Quantitative Relationship Between Cumulative Risk Alleles Based on Genome-Wide Association Studies and Type 2 Diabetes Mellitus: A Systematic Review and Meta-analysis
Open accessAbstract
Many epidemiological studies have assessed the genetic risk of having undiagnosed or of developing type 2 diabetes mellitus (T2DM) using several single nucleotide polymorphisms (SNPs) based on findings of genome-wide association studies (GWAS). However, the quantitative association of cumulative risk alleles (RAs) of such SNPs with T2DM risk has been unclear. The aim of this meta-analysis is to review the strength of the association between cumulative RAs and T2DM risk. Systematic literature searches were conducted for cross-sectional or longitudinal studies that examined odds ratios (ORs) for T2DM in relation to genetic profiles. Logarithm of the estimated OR (log OR) of T2DM for 1 increment in RAs carried (1-ΔRA) in each study was pooled using a random-effects model. There were 46 eligible studies that included 74,880 cases among 249,365 participants. In 32 studies with a cross-sectional design, the pooled OR for T2DM morbidity for 1-ΔRA was 1.16 (95% confidence interval [CI], 1.13-1.19). In 15 studies that had a longitudinal design, the OR for incident T2DM was 1.10 (95% CI, 1.08-1.13). There was large heterogeneity in the magnitude of log OR (P < 0.001 for both cross-sectional studies and longitudinal studies). The top 10 commonly used genes significantly explained the variance in the log OR (P = 0.04 for cross-sectional studies; P = 0.006 for longitudinal studies). The current meta-analysis indicated that carrying 1-ΔRA in T2DM-associated SNPs was associated with a modest risk of prevalent or incident T2DM, although the heterogeneity in the used genes among studies requires us to interpret the results with caution.
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Advancing age, increasing BMI and racial group are associated with the high prevalence of gestational diabetes mellitus in Asia.
“Therefore, advancing age, increasing BMI and racial group are associated to the high prevalence of GDM in Asia.”
From Prevalence and risk factors of gestational diabetes mellitus in Asia: a systematic review and meta-analysis (2018) · cites this paper as [158]
The Discussion and Results address how BMI, ethnicity and age relate to genetic risk associations for type 2 diabetes, not the prevalence of gestational diabetes in Asia. Searches for gestational diabetes, GDM and pregnancy found no passage addressing the claimed association; page numbers were not supplied in our copy. (LLM, conf=0.77)
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Cites
Hu, F. B. (2011) · Diabetes Care · doi:10.2337/dc11-0442 · Cited by 1,954 · see citing works
Vazquez, G., Duval, S., Jacobs, D. R., & Silventoinen, K. (2007) · Epidemiologic Reviews · doi:10.1093/epirev/mxm008 · Cited by 976 · see citing works
Clinical risk factors, DNA variants, and the development of type 2 diabetes
Lyssenko, V., Jonsson, A., Almgren, P., Pulizzi, N., Isomaa, B., Tuomi, T., Berglund, G., Altshuler, D., Nilsson, P., & Groop, L. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0801869 · Cited by 938 · see citing works
Genotype score in addition to common risk factors for prediction of type 2 diabetes
Meigs, J. B., Shrader, P., Sullivan, L. M., McAteer, J. B., Fox, C. S., Dupuis, J., Manning, A. K., Florez, J. C., Wilson, P. W. F., D'Agostino, R. B., et al. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa0804742 · Cited by 759 · see citing works
Meisinger, C., L�wel, H., Thorand, B., & D�ring, A. (2005) · Diabetologia · doi:10.1007/s00125-004-1604-3 · Cited by 209 · see citing works
Waters, K. M., Stram, D. O., Hassanein, M. T., Le Marchand, L., Wilkens, L. R., Maskarinec, G., Monroe, K. R., Kolonel, L. N., Altshuler, D., Henderson, B. E., et al. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001078 · Cited by 191 · see citing works
Villegas, R., Goodloe, R. J., McClellan, B. E., Boston, J., & Crawford, D. C. (2014) · BMC Genetics · doi:10.1186/1471-2156-15-69 · Cited by 34 · see citing works
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Research works printed but not linked: 67
- [1]Schellenberg ES, Dryden DM, Vandermeer B, Ha C, Korownyk C Lifestyle interventions for patients with and at risk for type 2 diabetes: a systematic review and meta-analysis. Ann Intern Med. 2013; 159: 543– 551 (in eng). 10.7326/0003-4819-159-8-201310150-00007 24126648 · DOI · Paper page
- [2]Kaprio J, Tuomilehto J, Koskenvuo M, Concordance for type 1 (insulin-dependent) and type 2 (non-insulin-dependent) diabetes mellitus in a population-based cohort of twins in Finland. Diabetologia. 1992; 35: 1060– 1067 (in eng). 10.1007/BF02221682 1473616 · DOI
- [3]Gloyn AL Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy. Hum Mutat. 2003; 22: 353– 362 (in eng). 10.1002/humu.10277 14517946 · DOI
- [4]Pearson TA, Manolio TA How to interpret a genome-wide association study. JAMA. 2008; 299: 1335– 1344 (in eng). 10.1001/jama.299.11.1335 18349094 · DOI
- [5]McCarthy MI Genomics, type 2 diabetes, and obesity. N Engl J Med. 2010; 363: 2339– 2350 (in eng). 10.1056/NEJMra0906948 21142536 · DOI · Paper page
- [7]International HapMap Consortium The International HapMap Project. Nature. 2003; 426(6968): 789– 796. 10.1038/nature02168 14685227 · DOI · Paper page
- [8]Zhang SL, Lu WS, Yan L, Association between peroxisome proliferator-activated receptor-gamma coactivator-1alpha gene polymorphisms and type 2 diabetes in southern Chinese population: role of altered interaction with myocyte enhancer factor 2C. Chin Med J (Engl). 2007; 120: 1878– 1885 (in eng). 18067759
- [9]Miettinen O Estimability and estimation in case-referent studies. Am J Epidemiol. 1976; 103: 226– 235 (in eng). 10.1093/oxfordjournals.aje.a112220 1251836 · DOI
- [10]Berlin JA, Longnecker MP, Greenland S Meta-analysis of epidemiologic dose-response data. Epidemiology. 1993; 4: 218– 228 (in eng). 10.1097/00001648-199305000-00005 8512986 · DOI
- [11]Orsini N, Bellocco R, Greenland S Generalized least squares for trend estimation of summarized dose-respnse data. Stata J. 2006; 6: 40– 57.
- [12]DerSimonian R, Laird N Meta-analysis in clinical trials. Control Clin Trials. 1986; 7: 177– 188 (in eng). 10.1016/0197-2456(86)90046-2 3802833 · DOI · Paper page
- [13]Higgins JP, Thompson SG Quantifying heterogeneity in a meta-analysis. Stat Med. 2002; 21: 1539– 1558 (in eng). 10.1002/sim.1186 12111919 · DOI · Paper page
- [14]Begg CB, Mazumdar M Operating characteristics of a rank correlation test for publication bias. Biometrics. 1994; 50: 1088– 1101 (in eng). 10.2307/2533446 7786990 · DOI · Paper page
- [15]Egger M, Davey Smith G, Schneider M, Minder C Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997; 315: 629– 634 (in eng). 10.1136/bmj.315.7109.629 9310563 PMC2127453 · DOI · Paper page
- [16]Duval S, Tweedie R Trim and fill: A simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis. Biometrics. 2000; 56: 455– 463 (in eng). 10.1111/j.0006-341X.2000.00455.x 10877304 · DOI · Paper page
- [17]Talmud PJ, Cooper JA, Morris RW, Sixty-five common genetic variants and prediction of type 2 diabetes. Diabetes. 2015; 64: 1830– 1840 (in eng). 10.2337/db14-1504 25475436 PMC4407866 · DOI
- [18]Qian Y, Lu F, Dong M, Cumulative effect and predictive value of genetic variants associated with type 2 diabetes in Han Chinese: a case-control study. PLoS One. 2015; 10: e0116537. 10.1371/journal.pone.0116537 25587982 PMC4294637 · DOI
- [20]Langenberg C, Sharp SJ, Franks PW, Gene-lifestyle interaction and type 2 diabetes: the EPIC interact case-cohort study. PLoS Med. 2014; 11: e1001647 (in eng). 10.1371/journal.pmed.1001647 24845081 PMC4028183 · DOI
- [21]Chen Z, Pereira MA, Seielstad M, Joint effects of known type 2 diabetes susceptibility loci in genome-wide association study of Singapore Chinese: the Singapore Chinese health study. PLoS One. 2014; 9: e87762 (in eng). 10.1371/journal.pone.0087762 24520337 PMC3919750 · DOI
- [22]Tam CH, Ho JS, Wang Y, Use of net reclassification improvement (NRI) method confirms the utility of combined genetic risk score to predict type 2 diabetes. PLoS One. 2013; 8: e83093 (in eng). 10.1371/journal.pone.0083093 24376643 PMC3869744 · DOI
- [23]Robiou-du-Pont S, Bonnefond A, Yengo L, Contribution of 24 obesity-associated genetic variants to insulin resistance, pancreatic beta-cell function and type 2 diabetes risk in the French population. Int J Obes (Lond). 2013; 37: 980– 985 (in eng). 10.1038/ijo.2012.175 23090577 · DOI
- [24]Ramya K, Ayyappa KA, Ghosh S, Mohan V, Radha V Genetic association of ADIPOQ gene variants with type 2 diabetes, obesity and serum adiponectin levels in south Indian population. Gene. 2013; 532: 253– 262 (in eng). 10.1016/j.gene.2013.09.012 24055485 · DOI
- [25]Imamura M, Shigemizu D, Tsunoda T, Assessing the clinical utility of a genetic risk score constructed using 49 susceptibility alleles for type 2 diabetes in a Japanese population. J Clin Endocrinol Metab. 2013; 98: E1667– E1673 (in eng). 10.1210/jc.2013-1642 23956346 · DOI
- [26]Anand SS, Meyre D, Pare G, Genetic information and the prediction of incident type 2 diabetes in a high-risk multiethnic population: the EpiDREAM genetic study. Diabetes Care. 2013; 36: 2836– 2842 (in eng). 10.2337/dc12-2553 23603917 PMC3747911 · DOI
- [27]Kalnina I, Zaharenko L, Vaivade I, Polymorphisms in FTO and near TMEM18 associate with type 2 diabetes and predispose to younger age at diagnosis of diabetes. Gene. 2013; 527: 462– 468 (in eng). 10.1016/j.gene.2013.06.079 23860325 · DOI
- [28]Peters KE, Beilby J, Cadby G, A comprehensive investigation of variants in genes encoding adiponectin (ADIPOQ) and its receptors (ADIPOR1/R2), and their association with serum adiponectin, type 2 diabetes, insulin resistance and the metabolic syndrome. BMC Med Genet. 2013; 14: 15 (in eng). 10.1186/1471-2350-14-15 23351195 PMC3598639 · DOI
- [29]Cauchi S, Ezzidi I, El Achhab Y, European genetic variants associated with type 2 diabetes in North African Arabs. Diabetes Metab. 2012; 38: 316– 323 (in eng). 10.1016/j.diabet.2012.02.003 22463974 · DOI
- [30]Cooke JN, Ng MC, Palmer ND, Genetic risk assessment of type 2 diabetes-associated polymorphisms in African Americans. Diabetes Care. 2012; 35: 287– 292 (in eng). 10.2337/dc11-0957 22275441 PMC3263882 · DOI
- [31]Gamboa-Meléndez MA, Huerta-Chagoya A, Moreno-Macías H, Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population. Diabetes. 2012; 61: 3314– 3321. 10.2337/db11-0550 22923468 PMC3501881 · DOI
- [32]Iwata M, Maeda S, Kamura Y, Genetic risk score constructed using 14 susceptibility alleles for type 2 diabetes is associated with the early onset of diabetes and may predict the future requirement of insulin injections among Japanese individuals. Diabetes Care. 2012; 35: 1763– 1770 (in eng). 10.2337/dc11-2006 22688542 PMC3402252 · DOI
- [33]Long J, Edwards T, Signorello LB, Evaluation of genome-wide association study-identified type 2 diabetes loci in African Americans. Am J Epidemiol. 2012; 176: 995– 1001 (in eng). 10.1093/aje/kws176 23144361 PMC3571243 · DOI
- [34]Vassy JL, Durant NH, Kabagambe EK, A genotype risk score predicts type 2 diabetes from young adulthood: the CARDIA study. Diabetologia. 2012; 55: 2604– 2612 (in eng). 10.1007/s00125-012-2637-7 22782289 PMC3434294 · DOI
- [35]Vassy JL, Dasmahapatra P, Meigs JB, Genotype prediction of adult type 2 diabetes from adolescence in a multiracial population. Pediatrics. 2012; 130: e1235– e1242. 10.1542/peds.2012-1132 23071215 PMC3483893 · DOI
- [36]Villegas R, Delahanty R, Gao YT, Joint effect of genetic and lifestyle risk factors on type 2 diabetes risk among Chinese men and women. PLoS One. 2012; 7: e49464 (in eng). 10.1371/journal.pone.0049464 23185337 PMC3504028 · DOI
- [37]Yamakawa-Kobayashi K, Natsume M, Aoki S, The combined effect of the T2DM susceptibility genes is an important risk factor for T2DM in non-obese Japanese: a population based case-control study. BMC Med Genet. 2012; 13: 11 (in eng). 10.1186/1471-2350-13-11 22364391 PMC3313886 · DOI
- [38]Li S, Zhao JH, Luan J, Genetic predisposition to obesity leads to increased risk of type 2 diabetes. Diabetologia. 2011; 54: 776– 782 (in eng). 10.1007/s00125-011-2044-5 21267540 PMC3052481 · DOI
- [39]Martínez-Gómez LE, Cruz M, Martínez-Nava GA, A replication study of the IRS1, CAPN10, TCF7L2, and PPARG gene polymorphisms associated with type 2 diabetes in two different populations of Mexico. Ann Hum Genet. 2011; 75: 612– 620. 10.1111/j.1469-1809.2011.00668.x 21834909 · DOI
- [40]Rees SD, Hydrie MZ, Shera AS, Replication of 13 genome-wide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations. Diabetologia. 2011; 54: 1368– 1374 (in eng). 10.1007/s00125-011-2063-2 21350842 · DOI
- [41]Tabara Y, Osawa H, Kawamoto R, 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; 60: 1634– 1640 (in eng). 10.1016/j.metabol.2011.03.014 21550079 · DOI
- [42]Uusitupa MI, Stancáková A, Peltonen M, Impact of positive family history and genetic risk variants on the incidence of diabetes: the Finnish Diabetes Prevention Study. Diabetes Care. 2011; 34(2): 418– 423. 10.2337/dc10-1013 20980412 PMC3024360 · DOI
- [43]Fontaine-Bisson B, Renström F, Rolandsson O, Evaluating the discriminative power of multi-trait genetic risk scores for type 2 diabetes in a northern Swedish population. Diabetologia. 2010; 53(10): 2155– 2162. 10.1007/s00125-010-1792-y 20571754 PMC2931645 · DOI
- [44]Qi Q, Li H, Wu Y, Combined effects of 17 common genetic variants on type 2 diabetes risk in a Han Chinese population. Diabetologia. 2010; 53: 2163– 2166 (in eng). 10.1007/s00125-010-1826-5 20556352 · DOI
- [45]Rotger M, Gsponer T, Martinez R,; Swiss HIV Cohort Study Impact of single nucleotide polymorphisms and of clinical risk factors on new-onset diabetes mellitus in HIV-infected individuals. Clin Infect Dis. 2010; 51(9): 1090– 1098. 10.1086/656630 20879858 · DOI
- [46]Wang J, Stancáková A, Kuusisto J, Laakso M Identification of undiagnosed type 2 diabetic individuals by the finnish diabetes risk score and biochemical and genetic markers: a population-based study of 7232 Finnish men. J Clin Endocrinol Metab. 2010; 95: 3858– 3862. 10.1210/jc.2010-0012 20463095 · DOI
- [48]Xu M, Bi Y, Xu Y, Combined effects of 19 common variations on type 2 diabetes in Chinese: results from two community-based studies. PLoS One. 2010; 5: e14022 (in eng). 10.1371/journal.pone.0014022 21103332 PMC2984434 · DOI
- [49]Cornelis MC, Qi L, Zhang C, 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; 150: 541– 550 (in eng). 10.7326/0003-4819-150-8-200904210-00008 19380854 PMC3825275 · DOI
- [50]Hu C, Zhang R, Wang C, PPARG, KCNJ11, CDKAL1, CDKN2A-CDKN2B, IDE-KIF11-HHEX, IGF2BP2 and SLC30A8 are associated with type 2 diabetes in a Chinese population. PLoS One. 2009; 4: e7643 (in eng). 10.1371/journal.pone.0007643 19862325 PMC2763267 · DOI
- [51]Lin X, Song K, Lim N, Risk prediction of prevalent diabetes in a Swiss population using a weighted genetic score—the CoLaus Study. Diabetologia. 2009; 52: 600– 608 (in eng). 10.1007/s00125-008-1254-y 19139842 · DOI
- [52]Miyake K, Yang W, Hara K, Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association. J Hum Genet. 2009; 54: 236– 241 (in eng). 10.1038/jhg.2009.17 19247372 · DOI
- [53]Nordman S, Ostenson CG, Efendic S, Gu HF Loci of TCF7L2, HHEX and IDE on chromosome 10q and the susceptibility of their genetic polymorphisms to type 2 diabetes. Exp Clin Endocrinol Diabetes. 2009; 117: 186– 190 (in eng). 10.1055/s-0028-1100419 19053027 · DOI
- [54]Rong R, Hanson RL, Ortiz D, Association analysis of variation in/near FTO, CDKAL1, SLC30A8, HHEX, EXT2, IGF2BP2, LOC387761, and CDKN2B with type 2 diabetes and related quantitative traits in Pima Indians. Diabetes. 2009; 58: 478– 488 (in eng). 10.2337/db08-0877 19008344 PMC2628623 · DOI
- [55]Schulze MB, Weikert C, Pischon T, Use of multiple metabolic and genetic markers to improve the prediction of type 2 diabetes: the EPIC-Potsdam Study. Diabetes Care. 2009; 32: 2116– 2119 (in eng). 10.2337/dc09-0197 19720844 PMC2768223 · DOI
- [56]Cauchi S, Meyre D, Durand E, Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value. PLoS One. 2008; 3(5): e2031. 10.1371/journal.pone.0002031 18461161 PMC2346547 · DOI
- [59]Vaxillaire M, Veslot J, Dina C,; DESIR Study Group Impact of common type 2 diabetes risk polymorphisms in the DESIR prospective study. Diabetes. 2008; 57(1): 244– 254. 10.2337/db07-0615 17977958 · DOI
- [60]Scott LJ, Bonnycastle LL, Willer CJ, Association of transcription factor 7-like 2 (TCF7L2) variants with type 2 diabetes in a Finnish sample. Diabetes. 2006; 55: 2649– 2653 (in eng). 10.2337/db06-0341 16936217 · DOI
- [61]Hansen SK, Nielsen EM, Ek J, Analysis of separate and combined effects of common variation in KCNJ11 and PPARG on risk of type 2 diabetes. J Clin Endocrinol Metab. 2005; 90(6): 3629– 3637. 10.1210/jc.2004-1942 15797964 · DOI
- [62]Zacharova J, Chiasson JL, Laakso M; STOP-NIDDM Study Group The common polymorphisms (single nucleotide polymorphism [SNP] +45 and SNP +276) of the adiponectin gene predict the conversion from impaired glucose tolerance to type 2 diabetes: the STOP-NIDDM trial. Diabetes. 2005; 54(3): 893– 899. 10.2337/diabetes.54.3.893 15734870 · DOI
- [63]Uusitupa M Gene-diet interaction in relation to the prevention of obesity and type 2 diabetes: evidence from the Finnish Diabetes Prevention Study. Nutr Metab Cardiovasc Dis. 2005; 15: 225– 233. 10.1016/j.numecd.2005.03.004 15955472 · DOI
- [64]Chen Y, Kittles R, Zhou J, Calpain-10 gene polymorphisms and type 2 diabetes in West Africans: the Africa America Diabetes Mellitus (AADM) Study. Ann Epidemiol. 2005; 15: 153– 159 (in eng). 10.1016/j.annepidem.2004.05.014 15652721 · DOI
- [65]Grarup N, Sandholt CH, Hansen T, Pedersen O Genetic susceptibility to type 2 diabetes and obesity: from genome-wide association studies to rare variants and beyond. Diabetologia. 2014; 57: 1528– 1541 (in eng). 10.1007/s00125-014-3270-4 24859358 · DOI
- [66]Loos RJ, Yeo GS The bigger picture of FTO: the first GWAS-identified obesity gene. Nat Rev Endocrinol. 2014; 10: 51– 61 (in eng). 10.1038/nrendo.2013.227 24247219 PMC4188449 · DOI
- [67]Patsopoulos NA, Tatsioni A, Ioannidis JP Claims of sex differences: an empirical assessment in genetic associations. JAMA. 2007; 298: 880– 893 (in eng). 10.1001/jama.298.8.880 17712072 · DOI · Paper page
- [68]Jeon CY, Lokken RP, Hu FB, van Dam RM Physical activity of moderate intensity and risk of type 2 diabetes: a systematic review. Diabetes Care. 2007; 30: 744– 752 (in eng). 10.2337/dc06-1842 17327354 · DOI · Paper page
- [70]Perreault L, Ma Y, Dagogo-Jack S, Sex differences in diabetes risk and the effect of intensive lifestyle modification in the Diabetes Prevention Program. Diabetes Care. 2008; 31: 1416– 1421 (in eng). 10.2337/dc07-2390 18356403 PMC2453677 · DOI
- [72]Tabara Y, Osawa H, Kawamoto R, Replication study of candidate genes associated with type 2 diabetes based on genome-wide screening. Diabetes. 2009; 58: 493– 498 (in eng). 10.2337/db07-1785 19033397 PMC2628625 · DOI
- [73]Linder K, Wagner R, Hatziagelaki E, Allele summation of diabetes risk genes predicts impaired glucose tolerance in female and obese individuals. PLoS One. 2012; 7: e38224. 10.1371/journal.pone.0038224 22768041 PMC3387191 · DOI
- [74]Stevens JW, Khunti K, Harvey R, Preventing the progression to type 2 diabetes mellitus in adults at high risk: a systematic review and network meta-analysis of lifestyle, pharmacological and surgical interventions. Diabetes Res Clin Pract. 2015; 107: 320– 331 (in eng). 10.1016/j.diabres.2015.01.027 25638454 · DOI
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Lee, K. W., Ching, S. M., Ramachandran, V., Yee, A., Hoo, F. K., Chia, Y. C., Wan Sulaiman, W. A., Suppiah, S., Mohamed, M. H., & Veettil, S. K. (2018) · BMC Pregnancy and Childbirth · doi:10.1186/s12884-018-2131-4 · Cited by 546 · see citing works
- Authors
- Kodama, S., Fujihara, K., Ishiguro, H., Horikawa, C., Ohara, N., Yachi, Y., Tanaka, S., Shimano, H., Kato, K., Hanyu, O., & Sone, H.
- Affiliations
- Niigata University (JP)
- University of Niigata Prefecture (JP)
- Yamanashi Gakuin University (JP)
- Kyoto University Hospital (JP)
- University of Tsukuba (JP)
- ORCID
- Venue
- Journal of Epidemiology
- Publisher
- Japan Epidemiological Association
- Published
- 2018
- Volume
- 28
- Issue
- 1
- Pages
- 3-18
- ISSN
- 0917-5040 (ISSN-L)
- 1349-9092
- PMC
- PMC5742374
- OpenAlex
- W2766539614
- Cited by
- 18
- References
- 7
- Citations by year
- 2025: 3 · 2024: 3 · 2023: 1 · 2022: 2 · 2020: 2 · 2019: 3 · 2018: 4
- FWCI
- 0.32
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Journal of Epidemiology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Terrestrial Environment Research Center (University of Tsukuba) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Japan Society for the Promotion of Science (16H03260, 16K16296, 16H06808)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Keywords
- type 2 diabetes, single nucleotide polymorphisms, genetic risk, diabetes risk prediction, genetic susceptibility, new-onset diabetes
- MeSH terms
- Alleles, Diabetes Mellitus, Type 2, Humans, Genetic Predisposition to Disease, Genome-Wide Association Study
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