Copyright: ©Author(s) 2026.
World J Diabetes. Nov 15, 2026; 17(11): 123851
Published online Nov 15, 2026. doi: 10.4239/wjd.123851
Published online Nov 15, 2026. doi: 10.4239/wjd.123851
Table 1 Summary of study design, modeling techniques, and validation strategies in type 2 diabetes mellitus models
| Characteristic | Category | n | Percentage (%) | |
| Overall | Studies included | 82 | ||
| Country/region | China | 30 | 36.6 | |
| Japan | 12 | 14.6 | ||
| South Korea | 4 | 4.9 | ||
| Iran | 3 | 3.7 | ||
| Mexico | 3 | 3.7 | ||
| United States | 3 | 3.7 | ||
| Germany | 2 | 2.4 | ||
| Qatar | 2 | 2.4 | ||
| Singapore | 2 | 2.4 | ||
| United Kingdom | 2 | 2.4 | ||
| United Arab Emirates | 2 | 2.4 | ||
| Other1 | 17 | 20.7 | ||
| Study design | Prospective cohort | 39 | 47.6 | |
| Cross-sectional | 20 | 24.4 | ||
| Retrospective cohort | 14 | 17.1 | ||
| Mathematical modeling | 2 | 2.4 | ||
| Case-control | 2 | 2.4 | ||
| Population-based cohort | 2 | 2.4 | ||
| Nested case-control | 1 | 1.2 | ||
| Multi-cohort prospective | 1 | 1.2 | ||
| Meta-analysis + prospective cohort validation | 1 | 1.2 | ||
| Modeling method | Traditional regression | Logistic regression | 42 | -2 |
| Cox proportional hazards model | 32 | - | ||
| Regularized regression | LASSO/elastic net | 17 | - | |
| Machine learning | Support vector machine | 5 | - | |
| Decision tree | 4 | - | ||
| Neural network | 2 | - | ||
| Random forest | 1 | - | ||
| Competing risk model | Fine–Gray model | 2 | - | |
| Other methods | Meta-analysis–based model | 1 | - | |
| Model validation | Internal validation | 67 | - | |
| Bootstrap | 21 | - | ||
| Cross-validation | 13 | - | ||
| Split-sample | 32 | - | ||
| External validation | 28 | - | ||
| Both internal and external validation | 15 | - | ||
| No validation | 0 | - | ||
Table 2 Methodological characteristics and predictive performance of the included type 2 diabetes mellitus prediction models
| Ref. | Country/region | Study design | Sample size | Modeling method | Key predictors | AUC (95%CI) | Sensitivity (95%CI) | Specificity (95%CI) | Validation | Model format | Target population |
| Bernabe-Ortiz et al[17], 2016 | Peru | Derivation: Cross-sectional national survey (ENINBSC); validation: Prospective cohort (CRONICAS) | Derivation: 2472 (48 events); validation: 2945 (85 events at baseline; 121 incident cases) | Logistic regression with stepwise backward elimination | Age, family history of diabetes, WC | Derivation: 0.73 (0.65–0.78) | Derivation: 69.6% | Derivation: 65.8% | Internal validation: Bootstrap; external validation: CRONICAS cohort | Points-based scoring system | Peruvian adults aged ≥ 35 years |
| Validation (cross-sectional): 0.68 (0.62–0.73) | Validation: 70.2% | Validation: 58.9% | |||||||||
| Validation (incident): 0.66 (0.61–0.71) | |||||||||||
| Liu et al[14], 2016 | China | Prospective cohort (Beijing Longitudinal Study of Ageing) | 1857 (144 events over 20 years) | Subdistribution hazards model (Fine–Gray) accounting for competing risk of non-diabetes death | Age, BMI, FPG, self-rated health, physical activity | 0.76 (0.72–0.80) | 0.74 | 0.65 | Internal validation by bootstrapping | Points-based scoring system | Community-dwelling Chinese adults aged ≥ 55 years |
| Zhang et al[60], 2016 | China | Prospective cohort (rural Henan province) | Derivation: 11564 (659 events); validation: 1285 (70 events) | Cox proportional hazards with forward selection | Age, BMI, TG, FPG | Derivation: 0.768 (0.760–0.776) | Derivation: 66.7% | Derivation: 74.0% | Internal validation: Random split (90/10); external validation: Compared with 5 existing models in validation set | Risk score formula | Rural Chinese adults aged ≥ 18 years |
| Validation: 0.766 (0.742–0.789) | Validation: 70.0% | Validation: 72.5% | |||||||||
| Han et al[49], 2016 | China | Derivation: Cross-sectional (HDNNCDS); validation: Prospective cohort (HPHS) | Derivation: 8764 (1096 prevalent cases); validation: 3430 (394 incident cases over 4.2 years) | Multivariable logistic regression with backward selection | Classic model: Age, sex, hypertension, family history of diabetes, alcohol consumption, regular exercise, BMI, WC | Derivation (classic): 0.78 (0.77–0.80) | External validation in independent cohort (HPHS) | Points-based scoring system | Northern Chinese adults aged 20–74 years | ||
| Validation (classic): 0.76 (0.73–0.78) | |||||||||||
| Diet model: Above + staple foods, livestock, eggs, potato, fresh fruit, fresh vegetables, dairy products | Derivation (diet): 0.81 (0.79–0.82) | Derivation (diet): 57.6% | Derivation (diet): 84.5% | ||||||||
| Validation (diet): 0.79 (0.77–0.81) | Validation (diet): 49.0% | Validation (diet): 85.8% | |||||||||
| Miyakoshi et al[20], 2016 | Japan | Retrospective cohort (health examinees) | Total: 4159 (279 events); derivation: 2080 (138 events); validation: 2079 (141 events) | Multivariate Cox proportional hazards with backward stepwise selection | RSFull: Age, family history of diabetes, SBP, sex, smoking, FPG, 2hPG, HbA1c | RSFull: 0.80 (0.76–0.84) | NR | NR | Internal validation (random split 50/50) | Points-based scoring system | Japanese adults undergoing health checkups (baseline non-diabetic) |
| RS-2hPG: Age, family history of diabetes, SBP, sex, FPG, HbA1c, TG | RS-2hPG: 0.75 (0.70–0.78) | ||||||||||
| RSNI: Age, family history of diabetes, SBP, sex, BMI | RSNI: 0.68 (0.63–0.72) | ||||||||||
| Zhang et al[55], 2017 | China | Prospective cohort (rural Henan, 6-year follow-up) | Total: 15768 (702 events); derivation: 12654; validation: 3114 | Cox proportional hazards with forward selection; scores = β × 10 (rounded down) | Drinking tea, BMI, WHtR, TG, FPG | Derivation: 0.791 (0.783–0.799) | 69.6% (derivation) | 75.6% (derivation) | Internal validation: Random split (80/20) | Points-based scoring system | Rural Chinese adults aged ≥ 18 years |
| Validation: 0.731 (0.713–0.748) | |||||||||||
| Asadollahi et al[18], 2017 | Iran | Cross-sectional (populationbased survey) | Derivation: 2158 (254 diabetes, 168 IFG); validation: 404 | Multivariate logistic regression with univariate prescreening | Family history of diabetes, place of life, age, hypertension, daily exercise, marital status, sex, WC, smoking, BMI | Derivation: 0.71 | Range: 12.9%–30.7% (for diabetes at different score cut-offs) | Range: 72.8%–88% (for diabetes at different score cut-offs) | External validation in independent clinical sample (n = 404) | Points-based scoring system | Iranian adults aged ≥ 25 years |
| Validation: 0.872 | |||||||||||
| Hippisley-Cox and Coupland[32], 2017 | United Kingdom (England) | Prospective open cohort (QResearch database) | Derivation: 8186705 (178314 events); validation: 2629940 (62326 events) | Cox proportional hazards with fractional polynomials; multiple imputation for missing data | Model A: Age, ethnicity, deprivation, BMI, smoking, family history of diabetes, CVD, treated hypertension, corticosteroids, atypical antipsychotics, statins, schizophrenia/bipolar disorder, learning disability, gestational diabetes, PCOS | Model A: Women: Harrell’s C 0.834 (0.832–0.837); men: 0.814 (0.812–0.816) | Model A (threshold 5.6%): 68.1% (top 20%) | Model A: 81.1% (top 20%) | External validation in separate set of 363 practices (not used in derivation) | Cox regression equations; web calculator (qdiabetes.org) | United Kingdom adults aged 25–84 years without diabetes |
| Model B: Model A + FPG | Model B: Women: 0.889 (0.887–0.891); men: 0.866 (0.863–0.868) | ||||||||||
| Model C: Model A + HbA1c | Model C: Women: 0.878 (0.875–0.881); men: 0.855 (0.849–0.861) | ||||||||||
| Chen et al[50], 2017 | China | Prospective cohort (Rural Deqing Cohort Study) | Whole cohort: 28251 (387 events over mean 4.2 years); sub-cohort: 3043 (191 events over mean 8.7 years) | Cox proportional hazards; scores based on β-coefficients | Non-invasive model: Age, BMI, family history of diabetes, meat diet, hypertension | Non-invasive: Whole cohort: 0.705; subcohort: 0.638 | Noninvasive: 70.4% | Noninvasive: 60.4% | Internal validation: Bootstrap; external validation: Subcohort validation | Points-based scoring system | Rural Chinese adults aged ≥ 18 years |
| Plus-FPG model: Age, BMI, family history of diabetes, meat diet, hypertension, IFG | Plus-FPG: Whole cohort: 0.754; sub-cohort: 0.667 | Plus-FPG: 63.0% | Plus-FPG: 73.1% | ||||||||
| Tian et al[72], 2017 | China | Cross-sectional (oil field workers) | 1995 (776 dysglycemia) | Multivariable logistic regression | Sex, age, BMI, HHBG, smoking, TG, FPG | 0.791 (0.773–0.809) | 0.736 | 0.735 | Internal validation; compared with m-FINDRISC) | Pointsbased scoring system | Chinese oil field workers aged 20–64 years |
| Yatsuya et al[15], 2018 | Japan | Prospective cohort (Aichi Workers’ Cohort Study) | 3540 (342 events over median 12.2 years) | Cox proportional hazards with backward selection; Framingham point system method | Age, BMI, smoking status, family history of diabetes, TG, FPG | C-index: 0.77 | 0.66 | 0.76 | Internal validation; cross-validated with Ibaraki model | Points-based scoring system | Japanese male workers aged 35–64 years |
| Abdullah et al[26], 2017 | Malaysia | Casecontrol (nested within Malaysian Cohort Project) | Total: 4077 (cases: 1962; controls: 2115); Malay: 1323, Chinese: 1344, Indian: 1410 | Multivariable logistic regression; GRS based on 62 T2DM-associated SNPs | Environmental model: Sex, age, WHR, physical inactivity | Environmental only: Malay: 0.75 (0.72–0.78); Chinese: 0.83 (0.80–0.86); Indian: 0.78 (0.75–0.81); Combined: 0.79 (0.77–0.81) | NR | NR | Internal validation; compared model fit with/without GRS) | GRS combined with environmental risk factors in logistic regression model | Multiethnic Malaysian adults (Malay, Chinese, Indian) aged 35–70 years |
| Full model: Environmental + GRS | Environmental + GRS: Malay: 0.77 (0.73–0.80); Chinese: 0.84 (0.82–0.87); Indian: 0.79 (0.76–0.82); Combined: 0.80 (0.78–0.82) | ||||||||||
| Wang et al[65], 2018 | China | Prospective cohort (health checkup attendees) | 9735 (1099 events over 3 years) | Cox regression (HR); logistic regression for prediction models (full, stepwise, MFP) | Male: Age, hypertension, 2hPG, FPG, TG | Male (stepwise model): 0.779 (0.759–0.799) | Male: 74% | Male: 67% | Internal validation using 500 bootstrap resamples | Nomogram; points-based scoring system (separate for male and female) | Chinese adults (aged 17–96 years) attending annual health check-ups in Wuhan, China |
| Female: Age, FPG, 2hPG, TG | Female (stepwise model): 0.860 (0.836–0.883) | Female: 88% | Female: 69% | ||||||||
| Han et al[37], 2018 | China | Prospective cohort (Dongfeng-Tongji cohort) | 17690 (1390 events over 5 years) | Cox proportional hazards | BMI, FPG, hypertension, hyperlipidemia, current smoking, family history of diabetes | 0.751 (0.737–0.764) | 0.656 | 0.729 | Internal validation using 90/10 random split (repeated 10 times) | Points-based scoring system | Middle-aged and older Chinese adults (mean age 63.3 years, retired workers) |
| Sulaiman et al[19], 2018 | United Arab Emirates | Cross-sectional (United Arab Emirates National Diabetes and Lifestyle Study) | 872 (219 undiagnosed diabetes) | Stepwise forward logistic regression | Age, family history of diabetes, hypertension, BMI, WHR | 0.82 (0.78–0.86) | 0.754 | 0.7 | External validation in a separate sample of Arab non-UAE citizens residing in the UAE (n = 631) | Pointsbased scoring system | United Arab Emirates citizens aged ≥ 18 years (without known diabetes) |
| Hu et al[83], 2018 | Japan | Prospective cohort (J-ECOH Study) | Total: 46198 (3385 events over 7 years); derivation: 30500 (2216 events); validation: 15698 (1169 events) | Cox proportional hazards with backward selection | Noninvasive: Sex, age, BMI, abdominal obesity, smoking, hypertension | Noninvasive: 0.73 (0.72–0.74) | NR | NR | Internal validation (random split 2/3-1/3) | Cox regression equations; risk calculators and charts | Japanese employees aged 30–59 years |
| Invasive: Age, BMI, smoking, hypertension, dyslipidemia, FPG, HbA1c | Invasive: 0.89 (0.89–0.90) | ||||||||||
| Félix-Martínez and Godínez-Fernández[84], 2018 | Mexico | Cross-sectional (National Health and Nutrition Surveys) | Model 1 (2006): 8743 (258 UDM); model 2 (2012): 5103 (63 UDM) | Multivariable logistic regression with backward stepwise selection (AIC-based, 10-fold CV) | Model 1: Age, WC, SBP | Model 1: 0.73 (validation) | Model 1: 74% | Model 1: 62% | external validation in NHS 2000 (n = 28913) | Logistic regression equation; interactive web applications | Mexican adults aged ≥ 20 years |
| Model 2: Age, WC, height, family history of diabetes | Model 2: 0.71 (validation) | Model 2: 76% | Model 2: 55% | ||||||||
| Kim et al[77], 2019 | Korea | Prospective cohort (KoGES) | Clinical model: 7912 (1345 events); integrated model: 6818 (1162 events) | Cox proportional hazards with backward elimination (clinical) + forward selection (SNPs) | Clinical model: Age, sex, FBS, ALT, γ-GTP, HDL, TG, SBP, BMI, parental history of DM | Clinical model (validated C-index): 5-year 0.744, 7-year 0.732, 10-year 0.732 | NR | NR | Internal validation (bootstrap 200 iterations) | Cox regression equations; points-based scoring system | Korean adults aged 40–69 years (urban/rural) |
| Integrated model: Above + 5-SNP point score | Integrated model (validated C-index): 5-year 0.747, 7-year 0.736, 10-year 0.738 | ||||||||||
| Zhang et al[51], 2019 | China | Crosssectional (community-based) | 1432 (142 newly diagnosed diabetes) | Multivariable logistic regression | Age, family history of diabetes, hypertension, WC, BMI, smoking, vegetable intake, fruit intake | 0.758 (0.714–0.803) | 0.831 | 0.6 | Internal validation | Pointsbased scoring system | Chinese communitydwelling adults aged 18–60 years without known diabetes |
| Wang et al[38], 2019 | China | Prospective cohort (3-year followup) | Training: 5557 (595 events); validation: 1870 (206 events) | Multivariable logistic regression with stepwise selection | Female: Age, BMI, FPG, TG | Training: Female 0.863 (0.837–0.888); male 0.751 (0.729–0.774) | Training: Female 82.6%; male 73.8% | Training: Female 79.1%; male 65.7% | Internal validation (500 bootstrap); temporal validation using later cohort | Nomogram | Central Chinese adults attending annual health check-ups |
| Male: Age, BMI, FPG, HDL-C, TG | Validation: Female 0.847 (0.801–0.892); male 0.755 (0.717–0.794) | Validation: Female 90.2%; male 63.3% | Validation: Female 66.7%; male 76.0% | ||||||||
| Kraege et al[41], 2019 | Switzerland | Prospective cohort (CoLaus/PsyCoLaus) | 5277 (405 events over mean 10.9 years) | Logistic regression with bivariate prescreening | Age, sex, WC, family history of diabetes, hypertension, physical inactivity | 0.772 (0.752–0.792) | 0.605 | 0.771 | External validation in 3 cohorts: EPIC-Europe (n = 26270), Tlalpan 2020 (Mexico, n = 1076), Shahedieh (Iran, n = 904) | Points-based scoring system | European adults aged 35–75 years, generalizable to populations with different diabetes prevalence |
| Xie et al[80], 2019 | United States | Cross-sectional (BRFSS 2014) | 138146 (20467 T2DM) | Multiple machine-learning methods: SVM, decision tree, logistic regression, random forest, neural network, Naïve Bayes | Age, BMI, income, marital status, race/ethnicity, sleep duration, check-up frequency, physical activity, smoking, etc. (27 variables) | Neural network: 0.795 | Decision tree: 51.6% (highest) | Neural network: 90.2% (highest) | Internal validation (random split 2/3 training, 1/3 test) | Machine learning models | United States adults aged ≥ 30 years (Behavioral Risk Factor Surveillance System) |
| Logistic regression: 0.793 | |||||||||||
| Linear SVM: 0.781 | |||||||||||
| Rbf SVM: 0.779 | |||||||||||
| Random forest: 0.761 | |||||||||||
| Naïve Bayes: 0.760 | |||||||||||
| Polynomial SVM: 0.759 | |||||||||||
| Decision tree: 0.718 | |||||||||||
| Pei et al[82], 2019 | China | Cross-sectional (retrospective, health checkup data) | 10436 (1570 with diabetes) | Decision tree (J48 algorithm, C4.5) | Age, BMI, family history of diabetes, work-related stress, physical activity, salty food preference, hypertension, sex, history of CVD/stroke | 0.948 | 0.942 | 94.2% (accuracy) | Internal validation (random split 70/30) | Decision tree with 19 IF-THEN rules | Chinese adults undergoing annual health check-ups in Shenyang, China |
| Wang et al[29], 2020 | Singapore | Nested case-control within prospective cohort (Singapore Chinese Health Study) | 485 cases, 485 controls (matched on age, sex, dialect, date of blood collection) | Weighted biomarker score based on logistic regression β coefficients; 10-fold cross-validation | TG/HDL ratio, ALT, ferritin, adiponectin (all in quartiles) | Base model + biomarker score: 0.83 (0.81–0.86); increment from base model (AUC 0.81) significant (P = 0.002) | NR | NR | Internal validation (10-fold cross-validation) | Weighted biomarker score | Singapore Chinese adults aged 45–74 years |
| Wu et al[76], 2019 | China | Crosssectional (Shanghai Nicheng Cohort) | 15309 (2344 prevalent undiagnosed diabetes) | Multivariable logistic regression with backward stepwise selection | Age group, family history of diabetes, hypertension, overweight/obesity (BMI ≥ 25 kg/m2), central obesity (WC ≥ 90/85 cm) | Exploratory: 0.654 (0.637–0.670) | 0.655 | 0.587 | Internal validation (random split 50/50) | Pointsbased scoring system | Middleaged and elderly Chinese (45–70 years) in suburban Shanghai |
| Validation: 0.669 (0.653–0.686) | |||||||||||
| Arellano-Campos et al[67], 2019 | Mexico | Prospective cohort (metabolic syndrome cohort) | 6144 (331 events over median 2.4 years) | Cox proportional hazards; points based on β-coefficient categories | Office-based model: Age, family history of diabetes, WHtR, hypertension, BMI | Office-based model: C-statistic 0.656 (after cross-validation) | NR | NR | Internal validation (k-fold cross-validation, bootstrap) | Points-based scoring system | Middle-aged Mexican adults (≥ 20 years, urban settings) |
| Biochemical model: Age, TG, FPG, hypertension, abdominal obesity | Biochemical model: C-statistic 0.741 (after cross-validation) | ||||||||||
| Cai et al[23], 2020 | China | Retrospective cohort (Rich Healthcare database) | Total: 1688 (103 events); derivation: 1273 (81 events); validation: 415 (22 events) | LASSO regression for feature selection; multivariate Cox regression | Age, BMI, FPG, TC | Derivation: AUC 0.878 (0.861–0.895), C-index 0.862 (0.830–0.894) | NR | NR | Internal validation (random split 75/25); 1000 bootstrap resampling | Nomogram (continuous variables; no simplified pointsbased score) | Chinese adults with hypertension (aged ≥ 20 years) without baseline diabetes |
| Validation: AUC 0.855 (0.836–0.874), C-index 0.841 (0.817–0.865) | |||||||||||
| Bahijri et al[85], 2020 | Saudi Arabia | Cross-sectional (communitybased, stratified 2-stage cluster sampling) | 1403 (328 with dysglycemia: 69 diabetes, 259 prediabetes) | Multivariable logistic regression; points assigned based on β-coefficient categories | Sex, age, WC, history of hyperglycemia, family history of diabetes | 0.76 (0.73–0.79) | Approximately 70% (at cutoff 5 or 6) | Approximately 70% (at cutoff 5 or 6) | Internal validation; model performance assessed on development sample | Pointsbased scoring system (range 0–15) | Saudi adults aged ≥ 20 years without known diabetes |
| Hu et al[86], 2020 | China | Prospective cohort (Dongfeng-Tongji cohort) | 4833 (171 events over 4.6 years) | Cox proportional hazards; restricted cubic splines; Youden index for optimal cut-offs | Age, sex, smoking, physical activity, BMI, TG, FPG | 0.75 (0.70–0.81) | 44.9% (BMI ≥ 24 kg/m2) | 75.4% (BMI ≥ 24 kg/m2) | Internal validation | Cox regression model (no simplified pointsbased score) | Chinese adults aged ≥ 50 years without major underlying diseases (relatively low-risk population) |
| 46.3% (TG ≥ 1.1 mmol/L) | 67.6% (TG ≥ 1.1 mmol/L) | ||||||||||
| 52.9% (FPG ≥ 5.89 mmol/L) | 81.7% (FPG ≥ 5.89 mmol/L) | ||||||||||
| Liu et al[58], 2020 | China | Prospective cohort (Beijing Health Management Cohort) | 43404 (2623 events over median 6.8 years) | Logistic regression with forward selection | Age, education, parental history of diabetes, WHR, BMI, sleep duration, FPG | Comprehensive nomogram: C-index 0.74 (0.71–0.76) in test set | NR | NR | Internal validation (bootstrap); random split (80/20) | Nomogram (points-based scoring system; risk groups defined) | Chinese adults aged 18–80 years from urban Beijing |
| Concise nomogram: C-index 0.73 (0.71–0.75) | |||||||||||
| Wilkinson et al[61], 2020 | United States | Prospective cohort (REGARDS, ARIC) | Development: 12043 (1602 events) over approximately 10 years; validation: 9710 (927 events) | Bayesian logistic regression with weakly informative Cauchy priors | Age, sex, race, BMI, TG, HDL, SBP, DBP, blood glucose | Development (REGARDS): 0.79 (0.78–0.80) | NR | NR | External validation in ARIC (independent cohort) | Bayesian logistic regression equation; probability calculation formula provided | United States Black and White adults aged ≥ 45 years (REGARDS) and 45–64 years (ARIC) |
| External validation (ARIC): 0.85 (0.83–0.86) | |||||||||||
| Zhang et al[78], 2020 | China | Cross-sectional (Henan Rural Cohort) | 36652 (3356 T2DM) | Multiple machine-learning methods: LR, CART, ANN, SVM, RF, GBM; SMOTE for class imbalance | 60 variables including sociodemographic, lifestyle, anthropometric, laboratory, and medical history variables. Top 10: Sweet flavor, urine glucose, age, heart rate, creatinine, WC, uric acid, pulse pressure, insulin, hypertension | GBM (with laboratory data): 0.872 | GBM: NR | GBM: 81.7% | Internal validation (10-fold cross-validation, repeated 100 times) | Machine learning models | Rural Chinese adults aged 18–79 years |
| RF: 0.868 | RF: NR | ||||||||||
| ANN: 0.858 | ANN: Highest sensitivity among all models | ||||||||||
| LR: 0.841 | |||||||||||
| SVM: 0.835 | |||||||||||
| CART: 0.811 | |||||||||||
| Non-laboratory models ranged from 0.767 to 0.817 | |||||||||||
| Shao et al[36], 2020 | China | Prospective cohort (China Health and Nutrition Survey, 2004-2015) | Total: 6023 (349 events over 10 years); derivation: 4498 (257 events); validation: 1525 (92 events) | Multivariable logistic regression; LASSO for feature selection; nomogram | Model A: Age, sex, ethnicity, hypertension, smoking, alcohol, WC, BMI | Model A: 0.788 (0.761–0.816) derivation; 0.818 (0.775–0.861) validation | Model A: 74.7% | Model A: 71.2% | Internal validation: Bootstrap; external validation: Validation in independent provinces | Nomogram (4 separate models with increasing complexity) | Chinese adults aged 20–80 years |
| Model B: Model A + education, soft drinks, tea, physical activity, calories, carbohydrates, fat, protein, triceps skinfold, sleep hours | Model B: 0.807 (0.780–0.834) derivation; 0.823 (0.780–0.865) validation | Model B: 77.5% | Model B: 70.8% | ||||||||
| Model C: Model B + LDL, HDL, TC, TG, insulin, FPG, HbA1c | Model C: 0.905 (0.879–0.932) derivation; 0.915 (0.877–0.953) validation | Model C: 84.1% | Model C: 83.0% | ||||||||
| Model D: LDL, HDL, TC, TG, insulin, FPG, HbA1c | Model D: 0.882 (0.853–0.912) derivation; 0.862 (0.813–0.912) validation | Model D: 73.1% | Model D: 92.3% | ||||||||
| Wang et al[87], 2020 | Japan | Retrospective cohort (DRYAD database, Murakami Memorial Hospital, 2004–2015) | Total: 11113 (373 events); training: 8296 (275 events); validation: 2817 (98 events) | Multivariable Cox regression; nomogram | Age, WC, smoking, fatty liver, FPG, HbA1c | Training: 0.87 (0.85–0.89) | Training: 82% | Training: 79% | Internal validation (random split 75/25) | Nomogram (points-based scoring system) | Japanese adults attending annual health checkups (healthy at baseline) |
| Validation: 0.87 (0.86–0.90) | Validation: 87% | Validation: 73% | |||||||||
| Yang et al[88], 2020 | United States | Crosssectional (NHANES 2011–2016) | Total: 8057 (1336 T2DM); training: 4246 (664 T2DM); test: 1060 (165 T2DM); validation: 2751 (507 T2DM) | Multiple machine-learning methods: LDA, RF, SVM; easy ensemble methods with 100 base models | Age, sex, WC, sagittal abdominal diameter, relative leg length, 60-second pulse, smoking, alcohol, hypertension, family history, general health condition, weight control or loss | LDA ensemble: 0.849 (validation) | LDA ensemble: 81.9% | LDA ensemble: 70.9% | Internal validation (random split 80/20); external validation using NHANES 2015–2016 | Machine-learning models | United States adults aged 18–80 years |
| RF ensemble: 0.836 (validation) | RF ensemble: 81.3% | RF ensemble: 71.3% | |||||||||
| SVM ensemble: 0.848 (validation) | SVM ensemble: 82.4% | SVM ensemble: 71.4% | |||||||||
| Del Razo-Olvera et al[33], 2020 | Mexico | Prospective cohort (derivation: Metabolic syndrome cohort; validation: INPer-IMSS cohort) | Derivation: 3161 (147 events over 2.4 years); Validation: 925 (97 events over 2.8 years) | Cox proportional hazards; stepwise selection; points based on β-coefficients (Framingham method) | History of gestational diabetes, BMI, hypertriglyceridemia, FPG | Derivation: 0.75 (0.73–0.80) | 73% (at cut-off ≥ 15) | 67% (at cut-off ≥ 15) | External validation in independent cohort (INPer-IMSS) | Points-based scoring system | Mexican women of reproductive age (20–49 years) |
| Validation: 0.91 (0.87–0.95) | |||||||||||
| Katsimpris et al[52], 2021 | Germany | Crosssectional (KORA FF4 study) | 1591 (139 T2DM) | Elastic net-penalized regression with bootstrap (5000 samples); logistic regression | Potatoes, mushrooms, onions and garlic, whipping cream, cookies, soft drinks, coffee, tomato sauce, mayonnaise, xylitol, galactose | 0.79 (0.76–0.83) | 10%–90% (range across thresholds) | 53%–98% (range across thresholds) | Internal validation (5-fold crossvalidation; bootstrap) | Logistic regression equation (coefficients provided) | German adults aged 39–88 years |
| Rhee et al[34], 2021 | Korea | Prospective cohort (NHIS-HEALS) | Total: 335302 (23420 events over 10.4 years); training: 268241; validation: 67061 | Deep learning (RNNLSTM); Cox longitudinal summary model for comparison | Age, sex, BMI, SBP, DBP, FPG, TC, hemoglobin, AST, ALT, GGT, proteinuria, smoking, alcohol, exercise, personal history (hypertension, heart disease, stroke, others), family history (hypertension, heart disease, stroke, DM, others) | DL model 5-year: 0.877 (0.869–0.885) | DL 5-year: 81.6% | DL 5-year: 76.5% | Internal validation (random split 80/20) | Deep learning (RNN-LSTM) algorithm | Korean adults aged ≥ 40 years |
| DL model 10-year: 0.827 (0.821–0.833) | DL 10-year: 75.1% | DL 10-year: 74.0% | |||||||||
| Cox model 5-year: 0.842 (0.832–0.852) | |||||||||||
| Cox model 10-year: 0.807 (0.801–0.813) | |||||||||||
| Awad et al[24], 2021 | Qatar | Mathematical modeling (simulated population based on epidemiological model) | 5000 simulated individuals per time point (2020, 2030, 2050) | Logistic regression on simulated samples | Age, sex, obesity, smoking, physical inactivity | 2020: 0.79 (0.77–0.80) | 2020: 79.0% | 2020: 66.8% | External validation using 2012 Qatar STEPwise survey data | Pointsbased scoring system | Qatari adults aged 15–79 years |
| 2030: 0.78 (0.76–0.79) | 2030: 77.5% | 2030: 65.8% | |||||||||
| 2050: 0.76 (0.75–0.78) | 2050: 74.4% | 2050: 64.5% | |||||||||
| Cai et al[63], 2021 | Japan | Retrospective cohort (NAGALA database) | Total: 12940 (201 events); derivation: 9651 (154 events); validation: 3289 (47 events) | LASSO regression for feature selection; multivariate Cox regression | Age, fatty liver, GGT, TG, HbA1c, FPG | Derivation: C-index 0.906 (0.878–0.934), AUC 0.916 (0.889–0.943) | NR | NR | Internal validation (random split 75/25); 1000 bootstrap resampling | Nomogram (continuous variables) | Japanese nonobese adults (BMI < 25 kg/m2) attending health checkups |
| Validation: C-index 0.837 (0.760–0.914), AUC 0.829 (0.753–0.905) | |||||||||||
| Wang et al[89], 2021 | China | Crosssectional (national health examination) | Total: 458153 (38335 T2DM); development: 366523 (30758 T2DM); validation: 91630 (7577 T2DM) | LASSO regression for feature selection; multivariable logistic regression | Age, family history of T2D, WC, TC, TG, BMI, HDL-C, hypertension | Male: Dev 0.864 (0.861–0.866), Val 0.865 (0.859–0.871) | Male: 80.1% | Male: 77.7% | Internal validation (random split 80/20) | Nomogram (sex-specific) | Adults in Western Xinjiang, China (aged ≥ 19 years) |
| Female: Dev 0.816 (0.813–0.819), Val 0.815 (0.808–0.821) | Female: 77.9% | Female: 70.7% | |||||||||
| Cai et al[21], 2021 | Japan | Retrospective cohort (NAGALA database) | Total: 2741 (223 events over 8 years); training: 2058 (157 events); validation: 683 (66 events) | LASSO regression for feature selection; multivariate Cox regression | Smoking status, WC, FPG, HbA1c | Training: C-index 0.839 (0.804–0.874), AUC 0.811 | Training: 77.5% | Training: 72.4% | Internal validation (random split 75/25); 1000 bootstrap resampling | Nomogram (continuous variables) | Japanese adults with NAFLD attending health check-ups |
| Validation: C-index 0.822 (0.777–0.868), AUC 0.805 | Validation: 69.9% | Validation: 75.6% | |||||||||
| de Sousa Tavares and Jorge[90], 2021 | Portugal (Azores) | Cross-sectional (retrospective, primary care data) | 6834 (4661 with T2DM) | Binary logistic regression with interaction terms; backward selection | CVD history, hypertension history, sex, age, BMI, TG, glucose | 0.863 (0.854–0.872) | NR | NR | Internal validation (bootstrapping) | Logistic regression equation with interaction terms | Azorean adults aged ≥ 18 years |
| Mustafina et al[39], 2021 | Russia | Prospective cohort (HAPIEE) | 7739 (915 events over 14 years) | Cox proportional hazards | Full model: Age, BMI, WC, FPG, TG, HDL-C, BP, family history of T2DM | Full model: NR | Full model: Male 76.0%, female 71.7% | Full model: Male 71.5%, female 69.2% | Internal validation; performance assessed on development sample | Points-based scoring system | Russian adults aged 45–69 years |
| Simplified model: WC, hypertension, family history of T2DM | Simplified model: 0.71 | Simplified model: 74.7% | Simplified model: 60.0% | ||||||||
| Deberneh and Kim[91], 2021 | Korea | Retrospective cohort (EHRs) | 253395 subjects; after preprocessing: 17131 per class for training, 200 per class for testing | Machine learning (LR, RF, SVM, XGBoost, CIM, stacking, soft voting) with ANOVA, χ2, RFE feature selection | FPG, HbA1c, TG, BMI, γ-GGT, age, uric acid, sex, smoking, drinking, physical activity, family history | Test: 0.71–0.73 (accuracy-based, no AUC reported) | Test: 71%–74% (accuracy) | Test: 71%–74% (accuracy) | Internal validation: 10-fold cross-validation | Machine-learning models | Korean adults attending health check-ups |
| Oh et al[40], 2021 | Korea | Prospective cohort (KoGES) | Derivation: 3973 (NR); validation: 1700 (NR) | Multivariable logistic regression; points based on β coefficients | KDR: Age, living location, WC, hypertension, family history of T2D, smoking | KDR: 0.657 (0.626–0.715) | NR | NR | Internal validation (random split 70/30) | Points-based scoring system (sex-specific risk scorecard with 10-year risk table) | Korean adults aged 40–69 years without diabetes |
| KDR + FPG: KDR + FPG | KDR + FPG: 0.690 (0.660–0.720) | ||||||||||
| KDR + HbA1c: KDR + HbA1c | KDR + HbA1c: 0.746 (0.717–0.775) | ||||||||||
| Stiglic et al[12], 2021 | 12 European countries (Austria, Belgium, Denmark, France, Germany, Greece, The Netherlands, Israel, Italy, Spain, Sweden, Switzerland) | Prospective cohort (SHARE survey) | 16363 (1360 events over 10 years) | LASSO logistic regression with inverse probability weighting | Global model: BMI, alcohol consumption, physical activity, CASP score, orientation in time, chronic health problems, hypertension, high cholesterol, self-rated health, country indicators (Spain, Israel, Italy) | 0.702 (0.698–0.706) | 0.642 (0.633–0.650) | 0.648 (0.643–0.652) | Internal validation (repeated 10-fold cross-validation with 10 runs) | LASSO logistic regression equation | European adults aged ≥ 50 years without diabetes at baseline |
| Al-Lawati et al[92], 2022 | Oman | Cross-sectional (WHS 2008 for development; Sur Survey 2006 for validation) | Development: 2720 (315 T2DM); validation: 1355 (189 T2DM) | Multivariable logistic regression with backward stepwise elimination | Age, male sex, no education, marital status, urban residence, hypertension, BMI, current tobacco use | Development: 0.80 (0.78–0.82); Validation: 0.74 (0.70–0.78) | Development: 71.1%; Validation: 54.0% | Development: 74.4%; Validation: 79.0% | External validation in independent cohort (Sur Survey 2006) | Points-based scoring system; risk assessment table provided | Omani adults aged ≥ 20 years |
| Sulistiowati and Pradono[93], 2022 | Indonesia | Prospective cohort (Bogor Cohort Study) | 4418 (568 events over 6 years) | Multivariable logistic regression | Age, obesity, central obesity, hypertension, physical activity | 0.70 (0.675–0.721) | 0.766 | 0.503 | Internal validation (split-sample not specified) | Bogor Diabetes Risk Prediction Chart | Indonesian adults aged 25–60 years without diabetes at baseline |
| Tan et al[48], 2022 | Japan | Prospective cohort (NAGALA) | 2012 (incident T2DM 6.81%) | LASSO regression; Cox proportional hazards | WC, HbA1c, FPG, HDL, TG, smoking | Training: 0.819 (0.776–0.858); validation: 0.853 (0.820–0.886) | Training: 74.7%; validation: 77.6% | Training: 77.0%; validation: 88.1% | Internal validation (random split 70/30 with 1000 bootstrap resampling) | Nomogram; online calculator | Japanese adults with abdominal obesity |
| Wang et al[35], 2022 | China | Prospective cohort (Guangzhou Biobank Cohort Study) | 15934 (1302 events over mean 4.1 years) | Bayesian network with structural expectation maximization algorithm | Hypertension, impaired fasting glucose, WC, age, sex, education, occupation, family income, smoking, drinking, physical activity, daytime napping, snoring, self-rated health, heart rate, lipid-lowering drugs, coronary heart disease history, family history of diabetes, BMI, WHR, TG, HDL-C, LDL-C | 0.746 (0.732–0.760) | 0.727 (0.703–0.752) | 0.660 (0.652–0.667) | Internal validation (5-fold cross-validation) | Bayesian network with conditional probability table; post-test probability table for risk combinations | Chinese adults aged ≥ 50 years without diabetes at baseline |
| Nicolaisen et al[28], 2022 | Denmark | Population-based cohort (Danish National Health Survey linked to healthcare registries) | 26007 with incident HbA1c-defined pre-diabetes (2449 progressed to T2D within 5 years) | Fine–Gray competing risk survival model with LASSO variable selection | Baseline HbA1c, age, sex, BMI, antihypertensive drug use, pancreatic disease, cancer, self-reported unhealthy diet, doctor’s advice to lose weight/change diet, lack of social support, good self-rated health | 72.7 (71.2–74.3) | 68.3 (63.9–72.7) | 66.3 (65.4–67.1) | Internal validation (random split 80/20) | Fine–Gray competing risk regression model | Danish adults aged ≥ 30 years with incident HbA1c-defined pre-diabetes |
| Zhao et al[44], 2022 | China | Prospective cohort (Rural Chinese Cohort Study) | 9860 (653 events over median 6.01 years) | Cox proportional hazards | Age, sex, BMI, WC, SBP, family history of diabetes | 0.675 (0.666–0.684) | 72.6% (at cut-off 24) | 53.6% (at cut-off 24) | External validation of existing New Chinese Diabetes Risk Score in independent cohort | New Chinese Diabetes Risk Score: Points-based scoring system | Chinese rural adults aged 20–74 years without diabetes at baseline |
| Sadek et al[94], 2022 | Qatar | Cross-sectional (Qatar Biobank) | Development: 1660 (169 T2DM); Validation: 930 (61 T2DM) | LASSO logistic regression | Age, sex, WHR, history of hypertension, history of hyperlipidemia, education level | Development: 0.870 (0.843–0.896); validation: 0.815 (0.765–0.864) | Development (cut-off 26): 84.6%; Validation: NR | Development: 76.2%; validation: NR | External validation in independent QBB cohort (n = 930) | Qatari Diabetes Mellitus Risk Score: Points-based scoring system | Qatari adults aged 18–89 years |
| Edlitz and Segal[16], 2022 | United Kingdom | Prospective cohort (United Kingdom Biobank) with external validation in Israeli Clalit cohort | Development: 44709 (1.79% incident T2D over mean 7.3 years); validation: 17132 (4.1% T2D) | Logistic regression; Cox regression; scorecard based on β coefficients | Anthropometric model: Age, sex, weight, height, WC, hip circumference, BMI, WHR | Anthropometric: 0.81 (0.77–0.84) | NR | NR | Internal validation (train 56%/val 24%/test 20%); external validation of 4-blood-test model only | Scorecard (points-based); logistic regression; Cox regression | United Kingdom adults aged 40–69 years without diabetes at baseline |
| Four-blood-test model: Age, sex, HbA1c, GGT, HDL, TG | Four blood test: 0.87 (0.85–0.90); external validation: 0.75 (0.74–0.75) | ||||||||||
| Liu et al[22], 2022 | China | Retrospective cohort (health screening data, Wuhan) | 127031 (8298 incident T2D over 2 years) | LASSO feature selection; machine-learning algorithms: LR, DT, RF, XGBoost | Age, sex, education, marital status, hypertension, exercise, current smoking, current drinking, WC, SBP, FPG, TC, TG, HDL-C, LDL-C, ALT, AST, TBIL, Scr, BUN, uric acid | XGBoost: 0.7805; RF: 0.7772; LR: 0.7601; DT: 0.7280 | XGBoost: 0.6452; RF: 0.6428; LR: 0.6320; DT: 0.5821 | XGBoost: 0.7577; RF: 0.7524; LR: 0.7636; DT: 0.7633 | Internal validation (random split 80/20) | Machine learning models (no simplified scoring system); SHAP for feature importance | Chinese adults aged ≥ 65 years without diabetes at baseline |
| Martínez-Hervás et al[95], 2022 | Spain | Prospective cohort | 2408 (156 incident T2D over 7.5 years) | CHAID decision tree algorithm | FPG, fasting TG, age, sex, BMI | 0.764 (0.722–0.807) for FPG alone; model correctly classified 93.5% | NR | NR | Internal validation (cross-validation) | CHAID decision tree diagram with risk stratification nodes | Spanish adults aged ≥ 18 years without diabetes at baseline |
| Dong et al[57], 2022 | China (Hong Kong) | Cross-sectional (Hong Kong Population Health Survey 2014/15) | 1857 (280 newly detected DM/pre-DM) | Logistic regression (AIC stepwise) | Age, BMI, WHR, smoking, sleep duration, vigorous recreational activity time, fruit consumption | LR: 0.812 (0.769–0.853) | LR at 15% threshold: 77.6% | LR: 68.1% | Internal validation (random split 2/3 development, 1/3 validation) | Logistic regression equation; online risk calculator | Chinese adults aged 18–84 years without self-reported DM/pre-DM or major chronic diseases |
| XGBoost with isotonic calibration | Age, BMI, WHR, SBP, WC, sleep duration, smoking, vigorous recreational activity time | XGBoost: 0.822 (0.779–0.863) | XGBoost at 15% threshold: 72.4% | XGBoost: 77.9% | XGBoost model with SHAP interpretation; online risk calculator | ||||||
| Tong et al[75], 2022 | China | Retrospective cohort (Beijing Health Management Cohort) | 44852 (2912 incident T2D over median 3.58 years) | Multivariable Cox regression | Sex, age, BMI, FPG, hypertension, dyslipidemia, sCr | Dynamic nomogram: 0.909 (0.897–0.920) (10-fold CV) | NR | NR | Internal validation (random split 70/30); 10-fold cross-validation | Dynamic nomogram | Urban Chinese current or retired employees aged 16–68 years without diabetes at baseline |
| Boersma et al[59], 2022 | Netherlands | Prospective cohort (Lifelines) | Derivation: 58377 (2146 new diabetes) | Multivariable logistic regression | Model 1: Age group, BMI group, SAF group | Model 1: 0.783 (0.774–0.793) | Model 1: 78 | Model 1: 66 | Internal validation (bootstrapping); external validation comparison to concise FINDRISC model | Points-based scoring system | Dutch general population adults (aged 25–50 years and their family members) |
| Model 2: Age group, BMI group, SAF group, parental history of diabetes | Model 2: 0.792 (0.783–0.802) | Model 2: 74 | Model 2: 70 | ||||||||
| Wang et al[54], 2023 | China | Cross-sectional | Pre-SMOTE: 4106 (149 T2DM); Post-SMOTE: 8013 (4023 T2DM) | BP neural network, logistic regression, SVM, CART, C4.5, DNN | Age, DBP, FPG, TC, TG, HDL-C, LDL-C, drinking, consumption frequency of cereals, potatoes, beans, fruits, eggs, milk, poultry, fish | BPNN: 0.977 LR: 0.962 SVM: 0.911 CART: 0.906 C4.5: 0.888 DNN: 0.845 | BPNN: 92.8 LR: 86.0 SVM: 89.0 CART: 84.8 C4.5: 84.9 DNN: 82.9 | BPNN: 94.6 LR: 93.0 SVM: 93.3 CART: 93.3 C4.5: 92.7 DNN: 86.1 | Internal validation (10-fold cross-validation, random split 70/30) | Machine learning models; logistic regression equation provided | Chinese adults aged ≥ 18 years in Dongguan, China |
| Zheng et al[46], 2023 | China | Prospective cohort (Kailuan Study) | Total: 18384 (5697 events); training: 12870; internal validation: 5514; external validation: 10620 + 8513 | Cox regression with 2-step selection (univariate + LASSO-Cox) | Age, BMI, WC, DBP, TG, FPG, fatty liver | Men: 0.741 (0.723–0.760) | NR | NR | Internal validation (random split 70/30) + external validation (2 independent cohorts) | Points-based scoring system; Web calculator | Chinese adults with IFG |
| Women: 0.762 (0.720–0.802) | |||||||||||
| Yonel et al[74], 2023 | Germany | Population-based cohort (SHIP-TREND-0 for development; SHIP-START-0 for external validation) | Development: 3339 (329 events); external validation: 2381 (403 events) | Logistic regression with backward selection; Heuristic shrinkage | Age, sex, BMI, smoking status, first-degree relative with diabetes, presence of dental prosthesis, presence of mobile teeth, history of periodontal treatment, probing pocket depths ≥ 5 mm | Development: 0.72 (0.69–0.75) | Point score (development): 77.0 (76.8–77.2) | Point score (development): 51.5 (51.4–51.7) | Internal validation (backward selection with multiple imputation, heuristic shrinkage); external validation in independent cohort | Full model (coefficients); Simplified point-based scoring system | German adults aged ≥ 40 years without known diabetes, attending dental settings |
| External validation (full model): 0.69 (0.67–0.72) | Point score (external validation): 79.2 (79.0–79.4) | Point score (external validation): 49.9 (49.8–50.0) | |||||||||
| External validation (point score): 0.69 (0.66–0.71) | |||||||||||
| Hu et al[62], 2023 | China | Retrospective cohort | Total: 184188 (19699 events); training: 92177; validation: 92011 | LASSO regression (compared with full Cox, stepwise Cox, MFP, XGBoost) | Age, BMI, FPG, TG, SBP, Scr | Training: 0.7341 (0.7290–0.7392) | Training: 68.00 | Training: 67.13 | Internal validation (random split 50/50) | Nomogram; Risk prediction formula | Chinese adults aged ≥ 20 years without prediabetes at baseline |
| Validation: 0.7336 (0.7285–0.7387) | Validation: 65.35 | Validation: 69.91 | |||||||||
| Yang et al[96], 2024 | China | Prospective cohort (physical examination center) | Total: 4602 (760 events); training: 3221; test: 1381 | Logistic regression with stepwise selection | Age, sex, BMI, FPG, HDL-C, LDL-C, fatty liver, liver dysfunction (ALT > 50 U/L and AST > 40 U/L) | Training: 0.787 (0.765–0.808) | NR | NR | Internal validation (random split 70/30; 1000 bootstrap resampling) | Nomogram; logistic regression equation | Chinese adults aged ≥ 20 years with newly diagnosed prediabetes |
| Test: 0.800 (0.770–0.829) | |||||||||||
| Ojurongbe et al[27], 2024 | Nigeria | Case-control (hospital-based) | Total: 444 (172 cases, 272 controls); training: 312; test: 132 | Penalized logistic regression with nested cross-validation and sequential backward feature selection | WHR, TG, catalase, atherogenic indices of plasma | Training: 0.99 (0.97–1.00) | Training: 96 | Training: 93 | Internal validation (10-fold nested cross-validation with 20 repetitions) | Web-based application; logistic regression equation | Nigerian adults aged > 18 years attending a diabetes clinic |
| Test: 0.94 (0.89–0.99) | Test: 94 | Test: 88 | |||||||||
| Hafezi et al[68], 2024 | Iran | Prospective cohort (MASHAD study) | Total: 6710 (1256 events); training: 5032; test: 1678 | Logistic regression; decision tree (CHAID) | Model A: BMI, VAI, LAP, abdominal volume index | Model A (LR): Approximately 0.67 | NR | Model A (train): 99%; model A (test): 100% | Internal validation (random split 75/25) | Logistic regression equations; Decision tree with 14 IF-THEN rules | Iranian adults aged 35–65 years without diabetes at baseline |
| Model B: Model A + age, sex, physical activity level, anxiety, depression, smoking, dietary composition, energy intake | Model B (LR): Approximately 0.70 | Model B (train): 99%; model B (test): 100% | |||||||||
| Xu et al[97], 2024 | Japan | Prospective cohort (JPHC Study) | Development: 10986 (707 events); external validation: 11345 (673 events) | Logistic regression with backward selection | Model 1 (non-invasive): Sex, BMI, family history of DM, DBP | Model 1: 0.643 | NR | NR | Internal validation (bootstrap, 1000 iterations); internal –external cross-validation (leave-one-area-out); external validation (J-ECOH Study) | Logistic regression equations; Excel spreadsheet for risk calculation | Japanese adults aged 46–75 years without diabetes at baseline |
| Model 2 (invasive): Family history of DM, HbA1c | Model 2: 0.786 | ||||||||||
| Model 3 (invasive): Family history of DM, HbA1c, FPG | Model 3: 0.845 | ||||||||||
| Lin et al[70], 2024 | China | Retrospective cohort | Total: 2235 (99 events); training: 1564; validation: 671 | LASSO logistic regression | Age, sex, BMI, FPG, TG, ALT, ALT/AST, BUN, Hb | Training: 0.824 (0.765–0.883) | NR | NR | Internal validation (random split 70/30; 1000 bootstrap resampling) | Dynamic online nomogram; logistic regression equation | Chinese older adults (≥ 60 years) with normal FBG |
| Validation: 0.809 (0.732–0.886) | |||||||||||
| Kawasoe et al[64], 2025 | Japan | Retrospective cohort | Total: 31084 (1548 events); derivation: 15542; validation: 15542 | Logistic regression | Model 1 (invasive): Age, sex, BMI, FPG, HbA1c | Model 1: 0.89 | Model 1: 81 | Model 1: 81 | Internal validation (random split 50/50) | Logistic regression equations | Japanese adults aged 30–69 years without diabetes at baseline |
| Model 2 (non-invasive): Age, sex, BMI, hypertension | Model 2: 0.71 | Model 2: 75 | Model 2: 54 | ||||||||
| Xie et al[13], 2025 | United Kingdom/Germany | Prospective cohort (United Kingdom Biobank; ESTHER) | Development: 60362 (2477 events); internal validation: 25870 (1059 events); external validation: 4383 (495 events) | LASSO-Cox regression with bootstrap (1000 resamples) | Clinical CDRS: Age, sex, BMI, smoking, family history of diabetes, antihypertensive medication, steroid medication, HbA1c; plus 11 metabolites (glucose, citrate, lactate, pyruvate, 3-hydroxybutyrate, acetate, glutamine, tyrosine, IDL-CE-pct, M-LDL-TG-pct, LA-pct) | Clinical CDRS: 0.815 (0.800–0.829) | NR | NR | Internal validation (random split 70/30); external validation (ESTHER cohort) | Cox regression equations | European adults (United Kingdom and Germany) aged 50–69 years without diabetes at baseline |
| United Kingdom Biobank-DRS (full): 0.834 (0.820–0.847) | |||||||||||
| United Kingdom Biobank-DRS (concise): 0.830 (0.815–0.844) | |||||||||||
| Wang et al[98], 2025 | Japan | Prospective cohort (NAGALA) | Total: 15464 (262 events) | Cox proportional hazards regression | Age, WC, ALT, HbA1c, FPG, fatty liver, current smoking, heavy alcohol consumption, HDL-C | Combined model: 0.90 (0.88–0.92) | 86.3 | 82.8 | Internal validation (not specified) | Risk score combining 9 factors | Japanese adults without diabetes at baseline (mean age 43.7 years) |
| Shahraki et al[66], 2025 | Iran | Prospective cohort (Isfahan Diabetes Prevention Study) | Total: 1765 (diabetes: 7.4%; prediabetes: 32.6%) | Cox proportional hazards regression with optimal cutoff categorization | Diabetes Model 1: WHR, HbA1c, OGTT-AUC, lipid index | Diabetes model 1: 0.71 (0.66–0.77) | Diabetes model 1: 78 | Diabetes model 1: 52 | Internal validation (ROC analysis; compared with FINDRISC) | Points-based scoring system | First-degree relatives of Iranian patients with type 2 diabetes, with normal glucose tolerance at baseline |
| Diabetes model 2: WHR, HbA1c, FPG, lipid index | Diabetes model 2: 0.69 (0.63–0.74) | Diabetes model 2: 77 | Diabetes model 2: 52 | ||||||||
| Chee et al[73], 2025 | Singapore | Cross-sectional | 1074 (65 confirmed diabetes, 83 confirmed prediabetes) | Logistic regression with stepwise variable selection | Model IV: BMI ≥ 23 kg/m2, family history of DM, smoking, stage III/IV periodontitis | Model IV: 0.717 (0.689–0.744) | Model IV: 71 | Model IV: 62 | Internal validation | Clinical risk model based on ORs; risk stratification using 4 simple factors | Asian dental patients (Singapore) aged ≥ 21 years without prior diabetes diagnosis |
| Model V: BMI ≥ 23 kg/m2, family history of DM, smoking, severe periodontitis | Model V: 0.721 (0.693–0.748) | Model V: 71 | Model V: 60 | ||||||||
| Munekawa et al[47], 2025 | Japan | Retrospective cohort (Panasonic Cohort) | Development: 72124 (5133 events); external validation: 12885 (712 events) | Cox proportional hazards model with interval censoring; natural cubic splines; bootstrap variable selection | Age, sex, BMI, SBP, log-TG, HDL, log-ALT, FPG, weight gain, smoking status | Internal validation (optimism-corrected C-index): 0.877 (0.852–0.882) | NR | NR | Internal validation (2000 bootstrap resamples); external validation (NAGALA cohort) | Cox regression equation | Japanese adults aged ≥ 40 years without diabetes at baseline |
| External validation C-index: 0.882 | |||||||||||
| Kiviniemi et al[30], 2025 | Finland | Multi-cohort prospective (FINRISK 1997-2012, NFBC1966) | Development: 4926 (96 events); validation: 17385 (397 events) | Logistic regression with penalization (ridge, elastic net, LASSO) and stepwise selection | Baseline model: Age, sex, BMI, WC, systolic/diastolic BP, HDL-C, TC, TG, glucose, current smoking, BP medication, lipid medication, diabetes family history | Baseline model: 0.832–0.913 (validation cohorts) | NR | NR | External validation (4 independent cohorts) | Logistic regression equations | Finnish adults aged 25–74 years without diabetes at baseline |
| Extended models: Baseline + 154 NMR metabolites | Best extended model: 0.840–0.915 (validation cohorts) | ||||||||||
| Alareeki et al[25], 2025 | Jordan | Mathematical modeling (simulated population based on epidemiological model) | Derivation: 5000 simulated individuals per time point (2020, 2030, 2050) | Multivariable logistic regression | Age group, sex, obesity, smoking, physical inactivity | 2020: 0.79 (0.77–0.80) | 2020: 78.7 (77.5–79.8) | 2020: 64.2 (62.9–65.6) | Internal validation (compared with survey-based risk score in 2017 data); external validation comparison with regional and international risk scores | Points-based scoring system | Jordanian adults aged 20–79 years without known diabetes |
| 2030: 0.78 (0.77–0.80) | 2030: 76.1 (74.9–77.3) | 2030: 68.4 (67.1–69.6) | |||||||||
| 2050: 0.77 (0.76–0.79) | 2050: 74.2 (73.0–75.4) | 2050: 65.6 (64.2–66.9) | |||||||||
| Chen et al[99], 2025 | China (Taiwan) | Prospective cohort (Taiwan Biobank) | Development: 65112 (2485 events); external validation (United Kingdom Biobank): 86484 (1187 events); external validation (APHS): > 4300000 | LASSO logistic regression | HbA1c, blood glucose, PEF, PRS, age, WHR, family history of diabetes, BMI, TG, SGPT, prediabetes, self-reported hyperlipidemia, mixed hyperlipidemia (ICD) | Taiwan Biobank testing: 0.9058 (0.8915–0.9202) | Taiwan Biobank testing: 78.34 (71.65–86.61) | Taiwan Biobank testing: 85.88 (77.08–91.20) | External validation (United Kingdom Biobank, APHS) | Logistic regression coefficients; risk prediction equation | Han Chinese adults (Taiwan) aged ≥ 20 years without diabetes at baseline |
| United Kingdom Biobank external validation: 0.8869 (0.8543–0.9112) | United Kingdom Biobank external validation: NR | United Kingdom Biobank external validation: NR | |||||||||
| Han et al[31], 2025 | China | Meta-analysis + prospective cohort validation | Development: Meta-analysis of 70 studies; validation: 3 cohorts (Hongguang, Bao’an, Kailuan) | Pooled effect estimates from meta-analysis; Framingham method for risk scoring | Sex, age, smoking, central obesity, exercise, BMI, WHtR, hypertension, fatty liver, family history of diabetes, FPG, TG, TyG, HDL-C, uric acid | Hongguang: 0.783 | Hongguang: NR | Hongguang: NR | External validation (3 independent Chinese cohorts) | Points-based scoring system (iCARE-DM) | Chinese elderly adults (≥ 50 years) without diabetes at baseline |
| Bao’an: 0.766 | Bao’an: NR | Bao’an: NR | |||||||||
| Kailuan: 0.741 | Kailuan: NR | Kailuan: NR | |||||||||
| Zhang et al[53], 2025 | China | Prospective cohort (HAELS) | Total: 1127 (107 events); training/validation: Bootstrap resampling | Cox proportional hazards regression with stepwise selection (SLE/SLS = 0.1) | Age, exercise, WC, FPG, TG, SBP, dessert intake | Training: 0.752 | NR | NR | Internal validation (bootstrap resampling, 2 iterations) | Nomogram | Chinese older adults (≥ 65 years) with prediabetes (FPG 5.6–7.0 mmol/L) |
| Validation: 0.793 | |||||||||||
| Baynouna AlKetbi et al[71], 2025 | United Arab Emirates | Retrospective cohort (Weqaya screening program) | Total: 8699; analysis: 6772 (643 events) | Cox proportional hazards regression with stepwise variable selection | HbA1c, random blood glucose, BMI, current smoking, sex, age, mean BP, eGFR percentile, HDL, hypertension at baseline | Full model: 0.837 (0.818–0.856) | 75.1 | 78.1 | Internal validation (time-dependent ROC) | Cox regression HRs; risk score based on coefficients | United Arab Emirates adults (Emirati nationals) aged ≥ 18 years without diabetes at baseline |
| HBA1C alone: 0.784 (0.761–0.807) | |||||||||||
| RBS alone: 0.698 (0.672–0.723) | |||||||||||
| Satoh et al[45], 2025 | Japan | Retrospective cohort (SKDB) | Total: 463248 (78431 events); derivation: 308832 (52152 events); validation: 154416 (26279 events) | Cox proportional hazards regression with stepwise selection | Age, sex, BMI, SBP, TG, HDL-C, LDL-C, AST, γ-GTP, HbA1c, eGFR, urine protein, antihypertensive medication, dyslipidemia medication, heavy drinking, exercise habits | C-index (validation): 0.656 (0.652–0.659) | NR | NR | Internal validation (random split 2:1) | Points-based scoring system | Japanese adults aged ≥ 40 years without diabetes at baseline |
Table 3 Frequency of predictor variables across the included models
| Category | Predictor | Frequency |
| Non-modifiable | Age | 83 |
| Sex | 48 | |
| Family history of diabetes | 41 | |
| Education | 7 | |
| Race/ethnicity | 5 | |
| Obesity | Body mass index | 68 |
| Waist circumference | 28 | |
| Waisttohip ratio | 12 | |
| Obesity/central obesity | 5 | |
| Waist-to-height ratio | 3 | |
| Lifestyle | Smoking | 36 |
| Physical activity | 23 | |
| Dietary factors (e.g., fruit, vegetable, meat, dessert intake, tea) | 14 | |
| Alcohol | 11 | |
| Sleep duration | 5 | |
| Glycemic | Glucose (FPG or random glucose) | 51 |
| HbA1c | 24 | |
| Post-load glucose measures (2hPG or OGTT-AUC) | 4 | |
| Insulin | 3 | |
| Lipid | Triglycerides | 39 |
| HDL | 20 | |
| Total cholesterol | 9 | |
| LDL | 8 | |
| Hyperlipidemia/dyslipidemia medication use | 8 | |
| Lipid accumulation product/lipid indices | 3 | |
| Blood pressure | Hypertension | 34 |
| SBP | 15 | |
| DBP | 6 | |
| Liver | Liver dysfunction/ALT/AST | 8 |
| Fatty liver | 6 | |
| Metabolic | Uric acid | 4 |
| Creatinine/eGFR/renal function | 3 |
- Citation: Zhao XF, Tang SS, Ji HY, An XD, Kang XM, Jiang LL, Lian FM. Potentially modifiable predictors in models for undiagnosed and incident type 2 diabetes: A systematic review. World J Diabetes 2026; 17(11): 123851
- URL: https://www.wjgnet.com/1948-9358/full/v17/i11/123851.htm
- DOI: https://dx.doi.org/10.4239/wjd.123851