CREATING INDIVIDUALIZED HBA1C TARGETS USING PREDICTIVE MODELING
Author(s)
Karpati T1, Curtis BH2, Feldman B1, Strizek AA2, Leventer-Roberts M1, He X3, Raz I4, Levin Iaina N3, Rubin G5, Balicer RD6
1Clalit Health Services, Tel Aviv, Israel, 2Eli Lilly and Company, Sydney, Australia, 3Eli Lilly and Company, Indianapolis, IN, USA, 4Hadassah Medical Organization, Jerusalem, Israel, 5Eli Lilly and Company, Israel, Ra’anana, Israel, 6Clalit Research Institute, Tel Aviv, Israel
OBJECTIVES: Glycemic targets (HbA1c) have been recommended to guide therapeutic treatment for patients with type 2 diabetes mellitus (T2DM) and reduce the risk of primary and secondary complications. In this study, we describe a methodology using predictive models to create individualized glycemic target ranges that are associated with a greater reduction of the risk for complications. METHODS: The study population includes adult members of Clalit Health Services with three-seven years T2DM duration, without concurrent serious chronic conditions (cancer, chronic infections, and cirrhosis). We built a predictive model to assess the future risk of common T2DM complications (macro/microvascular diseases, hypoglycemic events and all-cause mortality), based on the index HbA1c, while controlling for baseline demographic and clinical information. Individualized HbA1c target ranges were simulated in order to determine which specific range would minimize each individual’s risk of complications as identified by the predictive models. The final sub-analyses compared rates of complications associated with the model-based individualized HbA1c target range to rates of complications among those individuals whose index HbA1c was or was not within the target range. RESULTS: We developed a new methodology for the calculation of an individualized glycemic target. The obtained targets yielded 20% more individuals within the recommended range, compared to the standard guidelines, while maintaining the same outcome rates, and have the potential to more accurately identify those at risk for future outcomes. CONCLUSIONS: We successfully created a tool to calculate individualized HbA1c target ranges. Target ranges can potentially reduce the need for intensive intervention in some populations and highlight other populations at greatest risk. Validation of the tool using an independent external dataset is required. This study is the first attempt to generate an individualized glycemic control target tool based on predictive modeling and establishes how precision medicine can be incorporated into diabetes care management.
Conference/Value in Health Info
2017-11, ISPOR Europe 2017, Glasgow, Scotland
Value in Health, Vol. 20, No. 9 (October 2017)
Code
PRM17
Topic
Clinical Outcomes, Methodological & Statistical Research, Real World Data & Information Systems
Topic Subcategory
Clinical Outcomes Assessment, Confounding, Selection Bias Correction, Causal Inference, Modeling and simulation, Reproducibility & Replicability
Disease
Cardiovascular Disorders, Diabetes/Endocrine/Metabolic Disorders, Multiple Diseases
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