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Early Type 1 Diabetes Detection Solutions

Type 1 Diabetes: Early detection saves lives

Type 1 Diabetes (T1D) affects millions worldwide, yet most cases aren't identified until irreversible beta-cell damage has already occurred. Screening for T1D autoantibodies can identify at-risk individuals months or even years before symptoms appear, enabling earlier intervention, preventing life-threatening emergencies, and supporting better long-term outcomes for patients and families.

National screening programmes are gaining momentum across Europe, with Italy becoming the first country to introduce a national T1D screening law, and studies underway in Sweden, Germany, Denmark, Portugal, and the UK.

At Revvity, we're bringing our decades of expertise in population screening to T1D, offering scalable, reliable autoantibody detection solutions for clinical laboratories and screening programmes.

Early Type 1 Diabetes detection solutions

References

  1. Ruiz-Grao, M. C., et al. (2024). Trends in the incidence of type 1 diabetes in European children and adolescents from 1994 to 2022: A systematic review and meta-analysis. PediatricDiabetes. https://doi.org/10.1155/2024/2338922
  2. Sims EK, et al. Screening for Type 1 Diabetes in the General Population: A Status Report and Perspective. Diabetes 2022;71:610–23.
  3. Simmons KM, Sims EK. Screening and prevention of type 1 diabetes: Where are we? J Clin Endocrinol Metab 2023;108:3067–79.
  4. Alonso GT, et al. Diabetic ketoacidosis at diagnosis of type 1 diabetes in Colorado children, 2010–2017. Diabetes Care 2020;43:117–21.
  5. T1D Exchange. (2023). FDA Approval of Teplizumab for Type 1 Diabetes. https://t1dexchange.org/articles/fda-approval-teplizumab-type-1-diabetes

GSP T1D 3plex kit is a CE marked in vitro diagnostic medical device, compliant with IVD Regulation (EU) 2017/746, certified by Notified Body number 0537.

Products may not be licensed in accordance with the laws in all countries, such as the United States. Please check with your local representative for availability.

Revvity Inc. does not endorse or make recommendations with respect to research, medication, or treatments. All information presented is for informational purposes only and is not intended as medical advice. For country specific recommendations, please consult your local health care professionals.  

Revvity Omics service has not been cleared or approved by the U.S. Food and Drug Administration. Testing services may not be licensed in accordance with the laws in all countries. The availability of specific test offerings is dependent upon laboratory location. The content of this presentation is provided for informational purposes only, not as medical advice. It is not intended to substitute the consultation, diagnosis, and/or treatment provided by a qualified licensed physician or other medical professional.

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