Effect of intensive blood pressure control on cognitive outcomes and brain structures in adults with type 2 diabetes: prespecified analysis of secondary outcomes of BPROAD randomised controlled trial.

BMJNov 12, 2026 (epub)

Weiqing Wang, Yu Xu, Fengmei Xu et al.

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In 30 seconds

This prespecified secondary-outcome analysis of the multicentre, open-label, outcome assessor-masked BPROAD randomised trial examined intensive versus standard systolic blood pressure treatment in adults aged 50 years or older with type 2 diabetes, raised blood pressure and increased cardiovascular risk. Among 12,434 participants without probable dementia at baseline, intensive treatment targeting SBP <120 mm Hg did not significantly reduce dementia or mild cognitive impairment over a median 3.8 years (hazard ratio 0.96, 95% CI 0.86 to 1.06; P=0.38). In the MRI substudy, it was associated with less increase in white matter lesion volume.

Key findings

  • Dementia or mild cognitive impairment occurred at 3.69 versus 3.89 events per 100 person years with intensive and standard treatment, respectively.
  • The primary cognitive outcome did not differ significantly between groups (hazard ratio 0.96, 95% CI 0.86 to 1.06; P=0.38).
  • Intensive treatment was associated with a smaller increase in white matter lesion volume (between-group difference -0.09 inverse hyperbolic sine (asinh) transformed cm 3, 95% CI -0.15 to -0.02; P=0.01).

Why it matters

In this population, more intensive blood pressure lowering did not demonstrate a reduction in the combined incidence of dementia or mild cognitive impairment over the observed follow-up. The MRI finding suggests a difference in white matter lesion progression, but this structural outcome should be distinguished from demonstrated cognitive benefit when interpreting the results.

What to keep in mind

The cognitive follow-up was a median of 3.8 years, and MRI outcomes were assessed in a subset of participants; the trial was open label, although outcome assessors were masked.

Source

Published in BMJ. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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