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Endocrine Abstracts (2025) 110 S39.3 | DOI: 10.1530/endoabs.110.S39.3

ECEESPE2025 Symposia Symposia (123 abstracts)

The impact of rare gene variants in common diabetes and obesity

Amélie Bonnefond 1


1Inserm/CNRS UMR 1283/8199, Pasteur Institute of Lille, France


The boundary between monogenic and polygenic type 2 diabetes (T2D) or oebsity is more fluid than previously thought. Emerging research has revealed an intermediate oligogenic form of T2D/obesity, which serves as a crucial genetic bridge between these two extremes. In this presentation, I will discuss recent scientific advances supporting the classification of genes involved in oligogenic T2D/obesity. While polygenic T2D/obesity research has significantly advanced our understanding of genetic susceptibility, it has faced limitations in pinpointing direct causal relationships between genetic signals and the molecular mechanisms driving the disease. In contrast, studies on oligogenic T2D/obesity have provided clearer causal links between specific genes and disease risk, uncovering novel therapeutic targets. By recognizing oligogenic T2D/obesity as a distinct genetic entity, we open new avenues for research and precision medicine, moving beyond broad genetic risk scores toward targeted therapeutic interventions.

Volume 110

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course

European Society of Endocrinology 
European Society for Paediatric Endocrinology 

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