A large-scale real-world dataset integrating longitudinal clinical, imaging, and outcomes data for patients receiving GLP-1–based therapies — including semaglutide, tirzepatide, liraglutide, and dulaglutide — across care settings.

CT abdomen (NIH color map) showing body composition changes pre- and post-GLP-1 treatment. Visceral and subcutaneous fat distribution visualized longitudinally. De-identified.




Structured EHR elements linked to imaging data and quantitative biomarkers, with timestamps aligned to treatment initiation and follow-up.

Endocrinology & Metabolism
Obesity · Type 2 Diabetes (T2D) · Obesity or overweight with comorbidity · T2D with inadequate glycemic control or CV risk
GLP-1 receptor agonists · Dual GIP/GLP-1 receptor agonists
DEXA (body composition, bone mineral) · MR abdomen (PDFF, elastography) · CT abdomen · CT coronary arteries · CT chest · US abdomen/liver
Demographics · diagnoses · procedures · medications · pharmacy dispensing · labs (HbA1c, lipids, liver enzymes)
Internal medicine · primary care · endocrinology · pharmacy dispensing · radiology (DICOM) · laboratory
Raw DICOMs and standardized derived measures · HIPAA de-identified · Provenance documentation built into acquisition · Timestamps aligned to treatment initiation and follow-up
The dataset covers patients receiving the following therapies, enabling comparative effectiveness analyses across molecules and formulations.

Ozempic® · Wegovy® · Rybelsus®
GLP-1 RA
Mounjaro® · Zepbound®
GIP / GLP-1 RA
Victoza® · Saxenda®
GLP-1 RA
Trulicity®
GLP-1 RA
From longitudinal outcomes assessment to AI model development.

Track GLP-1 effects on visceral fat, lean mass, and metabolic biomarkers over time, with imaging timestamps aligned to treatment initiation and follow-up milestones.
Characterize progression or regression of metabolic dysfunction-associated steatotic liver disease via PDFF, elastography, and liver steatosis grading across treatment cohorts.
Assess coronary artery calcium, aortic calcification, and epicardial adipose tissue changes as cardiovascular surrogate endpoints in GLP-1 treated populations.
Assess coronary artery calcium, aortic calcification, and epicardial adipose tissue changes as cardiovascular surrogate endpoints in GLP-1 treated populations.
Build predictive models using baseline imaging phenotypes to identify which patients are most likely to respond to specific GLP-1 therapies.
Monitor muscle loss, hepatic changes, and bone density in real-world populations. Develop AI models for automated imaging feature extraction in cardiometabolic disease.
Both raw DICOMs and standardized derived measures, with timestamps aligned to treatment initiation and follow-up. Biomarker selection is tailored to your programme's endpoints and therapeutic objectives.

