<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>41(6)</volume><submitter>Tsoi STF</submitter><funding>Hong Kong Government Health and Medical Research Fund</funding><funding>Hong Kong Research Grants Council</funding><pubmed_abstract>&lt;h4>Aims&lt;/h4>Accurate identification of individuals with maturity-onset diabetes of the young (MODY) can support precision diabetes management. However, diagnosing MODY is challenging due to overlapping clinical features with type 2 diabetes. We aimed to develop a prediction model for identifying Chinese with high likelihood of MODY for further genetic testing.&lt;h4>Methods&lt;/h4>We developed a logistic regression model using clinical data from an unselected cohort of 1021 Chinese with young-onset (age at diagnosis ≤ 40) non-type 1 diabetes enrolled in the Hong Kong Diabetes Register, 1.9% (n = 19) of whom had MODY (GCK-, HNF1A-, HNF4A- and HNF1B-MODY) by molecular confirmation. We validated the model in an independent local cohort of 822 Chinese with young-onset non-type 1 diabetes. We compared the performance of the new Chinese-specific MODY prediction model with an existing MODY probability calculator in the validation cohort.&lt;h4>Results&lt;/h4>The prediction model comprised the following clinical variables: current age, age at diagnosis, sex, body mass index, systolic blood pressure, HDL-cholesterol, LDL-cholesterol, triglyceride and fasting C-peptide. It demonstrated acceptable discrimination of patients with MODY in the validation dataset, with an area under the curve of 0.813 (95% confidence interval 0.647-0.979). At the probability cut-off of 50%, the model achieved a sensitivity of 72.7% and a specificity of 92.4%. It allows identification of one MODY case in every nine genetic tests conducted.&lt;h4>Conclusion&lt;/h4>We developed a comprehensive Chinese-specific MODY prediction model. This model can be used in unselected Chinese with young-onset non-type 1 diabetes to identify high-risk individuals for genetic testing.</pubmed_abstract><journal>Diabetes/metabolism research and reviews</journal><pagination>e70087</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12445802</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Development of a Chinese-Specific Clinical Model to Predict Maturity-Onset Diabetes of the Young.</pubmed_title><pmcid>PMC12445802</pmcid><pubmed_authors>Chow E</pubmed_authors><pubmed_authors>Ma RCW</pubmed_authors><pubmed_authors>So WY</pubmed_authors><pubmed_authors>Fan Y</pubmed_authors><pubmed_authors>Lau ESH</pubmed_authors><pubmed_authors>Kong APS</pubmed_authors><pubmed_authors>Fan B</pubmed_authors><pubmed_authors>O CK</pubmed_authors><pubmed_authors>Chan JCN</pubmed_authors><pubmed_authors>Tsoi STF</pubmed_authors><pubmed_authors>Lim CKP</pubmed_authors><pubmed_authors>Luk AOY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of a Chinese-Specific Clinical Model to Predict Maturity-Onset Diabetes of the Young.</name><description>&lt;h4>Aims&lt;/h4>Accurate identification of individuals with maturity-onset diabetes of the young (MODY) can support precision diabetes management. However, diagnosing MODY is challenging due to overlapping clinical features with type 2 diabetes. We aimed to develop a prediction model for identifying Chinese with high likelihood of MODY for further genetic testing.&lt;h4>Methods&lt;/h4>We developed a logistic regression model using clinical data from an unselected cohort of 1021 Chinese with young-onset (age at diagnosis ≤ 40) non-type 1 diabetes enrolled in the Hong Kong Diabetes Register, 1.9% (n = 19) of whom had MODY (GCK-, HNF1A-, HNF4A- and HNF1B-MODY) by molecular confirmation. We validated the model in an independent local cohort of 822 Chinese with young-onset non-type 1 diabetes. We compared the performance of the new Chinese-specific MODY prediction model with an existing MODY probability calculator in the validation cohort.&lt;h4>Results&lt;/h4>The prediction model comprised the following clinical variables: current age, age at diagnosis, sex, body mass index, systolic blood pressure, HDL-cholesterol, LDL-cholesterol, triglyceride and fasting C-peptide. It demonstrated acceptable discrimination of patients with MODY in the validation dataset, with an area under the curve of 0.813 (95% confidence interval 0.647-0.979). At the probability cut-off of 50%, the model achieved a sensitivity of 72.7% and a specificity of 92.4%. It allows identification of one MODY case in every nine genetic tests conducted.&lt;h4>Conclusion&lt;/h4>We developed a comprehensive Chinese-specific MODY prediction model. This model can be used in unselected Chinese with young-onset non-type 1 diabetes to identify high-risk individuals for genetic testing.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-03T14:57:37.259Z</modification><creation>2026-04-28T03:11:32.416Z</creation></dates><accession>S-EPMC12445802</accession><cross_references><pubmed>40966384</pubmed><doi>10.1002/dmrr.70087</doi></cross_references></HashMap>