Comparison of five different risk scores to predict incident type 2 diabetes in the Swiss HIV cohort study

Author:

Blondet Fanny1,Kraege Vanessa12,Cavassini Matthias3,Damas Fernandez José3,Vollenweider Peter1,Wandeler Gilles4,Hoffman Matthias5,Calmy Alexandra6,Stoeckle Marcel7,Bernasconi Enos8,Hasse Barbara9,Marques-Vidal Pedro1,Méan Marie1

Affiliation:

1. Department of Medicine, Internal medicine, Lausanne University hospital, University of Lausanne

2. Medical Directorate, Lausanne University Hospital

3. Division of Infectious Diseases, Lausanne University hospital, University of Lausanne, Lausanne

4. Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern

5. Division of Infectious Diseases, Cantonal Hospital St. Gallen, St. Gallen

6. Division of Infectious Diseases, Geneva University Hospital, University of Geneva, Geneva

7. Division of Infectious Diseases and Hospital Epidemiology, Basel University Hospital, University of Basel, Basel

8. Division of Infectious diseases, Ente Ospedaliero Cantonale, Lugano, University of Geneva, and University of Southern Switzerland, Lugano

9. Division of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.

Abstract

Objective: People with HIV (PWH) have a higher risk of type 2 diabetes (T2D) than HIV-negative individuals. In the general population, diabetes risk scores are used to identify persons at risk of developing T2D, but little is known regarding their performance in PWH. Design: Assessment of the capacity of five diabetes risk scores to predict T2D in PWH. Methods: A prospective study including all Swiss HIV cohort study (SHCS) participants followed between 2009 and 2019. Five diabetes risk scores were assessed: FINDRISC versions 1 and 2, Balkau, Swiss Diabetes Association (SDA), and Kraege. Results: Three thousand eight hundred fifty-three T2D-free PWH (78.5% men, 39.9 ± 11.3 years) were included. After a median follow-up of 4.8 years (interquartile range 2.2–7.8), 62 participants (1.6%) developed T2D, corresponding to an incidence rate of 3.18 per 1000 person-years (95% confidence interval = 2.47–4.08). Participants who developed T2D were older (48.7 ± 12.4 vs. 39.8 ± 11.2 years), more likely to be obese (22.6% vs. 7.4%), abdominally obese (9.7% vs. 1.5%), and to have a family history of diabetes (32.3% vs. 19.1%) than those without T2D. The AUC for incident T2D ranged between 0.72 (Kraege 16) and 0.81 (SDA, FINDRISC2 and Balkau). Sensitivity ranged between 3.2% (Balkau) and 67.7% (FINDRISC1) and specificity between 80.9% (FINDRISC1) and 98.3% (Balkau). Positive predictive values of all scores were below 20%, while negative predictive values were above 98%. Conclusion: Our study shows that the performance of conventional diabetes risk scores in PWH is promising, especially for Balkau and FINDRISC2, which showed good discriminatory power. These scores may help identify patients at a low risk of T2D in whom careful assessment of modifiable T2D risk factors can be spared.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Infectious Diseases,Immunology,Immunology and Allergy

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