Key result
Higher SBP is linked more strongly to urinary albumin excretion in prediabetes than normal glucose metabolism.
Why the study?
Does glucose metabolism status modify the association of blood pressure with retinal arteriolar narrowing and urinary albumin excretion?
Cross-Sectional (n=6,594)
Does glucose metabolism status modify the association of blood pressure with retinal arteriolar narrowing and urinary albumin excretion?
Answers are grounded in this paper and cite their sources.
Prediabetes and diabetes exacerbate the adverse effects of higher blood pressure on retinal and glomerular microvasculature, highlighting the need for early dual risk factor control.
OBJECTIVE: Hypertension and diabetes frequently coexist and may interact to induce organ damage. Herein, we evaluated whether persons with prediabetes already have impaired retinal and glomerular autoregulatory responses to higher blood pressure. METHODS: We used cross-sectional, population-based data of 6594 participants [4206 with normal glucose metabolism (NGM), 1023 with prediabetes, and 1365 with type 2 diabetes (oversampled); mean age 59.8 ± 8.6 years; 50.2% men] of the Maastricht Study. Using multiple linear regression models, we tested if glucose metabolism status modified the associations of 24 h systolic and diastolic blood pressure (SBP/DBP) with retinal arteriolar and venular diameters (CRAE/CRVE) and urinary albumin excretion (uAE). RESULTS: The total modification for CRAE was significant for diabetes but not for prediabetes. The association of SBP with CRAE was attenuated by prediabetes ( Pinteraction = 0.098) and diabetes ( Pinteraction < 0.001) in females (but not males), with a beta of -0.21 SD per 10 mmHg (95% CI: -0.25; -0.16), -0.14 (-0.24; -0.05) and -0.04 (-0.14; 0.07) for NGM, prediabetes, and diabetes, respectively. The association of SBP with uAE was stronger in prediabetes ( Pinteraction = 0.002) and diabetes ( Pinteraction < 0.001) than in NGM, for the whole study population (no sex difference). The corresponding beta was 0.13 (0.11; 0.16), 0.20 (0.15; 0.26), and 0.24 (0.18; 0.29) for NGM, prediabetes and diabetes, respectively. No substantial changes were observed when replacing SBP by DBP. CONCLUSIONS: Our findings suggest that retinal and glomerular autoregulatory responses to higher blood pressure are impaired in persons with prediabetes and with diabetes. This emphasizes the importance of both blood pressure and glycemic control already in those with prediabetes.
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Wang et al. (2025) conducted a cross-sectional in Prediabetes and Type 2 Diabetes (n=6,594). Higher systolic and diastolic blood pressure vs. Normal glucose metabolism was evaluated on Urinary albumin excretion (uAE) associated with systolic blood pressure (beta 0.20, 95% CI 0.15-0.26, p=0.002 for interaction). The association of higher systolic blood pressure with urinary albumin excretion was stronger in prediabetes (beta 0.20; 95% CI 0.15-0.26) than in normal glucose metabolism (Pinteraction=0.002).
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