This was a retrospective cohort study of 245 patients with coexisting Type 2 Diabetes Mellitus and hypertension. Patients were assigned to either combination therapy (valsartan 80 mg/day + dapagliflozin 10 mg/day; n=102) or monotherapy (valsartan 80 mg/day; n=102) with a 24-week follow-up.
The combination group showed a greater reduction in systolic blood pressure (134.86 ± 6.37 mmHg vs. 139.68 ± 6.82 mmHg; P < 0.001) and diastolic blood pressure (83.12 ± 4.58 mmHg vs. 86.29 ± 4.79 mmHg; P < 0.001). Fasting plasma glucose was lower in the combination group (6.79 ± 1.02 mmol/L vs. 7.58 ± 1.10 mmol/L; P < 0.001), as was the 2-hour postprandial glucose (9.71 ± 1.68 mmol/L vs. 11.24 ± 1.84 mmol/L; P < 0.001). Glycemic variability indices also improved more with combination therapy (P < 0.001).
Inflammatory and cardiac biomarkers showed a more marked decline in the combination group (P < 0.05). Left ventricular ejection fraction improved significantly (60.12 ± 4.68% vs. 56.75 ± 4.96%; P < 0.05), and NT-proBNP, renal function, and fibrosis markers also improved more in the combination group (all P < 0.05). Multivariate analysis indicated combination therapy independently predicted better outcomes (OR = 2.417, 95% CI: 1.315–4.443, P = 0.004).
Safety and tolerability were not reported. The study was observational, limiting causal inference, and key details like primary outcome and practice relevance were not reported. These findings suggest potential benefits of combination therapy but require confirmation in randomized trials.
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BackgroundHypertension and Type 2 Diabetes Mellitus (T2DM) interact to increase cardiorenal risk. This study evaluated the cardiorenal efficacy of dapagliflozin combined with valsartan in patients with coexisting T2DM and hypertension.MethodsThis retrospective cohort study included 245 patients admitted between January 2023 and December 2024. Propensity score matching yielded 102 patients in the Monotherapy Group (valsartan 80 mg/day) and 102 in the Combination Group (valsartan 80 mg/day + dapagliflozin 10 mg/day). Outcomes assessed at baseline and 24 weeks included blood pressure, glycemic parameters (FPG, 2hPG, GluCV, PGE, LAGE, MAGE), inflammatory and cardiac biomarkers (hs-CRP, TNF-α, IL-6, IL-33, sST2, sICAM-1), echocardiographic measures (LVEF, LVEDD, LVESD, LAD, IVSd), NT-proBNP, renal function (eGFR, UACR, SCr, BUN), and fibrosis markers (PIIINP, C-IV, LN, TGF-β1).ResultsAt 24 weeks, the Combination Group showed greater reductions in systolic (134.86 ± 6.37 vs. 139.68 ± 6.82 mmHg) and diastolic blood pressure (83.12 ± 4.58 vs. 86.29 ± 4.79 mmHg), FPG (6.79 ± 1.02 vs. 7.58 ± 1.10 mmol/L), 2hPG (9.71 ± 1.68 vs. 11.24 ± 1.84 mmol/L), and glycemic variability indices (all P < 0.001). Inflammatory and cardiac biomarkers declined more markedly (P < 0.05). Significant improvements were also observed in LVEF (60.12 ± 4.68% vs. 56.75 ± 4.96%), NT-proBNP, eGFR, UACR, and fibrosis markers (all P < 0.05). Multivariate analysis showed combination therapy independently predicted better outcomes (OR = 2.417, 95% CI: 1.315–4.443, P = 0.004).ConclusionThe addition of dapagliflozin to valsartan was associated with superior cardiorenal outcomes compared to valsartan monotherapy in patients with T2DM and hypertension, as evidenced by enhanced improvements in blood pressure, glycemic control, inflammation, cardiac function, and renal parameters.