significance of the interactions found in this study. Larger independent studies will be needed to conclusively demonstrate whether the models we have identified here are true examples of effect modification. In addition the SNPs used to construct the GRS do not include many SNPs identified by GWAS studies in Chinese populations. When we did our SNP selection from the GWAS catalogue the majority of the studies had been conducted in white populations. We included SNPs from one study [27] that was published at the time. Other studies have been published since then, including a meta-analysis conducted in East Asian populations [28].

Another limitation is that the study subjects come from different studies and thus it is possible that the heterogeneous study population may have introduced bias in the association tests.

In summary, our study found associations between the GRS and T2D risk. We also found that a joint effect between genetic and modifiable risk factors although the interaction test failed to reach significance. The GRS provides a measure of the combined genetic effect of T2D associated loci.

Acknowledgments

We thank the participants and research staff of the Shanghai Women’s Health Study, Shanghai Men Health Study and Shanghai Breast Cancer Study for their contributions to the study.

Author Contributions

Conceived and designed the experiments: WZ XS. Performed the experiments: YG JL YX HL FH QC. Analyzed the data: RV RD SW HC. Wrote the paper: RV. Provided critical review of the manuscript: RD YG JL SW YX HL FH QC WZ XS.

References

  1. 1. Frayling TM. Genome-wide association studies provide new insights into type 2 diabetes aetiology. Nat Rev Genet 2007 Sep 8(9): 657–62. doi: 10.1038/nrg2178
  2. 2. Qi L, Cornelis MC, Kraft P, Stanya KJ, Linda Kao WH, et al. Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. Hum Mol Genet 2010 Jul 1 19(13): 2706–15.
  3. 3. Rung J, Cauchi S, Albrechtsen A, Shen L, Rocheleau G, et al. Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. Nat Genet 2009 Oct 41(10): 1110–5. doi: 10.1038/ng.443
  4. 4. Scott LJ, Mohlke KL, Bonnycastle LL, Willer CJ, Li Y, et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science 2007 Jun 1; 316(5829): 1341–5.
  5. 5. Shu XO, Long J, Cai Q, Qi L, Xiang YB, et al. Identification of new genetic risk variants for type 2 diabetes. PLoS Genet 2010; 6(9).
  6. 6. Sladek R, Rocheleau G, Rung J, Dina C, Shen L, et al. A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature 2007 Feb 22; 445(7130): 881–5.
  7. 7. Zeggini E, Weedon MN, Lindgren CM, Frayling TM, Elliott KS, et al. Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Science 2007 Jun 1; 316(5829): 1336–41.
  8. 8. Zeggini E, Scott LJ, Saxena R, Voight BF, Marchini JL, et al. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 2008 May 40(5): 638–45.
  9. 9. Cooke JN, Ng MC, Palmer ND, An SS, Hester JM, et al. Genetic risk assessment of type 2 diabetes-associated polymorphisms in african americans. Diabetes Care 2012 Feb 35(2): 287–92. doi: 10.2337/dc11-0957
  10. 10. Tabara Y, Osawa H, Kawamoto R, Onuma H, Shimizu I, et al. Genotype risk score of common susceptible variants for prediction of type 2 diabetes mellitus in Japanese: the Shimanami Health Promoting Program (J-SHIPP study). Development of type 2 diabetes mellitus and genotype risk score. Metabolism 2011 Nov 60(11): 1634–40. doi: 10.1016/j.metabol.2011.03.014
  11. 11. Lin X, Song K, Lim N, Yuan X, Johnson T, et al. Risk prediction of prevalent diabetes in a Swiss population using a weighted genetic score–the CoLaus Study. Diabetologia 2009 Apr 52(4): 600–8. doi: 10.1007/s00125-008-1254-y
  12. 12. Cornelis MC, Qi L, Zhang C, Kraft P, Manson J, et al. Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestry. Ann Intern Med 2009 Apr 21 150(8): 541–50. doi: 10.7326/0003-4819-150-8-200904210-00008
  13. 13. Qi Q, Li H, Wu Y, Liu C, Wu H, et al. Combined effects of 17 common genetic variants on type 2 diabetes risk in a Han Chinese population. Diabetologia 2010 Oct 53(10): 2163–6. doi: 10.1007/s00125-010-1826-5
  14. 14. Hivert MF, Jablonski KA, Perreault L, Saxena R, McAteer JB, et al. Updated genetic score based on 34 confirmed type 2 diabetes Loci is associated with diabetes incidence and regression to normoglycemia in the diabetes prevention program. Diabetes 2011 Apr 60(4): 1340–8. doi: 10.2337/db10-1119
  15. 15. Zheng W, Chow WH, Yang G, Jin F, Rothman N, et al. The Shanghai Women’s Health Study: rationale, study design, and baseline characteristics. Am J Epidemiol 2005 Dec 1 162(11): 1123–31. doi: 10.1093/aje/kwi322
  16. 16. Zheng W, Long J, Gao YT, Li C, Zheng Y, et al. Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. Nat Genet 2009 Mar 41(3): 324–8. doi: 10.1038/ng.318
  17. 17. Cai H, Zheng W, Xiang YB, Xu WH, Yang G, et al. Dietary patterns and their correlates among middle-aged and elderly Chinese men: a report from the Shanghai Men’s Health Study. Br J Nutr 2007 Nov 98(5): 1006–13. doi: 10.1017/s0007114507750900
  18. 18. Cai H, Zheng W, Xiang YB, Xu WH, Yang G, et al. Dietary patterns and their correlates among middle-aged and elderly Chinese men: a report from the Shanghai Men’s Health Study. Br J Nutr 2007 Nov 98(5): 1006–13. doi: 10.1017/s0007114507750900
  19. 19. Zhang X, Shu XO, Gao YT, Yang G, Matthews CE, et al. Anthropometric predictors of coronary heart disease in Chinese women. Int J Obes Relat Metab Disord 28(6): 734–40. doi: 10.1038/sj.ijo.0802634
  20. 20. Matthews CE, Shu XO, Yang G, Jin F, Ainsworth BE, et al. Reproducibility and validity of the Shanghai Women’s Health Study physical activity questionnaire. Am J Epidemiol 158(11): 1114–22. doi: 10.1093/aje/kwg255
  21. 21. Jurj AL, Wen W, Xiang YB, Matthews CE, Liu D, et al. Reproducibility and validity of the Shanghai Men’s Health Study physical activity questionnaire. Am J Epidemiol 2007 May 15 165(10): 1124–33. doi: 10.1093/aje/kwk119
  22. 22. Hindorff LA, Junkins HA, Mehta JP, Manolio TA. A catalog of published genome-wide association studies. Available at: http: //www.genome.gov/gwastudies. Accessed: 10/12/2010.
  23. 23. Dupont WD, Plummer WD, Jr. Power and sample size calculations. A review and computer program. Control Clin Trials 1990 Apr 11(2): 116–28.
  24. 24. WHO SG. Report on Diabetes Mellitus. Technical Report Series 727. Geneva: 1985.
  25. 25. Rees SD, Hydrie MZ, Shera AS, Kumar S, O’Hare JP, et al. Replication of 13 genome-wide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations. Diabetologia 2011 Jun 54(6): 1368–74. doi: 10.1007/s00125-011-2063-2
  26. 26. Xu M, Bi Y, Xu Y, Yu B, Huang Y, et al. Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies. PLoS One 5(11): e14022. doi: 10.1371/journal.pone.0014022
  27. 27. Tsai FJ, Yang CF, Chen CC, Chuang LM, Lu CH, et al. A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. PLoS Genet 6(2): e1000847. doi: 10.1371/journal.pgen.1000847
  28. 28. Cho YS, Chen CH, Hu C, Long J, Hee Ong RT, et al. Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat Genet 44(1): 67–72.