Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Year in Review
  • Published:

PERSONALIZED MEDICINE FOR T2DM IN 2019

Harnessing heterogeneity in type 2 diabetes mellitus

Personalized, or precision, medicine in type 2 diabetes mellitus is becoming a reality with new insights into the contributions of subgroup analyses. The roadmap to future implementation must take into account individual and subgroup variability in genetic architecture, environment, clinical measures, lifestyle, cost-effectiveness and treatment burden.

Key advances

  • Subgroup analyses have divided patients with type 2 diabetes mellitus (T2DM) into at least five clusters that differ with regard to genetics, insulin secretion, disease progression and disease complications4,7.

  • Specific phenotypic measures of readily measured continuous clinical features can help predict specific outcomes such as fatty liver disease or neuropathy4.

  • Autoimmunity screening might be beneficial in all patients with T2DM7.

  • Deep longitudinal omics profiling can lead to prediction models of insulin resistance with increased acceptance of diet and exercise changes in research participants8.

  • Individuals with biomarkers of insulin resistance can benefit from targeted treatments with PPAR γ agonists as opposed to sulfonylureas to address cardiovascular protection9.

  • Models based on multi-criteria decision analyses that include disease outcomes, patient preferences and medication characteristics can improve personalized treatments10.

This is a preview of subscription content, access via your institution

Relevant articles

Open Access articles citing this article.

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

References

  1. Gale, E. A. Is type 2 diabetes a category error? Lancet 381, 1956–1957 (2013).

    Article  Google Scholar 

  2. Udler, M. S. et al. Genetic risk scores for diabetes diagnosis and precision medicine. Endocr. Rev. 40, 1500–1520 (2019).

    Article  Google Scholar 

  3. Del Prato, S. Heterogeneity of diabetes: heralding the era of precision medicine. Lancet Diabetes Endocrinol. 7, 659–661 (2019).

    Article  Google Scholar 

  4. Dennis, J. M. et al. Disease progression and treatment response in data-driven subgroups of type 2 diabetes compared with models based on simple clinical features: an analysis using clinical trial data. Lancet Diabetes Endocrinol. 7, 442–451 (2019).

    Article  Google Scholar 

  5. Ahlqvist, E. et al. Novel subgroups of adult-onset diabetes and their association with outcomes: a data-driven cluster analysis of six variables. Lancet Diabetes Endocrinol. 6, 361–369 (2018).

    Article  Google Scholar 

  6. Udler, M. S. et al. Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: a soft clustering analysis. PLOS Med. 15, e1002654 (2018).

    Article  Google Scholar 

  7. Zaharia, O. P. et al. Risk of diabetes-associated diseases in subgroups of patients with recent-onset diabetes: a 5-year follow-up study. Lancet Diabetes Endocrinol. 7, 684–694 (2019).

    Article  Google Scholar 

  8. Schüssler-Fiorenza Rose, S. M. et al. A longitudinal big data approach for precision health. Nat. Med. 25, 792–804 (2019).

    Article  Google Scholar 

  9. Vaccaro, O. et al. Cardiovascular effects of pioglitazone or sulfonylureas according to pretreatment risk: moving toward personalized care. J. Clin. Endocrinol. Metab. 104, 3296–3302 (2019).

    Article  Google Scholar 

  10. Choi, S. E. et al. Personalizing second-line type 2 diabetes treatment selection: combining network meta-analysis, individualized risk, and patient preferences for unified decision support. Med. Decis. Making 39, 239–252 (2019).

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Louis H. Philipson.

Ethics declarations

Competing interests

The author declares no competing interests.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Philipson, L.H. Harnessing heterogeneity in type 2 diabetes mellitus. Nat Rev Endocrinol 16, 79–80 (2020). https://doi.org/10.1038/s41574-019-0308-1

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41574-019-0308-1

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing