Predicting responsiveness to GLP-1 pathway drugs using real-world data

BMC Endocr Disord. 2024 Dec 18;24(1):269. doi: 10.1186/s12902-024-01798-9.

Abstract

Background: Medications targeting the glucagon-like peptide-1 (GLP-1) pathway are an important therapeutic class currently used for the treatment of Type 2 diabetes (T2D). However, there is not enough known about which subgroups of patients would receive the most benefit from these medications.

Objective: The goal of this study was to develop a predictive model for patient responsiveness to medications, here collectively called GLP-1 M, that include GLP-1 receptor agonists and dipeptidyl peptidase-4 (DPP4) inhibitors (that normally degrade endogenously-produced GLP-1). Such a model could guide clinicians to consider certain patient characteristics when prescribing second line medications for T2D.

Methods: We analyzed de-identified electronic health records of 7856 subjects with T2D treated with GLP-1 M drugs at Vanderbilt University Medical Center from 2003-2019. Using common clinical features (including commonly ordered lab tests, demographic information, other T2D medications, and diabetes-associated complications), we compared four different models: logistic regression, LightGBM, artificial neural network (ANN), and support vector classifier (SVC).

Results: Our analysis revealed that the traditional logistic regression model outperforms the other machine learning models, with an area under the Receiver Operating Characteristic curve (auROC) of 0.77.Our model showed that higher pre-treatment HbA1C is a dominant feature for predicting better response to GLP-1 M, while features such as use of thiazolidinediones or sulfonylureas is correlated with poorer response to GLP-1 M, as assessed by lowering of hemoglobin A1C (HbA1C), a standard marker of glycated hemoglobin used for assessing glycemic control in individuals with diabetes. Among female subjects under 40 taking GLP-1 M, the simultaneous use of non-steroidal anti-inflammatory drugs (NSAIDs) was associated with a greater reduction in HbA1C (0.82 ± 1.72% vs 0.28 ± 1.70%, p = 0.008).

Conclusion: These findings indicate a thorough analysis of real-world electronic health records could reveal new information to improve treatment decisions for the treatment of T2D. The predictive model developed in this study highlights the importance of considering individual patient characteristics and medication interactions when prescribing GLP-1 M drugs.

1. Patient characteristics such as poorer blood glucose control, higher body mass, and shorter duration of diabetes predict better response to medications that target the GLP-1 pathway. 2. Simultaneous use of NSAIDs (for example ibuprofen) was associated with better responsiveness in women under 40.3. Combining GLP-1 pathway medications with some other commonly used T2D medications (for example thiazolidinediones or sulfonylureas) may not have an additional benefit.

Keywords: Electronic health record; GLP-1; HbA1c; Predictive model; Type 2 diabetes.

MeSH terms

  • Aged
  • Biomarkers / analysis
  • Diabetes Mellitus, Type 2* / drug therapy
  • Diabetes Mellitus, Type 2* / metabolism
  • Dipeptidyl-Peptidase IV Inhibitors* / therapeutic use
  • Female
  • Glucagon-Like Peptide 1*
  • Glucagon-Like Peptide-1 Receptor* / agonists
  • Glycated Hemoglobin / analysis
  • Glycated Hemoglobin / metabolism
  • Humans
  • Hypoglycemic Agents* / therapeutic use
  • Machine Learning
  • Male
  • Middle Aged
  • Prognosis

Substances

  • Hypoglycemic Agents
  • Dipeptidyl-Peptidase IV Inhibitors
  • Glucagon-Like Peptide 1
  • Glucagon-Like Peptide-1 Receptor
  • Glycated Hemoglobin
  • Biomarkers
  • hemoglobin A1c protein, human