Team-based diabetes care may improve blood sugar, blood pressure, and albuminuria
Key takeaway:
In 355 people with type 2 diabetes and early diabetic kidney disease, a multidisciplinary care program was linked with improved HbA1c, blood pressure, lipids, and albuminuria.
Study at a glance
What was studied
An integrated multidisciplinary care and education program for type 2 diabetes with early DKD.
Study type
non-randomized clinical trial (non-RCT or NRCT)
duration
Medium-Term (3–12 mo)
Intervention
Integrated multidisciplinary diabetes and kidney care program
Outcomes
HbA1c, Systolic blood pressure, Diastolic blood pressure, Total cholesterol, LDL cholesterol, HDL cholesterol, Albuminuria, Estimated glomerular filtration rate
Funding
Non-industry sponsored
Main effects
↓ HbA1c decreased from 7.51% to 7.10%
↓ Systolic and diastolic blood pressure decreased from baseline
↓ Total cholesterol, LDL cholesterol, and albuminuria decreased
Evidence Suggest
- A coordinated multidisciplinary care program may support better glycemic and cardiometabolic risk marker control in early DKD
- Albuminuria improved, but eGFR declined modestly during follow-up and needs cautious interpretation
- Medication changes occurred during the program, so non-drug education effects cannot be separated from treatment intensification
Who this applies to
Adults with type 2 diabetes and early-stage diabetic kidney disease
Keep in Mind
The study shows before-and-after changes, not definitive cause-and-effect evidence
Between the Lines
- Retrospective design with no concurrent comparison group
- Single-hospital setting limits generalizability
- The packaged intervention prevents attribution to any one component
- Long-term kidney failure or cardiovascular outcomes were not evaluated
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Journal Reference
Lo WC, Huang YJ, Tasi YL, Chen JF, Mai HC, Hung YL, Chio YH, Chen CY, Ou YL, Chen SC. Analysis of the association of multidisciplinary team care and education intervention in patients with early-stage diabetic kidney disease in Taiwan. Endocr J. 2026;73(4):517-527. doi:10.1507/endocrj.ej25-0418
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