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May 14, 2026Diabetes Care2 citations

Precision Medicine to Redefine Insulin Secretion and Monogenic Diabetes (PRISM): A Randomized Controlled Trial in Chinese Patients With Young-Onset Diabetes

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ALAndrea O.Y. LukCOChun Kwan OBFBaoqi Fan

Key Points

  • The study aimed to assess the effectiveness of precision medicine in managing young-onset type 2 diabetes.
  • Randomized controlled trial conducted over 3 years in Chinese individuals aged 18-50 years.
  • Participants assigned to either intervention (JADE-PRISM) or usual care (JADE only).
  • Intervention included assessment of biogenetic markers and algorithm-based treatment.
  • Primary end point developed in 116 participants (26.3%) in the JADE-PRISM group versus 125 (28.2%) in the JADE-only group (odds ratio 0.908, 95% CI 0.675–1.221).
  • 104 participants (23.8%) in the JADE-PRISM group reached three or more treatment targets compared to 54 (12.2%) in the JADE-only group (P < 0.001).
  • Improved proxies of β-cell function and reduced emotional distress observed in the JADE-PRISM group.

Abstract

OBJECTIVE Young-onset type 2 diabetes (YOD) results from complex causes, calling for precision management. RESEARCH DESIGN AND METHODS The Precision Medicine to Redefine Insulin Secretion and Monogenic Diabetes (PRISM) study was a single-center, two-arm, 3-year randomized controlled trial in which Chinese individuals aged 18 to 50 years with non–type 1 diabetes diagnosed at age ≤40 years were randomly assigned to intervention (Joint Asia Diabetes Evaluation JADE–PRISM) or usual clinic-based care (JADE only). The intervention included technologically guided assessment and use of biogenetic markers (autoantibodies, C-peptide, and common and rare genetic variants) to classify diabetes for 1-year intensified, algorithm-based treatment followed by two annual reviews by an endocrinologist-led multidisciplinary team. The primary end point was a composite of incident or progression of all diabetes-related complications. Secondary end points included attainment of three or more treatment targets (HbA1c 6·2%, blood pressure 120/75 mmHg, LDL cholesterol 1.2 mmol/L, triglycerides 1.2 mmol/L, and waist circumference 80 women or 85 cm men), proxies of β-cell function, and patient-reported outcome measures (PROMs). RESULTS During 2020 to 2021, 884 participants (mean SD age 40.7 6.5 years; mean SD age at diagnosis 32.5 6.8 years; autoantibody positivity n = 46; monogenic diabetes n = 23; C-peptide 200 pmol/L n = 82; central obesity n = 699; dyslipidemia n = 669; hypertension n = 588; albuminuria n = 313; insulin treated n = 250) were randomly assigned to the JADE-PRISM (n = 441) or JADE-only group (n = 443). During the 3-year study, the primary end point developed in 116 participants (26.3%) in the JADE-PRISM group versus 125 (28.2%) in the JADE-only group (odds ratio 0.908 95% CI 0.675–1.221). In the JADE-PRISM group, 104 participants (23.8%) versus 54 in the JADE-only group (12.2%; P 0.001) reached three or more treatment targets, with improved proxies of β-cell function and reduced emotional distress. CONCLUSIONS A 3-year technology-enhanced, multicomponent program improved cardiometabolic status, proxies of β-cell function, and PROMs in individuals with YOD but did not reduce complications.

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Cite This Study

Luk et al. (2026) studied this question.

synapsesocial.com/papers/6a056838a550a87e60a209aahttps://doi.org/10.2337/dc26-0114
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